Pharma / Medical

On behalf of our customer,  a pharmaceutical company based in Lugano area, we are looking for the following profile, to join their plant in Ticino:


Main responsibilities and activities:

  • Oversee the generation, review, and archival of documents used to support Good Manufacturing Practice manufacture of Final Product.
  • Perform internal and external audits as assigned
  • Review and release raw materials, intermediate products and finished products
  • Perform review and approval of OOS, deviations, nonconformance, and investigation as required
  • Ensure systems are in compliance with current SOPs
  • Assist investigations and resolve potential product quality issues to improve efficiency
  • Assist with writing, revising, and approving standard operating procedures
  • Review and approve SOP, protocols and reports as necessary


  • Master degree in Chemistry, Biochemistry, Biology or similar
  • at least 3-4 years of experience in a similar role
  • Experience with implementation of corrective action programs
  • Strong computer skills including Microsoft Office, QA applications and databases
  • Solid knowledge of tools, concepts and methodologies of QA
  • Good english

Interested? Click here

Your application will be treated professionally and reservedly.

We will only reply to candidates who fulfill criteria mentioned above.