Executes manufacturing activities in the area of Drug Product according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution.
Provides front line technical and procedural support, working with the manufacturing team.
Securing each batch is manufactured safely, on time, in compliance with the batch instructions and quality requirements
Responsible for establishing timely and with high quality the required production documentation (preparation, execution, review of batch records)
Supports process related investigations and assists in decision making on production issues
Supports process changes and CAPAs related to processes within required timelines
Performs training activities of relevant areas as operator and supports others and new joiners.
Operating, setting up and cleaning production equipment and premises for the production of liquid and freeze-dried drug forms (compounding, parts washing, autoclaving, filter integrity testing, visual inspection)
Your background:
2-4 years of experience GMP environment on the shopfloor (preferably in sterile manufacturing of Drug Product)
Familiarity with GMP requirements, quality procedures and SOP execution
Strong team orientation * IT knowledge and knowledge in SAP and MES is a benefit
Prepared to work in 2 shifts pattern
Willing to perform on-call duty
Expected salary
Location
Valais
Job date
Sat, 05 Jul 2025 06:29:24 GMT
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