QA Specialist (m/f/d) 100%.

job details

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  • specialism
    industry
  • contact
    Nikolina Babic
  • reference number
    142523-1707

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job details

For Lonza AG in Visp we are looking for a QA Specialist (m/f/d) 100%. This role is temporary for a minimum of 6 months.

Lonza in Visp, Switzerland, is one of the company's largest sites and a key hub for innovation and production. The site specializes in the development and manufacturing of pharmaceutical ingredients, biopharmaceuticals, and chemical intermediates. With a broad range of technologies and services, Lonza Visp supports clients in the pharmaceutical, biotechnology, and specialty chemicals sectors, providing tailored solutions for drug and specialty product manufacturing. The site plays a central role in Lonza's global value chain and drives innovation in the life sciences industry.

Key responsibilities:

  • Verification of the company's compliance with ISO/cGMP quality system requirements as well as knowledge of PICS Guide to Good Manufacturing Practices
  • Make independent quality-related decisions based on regulatory and compliance knowledge and provide independent quality support to project teams
  • Audit internal quality system elements in manufacturing and operational support areas.
  • Provide oversight for compliance of Change Controls, CA/PA and investigations, OOS and deviations
  • Independently identify and manage special projects or QA compliance functions as agreed upon with QA management
  • Review and approve validation documents

For Lonza AG in Visp we are looking for a QA Specialist (m/f/d) 100%. This role is temporary for a minimum of 6 months.

Lonza in Visp, Switzerland, is one of the company's largest sites and a key hub for innovation and production. The site specializes in the development and manufacturing of pharmaceutical ingredients, biopharmaceuticals, and chemical intermediates. With a broad range of technologies and services, Lonza Visp supports clients in the pharmaceutical, biotechnology, and specialty chemicals sectors, providing tailored solutions for drug and specialty product manufacturing. The site plays a central role in Lonza's global value chain and drives innovation in the life sciences industry.

Key responsibilities:

  • Verification of the company's compliance with ISO/cGMP quality system requirements as well as knowledge of PICS Guide to Good Manufacturing Practices
  • Make independent quality-related decisions based on regulatory and compliance knowledge and provide independent quality support to project teams
  • Audit internal quality system elements in manufacturing and operational support areas.
  • Provide oversight for compliance of Change Controls, CA/PA and investigations, OOS and deviations
  • Independently identify and manage special projects or QA compliance functions as agreed upon with QA management
  • Review and approve validation documents

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Nikolina Babic

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