Jobs in Exeter

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 London, 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. 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

Hips Lifecycle Management Leader

The Hips Lifecycle Management Leader role involves leading the lifecycle management of hip joint products within the MedTech Orthopaedics business. Responsibilities include strategic planning, product development, and collaboration with cross-functional teams to drive innovation and improve patient outcomes.

Johnson & Johnson MedTech

On-site Permanent

Manager, Clinical Operations

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 High Wycombe, United Kingdom

VELYS Trauma Marketing Manager

The VELYS Trauma Marketing Manager will lead the launch and establishment of the new VELYS Trauma system within the DPS International business and Trauma Platforms. Key responsibilities include developing and executing international strategies, partnering with cross-functional teams, and ensuring market access and clinical evidence strategies are in place.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Director, Major Markets Europe & Canada

The Director, Major Markets Europe & Canada, provides strategic regulatory leadership across key European and Canadian markets. This role ensures compliance with local and regional regulatory requirements, manages regulatory risk, and supports business growth in highly regulated markets. Key responsibilities include leading regulatory affairs strategy, ensuring compliance, and partnering with cross-functional teams to manage product registrations and lifecycle management.

Johnson & Johnson MedTech Leeds, United Kingdom

Hybrid 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 Leeds, United Kingdom

On-site Permanent

Spine and Biomaterials Marketing Manager

The Spine and Biomaterials Marketing Manager will lead the marketing strategy for the Spine and Biomaterials portfolio across international regions, driving brand visibility and market penetration. Key responsibilities include strategic development, campaign activation, product launches, performance analysis, and cross-functional collaboration to optimize market impact.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

EMEA HEMA Associate Manager

The EMEA HEMA Associate Manager supports the regional development and execution of Health Economics & Market Access activities across EMEA. Key responsibilities include coordinating EMEA initiatives, supporting evidence generation, and ensuring consistent market access strategies across multiple countries.

Johnson & Johnson MedTech

On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular review cycles.

Johnson & Johnson MedTech United States

On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include active participation in study activities, maintaining clinical quality plans, and facilitating regular risk reviews and updates.

Johnson & Johnson MedTech

On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and communicating risk updates to stakeholders through regular review cycles.

Johnson & Johnson MedTech

On-site Permanent

Director, 3rd Party RM. Program (BPO)

The Director, 3rd Party RM Program (BPO) leads the development and implementation of a global third-party risk management program, focusing on anti-bribery and anti-corruption. Key responsibilities include strategic governance, risk assessment, due diligence, and technology integration to ensure compliance and sustainable growth.

Johnson & Johnson MedTech

On-site Permanent

Specialist, Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech Belgium

On-site Permanent

EMEA HEMA Associate Manager

The EMEA HEMA Associate Manager supports the regional development and execution of Health Economics & Market Access activities across EMEA. Key responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with governance and regulatory standards.

Johnson & Johnson MedTech Switzerland

On-site Permanent