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    CQV Engineer (Pharma)

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Location: Breda    
Language: English
Industry: Pharmaceuticals
Start date: In consultation, preferred ASAP

The Company
My client believes in reducing the burden of disease in society through innovative medicines for serious diseases. Based in the North Brabant region, they develop medicine for complex illnesses using biotechnology.

The Role
As a CQV Engineer, you will develop system commissioning qualification and validation documentation for Secondary Pacakging. This hands on role will allow you to demonstrate your qualification skills under minimal supervision and report to the Validation Manager of site engineering.

- Create commissioning, qualification and validation plans
- Create CQV summary reports
- Lead CQV test activities
- Guide the implementation of validation plans
- At least 5 years’ experience in CQV
- Experience with Computerized System Validation
- Experienced working in a pharmaceutical manufacturing environment
Does this role interest you? Questions? Simply apply to this vacancy and I will be in touch.