Latest product manager Jobs

Manager, Trial Delivery Management

This role involves managing the end-to-end delivery of global clinical trials, with responsibility for trial-specific documentation, vendor oversight, budget management, and regional coordination. The position ensures alignment of feasibility strategies, conducts risk reviews, and supports compound training across multi-functional, global teams. It plays a key role in maintaining compliance, driving process improvements, and preparing for health authority inspections.

Johnson & Johnson MedTech €61,800 – €106,260 pa

On-site Permanent

Manager, Trial Delivery Management

This role involves managing the execution of clinical trials, including creating trial-specific documentation, overseeing vendor activities, and coordinating regional trial operations. The manager ensures alignment of feasibility strategies, conducts risk reviews, and supports compound training initiatives across global teams. It emphasizes operational oversight, compliance, and cross-functional collaboration in a matrixed environment.

Johnson & Johnson MedTech PLN 251,000 – PLN 483,000 pa

On-site Permanent

QMS Specialist

As a QMS Specialist, you will ensure the Quality Management System meets global medical device regulations, support key QMS processes, and collaborate with cross-functional teams to maintain audit readiness. Your role involves interpreting regulatory requirements, conducting data analysis, and driving continuous improvement to ensure high-quality, compliant products.

Smith & Nephew Goole, United Kingdom

Hybrid Permanent

Complex Wound Specialist

This role involves serving as a clinical specialist for advanced wound care, providing hands-on support and education to healthcare professionals in the community setting. The specialist will drive appropriate use of complex wound therapies, build clinical relationships, and ensure patients receive timely, effective treatments across North Wales and the Midlands. A field-based position combining clinical expertise with sales and training responsibilities.

Smith & Nephew Stoke-on-Trent, United Kingdom

Hybrid Permanent

Medical Affairs Specialist

The Medical Affairs Specialist supports the use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIRs). They ensure optimal clinical outcomes by providing expert-level support to healthcare professionals and collaborating with various teams to analyze and improve patient outcomes.

Johnson & Johnson MedTech

Hybrid Permanent Flexible

Medical Affairs Specialist

The Medical Affairs Specialist supports the clinical use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIRs). They ensure optimal patient outcomes by providing expert-level clinical support, generating performance reports, and assisting with new product introductions and clinical studies.

Johnson & Johnson MedTech

Hybrid Permanent

Medical Affairs Specialist

The Medical Affairs Specialist supports the use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIR). They ensure optimal clinical outcomes by providing expert-level support to healthcare professionals and collaborating with various teams to analyze and improve patient outcomes.

Johnson & Johnson MedTech

Hybrid Permanent

Medical Affairs Specialist

The Medical Affairs Specialist supports the clinical use of Intraocular Lenses (IOLs) through case analysis, proctoring, and managing Medical Information Requests (MIRs). They ensure optimal patient outcomes by providing expert-level clinical support, analyzing sub-optimal results, and collaborating with various stakeholders to improve product performance and clinical practices.

Johnson & Johnson MedTech

Hybrid Permanent

Medical Affairs Specialist

The Medical Affairs Specialist supports the use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIR). They ensure optimal clinical outcomes by providing expert-level support to healthcare professionals and collaborating with various teams to analyze and improve patient outcomes.

Johnson & Johnson MedTech

Hybrid Permanent Flexible

Medical Affairs Specialist

The Medical Affairs Specialist supports the clinical use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIRs). They ensure optimal patient outcomes by providing expert-level clinical support, analyzing sub-optimal results, and collaborating with various stakeholders to improve product performance and clinical workflows.

Johnson & Johnson MedTech

Hybrid Permanent Flexible

Senior Process Engineer - Orthopaedics

The Senior Process Engineer will lead the optimization of manufacturing value streams for medical devices, ensuring safety, compliance, and cost-effectiveness. Key responsibilities include hands-on engineering leadership, process development and validation, quality improvement, and collaboration with cross-functional teams to drive innovation and continuous improvement.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Sr Director, External Scientific Innovation Transactions

The Sr Director, External Scientific Innovation Transactions leads business development activities, including transactions, research collaborations, licensing, and asset acquisitions. They focus on identifying and securing top scientific innovations, primarily in the APAC region, and work closely with R&D, finance, legal, and IP teams to develop and execute complex deals.

Johnson & Johnson MedTech London, 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

CQ Lead and RP Surgery UK/Ireland

This role involves leading the quality management framework and system for Johnson & Johnson's Surgery division in the UK and Ireland. Responsibilities include managing quality systems, ensuring compliance, leading regional projects, and integrating quality management across multiple markets. The position requires strategic leadership and interaction with global projects and regulatory bodies.

Johnson & Johnson MedTech United Kingdom

On-site Permanent