Downstream Process Specialist – GMP (Biotech)

Randstad Switzerland; Luzern; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Zusammenfassung

Randstad Switzerland is assisting an international pharmaceutical client in finding an Associate Process Specialist - Downstream Operations for a 12‑month, onsite assignment in the Lucerne region. The role requires full-time presence at site to integrate into the team and support GMP manufacturing.

The candidate will work on downstream processing, SOPs, batch records, and process improvements, and must have 1–2 years in pharma/biotech with English and German fluency, plus a valid driving license

Qualifikationen

• 1–2 years of pharma/biotech experience.
• Ability to solve problems in a GMP environment.
• Willingness to learn and adapt with stakeholders.

Aufgaben

• Set up and troubleshoot downstream processes under GMP.
• Maintain GMP/EHS compliance and SOP master records.
• Support process transfers, documentation reviews, and batch records.
• Participate in sampling activities and on-call duties as needed.

Kenntnisse

English

German

Ausbildung

Bachelor's or Master’s degree in a relevant discipline

Tools

DeltaV

PAS-X

Jobbeschreibung

Randstad Switzerland is assisting an international pharmaceutical client in finding an Associate Process Specialist - Downstream Operations for a 12‑month, onsite assignment in the Lucerne region. The role requires full-time presence at site to integrate into the team and support GMP manufacturing.

The candidate will work on downstream processing, SOPs, batch records, and process improvements, and must have 1–2 years in pharma/biotech with English and German fluency, plus a valid driving license