CQV Engineer

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.

Start Date: ASAP
Duration: 1 year 
Hours: 40 per week 

Role:

• 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

Skills:

• 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)

Interview process: 1 stage interview process via Teams this week

Interested? Get in touch by sending CV to c.girdwood@panda-int.com ASAP and I'll give you a call.