Latest regulatory affairs Jobs

Product Design Mechanical Engineer - Medical Device - Warwick

This role involves designing and developing medical devices as part of a multidisciplinary engineering team. The engineer will work on life-saving and life-improving products, contributing to full product development cycles within a regulated environment. The company emphasizes innovation, staff growth, and career progression.

Newton Colmore Warwick, United Kingdom

On-site Permanent

Medical Devices - Senior Mechanical Design Engineer - Cambridge

This role involves contributing to the development and improvement of life-saving medical devices, collaborating with experts in electronics, software, and other medical fields. You will work on complex challenges, including fluidics, mechanism design, and thermal issues, using 3D CAD tools like SolidWorks. Your work will have a significant impact on the company's success and projects.

Newton Colmore Cambridge, United Kingdom

On-site Permanent

Manager Regulatory Medical Writing XTA

This role involves leading the preparation and finalization of clinical and regulatory documents within a global medical writing team, with a focus on strategic content planning and cross-functional collaboration. The manager will oversee writing projects across multiple therapeutic areas, mentor junior staff, ensure compliance with regulatory standards, and contribute to process improvements. Based in High Wycombe with a hybrid working model, the position requires strong scientific communication, project leadership, and regulatory expertise.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Manager Regulatory Medical Writing X-TA

This role involves leading the preparation and finalization of clinical and regulatory documents within a cross-functional environment, ensuring scientific accuracy and compliance with regulatory standards. The manager will guide teams, mentor junior staff, and drive process improvements in medical writing, with a strong focus on strategic planning and cross-departmental collaboration.

Johnson & Johnson MedTech €60,400 – €103,960 pa

Hybrid Permanent

Laboratory Analyst 2

This role involves performing analytical testing of raw materials, intermediates, and finished medical products using techniques like ICP, GC, IR, UV-Vis, and TOC. The Laboratory Analyst 2 supports quality assurance by maintaining methods, investigating out-of-specification results, validating processes, and ensuring compliance with safety and regulatory standards. The position also includes mentoring junior staff, driving continuous improvement, and contributing to method development and equipment validation.

Smith & Nephew Goole, United Kingdom

Hybrid Permanent

Site Director, Hull & Melton

Leads a strategically important manufacturing site for wound care products, driving long-term strategy, operational excellence, and large-scale transformation within a highly regulated environment. Champions cultural change, compliance, and innovation while leading cross-functional teams in manufacturing, quality, R&D, and regulatory. Plays a key role in global operations leadership, influencing supply chain strategy beyond the site.

Smith & Nephew Goole, United Kingdom

On-site Permanent

Scientist 2 - Lab Services

Scientist II - Laboratory ServicesLocation: Deeside, UKContract Type: Contract (5 Months)Start Date: ASAPPay Rate: £142.32 per day (PAYE)About the RoleWe are seeking a Scientist II - Laboratory Services to join our Technology & Innovation team at our Global Development Centre...

Carbon 60 Deeside, Clwyd, United Kingdom £141 – £142 pd

Bioinformatics Software Test Engineer

To work within the Customer Analysis Workflows and Applied Development groups specialising in biopharma and clinical analysis workflows. The role involves testing EPI2ME software products, developed by the EPI2ME software developers, to ensure that workflows are running as expected, that...

Oxford Nanopore Technologies Oxford, United Kingdom

QA Specialist - NPI

This role involves leading Quality Assurance for new product introductions across a global network of external manufacturers. The specialist ensures compliance with GMP and regulatory standards during technology transfer, supports clinical trial manufacturing, and acts as the QA lead during audits and inspections. Key responsibilities include oversight of CMOs, risk management, and continuous improvement of quality processes.

GE HealthCare Chalfont St Giles, Buckinghamshire, United Kingdom

Hybrid Permanent

Biomedical Engineer- Site Based

The Biomedical Engineer – Site Based provides on-site technical support for the maintenance and repair of medical equipment within healthcare facilities. This role ensures device safety, regulatory compliance, and optimal performance through preventive and corrective maintenance, accurate documentation, and collaboration with clinical staff and engineering teams. The position requires strong technical skills, customer communication, and adherence to quality and safety standards in a clinical environment.

GE HealthCare Remote, Null, United Kingdom

Laboratory Technician

Laboratory TechnicianLocation: Folkestone, KentStart Date: 10th August 2026Hours: 6:00am - 6:00pm - 4 on 4 offPay Rate: £CompetativeDuration: Temp to PermJoin Our Clients Team!Are you passionate about quality control? We are seeking a dedicated Laboratory Technician to join our dynamic...

Office Angels Folkestone, Kent, United Kingdom

Senior Design Assurance Engineer

ABOUT ORGANOX:OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and...

OrganOx Oxford, United Kingdom

On-site Permanent

Logistics Specialist

ABOUT ORGANOX:OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and...

OrganOx Oxford, United Kingdom

On-site Permanent

Senior Technical Consultant

This role involves providing clinical and technical support during cranial and spinal surgical procedures, working directly in operating theatres to assist clinical teams with implantable devices and technologies. The consultant collaborates with sales and medical staff to ensure proper use of Medtronic’s portfolio, supports training for healthcare professionals, and manages inventory and case coverage across the North of England. It requires strong technical knowledge, clinical experience, and the ability to operate independently in a fast-paced hospital environment.

Medtronic Manchester, United Kingdom £52,000 – £78,000 pa

On-site Permanent

Sales Specialist - IGT D Coronary

This role involves driving sales of advanced cardiology and vascular imaging products across Scotland, combining technical expertise with strategic account management. The specialist will train existing customers, identify new business opportunities, and deliver clinical value propositions to healthcare providers. It requires deep product knowledge, CRM proficiency, and collaboration with marketing and clinical teams to support tender strategies and market expansion.

Philips Edinburgh, Alba / Scotland, United Kingdom

Hybrid Permanent Clearance Required