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CK Group
cambridgeshire
Job Description 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 en
Job Source: CK GroupCK 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
cambridge
Job Description Blackfield Associates are partnered with a CDMO client based in the Cambridge area looking for a Validation Manager on a permanent basis. The Validation Manager will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In additio
Job Source: Blackfield AssociatesBlackfield Associates
Cambridge, England, United Kingdom
Blackfield Associates are partnered with a CDMO client based in the Cambridge area looking for a Validation Manager on a permanent basis. The Validation Manager will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be s
Job Source: Blackfield AssociatesServe Talent
Bury St. Edmunds
Job Title: Validation Engineer (Medical Device Manufacturing) Location: Suffolk, UK Company Overview: Join our dynamic client, a leading medical device manufacturing company. They are specialists in developing cutting-edge medical devices that meet the highest quality and regulatory standards. Position Overview: We are seeking a talented Val
Job Source: Serve TalentPolytec Personnel Ltd
Cottenham
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 LtdVector Recruitment Ltd
Royston, Hertfordshire
Senior Verification & Validation Engineer Cambridgeshire £40k - £55k (dep on exp) + bonus and excellent benefits! A fantastic opportunity for a Senior Verification & Validation Engineer has arisen at a Cambridge based cutting edge leading medical device development company whose innovative technology is reshaping the medical, life science and diag
Job Source: Vector Recruitment LtdNot found
Cambridgeshire
Growing IC design team seeks experienced engineer This smart and supportive silicon team are looking for someone to help with the verification and validation of their mixed signal IC designs. You will be creating and updating a test suite that covers the whole IC development process from simulation through FPGA prototyping to post-tapeout silicon a
Job Source: Not foundcambridgeshire, 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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