Engineering

AbbVie

Software Engineer - Information Security (Hybrid)

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

As a **Full Stack Software Engineer within the Information Security and Risk Management (ISRM) team**, you will contribute to the design, development, and maintenance of internal software applications and tools that support operational excellence and increased security maturity. As a member of the Application Security (AppSec) Platform Engineering team, you will build tools and capabilities to enhance AppSec processes. In addition, you will partner closely with other teams across ISRM such as program management, finance, etc. to build practical, high-quality solutions based on their specific needs. Projects will range from building application security program tooling to developing tools and capabilities that help us operate better as an organization. You will apply modern full-stack development practices and leverage artificial intelligence to accelerate development and embed intelligent features into the solutions you build.

**Responsibilities**

- Design, develop, and maintain full-stack web applications, internal tools, and API-driven solutions that support application security program management, including vulnerability discovery and tracking, data aggregation, risk reporting, and workflow automation.

- Build and support applications and tooling to enhance the efficiency of key support processes such as financial planning, project tracking, and headcount management.

- Leverage AI-assisted development tools (e.g., Claude Code, GitHub Copilot, ChatGPT Codex, or similar) to accelerate coding, testing, and documentation workflows.

- Use CI/CD pipelines (e.g., GitHub Actions, Jenkins, or similar) to build, test, and deploy solutions.

- Integrate AI/ML capabilities into applications to enable features such as intelligent alerting, anomaly detection, natural language interfaces, or automated triage to enhance the value of solutions delivered.

- Write clean, well-documented, secure, and maintainable code in modern languages such as Python and JavaScript/TypeScript across both backend and frontend layers.

- Collaborate with stakeholders to gather requirements, translate business needs into technical specifications, iterate rapidly on working solutions, and advance working prototypes into production applications.

- Participate in code reviews, contribute to team engineering standards, and support peer learning across the team.

- Manage and prioritize a personal backlog of application enhancements and bug fixes, communicating status clearly to stakeholders.

- Understand and adhere to corporate solution development standards including security and quality requirements.

Qualifications

- Bachelor's Degree and 6 years of experience OR Master's Degree and 5 years of experience OR PhD and 0 years of experience.
- Proficiency in Python (backend services, scripting, automation) and JavaScript/TypeScript (frontend and/or Node.js backend).
- Demonstrated experience building and deploying resilient and secure full-stack web applications, including frontend frameworks (e.g., React, Vue, or similar), REST APIs, and relational or NoSQL databases.

- Hands-on experience using AI-assisted development tools to improve code quality, velocity, and documentation.

- Familiarity with application security concepts and secure coding practices (e.g., OWASP Top 10).

- Familiarity with DevOps/DevSecOps practices, CI/CD pipelines, and infrastructure-as-code to facilitate code build, test, and deployment activities.

- Familiarity with deploying production applications via cloud and containerized models as appropriate.

- Ability to work independently on multiple concurrent projects with minimal supervision.

- Strong written and verbal communication skills, with the ability to engage and partner with both technical and non-technical stakeholders.

**Preferred:**

- Experience integrating AI capabilities into production applications to enable enhanced usability, data insights, and autonomous/agentic workflow automation.

- Experience building solutions using low- and no-code platforms such as MS Power Apps, OutSystems, etc.

- Experience with project/operational tooling such as Jira, ServiceNow, or similar platforms.

- Experience building or using solutions to detect, prevent, or remediate security issues.

- Experience in large corporate or enterprise environments, ideally within technology, healthcare, or a regulated industry.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Illinois

Senior Director Process Engineering

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

Position Summary

The Sr Director Process Engineering BDS CGT sets enterprise direction and senior technical governance for process engineering strategy, process platform deployment, process package design, technical assurance, manufacturing technology interfaces and project delivery for biologics drug substance and cell and gene therapy manufacturing within AbbVie Strategic Investment.

The role supports Strategic Investments through engineering leadership, technical expertise, standards development, technical governance and project execution support across multiple manufacturing sites, strategic investments and technology platforms.

The role supports engineering activities associated with new biologics drug substance and cell and gene therapy manufacturing facility investments, new production capabilities, strategic capacity creation, advanced manufacturing platforms and new technology deployments across the Strategic Investment portfolio.

The role partners with Strategic Investments, manufacturing sites, operations, quality, EHS, validation / CQV and external engineering partners to deliver technically robust and business-aligned engineering solutions.

**Strategic Investment Context**

Strategic Investment provides engineering leadership, technical governance, standards development and project execution support across AbbVie’s Strategic Investments and strategic capital portfolio.

The organization supports new biologics drug substance and cell and gene therapy manufacturing facilities, new platform deployments, strategic capacity creation, advanced biologics and CGT manufacturing capabilities and standards development for emerging technologies across Strategic Investments.

Strategic Investment roles are expected to promote common standards, transfer lessons learned across regions and sites, and enable consistent engineering delivery across strategic capital investments.

**Key Responsibilities**

**Strategic Investment Governance and Standards**

- Establish, maintain and deploy global engineering standards, technical practices and governance expectations for biologics drug substance and cell and gene therapy process engineering strategy, process platform deployment, process package design, technical assurance, manufacturing technology interfaces and project delivery.

- Drive consistent application of technical standards, design principles, lessons learned and engineering playbooks across regions, sites and capital projects.

- Define enterprise standards, engineering requirements and technical guardrails for new biologics drug substance and cell and gene therapy technologies, including requirements for consistent design, deployment, qualification, operation and scale-up across Strategic Investments.

- Ensure discipline strategies support AbbVie’s long-range Strategic Investment objectives, strategic investment programs and adoption of new technologies across future manufacturing platforms.

- Provide governance and escalation for technical decisions with material safety, quality, compliance, cost, schedule, operability or lifecycle impact.

**Strategic New Technology and Capital Investment Support**

- Provide engineering leadership for strategic capital investments, including new biologics drug substance and cell and gene therapy facility builds, technology platform deployments, new production capabilities, strategic capacity projects and lifecycle technology upgrades.

- Support front-end engineering, facility concept development, investment option evaluation, manufacturing capability assessments and site / platform planning activities for biologics drug substance and cell and gene therapy assets.

- Partner with Strategic Investments and project leadership to ensure technical assumptions, deliverables, risks and resource needs are integrated into capital program plans.

- Apply Strategic Investment lessons learned and standards to improve project quality, speed, reliability and readiness across the portfolio.

**Technical Leadership and Delivery**

- Lead or support technical decision-making for biologics drug substance and cell and gene therapy process engineering strategy, process platform deployment, process package design, technical assurance, manufacturing technology interfaces and project delivery across multiple manufacturing sites, capital projects and technology platforms.

- Ensure engineering deliverables support safety, quality, compliance, operability, maintainability, reliability, sustainability and operational readiness.

- Coordinate technical input from project teams, site SMEs, external engineering partners, vendors and cross-functional stakeholders.

- Drive timely resolution of technical issues and ensure suitable escalation when decisions have broader project, network or business impact.

**Cross-Functional Integration**

- Partner with Strategic Investments, manufacturing operations, quality, validation / CQV, EHS, site engineering, MS&T, supply chain, finance and related engineering disciplines.

- Ensure discipline decisions are integrated with biologics drug substance and cell and gene therapy manufacturing strategy, network capacity, technology platform deployment, regulatory expectations and site handover needs.

- Facilitate collaboration across Strategic Investments, sites and project teams to avoid fragmented solutions and drive consistency across the strategic capital portfolio.

- Represent Strategic Investment in technical reviews, project forums and risk discussions relevant to assigned scope.

**Capability Building and Continuous Improvement**

- Share engineering best practices, lessons learned and technical knowledge across sites, regions and projects.

- Build capability through coaching, mentoring, technical review discipline and development of reusable engineering practices.

- Promote a culture of engineering excellence, safety, quality, reliability, collaboration, accountability and proactive risk management.

- Support continuous improvement of Strategic Investment standards, templates, knowledge management and project delivery approaches.

**Strategic Investment Leadership Expectations**

- Collaborate across Strategic Investments to identify, develop and deploy best practices, technical standards, lessons learned and capability-building initiatives.

- Promote consistency, quality, reliability, sustainability and project delivery performance across regions, sites and capital projects.

- Support long-range manufacturing strategy, strategic investment planning and Strategic Investment capability development.

- Build technical capability through coaching, mentoring, standards governance, knowledge management and cross-functional collaboration.

**Stakeholder Interfaces**

**Strategic Investments:** Investment planning, portfolio alignment, technical assumptions, front-end engineering, biologics drug substance and cell and gene therapy technology deployment standards and strategic capital program support.

