10 Medical Devices Regulation Jobs in Warwick
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Systems Engineer ( MedTech / Medical Devices ) Quanta Dialysis Technologies - The Woods, CV34 5AH, Warwick, United Kingdom Skilled in either systems thinking, systems engineering, systems assurance, or systems integration in a commercial product development environment including but not limited to MedTech, Defence, Automotive... £35000 - £45000/annum 9 days ago
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Systems Engineering Team Lead JAM Recruitment Ltd - Warwick, Warwickshire, United Kingdom As a Lead Systems Engineer, you'll take ownership of systems development of the company's products ensuring full compliance with medical device regulations and standards. You'll, also, be heavily involved... 13 days ago
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Product Design Mechanical Engineer – Medical Device – Warwick Newton Colmore Consulting - Warwick, England, UK The ideal candidate would have a few years of industry experience and might be seeking their second role to advance their career. While a relevant degree in Mechanical Engineering or a related field is... Negotiable 14 days ago
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Systems Engineer JAM Recruitment Ltd - Warwick, Warwickshire, United Kingdom As a Systems Engineer, you'll contribute to systems development of the company's products ensuring full compliance with medical device regulations and standards. You'll, also, be involved with the feasibility... £35000 - £45000/annum 27 days ago
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Lead Systems Engineer JAM Recruitment Ltd - Warwick, Warwickshire, United Kingdom As a Lead Systems Engineer, you'll take ownership of systems development of the company's products ensuring full compliance with medical device regulations and standards. You'll, also, be heavily involved... 27 days ago
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Director / associate director regulatory affairs Birmingham, United Kingdom As we navigate through the transition to the Medical Device Regulation (MDR), we are seeking a highly skilled and experienced professional to join our team as Associate Director of Regulatory Affairs. Today
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Senior/principal eu regulatory consultant Namsa - Birmingham, United Kingdom biological safety and medical writing) to ensure documentation meets MDR requirements · Supporting MDR clients reviewing and drafting responses to notified body non-conformances · Advising on strategies... Today
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Regulatory Affairs and Quality Manager coventry, england, United Kingdom This role is responsible for the delivery of the company’s development regulatory roadmap. This will be achieved through leading the regulatory elements of the company’s product development efforts and... More than 30 days ago
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Regulatory affairs specialist - medical device Birmingham, United Kingdom Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remote Company Description: We are a leading healthcare company dedicated to improving patient outcomes through innovative medical... Today
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Director of engineering Skills Alliance - Birmingham, United Kingdom Your role will be to collaborate with the Executive Team; CEO, Chief Scientific Officer, Chief Medical Officer etc, to lead the development of these Medical Imaging Software products, grow the engineering... Today
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