Currently supporting my Biotech Client in noord Holland who are searching for a Qualification/Validation Engineer to support their teams due to an increase in projects and workload. This is an opportunity to become part of a diverse and ambitious team, and work within a cutting edge company.
: 40 per week
- Support the CQV teams with validation and qualification activities on the site
- Must be hands-on in your role, and be heavily involved with the qualification/validation of equipment
- Most of the IOQs are already written, but you will execute and review them accordingly
- Also be involved in writing of IOQs as required
- Strong background in CQV/Qualification and Validation withing the Biopharma GMP sector
- Able to review/execute protocols (IOQs and PQs)
- Work cross-functionally in team and get stuck in with hands-on work
- Languages: English (Dutch is a nice to have)
1 stage interview process via Teams this week
Get in touch by sending CV to email@example.com ASAP and I'll give you a call.