Job Description
LHH is seeking a GMP Documentation Specialist (m/w/d) in Luzern, Switzerland, to support clinical biologics manufacturing. This role involves reviewing executed batch records, ensuring compliance with ALCOA+ standards, and enhancing documentation practices.
The candidate must have a Bachelor’s degree in life sciences and experience in GMP environments. Key responsibilities include operational reviews, documentation updates, and support for manufacturing deviations.
This is a temporary 12-month contract role starting in July 2026.
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