Quality Assurance Technician - Parenteral Manufacturing | Chemiker (m/w/d)
Lilly Deutschland GmbH
Job Summary
This role offers the unique opportunity to join a global healthcare leader, Eli Lilly, as part of a start-up team building a high-tech production facility from the ground up in Alzey, Germany. As a Quality Assurance Technician, you will initially support the qualification and commissioning of the new site before transitioning into a shift-based operational role. Your daily responsibilities will involve on-site quality monitoring of aseptic filling, formulation, and visual inspection processes. You will be a critical decision-maker regarding production deviations, lead minor investigations, and ensure strict adherence to Good Manufacturing Practice (GMP) standards. This position is ideal for professionals who thrive in cross-functional environments and want to play a direct role in delivering life-changing injectable medicines to patients worldwide. The role evolves from site setup to active production oversight, making it a dynamic career path within a growing international organization.
Required Skills
Education
Degree or vocational qualification in Chemistry, Pharmacy, or a related technical/scientific field (implied by 'Chemiker' and 'Technician' context).
Experience
- Professional experience in quality assurance or quality control within a pharmaceutical environment
- Experience in aseptic filling or parenteral drug manufacturing processes
- Proven experience working within a regulated GMP environment
- Experience in handling deviations and conducting quality investigations
- Experience in creating, reviewing, and approving GMP documentation
Languages
Additional
- Willingness to work in a shift system (shift-accompanying support); ability to work on-site in Alzey, Germany; experience with digital systems like Veeva and MES is required.
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