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