£80 per hour
11 months ago
My client, a Global pharmaceutical company based in Utrecht are looking for a CQV Engineer for an initial 12 months.
Title: CQV Engineer
Essential Duties and Responsibilities for this CQV role include, but are not limited to, the following:
Responsible for generating CQV test documentation which includes VQAs, VTP, DRRs and test scripts.
Execute testing and verification in the field on upstream and downstream processing equipment.
Experience with upstream or downstream single use manufacturing processes is preferred.
Experience with delta V Manufacturing control systems is required.
Raise and close validation deviations where required. Understanding of ASTM 2500 risk based verification approach for clean utilities, black utilities, downstream and upstream processes.
If this role is of interest, please apply now!
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Catalyst Life Sciences
Catalyst Life Sciences are a global recruitment company operating in the Life Sciences space, with specialist consultants working within the technical and regulatory areas. This includes the following markets;
- Pharmacovigilance/Drug Safety
- Regulatory Affairs
- Quality Assurance
- Quality Control
- Medical Information
- Medical Writers
- Medical Affairs
- Clinical Trials
- Clinical Research
- Project Management
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I personally specialise in recruiting QA and validation professionals for roles globally so please do get in touch should you be considering new roles, or looking to fill ones at your current company!