QA Specialist
Job in
4800, Breda, Noord-Brabant, Netherlands
Listed on 2026-06-03
Listing for:
Panda International
Full Time
position Listed on 2026-06-03
Job specializations:
-
Pharmaceutical
-
Quality Assurance - QA/QC
Job Description & How to Apply Below
Overview
Description As a Specialist QA / Qualified Person, you will play a key role in ensuring that medicinal products released from the site comply with EU GMP and international regulatory standards. You will work closely with Production, Supply Chain, and Distribution teams, acting as a key quality partner while also contributing to continuous improvement and digital innovation initiatives. This role offers strong exposure across the business and is ideal for someone looking to develop further as a QP within a leading biotech environment.
Sectors Pharmaceutical Biotechnology Company Size & Type Large multinational biotech Highly regulated GMP manufacturing environment
- Eligible to act as a Qualified Person (QP) under EU Directive 2001/83/EC Article 49
- Master’s degree in:
Pharmacy Life Sciences (e.g. Biology, Chemistry, Pharmaceutical Sciences, Medicine, Veterinary Medicine) - Minimum 2+ years GMP experience in a pharmaceutical environment
- Strong understanding of GMP, regulatory requirements, and batch release processes
- Experience with deviations, CAPA, and quality systems
- Strong analytical and risk-based decision-making skills
- Excellent communication and stakeholder management skills
- Experience in biotech manufacturing environments
- Exposure to digital transformation / continuous improvement projects
- Experience supporting regulatory submissions and QP declarations
- Experience working in cross-functional/global teams
- Perform batch certification for medicinal and investigational products in line with EU and international regulations
- Act as QA partner to Production, Warehouse/Distribution, and Supply Chain
- Serve as key QA contact for Deviations and CAPAs, ensuring proper investigation and closure
- Write, review, and approve SOPs, procedures, and job aids
- Review and sign QP declarations and regulatory documentation
- Drive and contribute to continuous improvement and digital innovation initiatives
- Ensure compliance with corporate, site, and regulatory requirements
Interested? Send your CV to Daria at or call .
#J-18808-LjbffrNote that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
Search for further Jobs Here:
×