Full-time
On‑Site Pharma Process Specialist – GMP & Documentation Lead
Posted by headcount • Switzerland, Basel-Stadt, Switzerland
About the Role
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.
#J-18808-Ljbffr
#J-18808-Ljbffr
Ready to Apply?
Submit your application today and take the next step in your career journey with headcount.
Apply Now