GLP Global Quality Assurance Specialist – Switzerland

Full Time
Switzerland
Posted 9 months ago

We have just received instruction from our client, a leading global pharma company to search for a Global Quality Manager to join their organisation.

Location: Switzerland

Reporting Line: Head Innovation Quality.

Key Responsibilities:

  • Manage the Audit Program for GLP activities
  • Perform External and Internal Audits and reviews of documents
  • Act as GLP Subject Matter Expert for nonclinical and clinical activities
  • Contributes to the development and follow-up of the Quality Management System
  • Design, update and maintain internal and external audits and documents review program
  • Prepares trends analyses and recommends corrective actions to Quality management
  • Performs Documents Review (e.g. Protocols, study plans, reports)
  • Performs Quality Documents Review (e. g SOPs, instructions)
  • Conducts Internal audits (activities, processes and systems)

Requirements:

  • 10 years in industry (Pharmacy, Chemistry, Cosmetics, Food Processing, Medical De-vice) and solid experience in Quality and GLP
  • Experience of internal and external audits in an international environment.
  • Clinical Development.

Education:

  • Masters of Sciences or equivalent

Referrals:

If you feel this opportunity is suitable for someone you know, please feel free to refer them to me.

We offer £250 as a referral reward if the candidate referred is successful in securing the position.

Send your CV to info@acr-uk.com using the job title as the email subject line or ring us on +44 (0) 114 270 1741.