Medical Technology Jobs

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

Principal Affera Therapy Specialist

This role involves providing expert clinical and technical support for cardiac ablation systems, training physicians and EP Lab Staff, and driving sales. The position is critical for launching new products and ensuring technology acceptance across hospital stakeholders.

Medtronic Watford, United Kingdom £68,640 – £102,960 pa

On-site Permanent

Site Director, Hull & Melton

Lead and transform a strategically important manufacturing site within a highly regulated medical technology environment. Drive operational excellence across manufacturing, quality, regulatory, R&D, and finance functions while fostering a culture of innovation and continuous improvement. Serve as a key member of the global operations leadership team, influencing broader supply chain strategy and large-scale transformation initiatives.

Smith & Nephew Melton, 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

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

Import/Export Operations Specialist

The Import/Export Operations Specialist ensures the compliant and efficient movement of medical devices across international borders. Responsibilities include managing customs processes, preparing trade documentation, and coordinating with freight forwarders and internal stakeholders to resolve shipment issues and maintain regulatory compliance.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Manager, Trial Delivery Management

This role involves managing the execution of clinical trials, including creating trial-specific documentation, overseeing vendor activities, and coordinating regional trial operations. The manager ensures alignment of feasibility strategies, conducts risk reviews, and supports compound training initiatives across global teams. It emphasizes operational oversight, compliance, and cross-functional collaboration in a matrixed environment.

Johnson & Johnson MedTech PLN 251,000 – PLN 483,000 pa

On-site Permanent

Lead, Trial Delivery Management

This role involves leading the execution of clinical trial activities, including managing trial-specific documentation, overseeing vendor operations, and coordinating country or regional trial management efforts. The position requires input into operational strategies, risk mitigation, and support for compound training development, with a focus on ensuring compliance and efficient study delivery across global teams. It also includes mentoring team members and contributing to process improvements across clinical trial functions.

Johnson & Johnson MedTech United States

On-site Permanent

Lead, Trial Delivery Management

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...

Johnson & Johnson MedTech Canada

Lead, Trial Delivery Management

This role leads the execution of clinical trial activities, including managing trial-specific documentation, vendor oversight, and regional operational delivery. The position ensures alignment of feasibility strategies, conducts risk reviews, and supports compound training across global teams. It involves mentoring team members and contributing to process improvements within a matrixed, global environment.

Johnson & Johnson MedTech €72,500 – €115,230 pa

Hybrid Permanent

Lead, Trial Delivery Management

This role involves leading the execution of clinical trial activities, managing trial-specific documentation, overseeing vendor operations, and coordinating regional delivery efforts. The position ensures alignment of feasibility strategies, conducts risk assessments, and supports compound training development across global teams. It also includes mentoring team members and contributing to process improvements in clinical trial management.

Johnson & Johnson MedTech €48,600 – €77,395 pa

On-site Permanent

Lead, Trial Delivery Management

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...

Johnson & Johnson MedTech Belgium

Lead, Trial Delivery Management

This role involves leading the execution of clinical trial activities, including managing trial-specific documentation, overseeing vendor operations, and coordinating regional trial delivery. The candidate will support compound training, contribute to operational strategies, and ensure compliance with regulatory and quality standards across global studies. They will also mentor team members and support process improvements and health authority inspections.

Johnson & Johnson MedTech €55,400 – €87,860 pa

Hybrid Permanent

Content Compliance Specialist

This role involves managing and improving content compliance and copy review processes across EMEA markets for MedTech promotional materials. The specialist ensures regulatory adherence, supports audit readiness, and drives process efficiency through digital tools, AI, and automation. They provide guidance to submitters, maintain documentation, and contribute to system enhancements in a multilingual, cross-regional environment.

Johnson & Johnson MedTech €67,500 – €106,835 pa

Hybrid Permanent

Associate Director, Safety Analysis Scientist

This role involves leading the scientific safety assessment of pharmaceutical products across development and post-marketing stages, with responsibility for analyzing complex medical data, supporting global safety strategy, and contributing to regulatory compliance. The scientist will lead safety evaluations, guide cross-functional teams, and ensure high-quality reporting while acting as a subject matter expert during audits and inspections. Innovation in data presentation and process improvement is emphasized within a hybrid work environment.

Johnson & Johnson MedTech Belgium

Hybrid Permanent