Scientist - QA
Eli Lilly and Company, Durham, NC, United States
Position Description
The Scientist - QA for the Device Assembly and Packaging team provides daily oversight, assistance, and guidance to issues such as non-conformance investigations, change control proposals, procedure revisions, validations, batch disposition, commissioning, and qualification activities. The Scientist‑QA position is essential for maintaining GMP compliance and providing support during preparation for General Inspections by various regulatory agencies.
Key Responsibilities
Responsible for adhering to safety rules and maintaining a safe work environment by supporting HSE corporate and site goals.
Lead, mentor, and coach QA floor teams, operations, and support personnel, fostering a culture of safety, quality, compliance, and continuous improvement.
Ensure regular presence in device assembly and packaging areas to monitor GMP programs and quality systems.
Active on local process teams or indirect participation through project support activities.
Assess and triage deviations that occur within the device assembly and packaging areas.
Effectively review and/or redline to ensure quality attributes are met (e.g., deviations/observations, procedures, technical studies, validation protocols, change controls, and engineering documents).
Work with Lilly support groups and external partners to resolve or provide advice on product‑related issues.
Participate in self‑led inspections and provide support during internal/external regulatory inspections.
Technical Responsibilities
Provide continuous quality improvement oversight to regulated processes, practices, and documentation.
Review and approve GMP documentation, including procedures, deviations, technical reports, and change controls to ensure compliance with Lilly Global Quality Standards and regulatory requirements.
Network with global device assembly and packaging sites to share best practices, improve processes, and resolve product‑related issues.
Work cross‑functionally with process teams for metrics reviews, operational support, and deviation management.
Provide guidance and share technical knowledge in operational areas to ensure robust Quality Systems and GMP compliance.
Participate in inspections from regulatory agencies and corporate audits, and manage responses to findings.
Ensure compliance with corporate, local, and regulatory agency policies, procedures, and guidelines.
Provide QA oversight of device assembly and packaging operations.
Lead or participate in non‑routine investigations, root cause analysis, and corrective/preventive actions.
Minimum Requirements
Bachelor’s or Master’s degree in Engineering, Life Sciences, or related field.
5+ years of experience in Quality Assurance.
Demonstrated strong experience and proficiency with pharmaceutical manufacturing and working knowledge of Quality Management Systems and applicable regulatory requirements.
Demonstrated attention to detail and ability to maintain quality systems.
Previous experience working effectively with a cross‑functional group.
Demonstrated strong technical aptitude and ability to train and mentor others.
Demonstrated decision‑making and problem‑solving skills.
Demonstrated ability to organize and prioritize multiple tasks.
Demonstrated strong oral and written communication and interpersonal skills.
Additional Preferences
Previous experience with highly automated device assembly and/or packaging processes.
Previous experience with Manufacturing Execution Systems and electronic batch release.
CQM, CQE, or CQA certification from the American Society for Quality (ASQ).
Previous experience with Trackwise, SAP, Veeva, etc.
Experience with US/EU regulations and notified bodies.
Additional Information
The schedule for this position is Monday - Friday, day shift.
After‑hours contact may be required for escalation issues.
Accommodations Request
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 ) 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.
Equal Employment Opportunity Statement
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.
Benefits and Compensation
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400.
Full‑time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). 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.
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The Scientist - QA for the Device Assembly and Packaging team provides daily oversight, assistance, and guidance to issues such as non-conformance investigations, change control proposals, procedure revisions, validations, batch disposition, commissioning, and qualification activities. The Scientist‑QA position is essential for maintaining GMP compliance and providing support during preparation for General Inspections by various regulatory agencies.
Key Responsibilities
Responsible for adhering to safety rules and maintaining a safe work environment by supporting HSE corporate and site goals.
Lead, mentor, and coach QA floor teams, operations, and support personnel, fostering a culture of safety, quality, compliance, and continuous improvement.
Ensure regular presence in device assembly and packaging areas to monitor GMP programs and quality systems.
Active on local process teams or indirect participation through project support activities.
Assess and triage deviations that occur within the device assembly and packaging areas.
Effectively review and/or redline to ensure quality attributes are met (e.g., deviations/observations, procedures, technical studies, validation protocols, change controls, and engineering documents).
Work with Lilly support groups and external partners to resolve or provide advice on product‑related issues.
Participate in self‑led inspections and provide support during internal/external regulatory inspections.
Technical Responsibilities
Provide continuous quality improvement oversight to regulated processes, practices, and documentation.
Review and approve GMP documentation, including procedures, deviations, technical reports, and change controls to ensure compliance with Lilly Global Quality Standards and regulatory requirements.
Network with global device assembly and packaging sites to share best practices, improve processes, and resolve product‑related issues.
Work cross‑functionally with process teams for metrics reviews, operational support, and deviation management.
Provide guidance and share technical knowledge in operational areas to ensure robust Quality Systems and GMP compliance.
Participate in inspections from regulatory agencies and corporate audits, and manage responses to findings.
Ensure compliance with corporate, local, and regulatory agency policies, procedures, and guidelines.
Provide QA oversight of device assembly and packaging operations.
Lead or participate in non‑routine investigations, root cause analysis, and corrective/preventive actions.
Minimum Requirements
Bachelor’s or Master’s degree in Engineering, Life Sciences, or related field.
5+ years of experience in Quality Assurance.
Demonstrated strong experience and proficiency with pharmaceutical manufacturing and working knowledge of Quality Management Systems and applicable regulatory requirements.
Demonstrated attention to detail and ability to maintain quality systems.
Previous experience working effectively with a cross‑functional group.
Demonstrated strong technical aptitude and ability to train and mentor others.
Demonstrated decision‑making and problem‑solving skills.
Demonstrated ability to organize and prioritize multiple tasks.
Demonstrated strong oral and written communication and interpersonal skills.
Additional Preferences
Previous experience with highly automated device assembly and/or packaging processes.
Previous experience with Manufacturing Execution Systems and electronic batch release.
CQM, CQE, or CQA certification from the American Society for Quality (ASQ).
Previous experience with Trackwise, SAP, Veeva, etc.
Experience with US/EU regulations and notified bodies.
Additional Information
The schedule for this position is Monday - Friday, day shift.
After‑hours contact may be required for escalation issues.
Accommodations Request
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 ) 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.
Equal Employment Opportunity Statement
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.
Benefits and Compensation
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400.
Full‑time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). 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.
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