Quality Auditor 80-100 % (m/f/d)

Lucerne Interim View Job Description
Our client, a leading global player in the pharmaceutical industry Lucerne area is looking for a service and customer oriented Quality Auditor (m/f/d) who will support the Quality Operations and Compliance organization on clinical quality activities accountability for Good Manufacturing Practice (GMP) compliance, ensuring clinical supply functions operate within GMP requirements and compliant clinical drug substance and drug product supply.

Added 16/01/2025

  • International pharmaceutical company
  • Six months as part of temporary employment to cover maternity leave

About Our Client

Our client, a leading global player in the pharmaceutical industry Lucerne area is looking for a service and customer oriented Quality Auditor (m/f/d) who will support the Quality Operations and Compliance organization on clinical quality activities accountability for Good Manufacturing Practice (GMP) compliance, ensuring clinical supply functions operate within GMP requirements and compliant clinical drug substance and drug product supply.

Job Description

The selected candidate will be responsible for the primary following activities:

  • You will be responsible for the oversight and support of certain quality assurance activities in the space of Quality Operations and Compliance.
  • Conduct quality review and approval of GMP documentation (e.g. calibration activity documentation, equipment periodic review, logbooks, training plans and records, SOPs)
  • Support quality oversight activities under the responsibility of the Quality Operations and Compliance area (e.g. calibration, equipment periodic review, logbooks, management for training plans and training records, SOPs, quality on the floor)
  • Assure and maintain compliance with GMP regulations in the defined scope of work
  • Provide support to projects and source areas as Quality Assurance Representative

The Successful Applicant

To be considered for this position, the ideal candidate must have:

  • BA/BS or higher academic education
  • 3+ years of experience in a regulated industry, preferably in pharmaceuticals, biotechnology, or medical technology
  • Experience in conducting quality oversight activities
  • Focus on quality and compliance
  • Service- & customer-oriented mindset
  • Excellent communication skills and fluency in English, German is a plus

What's on Offer

This is a unique opportunity to immediately join a renowned international company and become an integral part of the team.

Contact
Christoph Schultz
Quote job ref
JN-012025-6637084

Job summary

Job Function
Healthcare & Life Sciences
Specialisation
Pharmaceutical
Industry
Healthcare / Pharmaceutical
Location
Lucerne
Contract Type
Interim
Consultant name
Christoph Schultz
Job Reference
JN-012025-6637084

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