Upstream Bioprocess Team Lead — Innovate & Deliver

Lonza Group Ltd.

Oberwallis

Vor Ort

CHF 140.000 - 190.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

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Benefits dieser Stelle

Relocation assistance

Zusammenfassung

Lonza Group Ltd. is seeking a Team Lead for Upstream Processing (USP) at our Visp site in Switzerland.

You will provide technical leadership to a team of Bioprocess Engineers, drive manufacturing campaigns, ensure cGMP compliance and support technology transfers and process validation. The role requires a Bachelor’s or Master’s degree in a related field and over 5 years of biotech/manufacturing experience, with strong English and German language skills.

Qualifikationen

  • Requires Bachelor’s or Master’s in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences or related discipline.
  • Minimum 5 years of experience in biotechnology or biopharmaceutical manufacturing, process engineering or USP operations.
  • Strong technical expertise in mammalian cell culture and GMP‑regulated manufacturing environments.

Aufgaben

  • Accountable for planning, execution and documentation of manufacturing campaigns within the USP area.
  • Provides technical leadership and expertise for mammalian cell culture manufacturing operations.
  • Supports technology transfers, process validation, process monitoring and lifecycle management activities.
  • Ensures manufacturing activities are performed in accordance with cGMP requirements and approved procedures.
  • Leads and develops Bioprocess Engineers; manages resources and performance.

Kenntnisse

Leadership
Communication
Problem solving
Stakeholder management
GMP experience

Ausbildung

Bachelor's or Master's in Biotechnology/Life Sciences

Tools

Mammalian cell culture
Process engineering

Jobbeschreibung

Lonza Group Ltd. is seeking a Team Lead for Upstream Processing (USP) at our Visp site in Switzerland.

You will provide technical leadership to a team of Bioprocess Engineers, drive manufacturing campaigns, ensure cGMP compliance and support technology transfers and process validation. The role requires a Bachelor’s or Master’s degree in a related field and over 5 years of biotech/manufacturing experience, with strong English and German language skills.

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