Latest Managed Services Jobs

Senior Manager, HCC EMEA Regional Office & Risk Management COE – Orthopaedics

This role involves providing strategic healthcare compliance leadership across EMEA for Johnson & Johnson MedTech’s Orthopaedics division. The Senior Manager will act as a compliance advisor to regional business functions, embed compliance into commercial processes, lead risk management initiatives, and monitor evolving regulations. The position plays a key role in maintaining integrity and compliance maturity across diverse markets ahead of the planned spin-off of the Orthopaedics business into DePuy Synthes.

Johnson & Johnson MedTech

Hybrid Permanent

Senior Manager, HCC EMEA Regional Office & Risk Management COE – Orthopaedics

This role leads healthcare compliance and risk management for Johnson & Johnson MedTech’s Orthopaedics business across EMEA. The Senior Manager will advise regional stakeholders on compliance integration, drive risk mitigation strategies, and strengthen controls within commercial operations. The position plays a key role in maintaining integrity across regulated markets and will transition to the new standalone orthopaedics company, DePuy Synthes, upon separation.

Johnson & Johnson MedTech

Hybrid Permanent

Medical Affairs Senior Program Manager

Lead the planning and execution of strategic medical affairs programs, working cross-functionally to translate scientific objectives into actionable initiatives. Support evidence generation, publication planning, and medical education activities aligned with Medtronic's therapies. Operate in a global environment with frequent international travel and collaboration across clinical, regulatory, and commercial teams.

Medtronic €95,920 – €143,880 pa

Medical Affairs Senior Program Manager

Lead the planning and execution of strategic Medical Affairs programs, working cross-functionally to deliver scientific initiatives that support the safe and effective use of Medtronic therapies. Drive project timelines, stakeholder alignment, and process improvements within a global healthcare technology environment.

Medtronic

On-site Permanent

Senior Design Assurance Engineer

The Senior Design Assurance Engineer leads risk management activities across the full product lifecycle for Class II and III medical devices, ensuring compliance with ISO 14971 and regulatory standards. This role involves developing and maintaining risk documentation, facilitating cross-functional risk reviews, and integrating risk controls into design verification. The position supports ongoing product improvement by monitoring post-market data and contributing to quality processes within a growing medical technology team.

OrganOx Oxford, United Kingdom

On-site Permanent

System Test Technician

The role involves executing system-level testing across electrical, mechanical, software, and medical components for Class 3 medical devices used in organ perfusion. The technician will perform functional, safety, and reliability testing, maintain documentation for regulatory compliance, build test fixtures, and support continuous improvement of test procedures within an ISO 13485 and MDR-regulated environment.

OrganOx Oxford, United Kingdom

On-site Permanent

Quality Engineering Lead

Lead quality engineering efforts for medical devices, focusing on statistical process control, root cause analysis, and continuous improvement using Lean Six Sigma methodologies. Provide technical leadership during audits, validations, and new product introductions while mentoring junior engineers. Work cross-functionally to ensure compliance with ISO13485 and reduce cost of poor quality through data-driven initiatives.

Smith & Nephew Goole, United Kingdom

Hybrid Permanent

Senior Regulatory Affairs Specialist

This role involves managing regulatory compliance for advanced wound care medical devices throughout their lifecycle, including preparing global regulatory submissions, guiding product development teams, and liaising with regulatory authorities. The specialist ensures adherence to standards such as ISO 13485, FDA 21 CFR Part 820, cGMP, and cGDP, while reviewing product documentation and supporting continuous improvement. Based in Hull, the position operates within a collaborative, global team environment focused on bringing innovative healthcare products to market.

Smith & Nephew United Kingdom

Hybrid Permanent

Manufacturing Engineer

This role involves designing and optimizing manufacturing processes for medical devices, with a focus on instrumentation and electromechanical systems. The engineer will lead process improvements, support verification and validation at contract manufacturing organizations (CMOs), and ensure compliance with quality standards. Key responsibilities include driving design for manufacturability, managing technical projects, and maintaining rigorous documentation within a regulated environment.

GxPeople Global Trowbridge, Wiltshire, BA14 8EY, United Kingdom £55,000 – £65,000 pa

Production Chemist

The role involves manufacturing high-accuracy calibration and reference gases using gravimetric methods, preparing gas cylinders, and ensuring strict adherence to quality and safety standards. The chemist will work within a production team to meet customer specifications and support logistics, maintaining compliance with ISO 6142 and ISO 17034. The position offers structured training and career progression within a global industrial gases company.

Pertemps Leeds Uttoxeter, Staffordshire, United Kingdom £31,000 – £34,000 pa

Area Sales Representative (MedTech)

This role involves selling MedTech devices to healthcare, research, and pharmaceutical clients across South London, Surrey, and Kent. The successful candidate will work autonomously, managing a local patch with a 60/40 split between new business development and account management. After comprehensive training, they will demonstrate equipment, generate leads, and drive sales within a globally respected biomedical laboratory equipment company.

Ernest Gordon Recruitment Guildford, Surrey, United Kingdom £45,000 – £50,000 pa

Hardware Design Engineer - TechBio

Design and develop advanced hardware systems for a programmable TechBio platform, focusing on sensor integration, mixed-signal PCB design, and full-cycle electronics development from concept to field deployment. Work closely with cross-functional teams to innovate and industrialise novel electrochemical and optical sensing solutions. This role requires deep expertise in analog front-end design, Altium, and hands-on validation of complex sensor systems.

Newton Colmore Guatemala

Regulatory Affairs Specialist

This role involves ensuring product compliance with UK and international regulations, particularly in food contact materials and packaging legislation. The specialist will interpret evolving regulatory requirements, assess compliance for raw materials and finished products, and support new product development. Collaboration with technical, R&D, production, and commercial teams is central to providing practical regulatory solutions that align with business objectives.

Cranleigh Scientific Carlisle, Cumbria, CA3 8LU, United Kingdom

Clinical Trials Assistant

Support the delivery of ophthalmic clinical trials by assisting with participant coordination, data management, imaging, and sample processing within a private eye clinic. Gain hands-on experience in clinical research procedures including OCT and retinal imaging, phlebotomy, and Good Clinical Practice compliance. Work alongside leading clinicians in a technology-rich, on-site environment with structured training and career development opportunities.

IDA Recruitment Ltd Cavendish Square, London, United Kingdom £28,000 – £30,000 pa

On-site Permanent

Delivery Lead

This role involves leading the end-to-end delivery of platform features and releases for a clinical technology platform used in global trials. The Delivery Lead will coordinate cross-functional teams including Engineering, Testing, and Operations, ensuring timely, high-quality releases with strong focus on operational readiness, change management, and continuous improvement. The position requires proactive risk management, stakeholder alignment, and optimisation of delivery processes within an Agile environment.

Leo Technology London, United Kingdom £70,000 – £90,000 pa