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PV Auditor QA Systems
Prothya Biosolutions Netherlands B.V.
What you'll do
Plan, prepare, conduct, and report GMP and Pharmacovigilance (PV) audits
Assess compliance with applicable regulations, internal procedures, and quality standards
Identify risks, non-conformities, and improvement opportunities
Follow up on CAPAs (Corrective and Preventive Actions)
Support inspection readiness activities
Collaborate with internal stakeholders and external partners
Maintain accurate audit documentation and records
Contribute to the development and improvement of quality systems and processes
Provide guidance and training related to QA/PV compliance when required
What you'll bring
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Quality Management, or related field
Proven experience in GMP and/or Pharmacovigilance auditing
Strong knowledge of applicable GxP regulations and quality systems
Excellent analytical and communication skills
Ability to work independently and manage multiple priorities
Strong attention to detail and problem-solving mindset
Fluent in English; additional languages are considered an asset
What's on offer
A fulltime employment of 40 hours per week
A market-rate salary
A budget of 16,66% (holiday allowance and year-end bonus) of your gross salary, yours to spend or to save monthly
A personal training budget of €2,100 every three years to foster professional growth and development.
Flexible working hours after deliberation
Your own place in a close-knit and expert team with an employer that stimulates growth and personal development
Contribution to travel expenses from the first kilometer
Excellent accessibility by public transport and private parking available.
Sound pension provision.