**Manufacturing Sites and Operations:**  Network needs, site readiness, operability, maintainability, startup, handover and operational performance support.

**Quality, Validation / CQV and EHS:** Compliance expectations, validation strategy, qualification readiness, safety, risk review and inspection readiness interfaces.

**Strategic Investment Disciplines:**  Cross-discipline technical integration, standards, design reviews, technical issue resolution and lessons learned.

**External Engineering Partners, EPCM Firms, Vendors and OEMs**: Technical oversight, deliverable review, issue escalation, supplier alignment and execution quality.

Qualifications

- Bachelor’s degree in Engineering, Science or a relevant technical discipline required; advanced degree preferred where relevant.
- Typically 15+ years of relevant engineering, manufacturing, capital project, technical operations or regulated manufacturing experience.
- Demonstrated technical capability in biologics drug substance and cell and gene therapy process engineering strategy, process platform deployment, process package design, technical assurance, manufacturing technology interfaces and project delivery.
- Experience supporting biologics drug substance, cell therapy, gene therapy, viral vector, mRNA, sterile biologics or similarly regulated biopharmaceutical manufacturing environments preferred.
- Demonstrated ability to work across global functions, manufacturing sites, project teams, suppliers, vendors and external engineering partners.
- Strong communication, risk management, technical judgment, stakeholder engagement and structured problem-solving skills.

**Technical Competencies**

- Biologics drug substance and cell and gene therapy process design and process package review
- Front-end engineering and concept development
- Biologics and CGT technology transfer, platform deployment and manufacturing scale-up
- Process safety and CQV interfaces
- Strategic Investment support
- Strategic capital investment and new biologics / CGT technology deployment support
- Engineering governance and standards
- Development of engineering standards and deployment requirements for emerging biologics drug substance and cell and gene therapy manufacturing technologies
- Technical understanding of bioreactor, harvest, purification, single-use, closed processing, aseptic processing, viral vector, cell processing and cryogenic / cold-chain interfaces as applicable to biologics and CGT platforms
- Technical risk management
- Project execution support
- Stakeholder management
- Vendor / partner technical coordination
- GMP and regulated manufacturing awareness
- Operational readiness and handover support

**Leadership Competencies**

- Strategic thinking and enterprise mindset
- Matrix leadership and influence without direct authority
- Clear technical communication and executive-ready recommendations
- Risk-based decision making and issue escalation
- Collaboration across functions, sites, regions and external partners
- Capability building, mentoring and knowledge sharing
- Lead, coach and develop a high-performing technical engineering team with clear priorities, accountability, development plans and delivery expectations aligned to Strategic Investment objectives.
- Set technical direction for the engineering team, ensuring work is prioritized against safety, quality, compliance, business value, capital delivery needs and long-range manufacturing strategy.
- Build technical bench strength by identifying capability gaps, developing succession depth, mentoring senior engineers and enabling knowledge transfer across sites, projects and technology platforms.
- Create an inclusive, disciplined technical decision-making environment where engineers challenge assumptions, manage risk transparently and escalate decisions with material safety, compliance, cost, schedule or operability impact.
- Align team performance with enterprise standards by reinforcing consistent engineering practices, structured technical reviews, lessons learned adoption and measurable delivery outcomes.
- Continuous improvement and commitment to safety, quality and compliance

**Working Relationships**

This role works globally with Strategic Investments, Strategic Investment disciplines, biologics drug substance and cell and gene therapy manufacturing sites, quality, validation / CQV, EHS, operations, MS&T, supply chain, finance, external engineering firms, technology vendors and equipment suppliers. The role is expected to operate across multiple projects, manufacturing sites and technology platforms, supporting new biologics and CGT manufacturing investments, new production capabilities and enterprise standards for emerging biologics drug substance and cell and gene therapy technologies.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Principal Engineer I, Process Development

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube](<https://www.youtube.com/user/AbbVie>).

Job Description

AbbVie's PDS&T organization is seeking a highly motivated, talented Principal Engineer I, Process Development with a proven track record and expertise in developing small molecule drug products for our site based in North Chicago, IL. This individual will serve as a technical expert by leading studies aimed at delivering robust pipeline assets and commercial products. The candidate is also expected to foster productive collaboration and demonstrate effective communication within scientific teams.

**Responsibilities**

- Lead project cross functional teams to deliver robust process for late-stage small molecule solid dosage assets and commercial products by solving complex engineering challenges
- Collaborate within functions to integrate scientific objectives into activities associated with development of new/improved products or technology.
- Function as a technical expert by anticipating, recognizing, and resolving problems. Demonstrate understanding of the issues relevant to the broad organization and business.
- Conceptualize and implement novel approaches using combinations of engineering scientific principles.
- Design and coordinate experiments to test hypothesis related to project outcomes; extract the full relevance of scientific observations while assuring experimental quality through sound experimental design and provides advice on experimental design.
- Champion new technologies and demonstrate applicability departments/business units. Implement new technical alternatives for research from literature review, industry knowledge, and extensive development experience. Proactively advise and share knowledge and expert opinions with subordinates, peers, and senior management. Mentor and train functional colleagues.
- Consistently and effectively present complex technical data to large and diverse groups. Author technical report, documentation and regulatory submission.
- Maintain and develop broad external and internal contacts to maintain technical knowledge as required to accomplish strategic needs of the business.
- Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

Qualifications

- Bachelors, Masters, or PhD in Chemical Engineering, Mechanical Engineering, Bioengineering, Pharmaceutical Sciences, or related field with 14+ (Bachelors), 12+ (Masters), or 6+ (PhD) years of related work experience with strong engineering background.
- Deep technical background in pharmaceutical development. Solid oral dosage process development experience is highly preferred. Must be very experienced in the lab as well as in the production environment.
- Demonstration of creative 'out of the box' thinking to solve complex technical problems and champion new technologies to achieve project goals.
- Interacts well with diverse groups within function and maintains strong working relationships with internal and external collaborators. Demonstrated ability to influence others across areas of scientific disciplines.

**Key Competencies**

- Delivers business results while also positioning AbbVie for long-term success.
- Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance.
- Learns fast, grasps the "essence”, and can change course quickly where indicated.
- Raises the bar and is never satisfied with the status quo.
- Creates a learning environment, open to suggestions and experimentation for improvement.
- Embraces the ideas of others, nurtures innovation and manages innovation to reality.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Transformation Project Engineering Lead - API

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

The Operations Transformation organization's mission is to accelerate future-ready Operations through purposeful transformation and drive excellence through new technology and enhanced cross-functional collaboration. The Strategic Capital Deployment team leads AbbVie Operations' long-term strategic investments and investment roadmaps, while executing large-scale capital projects through optimized delivery, technology adoption, and cross-functional collaboration.

The Transformation Project Engineering Lead will lead the project engineering sub-team on a Strategic Capital Project. They are accountable to the Project Director and will be responsible for driving the schedule, execution, risk management, and reporting for the team.

An engineering professional who, working with little or no supervision, applies advanced scientific knowledge, engineering knowledge, mathematics, and ingenuity to complete complex assignments related to a specific technical field or discipline. A Principal Engineer has full knowledge of other related disciplines beyond their own area of expertise.

Responsibilities

- Responsibilities of this engineering grade level inherently include and expand upon the responsibilities established for lower engineering grade levels.
- Responsible for compliance with applicable policies and procedures. Ensures quality and effectiveness of key results of major projects within function through sound design, early risk assessments, and implementation of fallback strategies. Has full awareness of the potential consequences (defects and failure modes) of design changes to established processes. Mitigates risk within functions through sound design, early risk assessments and implementation of fallback strategies.
- Identifies, plans, and conducts medium- to large-size projects within engineering specialty requiring custom, risk-managed execution plans, investigations, and/or equipment. Manages multiple, often concurrent, projects and meets deadlines.
- Maintains project controls and reporting for cost, scope and schedule; develops execution strategy including procurement; balances multiple demands within an Understands the business needs of the company, and has a thorough knowledge of the customer and clinical needs when developing a project scope. Incorporates business foresight of emerging technological trends.
- Works with marketing, product development, and manufacturing to establish scope, priorities, and schedules on multiple projects. - Independently performs economic analysis and feasibility studies related to complex and often multiple competing project alternatives. Responsible for achieving the project's financial targets in support of business objectives.
- Analyzes business forces (customers, suppliers, competitors, technologies, government regulations) in major markets to identify trends and recommend responses. Independently executes, and/or directs others in the execution of: the design of products/processes/equipment/systems/facilities by applying novel engineering theories, concepts, and techniques within the disciplines. experiments, often with multiple variables, gathers data, and performs detailed analysis. A
- Designs and leads complex experiments, often with multiple variables, gathers data, and performs detailed analysis. Assesses relevance. Conceptualizes complete solutions. Creates or coordinates the design solutions for novel or complex problems; integrates regulatory and operational needs; assesses cost benefit. Explores multiple alternatives. Structures studies and integrate cross-disciplinary and cross-functional issues to arrive at optimal cause of action.
- Applies technology in innovative ways. Combines technologies to anticipate or address customer needs; shares solutions across sites; employs proven solutions to increase effectiveness of engineering methodology or manufacturing process. Mentors others by sharing technical expertise and providing feedback and guidance.
- Where appropriate, provides tasks/project assignment opportunities for employee development and evaluates performance. Represents the organization as the prime technical contact on contracts and projects.
- Interacts with both senior management and external personnel on significant technical matters often requiring coordination between organizations. Submits articles for internal or external publication. Acts as a trusted advisor. Balances bottom line objectives of a project with long-term interest of customer. Is identified as a Subject Matter Expert in the discipline. Participates in internal teams to develop and align procedures and standards. May influence validation strategy.

