Latest medical device engineer Jobs

Associate Director, Safety Analysis Scientist

This role involves leading scientific safety evaluations for pharmaceutical products across development and post-marketing stages, with a focus on analyzing complex medical data, shaping safety strategies, and supporting regulatory compliance. The scientist will serve as a subject matter expert, lead cross-functional safety reviews, contribute to key clinical documents, and drive innovation in safety analysis methodologies. Emphasis is placed on proactive risk assessment, collaboration with global teams, and ensuring high-quality, timely safety reporting.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Associate Director, Safety Analysis Scientist

This role involves leading the scientific safety assessment of pharmaceutical products across development and post-marketing stages, with responsibility for analyzing complex medical data, supporting global safety strategy, and contributing to regulatory compliance. The scientist will lead safety evaluations, guide cross-functional teams, and ensure high-quality reporting while acting as a subject matter expert during audits and inspections. Innovation in data presentation and process improvement is emphasized within a hybrid work environment.

Johnson & Johnson MedTech Belgium

Hybrid Permanent

Director, Global R&D, Clin/Med and BD

This role involves leading the global Health Care Compliance program for Clinical Research, Medical Affairs, R&D, and Business Development. Responsibilities include strategic oversight, risk assessment, and ensuring compliance with regulatory requirements across various business activities, including mergers and acquisitions.

Johnson & Johnson MedTech United States

Hybrid Permanent

Director, 3rd Party RM. Program (BPO)

The Director, 3rd Party RM Program provides strategic leadership for an enterprise-wide third-party risk management program, focusing on anti-bribery and anti-corruption risks. Key responsibilities include setting global standards, developing risk assessment frameworks, overseeing due diligence processes, and partnering with Legal and IT to implement technology solutions.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Director, 3rd Party RM. Program (BPO)

The Director, 3rd Party RM Program (BPO) leads the development and implementation of a global third-party risk management program, focusing on anti-bribery and anti-corruption. Key responsibilities include strategic governance, risk assessment, due diligence, and technology integration to ensure compliance and sustainable growth.

Johnson & Johnson MedTech

On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, CSRs, and IB updates. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Medical Advisor/Sr. Medical Advisor

This role involves providing high-quality medical input and leadership in oncology, collaborating with cross-functional teams to drive medical strategy and patient outcomes. Responsibilities include building expertise in oncology, gathering field insights, and contributing to evidence generation and medical affairs projects.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, CSRs, and IB updates. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead on specific projects under supervision.

Johnson & Johnson MedTech Canada

Remote Permanent

Medical Writer II, Oncology

The Medical Writer II, Oncology role involves writing and coordinating clinical and regulatory documents, such as Phase 1-3 protocols, CSRs, and IB updates. You will work in a team environment, applying internal standards and regulatory guidelines, and participate in process working groups to support the development of oncology treatments.

Johnson & Johnson MedTech Switzerland

On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, clinical study reports, and initial IBs. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech Belgium

On-site Permanent

Medical Governance Manager

This role involves implementing and maintaining the UK medical governance framework, reviewing and certifying materials, and providing compliance training. The position is pivotal in ensuring high ethical standards and compliance with the ABPI Code of Practice, working closely with cross-functional teams.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Medical Science Liaison

The Medical Science Liaison role involves providing scientific and medical support to key opinion leaders and internal teams, focusing on the Haematology franchise. You will work in the field, sharing knowledge and insights to optimize brand and therapy strategies, contributing to the development of innovative treatments.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Remote Permanent

Medical Writer II, Oncology

This role involves writing and coordinating clinical documents, such as Phase 1 protocols and clinical study reports, for oncology treatments. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech United States

On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating basic clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, and initial IBs. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech

Hybrid Permanent

Medical Writer II, Oncology

The Medical Writer II, Oncology role involves writing and coordinating clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, and initial IBs. You will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech

Hybrid Permanent