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Serve 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 TalentVector Recruitment Ltd
Royston, Hertfordshire
Compliance / Quality Administrator – Medical Devices We are looking for a Compliance / Quality Administrator to join a dynamic company developing an array of products for the medical and healthcare industry. The company is growing and offering many opportunities for personal career development in addition to a wide variety of new projects to work o
Job Source: Vector Recruitment LtdVector Recruitment Ltd
Royston
Compliance / Quality Administrator – Medical Devices Read all the information about this opportunity carefully, then use the application button below to send your CV and application. We are looking for a Compliance / Quality Administrator to join a dynamic company developing an array of products for the medical and healthcare industry. The company
Job Source: Vector Recruitment LtdMantell Associates
cambridgeshire, england, United Kingdom
Mantell Associates is currently partnered with an up and coming Medical Device organisation in their search for an Associate Director of Business Development to join their Commercial team. Associate Director of Business Development - Responsibilities: Look after a team of talented and highly scientific Business Development / Sales Account Managers
Job Source: Mantell 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 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 GroupLEX Diagnostics
Cambridge, England, United Kingdom
LEX is currently seeking a Verification and Validation Engineer who will actively engage in hands-on testing of the LEX diagnostic system. You will be working closely with the head of Quality and Engineering team and will be responsible for defining, designing, and executing verification and validation activities for the LEX 5-minute PCR diagnostic
Job Source: LEX DiagnosticsBlueGate Consulting
cambridgeshire, england, United Kingdom
IC Test and Automation Engineer, Cambridge, salary negotiable, dependent upon experience. An excellent opportunity for a capable IC Design for test Engineer to join a well funded, high calibre multi-disciplined R & D driven technology company whose IP and technology is used in high end mobile devices, drones, autonomous vehicles and consumer elect
Job Source: BlueGate ConsultingCambridge
Validation Engineer - Medical Devices
A growing medical devices company based in Cambridgeshire are in the process of expansion and are actively looking for an experienced Validation Engineer to join the team.
The role as Validation Engineer will give you the opportunity to work on novel and complex medical devices whilst working closely with R&D Engineers, external consultants, and suppliers to ensure the company's reputation and quality of products remain market leading.
Your work will be vitally important in ensuring the successful execution of validation and verification activities required ahead of regulatory approval, product launch, and mass manufacturing.
You will be heavily involved in readying the company's product for clinical trial, and the verification and validation test plans and protocols for the product, documenting all activities within the Quality Management System. Another key part of the role is the contribution to the Standard Operating Procedures.
To be considered for the Validation Engineer you will need to have prior experience with medical devices and an ISO 13485 environment, coupled with expertise in writing test protocols and familiarity with QMS.
The company are passionate about delivering a step-change for patients with their technology and they need great people to help them.
In return for your hard work the company offer a salary, tailored to your experience level, and a benefits package that includes bonuses, industry leading pension contributions, 25 days holiday and much more.
Matt Lowdon is taking lead on this assignment and so please do make a confidential application for more details.
Matt has been working with this company for over 12 years and can offer deep insights and knowledge throughout the interview process, with the aim of maximising your chances of securing this role.
Newton Colmore is a specialist executive search and talent solutions company dedicated to the medical devices and biotechnology sectors. Founded in 2015, we have helped our clients find expert scientists and engineers across the globe.
Validation Engineer - Medical Devices jobs in Cambridge
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