Qualifications

- A Bachelors Degree in Engineering, science, or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 8+ years of significant engineering and/or operational experience. A post-graduate education/degree is desired, and may contribute towards the desired years of experience.Has demonstrated competency within a discipline.
- Has a career history marked by a consistent series of technical contributions and accomplishments. Significant contribution to product or process development or improvement through creative application of technical effort will equally be recognized.
- Possesses a strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors. Exercises judgment and advises management as to the appropriate actions.
- Interacts well with diverse groups within engineering and maintains strong working relationships with internal and external collaborators.
- Listens to and understands others' points of view and articulates tactfully and respectfully one's own perspective orally, in writing, and in presentations.
- Works well with other engineers in a collaborative, fast-paced goal-driven environment.
- Possesses interpersonal skills to negotiate and reconcile differences.
- Has a technical background in health care, medical devices, pharmaceutical, biologics, or similar industries (preferred).
- Has demonstrated competency with financial systems and in fiscal control.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Principal Electrical Engineer, Connected Systems & Combination Product Development, R&D

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

We are seeking an experienced Sr. Electrical Engineer to support the development of innovative drug-device combination products and connected medical technologies within our Combination Product Development team in R&D. In this role, you will lead and support electrical engineering activities for advanced drug delivery and medical device systems, with particular emphasis on connected and intelligent devices leveraging IoT, AI-enabled engineering approaches, Bluetooth, Wi-Fi, NFC, NB-IoT, and related wireless technologies.

This position will contribute to the development of new device and platform technologies, ensuring strong technical execution and compliance with applicable quality and regulatory requirements. The individual will work closely with cross-functional engineering and development teams, as well as external partners, throughout the product development lifecycle.

Responsibilities

Design and Development

- Lead and support electrical and electronic design activities for drug delivery systems, connected devices, and other electromechanical medical products.
- Execute feasibility and early-stage development activities, including user needs translation, requirements development, concept evaluation, technology assessment, and system architecture definition.
- Evaluate electrical system architectures, including sensing, power, embedded electronics, communications, and subsystem integration.
- Perform electronics design assessments, including circuit design, PCB review, component selection, design margin analysis, and test strategy development.
- Support development of connected device architectures incorporating Bluetooth, NFC, NB-IoT, Wi-Fi and related wireless communication technologies.
- Contribute to robust, manufacturable, scalable designs from concept through clinical development and commercial launch.

Technical Analysis and Validation

- Support system integration, reliability assessments, verification testing, and design validation activities.
- Develop and support engineering documentation, including design inputs, design outputs, protocols, risk assessments, FMEAs, and traceability documentation.
- Partner with lab and verification teams on test methods, test setups, engineering investigations, and confidence testing.
- Review schematics, PCB layouts, and interface definitions to identify technical risks and recommend solutions.
- Support troubleshooting, root cause analysis, complaint investigations, and reliability assessments for development and fielded products.
- Ensure designs address electrical safety, EMC, manufacturability, testability, and long-term reliability.

Connected Systems and Digital Capability

- Drive evaluation and application of connected medical device technologies that improve usability, adherence, data access, and system intelligence.
- Contribute to development of devices that interface with digital health ecosystems, mobile applications, cloud-connected environments, and remote monitoring platforms.
- Apply appropriate IoT architectures, connectivity strategies, and cybersecurity-aware design principles for regulated medical products.
- Provide technical depth in wireless and short-range communication technologies, especially Bluetooth, NFC, Wi-Fi and NB-IoT.
- Evaluate and leverage AI-assisted engineering tools and intelligent development methods to improve design, analysis, prototyping, and testing workflows.

Cross-Functional Collaboration

- Collaborate with clinical, regulatory, quality, operations, software, systems, and mechanical engineering teams, as well as external development partners.
- Work across engineering disciplines to drive technical alignment and execution of integrated product solutions.
- Partner with stakeholders to ensure development deliverables, documentation, and timelines meet quality and regulatory expectations.
- Support technical reviews with suppliers, contract manufacturers, and external partners.

Continuous Improvement

- Maintain awareness of emerging technologies relevant to combination products, connected devices, and digital health.
- Monitor industry trends in IoT, AI-enabled engineering, wireless medical systems, and connected care technologies.
- Contribute to continuous improvement initiatives focused on engineering quality, process efficiency, and innovation.
- Apply appropriate project management and stage-gate development practices to support successful execution.

Qualifications

- BS in Electrical Engineering or equivalent discipline with typically 10+ years of relevant industry experience; or MS in Electrical Engineering or equivalent discipline with typically 8+ years of relevant experience.
- Demonstrated experience in medical devices, drug-device combination products, or other regulated electromechanical systems.
- Strong experience designing and developing electrical systems from concept through verification, validation, and product launch.
- Experience with connected medical devices, digital health technologies, or wireless-enabled products is highly desirable.
- Experience working with external development partners, suppliers, and cross-functional product development teams is preferred.

Technical Skills

- Expertise in analog, digital, and mixed-signal electrical system design.
- Strong understanding of embedded systems, microcontrollers, communication interfaces, and subsystem integration.
- Experience with circuit design, PCB design and review, schematic capture, component selection, and design for manufacturability/testability.
- Strong knowledge of communication protocols such as SPI, I2C, UART/RS-xxx, USB, and related embedded interfaces.
- Experience with wireless and IoT technologies, especially Bluetooth, NFC, Wi-Fi and NB-IoT.
- Experience evaluating or developing connected device architectures in medical or regulated product environments.
- Understanding of IEC 60601, IEC 60601-2-24, 21 CFR 820.30, ISO 13485, ISO14971 and related medical device standards and requirements.
- Experience with design verification and validation in regulated environments.
- Proficiency with engineering tools, lab equipment, simulation tools, and analytical problem-solving methods.
- Experience using AI-assisted tools to enhance engineering productivity is desirable.

Competencies

- Strong technical leadership and engineering judgment.
- Ability to solve complex problems involving multiple design constraints and tradeoffs.
- Excellent cross-functional collaboration and communication skills.
- Strong project management capability and ability to manage multiple priorities.
- Proactive approach to identifying and resolving technical and project risks.
- Self-motivated with the ability to work independently and effectively within teams.

Key Stakeholders

- R&D engineering teams, including electrical, software, systems, and mechanical engineering
- Regulatory Affairs and Quality Assurance
- Operations, Manufacturing, and Supply Chain
- Clinical and Commercial teams
- External development partners, suppliers, and contract manufacturers
- Project and cross-functional leadership across internal and external development ecosystems in a regulated environment

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

California

Director – Process Engineering / Senior Principal Research Scientist

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

Are you a passionate engineer who thrives at the intersection of science, innovation, and impact? AbbVie's Research and Development Process Engineering team is on the front lines of transforming cutting-edge science into life-changing medicines — and we're looking for a **Senior Principal Research Scientist or Director, Process Engineering** to help us push the boundaries of what's possible in drug product development. This position is being posted at two potential levels — Principal Research Scientist I and Associate Director — and we welcome candidates who feel they are a strong fit for either level to apply. Join us at our North Chicago, IL hub and be part of something bigger.

This isn't just a role — it's an opportunity to shape the future of drug manufacturing. Whether you join as a Sr Principal Research Scientist or step in at the Director level, you'll bring your proven project leadership in drug product development to drive synthetic molecule candidates from concept to commercial-ready processes, making real decisions that accelerate medicines to patients who need them most. At the Associate Director level, this role also carries broader accountability for setting technical strategy and may include direct people leadership responsibilities across the Process Engineering function.

