We are seeking an experienced
QA Specialist to support our biotech client in the Netherlands. You will be responsible for overseeing Quality Management Systems (QMS), handling change controls (CCs), corrective and preventive actions (CAPAs), and leading batch release reviews. The role requires a hands-on approach to help manage the backlog and support the team in maintaining compliance.
On vs off site: On-site for onboarding during first week, can work predominantly remotely thereafter and visit site once per week (or similar construction)
Start Date: ASAP
Duration: 6 months (extension possible thereafter)
Key Responsibilities:
- Oversee QMS Trackwise system
- Manage CCs, CAPAs, and support with BRR if needed
- Provide senior guidance to the business from a QA perspective
- Ensure compliance with GMP standards
- Work closely with internal teams to resolve any product-related issues
Requirements:
- Strong experience in QA, within biopharma GMP environments
- Expertise in QMS (Trackwise), BRR, CAPAs and remediation of backlogs
- Self-starter with the ability to work independently
- Fluent in English; Dutch is a plus
- Flexibility to adapt to the evolving needs of a growing company
Interview Process:
- Teams interview (30-45 minutes)
- Rapid feedback and potential same-day decision
Get in touch by sending CV to c.girdwood@panda-int.com