Join the QC BioPharma Protein Analysis team and support the GMP-compliant release testing of biopharmaceutical active ingredients for clinical and commercial use.

Requirements: 

• On site presence in Visp
• German speaking (English is a bonus)
• Minimum 1 year industry working experience 
• GMP 
• Qualifications: Internship or BSc

Key Responsibilities

• Plan and support execution of release analyses

• Implement, optimise, transfer, and validate biochemical analytical methods

• Provide technical expertise on analytical and laboratory topics

• Evaluate analytical data and prepare reports and presentations

• Manage GMP change controls and deviations

• Create, review, and approve GMP documentation

You will work closely with QC teams, research, production, and quality assurance, ensuring projects are delivered on time, on budget, and in full regulatory compliance while taking ownership within your projects.