You'll be a master of drug product manufacturing platforms — direct compression, wet & dry granulation, hot melt extrusion, tableting, encapsulation, and film coating — and you'll apply your deep understanding of powder material properties to unlock new levels of manufacturability and product performance. When challenges arise, you're the person who steps up to troubleshoot complex process and material issues with creativity and rigor. And when it's time to go big, you'll translate bench-scale breakthroughs into pilot plant realities through expert scale-up execution.

At AbbVie, we celebrate bold ideas, encourage experimentation, and give talented engineers and leaders the resources and autonomy to actually innovate. If you're ready to raise the bar, lead with influence, and leave your mark on some of the world's most important medicines — at either an individual-contributor or people/technical leadership level — we want to hear from you.

**Key responsibilities include:**

- Lead drug product manufacturing process early phase development for synthetic molecule development candidates within the AbbVie pipeline.
- Collaborate with development CMC teams to ensure manufacturing processes are aligned with intended commercial manufacturing sites.
- Advance scientific expertise within the function — mentoring peers and influencing senior leadership with your expert insights; at the Associate Director level, this includes providing technical leadership and, where applicable, direct oversight/management of team members.
- Drive the development of technologies and scientific innovations that expand AbbVie's small molecule formulation capabilities.
- Partner cross-functionally to build strategies that directly power AbbVie's drug discovery and development programs; at the Associate Director level, help shape department- and function-level strategy in partnership with senior leadership.
- Champion compliance with AbbVie's safety, quality, and regulatory standards.

Qualifications

- Bachelor’s Degree in Science related field with 18 years of related work; Master’s Degree Science or PharmD with 16 years of related work; PhD in Science or related field with 10 years of related work experience.
- Proven ability to innovate with a history of new or improved product releases.
- Interacts well with diverse groups within function and maintains strong working relationships with internal and external collaborators.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Future Opportunities, Join our Talent Community for Senior Scientist I, R&D Process Engineering

Job Description

Process Engineering, a part of AbbVie R&D’s Development Sciences organization, is responsible for designing and developing scalable processes to make drug substances and drug products, including small molecules, peptides, and antibody drug conjugates (ADCs), throughout pre-clinical and clinical development stages. Process Engineering also partners with Biologics CMC (Chemistry, Manufacturing, and Controls) Development and Aesthetics R&D functions to provide active engineering support to enable robust process scale-up and manufacturing of biologics drug substances and drug products including toxins and cosmetic active ingredients (CAIs). We contribute to the development of innovative engineering technologies and create valuable intellectual property through the composition of matter, chemical processes, and technologies resulting in cost-effective commercial manufacturing processes. We support the development of the supply chain for pipeline molecules and help prepare and defend CMC regulatory content.

Chemical/Bio Engineers within R&D Process Engineering support pipeline projects through all phases of development. Early in development, engineers focus on establishing an enabling process that can be scaled up successfully. In the later stages of development, engineers optimize the drug substance and drug product processes and lead manufacturing campaigns. Engineers also work cross-functionally to transfer the optimized process to manufacturing sites, develop control strategy, and prepare reports to support regulatory filings.

**Role Overview**

The successful engineering candidate will play a key role in the R&D Process Engineering function. The core deliverable of R&D Process Engineering is to develop robust manufacturing processes and advance innovative technologies using strong engineering fundamentals. The ideal candidate will have a passion for hands-on laboratory process development. The candidate is also expected to lead the identification and development of novel approaches and technologies to enhance process development efficiency and commercialization. The candidate must exhibit a collaborative nature in identifying process challenges on a wide range of projects and take part in a cross-functional team to deliver specific project needs.

**Key Responsibilities:**

- Develop robust manufacturing processes, supporting assets through all phases of development.
- Participate in development and characterization of new assets.
- Establish, communicate, and execute research plans.
- Develop commercial ready manufacturing processes in the laboratory and demonstrate the processes in the pilot plant.
- Address challenging problems with reactions, separations, and/or isolations using expertise in reaction kinetics, transport phenomena, and mathematical modeling.
- Author and/or review technical documents summarizing process development efforts and contribute to regulatory filings.
- Exhibit a collaborative nature in identifying process challenges on a wide range of projects and communicate findings and recommendations effectively by multi-disciplinary interactions with organic chemists, analytical chemists, process development engineers, pilot plant engineers, drug product development scientists, program managers, and regulatory affairs specialists.
- Author publications and present at scientific conferences.

Qualifications

- BS, MS, or PhD in Chemical/Bio Engineering or a related field and 10+ (BS), 8+ (MS), or 0+ (PhD) years of relevant industrial experience.
- Job level will be commensurate with academic and/or industrial work experience.
- Candidates are expected to have a strong background in chemical engineering and the proven ability to demonstrate their skills in this field.
- The candidate is expected to demonstrate the ability to solve difficult technical problems and champion new technologies to achieve project goals.
- The candidate is required to be a strong team player and possess effective oral and written communication skills.

**Preferred:**

- Working knowledge of analytical techniques such as UV/Vis, HPLC, FTIR, Raman, mass spectrometry, and microscopy.
- Experience with laboratory experimentation and process scale-up.
- Experience with mechanistic and/or process modeling or computational fluid dynamics.
- Experience with design of experiments and statistical tools.
- Familiarity with operation of chemical/biochemical process equipment and systems.
- Experience with control strategy development, risk assessments, and tech transfer.
- Experience with GxP compliance.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Project Engineer - API Pilot Plant

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

AbbVie’s API Pilot Plant in North Chicago, IL is seeking a project engineer to provide capital project management and technical support to the pilot plant and laboratories within AbbVie’s Synthetic Molecule CMC organization. The API Pilot Plant supports the pharmaceutical pipeline through process development and manufacturing of Active Pharmaceutical Ingredients (APIs) for pre-clinical toxicology studies, clinical trials, formulation development, and registration runs.

This function will primarily lead the planning and execution of small to medium sized capital projects related to process equipment, facilities, and utilities for the API Pilot Plant. In addition, this role will support AbbVie’s R&D pipeline by providing day-to-day technical support of the plant and collaborating with process engineers, chemists, and operations technicians on the introduction of new processes and plant improvements.

**Core Job Responsibilities**

- Plans and conducts small to medium sized capital projects within an engineering specialty and through all aspects of the project life cycle including scope development, cost estimating, execution planning, preparation of requests for capital expenditure, design, procurement, construction, cost/schedule control, commissioning, qualification, operator training, startup, and financial closeout.
- Responsible for the successful completion of projects within the stated parameters of scope, cost, and schedule with the assurance that all functional, regulatory, end-user, and good engineering practice requirements are met.
- Monitors project progress to plan and implement corrective actions or contingencies as needed to maintain commitments. Provides management with regular project status updates and variances to plan.
- Leads the design of process equipment, facilities, and utilities by applying standard engineering theories, concepts, and techniques. Leads the procurement and installation of process equipment through development of equipment specifications and participation in FATs and SATs.
- Supports the commissioning and qualification of equipment, facilities and utilities including development of user/system/functional requirement specifications and execution of installation and operational qualification protocols.
- Provides technical support for the pilot plant including troubleshooting of equipment problems, performing root cause analysis, and identifying corrective actions.
- Support AbbVie’s quality policies through engineering support of investigations and implementation of corrective actions.
- Assist AbbVie in achieving environmental, health, safety, and energy (EHS&E) goals by working safely, participating in Process Hazard Analysis and Pre-Startup Safety Reviews (PSSRs), complying with process safety management of change procedures, and observing all corporate and department safety policies.

Qualifications

- Bachelor’s degree in chemical or mechanical engineering or equivalent with a desired 2+ years of relevant engineering and/or operational experience. Additional post-graduate education may contribute towards the desired years of experience.
- Possesses a working technical knowledge and application of concepts, practices, and procedures. Ability to work on problems of moderate scope where analysis of situations or data requires a review of identifiable factors. Demonstrates judgment within defined procedures and practices to determine appropriate action.
- Working knowledge in the areas of process equipment and system design, P&ID development, process equipment sizing and selection, preparation of equipment specifications, instrumentation, and control systems.
- Strong teamwork skills and the ability to establish and maintain constructive relationships with personnel from various disciplines at all levels in the organization.
- Strong verbal and written communication skills.
- Technical background in health care, medical devices, pharmaceuticals, biologics, or similar industries (preferred).

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this roleat the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on manyfactors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount isearned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that areallocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolutediscretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Principal Research Scientist I - Process Engineering

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

Are you a passionate engineer who thrives at the intersection of science, innovation, and impact? AbbVie's **Research and Development Process Engineering** team is on the front lines of transforming cutting-edge science into life-changing medicines — and we're looking for a **Principal Research Engineer I**/II to help us push the boundaries of what's possible in drug product development. Join us at our North Chicago, IL hub and be part of something bigger.

