Regulatory Affairs Specialist Jobs in Minneapolis, Minnesota

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63 Minneapolis, MN Regulatory Affairs Specialist jobs found on Monster.

Jobs 1 to 20 of 63
COMPANY OVERVIEW: Vital Images, Inc., a Toshiba Medical Systems Group Company, is a market leader in advanced visualization software solutions for physicians and healthcare specialists. The company's sophisticated technology gives radiologists, cardiologists, oncologists and other medical specialists productivity and communications tools that can be accessed throughout the enterprise and via the ...
COMPANY OVERVIEW: Vital, a Toshiba Medical Systems Group Company, is a market leader in advanced visualization software solutions for physicians and healthcare specialists. The company's sophisticated technology gives radiologists, cardiologists, oncologists and other medical specialists productivity and communications tools that can be accessed throughout the enterprise and via the Web at anytim...
This position is responsible for: developing strategies for worldwide regulatory approval and introduction of new products to market. Provide regulatory support on product development teams for regulatory issues and questions. Prepares U.S. and international submissions and provides support for major market regulatory approvals. Provides post-market support and ensures regulatory compliance ...
Description: We're changing the way health care works for the better. That means consulting with our members, partnering with our physicians, and delivering drugs in the most efficient and effective way. Join us and start doing your life's best work.(sm) The Manager, Regulatory Affairs has responsibility for managing strategic regulatory operations and providing expert advice on the guidelines a...
American Medical Systems Holdings, Inc. Minneapolis, MN, 55415
POSITION SUMMARY: The Senior Regulatory Affairs Specialist originates appropriate documents to obtain and maintain clinical and/or marketing privileges consistent with applicable government requirements where AMS conducts business. All positions are responsible for following applicable AMS policies and procedures as defined by their manager. PRINCIPAL DUTIES AND RESPONSIBILITIES: • Plans, coor...
Medtronic Fridley, MN
The Regulatory Affairs Specialist is responsible for developing pre- and post-market regulatory strategies, preparing U.S. and international submissions and obtaining approval for products and therapies to markets worldwide.• Define the regulatory strategy and manage regulatory submission activities for new product development activities and product maintenance for existing approved products. • T...
Medtronic Fridley, MN
The Senior Regulatory Affairs Specialist is responsible for developing regulatory strategy, preparing U.S. and international submissions and obtaining approval to introduce new products and therapies to markets worldwide.• Provide support to currently-marketed products as necessary. This includes reviewing labeling, promotional material, product changes and documentation for changes requiring gove...
Medtronic Fridley, MN
The Senior Regulatory Affairs Specialist is responsible for developing regulatory strategy, preparing U.S. and international submissions and obtaining approval to introduce new products and therapies to markets worldwide.• Provide support to currently-marketed products as necessary. This includes reviewing labeling, promotional material, product changes and documentation for changes requiring gove...
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 character, and working with passion, we all have a role to pla...
St. Jude Medical Saint Paul, MN, 55102
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 character, and working with passion, we all have a role to pla...
This position is responsible for: developing strategies for worldwide regulatory approval and introduction of new products to market. Provide regulatory support on product development teams for regulatory issues and questions. Prepares U.S. and international submissions and provides support for major market regulatory approvals. Provides post-market support and ensures regulatory compliance of ma...
This position is responsible for: developing strategies for worldwide regulatory approval and introduction of new products to market. Provide regulatory support on product development teams for regulatory issues and questions. Prepares U.S. and international submissions and provides support for major market regulatory approvals. Provides post-market support and ensures regulatory compliance ...
Medtronic Inc. Fridley, MN, 55432
Position Description The Regulatory Affairs Specialist is responsible for developing pre- and post-market regulatory strategies, preparing U.S. and international submissions and obtaining approval for products and therapies to markets worldwide. Position Responsibilities • Define the regulatory strategy and manage regulatory submission activities for new product development activities and produ...
Smiths Group St. Paul, MN
Job Title: Regulatory Affairs Specialist II Requisition Number: Dom1385 Job Family: Regulatory Affairs and Quality Assurance Position Type: Regular Standard Hours: Full Time (40 hours) City: St. Paul State / Province: Minnesota Country: U.S. Opportunity: Job Purpose: Position provides regulatory expertise for the Smiths Medical site based in St. Paul, Minnesota. The incumbent will also b...
Baxter International Inc St Paul, MN
DescriptionThis position is responsible for: developing strategies for worldwide regulatory approval and introduction of new products to market. Provide regulatory support on product development teams for regulatory issues and questions. Prepares U.S. and international submissions and provides support for major market regulatory approvals. Provides post-market support and ensures regulatory compl...
Baxter International Inc St Paul, MN
DescriptionThis position is responsible for: developing strategies for worldwide regulatory approval and introduction of new products to market. Provide regulatory support on product development teams for regulatory issues and questions. Prepares U.S. and international submissions and provides support for major market regulatory approvals. Provides post-market support and ensures regulatory compl...
St. Jude Medical, Inc. St, MN
Description We are seeking an experienced, high caliber Regulatory Affairs Specialist to be responsible for regulatory submissions work for an assigned project effort. 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 work culture that ...
St. Jude Medical, Inc. St, MN
Description We are seeking an experienced, high caliber Senior Regulatory Affairs Specialist. This position supports new product development and on-going regulatory support for approved structural heart implantable devices, specifically transcatheter heart valve technologies. Employees act on their strong desire to make a difference, partner with others and put ideas into action. Employees are e...
St. Jude Medical, Inc. St, MN
Description We are seeking an experienced, high caliber Regulatory Affairs Specialist to join our team. Working without appreciable direction, the RA Specialist prepares and submits worldwide regulatory applications for neuromodulation products. Employees act on their strong desire to make a difference, partner with others and put ideas into action. Employees are engaged by a work culture that i...
Medtronic Mounds View, MN
The Regulatory Affairs Specialist is responsible for providing assistance in supporting the process of meeting requirements established by FDA and major market regulatory agencies in introducing new products to market and supporting market-released products.• Provide assistance to more senior Regulatory Affairs Specialists in developing product submissions for FDA and other major market regulatory...

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Legal Career Tools

Regulatory Affairs Associate

Salaries

$38,760.00 - $94,500.00
Typical Salary for Regulatory Affairs Associate in Minneapolis
(111 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
38.8%
Master's
38.8%
Associates
9%
Some College Coursework Completed
4.5%
High School
3%
Doctorate
3%
(67 Respondents)
Source: Monster.com Careerbenchmarking Tool

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