Location: Visp

Contract end date: 30.06.2026

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.

**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:**

- **Fluent German and English**
- Experience in biopharmaceutical QC laboratories, preferably within a GMP-regulated environment.
- Knowledge 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.