Validation Engineer Manufacturing - Macclesfield

CK Group
25 Apr 2018
26 May 2018
Contract Type
Full Time
Natasha Young at CK Group is recruiting for a Validation Engineer (Manufacturing) to work with a pharmaceutical company at their manufacturing operations site based in Macclesfield. This is a contract opportunity to join a company with a broad range of human healthcare products for an initial duration of 12 months.

The Validation Engineer (Manufacturing) work with the local projects team to develop, produce and execute qualification documentation, commissioning, IQ and OQ protocols. This role will also review technical content of equipment supplier test protocols, lead the execution of test activities for C & Q elements throughout all phases of the project and ensure that computer validation will be considered appropriately.

Validation Engineer (Manufacturing) should have the following skills and experience:
· Working knowledge of ISO, USP and other regulatory guidelines
· Must have GMP and GEP experience.
· Broad experience of writing Commissioning, IQ and OQ protocols.
· Experience of executing FAT, SAT, Commissioning, IQ and OQ protocols.
· Must be competent in the use of electronic document management systems.
· Must have in depth knowledge of all C&Q elements and associated criticality in line with ISPE recommended deliverables.

Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference TC41952 in all correspondence.

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