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QA Manager Clinical GCP – audits and compliance

vor 3 Monaten


Zürich, Zürich, Schweiz gloor&lang AG Vollzeit
12-month Contractor Role in Zurich

Our client, a research and development-driven biopharmaceutical company based in Zurich, specializes in Immune Response diseases and collaborates with major pharmaceutical companies for clinical development. To support the expanding Quality Assurance (QA) activities, we are looking to hire a skilled QA professional familiar with GCP audit tasks for a temporary position that may transition into a permanent role later this year. We need a self-sufficient, hands-on expert capable of overseeing GXP compliance, managing QA processes, coordinating internal training sessions, handling related projects, and supporting cross-functional teams. The role requires on-site presence for up to 4 days a week.

Your tasks:
  • Oversight for Quality Management System (QMS)
  • Providing Quality Oversight throughout clinical trials
  • Leading GCP/GMP/GLP Vendor Qualifications
  • Organizing and conducting audits at GCP/GMP vendors
  • Coordinating internal audits and regulatory inspections

Your profile:

  • B.Sc or M.Sc in Life Sciences
  • 3-5 years of experience in Clinical QA Operations
  • Experience in CRO and Clinical Vendor Management
  • Thorough knowledge of GCP and GMP regulations

Your autonomy, integrity, and proactive attitude are highly valued. Your customer-oriented mindset will facilitate communication with all stakeholders. Become the newest reliable team member in this welcoming work environment near public transportation in Zurich.