This isn't just a role — it's an opportunity to **shape the future of drug manufacturing**. You'll bring your **proven project leadership in drug product development** to drive synthetic molecule candidates from concept to commercial-ready processes, making real decisions that accelerate medicines to patients who need them most.

You'll be a master of **drug product manufacturing platforms** — direct compression, wet & dry granulation, hot melt extrusion, tableting, encapsulation, and film coating — and you'll apply your deep understanding of **powder material properties** to unlock new levels of manufacturability and product performance. When challenges arise, you're the person who steps up to **troubleshoot complex process and material issues** with creativity and rigor. And when it's time to go big, you'll translate bench-scale breakthroughs into pilot plant realities through expert **scale-up execution**.

At AbbVie, we celebrate bold ideas, encourage experimentation, and give talented engineers the resources and autonomy to *actually innovate*. If you're ready to raise the bar, lead with influence, and leave your mark on some of the world's most important medicines — we want to hear from you.

**Key responsibilities include:**

- Lead drug product manufacturing process early phase development for synthetic molecule development candidates within the AbbVie pipeline.
- Collaborate with development CMC teams to ensure manufacturing processes are aligned with intended commercial manufacturing sites.
- Advance scientific expertise within the function — mentoring peers and influencing senior leadership with your expert insights.
- Drive the development of technologies and scientific innovations that expand AbbVie's small molecule formulation capabilities.
- Partner cross-functionally to build strategies that directly power AbbVie's drug discovery and development programs.
- Champion compliance with AbbVie's safety, quality, and regulatory standards.

Qualifications

- BS (+14 yr experience) MS (+12 yr. experience) or PhD (+6 yr experience) in Chemical Engineering, or equivalent scientific/engineering degrees
- Strong project leadership experience for drug product development.
- Advanced understanding drug product manufacturing platforms with direct compression, wet & dry granulation, and hot melt extrusion which include tableting, encapsulation and film coating.
- Advanced understanding of powder material properties and their impact on drug product manufacturability and final product performance.
- Ability to apply/interpret models during drug product development to optimize development.
- Experience writing regulatory submissions and generating the data required to gain approval
- Demonstrated ability to troubleshoot process/material issues.
- Apply techniques to scale-up the development process to pilot plant equipment.
- Displays technical awareness in various aspects of drug development, adherence to rigorous scientific methods, and commitment to the scientific process.
- Strong drive for learning new techniques and technologies.
- Excellent oral and written communication skills.
- Demonstrated ability to work collaboratively in a cross-functional team setting.

Preferred:

- Drug Substance Crystallization development knowledge

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Senior Scientist I/II, Process Engineering

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

Process Engineering, a part of AbbVie R&D’s Small Molecule CMC Development organization, is responsible for designing and developing scalable processes to make small molecule drug substances and drug products, including antibody drug conjugates (ADCs), throughout pre-clinical and clinical development stages. Process Engineering also partners with Biologics CMC Development and Aesthetics R&D functions to provide active engineering support to enable robust process scale-up and manufacturing of biologics drug substances and drug products, including toxins and cosmetic active ingredients (CAIs). We contribute to the development of innovative engineering technologies and create valuable intellectual property through the composition of matter, chemical processes, and technologies resulting in cost-effective commercial manufacturing processes. We support the development of the supply chain for pipeline molecules and help prepare and defend CMC regulatory content.

Chemical/Bio Engineers support pipeline projects through all phases of development. Early in development, engineers focus on ensuring that the process can be run safely, identifying and addressing scale-up issues, enabling processes that can be scaled-up successfully. In the later stages of development, engineers optimize the drug substance and drug product processes and lead manufacturing campaigns. Engineers also work cross-functionally to transfer the optimized process to manufacturing sites, develop control strategy, and prepare reports to support regulatory filings.

**Role Overview**

The successful candidate will play a key role in the Center of Excellence in Crystalline Drug Substance and Drug Product (CrySP), a part of Process Engineering function. The core deliverable of Process Engineering is to develop robust processes to manufacture small molecule Active Pharmaceutical Ingredients (API), Antibody Drug Conjugates (ADCs), toxins, cosmetic active ingredients (CAIs), and drug products utilizing strong engineering fundamentals. The idea candidate will have background in crystallization fundamentals and crystallization process development. Process Engineering also leads the development of isolation and purification strategies for both small and large molecule compounds. The ideal candidate will have a passion for hands-on laboratory process development and a proven track record in research and development. The candidate is also expected to lead the identification and development of novel approaches and technologies to enhance process development efficiency and commercialization. The candidate must exhibit a collaborative nature in identifying process challenges on a wide range of projects and participate in a cross-functional teams to deliver against specific project needs.

**Key Responsibilities:**

- Develop robust scale up and manufacturing processes, supporting small and/or large molecule assets through all phases of development.
- Perform laboratory experiments and process modeling to support process understanding and optimization.
- Address challenging problems with separations, and/or isolations using expertise in thermodynamics, crystallization fundamentals, transport phenomena, and mathematical modeling.
- Author and/or review technical documents summarizing process development efforts.
- Exhibit a collaborative nature in identifying process challenges on a wide range of projects and communicate findings and recommendations effectively by multi-disciplinary interactions with organic chemists, analytical chemists, process development engineers, pilot plant engineers, drug product development scientists, program managers, and regulatory affairs specialists.
- Author publications and present at scientific conferences.

Qualifications

- BS, MS, or PhD in Chemical Engineering or a related field and 10+ (BS), 8+ (MS), or 0+ (PhD) years of relevant industrial experience.
- Job level will be commensurate with academic and/or industrial work experience.
- Candidates are expected to have a strong background in chemical engineering and the proven ability to demonstrate their skills in this field.
- The candidate is expected to demonstrate the ability to learn, understand, and master new experimental techniques.
- The candidate is required to possess effective oral and written communication skills and be a strong team player.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

China AI/ML, Automation, and Capability Expansion Lead, Biotherapeutics and Genetic Medicine

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

The Biotherapeutics and Genetic Medicine (BGM) team at AbbVie is a critical discovery engine supporting our ambition to become the top biopharma company in the world. BGM China expands the team’s access to China’s rapidly advancing scientific and technology ecosystem, connecting differentiated external capabilities with global discovery priorities to accelerate the delivery of transformational large-molecule candidates to patients.

Reporting to the Director of China Strategy BGM, the China AI/ML, Automation, and Capability Expansion Lead will identify, evaluate, and help translate China-based AI/ML, automation, and emerging technical capabilities into practical value for BGM. The role will prioritize biotherapeutic discovery applications—including antibody design, protein engineering, and discovery workflow automation—while assessing relevance to genetic medicine where appropriate. Working closely with global BGM teams, this lead will support technology learning, external diligence, and collaboration models that strengthen BGM’s future capability with AI/ML and automation.

This individual will also work closely with other partner functions in the Discovery and Development organizations.

Responsibilities:

- Scout and access potential China-based partners in AI/ML and automation, including both service providers and biotech companies, and coordinate with CIE on selected opportunities.
- Work closely with global BGM stakeholders to track and assess emerging AI/ML applications in biotherapeutic discovery, including antibody design, protein engineering, enzyme evolution, and data-enabled experimental optimization.
- Work closely with global BGM stakeholders to assess discovery-stage automation solutions and customized automation systems that can improve speed, quality, and throughput in priority workflows.
- Evaluate other China-based external technology platforms, service models, and technical partners for scientific quality, operational fit, scalability, and strategic relevance to BGM.
- Facilitate learning and technology translation from China-based external partners to the global BGM team and other partner functions in R&D.
- Contribute to external diligence activities related to scientific feasibility, execution risk, and capability fit.
- Maintain close communication and alignment with global stakeholders to translate internal requirements into external evaluation criteria, and to convert external learning into internal capability building.
- Work closely with the broader AbbVie partnership ecosystem as needed, including AI S&P, BD, S&E, TLC, and other relevant functions, to ensure alignment on external scouting, evaluation, and translation priorities.

