Latest Regulatory Affairs Specialist Jobs

Development & Regulatory Chemist

This role involves developing and validating analytical methods for APIs, authoring and maintaining ASMFs, and supporting regulatory submissions. The chemist will work closely with cross-functional teams to ensure high-quality documentation and compliance with ICH and GMP standards.

SRG Hitchin, Hertfordshire, SG5 1HP, United Kingdom

On-site Permanent

Medical Device Programme Lead

Balance technical, regulatory and commercial challenges in this fulfilling roleThis highly regraded Cambridge-based medical technologies company is seeking a proven engineering leader to help guide high-value development programmes from concept through to transfer to manufacture. Your leadership will accelerate development...

ECM Selection Cambridge, United Kingdom

Quality Control Release Specialist 2

This role involves ensuring compliance with regulatory requirements and company procedures for the release of manufactured medical products. Responsibilities include leading the coordination and training of QC Release personnel, managing quality processes, and supporting continuous improvement initiatives.

Smith & Nephew Goole, United Kingdom

On-site Permanent

Quality Technician

QA TechnicianShift Pattern - Mon - Thurs (6am - 6pm)Position Summary:The QA Technician is responsible for ensuring that all products manufactured meet the highest quality standards and comply with regulatory requirements for medical devices. This role involves performing inspections, testing,...

SRG Shotwick, Cheshire, CH1 6HZ, United Kingdom £38,000 – £43,000 pa

On-site Permanent Shift-work

Technical Engineer

This role involves leading the calibration, maintenance, and repair of medical devices to ensure they meet manufacturer and regulatory standards. You will work both in the field and at the Oxford site, managing audits, approving certificates, and building strong client relationships. The position offers a mix of technical, customer-facing, and leadership responsibilities, supporting the growth of a leading medical device services company.

Progress Sales Recruitment Banbury, Oxfordshire, United Kingdom £40,000 – £50,000 pa

Hybrid Permanent

Instrument Software Validation Analyst

This role involves maintaining validated systems through structured validation processes (IQ/OQ/PQ) and bridging technical software testing with regulatory compliance. Responsibilities include ensuring adherence to FDA, EMA, and GMP regulations, 21 CFR Part 11, GAMP 5 guidelines, and data integrity principles, with a focus on laboratory systems like LIMS and Chromatography Data Systems.

Access Computer Consulting Brussels, Belgium £302 – £345 pd

On-site Permanent

Lead Development Engineer

This role involves leading the design and development of next-generation orthopaedic implants and instrumentation. Responsibilities include creating detailed designs using CAD, FEA, and PLM, mentoring team members, managing design control documentation, and collaborating with manufacturing, quality, and regulatory teams. The position offers opportunities to work with cutting-edge technologies and contribute to impactful medical innovations.

Corin Group Cirencester, gloucestershire, United Kingdom

On-site Permanent

Senior Manufacturing Engineer - CMO

As a Senior Manufacturing Engineer - CMO, you will lead strategic initiatives and projects to enhance the Advanced Wound Management portfolio. You will manage complex changes, collaborate with cross-functional teams and external partners, and ensure regulatory compliance and quality. The role involves developing and implementing key projects to drive product sustainment and value creation, while also providing engineering support to key suppliers and maintaining manufacturing resilience.

Smith & Nephew United Kingdom

Hybrid Permanent

Optical Systems Engineer - Medical Devices - Cambridge

This role involves designing and integrating optical systems into complex medical technologies, from early feasibility to product launch. You will collaborate with a multidisciplinary team to develop devices that improve diagnostics, treatment, and patient outcomes, with a focus on precision, creativity, and regulatory compliance.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Mechanical Design Engineer

This role involves designing and developing mechanical components for wearable medical devices, from concept to production. You will create detailed 3D CAD models, support prototyping and testing, and ensure compliance with regulatory requirements. Working closely with multidisciplinary teams, you will play a key role in transitioning early-stage concepts into robust, manufacturable products.

Cure Talent Loughborough, Leicestershire, LE11 2QG, United Kingdom £30,000 – £40,000 pa

On-site Permanent

Chief Technology Officer

The Chief Technology Officer will lead the technology and product development strategy for a rapidly growing MedTech company. Key responsibilities include guiding multidisciplinary teams, translating customer and commercial requirements into product priorities, and ensuring regulatory compliance. The role involves close collaboration with executive leadership and external stakeholders.

Cure Talent Nottingham, Nottinghamshire, United Kingdom £100,000 – £120,000 pa

On-site Permanent

Senior Project Manager

The Senior Project Manager will lead complex projects across the Specialty Diagnostics Group, focusing on business transformation and change control. Key responsibilities include managing project tasks, budgets, risks, and documentation, as well as mentoring staff and contributing to strategic direction.

Manpower Basingstoke, Hampshire, United Kingdom £40 – £500 ph

Hybrid Permanent Flexible

Mechanical Design Engineer

The Mechanical Design Engineer will support the design and development of advanced packaging and automation equipment, from initial concept to final commissioning. Responsibilities include creating design specifications, selecting materials, producing CAD drawings, and ensuring compliance with regulatory standards.

Recruit 2 You Castle Donington, Leicestershire, United Kingdom £35,000 – £45,000 pa

On-site Permanent

Global Clinical Study Manager

The Global Clinical Study Manager will oversee the end-to-end delivery of complex clinical studies, ensuring milestones, timelines, and budgets are met. Key responsibilities include managing cross-functional teams, coordinating with vendors, and ensuring compliance with regulatory requirements. This role requires strong leadership and project management skills, with a focus on driving high-quality study execution in a fast-paced environment.

Carbon 60 London, United Kingdom £500 – £615 pd

Remote Temporary Flexible

Supplier Quality Engineer

As a Supplier Quality Engineer, you will lead the supplier quality management programme, ensuring suppliers meet regulatory and quality standards. You will work closely with Engineering, Manufacturing, and Quality teams, conduct supplier audits, manage quality agreements, and support design reviews and risk management. This role involves regular UK and international travel and offers a hybrid working model with 3 days on-site per week.

ProTech Recruitment Ltd Oxfordshire, United Kingdom £50,000 – £55,000 pa

Hybrid Permanent