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CK Group- Science, Clinical and Technical
Cambridge
CK Group are recruiting for a Validation Manager on behalf of a growing Cell Therapy CDMO to be based at their site in Cambridge on a permanent basis. The Role: Reporting to the Head of Quality, you will be responsible for leading the Validation function by building the team and developing its capabilities. This will include ensuring activities a
Job Source: CK Group- Science, Clinical and TechnicalBlackfield Associates
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Job Source: Blackfield AssociatesServe Talent
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Job Source: Matchtech MobilityPolytec Personnel Ltd
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Location: Cambridge (CB24) Duration: Permanent Hours: 9am until 5pm (Monday to Friday) Salary: Up to £55,000 Job Reference: 35053 Polytec are looking for a Design Validation Engineer for our client based just north of Cambridge. Responsibilities: * Develop comprehensive test plans and test to verify performance and functionality * Produce clear
Job Source: Polytec Personnel LtdNot found
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Job Source: Not foundNewton Colmore Consulting Ltd
Cambridge
Validation Engineer - Medical Devices A growing medical devices company based in Cambridgeshire are in the process of expansion and are actively looking for an experienced Validation Engineer to join the team. The role as Validation Engineer will give you the opportunity to work on novel and complex medical devices whilst working closely with R&D E
Job Source: Newton Colmore Consulting Ltdcambridgeshire, england, United Kingdom
CK Group are recruiting for a Validation Manager on behalf of a growing Cell Therapy CDMO to be based at their site in Cambridge on a permanent basis.
The Role:
Reporting to the Head of Quality, you will be responsible for leading the Validation function by building the team and developing its capabilities. This will include ensuring activities associated with manufacturing and lab equipment, facilities, utilities, laboratory, and computer systems are completed, in accordance with GMP requirements
Responsibilities :
Manage a team and ensure validation master plans (VMPs), protocols and procedures are established
To prepare and maintain validation plans (VPs) and identifying validation requirements.
Assist in the authoring of User Requirement Specifications, DQ/IQ/OQ/PQ protocols, and reports for validation purposes.
Working with external companies and project teams to ensure activities that require specialist knowledge are completed
Executing validation protocols for equipment, facilities and utilities
Your Background:
Degree (or equivalent) in a Science or related discipline
Qualifications related to validation and quality compliance (GMP/ ICH/ FDA/ USP/ EP policies).
Experience of validating manufacturing/laboratory equipment, facilities/utilities and processes, including the generation of lifecycle documents (URS, DQ, IQ, OQ & PQ) in a biopharmaceutical.
Significant experience leading validation activities within the biopharmaceutical or ATMP sectors
Understanding and experience of aseptic processing and cleanroom technologies
Proven track record of establishing validation master plans (VMPs)
Apply :
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 99463 in all correspondence
Validation Manager jobs in cambridgeshire, england, United Kingdom
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