Latest Managed Services Jobs

CAP Sr. Mgr OTC BPO Depuy

This role involves leading the Order-to-Cash (OTC) process globally for DePuy Synthes, ensuring end-to-end process design, governance, and performance. The manager will partner with supply chain, finance, and commercial teams to drive continuous improvement, compliance, and operational excellence in a complex, regulated medical technology environment.

Johnson & Johnson MedTech United States

On-site Permanent

CAP Sr. Mgr OTC BPO Depuy

This role involves leading the Order-to-Cash (OTC) process globally, ensuring end-to-end ownership, standardization, and continuous improvement. The Sr. Manager will partner with various teams to drive operational excellence, customer satisfaction, and financial performance, while also supporting system implementations and compliance with regulatory standards.

Johnson & Johnson MedTech

On-site Permanent

Affera Regional Clinical Educator

The Affera Regional Clinical Educator role involves driving clinical excellence among Affera Mapping Specialists in the UK. Responsibilities include in-field training, coaching, and support for the rollout of the Affera Mapping System and other electrophysiology technologies. The role requires strong expertise in electrophysiology and cardiac mapping, as well as the ability to develop and deliver tailored training programs.

Medtronic Watford, United Kingdom

On-site Permanent

Clinical Development Specialist

This role involves leading the launch and adoption of the Affera Mapping System and Cardiac Ablation Solutions (CAS) portfolio. Responsibilities include site initiations, providing clinical and technical expertise, training clinicians, and ensuring regulatory compliance. The role requires a strong background in electrophysiology and ablation technologies, with a focus on 3D mapping systems and complex EP procedures.

Medtronic Watford, United Kingdom

On-site Permanent

Senior Specialist, Evidence Evaluation

In this role, you will create robust clinical evidence documentation to support the CE registration of medical devices, working closely with cross-functional teams to ensure product safety and performance. You will act as a subject matter expert, engaging in regulatory interactions and strategic business decisions.

Smith & Nephew Cannock Chase, United Kingdom

Hybrid Permanent

Contract Excellence Lead - International

Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We are looking for a Contract Excellence Lead for our International region to join our Commercial Centre of Excellence. In this influential role, you will shape...

Smith & Nephew Watford, United Kingdom

Biosurgery Sales Specialist| J&J MedTech | Surgery | Midlands

This role involves driving sales growth for Johnson & Johnson MedTech's Biosurgery portfolio in key private and NHS centres across the Midlands. Responsibilities include account planning, market analysis, and collaboration with the wider J&J MedTech team to maximize sales opportunities and adopt new technologies.

Johnson & Johnson MedTech Birmingham, United Kingdom

On-site Permanent

Associate Director, Regulatory Policy

The Associate Director, Regulatory Policy, provides leadership in regulatory compliance and policy, ensuring alignment with global and regional requirements. Key responsibilities include interpreting regulatory policies, developing internal guidelines, and supporting cross-functional teams to manage regulatory risks and enable informed decision-making.

Johnson & Johnson MedTech United Kingdom

On-site Permanent

Principal Portfolio Lead Clin Prog

This role involves formulating and executing the clinical programming strategy for a portfolio of medium to high complexity clinical trials. Responsibilities include planning, resource allocation, cross-functional collaboration, and ensuring compliance with quality and regulatory standards.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Biosurgery Sales Specialist| J&J MedTech | Surgery | East Midlands

This role involves driving sales growth for Johnson & Johnson MedTech's Biosurgery portfolio in key surgical centers across the West Midlands. Responsibilities include account planning, market analysis, and building strong relationships with healthcare professionals to promote the adoption of new surgical technologies and solutions.

Johnson & Johnson MedTech United Kingdom

On-site Permanent

New Technology Specialist - Midlands - Johnson & Johnson MedTech | Electrophysiology

This role involves driving the adoption of new electrophysiology technologies in the Midlands region by providing expert clinical and technical support during product launches and in-field procedures. The specialist will lead training, design clinical evaluations, and act as a liaison between customers and internal teams to ensure successful implementation of new products like CARTO. A strong background in electrophysiology and a proven track record in field-based technical sales are essential.

Johnson & Johnson MedTech

Hybrid Permanent

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, CSRs, and IB updates. 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 High Wycombe, United Kingdom

On-site Permanent

Senior Clinical Trial Leader

The Senior Clinical Trial Leader role involves planning and executing clinical trials for innovative medical devices, working closely with cross-functional teams, clinical sites, and external partners. The position focuses on advancing clinical research and ensuring quality and compliance in the development of medical devices that improve patient outcomes.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, CSRs, and IB updates. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead on specific projects under supervision.

Johnson & Johnson MedTech Canada

Remote Permanent

Medical Writer II, Oncology

The Medical Writer II, Oncology role involves writing and coordinating clinical and regulatory documents, such as Phase 1-3 protocols, CSRs, and IB updates. You will work in a team environment, applying internal standards and regulatory guidelines, and participate in process working groups to support the development of oncology treatments.

Johnson & Johnson MedTech Switzerland

On-site Permanent