Senior Regulatory Affairs Specialist - Plymouth, MN

This role involves preparing regulatory submissions for new products changes renewals to support global market access collaborating with cross-functional teams ensuring product documentation aligns with applicable regulatory requirements. · ...

We believe that great healthcare is an essential safeguard of human dignity. · At Laborie, we know the work we do matters – it's what fuels our motivation and contributes to our success.This role involves hands-on development of regulatory strategies, preparation of submissions, ...

We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters – it's what fuels our motivation and contributes to our success. · If you're ready to make a positive impact in the lives of patients across the globe, we'd lik ...

We are seeking a passionate and experienced Senior Regulatory Affairs Specialist to join our team on-site in Plymouth, MN. This role will lead the preparation and submission for regulatory approvals and identify and resolve problems. · ...

The primary purpose of this job is to strategically plan, execute and provide oversight to regulatory activities necessary to obtain and maintain regulatory approvals within the United States and International markets and ensure compliance with relevant FDA, EU, ISO, and other re ...

The primary purpose of this job is to strategically plan, execute and provide oversight to regulatory activities necessary to obtain and maintain regulatory approvals within the United States and International markets and ensure compliance with relevant FDA, EU, ISO, and other re ...

The primary purpose of this job is to strategically plan, execute and provide oversight to regulatory activities necessary to obtain and maintain regulatory approvals within the United States and International markets. · We create better solutions · Collaboration · We create suc ...

The primary purpose of this job is to provide team support to Regulatory Affairs managers and department management in being responsible for ensuring compliance to all relevant regulations and standards. · You adhere to Integer's Values and all safety, environmental, security and ...

Abbott is seeking a Regulatory Affairs Specialist II to join our team on-site in Plymouth, MN.In this role, you will perform specialized level work assignments and/or analyses · ...

Abbott is recruiting for a Regulatory Affairs Specialist III to join their team on-site in Plymouth, MN.This new team member will support manufacturing/operations day-to-day activities for change control and provide regulatory direction on team activities. · ...

+As an individual contributor, this position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for regulatory registration. · ...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. · Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic med ...

+ Serve as a regulatory affairs specialist supporting product corrections and recalls in collaboration with the Field Action Team. · + Coordinate communication with internal OUS regulatory partners and external regulatory authorities for recall-related activities. · + Manage Prod ...

We are seeking a highly skilled Principal Regulatory Affairs Specialist to join our Interventional Cardiology and Vascular Therapies Division. · ...

The Sr. Regulatory Affairs Specialist (SRA) will develop US, EU, and Canada strategies, assessments and submissions for complex projects across multiple business units and review issues related to regulatory documents. · ...

The Sr. Regulatory Affairs Specialist will develop US EU and Canada strategies assessments and submissions for complex projects across multiple business units. · Conduct appropriate research using standards guidance documents previous assessments and other resources to develop st ...

+At Boston Scientific we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees tackling some of the most important health industry challenges with access to the latest tools information and training we'll help yo ...

We are seeking a highly skilled and experienced Principal Regulatory Affairs Specialist to join our Interventional Cardiology and Vascular Therapies Division. · This role follows a hybrid work model requiring employees to be in our local office at least three days per week.Boston ...

The Sr. · Regulatory Affairs Specialist (SRA) will develop US, EU, · & Canada strategies, assessments and submissions for complex projects across multiple business units and review issues related to regulatory documents, · investigations, product development planning and regulat ...

Join our Vascular Therapies Regulatory Team where we develop innovative technologies to treat peripheral vascular disease. Our products improve patient outcomes and enhance lives by delivering some of the most advanced and comprehensive therapy solutions on the market. · ...