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Commercial Education Mgr – Knee & VELYS

This role involves designing and delivering high-impact education programs for knee reconstruction and robotic-assisted surgery technologies, including the VELYS platform. The manager will train sales teams and healthcare professionals, develop digital and simulation-based learning materials, and support product launches. It requires strong collaboration across clinical, commercial, and marketing teams to improve training effectiveness and drive adoption of innovative MedTech solutions.

Johnson & Johnson MedTech Leeds, 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
Smith & Nephew logo

QC Release Specialist 2

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.Smith+Nephew is hiringQC Release Specialist 2 .The Quality Compliance release team is focused on ensuring that Smith + Nephew complies with key regulatory requirements and Smith...

Smith & Nephew Goole, United Kingdom
Smith & Nephew logo

Laboratory Analyst 1

This role involves conducting QA testing of medical products and devices using analytical techniques such as ICP, GC, IR, UV-Vis, and TOC. The Laboratory Analyst ensures compliance with safety, quality, and regulatory standards by testing raw materials, intermediates, and finished products, maintaining equipment, and updating procedures. The position supports continuous improvement and contributes to maintaining high standards in a regulated manufacturing environment.

Smith & Nephew Goole, 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

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