Science Regulatory Jobs in Minneapolis, Minnesota

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527 Minneapolis, MN Science Regulatory jobs found on Monster.

Jobs 1 to 20 of 527
We have been engaged by our client to search for a Director of Regulatory Affairs. Primary responsibilities include developing and implementing regulatory strategy/tactics and ensuring alignment of regulatory strategy to business strategy in order to accelerate the development and commercialization of Company's products. Candidate will additionally provide regulatory insight (raising potential iss...
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...
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 ...
Regulatory Affairs Specialist Arden Hills, MN Kelly Services is currently seeking a Regulatory Affairs Specialist for one of our top clients in Arden Hills, Minnesota. As a Regulatory Affairs Specialist placed with Kelly Services, you provide regulatory affairs representation on development teams with emphasis on preparation of documents for regulatory submissions for the Medical Device Industry...
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...
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...
Job ID: 71968 3M is seeking a Regulatory Affairs Associate for the Materials Resource Division (MRD) located in Maplewood, Minnesota. Be part of what’s next! Job Summary : The person hired for the position of Regulatory Affairs Associate will primarily be responsible for global product regulatory compliance, hazard communication and life cycle management support activities for Materials Resourc...
POSITION SUMMARY: The Senior Manager Regulatory Affairs Franchise Lead provides direction and oversight within Regulatory Affairs and other departments to assure achievement of franchise objectives worldwide. This individual is the RA single-point-of-contact for their respective franchises; member of the franchise business team, PST, NPD portfolio management team, Change Control Board and CAPA Re...
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...
Manages specific tasks of assigned research, education or operational projects or programs. Develops and executes plans and strategies to ensure the delivery of quality programming, services, tools and/or materials. Possesses a specialized set of skills and knowledge related to a specific area of focus. Education/Experience: Bachelor’s degree or specialized training equivalent and minimum two year...
The RA Project Manager position is responsible for the hands-on regulatory activities required to submit, approve and launch new products and for the maintenance of existing commercialized products for the Prescription Drug business unit. The Project Manager executes regulatory activities according to project plans to assure new products meet submission, approval and commercial launch goals. Relat...
Actuary - Life Risk & Regulatory Consulting Position Overview As an Actuarial Consultant you will work with a team of industry professionals on regulatory consulting engagements. This position has significant opportunity for advancement as well as personal and professional growth. Specific Duties and Responsibilities Serve as the actuarial subject matter expert on client engagements including...
An exciting leadership opportunity is currently available at Perrigo’s facilities just outside of Minneapolis, Minnesota. We are currently searching for an experienced manager to take on this leadership role and manage a team of Regulatory professionals. In addition to managing the team, the RA Manager will manage regulatory activities and collaborate with the project team to develop regulatory st...
IT Auditor Risk & Regulatory Insurance Consulting Position Overview The IT Auditor is responsible for supporting Risk & Regulatory Consulting in the overall growth and management of their functional area. The IT Auditor is responsible for all aspects of client project management and delivery, as well as supporting Practice and People development. Specific Duties and Responsibilities (Responsi...
We are always hiring, because Vascular Solutions is always growing. Successful both clinically and financially, we provide meaningful work, financial rewards and rapid growth opportunities for employees who want a chance to achieve based on their own merits. Please review the responsibilities and requirements of the position below. If you would like to join the nation’s fastest growing medical de...
Smiths Group St. Paul, MN
Job Title: Sr. Regulatory Affairs Specialist Requisition Number: RAQA1823 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...
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...
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...
Medtronic Mounds View, MN
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 international ...

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Science Career Tools

Science Regulatory/Quality Assurance, Other

Salaries

$24,960.00 - $79,040.00
Typical Salary for Science Regulatory/Quality Assurance, Other in Minneapolis
(51 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
51.1%
Master's
22.2%
Associates
15.6%
Doctorate
6.7%
Some College Coursework Completed
4.4%
(45 Respondents)
Source: Monster.com Careerbenchmarking Tool

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