Remote Regulatory Specialist – Active Medical Devices

A premier certification body is seeking a home-based Technical Specialist & Scheme Manager to evaluate medical devices for compliance and support manufacturers throughout their certification life cycle. The position requires at least 5 years of experience with active medical devices, a relevant degree, and a deep understanding of regulatory requirements....

A premier certification body is seeking a home-based Technical Specialist & Scheme Manager to evaluate medical devices for compliance and support manufacturers throughout their certification life cycle. The position requires at least 5 years of experience with active medical devices, a relevant degree, and a deep understanding of regulatory requirements....

Great that you're thinking about a career with BSI! Job title: Technical Specialist & Scheme Manager - Active Devices Location: Home-based position located in the UK or Europe with up to 20% travel for training. BSI is seeking experienced R&D Engineers to join our Active Medical Devices team as a home-based Technical Specialist & Scheme Manager (Technical...

A leading global certification company is looking for a Senior Product Assessor for Active Medical Devices. This remote role involves managing a team, conducting compliance assessments, and ensuring the highest standards. Candidates should have significant experience in medical devices and relevant technical knowledge. The company promotes innovation and...

Great that you're thinking about a career with BSI! Job title: Technical Specialist & Scheme Manager - Active Devices Location: Home-based position located in the UK or Europe with up to 20% travel for training. BSI is seeking experienced R&D Engineers to join our Active Medical Devices team as a home-based Technical Specialist & Scheme Manager (Technical...

Job Title Technical Specialist & Scheme Manager - Active Devices Location Home-based position located in the UK or Europe with up to 20% travel for training. Responsibilities Review and evaluate medical device technical and clinical documentation in your areas of competence to assess compliance with MDD 93 / 42 / EEC, MDR 2017 / 745 and UK MDR 2012 schemes....

A leading medical technology company is seeking an Advanced Regulatory Affairs Specialist in Rome, Italy. You will be responsible for regulatory activities related to product registrations and compliance across EMEA. The ideal candidate has a Bachelor’s degree in Science or Engineering, at least 5 years of experience in regulatory affairs, and excellent...

Are you ready to take your career to the next level? If you have a strong background as a Product Assessor within an EU notified body conducting MDD / MDR technical documentation review then we have an exhilarating opportunity for you! Join our dynamic team at SGS and become a Senior Product Assessor - Active Devices. This role will allow you to make a...

A leading global healthcare company is seeking an Advanced Regulatory Affairs Specialist in Vimercate, Italy. In this role, you will participate in regulatory activities tied to the import and distribution of medical devices across the EMEA region. The ideal candidate has a Bachelor's Degree in Science or Engineering and at least 5 years of relevant...

A global healthcare technology firm in Italy is looking for an Advanced Regulatory Affairs Specialist to join their team. You will participate in all regulatory activities related to the import and distribution of medical devices within the EMEA region, ensuring compliance with regulations. The role requires a Bachelor's degree and experience in the medical...