Location: Visp
Contract duration: 6 months
Responsibilities:
1. Plan and support the implementation of release testing for biopharmaceutical products.
2. Perform, optimize, transfer, and validate analytical methods, with a strong focus on biochemical and protein analysis techniques.
3. Provide technical expertise on analytical and laboratory-related topics.
4. Extract, analyze, and interpret analytical data, and prepare clear reports and presentations.
5. Manage and document change requests and deviations in accordance with GMP requirements.
6. Create, review, and approve technical and regulatory documentation to ensure compliance with applicable guidelines.
7. Ensure the quality-compliant and timely execution of assigned tasks within budget.
8. Work independently within project frameworks while taking ownership and responsibility for deliverables.
9. Collaborate closely with QC teams, research, production, and quality assurance to ensure smooth cross-functional processes.
Requirements:
10. Bachelor’s or Master’s degree in Biochemistry, Biotechnology, Molecular Biology, Pharmaceutical Sciences, or a related field.
11. Fluent German and English
12. Experience in biopharmaceutical QC laboratories, preferably within a GMP-regulated environment.
13. Knowledge of protein and biochemical analytical techniques (e.g., HPLC/UPLC, electrophoresis, ELISA, spectroscopy).
14. Experience with analytical method development, transfer, and validation.
15. Familiarity with GMP documentation, including deviations, change controls, and SOP management.