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Blackfield 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 AssociatesCK 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- 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
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 GroupServe 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 TalentMatchtech Mobility
GB
This role can be OUTSIDE IR35 Cambridgeshire based - Requirement to work on site. SYSTEM VALIDATION ENGINEER We are seeking a talented System Validation Engineer to join our team and contribute to the comprehensive testing of our Automotive product lines. Job Description: We are seeking a talented System Validation Engineer to join our team and co
Job Source: Matchtech MobilityPolytec 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 LtdCambridge, 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 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, England, United Kingdom
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