Mes Expert Drug Product 80-100% (m/f/d)

Lonza Group

Visp, Switzerland
**
Mes recipe authoring experience
Gmp validation documentation (iq/oq/pq)
Regulated environment knowledge
** Lonza Group is seeking a dedicated MES Drug Expert to optimize drug product manufacturing at their Visp, Switzerland location. The ideal candidate should have experience in MES recipe authoring and a background in pharmaceutical technology, chemistry, or pharmacy, with a strong commitment to quality and regulatory compliance. **

Job Summary

  • The role involves authoring and adapting MES/PCS recipes to optimize drug product manufacturing processes.
  • Candidates will lead process-related investigations, critical deviations, and manage CAPAs within required timelines.
  • Relocation assistance is available for eligible candidates and their families to join the team in Visp, Switzerland.

Matching Summary

Match Score: 75

** Lonza Group is seeking a dedicated MES Drug Expert to optimize drug product manufacturing at their Visp, Switzerland location. The ideal candidate should have experience in MES recipe authoring and a background in pharmaceutical technology, chemistry, or pharmacy, with a strong commitment to quality and regulatory compliance. **

Skills & Requirements

Must-have

  • MES recipe authoring experience
  • GMP validation documentation (IQ/OQ/PQ)
  • Regulated environment knowledge
  • Process investigation leadership
  • CAPA management in Trackwise

Nice-to-have

  • Emerson Syncade expertise
  • DeltaV system familiarity
  • Sterile drug product process knowledge
  • German language proficiency
  • Customer audit support experience

Key Requirements

  • Studies in Pharmaceutical Technology, Chemistry, or Pharmacy
  • Proficiency in German and English
  • Knowledge of cGMP and 21 CFR Part 11

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter