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Audit & CAPA Lead Consultant (6-Month Contract)

Debiopharm · Lausanne

Nouveau
Contrat Senior 🇬🇧 English
Veeva Ennov CAPA GxP GCP GLP ICH Q9 ICH E6(R3) ICH E8(R1)

Description du poste

About the role

Debiopharm is looking for an Audit & CAPA Lead Consultant for a 6-month contract in Lausanne. You will strengthen quality oversight, support inspection readiness and drive continuous improvement for its clinical trials programmes across GxP activities, especially GCP/GcLP. You will act as the global Audit & CAPA process and system owner and single point of contact for business representatives.

Key responsibilities

  • Define a risk-based audit strategy with GxP Quality Leads and Business Partners, and create, maintain and run the Master Audit Plan covering third parties, systems, studies and documents
  • Perform internal audits of clinical trials, programmes and internal processes, mainly in GCP
  • Select and manage outsourced auditors when appropriate
  • Embed ICH Q9 quality risk management across the audit and CAPA lifecycle, using trend analysis and quality indicators to escalate critical issues
  • Lead preparation and conduct of regulatory authority inspections and partner with Quality Leads on timely CAPAs
  • Develop Audit/CAPA metrics and drive continuous improvement
  • Carry out targeted audits on behalf of Debiopharm International S.A.

Required profile

  • University degree: Pharmacist diploma, PhD, MSc or BSc in science (or equivalent experience)
  • 5 to 8 years managing quality assurance in pharma/biotech; hybrid experience in large and smaller structures is an asset
  • Minimum 5 years auditing and supervising audits in GCP environments; recent experience leading GCP inspection preparation (FDA, EMA, MHRA etc.) is required
  • Minimum 3 years tracking CAPAs, deviations and changes (CROs, TMF, sites, CSRs); experience with validated electronic quality tools such as Veeva or Ennov is highly desirable

Required skills

  • Solid knowledge of GxP and risk-based approaches such as ICH Q9
  • Experience implementing risk-based approaches under ICH E6(R3) and ICH E8(R1)
  • Maintaining quality SOPs and building an inspection-ready programme
  • Agile communication in matrix organisations and cross-functional teams

The recruitment process involves interviews with Talent Acquisition and the Hiring Manager, a panel interview and reference checks. Unsolicited applications from agencies or recruiters are not accepted.

Questions fréquentes

Le salaire n'est pas communiqué publiquement par le recruteur. Vous pouvez postuler et négocier directement avec Debiopharm.
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Le contrat proposé est un Contrat basé à Lausanne.
Source : ats:workable

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Debiopharm

Lausanne