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Science Regulatory Jobs in Minneapolis, Minnesota

Currently, there are no Science Regulatory jobs available in Minneapolis, Minnesota which match this search. You may wish to explore similar job titles on the Science jobs in Minnesota page or view related jobs below.
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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...
Category : Biotech/R&D/Science Location/City : MN - Minneapolis Id : 1684 Pace Division: Labops Summary: The Regulatory Specialist will provide regulatory support and advice to our customers on regulatory matters throughout a product's lifecycle (formulation, development, packaging design, and retail sales.) Responsibilities: Author Safety Data Sheets (SDS) Review labels for compliance with...
Qualifications All required qualifications must be documented on application materials . Required Qualifications : Bachelor’s degree in related health science field plus 2 years’ experience in research including assisting in protocol activation of research studies including preparing and submitting IRB applications, budgets and regulatory files; or a combination of related education and work ex...
Qualifications Required Qualifications: Qualified candidates will have completed a Doctoral Degree in Psychology or related field and a publication record in the area of tobacco regulatory science. Individual must have skills in conducting tobacco regulatory research, data analysis and writing scientific articles. Must have the skills and ability to work independently. Preferred Qualifications:...
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...
Primary Location: US-MN-Maple Grove Additional Locations: US-IL-Chicago; US-MA-Boston; US-MA-Marlborough; US-MI-Detroit; US-MN-Arden Hills; US-MN-Maple Grove; US-MO-St. Louis Requisition ID: 135257 At Boston Scientific, our products and technologies are used to diagnose or treat a wide range of medical conditions including heart, digestive, pulmonary, vascular, urological, women's health, and c...
Primary Location: US-MN-Maple Grove Additional Locations: US-IL-Chicago; US-MA-Boston; US-MA-Marlborough; US-MI-Detroit; US-MN-Arden Hills; US-MN-Maple Grove; US-MO-St. Louis Requisition ID: 135257 At Boston Scientific, our products and technologies are used to diagnose or treat a wide range of medical conditions including heart, digestive, pulmonary, vascular, urological, women’s health, and c...
Job ID: 105299 3M is seeking a Regulatory Affairs Associate for the Critical and Chronic Care Solutions Division (C3SD) located in Maplewood, MN. Ready to be part of what’s next? Job Summary : The person hired for the position for the Regulatory Affairs Associate wilI lead medical device and combination product registration activities globally. Primary Responsibilities include but are not limi...
Category : Biotech/R&D/Science Location/City : MN - Maplewood Id : 1757 Pace Division: LabOps Summary: Candidate will analyze customer products in regards to human health effects and product compliance, and make recommendations for environmental health and safety in this scientific, non-laboratory position. Responsibilities: Work as part of team that provides product EHS support and leaders...
Job ID: 105340 3M is seeking an International Regulatory Affairs Associate for the Healthcare Business Group located in Maplewood, MN. Be part of what’s next! Job Summary : The person hired for the position of International Regulatory Affairs Associate will be responsible for supporting international projects in order to support our growth globally. The position will work closely with 3M Region...
Job ID: 104783 3M is seeking a Regulatory Affairs Associate for the Critical and Chronic Care Solutions Division (C3SD) located in Maplewood, MN. Ready to be part of what’s next? Job Summary : The person hired for the position of Regulatory Affairs Associate wilI lead medical device registration activities globally. Primary Responsibilities include but are not limited to the following: - Prov...
Job ID: 103241 3M is seeking a Regulatory Affairs Associate for the Oral Care Solutions Division located in Maplewood, MN. Ready to be part of what's next? Job Summary : The person hired for the position of Regulatory Affairs Associate will provide regulatory support to marketed device product teams and new product introductions with focus on Dental and Orthodontic medical device products. Pri...
Category : Biotech/R&D/Science Location/City : MN - Maplewood Id : 1699 Pace Division: LabOps Summary: Candidate will provide product Hazard Communication and Product Regulatory Support to our customers. If you are a scientist who wishes to apply their technical knowledge to achieve business and safety goals, this is an excellent career opportunity. Responsibilities: Generate SDS's and prod...
Job ID: 100688 3M is seeking a Regulatory Affairs Associate for the Infection Prevention Division located in Maplewood, MN. Be part of what’s next! Job Summary : The person hired for the position of Regulatory Affairs Associate will provide regulatory support to marketed device product teams and new product introductions with focus on device hardware and consumable products. Primary Responsibi...
Actuary - Life Risk & Regulatory Consulting 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. Serve as the actuarial subject matter expert on client engagements including; coordinate internal resources, advise project team on p...
IT Auditor Risk & RegulatoryInsurance Consulting The IT Auditor is responsible for supporting Risk & Regulatory Consultingin 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. (Responsibilities will vary slightly depending on seniority level) ...
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...
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...
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...