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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

Associate Director, RA UK & Ireland

The role involves leading and overseeing regulatory affairs activities for the UK market, ensuring compliance with UK and EU regulations, and managing regulatory risk. The Associate Director will partner with various teams to support product registrations, lifecycle management, and business initiatives, while also leading the UKCA marking strategy and coaching regulatory team members.

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, working closely with country HEMA Leads. Responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with governance standards.

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

D&A and Master Data Specialist

The role involves managing the accuracy and consistency of master data across various commercial systems, implementing data governance practices, and ensuring compliance with regulations like GDPR. Responsibilities include collaborating with internal stakeholders, developing data management strategies, and utilizing tools like Power BI and Excel to create analytical reports and dashboards.

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

Export Control Analyst

The Export Control Analyst role involves supporting global trade compliance activities, ensuring products and data are exported in line with export control laws. Responsibilities include screening, classification, and transaction reviews, maintaining records, and providing guidance to various teams.

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

HEMA Lead UK

The HEMA Lead UK is responsible for shaping and executing health economics and market access strategies for DePuy Synthes in the United Kingdom. Key responsibilities include leading payer and HTA engagement, developing value dossiers, and ensuring successful reimbursement and adoption of innovative orthopaedic solutions. The role involves cross-functional collaboration and compliance with regulatory requirements.

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

Sr. Source Reg Compliance Specialist

The Sr. Source Regulatory Compliance Specialist is responsible for ensuring suppliers and externally provided processes comply with regulatory requirements and quality standards. Key responsibilities include executing supplier audits, supporting compliance oversight, and maintaining documentation. The role involves close collaboration with Quality, Regulatory Affairs, Supply Chain, and Procurement teams to maintain product quality and supply continuity.

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

Product Manager

The Product Manager will join a dynamic AI & Digital team focused on transforming the orthopaedics supply chain with innovative, scalable AI and digital solutions. The role involves strong organizational engagement, cross-functional collaboration, and implementing data-driven solutions to meet the growing demand for personalized care in the medical device industry.

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

Staff Scientist – Microbiology & Sterility Assurance (Supplier / External Manufacturing)

This role involves ensuring microbiological quality and sterility assurance across external manufacturing sites and suppliers for medical devices. The scientist will lead contamination control, sterilization validation, and audit readiness, providing technical expertise on regulatory compliance and supporting investigations and risk assessments. They will work closely with global partners to maintain high standards in controlled environments and drive continuous improvement in quality systems.

Johnson & Johnson MedTech Leeds, United Kingdom
Hybrid 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 Leeds, United Kingdom
On-site 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

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

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