Latest Regulatory Affairs Medical Devices jobs (page 3)

83 Regulatory Affairs Medical Devices Jobs - page 3

Senior Director of Quality, Regulatory and Clinical Affairs Waters Corporation - Wilmslow SK9, Cheshire, North West Lead the Global Design Quality Assurance, Regulatory & Clinical Affairs functions for Waters Clinical Business Unit, with emphasis on global strategy for in vitro diagnostic clinical business activities... 125.00-150.00 day 4 days ago
QARA / Quality Assurance and Regulatory Affairs Director Cpl Life Sciences - Wales, United Kingdom The Quality Assurance and Regulatory Affairs Director will be responsible for developing, implementing, and maintaining quality and regulatory systems in compliance with FDA, ISO, and other global regulatory... 10 days ago
Senior Quality Assurance Officer Jackson Hogg - Newcastle upon Tyne, United Kingdom Work on site projects to support the progression of the most viable commercial/strategic opportunities for New Product Development (NPD) or Product Lifecycle Management (PLCM) Extensive knowledge of international... 13 days ago
Regulatory CMC (Chemistry, Manufacturing, Controls) Manager Vertex - London EC1A, City of London, London Reviews CMC sections of regulatory submissions, as well as the interactions and responses with regulatory agencies Bachelor's degree in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics... 125.00-150.00 day 5 days ago
Regulatory Affairs Manager Stannah - Andover, Hampshire, England As Regulatory Affairs Manager, you will play a central role in ensuring our products comply with international regulations and standards throughout their lifecycle. From product classification, documentation... $ 0.00 - $ 0.00 Per 5 days ago
Quality Assurance Specialist GENinCode Predictive Genetics - Hammersmith, United Kingdom Work with the Development team to ensure smooth and timely introduction of new products, participating in the product design stages including design reviews and product verification and validation for... 13 days ago
Lead Regulatory Affairs Coordinator Calibre Scientific - Reading, United Kingdom Lead the IVDR certification process for all registered products, including the development and maintenance of an ‘IVDR Master Plan’ with clearly defined timelines, milestones, resource needs, and cost... 9 days ago
Principal Consultant (CMC) Scendea Ltd Contribute to technical authorship and review of development regulatory documents including Regulatory Strategy Plans, Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice... 150.00-200.00 day 10 days ago
Regulatory Affairs Specialist Tata Consultancy Services - Leeds, United Kingdom As a Regulatory Affairs Specialist, you will be providing support to registration activities, CE marking and regulatory submissions as directed by project requirements and worldwide product registration... 10 days ago
Regulatory Affairs Specialist (Sports Medicine) Smith & Nephew - United Kingdom This is ideal for an eager regulatory affairs professional who has Medical Device Regulatory Submissions experience, who will implement regulatory activities to support currently marketed devices and new... Competitive 9 days ago

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