Quality Assurance Specialist at Haarlem, Noord-Holland

Details of the job offer

  2026-06-12

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.

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.


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


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


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

E: audrey.poluakan@gigroup.com


#LI-SS1

  Manufacturing
  Pharmaceutical and biotechnology
  7970
CONTACT NOW
miguel.mendes@gigroup.com
Quality Assurance Specialist
Temporary / Haarlem
Place of work - City:
Haarlem
Industrial sector:
Manufacturing
Professional area:
Pharmaceutical and biotechnology
Number of vacancies:
1
Reference code:
6296
Salaris per:
Job offer insertion date:
2026-06-12

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.

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.


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


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


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

E: audrey.poluakan@gigroup.com


#LI-SS1

Call us now to book an interview.

Mendes Miguel
miguel.mendes@gigroup.com

https://nl.gigroup.com/job-detail/haarlem-noord-holland-quality-assurance-specialist/6296/