Compliance with relevant SOPs (Standard Operating Procedures) and regulations (e.g., hygiene concept, safety regulations)
Independent operation of production systems and equipment, including preparation, operation and follow‑up according to SOPs
Execution of manufacturing activities according to cGMP guidelines in the area of buffer and media preparation for mammalian cell production, including operation of the small‑parts washer and autoclave
Monitoring of production processes, identifying and reporting potential issues and actively contributing to continuous improvement initiatives
Performing GMP‑compliant work and timely documentation of activities (e.g. in computer systems such as MES or in logbooks)
Sampling, performing in‑process controls, and evaluating test results
Responsibility for training production staff on specific equipment or standard pr...
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