Latest Life Sciences Jobs

Associate Director, Safety Analysis Scientist

This role involves leading the scientific safety assessment of pharmaceutical products, supporting safety management teams, and ensuring regulatory compliance through high-quality safety evaluations and reporting. The individual will analyze complex medical-scientific data, contribute to risk-benefit assessments, and act as a subject matter expert during audits. The position emphasizes leadership, cross-functional collaboration, and innovation in safety data interpretation and presentation within a hybrid work environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Medical Writer III, X-TA

The Medical Writer III role involves writing and coordinating clinical and regulatory documents, leading cross-functional document planning and review meetings, and mentoring junior staff. The position is hybrid, with 3 days onsite weekly, and supports key therapeutic areas within the Integrated Data Analytics & Reporting (IDAR) business.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Digital Health Director – Western Europe

As Digital Health Director, you will lead the commercial growth and adoption of connected care solutions across Western Europe, partnering with healthcare leaders to advance digital transformation. You will develop and execute commercial strategies, manage a team, and influence the future direction of digital health products.

Medtronic London, United Kingdom

Senior Training and Education Specialist

The Senior Training & Education Specialist designs, develops, and implements learning solutions to support operational processes, workforce capability, and business performance. The role involves conducting needs analyses, developing curricula, managing projects, and facilitating training sessions across diverse customer and business environments.

Medtronic Watford, United Kingdom

Manager, Global Labeling Product Leader

This role involves leading the development and maintenance of product labeling documents, providing guidance on labeling content and processes, and contributing to the global labeling strategy. The position requires a strong understanding of regulatory affairs and pharmaceutical drug development, with a focus on ensuring high-quality and compliant labeling.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Medical Writer III, Oncology

The Medical Writer III role involves writing and coordinating complex clinical and regulatory documents for oncology, leading cross-functional document planning and review meetings, and mentoring junior staff. The position requires 6+ years of pharmaceutical/scientific industry experience, including 4+ years in regulatory medical writing, and proficiency in internal systems and processes.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Manager, Medical Writing, Immunology

This role involves leading the development and finalization of clinical and regulatory documents within the Immunology therapeutic area, with a focus on scientific strategy, team leadership, and cross-functional collaboration. The manager will oversee medical writing projects from planning to delivery, mentor junior staff, and ensure compliance with regulatory standards such as ICH guidelines. The position also includes direct people management, process improvement, and coordination across global teams in a patient-centered innovation environment.

Johnson & Johnson MedTech Switzerland

On-site Permanent

Manager, Global Labeling Product Leader

This role involves leading the development, revision, and maintenance of product labeling documents, ensuring compliance and high quality. Responsibilities include coordinating the resolution of labeling issues, contributing to global labeling strategy, and improving the end-to-end labeling process.

Johnson & Johnson MedTech United States

Manager, Global Labeling Product Leader

This role involves leading the development, revision, and maintenance of product labeling documents for pharmaceuticals, ensuring compliance and high quality. Responsibilities include coordinating labeling issues, contributing to global labeling strategy, and improving labeling processes.

Johnson & Johnson MedTech

Manager, Global Labeling Product Leader

This role involves leading the development and maintenance of product labeling documents, ensuring compliance and quality. Responsibilities include coordinating labeling processes, providing guidance on content and timelines, and contributing to the global labeling strategy.

Johnson & Johnson MedTech

Manager, Medical Writing, Immunology

Lead and manage medical writing activities for immunology clinical documents, including planning, authoring, and mentoring junior staff. Guide cross-functional teams, ensure regulatory compliance, and drive process improvements in a global healthcare environment.

Johnson & Johnson MedTech Belgium

On-site Permanent

Manager, Medical Writing, Immunology

Lead and manage the development of clinical and regulatory medical writing deliverables within the Immunology therapeutic area, providing scientific and strategic input across the product lifecycle. This role involves direct supervision of medical writers, mentoring junior staff, leading cross-functional writing teams, and ensuring compliance with regulatory standards. The position requires deep expertise in medical writing processes, ICH guidelines, and clinical documentation, with a strong emphasis on leadership, project management, and process improvement.

Johnson & Johnson MedTech

On-site Permanent

Manager, Medical Writing, Immunology

Lead and manage the creation of clinical and regulatory documents within the Immunology therapeutic area, providing scientific and strategic direction for medical writing teams. This role involves mentoring junior staff, driving process improvements, and ensuring compliance with regulatory standards. The position also includes direct people management responsibilities and cross-functional collaboration across drug development programs.

Johnson & Johnson MedTech Canada

Remote Permanent

Medical Writer III, X-TA

This role involves writing and coordinating clinical and regulatory documents, leading cross-functional document planning and review meetings, and mentoring junior staff. The position is hybrid, with 3 days onsite weekly, and may be located in multiple European countries.

Johnson & Johnson MedTech Netherlands

Medical Writer III, X-TA

The Medical Writer III role involves writing and coordinating clinical and regulatory documents, leading cross-functional document planning meetings, and mentoring junior staff. The position is hybrid, with 3 days onsite weekly, and supports key therapeutic areas within the Integrated Data Analytics & Reporting (IDAR) business.

Johnson & Johnson MedTech