Latest Life Sciences Jobs

Sr Director, C&SP - NS and Cardio-Pulmonary

The Senior Director, C&SP - Neuroscience & Cardio role involves leading a large, global team in Clinical & Statistical Programming, shaping the long-term strategy, and ensuring operational excellence across major therapeutic and regional portfolios. Responsibilities include guiding organizational evolution, making strategic decisions, and fostering collaboration across various functions to deliver clinical evidence to global health authorities.

Johnson & Johnson MedTech

Hybrid Permanent

Sr Director, C&SP - NS and Cardio-Pulmonary

As Senior Director of Clinical & Statistical Programming, you will lead a global team to shape the long-term strategy and technical capabilities for Johnson & Johnson's innovative healthcare solutions. Your role involves strategic decision-making, operational excellence, and people leadership across major therapeutic areas like neuroscience and cardiology.

Johnson & Johnson MedTech

Hybrid Permanent

Technical Consultant

As a Technical Consultant in the Cardiac Ablation Solutions (CAS) team, you will provide technical support, training, and education to customers, ensuring the successful introduction and market release of new products. Your role involves working closely with the clinical team, sales, and marketing to enhance Medtronic’s reputation and meet business targets.

Medtronic Cambridge, United Kingdom £42,000 – £63,000 pa

On-site Permanent

Regional Sales Manager UK&I

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeJoin...

Medtronic Watford, United Kingdom

Site Director, Hull & Melton

Lead and transform a strategically important manufacturing site within a highly regulated medical technology environment. Drive operational excellence across manufacturing, quality, regulatory, R&D, and finance functions while fostering a culture of innovation and continuous improvement. Serve as a key member of the global operations leadership team, influencing broader supply chain strategy and large-scale transformation initiatives.

Smith & Nephew Melton, United Kingdom

On-site Permanent

Account Manager (Wound Care)

This role involves managing key accounts in Central London for Smith & Nephew’s wound care portfolio, building relationships with NHS stakeholders, and delivering tailored solutions to improve patient outcomes. You'll develop strategic account plans, lead business reviews, and use CRM tools to drive growth in a competitive healthcare market. The position supports long-term partnerships through value-based selling and cross-functional collaboration.

Smith & Nephew London, W3 0BJ, United Kingdom

Hybrid Contract

Associate Director, Clinical Risk Management

This role involves leading clinical risk management across complex trials and programs, ensuring data integrity, patient safety, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, and advise on quality issues and corrective actions in a global, cross-functional environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Regulatory Affairs Executive

This role involves managing regulatory affairs activities for MedTech products in the UK, ensuring compliance with regulations and supporting submissions to health authorities. The candidate will develop local regulatory strategies, handle labelling documentation, and mentor junior colleagues while collaborating with cross-functional teams. A key focus is maintaining an inspection-ready culture and contributing to risk management and regulatory intelligence initiatives.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, 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 facilitating regular risk updates to R&D colleagues.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Medical Writer III

This role involves writing and coordinating clinical and regulatory documents such as clinical study reports, protocols, and regulatory responses within the Immunology therapeutic area. The Medical Writer III leads document planning and review meetings, collaborates with cross-functional teams, and ensures scientific accuracy and compliance with regulatory standards. The position operates in a hybrid work model, requiring onsite presence for part of the week while supporting global teams across time zones.

Johnson & Johnson MedTech United States US$109,000 – US$174,800 pa

Hybrid Permanent

Medical Writer III

This role involves writing and coordinating clinical and regulatory documents such as clinical study reports, protocols, and safety updates within the Immunology therapeutic area. The Medical Writer III will lead document planning and review meetings, mentor junior staff, and ensure compliance with internal processes and regulatory standards. The position operates in a hybrid model with global cross-functional collaboration.

Johnson & Johnson MedTech £109,000 – £174,800 pa

Hybrid Permanent

Medical Writer III

This role involves writing and coordinating clinical and regulatory documents such as CSRs, protocols, and regulatory responses within the Immunology therapeutic area. The Medical Writer III will lead document planning and review meetings with cross-functional teams, mentor junior staff, and ensure compliance with internal processes and regulatory standards. The position operates in a hybrid model with three days per week onsite and supports global teams across time zones.

Johnson & Johnson MedTech US$109,000 – US$174,800 pa

Hybrid Permanent

Medical Writer III

This role involves writing and coordinating clinical and regulatory documents such as clinical study reports, protocols, and regulatory responses within the Immunology therapeutic area. The Medical Writer III leads document planning and review meetings with cross-functional teams, ensures adherence to timelines and best practices, and may mentor junior staff. The position operates in a hybrid work model with global collaboration across diverse stakeholders.

Johnson & Johnson MedTech US$109,000 – US$174,800 pa

Hybrid Permanent

Manager Global Regulatory Scientist, Regulatory Affairs

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 Belgium

Manager Global Regulatory Scientist, Regulatory Affairs

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