Post market surveillance jobs in United Kingdom

Olympus is a global leader in the medical device and technology industry. For more than 100 years, we have focused on making people's lives healthier, safer, and more fulfilling. Our products and solutions help to diagnose, prevent, and treat illnesses, further scientific research and keep people...

Location: Doncaster Business: SARIAs UK operations have a market-leading presence in a wide range of sectors associated with the food chain. The Groups companies manufacture quality products for use in human and animal foodstuffs, agriculture, aquaculture, and industrial applications. The company...

Job Summary QA Specialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Directives, Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accord...

Job Summary RA Specialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accordingly. Responsibilities · R...

Junior Consultant - QA/RA Position Overview: We are seeking a motivated Junior Consultant with 2-5 years of experience in Regulatory Affairs. This role requires hands-on involvement with the management of technical files, post-market regulatory activities, global device registration, and formulat...

Are you up for the challenge of bringing disruptive new technologies to the market for patients with chronic medical conditions? We are rapidly expanding and are looking for an experienced Quality & Regulatory Affairs Manager with experience of managing Class I, II, medical devices. About Job: As...

A long term Medical Device client of ours based in West Yorkshire, are looking to add a Regulatory Specialist to their team to support their growing business. They are looking for an individual that is hard working and self-motivated to assist with all things regulatory. Responsibilities will ...

Regulatory Affairs Lead – Remote – Competitive Package BioTalent are exclusively supporting an innovative UK based start up AI-backed software medical device company in their search for an experienced Software as a Medical Device (SaMD) Regulatory Affairs Lead. The company aims to effect large-sc...

We’re on a journey to shape the future of policing across Herefordshire, Worcestershire, Shropshire, Telford and Wrekin which make up West Mercia Police Force and we want you to be part of it. We value difference and believe in creating an inclusive working environment where our employees feel sa...

Job title: Clinical Affairs Specialist Reports to: Global Head of QA/RA Location: Manchester Science Park / Hybrid working arrangement Contract Type: Permanent / Full-Time Salary & Benefits: Competitive Salary + Benefits Package About Yourgene Health: Yourgene Health is a leading integrated tec...

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 technologies. Our commitment to quality and compliance drives us to seek talented profession...

... Post Market Surveillance as a Clinical SME. The individual will support Marketing where needed and participate in device development from the start, with the insight they will have in market needs (e ...

Lead strategies for a large product portfolio including supporting new registrations, authoring technical files, and post-market surveillance. * A minimum of 8 years post-qualification experience in ...

... surveillance and ensure compliance with statutory requirements along with supporting health and ... Two years post qualification experience is preferable along with experience of working within an ...

ISO 13485 Auditing Qualification * Proven experience and knowledge of CAPA, Supplier Quality, Auditing, Change Management and Document Control * Risk Management & Post Market Surveillance experience ...

Head of Regulatory Affairs / Regulatory Director Salary : £150,000 - £200,000 per annum Benefits : Plus shares, non-contributory pension, and bonus Location : Remote / Hybrid (depending on your location) Must be UK based. About the Role : We are seeking a highly skilled and experienced Head of Re...

Job Title : Account Manager Industry : Security and Surveillance Job Type : Full time Location : on the road Company Overview Dahua Technology is a world-leading video-centric smart IoT solution and service provider. Based on technological innovations, Dahua Technology offers end-to-end security ...

Job Title: Senior Regulatory Affairs and Clinical Lead Job Type: Full-time, permanent position Location: West Oxfordshire, (On-site) Remuneration: £100,000 + This is an excellent opportunity to join a leading medical device manufacturing that is the world leader in Glucose Monitoring, their rangi...

As the Framatome group continues to grow, we are urgently recruiting for a Contract Manager for our secondment business, EPR-Engineering in Bristol. EDF EPR Engineering UK (EPR-E) is a venture between EDF and Framatome (Subsidiaries of Edvance), an EPCC established in 2018 in charge of the design...

Provision of advice according to established procedures relating to CAPA, Complaint, Post Market Surveillance and NCR and against the external requirements of the relevant regulatory authority (ISO13485, Medical Device Directive MDD 93/42/EEC/Medical Device Regulation (EU) 2017/745 and 21 CFR Par...

Business Development Manager – Japan (APAC Region) Location: Japan / Asia-Pacific territory – including significant travel Remuneration: JPN YEN / comprehensive and highly incentivised (JPN YEN 20m plus package including substantial basic + structured bonus + large company benefits) The Company H...

Head of Regulatory Affairs £150,000 - £200,000 per annum Plus shares, non-contributory pension and bonus Remote / Hybrid (depending on your location) Senior Leadership position with a fast-growing scale-up Medical Technology company. Core focus on providing vision, leadership, support, collaborat...

A long term Medical Device client of ours based in West Yorkshire, are looking to add a Regulatory Specialist to their team to support their growing business. They are looking for an individual that is hard working and self-motivated to assist with all things regulatory. Responsibilities will inc...