Qualifications

- Ph.D. with 5–10 years of industry experience or a master’s degree with 10–15 years of industry experience. An advanced degree is preferred.
- Background in life sciences, chemistry, computer science or a related discipline;
- With relevant industry experience in discovery technologies, or related biopharmaceutical R&D fields; direct experience in AI/ML-enabled discovery and laboratory automation is strongly preferred.
- Strong understanding of AI/ML methods, automation systems, data-enabled experimentation, or digital discovery workflows, with demonstrated ability to assess their relevance to real discovery applications.
- Experience evaluating or deploying AI/ML-driven solutions in biotherapeutic discovery, including applications in antibody design, protein engineering, enzyme evolution, or experimental optimization.
- Ability to assess technology maturity, scalability, implementation feasibility, and scientific value of external AI/ML or automation solutions and convert findings into actionable recommendations.
- Strong knowledge of China’s biotech and technology ecosystem, including AI/ML startups, automation solution providers, discovery technology companies, and service partners with relevant platform capabilities.
- Fluency in English and Chinese, with excellent written and verbal communication skills and the ability to work effectively across cultures and functions.
- This role is based in Shanghai, China. Candidates must be comfortable with travel (approximately 20–30%), external meetings, and conference participation.
- Background in biochemistry, protein science, bioinformatics, computational biology, or automation-related disciplines is preferred.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Other Non-US

Senior Scientist, Engineering (I/II) - Automation

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

**Organization Description**

The scientists and engineers within AbbVie's Synthetic Molecules Chemistry, Manufacturing, and Controls (SM CMC) organization within Development Sciences work in multi-functional teams to develop scalable processes and enable clinical supplies for safety testing, clinical trials, and formulation development. Scientists focus on ensuring the process can be run safely, identifying and addressing major scale-up issues, ensuring product quality, and developing a scientific understanding of key performance indicators. Later in development, scientists and engineers then work to optimize the process, develop a commercializable production strategy, and lead technology transfer activities. Throughout the development process, a focus on building process understanding, automation of experimental equipment, use of data-rich experimental tools, and modeling of experimental learnings are key. Team members create valuable intellectual property through composition of matter, processes, and technologies resulting in robust and effective manufacturing processes.

**Job Description**

The Senior Automation Engineer will play a key role in AbbVie’s laboratory automation development and deployment as we continue developing AbbVie’s Labs of the Future. Throughout the development lifecycle, lab automation, data analysis and data management play a significant role in gaining organizational efficiency and generating scientific insights. The vision of the automation team is to transform the culture and the way we do research to enhance safety, access new enabling capabilities, and gain efficiency in development of life-changing medicines with high-quality data through a deliberate and sustainable automation competency. The tools generated by this role will be instrumental in developing end-to-end automated solutions and data analytics to laboratory scientists, allowing them to reduce risk and make faster decisions that directly impact drug substance and drug product pipeline development.

We are seeking a talented Automation Scientist to develop robotics and automated solutions. In order to do so, the ideal candidate will integrate a combination of off-the-shelf and custom-built components to provide innovative platforms for AbbVie researchers to execute experiments. This role requires fluid communication in cross-functional teams to understand the essence of user needs while deploying powerful automated equipment to improve R&D productivity. The candidate will also facilitate collection, reporting, and analysis of performance data via online analytical tools and sensor data in an actionable form. As such, the candidate will integrate knowledge driven and first principles regression into the deliveries as well as applying data driven and AI/ML tools (Bayesian optimization, NN, NODE, DOE, etc.) in order to facilitate rapid optimization. As such, the candidate will not only build automated lab equipment but work towards fully autonomous solutions. Ideal candidates should possess a BS/MS/PhD degree in a discipline with a strong background on hardware integration, analytical tools, and data handling with experience in chemical process development.

**Responsibilities:**

- Lead delivery of custom and off-the-shelf automated laboratory systems to chemistry, engineering, and analytical team members.
- Proactively develop innovative automation and data handling solutions.
- Partner with technical staff to understand business challenges and effectively guide toward sustainable solutions.
- Partner with Development Sciences Digital Transformation team to develop and deploy scalable and maintainable performance reporting.
- Build robust, automated and autonomous end-to-end solutions for various workflows, e.g., from instrument measurement to a data warehouse.
- Apply an operational excellence mindset to help identify, devise, and recommend new opportunities to optimize current processes.
- Integrate modeling approaches with experimental tools to help scientists develop processes with increased efficiency.

Qualifications

- BS, MS, or PhD degree in Chemical Engineering, Chemistry, Robotics, Mechanical Engineering, Electrical Engineering, Systems Engineering or equivalent.
- BS, MS, or PhD in Chemical/Bio Engineering or a related field and 12+ (BS), 10+ (MS), or 4+ (PhD) years of relevant industrial experience. The final determination on the title and grade level will be based on the experience of the candidate.
- Experience coordinating technical projects through to delivery.
- Proven experience bringing new automation equipment and processes on-line, from initial startup to reaching targeted metrics such as rate, yield, deployment time, etc.
- Delivered projects into environments such as R&D labs, manufacturing, etc.
- Experience with various programming languages, such as Python, Visual Basic, C, C#, C++, etc and experience with automation ecosystems, such as Ignition.
- Proficiency using business/project management software like MS Excel, MS Project, Jira, Smartsheet, etc.
- Proven written and verbal communication skills and ability to succinctly summarize key findings.

**Key Competencies:**

- Partners with R&D scientific & technical staff to understand business challenges and effectively guide toward sustainable solutions.
- Develop group vision and objectives in collaboration with key stakeholders to support team strategies and goals.
- Act as a strong team player in a cross functional collaborative environment thriving for world class excellence.
- Learns fast, grasps the "essence" and can change course quickly where indicated.
- Raises the bar and is never satisfied with the status quo.
- Creates a learning environment, open to suggestions and experimentation for improvement.
- Ability to manage people and lead projects to deliver a common set of objectives.
- Embraces the ideas of others, nurtures innovation and manages innovation to reality.
- Demonstrate excellent communication skills and specifically
  - Illustrate strong oral and written technical communications
  - Seamlessly present automation solutions to multifunctional teams
  - Educate and train colleagues on various tools and techniques

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Principal Research Scientist II, Process Chemistry

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

AbbVie Process Chemistry is responsible for the chemical development of AbbVie’s clinical candidates. We are looking for a highly motivated Principal Research Scientist II who can make scientific contributions and develop strategies, timelines and key activities across drug substance modalities, including small molecules. The candidate must be able to mentor and develop staff with experimental approaches to solve difficult scientific and technical challenges. The candidate will be an integral part of project teams and will be responsible for developing the synthetic process and executing activities required for drug substance process development. Working with cross-functional colleagues, the candidate will develop productive collaborations and communications with scientific teams.

**Responsibilities:**

- The candidate will participate and/or lead project teams associated with drug substance process development and characterization.
  - Develop and characterize drug substance processes in the laboratory and translate them to scalable processes.
  - Proactively advise and share knowledge and expert opinions with subordinates, peers, and senior management. Mentor staff in troubleshooting strategic and experimental issues.
  - Author and review key regulatory documents, laboratory data, technical memos and reports.
- The position involves multi-disciplinary interactions with organic chemists, analytical chemists, engineers, drug product development, and program management.
- The candidate will identify and nurture ideas for continuous improvement activities and initiatives within the department.
- The candidate will be responsible for setting project strategies, defining project responsibilities and timelines, developing control strategies, providing leadership in a matrixed team setting and developing robust processes for cGMP manufacturing.

Qualifications

- BS (16+ years); MS (14+ years) or PhD (8+ years) in Chemistry or allied field, with 8+ years of previous work experience in a pharmaceutical laboratory setting.
- Proven scientific leadership; strong interpersonal and communication skills for facilitating collaborations and a demonstrated ability to lead cross-functional process development teams.
- Experience with GMP drug substance manufacturing and process development.
- Experience in managing and developing scientific leaders.
- The successful candidate will have a strong understanding of modern organic chemistry, mechanistic theory, process development, control strategy development, and regulatory starting material strategies.

*Key AbbVie Competencies:*

Interacts well with diverse groups within function and maintain strong working relationships with internal and external collaborators to enable higher performance.

- Learns fast, grasps the "essence" and can change course quickly where indicated.
- Raises the bar and is never satisfied with the status quo.
- Creates a learning environment, open to suggestions and experimentation for improvement.
- Embraces the ideas of others, nurtures innovation and manages innovation to reality.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Senior Electrical Engineer, Combination Product Development

Company Description

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](<http://www.abbvie.com/>). Follow @abbvie on [LinkedIn,](<https://www.linkedin.com/company/abbvie/>) [Facebook](<https://www.facebook.com/AbbVieGlobal/>), [Instagram](<https://www.instagram.com/abbvie/>), [X](<https://twitter.com/abbvie>) and [YouTube.](<https://www.youtube.com/user/AbbVie>)

Job Description

**Sr. Electrical Engineer, Combination Product Development, R&D**

We are seeking an experienced Sr. Electrical Engineer to support the development of innovative drug-device combination products within our Combination Product Development team in R&D. In this role, you will lead electrical system design efforts for clinical development of advanced drug delivery systems, including on-body injectors, subcutaneous ambulatory infusion pumps, and other electromechanical systems.

