Senior QA Specialist, QMS & Compliance (Visp)

Lonza

Oberwallis

Remote

CHF 120,000 - 150,000

Full time

32 hours ago
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Benefits offered by this job

Relocation assistance

Job summary

Lonza Visp, Switzerland, seeks a Senior QA Specialist, Quality Systems, to support the quality management system and participate in audits. You will collaborate with multiple functions to harmonize QMS topics and drive improvement of quality processes. The role requires GMP experience and strong English communication.

Relocation assistance is available for eligible candidates. The position offers a dynamic working culture and opportunities to influence compliance across the site.

Qualifications

  • Academic degree in Chemistry/ Biology/ Biochemistry/ Biotechnology or a comparable qualification.
  • Experience in GMP environment and manufacture of Drug Products is required.
  • Customer complaint management experience and Quality Council preparation are a must.
  • Quality escalation management and deviation trending are essential.
  • Excellent written and spoken English; German is an advantage.
  • Structured, self-driven and precise working style.

Responsibilities

  • Support oversight of the quality management system (QMS) at Lonza Visp site.
  • Generate and maintain compliant reports and trends for KPIs (non-conformities, CAPAs, changes, training).
  • Assist in implementing corporate documents at local level.
  • Collaborate with departments to harmonize QMS topics across the site.
  • Identify and manage QMS projects as required for the Visp site.
  • Participate in audits and inspections and follow-up actions.
  • Perform other duties as assigned.

Skills

GMP experience
Quality systems
Strong communication
Structured working

Education

Chemistry/Biology/Biochemistry/Biotechnology degree

Job description

Lonza Visp, Switzerland, seeks a Senior QA Specialist, Quality Systems, to support the quality management system and participate in audits. You will collaborate with multiple functions to harmonize QMS topics and drive improvement of quality processes. The role requires GMP experience and strong English communication.

Relocation assistance is available for eligible candidates. The position offers a dynamic working culture and opportunities to influence compliance across the site.

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