Latest regulatory affairs Jobs

Medical Writer III

This role involves writing and coordinating complex clinical and regulatory documents such as CSRs, protocols, and regulatory responses within the Immunology therapeutic area. The Medical Writer III leads document planning and review meetings with cross-functional teams, ensures scientific accuracy, and mentors junior staff. The position operates in a hybrid work model with a focus on process leadership and adherence to regulatory standards.

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 risk management plans within the Immunology therapeutic area. The Medical Writer III will lead document planning and review meetings with cross-functional teams, ensure adherence to timelines and regulatory standards, and may mentor junior staff. The position operates in a hybrid work model with a significant focus on collaboration, process leadership, and global stakeholder engagement.

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

Hybrid Permanent

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, 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

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

Medical Writer III

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

Medical Writer III

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

Medical Writer III

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 Switzerland

Manager, Medical Writing, Immunology

This role involves preparing and finalizing clinical documents for the Immunology therapeutic area, leading cross-functional teams, and guiding team members on processes and best practices. The Manager will work with a high level of independence, take a lead role on assigned projects, and recommend departmental process improvements.

Johnson & Johnson MedTech United States

On-site Permanent

Legal Director, UK, Ireland & Nordics

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 Leeds, United Kingdom

New Technology Specialist - Midlands - Johnson & Johnson MedTech | Electrophysiology

This role involves driving the adoption of new electrophysiology technologies in the Midlands region by providing expert clinical and technical support during product launches and in-field procedures. The specialist will lead training, design clinical evaluations, and act as a liaison between customers and internal teams to ensure successful implementation of new products like CARTO. A strong background in electrophysiology and a proven track record in field-based technical sales are essential.

Johnson & Johnson MedTech

Hybrid Permanent

Medical Safety Officer - PALM

This role involves leading the medical safety assessment of pharmaceutical products throughout their lifecycle, with a focus on proactive safety surveillance, risk management, and benefit-risk evaluation. The Medical Safety Officer provides expert medical input into clinical development and regulatory documentation, leads cross-functional Safety Management Teams, and ensures compliance with global pharmacovigilance standards. Key responsibilities include signal detection, risk mitigation strategy design, and communication of safety findings to internal leadership and health authorities.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Manager Clinical Data Transparency

This role involves leading the production of plain language summaries (PLS) for clinical trial results, ensuring scientific accuracy and compliance with regulatory standards while making content accessible to non-specialist audiences. The manager will oversee vendor performance, collaborate with cross-functional teams across therapeutic areas, and ensure adherence to health literacy principles and global disclosure requirements. Key responsibilities include maintaining robust PLS processes, addressing content issues, and supporting translation workflows.

Johnson & Johnson MedTech High Wycombe, United Kingdom €68,600 – €119,600 pa

Hybrid Permanent

Business Title Manager Clinical Data Transparency

This role involves leading the creation and oversight of plain language summaries (PLS) for clinical trial results, ensuring scientific accuracy while making content accessible to non-specialist audiences. The manager will coordinate with cross-functional teams, clinical stakeholders, and external vendors, ensuring compliance with regulatory standards such as the EU Clinical Trial Regulation. Key responsibilities include quality review, process improvement, and maintaining alignment with data transparency policies across global markets.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent