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Location: Midlands

Type: Contract

Rate: Negotiable


Reference: CVENG

Updated: 27/04/2018 17:04:49

New build pharma facility

Skill required:

A minimum of 5+ Years cGMP industrial experience, ideally performing Cleaning Validation.

Extensive experience working on autoclaves.

Experience of FDA and EU licensing and inspection.

Main Duties:

Generate, execute and complete cleaning validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria.

Ensure all aspects of Cleaning Validation adhere to required policies and procedures, including safety and training.

Drive/Support execution of cleaning validation studies including sample collection, manufacturing equipment inspections, load configuration and cycle development.

Prepare equipment for qualification studies and execute validation studies according to approved protocols and SOPs.

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