As a QA Associate, you will serve as the primary Quality contact within the Filling Cartridges Process Team, acting as a trusted partner to cross-functional teams and a key point of escalation for quality matters.
What You'll Do
Ensure consistent application of cGMP standards and Eli Lilly quality requirements across the area
Serve as the accountable escalation point for quality issues arising in the production area
Support preparation for Regulatory inspections and contribute to the site self-inspection program
Investigate deviations in the Cartridge area and perform Quality Assessments in Veeva QMS
Review and approve qualification protocols and procedures
Act as Media Fill observer and approve work orders where applicable
Actively contribute to site Quality Systems and Quality Culture initiatives
What We're Looking For
Master's Degree in a Scientific discipline
1-2 years of experience in pharmaceutical industry operations
Basic knowledge of current GMPs, pharmaceutical legislation, and regulatory requirements
Good command of English (minimum B2 CEFR level)
Strong communication and influencing skills
Collaborative mindset with a pragmatic, compliance-oriented approach
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