This role will contribute to the development of new device and platform technologies, maintaining technical rigor and ensuring compliance with regulatory standards. This role will work closely with engineering colleagues in R&D and cross-functional colleagues in a global organization as well as maintaining strong working relationships with external development partners throughout the product development process.

**Responsibilities**

**Design and Development Leadership:**

- Work closely with external development partners through design and development efforts associated with electronic components of drug delivery systems
- Execute feasibility and initial development activities including needs definition, requirements, assessment of design fundamentals, and technology landscaping
- Conduct system architecture evaluation, including assessment of system design, testing, and analysis of electrical components
- Perform electronics design assessments including circuit design, PCB assessment, circuit analysis, evaluation of design margins, and testing requirements definition

**Technical Analysis and Validation:**

- Support system integration activities, reliability assessments, verification testing, and design validation to ensure products are technically robust and meet reliably goals
- Provide engineering analysis and design history file documentation to support development activities, including Design Inputs, Design Outputs, Protocols, Task Analysis, and risk assessments
- Support the lab and design verification teams with test plans, test setups, methods, investigations, and engineering confidence tests

**Cross-Functional Collaboration:**

- Engage and collaborate with clinical, project development, regulatory, quality, and operations teams, as well as external engineering partners to ensure alignment throughout device development
- Work across engineering disciplines (mechanical, software, systems engineering) to drive consensus and support execution on technical solutions
- Partner with cross-functional stakeholders to ensure development deliverables and timelines meet regulatory standards and quality expectations

**Professional Development and Process Improvement:**

- Establish and maintain working knowledge of technology trends and assess their relevance to combination product development
- Partner with external vendors to understand and evaluate future technology roadmaps
- Participate in and drive department continuous improvement initiatives focused on maximizing process efficiencies and enhanced collaboration
- Use appropriate project management techniques and stage/gate processes to ensure successful completion of assigned projects

Qualifications

**Education and Experience:**

- BS in Electrical Engineering or equivalent discipline, with typically 10+ years of relevant industry experience; MS in Electrical Engineering with typically 8+ years of relevant experience;
- Demonstrated experience in medical devices or combination product development
- Prior experience with subcutaneous injection devices, electromechanical devices, or digital/connected health technologies is highly desirable

**Technical Skills and Knowledge:**

- Demonstrated expertise in electrical system design for drug delivery systems
- Advanced understanding of circuit design, PCB design, and embedded systems; experience having designed and developed electrical systems from concept through product launch is a plus
- Proficiency with design tools, simulation software, and analytical modeling techniques
- Solid knowledge of applicable global regulatory requirements and industry standards (e.g., 21 CFR 820.30, ISO 13485, MDR)
- Understanding of modern, lean product development methodologies and stage/gate processes
- Experience with design verification and validation protocols in regulated environments

**Competencies and Attributes:**

- Demonstrated ability to function as a technical leader, generating original technical ideas and development strategies
- Possesses strong technical judgment and ability to work on problems of complex scope with competing factors
- Excellent ability to work collaboratively with diverse groups within engineering and maintain strong working relationships with internal and external partners
- Outstanding written and verbal communication skills with ability to clearly articulate technical challenges and solutions to stakeholders
- Demonstrated project management capability and ability to balance multiple priorities
- Proactive approach to identifying and resolving technical and project risks
- Self-motivated with ability to operate independently

**Key Stakeholders and Working Relationships**

- R&D team members (mechanical engineering, software engineering, systems engineering)
- Regulatory and Quality Assurance functions
- Operations and Supply Chain teams
- Clinical and Commercial teams
- External development partners
- Project management and cross-functional leadership

**Additional Information**

- Travel (domestic and/or international) may be required depending on project assignments (estimated 5%-10%)
- This role requires strong attention to detail and commitment to quality and regulatory compliance
- The successful candidate will demonstrate a passion for advancing innovative drug delivery technologies

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit [https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html](<https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html>)

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

[https://www.abbvie.com/join-us/reasonable-accommodations.html](<https://www.abbvie.com/join-us/reasonable-accommodations.html>)

Associate Director, Process Technology

The Process Technology Lead is accountable for leading the Process Engineering Process Technology site team. This team is responsible for executing site Process Engineering projects, and for coordinating internal and external Process Engineering resource support for all site CAPEX and OPEX projects. The Process Technology team is responsible for all Process Engineering elements required to scope, develop, procure, construct, and qualify new equipment and facilities required to meet facility production throughput demands. This role manages a small to mid-sized team which may consist of both experienced professionals and managers. S(he) works closely with the Process Technology Leads at other sites. S/He coordinates routinely with Senior Director, Project Delivery and Director, Global Plasma Technology Ownership.

This position reports into Site Head of Process Engineering

**Project Responsibilities:**

• Leads multi-disciplinary project teams through life cycle activities to deliver capacity expansion capabilities to meet global and local strategic requirements.

• Develops Process Automation Strategy for project activities. Works closely with Execution Systems team to ensure that project instrumentation, automation, and alarm strategies align with industry standards and with product Quality by Design approach.

• Responsible for providing cGMP compliant processes and facilities suitable for FDA and global regulatory approval.

• Ensures that initiatives are aligned with the business objectives and strategic philosophy. • Oversees project teams responsible for completion of project lifecycle activities through turnover to routine commercial production.

• Oversees generation of regular project reports (financial updates, project schedules, risks and summary of current activities) for senior site management and Global Steering Committees. 2 Leadership Responsibilities:

**Leadership Responsibilities:**

• Directly oversees technical staff supporting a wide range of CAPEX and OPEX project responsibilities.

• Responsible for assessing the Process Technology project workload against the available resource pool and supplementing with contract resources. Manages and directs all contract resources in support of project activities.

• Responsible for mentoring and development of staff, including motivating in a manner that promotes the achievement of CSL’s business goals and objectives.

• Responsible for assessing the skillset of Process Technology team and bridging any gaps that are needed to support site project portfolio.

• Establishes performance goals and strategic/operational objectives for team. • Coaches, counsels, and appraises performance of personnel.

• Develops staff competencies & capabilities to enable business continuity, sustained success, and career development.

• Promotes high employee engagement and a positive work environment.

• Responsible for organizational design, resource requirements and staffing decisions.

• Recruits, retains, trains, and develops the team.

• Capable of influencing site and global leadership.

• Able to manage partnerships both internally and externally.

**Position Qualifications and Experience Requirements:**

Education:

• Undergraduate degree in Engineering/Science required.

• Advanced degree in Engineering/Science or MBA preferred.

Experience Required:

• 8+ years working in Process Engineering in Pharmaceutical, Chemical Manufacturing or similar industry.

• Demonstrated experience in process improvement development & execution.

• Strong communication and conflict management skills to influence project professionals and stakeholders, including non‐specialists, at all levels in the organization.

• Demonstrated experience in managing, organizing, developing and deploying best practice frameworks, processes, tools and templates in an Operations context, in alignment with Enterprise standards.

• 5 years or more experience working within a global matrix organization

• Involvement in cross-functional, multicultural and international teams.

Other Essential Knowledge

• Ability to work across a range of countries and cultures.

**Customer Orientation (Internal/External):**

• Creates strategies to stay ahead of industry-related changes. Drives alignment across the enterprise in order to serve customer needs. Spends time internally and externally with customers and stakeholders and genuinely seeks to understand their needs.

**Enterprise Results and Value Orientation:**

• Looks for outcomes that maximize the benefits for the enterprise, not just their department or function. Pursues value realization for the enterprise even if their function does not benefit.

**Collaboration and Influencing:**

• Champions a culture of inclusiveness and teamwork.

• Collaborates effectively with others and influences all stakeholders towards enterprise outcomes. Embraces conversations needed to deliver enterprise value.

**Strategic/Innovative:**

• Global perspective. Takes a broad view when approaching issues. Sees ahead to future possibilities & translates to breakthrough strategies. Collaborates to influence strategies of others and adapts own strategy towards enterprise value.

**Change Management:**

• Mobilizes others to initiate change; builds group momentum for change; embeds culture of change. Aligns change to enterprise strategies and direction.

**Interpersonal Savvy:**

• Relates well to all kinds of people, up, down, and sideways, inside and outside the organization; builds appropriate rapport; builds constructive and effective relationships; uses diplomacy and tact; can diffuse even high-tension situations comfortably.

