| Location | Amsterdam, Netherlands |
|---|---|
| Business Sector | Biotechnology |
| Contact name | Caitlin Girdwood |
| Contact email | |
| Job ref | 26300 |
| Published | 11 minutes ago |
We are supporting a leading biotech company in the search for an entry-level QA Documentation Officer to support GMP documentation processes within the Quality Assurance team. Unique opportunity to gain experience at an innovative Biotech in Amsterdam!
This is an ideal opportunity for someone early in their QA career looking to gain hands-on experience in a regulated GMP environment, particularly in document control systems (e.g., Veeva) and QA compliance support.
Key Details:
Start Date: 15th January
Contract Duration: 6 months (extension possible thereafter)
Location: On-site (100%)
Employment Type: Contractor / Freelance
Workload: Full-time
Key Responsibilities:
Archive and manage physical GMP logbooks in line with internal SOPs
Process, track, and manage electronic documentation using Veeva
Support the document control process under supervision of senior QA staff
Coordinate training activities related to document workflows and compliance
Ensure documentation is accurate, complete, and compliant with GxP guidelines
Work closely with experienced QA colleagues to ensure data integrity and readiness for audit
Ideal Candidate Profile:
Maximum 2 years experience in a GMP-regulated manufacturing environment (biotech/pharma)
Hands-on exposure to GxP documentation practices
Familiarity with Veeva or other electronic document management systems (EDMS) – even a few months' experience is a plus
Strong attention to detail and eagerness to learn
Comfortable working full-time on-site in a structured QA environment
Interviews + offer will happen next week Monday/Tuesday in the morning, so get in touch asap to discuss further!