Regulatory Affairs Specialist Jobs in Minnesota

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32 Minnesota Regulatory Affairs Specialist jobs found on Monster.

Jobs 1 to 20 of 32
POSITION SUMMARY: The Principal Regulatory Affairs Specialist originates appropriate documents to obtain and maintain clinical and/or marketing privileges consistent with applicable government requirements. All positions are responsible for following applicable AMS policies and procedures as defined by their manager. PRINCIPAL DUTIES AND RESPONSIBILITIES: · Primary regulatory representative on...
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 Principal Regulatory Affairs Specialist serves as a principal spokesperson related to new technological/technical research, functional thought leadership, and other significant advancements. Acts independently to uncover and resolve issues associated with the development and implementation of long range organizational goals. Determines and pursues courses of action necessary to obtain r...
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...
St. Jude Medical, Inc. Plymouth, 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 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 Plymouth, MN, 55447
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...
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...
Job Title: Regulatory Affairs Specialist Location: Minneapolis, MN Contract: 6+ months Pay: Open Job Description: Reviewing design and manufacturing changes for PMA products for FDA reportability and writing up reports and submissions as needed. Device regulatory experience mandatory; Healthcare regulatory experience highly desired. Engineering background highly desired. Scientific undergra...
A leading company in the medical device industry is currently seeking a Senior Regulatory Affairs Specialist to join their team. For the right candidate, this is a fantastic opportunity with great growth prospects. Details: 1) Assist in the development of regulatory strategy and update strategy based upon regulatory changes 2) Determine trade issues to anticipate regulatory obstacles 3) Determi...
Contract opportunity through 4/27/2015 Bachelors degree required Request Notes : -Reviewing design and manufacturing changes for PMA products for FDA reportability and writing up reports and submissions as needed. -Device regulatory experience mandatory; -Engineering background highly desired. -Scientific undergrad (ideally engineering) at a minimum. -Full time but flexible on this. -Flexi...
Our client in Minneapolis, MN is looking for Regulatory Affairs Specialist. This is a long term consulting position. If interested, Please apply to this ad . Job Title: Regulatory Affairs Specialist Job Location: Minneapolis, MN Job#: 14-01798 Job Description: Will review design and manufacturing changes for PMA devices to assess FDA reportability. Regulatory experience highly desired. Engi...
Johnson & Johnson Maple Grove, MN, 55369
REGULATORY AFFAIRS SPECIALIST I-5955141001 Description Johnson & Johnson and the Global Surgery Group is recruiting for a Regulatory Affairs Specialist at Sterilmed, located in Plymouth, MN. The Global Surgery Group is comprised of the following businesses within Johnson & Johnson: Ethicon Surgical Care, Ethicon Energy, Ethicon Biosurgery, Acclarent, Biosense Webster, Cordis, Mentor and Sterilm...
Title: Regulatory Affairs Specialist Company: Medical Device Duration: Contract, 10 months Location: Minneapolis, MN Join one of the world s largest medical technology companies! Role: Contractor will review design and manufacturing changes for PMA devices to assess FDA reportability. Regulatory assessment of post-market changes to PMA device components and manufacturing processes. Work wi...
Title: Regulatory Affairs Specialist Company: Medical Device Duration: Contract, 6 months Location: Minneapolis, MN Role: Reviewing design and manufacturing changes for PMA products for FDA reportability and writing up reports and submissions as needed. Prepare required documentation (510(k)s, technical files, dossiers) for domestic and foreign submissions and registrations. Attend design r...
Cantel Medical Plymouth, MN, 55447
Company Overview: MEDIVATORS (formerly Minntech Corporation), a Cantel Medical Company, is a medical technology innovator of life-impacting solutions for over 35 years. Having a broad range of competencies in medical disposables, medical solution manufacturing, hollow fiber filtration, chemical disinfection, high level disinfection and sterilization, the company serves the healthcare, therapeutic...
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...
American Medical Systems Holdings, Inc. Minneapolis, MN, 55415
POSITION SUMMARY: The Principal Regulatory Affairs Specialist originates appropriate documents to obtain and maintain clinical and/or marketing privileges consistent with applicable government requirements. All positions are responsible for following applicable AMS policies and procedures as defined by their manager. PRINCIPAL DUTIES AND RESPONSIBILITIES: • Primary regulatory representative on...
Medtronic Inc. Fridley, MN, 55432
Position Description The Senior Principal Regulatory Affairs Specialist serves as a principal spokesperson related to new technological/technical research, functional thought leadership, and other significant advancements. Acts independently to uncover and resolve issues associated with the development and implementation of long range organizational goals. Determines and pursues courses of action...

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Legal Career Tools

Regulatory Affairs Associate

Salaries

$38,760.00 - $94,500.00
Typical Salary for Regulatory Affairs Associate in Minnesota
(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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