GMP Manufacturing Specialist — Pilot Ops & Lean

Lonza

Oberwallis

Vor Ort

Vertraulich

Vollzeit

vor 22 Stunden
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

Mach aus dieser Rolle ein Vorstellungsgespräch — ein Lebenslauf und ein Anschreiben, die darauf ausgerichtet sind, was dieser Arbeitgeber sucht.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Relocation assistance
Competitive compensation
Inclusive culture

Zusammenfassung

Lonza in Visp, Switzerland, seeks a skilled professional to manage pilot and production campaigns, maintain plant operations, and provide technical support including on-call duties.

You will create and optimize cGMP documentation with MSAT and biotechnologists, ensuring early consideration of technical needs. Coordinate with engineering and workshop teams for investments and improvements, and drive Lean/6S-based process enhancements.

Qualifikationen

  • Very good German skills; English skills desirable.
  • Sound knowledge of process equipment and automation systems (DeltaV/MES).
  • Experience in GMP-regulated production environments.

Aufgaben

  • Support pilot and production campaigns; ensure plant operation and on-call technical support.
  • Create and maintain cGMP documentation (SOPs, HSPs, checklists) with MSAT and biotechnologists.
  • Ensure technical and operational requirements are considered early in planning and engineering phases.
  • Coordinate engineering, workshop and technical teams during investments and improvements.
  • Monitor production activities and initiate corrective actions for deviations.
  • Contribute to technical instruction and training of employees.

Kenntnisse

German language proficiency
Teamwork
Very good written and spoken English

Ausbildung

Bachelor’s or Master’s in biotechnology/pharmaceutical sciences or related
Vocational training in chemical/pharmaceutical tech or lab technician

Tools

DeltaV/MES

Jobbeschreibung

Lonza in Visp, Switzerland, seeks a skilled professional to manage pilot and production campaigns, maintain plant operations, and provide technical support including on-call duties.

You will create and optimize cGMP documentation with MSAT and biotechnologists, ensuring early consideration of technical needs. Coordinate with engineering and workshop teams for investments and improvements, and drive Lean/6S-based process enhancements.

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