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Quality Assurance Operations Technician

GXP CONSULTING Switzerland · Lausanne et périphérie

Nouveau
Mid 🇬🇧 English
GMP Deviation management

Description du poste

About the role

Join a dynamic Life Sciences consulting firm to support day‑to‑day quality assurance operations in a GMP‑regulated manufacturing environment. You will work closely with production, QC, and cross‑functional teams to ensure compliance and drive continuous improvement.

Key responsibilities

  • Review batch records and manufacturing documentation for GMP compliance.
  • Participate in shop‑floor QA activities and provide operational oversight to production teams.
  • Support deviation management, investigations, CAPAs, and change‑control processes.
  • Align procedures and documentation with internal quality standards and regulatory expectations.
  • Collaborate with Manufacturing, QC, MSAT and other functions to maintain inspection readiness.
  • Promote a quality‑focused culture throughout manufacturing operations.

Required profile

  • Technician degree or equivalent in Biotechnology, Life Sciences or related field.
  • Minimum 3 years of QA Operations experience in biotech or pharmaceutical settings.
  • Good understanding of GMP requirements and manufacturing processes.
  • Strong attention to detail, structured work style and ability to thrive in a fast‑paced environment.
  • Fluent in French and/or English.

Required skills

  • GMP knowledge
  • Batch record review
  • Deviation management
  • CAPA implementation
  • Change‑control procedures

What we offer

  • Human‑sized company with an open, collaborative culture.
  • International, multicultural work environment.
  • Exciting projects in the Life Sciences sector.
  • Professional development and learning opportunities.
  • Competitive compensation and attractive benefits.

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GXP CONSULTING Switzerland

Lausanne et périphérie