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Regulatory Affairs Specialist Jobs in Minneapolis, Minnesota

13 jobs

Position Description The Senior Regulatory Affairs Specialist (NDT) is responsible for developing global regulatory strategy, preparing submissions and obtaining approval to introduce Medtronic Inc. products and therapies. Position Responsibilities • Provide regulatory support for new products/therapies and changes to existing products. Work with other RAS, engineers and technical experts to re...
Together Medtronic and Covidien are working to improve how healthcare addresses the needs of more people, in more ways and in more places around the world. As one company, we can accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. This is the ideal opportunity to join us, and be part of our commitment to the health of ot...
Together Medtronic and Covidien are working to improve how healthcare addresses the needs of more people, in more ways and in more places around the world. As one company, we can accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. This is the ideal opportunity to join us, and be part of our commitment to the health of ot...
We are seeking an experienced, high caliber Regulatory Affairs Specialist I to join our international regulatory team, with fluency in Chinese (Mandarin preferred). Each employee can make a difference at St. Jude Medical and has the power, either individually or as a team, to influence the success of the company. We are team-oriented, fast-paced and progressive. We value people with great ideas w...
We are seeking an experienced, high caliber International Regulatory Affairs Specialist II to be responsible for regulatory submissions work for an assigned project effort. The Specialist prepares, reviews and coordinates project submissions for regulatory approvals. Employees act on their strong desire to make a difference, partner with others and put ideas into action. Employees are engaged by a...
We are seeking an experienced, high caliber International Regulatory Affairs Specialist II to be responsible for regulatory submissions work for an assigned project effort. The Specialsit prepares reviews and coordinates project submissions for regulatory approvals. Employees act on their strong desire to make a difference, partner with others and put ideas into action. Employees are engaged by a ...
Summary of Position with General Responsibilities: This position will be responsible for global adverse event reporting, world-wide regulatory submissions and ensuring compliance with all the required regulations for assigned projects. Essential Job Functions: Responsibilities: Participates in product development/line extension teams as required to ensure that the product is in compliance with...
Regulatory Affairs Specialist I - (150001VT) About Us At St. Jude Medical every one of us plays a role in our collective ability to save and improve lives. As an organization, we want to continue to grow and lead our industry in changing the way the world views the treatment of expensive, epidemic diseases. By seeing things from a different perspective, using our imagination, leading with charact...
International Regulatory Affairs Specialist II - (150001UU) About Us At St. Jude Medical every one of us plays a role in our collective ability to save and improve lives. As an organization, we want to continue to grow and lead our industry in changing the way the world views the treatment of expensive, epidemic diseases. By seeing things from a different perspective, using our imagination, leadi...
Together Medtronic and Covidien are working to improve how healthcare addresses the needs of more people, in more ways and in more places around the world. As one company, we can accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. This is the ideal opportunity to join us, and be part of our commitment to the health of ot...
Senior Regulatory Affairs Specialist - Interventional Lung Solutions (ILS) The Senior Regulatory Affairs Specialist is responsible for communications and submissions to global government agencies to support marketing approvals. This involves interfacing and supporting requests for information from global government agencies. The position is also responsible for supporting Design Control requireme...
Regulatory Affairs Specialist - International The International Regulatory Affairs Specialist develops and executes strategies for global regulatory approvals to introduce new and modified medical device products to the market. The Regulatory Affairs Specialist translates regulatory requirements into project/product requirements, prepares worldwide regulatory submissions and negotiates their appr...
The Senior Regulatory Affairs Specialist develops strategies for worldwide governmental approvals to introduce new and modified products to the market, prepares advice on regulatory requirements, prepares worldwide regulatory submissions and negotiates their approval. Responsibilities include developing regulatory strategies, preparing US FDA submissions, providing documentation for internat...