Latest medical device engineer Jobs

Lead Clinical Data Analyst

The Lead Clinical Data Analyst will coordinate timelines and resources for implementing and maintaining clinical systems, providing oversight for clinical study databases across various platforms. The role involves collaborating with Data Management leadership, supporting project deliverables, and assisting with vendor evaluation and selection.

Johnson & Johnson MedTech
On-site Permanent

Manager, Safety Analysis Scientist

The Manager, Safety Analysis Scientist role involves leading the safety assessment of assigned products, preparing scientific safety analyses, and collaborating with cross-functional teams to ensure regulatory compliance. The role requires in-depth product knowledge, mentoring team members, and supporting safety management teams.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid Permanent

Medical Affairs Specialist

The Medical Affairs Specialist supports the use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIRs). They ensure optimal clinical outcomes by providing expert-level support to healthcare professionals and collaborating with various teams to analyze and improve patient outcomes.

Johnson & Johnson MedTech
Hybrid Permanent Flexible

Medical Affairs Specialist

The Medical Affairs Specialist supports the clinical use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIRs). They ensure optimal patient outcomes by providing expert-level clinical support, generating performance reports, and assisting with new product introductions and clinical studies.

Johnson & Johnson MedTech
Hybrid Permanent

Medical Affairs Specialist

The Medical Affairs Specialist supports the use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIR). They ensure optimal clinical outcomes by providing expert-level support to healthcare professionals and collaborating with various teams to analyze and improve patient outcomes.

Johnson & Johnson MedTech
Hybrid Permanent

Medical Affairs Specialist

The Medical Affairs Specialist supports the clinical use of Intraocular Lenses (IOLs) through case analysis, proctoring, and managing Medical Information Requests (MIRs). They ensure optimal patient outcomes by providing expert-level clinical support, analyzing sub-optimal results, and collaborating with various stakeholders to improve product performance and clinical practices.

Johnson & Johnson MedTech
Hybrid Permanent

Medical Affairs Specialist

The Medical Affairs Specialist supports the use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIR). They ensure optimal clinical outcomes by providing expert-level support to healthcare professionals and collaborating with various teams to analyze and improve patient outcomes.

Johnson & Johnson MedTech
Hybrid Permanent Flexible

Medical Affairs Specialist

The Medical Affairs Specialist supports the clinical use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIRs). They ensure optimal patient outcomes by providing expert-level clinical support, analyzing sub-optimal results, and collaborating with various stakeholders to improve product performance and clinical workflows.

Johnson & Johnson MedTech
Hybrid Permanent Flexible

Manager, Medical Writing, Immunology

The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading cross-functional teams, and guiding team members on processes and best practices. The position focuses on the Immunology therapeutic area, working with a high level of independence to ensure timely and scientifically sound document delivery.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent

Manager, Medical Writing, Immunology

The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading team projects, and guiding cross-functional team members on processes and best practices. The position focuses on the Immunology therapeutic area and supports the development of transformational medicines for immunological disorders.

Johnson & Johnson MedTech Switzerland
On-site Permanent

Manager, Medical Writing, Immunology

The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading cross-functional teams, and guiding team members on processes and best practices. The position focuses on the Immunology therapeutic area, with responsibilities including content and scientific strategy, project management, and process improvements.

Johnson & Johnson MedTech Canada
Remote Permanent

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 in content and scientific strategy, and proactively recommend process improvements.

Johnson & Johnson MedTech Belgium
On-site Permanent

Manager, Medical Writing, Immunology

This role involves preparing and finalizing clinical documents, leading cross-functional teams, and guiding team members on processes and best practices. The Manager will work independently, take a lead role in content and scientific strategy, and drive departmental process improvements.

Johnson & Johnson MedTech
On-site Permanent

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

Lead Local Trial Manager

The Lead Local Trial Manager is responsible for managing and overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, maintaining high-quality data, and collaborating with internal and external stakeholders to deliver successful trials.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid Permanent