Latest regulatory affairs specialist Jobs

Regional Head of Technology - Electrophysiology and NeuroVascular - EMEA

This role involves leading a technology organization within the EMEA region, focusing on electrophysiology and neurovascular solutions. Responsibilities include shaping growth strategies, modernizing platforms, and delivering digital and AI capabilities. The leader will work closely with senior business leaders to align technology with business goals and ensure smooth operations and process improvements.

Johnson & Johnson MedTech

On-site Permanent

Regional Head of Technology - Electrophysiology and NeuroVascular - EMEA

This role involves leading a technology organization within the EMEA region, focusing on digital surgery, robotics, OR integration, and imaging. The Director will partner with senior leaders to shape growth strategies, modernize platforms, and deliver AI and digital capabilities, ensuring technology serves as a competitive advantage.

Johnson & Johnson MedTech

On-site Permanent

Medical Writer II, Oncology

The Medical Writer II, Oncology role involves writing and coordinating clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, and initial IBs. You will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech

Hybrid Permanent

Lead Local Trial Manager

The Lead Local Trial Manager is responsible for managing and overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, maintaining high-quality data, and collaborating with internal and external stakeholders to deliver successful trials.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Senior Local Trial Manager

The Senior Local Trial Manager is responsible for overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, managing site selection, and maintaining relationships with external and internal stakeholders. The role involves process improvement, mentoring team members, and delivering high-quality data.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

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

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

Director, Global R&D, Clin/Med and BD

This role involves leading the global Health Care Compliance program for Clinical Research, Medical Affairs, R&D, and Business Development. Responsibilities include strategic oversight, risk assessment, and ensuring compliance across various business activities, including mergers, acquisitions, and strategic partnerships.

Johnson & Johnson MedTech

Hybrid Permanent

Director, Global R&D, Clin/Med and BD

This role involves leading the global Health Care Compliance program for Clinical Research, Medical Affairs, R&D, and Business Development. Responsibilities include strategic oversight, risk assessment, and ensuring compliance with regulatory requirements across various business activities, including mergers and acquisitions.

Johnson & Johnson MedTech United States

Hybrid Permanent

Senior Director, Quality Systems (UK)

This role leads the global strategy and operation of Quality Management Systems (QMS) for Johnson & Johnson's Innovative Medicine and MedTech divisions. The Senior Director will drive digital transformation, ensure compliance with GxP and regulatory standards, and oversee core platforms like LMS, EDMS, and QMS workflows. They will lead a global team, align stakeholders, and deliver scalable, compliant quality systems in a highly regulated environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid 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

Technology Director, Make EMEA

The Technology Director, Make (EMEA) is a senior IT leader responsible for shaping and delivering manufacturing technology solutions across DePuy Synthes operations in the EMEA region. This role involves leading the EMEA manufacturing technology strategy, overseeing the delivery and lifecycle management of manufacturing systems, and ensuring compliance with regulatory requirements. The position also focuses on driving standardization, cybersecurity, and continuous improvement across manufacturing systems while leading regional teams and influencing global strategy.

Johnson & Johnson MedTech Leeds, United Kingdom

Hybrid Permanent

Global Process Owner - Machining & Finishing

This role involves leading global machining and finishing processes across DePuy Synthes manufacturing sites, driving standardization, innovation, and compliance. The individual will develop technology roadmaps, govern process changes, and act as a subject matter expert to improve manufacturing excellence in a regulated medical device environment.

Johnson & Johnson MedTech Leeds, United Kingdom

Hybrid Permanent

Manager, Safety Analysis Scientist

The Manager, Safety Analysis Scientist role involves leading the safety assessment of assigned products, preparing scientific safety analyses, and collaborating with cross-functional teams to ensure regulatory compliance. The role requires in-depth product knowledge, mentoring team members, and supporting safety management teams.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Product Manager - EMEA

As a Product Manager, you will lead cross-functional teams to develop innovative AI and digital solutions that transform the orthopaedics supply chain. You will collaborate with business partners to implement data-driven, scalable solutions that enhance patient care and streamline processes.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent