Latest regulatory affairs specialist Jobs

Quality Assurance & Regulatory Affairs Specialist - MedTech

This role involves ensuring quality assurance and regulatory compliance across the full lifecycle of advanced medical devices, from design through manufacturing, for global markets including Europe, North America, and APAC. The specialist will conduct internal audits, help shape regulatory strategy, and work with complex, innovative technologies in a high-autonomy environment. The role focuses on new product development, requiring strict adherence to ISO 13485, CE Marking, and other international standards.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £45,000 – £49,000 pa

On-site Permanent

Sr. Source Reg Compliance Specialist

The Sr. Source Regulatory Compliance Specialist is responsible for ensuring suppliers and externally provided processes comply with regulatory requirements and quality standards. Key responsibilities include executing supplier audits, supporting compliance oversight, and maintaining documentation. The role involves close collaboration with Quality, Regulatory Affairs, Supply Chain, and Procurement teams to maintain product quality and supply continuity.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Mechanical Engineer - Genomics Instrumentation - Cambridge

You will work within a multidisciplinary team to design and develop cutting-edge genomics instrumentation, contributing to high-throughput genomic workflows and precision diagnostics. Your role involves the full product lifecycle, from concept development to product launch.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Post Doctoral Researcher, Evaluation & Standards in Clinical Operations

This role involves developing evaluation frameworks and rubrics for AI agents in clinical operations and global development. Responsibilities include designing quality dimensions, running human evaluation protocols, and building benchmark datasets. The position requires a strong understanding of clinical operations, regulatory documentation, and AI systems.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Regulatory Affairs Manager

Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business...

Cure Talent Curbridge, Oxfordshire, United Kingdom

Quality & Regulatory Associate

This role involves supporting the Quality Management System (QMS) and Regulatory processes, including ISO13485 readiness and FDA 510(k) documentation. You will work closely with internal teams to maintain quality documentation, manage change controls, and promote continuous improvement.

Taylorollinson Manchester, United Kingdom £35,000 – £45,000 pa

Hybrid Permanent

Quality and Regulatory Labelling Program Manager

This role involves leading global labelling initiatives to ensure compliance with regulatory standards across various markets. The Program Manager will collaborate with cross-functional teams to manage change controls, mitigate risks, and drive continuous improvement in labelling processes.

Randstad Engineering Popley, Hampshire, RG24 9TW, United Kingdom £27 ph

Hybrid Contract

Technical Writer

The Technical Writer will create and maintain technical and customer-facing documents, ensuring accuracy and up-to-date information across Regulatory Affairs, Marketing, and Technical Services. The role involves working with multiple stakeholders, managing documentation, and supporting continuous improvement initiatives.

Talentmark Burgess Hill, West Sussex, United Kingdom £264 – £331 pd

Hybrid Contract Clearance Required

Plant Quality Manager

This role involves leading all Quality Assurance and Quality Control activities at a manufacturing site producing both cosmetic and medical device products. The Plant Quality Manager will ensure compliance with GMP, ISO 13485, and ISO 22716 standards, support regulatory audits, and drive a culture of quality across departments. The position requires close collaboration with operations, engineering, regulatory affairs, and R&D teams to maintain high-quality standards in a regulated environment.

New Appointments Group Ct201Jt, CT20 1JT, United Kingdom

On-site Permanent

Process Engineer, Validation

The Process Engineer, Validation leads and executes validation activities for new product ranges and changes to existing medical devices. They ensure all manufacturing processes, equipment, and test methods meet internal and external regulatory standards, working closely with cross-functional teams and external partners. The role involves developing validation strategies, authoring protocols, conducting risk assessments, and supporting regulatory submissions.

OrganOx Oxford, United Kingdom

On-site Permanent

Software Quality Engineer

The Software Quality Engineer supports software quality assurance by ensuring regulatory compliance in software lifecycle documentation, testing, and adherence to coding standards. They will work closely with R&D, Post-Market Engineering, and Quality teams to manage design and development, risk assessment, and change control processes.

OrganOx Oxford, United Kingdom

On-site Permanent

Global Medical Advisor - Hepatitis

This role involves leading global medical strategy for hepatitis therapies, shaping scientific direction across the product lifecycle. The advisor will drive cross-functional collaboration, engage with key external experts, and translate clinical insights into evidence-based strategies. It focuses on scientific excellence, compliance, and generating impactful data to support patient outcomes.

Norgine Uxbridge, UB8 1SB, United Kingdom

On-site Permanent

Medical Advisor

Want a 3D Career? Join Norgine.At Norgine, our colleaguesDare themselves to be different and try new things,Drive to achieve their goals and beyond, andDevelop themselves and their community.We call it the3D career at Norgine and it offers you a fully-rounded...

Norgine Uxbridge, UB8 1SB, United Kingdom

Hybrid

QA/RA Manager

This role involves leading the design and implementation of regulatory and quality management systems for a portfolio of Class I medical devices, ensuring compliance with ISO 13485, 21 CFR 820, and evolving global regulations. The candidate will oversee a digital EQMS, lead audits, manage post-market surveillance, and build a high-performing remote team. They will act as the primary liaison with regulatory authorities and embed a proactive compliance culture across R&D, supply chain, and commercial functions.

SRG London, United Kingdom

Hybrid Permanent

Regulatory Manager

As a Regulatory Manager, you will lead regulatory strategy for drug-device combination products, working closely with global regulatory bodies and clients. You will manage a small team, contribute to regulatory intelligence, and represent the regulatory function in senior meetings.

HAYS Specialist Recruitment Cheshire, United Kingdom

On-site Permanent