On‑Site Pharma Process Specialist – GMP & Documentation Lead

A leading pharmaceutical company is seeking a Process Specialist in Basel, Switzerland, for a hands-on role focused on process support within manufacturing. Responsibilities include batch record review, SOP updating, and ensuring GMP compliance. Ideal candidates will have 3-5 years of experience in pharma, a scientific degree, and must be fluent in both German and English. This is an on-site position requiring strong collaboration skills and the ability to adapt quickly to established processes.
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