Latest Medical Devices Jobs

Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation by leveraging deep surgical expertise and insights into the local healthcare ecosystem. Key responsibilities include stakeholder engagement, evidence strategy, and scientific leadership to support regulatory approval, market access, and clinical adoption of J&J MedTech products.

Johnson & Johnson MedTech Liverpool, United Kingdom
On-site Permanent

Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation by leveraging deep surgical expertise and insights into the local healthcare ecosystem. The role involves building strong stakeholder relationships, ensuring robust evidence for product approval and market access, and communicating scientific and clinical data effectively.

Johnson & Johnson MedTech Birmingham, United Kingdom
On-site Permanent
Medtronic logo

Product Portfolio Marketing Specialist

This role involves shaping the competitive landscape for bladder and bowel neurostimulation therapies, leading international product launches, and developing marketing strategies for the Pelvic Health business. You will collaborate with cross-functional teams to ensure successful market entry and drive growth through strategic initiatives and customer engagement.

Remote Permanent
Medtronic logo

Commercial Development Manager – OEM

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 Watford, United Kingdom

Associate Director, Safety Analysis Scientist

This role involves leading the scientific safety assessment of pharmaceutical products across development and post-marketing stages. The Associate Director will analyze complex medical data, lead safety evaluations, support regulatory submissions, and collaborate with cross-functional teams to shape safety strategies. They will also mentor junior staff, contribute to audits, and drive innovation in safety reporting processes.

Johnson & Johnson MedTech United States US$137,000 – US$235,750 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 a focus on analyzing complex medical data, supporting global safety teams, and contributing to regulatory compliance. The Associate Director acts as a subject matter expert, driving safety strategy, conducting proactive data reviews, and influencing cross-functional decisions. They also lead training, support health authority interactions, and innovate in safety reporting processes.

Johnson & Johnson MedTech US$137,000 – US$235,750 pa
Hybrid Permanent

Associate Director, Safety Analysis Scientist

This role involves leading safety evaluations for medical products, analyzing complex scientific data, and supporting regulatory compliance across the product lifecycle. The scientist will serve as a subject matter expert, guide cross-functional teams, and contribute to safety strategy, risk management, and health authority interactions. Emphasis is placed on innovation in data presentation and improving reporting efficiencies within a global safety framework.

Johnson & Johnson MedTech £137,000 – £235,750 pa
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

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

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

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, clinical study reports, 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 Belgium
On-site Permanent

Medical Governance Manager

This role involves implementing and maintaining the UK medical governance framework, reviewing and certifying materials, and providing compliance training. The position is pivotal in ensuring high ethical standards and compliance with the ABPI Code of Practice, working closely with cross-functional teams.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent

Medical Science Liaison

The Medical Science Liaison role involves providing scientific and medical support to key opinion leaders and internal teams, focusing on the Haematology franchise. You will work in the field, sharing knowledge and insights to optimize brand and therapy strategies, contributing to the development of innovative treatments.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Remote 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