Position: Mid-Senior level

Job type: Full-time

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Job content

Are you a QA specialist?

Are you looking for a new challenge in the pharmaceutical industry in Geneva?

This international client is looking for a QA manager to join the company.

You will be responsible to maintain and manage the R&D site’s Quality Assurance (QA) activities in compliance with GMPs, ensuring a constant state of regulatory compliance and quality services.

Your Responsibilities
  • You will manage the development, implementation and maintenance of the Quality System.
  • You will review/approve the issuance of quality documents (SOP’s, specifications protocols, reports..)
  • You will manage deviations with the concerned functions, the corrective and preventive actions (CAPA) and participate to quality investigations
  • You will manage the Change Control process: review and evaluate change control requests
  • You will review and approve validation and qualification protocols and reports, including CSV
  • You will review and approve stability protocols, reports and batch records
  • You will participate to risk Analysis
  • You will manage annual quality training and training plan
  • You will manage suppliers, subcontractors, external audits and inspection from Regulatory Authorities.
  • Manage the Quality Assurance Manager Assistant
Your Profile
  • You have a Bachelor, Master degree in Chemistry, Pharmacy, or Biochemistry
  • You have at least 7 years of experience in QA environment within Pharmaceutical or Biotechnology industry
  • You are fluent in English (both oral and written)
  • Extremely motivated, with rigorous work habits and problem-solving skills
  • Track record of successful inspection from regulatory authorities
  • Knowledge and experience of GLP is an asset
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Deadline: 09-06-2024

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