Latest regulatory affairs Jobs

Manager Regulatory Medical Writing X-TA

This role involves leading the preparation and finalization of clinical and regulatory documents within a cross-functional environment, with a focus on scientific strategy, submission planning, and team leadership. The manager will guide medical writing activities across multiple therapeutic areas, mentor junior staff, and ensure compliance with regulatory standards such as ICH. The position operates in a hybrid model, requiring collaboration with global teams and active participation in process improvement initiatives.

Johnson & Johnson MedTech

Hybrid Permanent

Manager, Medical Writing, Immunology

Leads medical writing activities for clinical documents in the Immunology therapeutic area, providing scientific and strategic leadership. Manages a team of medical writers, mentors junior staff, and collaborates cross-functionally to ensure regulatory compliance and high-quality documentation. Works within a global regulatory environment, contributing to process improvements and departmental best practices.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Business Development Director

£75,000 - £80,000 per annum + 20% Bonus + Car AllowanceOffice is based in Hampshire, close to the Surrey borderFull Time | PermanentRegular UK Travel requiredOur client is an established international manufacturing and engineering business supplying innovative material solutions to...

HR Dept (Recruitment Agency) Farnborough, Hampshire, GU14 7JT, United Kingdom £75,000 – £80,000 pa

Operations Lead

Lead manufacturing, logistics, and warehouse operations within a regulated life sciences environment, driving performance in safety, quality, and efficiency. Champion lean principles, continuous improvement, and operational transformation while developing teams and supporting site growth. Play a central role in strategic planning, change management, and cross-functional initiatives including new product introductions and scale-up activities.

Hays Procurement Jobs Llantrisant, Mid Glamorgan, United Kingdom £75,000 – £85,000 pa

Design Engineer

This role involves designing and developing injection-moulded products from concept to manufacturing, with a focus on innovation and regulatory compliance. The engineer will create prototypes, validate designs, and collaborate with global teams, particularly in Asia and the US. Work centres on medical or high-regulation applications requiring precision and adherence to quality standards.

Reed Sy164Le, United Kingdom £40,000 – £45,000 pa

Hybrid Permanent

Principal/Senior Scientist MSAT

Exciting Opportunity: Principal/Senior Scientist MSATAre you an experienced bioprocessing scientist looking to work at the interface of development and manufacturing? This organisation is seeking a Principal/Senio Scientist (MSAT) to lead complex projects, support process scale-up, and drive successful delivery into...

SRG Darlington, County Durham, United Kingdom £38,045 – £65,045 pa

Quality Manager

This role involves leading all quality operations at a precision manufacturing site, ensuring compliance with stringent regulatory standards, and driving continuous improvement across processes. The Quality Manager will manage audits, lead root cause investigations, and work closely with production and engineering teams to embed quality and safety into daily operations. The position plays a critical role in maintaining certifications and supporting global customer requirements in a highly regulated environment.

Yolk Recruitment Bridgwater, United Kingdom £50,000 – £55,000 pa

On-site Permanent

Product Design Engineer ( Manufacturing )

Lead the design and development of innovative medical devices from concept through to manufacture, using SolidWorks and applying consumer electronics expertise. Collaborate with cross-functional teams to optimise products for performance, reliability, and manufacturability while ensuring compliance with regulatory standards. Mentor junior engineers and drive continuous improvement within a highly regulated, innovation-driven environment.

Rise Technical Recruitment Warrington, United Kingdom £70,000 – £75,000 pa

On-site Permanent

Electronics Repair Technician

This role involves diagnosing, repairing, and calibrating high-value medical and electronic equipment such as MRI systems, ultrasound probes, and CT/X-ray devices to component level. Working in a specialist electronics laboratory, the technician will use advanced test equipment and reverse-engineer circuits where documentation is limited. The position emphasizes technical problem-solving, compliance with ISO and regulatory standards, and collaboration within an engineering team to extend the life of critical healthcare technology.

Focus Resourcing Theale, Berkshire, United Kingdom

On-site Permanent Clearance Required

Superintendent Pharmacist

This role involves providing clinical and regulatory leadership for a high-growth digital pharmacy processing over 50,000 prescriptions monthly. The Superintendent Pharmacist will shape governance strategy, ensure compliance with GPhC and MHRA standards, and drive innovation in automation and scalable processes within a rapidly expanding medical cannabis dispensing environment.

Montu Pharmaceatiucal Rg415Rb, RG41 5RB, United Kingdom £10,000 – £110,000 pa

Hybrid Permanent

Electronic Systems Engineer

Design and integrate electronic systems for advanced technology, translating requirements into hardware solutions and managing cross-disciplinary interfaces. Work across the full development lifecycle from concept to testing, ensuring compliance with safety and regulatory standards. Collaborate with engineering teams on complex integration challenges in a high-reliability environment.

Innovate Recruitment Stevenage, Hertfordshire, United Kingdom

Hybrid Permanent Clearance Required

Validation/ Quality Assurance Specialist, Pharmaceutical

The Validation Specialist will plan and execute validation activities, author and maintain validation protocols, and collaborate with cross-functional teams to ensure compliance with GMP standards. The role involves maintaining validated status, supporting regulatory inspections, and contributing to the Site Validation Master Plan.

Russell Taylor Group De118Je, DE11 8JE, United Kingdom £30,000 – £34,000 pa

On-site Permanent

Senior NPI Quality Engineer

Senior NPI Quality EngineerElectronics & Medical DevicesCompetitive Salary plus Bonus & BenefitsRelocation Assistance Provided (If Required)Step into a pivotal leadership role as a Senior NPI Quality Engineer and help bring high-quality, regulated products to life from first design through to...

Jonathan Lee Recruitment Jersey Marine, West Glamorgan, SA10 6JJ, United Kingdom

Automation Engineer

This role involves maintaining and improving PLC and control systems across a regulated manufacturing environment, with a focus on automation reliability, continuous improvement, and project delivery. The engineer will lead upgrades, integrate production systems, and ensure compliance with quality and change control standards. A key focus is driving OEE improvements and supporting technology modernisation across the site.

CV Technical Cornwall, United Kingdom £50,000 – £60,000 pa

On-site Permanent

Senior Clinical Trial Administrator

This role involves managing and maintaining Trial Master Files (TMF) and electronic TMFs in compliance with ICH-GCP and company SOPs, supporting clinical trials conducted through external vendors. The Senior Clinical Trial Administrator will lead TMF oversight, conduct quality checks on documentation, coordinate with vendors, and support audits and regulatory inspections. They will also mentor junior staff and contribute to cross-functional study team activities.

GE HealthCare Chalfont St Giles, Buckinghamshire, United Kingdom

Hybrid Permanent