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

Luzern 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.

hinzugefügt 16/01/2025

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

Firmenprofil

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.

Stellenbeschreibung

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

Anforderungsprofil

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

Sonstige Informationen

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

Kontakt
Christoph Schultz
Referenznummer angeben
JN-012025-6637084

Zusammenfassung

Berufsfeld
Healthcare & Life Sciences
Näheres Berufsfeld
Pharma-Industrie
Branche
Healthcare / Pharmaceutical
Ort
Luzern
Vertragsart
Interim
Beratername
Christoph Schultz
Referenznummer
JN-012025-6637084

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