This position is no longer open for applications

QA Auditing and Supplier Specialist

QA Auditing and Supplier Specialist (BBBH447858) Nyon, Suisse


For our client GSK, specialized in Consumer health products, localized in Nyon in Switzerland, we are looking for a :

QA Supplier Specialist
8-month temporary mission

Your mission
Ensure quality interface and key player in relationship between Nyon plant and suppliers or 3rd parties/service providers.

Your responsibilities

  • Suppliers and 3rd parties/service providers approval process, documentation management and monitoring: Issue and maintain up to date Quality Agreements, ensure the supply of the current technical specification to the supplier (PRS) or to the service providers (SRS), management of the QIR, maintain/update the list of approved suppliers & 3rd parties/service providers and participate to supplier monitoring process
  • Perform Quality Risk analysis for suppliers (Raw materials, packaging material, consumables) and 3rd parties/service providers
  • Manage changes related to suppliers & 3rd parties/service providers (Supplier notification, User /regulatory requirements, unsatisfactory audits outcome…) as QA Associate
  • Provide support to the Audit team in preparation to the annual supplier audit program, liaising with auditors for supplier information exchange and follow program completion
  • Participate to the annual program for QA supplier deliverables (QAA, PRS, Supplier monitoring, etc …) and ensure completion as per the plan.
  • Follow-up with supplier on complaints related with materials (raw materials, packaging materials, consumables and 3rd parties/service providers)
  • Ensure that system and organization is in place for collecting information / samples and complaints follow-up until fully solved and CAPA implementation at supplier (including CAPA effectiveness check)
  • Author and review Standard Operating Procedures related to QA supplier activity, as needed
  • Periodically report KPIs for QA Suppliers activity
  • Ensure that all records (Deviations, CC, CAPAs etc…) in which QA supplier oversight is involved is completed appropriately according to local SOP and on time
  • Participate to self-inspection as per plan
  • Support external inspections/audits on site



Your profile

  • University degree in sciences, Pharmacist
  • 5-year experience in pharmaceutical industry is preferred
  • 2-year experience in supplier related activities
  • Previous experience in GMP
  • Fluent in French and English



Your application
Please apply on-line. For more information, contact Ms Sophie Darthenay

;