GMP Laboratory Scientist - Validation, QC & CAPA

K-Recruiting GmbH; Schweiz; On-site; CHF 78,000 - 112,000; Full time

Job summary

K-Recruiting GmbH seeks a Scientist (M/F/D) for Neuchatel, Switzerland to perform laboratory investigations, material qualification, and method transfers. The role includes QC support, CAPA ownership, and adherence to cGMP, EHS standards, with emphasis on problem solving and regulatory compliance.

Required is a university or engineering degree in analytical chemistry, biotechnology, or biochemistry and 1–2 years GMP pharma experience, fluent in English and French, with strong IT skills.

Qualifications

• University or engineering degree in analytical chemistry, biotechnology, biochemistry.
• 1–2 years of GMP pharma experience, preferably in recombinant therapeutic product.
• Experience in GMP Laboratory activities.
• Good knowledge of method transfer and critical reagent qualification.
• Experience in problem solving and deviation management.
• Good knowledge of statistical tools.

Responsibilities

• Laboratory Investigations and CAPA ownership.
• Critical Material Qualification and qualification plans/reports.
• Laboratory Method Transfers and QC support.
• Support daily QC activities following cGMP, EHS requirements.
• Author transfer protocols and reports for assays.
• Oversee validation and qualification activities with analysts.
• Investigate problems and provide improvements.
• Risk assessments, root cause analysis and investigations.
• Participate in equipment lifecycle and CAPA processes.
• Support assays lifecycle management and regulatory compliance.

Education

University or engineering degree in analytical chemistry, biotechnology, biochemistry

Tools

Statistical tools

Job description

K-Recruiting GmbH seeks a Scientist (M/F/D) for Neuchatel, Switzerland to perform laboratory investigations, material qualification, and method transfers. The role includes QC support, CAPA ownership, and adherence to cGMP, EHS standards, with emphasis on problem solving and regulatory compliance.

Required is a university or engineering degree in analytical chemistry, biotechnology, or biochemistry and 1–2 years GMP pharma experience, fluent in English and French, with strong IT skills.