Für diese Stelle werden keine Bewerbungen mehr angenommen
- Ensuring timely, quality, and cost-optimized production of assigned products in compliance with relevant laws, regulations, and guidelines.
- Independently executing operational batch record reviews in accordance with internal work instructions.
- Preparing and executing or reviewing risk analyses in assigned projects and implementing resulting measures.
- Conducting production campaigns according to cGMP guidelines, including batch execution, test result evaluation, and troubleshooting.
- Documenting processes, process know-how, and preparing campaign reports.
- Continuously seeking improvement opportunities in processes, equipment, and procedures in collaboration with project teams.
- Implementing relevant GMP documents for the respective area and training employees for assigned products.
- Bachelor's or Master's degree in Chemistry, Biochemistry, or related field.
- 5-10 years of experience in production or quality control within a GMP environment.
- Experience in analytics for bioconjugates or related biopharmaceutical products is essential.
- Strong understanding of regulatory requirements and guidelines, particularly in GMP.
- Excellent communication skills and ability to work effectively in interdisciplinary teams.
- Proven track record of problem-solving and decision-making in a production environment.
Bio Process Engineer - Visp, Schweiz - headcount AG
Beschreibung
Bio Process EngineerLocation: Visp
Start: ASAP
Duration: 9 months
Workload: Full-time
On behalf of our client, a Swiss multinational manufacturing company for the pharmaceutical industry, we are looking for a Bioprocess Engineer.
The main objective of this position is to oversee and optimize the production of bioconjugates, ensuring compliance with regulations and delivering high-quality, cost-effective outcomes.
Your Tasks:
**Please only apply if you are eligible to work in Switzerland and the EU**
headcount AG