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As a Biotechnologist, you’ll be at the heart of the Drug Product manufacturing operations, ensuring every batch meets the highest standards of quality, safety, and compliance.
What You’ll Do
* Execute and oversee manufacturing activities for liquid and freeze-dried drug forms in a GMP-compliant environment.
* Troubleshoot equipment, resolve issues, and contribute to continuous process improvement.
* Ensure timely and accurate documentation of batch records and GMP-related documents.
* Support investigations, CAPAs, and process changes with a hands-on, solution-oriented mindset.
* Train and mentor team members, sharing your expertise and fostering a culture of excellence.
* Operate, clean, and set up production equipment (e.g., compounding, autoclaving, filter integrity testing, visual inspection).
What You Bring
* 2–4 years of hands-on experience in a GMP manufacturing environment (sterile Drug Product preferred).
* Fluent in English or German (ideally both).
* Strong understanding of GMP, SOPs, and quality systems.
* A collaborative spirit, structured mindset, and proactive attitude.
* IT-savvy, with knowledge of SAP and MES as a plus.
* Willingness to work in a 2-shift pattern and participate in on-call duties.
Seniority level
* Seniority level
Entry level
Employment type
* Employment type
Temporary
Job function
* Job function
Quality Assurance and Production
* Industries
Pharmaceutical Manufacturing
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