Biopharma Manufacturing Specialist - Upstream/Downstream

Lonza

Oberwallis

On-site

Vertraulich

Full time

8 days ago

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Benefits offered by this job

Relocation support

Job summary

Lonza in Visp, Switzerland, is seeking manufacturing professionals to support upstream or downstream operations in a cGMP environment. This site-based role emphasizes close collaboration and precise manufacturing practices to deliver life-changing biopharmaceutical products.

The position offers opportunities to work across upstream and downstream operations, involving equipment troubleshooting, documentation, and participation in CAPA and change controls.

Qualifications

  • Education in Biotechnology, Biology, Biochemical Engineering, or a related life sciences discipline.
  • Experience in biopharmaceutical manufacturing, including microbial or mammalian cell culture and/or protein purification.
  • Understanding of GMP principles and pharmaceutical manufacturing practices is beneficial.

Responsibilities

  • Support upstream or downstream manufacturing activities in compliance with cGMP and safety requirements.
  • Troubleshoot process equipment, evaluate results, and recommend appropriate solutions.
  • Contribute to environmental monitoring, safety initiatives, and risk assessment activities.
  • Prepare, review, and maintain manufacturing documentation, including batch records and SOPs.
  • Support investigations, deviations, change controls, and CAPA activities.
  • Participate in equipment commissioning and capital investment projects.
  • Train and support manufacturing personnel on equipment operation and standard manufacturing practices.

Skills

Fluency in English
German language
Strong problem-solving
Teamwork

Education

Biotechnology
Biology
Biochemical Engineering

Tools

DSP experience
Column Packing

Job description

Lonza in Visp, Switzerland, is seeking manufacturing professionals to support upstream or downstream operations in a cGMP environment. This site-based role emphasizes close collaboration and precise manufacturing practices to deliver life-changing biopharmaceutical products.

The position offers opportunities to work across upstream and downstream operations, involving equipment troubleshooting, documentation, and participation in CAPA and change controls.

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