Visp-Based Senior QA & GMP Project Lead

Lonza

Oberwallis

Vor Ort

Vertraulich

Vollzeit

vor 43 Stunden
Sei unter den ersten Bewerbenden
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Benefits dieser Stelle

Agile culture
Inclusive workplace
Competitive compensation
Role-based benefits

Zusammenfassung

Lonza in Visp, Switzerland is seeking a Senior QA Specialist to manage GMP-focused projects within BioConjugates. You will ensure API production complies with GMP, support contract manufacturing, and advise development, production, and analytical teams on quality systems.

You will review manufacturing documentation, drive change control, investigate deviations and OOS results, and contribute to continuous improvement of Quality Management Systems while acting as the quality contact during client

Qualifikationen

  • Academic degree in Life Sciences or related field.
  • Experience in GMP environments within biopharma.
  • Experience with project management and stakeholder management.
  • Strong communication and teamwork abilities.

Aufgaben

  • Ensure API production complies with GMP.
  • Support contract manufacturing and advise on GMP across departments.
  • Check manufacturing documentation for conformity and change control.
  • Investigate deviations and OOS results.
  • Contribute to continuous improvement of Quality Management Systems.
  • Serve as quality contact for client GMP audits.

Kenntnisse

Project management
Stakeholder management
Communication
Teamwork
Customer focus

Ausbildung

Life Sciences degree

Jobbeschreibung

Lonza in Visp, Switzerland is seeking a Senior QA Specialist to manage GMP-focused projects within BioConjugates. You will ensure API production complies with GMP, support contract manufacturing, and advise development, production, and analytical teams on quality systems.

You will review manufacturing documentation, drive change control, investigate deviations and OOS results, and contribute to continuous improvement of Quality Management Systems while acting as the quality contact during client

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