Overview
Quality Assurance Specialist Jobs in Haarlem, North Holland, Netherlands at Gi Group
Title: Quality Assurance Specialist
Company: Gi Group
Location: Haarlem, North Holland, Netherlands
Quality Assurance Specialist | Salary: up to €4,200 per month | Contract: Initial 12-month contract | Haarlem, on-site | Full-time, 40h/week
Join a major pharmaceutical company in Haarlem as a Quality Assurance Specialist, supporting key QA processes that ensure systems, data and suppliers meet quality and regulatory requirements.
Role
As a Quality Assurance Specialist, you’ll play a central role across Supplier Quality Management, Quality Agreements, and Stability coordination, with a strong focus on compliance, data accuracy and cross-functional collaboration.
Offer
- Salary: up to €4,200 per month;
- Location: Haarlem, Netherlands, on-site;
- Work Schedule: Monday to Friday, 08:30–17:00;
- Work Model: Full-time, 40 hours per week;
- Contract: Initial 12-Month temp contract with possibility of extension;
What you’ll do
- Execute Supplier Management activities, including supplier qualification and ongoing maintenance of supplier data in the Supplier Quality Management System (SQMS).
- Support the creation, management and lifecycle maintenance of Quality Agreements with suppliers, customers and internal functions.
- Coordinate stability samples and associated documentation to support the global stability program, including support in investigating stability-related events.
- Ensure processes, systems and documentation align with the Quality Management System (QMS), internal procedures and applicable regulations.
- Support governance activities linked to controlled printing, document control and archiving to protect records, prevent data loss and avoid Data Integrity issues
- Work effectively with internal stakeholders and external parties to deliver on multiple priorities and tight deadlines.
What you bring
- MBO or HBO/Bachelor degree;
- With MBO: minimum 3 years of relevant QA/regulated-industry experience;
- With HBO/Bachelor: 1–3 years of relevant QA/regulated-industry experience;
- Strong technical capability with computerized systems (e.g., QMS/SQMS, document management tools);
- High attention to detail and strong affinity with data quality;
- Clear communication skills in Dutch and English (written and verbal);
- Nice to have: experience in a GMP/regulated environment (pharma preferred);
- Nice to have (only if in scope): Pharmacovigilance data management / side effect reporting experience.
Interested?
Apply now by clicking “Easy Apply” and uploading your updated CV, and feel free to contact:
Audrey Poluakan Recruitment Consultant at Gi Life Sciences Recruitment
M: 0658069570
