Senior Freelance EU MDR Medical Device Regulatory Consultant

Senior Clinical Medical Device Consultant We are seeking a freelance Senior Clinical Medical Device Consultant who has experience conducting regulatory strategies for clinical trial start‑up activities for a variety of European countries including the UK and Germany. They should also be experienced with authoring and reviewing clinical documentation to...

Opportunity to join a 100% Medical Device-focused CRO and offer technical leadership with the preparation Clinical Evaluation Reports (CERs). **The Company:** An international CRO that accelerate product development through integrated laboratory, clinical and consulting services. They provide holistic support to clients from development to...

Opportunity to join a Medical Device manufacturer and provide market-leading Medical Writing support. **Senior Medical Writer Role:** - Conduct scientific literature reviews and compile reports, including annual literature updates and periodic safety updates, to provide to global regulatory agencies - Attends stakeholder meetings (internal and external)...

Hi I am currently partnered with a medical device company in London who are looking to expand their operation within their regulatory team. £55,000 **Requirements**: - Technical document writing - Prepare and maintain regulatory files such as STED and MDD/MDR Technical Files - Prepare technical files for CE certifications - Support with premarket...

A leading science-backed health and beauty brand is seeking a Quality Manager. You will develop and maintain a robust Quality Management System for medical devices. The ideal candidate has 5-7 years of experience in quality assurance within the medical device sector, expert knowledge of EU MDR and ISO 13485:2016, and strong leadership skills. This role...

Hi I am currently working with a medical device company who are looking for an experienced Quality Specialist to join their expanding operation. £45,0000 Must have experience in the following: EU/UK MDD/MDR experience ISO13485 Dealing with NCRs/CAPAs QMS Management Minimum 3 years in Medical Devices - They will not entertain profiles from another...

This is a fantastic opportunity for a Senior Principal Regulatory Specialist to join an established, global Medical Device company based near the South Coast in Hampshire. The business operates with hybrid flexibility of 3 days onsite/2 remote, and flexi hours too! The position is offering a six-figure salary with amazing benefits including 15% bonus,...

Get AI-powered advice on this job and more exclusive features. About Us The Medicines and Healthcare products Regulatory Agency (MHRA) enhances and improves the health of millions of people every day through effective regulation of medicines and medical devices, underpinned by science and research. The agency is made up of approximately 1,300 staff working...

At a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate, the success of large, complex global health companies requires regulatory leaders who are deeply steeped in the public and private levers that impact this industry. To remain competitive in this rapidly changing landscape,...

A national regulatory agency in the UK is seeking an Innovative Devices Regulation Lead within the Healthcare Quality and Access group. This full-time, permanent position requires oversight of medical device regulations and engagement with various stakeholders. The ideal candidate will have a degree in a science-related field, relevant experience in...