*The expected base salary range for this position at hiring is $177,000- $209,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed location as of the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.*

**About CSL Behring**

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit [https://www.csl.com/](<https://www.csl.com/>) and CSL Plasma at [https://www.cslplasma.com/](<https://www.cslplasma.com/>).

**Our Benefits**

For more information on CSL benefits visit [How CSL Supports Your Well-being | CSL](<https://www.csl.com/careers/your-well-being>).

**You Belong at CSL**

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

**Equal Opportunity Employer**

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit [https://www.csl.com/accessibility-statement](<https://www.csl.com/accessibility-statement>).

Eli Lilly and Company

Sr. Advisor/Director/Sr. Director, TSMS- Advanced Therapies

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

**Introduction:**

*At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.*

*Lilly is expanding its portfolio of advanced therapy medicines, spanning viral vector (AAV and lentiviral) and non-viral delivery (lipid nanoparticle and mRNA) platforms. These are among the most technically demanding modalities in our network, combining rapidly evolving science with a fast-moving regulatory landscape, and are manufactured across both internal Lilly sites and external manufacturing partners.*

**Job Title:** Senior Advisor / Director / Senior Director – Technical Services/Manufacturing Science, Advanced Therapies

**Organization Overview**

The TS/MS organization provides technical oversight to ensure robust and consistent biology and chemistry throughout all aspects of Lilly’s manufacturing process. Through cross functional collaboration, TS/MS ensures the quality and safety of our products through process monitoring and knowledge to control, prevent and mitigate variability to deliver a reliable supply of medicine. Within TS/MS, the central commercialization team provides global technical stewardship for products from early development through launch and across the commercial lifecycle, working across internal manufacturing sites and external partners.

**Responsibilities:**

The successful candidate will serve as the technical lead and global technical owner for assigned advanced therapy drug substance programs, leading the technical strategy from early development through commercial launch and lifecycle management. This is an individual contributor and technical leadership role supporting a growing portfolio of multiple advanced therapy modalities. The role focuses on drug substance, spanning both drug substance and drug product for lipid nanoparticle products where the two are closely coupled. Key responsibilities of the role include:

- Partnering with development organizations, define and own the product control strategy, support establishment of specifications, monitor process capability, and set the technical improvement agenda for assigned products
- Represent technical services on cross functional product and governance teams, providing technical positions on manufacturing readiness, process validation and ongoing product performance
- Provide technical oversight of external contract manufacturing partners, including technology transfer, process comparability assessments, technical content for quality and technical agreements, and on-site support during manufacturing campaigns
- Author and review CMC sections of regulatory submissions, manage responses to health authority questions, and support post-approval changes; apply global regulatory expectations and relevant ICH guidance for viral vector and nucleic acid products
- Provide technical leadership on viral vector manufacturing challenges including transfection and producer cell line performance, downstream purification, and full/empty capsid separation
- Provide technical leadership on lipid nanoparticle and mRNA manufacturing challenges including encapsulation efficiency, lipid analytics, and in vitro transcription performance
- Partner with analytical development on potency, infectivity and subvisible particulate characterization strategy, and address cryogenic handling and cold chain integrity requirements for frozen products
- Lead complex process-related investigations and assess technical impact; own or support large process-related change controls with greater risk, resource or complexity
- Partner closely with the quality assurance and quality control functions to provide technical oversight of the control strategy and ensure manufacturing processes remain in a state of control
- Teach, coach and mentor scientists and engineers across the network in an emerging field where platform knowledge and precedent are still developing, setting the standard for scientific curiosity and technical rigor

**Basic Requirements:**

- Master’s or PhD degree in biochemistry, molecular biology, chemical engineering, biotechnology, pharmaceutical sciences, or related scientific discipline
- Minimum of eight years of experience in biopharmaceutical drug substance manufacturing, process development or technical services within a GMP environment, in any biopharmaceutical modality.
- Hands-on technical experience with advanced therapy drug substance in either viral vector (AAV and/or lentiviral) or non-viral delivery (lipid nanoparticle / mRNA). Depth in one platform is acceptable, with the capability and willingness to develop breadth across both. This experience may have been gained in a development, laboratory or GMP manufacturing setting

**Additional Skills/Preferences:**

- Knowledge of viral vector drug substance manufacturing, including transient transfection, producer or packaging cell lines, and chromatographic and density-based purification
- Knowledge of non-viral delivery drug substance manufacturing, including in vitro transcription and mRNA production, microfluidic or impingement-jet lipid nanoparticle formation, and encapsulation analytics
- Experience spanning drug substance and drug product, particularly for lipid nanoparticle products where the two are closely coupled
- Experience providing technical oversight of contract manufacturing partners, including comparability and technology transfer
- Experience contributing to advanced therapy regulatory submissions and health authority interactions
- Knowledge of qualification and validation requirements and good manufacturing practices
- Demonstrated strong proclivity for technical leadership, teaching and mentoring, with the ability to transfer knowledge to all levels of the organization
- Self-starter with high initiative, a data-driven approach to problem-solving, and demonstrated adaptability working in fast paced environments where established precedent is limited

**Additional Information:**

- This position may be filled at a level commensurate with the successful candidate’s experience and technical depth
- Travel of up to 30% is expected, including travel to internal manufacturing sites, contract manufacturing partner sites, and external scientific and regulatory forums
- Role is Monday through Friday based. Must be flexible to accommodate collaboration across global time zones and to support manufacturing campaigns at internal and partner sites
- Location: Indianapolis, IN USA

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ([https://careers.lilly.com/us/en/workplace-accommodation](<https://careers.lilly.com/us/en/workplace-accommodation>)) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is

$151,500 - $264,000

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

\#WeAreLilly

Indiana

Engineer - Project Manager - GFD

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

The Global Facilities Delivery (GFD) Organization delivers new and renovated capital assets around the world. Our mission is accomplished through a highly leveraged organization of design, construction, and qualification contractors. Many of the assets delivered focus on medical innovation and delivering innovative solutions to patients. Some of the assets delivered will expand the supply of existing medicines or strengthen the supply chain.

**Key Objectives/Deliverables:**

- Project Management: Lead teams to deliver large programs of at least $50M USD or more in capital assets and/or support a workstream or node of a larger program of $200M or more in capital assets. These teams will consist of both Lilly and Non-Lilly professionals to safely achieve project objectives from front-end planning (conceptual design) in a Brownfield or Greenfield site through operational qualification (cradle to grave). Project objectives are defined as delivering asset capability or capacity with safety, cost, schedule, and quality assurance.
- Interface/Communication: Ability to work from a regional distance from corporate headquarters while developing and maintaining effective communication with GFD program leadership, the project team, governance teams, business partners, and other stakeholders. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.
- Compliance: Lead/influence with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.\\
- Safety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance with safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification.

**Minimum Requirements:**

- Bachelor of Science – Engineering field or related to project management
- Minimum of 5+ years of previous experience in capital project delivery in industrial or manufacturing facilities.
- Willingness to relocate and/or travel to locations outside of home state/country.
- Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

**Additional Preferences:**

- Project Size: Previous experience on projects or multiple projects of \>$10M.
- Previous experience managing greenfield projects.
- Pharma manufacturing experience.
- Capital Project Management Experience in Pharma manufacturing facilities, such as: Bulk API, sterile products, secondary packaging, Devices and to a lesser extent lab projects.
- Experience in the following areas: GMP manufacturing, LEAN, Automation, construction, construction quality, project controls, the engineering disciplines, safety, scheduling
- The capacity to achieve results and influence through people is critical.
- Demonstrated ability to work from long distances with little supervision.
- Must exhibit a good sense of judgment in decision making, without the need for management approval while at the same time keeping management informed and engaged on critical issues.
- Effective communication skills both written and verbal.
- Ability to influence personnel and organizations without having direct administrative responsibility for them
- Competency in a foreign language(s).
- Professional Engineer (PE) or equivalent technical certification.
- Project Management Professional (PMP) certification.
- Experience in working and/or living outside the U.S.
- Demonstrated willingness to embrace the concept of continuous improvement and be an agent for change.

**Additional Information:**

- Travel is required and will vary by project.
- Full relocation to one of the posting locations listed on this requisition is required for the duration of the project. Throughout the hiring process, you may share preferences and further detail about your mobility with the hiring team.
- This is an onsite role; onsite presence is required (this is NOT a remote role).
- Multiple job levels can be hired on this posting, and business title will vary based on job title (i.e. Engineer/Sr. Engineer/Principal Engineer/Sr Principal Engineer – Project Manager – GFD).

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ([https://careers.lilly.com/us/en/workplace-accommodation](<https://careers.lilly.com/us/en/workplace-accommodation>)) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is

$66,000 - $171,600

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

\#WeAreLilly