Associate Scientist _GMP Operations (6802)

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 German and English speaking Associate Scientist (GMP Operations) for a 11months’ 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.

Main Responsibilities:

·       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 ProNas 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

Qualifications and Experience:

·       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., ProNas 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 English and German mandatory.