Job Title: CSV Engineer
Job Type: Contract
Contract Length: 18 Months
Working Location: Berkshire, England
Main Tasks:

Prepare and execute validation protocols for range of production, laboratory equipment, facilities and utilities.
Ensure validation compliance is maintained in accordance with the site validation master plan.
Maintain validation compliance within the department through maintaining validation documentation.
Ensure all activities are carried out in a safe manner and comply with the site safety standards.
Perform periodic reviews on equipment and systems.
Support the site in maintaining its compliance objectives through timely closure of CAPA, Deviations and Change control Tasks.
Support other members of the validation team where required.
Active contribution to the meetings.
Proactive and smart contribution to the development of the validation strategies. Perform other duties as assigned.

Requirements:

Broad experience of validation lifecycle projects.
Broadly experienced in cell banking and analytical services departments.
Able to manage projects.
Experienced in created and managed documents, Experience in Quality records. Comprehensive understanding of GMP in Biopharmaceutical - EU and USA rules and guidelines.
Comprehensive understanding of validation principles and practices: risk-based approach.
Pharmaceutical Quality systems including change control, deviation, CAPAs.

Please apply within or email me a copy of your CV on redwan.sultan@biotalent.com if you are interested in the above position.