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Manufacturing Operator (Quality Control)
Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a Manufacturing Operator for a Contract position till end of 2025 (with possibility for extension) based in the Valais area, Switzerland.
The candidate should be already located in Switzerland and be prepared to work on-site in 2 shifts pattern (Monday to Friday, 6am-2pm and 2pm-11pm).
This position is about Quality Control on the shopfloor.
Main Responsibilities:
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 and review of batch records) or other relevant GMP documents for the assigned production area.
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 (e.g.: compounding, parts washing, autoclaving, filter integrity testing, visual inspection)
Qualifications and Experience:
Relevant working/residency permit or Swiss/EU-Citizenship required
2-4 years of experience GMP environment on the shopfloor (preferably in sterile manufacturing of Drug Product)
High school education sufficient
Fluent in either English or German (preferably both)
Familiarity with GMP requirements, quality procedures and SOP execution
Strong team orientation
Effective communication skills and interaction with a variety of interfaces within the organization
Structured, focused, and well-organized working attitude
High motivation and dynamic drive
IT knowledge and knowledge in SAP and MES is a benefit
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