Latest Managed Services Jobs

Clinical Specialist Trauma |Johnson & Johnson MedTech | Orthopedics| North- West

This role involves providing in-theatre support to orthopaedic consultants and nursing staff, ensuring the correct use of DePuy Synthes products. Responsibilities include training, stock management, customer education, and developing business opportunities across key accounts. The Clinical Specialist will also support medical education events and maintain strong relationships with clinical partners.

Johnson & Johnson MedTech

On-site Permanent

Sales Specialist Trauma |Johnson & Johnson MedTech | Orthopedics|

The Sales Specialist role involves achieving sales targets and promoting DePuy Synthes' orthopedic and trauma products to key stakeholders in secondary care. Responsibilities include developing business plans, managing customer relationships, and driving the adoption of new technologies while maintaining core business.

Johnson & Johnson MedTech United Kingdom

On-site Permanent

Senior Therapy Sales Specialist

This role involves working with the Acute Care & Monitoring (ACM) Team to drive sales and clinical education for Medtronic's Perioperative Complications product range in Scotland. Responsibilities include providing expert knowledge, building relationships with clinical stakeholders, and educating customers on the safe and effective use of Medtronic's products in operating rooms.

Medtronic Edinburgh, Alba / Scotland, United Kingdom £55,040 – £82,560 pa

On-site Permanent

Technical Consultant - Spine

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeThe...

Medtronic United Kingdom £42,000 – £63,000 pa

On-site Permanent Flexible

Surgical Training Technician

As a Surgical Training Technician, you will prepare and maintain laboratory spaces for surgical education, support live training sessions, and ensure compliance with regulatory frameworks. You will work closely with Medical Education, Marketing, and R&D teams, managing stock levels and maintaining inventory systems.

Smith & Nephew Watford, United Kingdom

On-site Permanent

Operational Quality 1

The Operational Quality 1 role involves maintaining high standards of quality and compliance in the manufacturing process. Responsibilities include reviewing and releasing product documentation, managing non-conformances, and supporting quality audits. The role also involves leading investigations and dispositions of defective materials and ensuring compliance with quality management systems.

Smith & Nephew Goole, United Kingdom

Hybrid Permanent

Senior Clinical Trial Leader

The Senior Clinical Trial Leader will support the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance while contributing to innovative medical device development that improves patient outcomes.

Johnson & Johnson MedTech United States

On-site Permanent

Senior Clinical Trial Leader

The Senior Clinical Trial Leader will support the planning and execution of clinical trials for DePuy Synthes, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance in the development of innovative medical devices that improve patient outcomes.

Johnson & Johnson MedTech

On-site Permanent

Senior Clinical Trial Leader

The Senior Clinical Trial Leader will support the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance while contributing to innovative medical device development that improves patient outcomes.

Johnson & Johnson MedTech

On-site Permanent

Senior Clinical Trial Leader

The Senior Clinical Trial Leader will support the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance while contributing to innovative medical device development that improves patient outcomes.

Johnson & Johnson MedTech

On-site Permanent

Clinical Trial Leader

The Clinical Trial Leader role involves supporting the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The position focuses on ensuring trials are conducted with quality and compliance, contributing to the development of innovative medical devices that improve patient outcomes.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Associate Director, RA UK & Ireland

The role involves leading and overseeing regulatory affairs activities for the UK market, ensuring compliance with UK and EU regulations, and managing regulatory risk. The Associate Director will partner with various teams to support product registrations, lifecycle management, and business initiatives, while also leading the UKCA marking strategy and coaching regulatory team members.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating clinical documents, such as Phase 1 protocols and clinical study reports, for oncology treatments. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech United States

On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating basic clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, and initial IBs. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech

Hybrid Permanent

Medical Writer II, Oncology

The Medical Writer II, Oncology role involves writing and coordinating clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, and initial IBs. You will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech

Hybrid Permanent