Latest Regulatory Affairs Specialist Jobs

Quality Engineer

The Quality Engineer is responsible for developing, implementing, and maintaining quality plans, metrics, processes, and systems to ensure Azenta Life Science products consistently meet the highest standards of reliability, performance, and regulatory compliance.This role serves as a technical quality leader,...

Azenta Life Sciences Partington, Manchester, United Kingdom

Head of Compliance - Medical Device

This senior leadership role involves shaping compliance strategy, strengthening regulatory frameworks, and overseeing global compliance activities for medical devices. You will provide expert guidance, ensure regulatory alignment, and drive quality-related activities in a fast-paced, evolving environment.

SRG United Kingdom

On-site Permanent

Biomedical Field Service Engineer

This role involves performing preventative maintenance and repairs on medical equipment in UK hospitals, ensuring minimal disruption to hospital operations. You will work closely with the site manager, maintain service documentation, and interact with customers and OEM staff, requiring strong communication and technical skills.

Focus Resourcing United Kingdom

On-site Permanent

Automation Engineer - Pharmaceutical

This role involves maintaining and troubleshooting automation and control systems in a GMP-regulated pharmaceutical manufacturing environment. You will participate in computerized system validation, support continuous improvement projects, and collaborate with cross-functional teams to ensure compliance and data integrity.

Smart4Sciences West Yorkshire, United Kingdom

On-site Permanent

Clinical Trial Associate

The Clinical Trial Associate role involves providing high-quality administrative and operational support to clinical, regulatory, and pharmacovigilance teams. Responsibilities include managing trial master files, coordinating site set-up, and supporting data management activities. This role offers hands-on experience in a regulated, quality-driven environment, contributing to the smooth running of multiple clinical studies.

Hyper Recruitment Solutions Gosmore Hill, Hertfordshire, United Kingdom

On-site Permanent

Principal Clinical Research Specialist

The Principal Clinical Research Specialist will lead and manage multi-site clinical studies for Pelvic Health across Europe, ensuring compliance with regulations and delivering high-quality clinical evidence. Responsibilities include designing study protocols, overseeing trial operations, and collaborating with investigators and cross-functional teams.

Medtronic Watford, United Kingdom £64,800 – £97,200 pa

Remote Permanent

Quality Engineer, Validation

The Quality Engineer, Validation is responsible for ensuring robust and repeatable manufacturing processes and test methods, leading validation activities for new and existing processes. This role involves close collaboration with Design Assurance, Operations, and Suppliers to develop validation plans, execute validation phases, and ensure compliance with ISO standards and regulatory requirements.

OrganOx Oxford, United Kingdom

On-site Permanent

Principal Embedded Software Engineer - 6-Month

As a Principal Embedded Engineer, you will work on expanding the feature set of existing medical devices and ensuring the codebase is maintainable. You will collaborate with multidisciplinary teams to develop and productize custom computing devices, optimize performance, and ensure robust and secure software for medical-grade systems.

Medtronic London, United Kingdom

On-site Contract

Band 6 Specialist Biomedical Scientist Histopathology

Job summaryWe have an exciting opportunity as Specialist Biomedical Scientist at Wycombe Hospital in the Histopathology Department of Buckinghamshire Healthcare NHS Trust. You will be work as registered Biomedical Scientist, supporting Senior and Lead Biomedical Scientists while leading the day-to-day...

NHS Professionals High Wycombe, Buckinghamshire, United Kingdom £26 ph

On-site Permanent

Sales and Applications Specialist - Mobile Surgery

This role involves promoting mobile surgery products, providing technical expertise during sales presentations and demonstrations, and supporting account managers in achieving business growth. The candidate will also train customers, maintain customer relationships, and stay updated on product developments and compliance standards.

Philips United Kingdom

Remote Permanent

Full Stack Developer

The Full Stack Developer role involves hands-on software engineering, focusing on building and maintaining high-quality applications and solutions across OrganOx's digital platforms. Responsibilities include coding, API design, database management, DevOps, and collaboration with internal and external teams to support regulated medical device and data solutions.

OrganOx Oxford, United Kingdom

On-site Permanent

Senior Counsel, Global R&D Commercial

This role involves providing strategic legal advice to R&D, IP, and commercial teams, drafting and negotiating complex agreements, and supporting product development and commercialization. The position plays a key role in managing legal risks and enabling business opportunities across global markets.

Smith & Nephew Watford, United Kingdom

Hybrid Permanent

Quality Engineer

As a Quality Engineer, you will lead quality initiatives in a manufacturing environment, ensuring the reliability and compliance of medical devices. You will apply statistical process control, conduct root cause analysis, and collaborate with cross-functional teams to drive continuous improvement and maintain quality standards.

Smith & Nephew Goole, United Kingdom

On-site Permanent

Field Service Engineer

This role involves providing technical support and maintenance for Philips Imaging's advanced healthcare equipment, including installation, repair, and preventive maintenance. The Field Service Engineer will work in a 5x7 rotation, supporting customers remotely and on-site, and must be based in the Newcastle, Durham, or Darlington area.

Philips United Kingdom

Remote Permanent Flexible Clearance Required

Validation Specialist

The Validation Specialist role involves enhancing validation practices, supporting compliance with regulatory inspections, and streamlining processes. You will identify risk areas and implement mitigation strategies to meet standards set by bodies like the MHRA and FDA.

Norgine Hengoed, CF82 7NL, United Kingdom

On-site Contract