QC Scientist: GMP Analytics & Method Transfers

Actalent; Neuenburg; On-site; CHF 90,000 - 120,000; Full time

Job summary

Actalent in Neuchâtel, Switzerland is seeking a Scientist to oversee lifecycle management of analytical assays in the QC Laboratories, focusing on Laboratory Investigations, Critical Material Qualification and Method Transfers.

You will author transfer protocols and qualification reports, lead validation activities and support quality control with regulatory standards. Fluent in English and French, starting ASAP for a temporary contract through August 2027.

Qualifications

• Requires GMP pharma experience or exposure.
• Knowledge of method transfer and critical reagent qualification preferred.
• Fluent in French and English (C1 written and spoken).

Responsibilities

• Author transfer protocols and reports for assays.
• Author qualification plans and reports for critical reagents.
• Oversee validation and qualification activities and provide training/support.
• Execute and document experiments.
• Investigate and troubleshoot problems; perform risk assessments and CAPAs.
• Own Laboratory Investigations and CAPA.
• Support regulatory compliance and provide technical/statistical input.

Skills

Fluent in French and English (C1)

Education

University or engineering degree in analytical chemistry/biotechnology/biochemistry

Job description

Actalent in Neuchâtel, Switzerland is seeking a Scientist to oversee lifecycle management of analytical assays in the QC Laboratories, focusing on Laboratory Investigations, Critical Material Qualification and Method Transfers.

You will author transfer protocols and qualification reports, lead validation activities and support quality control with regulatory standards. Fluent in English and French, starting ASAP for a temporary contract through August 2027.