Jobs in Exeter

Quality Assurance & Regulatory Affairs Administrator

Quality Assurance & Regulatory Affairs Administrator Sunbury-on-Thames £28,000 - £33,000 per year Full-time, Ongoing Temporary We are recruiting for a Quality Assurance & Regulatory Affairs Administrator to join a growing medical technology organisation supporting compliance and quality systems across its global product range. This is a great opportunity for someone...

The Workshop

London

Quality Manager (Medical Devices / ISO 13485)

(Medical Devices / ISO 13485) £55,000 - £65,000 + Training + Early Finish Friday + Private Medical + Enhanced Pension + Enhanced Holiday Belfast Are you a Quality Manager or Senior Quality Engineer with experience working within ISO 13485 regulated manufacturing environments looking to join a global market leader known...

Ernest Gordon Recruitment

Belfast

Market Structure & Regulatory Affairs Specialist (Vice President)

Market Structure & Regulatory Affairs Specialist (Vice President) ING Financial Markets, UK The Work Environment Financial Markets (FM) is one of the global product business lines of ING Wholesale Banking and is ING's gateway to secondary capital markets around the world. The FM Regulatory Centre of Expertise (Reg CoE) team...

ING Group

City of London

Market Structure & Regulatory Affairs Specialist (Vice President)

Market Structure & Regulatory Affairs Specialist (Vice President) ING Financial Markets, UK The Work Environment Financial Markets (FM) is one of the global product business lines of ING Wholesale Banking and is ING's gateway to secondary capital markets around the world. The FM Regulatory Centre of Expertise (Reg CoE) team...

ING

London

Clinical Trials Scientific Affairs Analyst

Clinical Trials Scientific Affairs Analyst page is loaded## Clinical Trials Scientific Affairs Analystlocations: ACM - Remote - UK: ACM - Remotetime type: Full timeposted on: Posted Yesterdayjob requisition id: REQ_231430Job Title: Clinical Trials Scientific Affairs AnalystDepartment: Study Set UpLocation: Remote | United KingdomHours Per Week: 37.5 hoursSchedule: Days; Monday –...

ACM Global Laboratories, Inc.

North Yorkshire

Clinical Trials and Innovative Medicines Lead Pharmacist

OverviewClinical Trials and Innovative Medicines Lead Pharmacist - Band 8b, University Hospital of North Midlands NHS Trust. Closing date: 26 March 2026. Average of 37.5 hours/week across a 7 day working rota (with a maximum weekend commitment of 1 in 4).This exciting post has been developed following investment in Pharmacy...

University Hospital of North Midlands NHS Trust

Stoke-on-Trent

Regulatory Affairs Manager

Overview Clinigen is a rapidly growing global specialty pharmaceutical services business with a unique combination of services across the pharmaceutical lifecycle. We currently have over 1,000 employees headquartered in the UK with global offices in the US, EU (Belgium, Germany, France), Asia Pacific and South Africa. Clinigen is growing rapidly...

Clinigen

Weybridge

Regulatory Affairs Officer

Regulatory Affairs OfficerLocation: Hybrid (3 days on-site)Salary:£26-28KSector: Scientific / Regulatory Affairs CY Partners are excited to be supporting a global organisation in recruiting an enthusiastic, scientifically minded graduate to join their experienced regulatory team. This is an excellent opportunity to work in chemical regulatory affairs, working with innovative product solutions...

Cypartners

Frimley

Senior Regulatory Affairs Consultant - Labelling (home or office based)

OverviewAbout The Role We are seeking an experienced Regulatory Affairs professional to join our team as a European Labelling & Promotional Regulatory Specialist. This key position provides expert guidance across a Therapeutic business unit, delivering both strategic and operational regulatory input to cross-functional teams. The role can be home or...

Parexel

Uxbridge

Senior Specialist- Regulatory Affairs

To be an integral member and significant contributor to project team(s) in the development and delivery of global compliance solutions to client companies, ensuring that client objectives are met and exceeded at all times. This will require the utilisation of a platinum standard approach to regulatory research, internal and external...

HIRANI

Belfast

Senior Digital Healthcare Account Leader

A leading creative agency is seeking a Senior Account Manager in Basingstoke to oversee digital projects in the healthcare sector. The ideal candidate will manage client relationships, drive account growth, and ensure project delivery meets financial targets. Expertise in the healthcare creative agency space and strong negotiation skills are essential....

HH Global

Basingstoke

Electronics Engineer - Programme Manager - Medical Devices

Electronics Engineer – Programme Manager – Medical Devices – Cambridge Due to a growth in company output, there is a need for a new Programme Manager who has an Electronics Engineering pedigree. Based in Cambridge, you will be leading several projects. Some projects will involve you offering support and mentorship...

Newton Colmore

Cambridge

Senior Regulatory Affairs Consultant - Labelling (home or office based)

Job Title: Senior Regulatory Affairs Consultant - Labelling (home or office based) Job Location: Uxbridge, UK Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Mid-Senior level About The Role We are seeking an experienced Regulatory Affairs professional to join our team as a European Labelling & Promotional...

Lifelancer

Uxbridge

Regulatory Affairs Manager

Barrington James are exited to post a fantastic opportunity for one of our close clients. This company is a Medical Device manufacturer. They are backed by some serious investors the industry and are looking for future support within their regulatory. This opportunity is perfect for someone who is ambitious, independent...

Barrington James Limited

Swindon

Backend Engineer: Medical Imaging & Health APIs

Your role at V7: Own and maintain backend infrastructure and processes dealing with the input, output, and consumption of both radiological and pathological medical imaging scans.Build out infrastructure for import/export of annotations to standard medical imaging formats like DICOM SEG/SR/RT, NIFTI, etc.Integrate with industry standard external storage like Google Healthcare...

V7

London