Latest Project Services Jobs

Manager, Global Transparency Reporting - EMEA

Lead and manage end-to-end global transparency reporting for Johnson & Johnson MedTech across EMEA, ensuring compliance with evolving regulations and industry codes. You will oversee data collection, validation, and submission processes while leading a team and driving process improvements through automation and analytics. This role involves close collaboration with compliance, legal, finance, and technology stakeholders to strengthen reporting governance and implement scalable digital solutions.

Johnson & Johnson MedTech

Hybrid Permanent

Manager, Global Transparency Reporting - EMEA

Lead and oversee end-to-end global transparency reporting for Johnson & Johnson MedTech across EMEA, ensuring compliance with local and international regulations. Manage a team, drive process improvements, and act as a compliance advisor to stakeholders. Leverage data analytics and digital tools to enhance reporting accuracy and efficiency while maintaining governance and audit readiness.

Johnson & Johnson MedTech

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

Medical Affairs Senior Program Manager

Leads strategic medical affairs programs and cross-functional initiatives, translating scientific objectives into actionable plans. Focuses on medical education, evidence generation, publication planning, and stakeholder alignment across global and regional teams. Works closely with leadership to enhance processes and support the safe, effective use of Medtronic's medical technologies, including robotic systems like Hugo™ RAS.

Medtronic

Principal Mechanical Design Engineer - Medical Devices

Principal Mechanical Design Engineer - Medical Devices - CambridgeA growing Medical Devices team, based in Cambridge, is currently seeking an experienced Mechanical Design Engineer to lead the development of cutting-edge Medical Devices in the fields of Health Technology, Biotech, and...

Newton Colmore Cambridge, United Kingdom

Permanent

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

Start Up Senior Trial Manager, Early Development

This role involves managing early development clinical trials in the UK, with dual responsibilities in trial management and study start-up activities. The candidate will oversee local trial operations, ensure compliance with regulatory and ethical standards, and coordinate UK regulatory submissions and approvals. They will act as a bridge between trial delivery and start-up teams, driving process improvements and mentoring junior staff in a hybrid working environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Associate Development Engineer

Design and develop new orthopaedic implants and surgical instruments for hip surgery, focusing on innovation, manufacturability, and patient impact. Work within a multidisciplinary R&D team to advance product development from concept to commercialization using engineering analysis, prototyping, and cross-functional collaboration.

Johnson & Johnson MedTech United States

On-site Permanent

Manager Medical Writing XTA

This role involves leading the preparation and finalization of clinical and regulatory documents across multiple therapeutic areas, with a focus on scientific strategy, project leadership, and cross-functional collaboration. The individual will act as a primary point of contact for medical writing activities, mentor junior staff, and ensure compliance with regulatory guidelines such as ICH. The position requires strong scientific communication, project management, and leadership skills within a hybrid work environment.

Johnson & Johnson MedTech United States US$117,000 – US$201,250 pa

Hybrid Permanent

Manager Medical Writing XTA

Leads the development and finalization of clinical and regulatory documents across multiple therapeutic areas, providing scientific and strategic direction for writing teams. Provides mentorship to junior staff, drives process improvements, and serves as a key liaison between medical writing and cross-functional teams. Works independently to ensure compliance with regulatory standards and supports submission activities.

Johnson & Johnson MedTech US$117,000 – US$201,250 pa

Hybrid Permanent

Manager Medical Writing XTA

Leads the preparation and finalization of clinical and regulatory documents within a cross-functional environment, providing scientific and strategic direction for medical writing activities across multiple therapeutic areas. Responsible for mentoring junior staff, driving process improvements, and ensuring compliance with regulatory standards such as ICH guidelines. Works closely with clinical teams to coordinate submissions and maintain high-quality documentation.

Johnson & Johnson MedTech US$117,000 – US$201,250 pa

Hybrid Permanent

Senior Research and Test engineer

This role involves leading the development and execution of test methods for medical implants and instrumentation, with a focus on kinematics and tribology. The engineer will perform verification and research testing, create test protocols, analyze data, and support regulatory submissions while ensuring compliance with quality standards. Collaboration with R&D, Quality, and global teams is key, along with mentoring staff and improving testing processes.

Johnson & Johnson MedTech Leeds, United Kingdom

Medical Affairs Tender Evidence Manager

Manages the end-to-end tender clinical evidence process across EMEA, ensuring submissions are scientifically robust, compliant, and optimized for quality scoring. Develops and coordinates evidence packages using scientific literature, collaborates cross-functionally with medical, clinical, and commercial teams, and supports evidence-based selling initiatives. Leads a regional team and serves as primary liaison for medical-scientific inquiries and tender readiness.

Johnson & Johnson MedTech Leeds, United Kingdom

Sr Manager Intl Clinical Research

This role involves leading international clinical evidence generation projects, supporting health technology assessments, and translating clinical data into actionable resources for market access and commercial teams. The position works across EMEA with a focus on orthopaedics, particularly joint reconstruction and digital surgery, while collaborating with global and regional stakeholders to align clinical strategies and disseminate scientific findings.

Johnson & Johnson MedTech Leeds, United Kingdom

Endomech Sales Specialist|Johnson & Johnson MedTech | Surgery| West Midlands

This role involves driving the adoption of advanced surgical technologies by building strong relationships with surgeons and healthcare professionals in the West Midlands. The specialist will lead account planning, deliver value-based selling, and support clinical education initiatives to grow market share. Focus is on consultative engagement, territory management, and promoting Johnson & Johnson's Endomech energy products within secondary care settings.

Johnson & Johnson MedTech Birmingham, United Kingdom

Hybrid Permanent