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Freelance​/QA GMP Specialist

Job in 1013 ML, Amsterdam, North Holland, Netherlands
Listing for: Propharma Group
Full Time, Contract position
Listed on 2026-06-18
Job specializations:
  • Pharmaceutical
    Pharma Engineer, Pharmaceutical Manufacturing, Regulatory Compliance Specialist
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 EUR Yearly EUR 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Freelance/Contract QA GMP Specialist
About Pro Pharma  For the past 20 years, Pro Pharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), Pro Pharma partners with its clients through an advise-build-operate model across the complete product lifecycle.

With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, Pro Pharma offers an end‑to‑end suite of fully customizable consulting solutions that de‑risk and accelerate our partners’ most high‑profile drug and device programs.

Role Overview  We are currently working with a global life‑sciences brand that is looking for additional support within their manufacturing operations based in the Netherlands. The position is for an independent freelancer/contractor to work for at least 6 months on a full‑time basis (1.0

FTE). The role offers hybrid working with at least 3 days onsite in Leiden, and it is to commence immediately.
Responsibilities   Support continuous improvement efforts within a GMP setting
Support and lead team members on performing CAPAs and deviations
Ensure these processes are correctly managed and timelines achieved
Support other quality operational tasks as and when needed
Work successfully across the QA team and provide key support for the continuous improvement mindset
Provide overall support and coaching of colleagues within the GMP
Qualifications   Ideally further educated to BSc or higher within a life‑sciences discipline or an applicable area
Must have demonstrated exposure to working within a GMP setting within the biological area (ATMP, CGT, etc.)
Can demonstrate key skills in QA GMP
Fluent in English Can work on a hybrid basis in Leiden
Can perform the project to the desired requirements set out in the job description
EEO Statement  We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits.
Equal Opportunity Employer. Pro Pharma Group does not accept unsolicited resumes from recruiters/third parties. Please do not call or email anyone regarding this posting.

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