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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 TechnicalCK Group
cambridgeshire, 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
Job Source: CK GroupCK 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
Job Source: CK GroupBlackfield 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 AssociatesCK 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 TechnicalPolytec Personnel Ltd
Cambridge
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 LtdPolytec 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 LtdServe Talent
IP28 7ASBury St. EdmundsBury St. EdmundsEast AngliaUnited Kingdom
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 Validation
Job Source: Serve TalentCambridge
Job 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 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: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.This is an excellent opportunity for anyone wanting to be involved with Advanced Therapy Medicinal Products (ATMP) manufacturing.
Validation Manager jobs in Cambridge
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