Associate Scientist; GMP Operations

Associate Scientist (GMP Operations) – 6802

Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a Associate Scientist (GMP Operations) for an 11‑month contract role with high chances of extension based in the Visp, Switzerland
.

This Scientist supports the timely, compliant, and high‑quality execution of projects within their assigned area of responsibility. The role operates in a cGMP‑regulated environment and contributes to laboratory, documentation, and coordination activities to ensure smooth project execution while maintaining strict adherence to quality and safety standards.

• Timely and cGMP‑compliant execution of assigned projects within the defined area of responsibility
• Interface and coordination with analytical representatives and cross‑functional stakeholders
• Review and approval of corrections in Pro Nas and creation and maintenance of label data
• Preparation of projects, including organization of special materials for aliquoting, verification of packing lists, and preparation of documentation folders
• Assistance with and execution of training activities in accordance with SOP and GMP requirements
• Issuance of reserve and stability samples following established procedures
• Ordering and management of laboratory materials and consumables
• Close collaboration with QC, QA, AD, PD, MSAT, Operations, and Logistics
• Compliance with all applicable quality, GMP, SOP, and safety regulations

• Relevant working/residency permit or Swiss/EU‑Citizenship required
• Degree in a scientific discipline (e.g., Chemistry, Biology, Biotechnology, Pharmaceutical Sciences) or equivalent practical experience
• Experience in a GMP‑regulated pharmaceutical, biotech, or laboratory environment preferred
• Familiarity with laboratory documentation systems and quality processes (e.g., Pro Nas or similar)
• Strong organizational skills with high attention to detail
• Ability to work independently as well as collaboratively in cross‑functional teams
• Good communication skills in a regulated environment

• Seniority level:
  Associate
• Employment type:
  
  Contract
• Job function:
  Science
• Industry: Pharmaceutical Manufacturing