Job Ref: 213080837

Date: 2021-01-26 15:04:38

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We are currently recruiting for a Validation Engineer for our client who are a global pharmaceutical company based in Milton Keynes.
The main purpose of the role is to support the effective management of the validation of processes / equipment / utilities / cleaning at the site.
Key roles include:
* Execute requalification of equipment, facilities and utilities and periodic review activities in accordance with the Validation Master Plan schedule
* Practical support during protocol execution where required and appropriate.
* Supervise validation testing performed by contractors to ensure work is accurately completed to the required standards
* Assists in developing programs and maintaining standard operating procedures (SOPs)
* Facilitation of the review and approval of validation documents.
* Lead and perform small to medium size validation activities by writing, reviewing, approving and executing documentation for new and current validation activities. This will include the validation of a new parts washer and the temperature mapping and cleaning validation of modified pipework.
* Generating validation technical reports related to systems, products and/or processes, in compliance with company standards and regulatory requirements.
* Review proposed Change Controls (low to mid complex changes) to assess the impact on the validated status and determine the validation strategy as required.
* Provision of advice and guidance on validation related topics and best practices.
* Communicate cross functionally regarding status of validation status and project timelines
* Identification and implementation of continuous improvement initiatives to ensure lean ways of working.
Candidates will ideally have an Engineering or scientific background.with Equipment Validation and sterilisation Validation experience

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