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CTC Resourcing Solutions AG offers specialized industry expertise to help companies source top talent and provide reliable HR and consulting services.
A global leader in life sciences and biotechnology operates across multiple locations worldwide, maintaining the highest standards of compliance, efficiency, and customer satisfaction.
Job OverviewWe seek a dedicated Manufacturing Specialist to join the Drug Product team at our client's Visp site on a 12-month contract, with chances of extension.
Key Responsibilities- Execute manufacturing activities for Drug Product production, adhering to cGMP guidelines.
- Conduct batch execution, evaluate test results, troubleshoot equipment, and provide resolution recommendations.
- Collaborate with the manufacturing team to ensure batches are produced safely, on time, and meet quality standards.
- Prepare, execute, and review production documentation, including batch records and GMP-related documents.
- Support process investigations and assist in decision-making for production issues.
- Implement process changes and corrective actions (CAPAs) within defined timelines.
- Perform training for operators and support onboarding for new team members.
- Operate, set up, and clean production equipment and premises for liquid and freeze-dried drug forms.
- Experience: 2-4 years in a GMP environment, preferably in sterile Drug Product manufacturing.
- Languages: Fluent in English or German (proficiency in both is preferred).
- Knowledge: Familiarity with GMP requirements, quality procedures, and SOP execution. IT proficiency and experience with SAP/MES systems are advantageous.
- Competencies: Strong team orientation, communication skills, and ability to interact across organizational interfaces.
- Attributes: Structured, focused, and highly motivated with a dynamic drive.
- Flexibility: Willingness to work flexible hours as needed.
