QC Scientist - Analytical Assays

About the role

A pharmaceutical company in Neuchâtel, Switzerland is looking for a QC Scientist to support the lifecycle management of analytical assays in its QC laboratories. The focus is on laboratory investigations, critical reagent qualification and analytical method transfers. The consultant is Robert Angrave of CK QLS.

Key responsibilities

• Lead laboratory investigations, including root cause analysis, risk assessments and CAPAs.
• Prepare analytical method transfer protocols and reports.
• Author qualification plans and reports for critical reagents.
• Oversee validation and qualification activities, providing training and technical support to analysts.
• Execute and document laboratory experiments.
• Provide technical and statistical support to daily QC activities.
• Ensure activities comply with cGMP, internal procedures and EHS requirements.

Required profile

• University or engineering degree in Analytical Chemistry, Biotechnology or Biochemistry.
• 1-2 years' experience in a GMP pharmaceutical environment, preferably involving recombinant therapeutic products.
• Experience working within a GMP laboratory.
• Fluent French and English, with C1 proficiency in written and spoken communication.
• Right to work in Switzerland.

Required skills

• Good knowledge of analytical method transfer and critical reagent qualification.
• Experience in troubleshooting, problem solving and deviation management.
• Good knowledge of statistical tools and proficiency with standard IT applications.
• Ability to work independently, manage competing priorities and escalate issues appropriately.

To apply, submit your CV or contact the consultant directly. Candidates must have the right to work in Switzerland.