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Job type: Contract

Discipline: Good Laboratory Practice (GLP)

Location: Switzerland

Drive quality excellence at a leading CMO where your QA expertise ensures every product meets the highest global standards.

��Ƶ is seeking a dedicated Scientist to support the timely and compliant execution of projects within a regulated environment. This role focuses on ensuring adherence to cGMP standards and quality protocols while collaborating with cross-functional teams. Proficiency in English and German is required, and candidates located near Visp or Bern, or willing to relocate, are encouraged to apply.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

Act as the interface with analytics representatives.
Approve corrections in ProNas and create label data.
Prepare special materials for aliquoting, check packing lists, and organize project folders.
Assist with and conduct training sessions.
Issue reserve and stability samples.
Order laboratory materials as needed.
Ensure compliance with quality SOPs, GMP, and safety regulations.

Key Skills and Requirements:

Proficiency in English and German.
Familiarity with QC software such as LIMS or Trackwise is advantageous but not mandatory.
Experience in a related field is beneficial.
Ability to work remotely if required.
Strong understanding of quality control processes and compliance standards.

If you are having difficulty in applying or if you have any questions, please contact Ria Tailor at r.tailor@proclinical.com.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

��Ƶ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ��Ƶ is acting as an Employment Agency in relation to this vacancy.

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