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Validation Manager
2 weeks ago
Cpl Life Sciences Cambridge, United KingdomValidation Managers I have a very exciting opportunity for you. · An exciting new opportunity has arisen for a Validation Manager, to join our clients QA Department. The role will be responsible for managing the validation programme and will report to the Group Quality Manager. T ...
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Validation Manager
4 days ago
CK Group cambridgeshire, United Kingdom Permanent, Full timeCK 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 ...
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Validation Manager
4 days ago
Blackfield Associates cambridge, United KingdomBlackfield 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 ...
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Validation Manager
4 days ago
Blackfield Associates cambridge, United KingdomJob DescriptionBlackfield 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 ...
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Validation Manager
4 days ago
CK Group cambridgeshire, United KingdomJob DescriptionCK 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 bu ...
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Validation Manager
3 weeks ago
Blackfield Associates Cambridge, Cambridgeshire, United KingdomJob Description Blackfield Associates are partnered with a CDMO client based in the Cambridge area looking for a Validation Manager on a permanent basis. · In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated ...
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Validation Manager
1 week ago
CK Group- Science, Clinical and Technical Cambridge, United Kingdom Full timeCK 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 d ...
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Validation Manager
2 weeks ago
Blackfield Associates Cambridge, Cambridgeshire, United KingdomBlackfield Associates are partnered with a CDMO client based in the Cambridge area looking for a Validation Manager on a permanent basis. · In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated departments to ...
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Validation Manager
1 week ago
CK Group Cambridge, United KingdomCK 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 t ...
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Validation Manager
2 weeks ago
CK GROUP Cambridge, Cambridgeshire, United KingdomCK 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. · Reporting to the Head of Quality, you will be responsible for leading the Validation function by building the team and developi ...
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Validation Manager
3 days ago
CK Group- Science, Clinical and Technical Cambridge, United KingdomCK 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 d ...
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Validation Manager
3 weeks ago
CK Group- Science, Clinical and Technical Cambridge, Cambridgeshire, United KingdomCK 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 a ...
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Validation Manager
3 weeks ago
CK Group Cambridgeshire, United KingdomCK 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 ...
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Validation Manager
1 week ago
Blackfield Associates Cambridge, United KingdomBlackfield 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 1 ...
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Validation Manager
3 days ago
SLS Services Limited Sawston, Cambridgeshire, United KingdomEnsure Compliance with GMP Requirements: The Validation Manager ensures that all validation activities related to manufacturing and lab equipment, facilities, utilities, laboratory, and company computer systems comply with Good Manufacturing Practice (GMP) requirements, specifica ...
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Validation Manager
3 days ago
SLS Services Limited Sawston, Cambridgeshire, United KingdomAre you looking to join a rapidly growing ATMO CDMO based in Sawston? This is the perfect role for someone to develop further experience in people management whilst perfecting their Validation knowledge. · Here are the key responsibilities and objectives of the Validation Manage ...
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Validation Manager
1 week ago
Blackfield Associates Ely, United KingdomJob DescriptionBlackfield 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 ...
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Validation Officer
2 weeks ago
Mundipharma Cambridge, United KingdomProvide Validation coordination and Executes validation projects, ensuring these are completed in line with GMP requirements, industry standards, company procedures and business requirements, collaborating with key stakeholders for the design, preparation, completion and final re ...
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Validation Specialist
3 weeks ago
CK GROUP Cambridge, United KingdomCK Group are recruiting for a Validation Specialist on behalf of a growing Cell Therapy CDMO to be based at their site in Cambridge on a permanent basis. · **About the Company**: · Our client is based in state of the art facilities for multi-product GMP manufacturing, they are cu ...
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Quality Specialist
2 weeks ago
BioTalent Cambridge, United KingdomI am currently working on an exciting **Quality Assurance CSV Specialist** position based in **Cambridge** within a rapidly growing and innovative Biotechnology company focussed on developing products for cell and gene therapies. · Your mission is to manage equipment and system v ...
Validation Manager - Cambridge, Cambridgeshire, United Kingdom - CK Group- Science, Clinical and Technical
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 ensuring activities associated with manufacturing and lab equipment, facilities, utilities, laboratory, and computer systems are completed, in accordance with GMP.
requirementsResponsibilities :
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 sectorsUnderstanding 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
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