Principal Associate

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Job Title: Principal Associate Computer Systems Quality Assurance (CSQA) for E-Systems

Location: Limerick, Ireland

Company: Eli Lilly & Company

About Us: Eli Lilly Limerick is a cutting-edge biotechnology company dedicated to revolutionizing the healthcare industry through the development and production of next-generation biopharmaceuticals. Our state-of-the-art manufacturing facility is at the forefront of innovation, employing the latest bioprocessing technologies to create life-saving therapies. We are seeking a highly motivated and detail-oriented CSQA Principal Associate to join our quality assurance team and ensure the highest standards of product quality and compliance for our electronic systems.

Position Summary: As a CSQA Principal Associate, you will play a critical role in developing, designing, maintaining the quality and regulatory compliance of our biopharmaceutical products within our next-generation manufacturing facility. You will work closely with cross-functional teams to implement and develop, design, uphold quality assurance standards, facilitate inspections and audits, and support continuous improvement initiatives.

Key Responsibilities:

1. Quality Assurance Design and Oversight:

Implement Global Quality Standards to the new Lilly Limerick site.

Provide quality direction and governance for QA-owned e-systems, site IT systems, and site laboratory systems.

Develop and maintain quality assurance procedures, policies, and systems.

Conduct routine self-inspections and monitoring assessments (time-on-the-floor) to ensure compliance with cGMP (current Good Manufacturing Practices) and other relevant regulations.

Investigate and address deviations, non-conformities, and CAPA (Corrective and Preventive Actions) to maintain quality.

Participate in IT and quality organizations to provide consistency across all computer systems areas.

Perform and support data flow mapping for production, analytical, and site-wide processes.

2. Regulatory Compliance:

Stay current with industry regulations, guidelines, and best practices.

Assist in the preparation and execution of regulatory inspections and audits.

Ensure compliance with periodic review, change control, deviation, back up and archive, security, and other support processes for IT systems.

Participate in quality meetings keeping the group updated on initiatives within the QA owned GMP IT systems.

3. Documentation and Reporting:

Maintain accurate and comprehensive quality records, change control documentation, and quality reports.

Develop common local procedures for computer systems and help the site consistently interpret and implement global policies across all computer systems areas.

Review and approval of key GMP documents such as GMP standard operating procedures and CSV deliverables as appropriate to area of responsibility.

Review and approval of GMP documents associated with qualification and validation including IQ/OQ/PQ & validation documents for facilities, equipment, computer systems, GMP utilities and system periodic review reports as appropriate to area of responsibility.

4. Quality Improvement Initiatives:

Identify areas for process improvement and work collaboratively with cross-functional process teams to implement changes.

Participate in risk assessments and quality improvement projects.

5. Training and Development:

Provide training to staff on all relevant aspects of computer system quality.

Stay informed about the latest developments in computer systems validation and quality assurance.

Qualifications:

BSc, Hons BSc, MSc, or PhD in Science, Engineering, Quality, or related discipline.

5+ years of experience in quality assurance within a biotechnology, pharmaceutical, or medical device manufacturing environment.

Strong knowledge of cGMP, FDA, Data Integrity, Quality Risk Management and other biopharmaceutical regulatory requirements.

Excellent problem-solving and analytical skills.

Detail-oriented with a strong commitment to maintaining high-quality standards.

Effective communication and teamwork skills.

Demonstrated initiative – able to work proactively without direct supervision and with a continuous improvement mind-set.

Experience with data flow mapping and within electronic quality management systems (e.g., TrackWise) and other pharmaceutical IT systems is a plus.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

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