- Ensuring Validation Master Plans (VMPs), protocols, and procedures are established to facilitate the delivery of validation activities to the require regulatory standards.
- Oversee User Requirement Specifications, DQ/IQ/OQ/PQ protocols, and reports for validation purposes.
- Supervise validation testing performed by vendors to ensure work is accurate, critically review results and work with vendors to report deviations.
- Manage requalification of systems and equipment in accordance with procedures to maintain validated states.
- Support implementation of a risk-based approach to the validation of systems to ensure compliance with Annex 11 and 15.
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Validation Manager
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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
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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
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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
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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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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 - Cambridge, Cambridgeshire, United Kingdom - Blackfield Associates
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 addition, they will be supporting multiple validation projects, liaising with the project departments and the associated departments to ensure work is completed in a timely manner.
Other responsibilities include:
This is an excellent opportunity for anyone wanting to be involved with Advanced Therapy Medicinal Products (ATMP) manufacturing.