Medical Technology Jobs

Technical Sourcing Program Manager

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 London, United Kingdom

Service Marketing Manager EMEA

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing...

Medtronic

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

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

Lead Product Analyst, IM SCT Deliver – Customer Order Experience

The Lead Product Analyst will manage IT solutions for customer order experiences, collaborating with business and technology teams to deliver user-centric, industry-leading strategies. Key responsibilities include driving integration with commercial and supply chain systems, evaluating industry capabilities, and fostering a culture of innovation and talent development.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Medical Advisor/Sr. Medical Advisor

This role involves providing high-quality medical input and leadership in oncology, collaborating with cross-functional teams to drive medical strategy and patient outcomes. Responsibilities include building expertise in oncology, gathering field insights, and contributing to evidence generation and medical affairs projects.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Sr. Manager, Safety/PSM

Leads environmental, health, safety, and Process Safety Management (PSM) programs at a manufacturing site, ensuring regulatory compliance and driving a strong safety culture. Focuses on risk-based safety integration, incident investigation, and continuous improvement in highly regulated MedTech environments.

Johnson & Johnson MedTech United States £122,000 – £245,000 pa

On-site Permanent

Sr. Manager, Safety/PSM

This role leads environmental, health, safety, and Process Safety Management (PSM) programs at a manufacturing site, ensuring regulatory compliance and driving a strong safety culture. The position acts as the site's PSM subject-matter expert, conducting hazard analyses, incident investigations, and risk mitigation in collaboration with operations and leadership. It focuses on continuous improvement of safety systems and fostering accountability across teams.

Johnson & Johnson MedTech US$122,000 – US$245,000 pa

On-site Permanent

D&A and Master Data Specialist

This role focuses on maintaining master data integrity across commercial systems, ensuring data accuracy, compliance, and consistency. The specialist will implement data governance practices, support MDM system implementations, and collaborate with cross-functional teams to improve data processes. Using tools like Power BI and Excel, they will generate insights and support data quality initiatives across regions.

Johnson & Johnson MedTech Germany €62,500 – €97,865 pa

Hybrid Permanent

Experienced Regulatory Affairs Professional EMEA

This role involves developing and executing regulatory strategies for pharmaceutical products in the EMEA region, with a focus on oncology. The professional will support submissions to health authorities, including clinical trial applications and marketing authorization dossiers, while collaborating with cross-functional teams and regulatory agencies. Key responsibilities span pre-authorization, authorization, and post-approval lifecycle management across solid tumour therapies.

Johnson & Johnson MedTech

Hybrid Permanent

Experienced Regulatory Affairs Professional EMEA

This role involves developing and executing regulatory strategies for solid tumour pharmaceutical products across Europe, the Middle East, and Africa. The professional will lead submissions to health authorities, support clinical trial applications, marketing authorizations, and lifecycle management, while collaborating with cross-functional teams and regulatory agencies. Expertise in EMA procedures and oncology regulations is central to ensuring compliance and timely product commercialization.

Johnson & Johnson MedTech

Hybrid Permanent

Experienced Regulatory Affairs Professional EMEA

This role involves developing and executing regulatory strategies for solid tumour products across Europe, the Middle East, and Africa, with a focus on clinical trial applications, marketing authorisation submissions, and lifecycle management. The professional will collaborate with cross-functional teams and regulatory agencies, ensuring compliance and timely approvals for oncology pharmaceuticals. Work includes drafting submissions, responding to health authority queries, and supporting scientific advice procedures.

Johnson & Johnson MedTech Poland PLN 121,000 – PLN 194,350 pa

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role leads clinical risk management across therapeutic areas, ensuring trial data integrity, patient safety, and regulatory compliance. The Associate Director drives risk-based oversight, inspection readiness, and quality assurance for clinical trials, working closely with global teams to identify, assess, and mitigate risks. They also support audits, develop quality strategies, and provide expert guidance on GCP and regulatory standards.

Johnson & Johnson MedTech United States US$122,000 – US$212,750 pa

Hybrid Permanent

Assoc Director, Clinical Risk Management

This role involves leading clinical risk management across multiple therapeutic areas, focusing on ensuring trial data integrity, patient safety, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, and guide cross-functional teams in implementing quality strategies throughout clinical development. A key aspect is providing expert advice on quality issues and leading continuous improvement in clinical trial quality systems.

Johnson & Johnson MedTech Switzerland

Hybrid Permanent

Associate Director, Clinical Risk Management

This role involves leading clinical risk management across multiple therapeutic areas, focusing on identifying, assessing, and mitigating quality risks in clinical trials to ensure patient safety, data integrity, and regulatory compliance. The position supports inspection readiness, drives risk-based oversight, and collaborates with cross-functional teams to implement effective quality strategies and corrective actions.

Johnson & Johnson MedTech Spain

Hybrid Permanent