Quality Control Associate m/f/d, Wallis As a member of QC BioPharma Protein Analysis team , you will contribute to the release testing of biopharmaceutical active ingredients intended for clinical and commercial use, ensuring full compliance with GMP standards and safety guidelines .
Location: Visp
Contract duration: 6 months
Responsibilities: - Plan and support the implementation of release testing for biopharmaceutical products.
- Perform, optimize, transfer, and validate analytical methods , with a strong focus on biochemical and protein analysis techniques .
- Provide technical expertise on analytical and laboratory- related topics.
- Extract, analyze, and interpret analytical data , and prepare clear reports and presentations .
- Manage and document change requests and deviations in accordance with GMP requirements .
- Create, review, and approve technical and regulatory documentation to ensure compliance with applicable guidelines.
- Ensure the quality- compliant and timely execution of assigned tasks within budget.
- Work independently within project frameworks while taking ownership and responsibility for deliverables.
- Collaborate closely with QC teams, research, production, and quality assurance to ensure smooth cross- functional processes.
Requirements: - Bachelor's or Master's degree in Biochemistry, Biotechnology, Molecular Biology, Pharmaceutical Sciences, or a related field .
- Fluent German and English
- Experience in biopharmaceutical QC laboratories , preferably within a GMP- regulated environment .
- K nowledge of protein and biochemical analytical techniques ( e. g., HPLC/ UPLC, electrophoresis, ELISA, spectroscopy).
- Experience with analytical method development, transfer, and validation .
- Familiarity with GMP documentation , including deviations, change controls, and SOP management .
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