Sr Regulatory Affair Principal - Somerville

+ Job Summary · Working cross-functionally with the Research and Development – ProFound team, the Sr.Regulatory Affairs Principal is responsible for developing and executing regulatory strategies, · ensuring compliance with global regulations and leading the process to obtain · a ...

Working cross-functionally with the Research and Development – ProFound team, the Sr. Regulatory Affairs Principal is responsible for developing and executing regulatory strategies, ensuring compliance with global regulations and leading the process to obtain and maintain market ...

Working cross-functionally with the Research and Development – ProFound team, the Sr. Regulatory Affairs Principal is responsible for developing and executing regulatory strategies, · ensuring compliance with global regulations and leading the process to obtain and maintain marke ...

We are seeking a Sr Regulatory Affairs Principal to develop and execute regulatory strategies for our high-risk products. The successful candidate will have experience with FDA regulations and submissions. ...

We are seeking a Sr. Regulatory Affairs Principal to join our team. This role will be responsible for developing and executing regulatory strategies to ensure compliance with global regulations and leading the process to obtain and maintain market approval for DeepHealth's high-r ...

The Sr. Regulatory Affairs Principal works cross-functionally with the Research and Development team to develop regulatory strategies for DeepHealth's high-risk products.Develops regulatory strategy for high-risk devicesProvides strategic input on product lifecycle planningLeads ...

The Sr Regulatory Affairs Principal - (Autonomous) will develop and execute regulatory strategies ensuring global regulations compliance leading market approval for DeepHealth high risk products including AI technologies. ...

Working cross-functionally with the Research and Development – ProFound team, the Sr. Regulatory Affairs Principal is responsible for developing and executing regulatory strategies. · ...

This Sr. Regulatory Affairs Principal role involves developing and executing regulatory strategies for DeepHealth's high-risk products. The ideal candidate will have strong knowledge of FDA Quality System Regulations and experience drafting regulatory filings. · ...

A global health consulting firm in Boston seeks a Principal Consultant to deliver key Medical Affairs projects and foster business growth. · All the relevant skills, qualifications and experience that a successful applicant will need are listed in the following description. · The ...

Cardinal Health is seeking a Principal Regulatory Affairs Specialist to support the Medical Solutions Regulatory Affairs team. · ...

Cardinal Health is seeking a Principal Regulatory Affairs Specialist. The selected candidate will provide regulatory support on medical devices.Regulatory lead for change development projects. · New product development, change assessment, US, EU and international regulatory submi ...

+Job summary · +Regulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. · +Responsibilities:Lead new and modified product development projects to establish and ...

This is a remote position and the ideal candidate will be located near Mansfield MA or Waukegan IL. The Principal Regulatory Affairs Specialist will support the Medical Solutions Regulatory affairs team responsible for regulatory activities associated with new product development ...

Acute Care TechnologyAt ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and tr ...

Acute Care TechnologyAt ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and tr ...

Acute Care TechnologyAt ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and tr ...

We are a growing family-owned innovative company founded in 1966. We operate directly in over 30 countries and have a workforce of more than 7, · 000 strong. · Participates as regulatory design team member for new products providing early input on analytical test requirements. · ...

Responsible to manage pre-market regulatory activities required to maintain compliance to US FDA, Health Canada and EU IVD Regulations (EU) 217/46, as well as other country regulatory agencies. · ...

This Senior/ Principal Regulatory Affairs Specialist will integrate with engineering and clinical teams to contribute to bench work design discussions early drafting of submissions This full-time permanent opportunity offers a competitive salary comprehensive benefits package qua ...