Latest Medical Devices Jobs

Medical Writer III

This role involves writing and coordinating 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 compliance with internal processes, and mentors junior staff. The position operates in a hybrid work model with a focus on global collaboration and adherence to regulatory standards.

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

Hybrid Permanent

Medical Writer III

This role involves writing and coordinating clinical and regulatory documents such as CSRs, protocols, and regulatory responses within the Immunology therapeutic area. The Medical Writer III will lead document planning and review meetings with cross-functional teams, ensure compliance with internal processes, and mentor junior staff. The position operates in a hybrid model with a focus on regulatory medical writing within a global, collaborative environment.

Johnson & Johnson MedTech £109,000 – £174,800 pa

Hybrid Permanent

Senior Consultant, AI & Knowledge Strategy, Integrated Health Solutions Eurasia

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing...

Medtronic Watford, United Kingdom

Senior Training and Development Specialist EMEA and APAC

Designs and delivers hands-on, field-based training programmes for clinical and sales teams across EMEA and APAC, translating complex clinical data into practical sales and procedural knowledge. Develops simulation tools and scenario-based learning to improve product understanding and customer engagement. Works cross-functionally with Medical Affairs, Marketing, and HCPs to support product launches and commercial effectiveness in the endoscopy space.

Medtronic

Manager Clinical Data Transparency

This role involves leading the production of plain language summaries (PLS) for clinical trial results, ensuring scientific accuracy and regulatory compliance while making complex data accessible to non-scientific audiences. The manager will oversee vendor quality, collaborate with cross-functional teams across therapeutic areas, and ensure adherence to global standards such as the EU Clinical Trial Regulation. A key focus is maintaining transparency and health literacy principles in clinical data disclosure.

Johnson & Johnson MedTech

Hybrid Permanent

Senior Scientist Clinical Pharmacokinetics

The Senior Scientist Clinical Pharmacokinetics role involves leading the end-to-end execution of Phase 1 clinical pharmacology studies, including protocol development, data analysis, and report writing. Additional responsibilities include supporting all phases of drug development with noncompartmental analysis and contributing to regulatory submissions.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Manager Clinical Data Transparency

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 Netherlands

Senior Scientist Clinical Pharmacokinetics

The Senior Scientist Clinical Pharmacokinetics role involves leading the end-to-end execution of Phase 1 clinical pharmacology studies, including protocol development, data analysis, and report writing. The role also supports non-compartmental analysis for all phases of drug development and ensures the quality and accuracy of pharmacokinetic/pharmacodynamic data.

Johnson & Johnson MedTech Belgium

On-site Permanent

Senior Scientist Clinical Pharmacokinetics

The Senior Scientist Clinical Pharmacokinetics role involves developing and analyzing clinical pharmacology protocols, performing pharmacokinetic/pharmacodynamic data analysis, and contributing to clinical study reports and regulatory submissions. The role also includes supporting all phases of drug development, from Phase 1 to Phase 4, with a focus on non-compartmental analysis and ensuring the accuracy and timeliness of PK/PD data.

Johnson & Johnson MedTech

On-site Permanent