Technical Assistant / Deputy Lab Coordinator | Technischer Assistent / stellv. Laborkoordinator | M/W/D - Referenz 001017
consult16 GmbH
Job Summary
This role involves providing technical expertise in sterility testing and method verification, including planning routine releases, verification, and special analytics under cGMP conditions. The successful candidate will ensure smooth laboratory operations, manage weekly sample planning for timely analysis release, and maintain sample turnaround times. Key responsibilities also include supporting projects, troubleshooting, special investigations, and studies, as well as processing deviations, changes, events, and OOX incidents. The position requires creating and revising regulations and GMP documents, working proactively to find solutions, optimize processes, and continuously improve lab efficiency. This is an excellent opportunity for a professional with a scientific background and cGMP experience to contribute to an international pharmaceutical company.
Required Skills
Education
Completed scientific degree (Master or Bachelor) or completed scientific training as a Biology Laboratory Technician, or comparable qualification acquired through relevant professional experience in the pharmaceutical sector.
Experience
- Initial relevant professional experience (for Master/Bachelor graduates) or many years of professional experience (for Biology Lab Technicians) in a scientific field, preferably pharmaceutical
- Initial professional experience in a cGMP environment
- Experience with GMP-compliant working methods and regulations (ICH, Pharmacopoeias)
- Experience in the technical guidance of multiple individuals or larger teams
- Experience in interface communication
Languages
Additional
- Temporary contract for 18 months. Ability to work on Saturdays in exceptional cases, with prior coordination. Work permit for Germany required.
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