Latest Life Sciences Jobs

Director, Pharmacovigilance Alliance Contracting and Management

This role involves leading the strategy, negotiation, and execution of global and local Pharmacovigilance Agreements, ensuring alignment with regulatory requirements and business objectives. The Director will manage a team responsible for alliance contracting, governance, compliance, and operational excellence, while fostering strong partnerships and driving continuous improvement and digital transformation.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Manager, Medical Writing, Immunology

Leads medical writing activities for clinical documents in the Immunology therapeutic area, providing scientific and strategic leadership. Manages a team of medical writers, mentors junior staff, and collaborates cross-functionally to ensure regulatory compliance and high-quality documentation. Works within a global regulatory environment, contributing to process improvements and departmental best practices.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Senior Sales Specialist

This role involves driving sales and clinical education activities for Medtronic's Perioperative Complications product range in Scotland. Responsibilities include building relationships with clinicians, providing in-theatre support, and developing new business opportunities.

Medtronic Edinburgh, Alba / Scotland, United Kingdom £55,040 – £82,560 pa

Business Development Manager

The Senior Market Development Manager will drive the adoption and growth of innovative cardiac therapies like Aurora EV-ICD™, OmniaSecure™, and CSP across the UK and Ireland. Key responsibilities include developing market strategies, optimizing patient referral pathways, and collaborating with healthcare stakeholders to support service development and pathway transformation.

Medtronic Watford, United Kingdom £70,320 – £105,480 pa

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 may be located in multiple European countries.

Johnson & Johnson MedTech

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 supports key therapeutic areas within the Integrated Data Analytics & Reporting (IDAR) business.

Johnson & Johnson MedTech

Manager, Global Labeling Product Leader

The Manager, Global Labeling Product Leader role involves leading the development, revision, and maintenance of product labeling documents across therapeutic areas and regions. Responsibilities include ensuring high-quality, compliant labeling, coordinating the resolution of labeling issues, and contributing to the global labeling strategy.

Johnson & Johnson MedTech Belgium

Manager, Global Labeling Product Leader

The Manager, Global Labeling Product Leader role involves leading the development, revision, and maintenance of product labeling documents across therapeutic areas and regions. Responsibilities include coordinating labeling processes, providing scientific advice, and contributing to the global labeling strategy.

Johnson & Johnson MedTech

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 pharmaceutical regulations and the ability to work independently within a matrix environment.

Johnson & Johnson MedTech Switzerland

Manager, Global Labeling Product Leader

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

Johnson & Johnson MedTech

Medical Writer III, Oncology

The Medical Writer III role involves writing and coordinating clinical and regulatory documents for oncology treatments, leading cross-functional teams, and mentoring junior staff. Responsibilities include document planning, content review, and process improvement.

Johnson & Johnson MedTech Belgium

Medical Writer III, Oncology

This role involves writing and coordinating complex clinical and regulatory documents for oncology treatments, leading cross-functional document planning, and mentoring junior staff. The position requires strong scientific writing skills, experience in regulatory medical writing, and the ability to collaborate with global teams.

Johnson & Johnson MedTech United States

Medical Writer III, Oncology

The Medical Writer III role involves writing and coordinating complex clinical and regulatory documents for oncology, leading cross-functional teams, and mentoring junior staff. Responsibilities include document planning, content review, and championing best practices in medical writing.

Johnson & Johnson MedTech Canada

Manager, Medical Writing, Immunology

Lead and mentor a team of medical writers while independently managing the development of clinical and regulatory documents for immunology therapies. Oversee project timelines, scientific strategy, and cross-functional collaboration, ensuring compliance with regulatory standards. Provide coaching, conduct performance reviews, and contribute to process improvements within the medical writing function.

Johnson & Johnson MedTech United States

On-site Permanent