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i-Pharm Consulting

Quality Assurance Specialist

i-Pharm Consulting
Netherlands · Contract · Associate

Contract: Initial 6-month contract with strong long-term potential

Work Structure: Monday to Friday + 1 weekend day shift per month

Salary: €51,000 – €56,000 per annum + shift allowance + travel allowance


Ready to elevate your QA career in a fast-paced, forward-thinking pharma environment? We’re seeking a Quality Assurance Specialist with hands-on review experience in either Quality Assurance or Manufacturing (MFG). This is an exciting opportunity to join a high-performing team where practical thinking, strong attention to detail, and a can-do attitude are highly valued.


About the Role:

As a QA Specialist, you’ll support the quality oversight of manufacturing and QC processes. Your core responsibility will be to review and prepare documentation for QP disposition, ensuring compliance with GMP and regulatory standards.


You’ll also be a key contributor in ensuring that systems, procedures, and documentation remain inspection-ready at all times.


Key Responsibilities:

  • Review manufacturing, quality control, and environmental monitoring data
  • Identify and escalate deviations from standard procedures
  • Prepare product documentation for QP review and release
  • Maintain strong compliance with GMP and internal quality systems
  • Support administrative tasks, including document control and records management


What We’re Looking For


Must-Have:

  • Experience reviewing QA or Manufacturing (MFG) documentation in the pharmaceutical industry
  • Experience with digital dossiers
  • Practically minded individual
  • A few years of experience in a GMP-regulated environment


Preferred:

  • Experience with ERP systems (e.g. EBS, SAP, TrackWise, MES)
  • Understanding of GMP, regulatory requirements, and compliance practices
  • Strong organisational skills, communication, and attention to detail


If you're ready to take the next step in your QA career, apply today!


Please note: You must be able to work in the Netherlands or the EU without restriction or sponsorship to be eligible for this role. If you are interested in finding out more about this role or others, please contact Jada Kirlew at [email protected] or call: +44 (0)20 7551 0727 / +31 208 089 982 (NL)

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Posted
Apr 15, 2025
Type
Contract
Level
Associate
Location
Schiphol

Industries

Pharmaceutical Manufacturing Biotechnology Research

Categories

Quality Assurance Science

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