Regulatory Relations Specialist jobs in Minneapolis, MN

Regulatory Relations Specialist files applications and interacts with governmental officials during the regulation and certification process for a plant or other facility. Assists in developing procedures to ensure regulatory compliance. Being a Regulatory Relations Specialist gathers data pertaining to organizational projects and their impact on the regulation process. May require a bachelor's degree. Additionally, Regulatory Relations Specialist typically reports to a supervisor or manager. To be a Regulatory Relations Specialist typically requires 4 to 7 years of related experience. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. (Copyright 2024 Salary.com)

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Regulatory Specialist
  • Patterson
  • Saint Paul, MN FULL_TIME
  • Patterson isn't just a place to work, it's a partner that cares about your success.

    One of the distinguishing marks of our company is the talented people who embrace the people-first, always advancing, and results-driven culture. Professional growth abounds in this motivating environment. We value the diverse talents and experiences our employees bring to Patterson and believe that they build a stronger and successful organization.

    This position supports Patterson’s Pharmaceutical Distribution business related to the Controlled Substance Monitoring Program (CSMP). The Specialist will be responsible for ensuring compliance to DEA regulations regarding controlled substances, State regulations of controlled substances and internal due diligence SOP’s. The duties for this position include, but are not limited to, conducting customer due diligence; leveraging tools, reports, and data; and documenting findings in accordance with CSMP policies and procedures.

    Responsibilities:

    • Conduct due diligence of prospective or existing customers related to controlled substances. Reviews may include conducting state license and DEA registration checks, open-source research, analysis of internal or external data or the use of other available information.
    • Performs thorough reviews of controlled substance orders of interest as part of the Suspicious Order Monitoring program. Determine whether to release, investigate or escalate a customer in accordance with SOM policies and procedures.
    • Review and analyze data to support due diligence efforts and identify/validate controlled substance trends or customer profiles.
    • Liaison with customers or Patterson Sales personnel to obtain additional information as needed.
    • Write reports, document due diligence activities and maintain customer due diligence files in accordance with CSMP policies and procedures.
    • Stay current on product and geographic abuse and diversion trends as well as industry trends, best practices and DEA guidance.
    • Seek opportunities to improve operational excellence of controlled substances related polices and procedures.
    • Performs other duties as assigned or requested;

    Minimum/Required Qualifications

    • 2 years experience in a related regulatory or investigative field.
    • Strong verbal and written communication skills, including writing reports.
    • Strong analytical and critical thinking skills.
    • The ability to analyze a variety of information sources to make informed decisions.
    • Organized and detailed oriented. Ability to effectively prioritize and multi-task.
    • Proficiency in use of Microsoft Office tools and the ability to learn new tools (i.e. Tableau).
    • Ability to develop trust and credibility at all levels of the organization and maintain confidentiality.
    • Highly motivated and self-driven with the ability to work efficiently with limited supervision.


    Preferred Qualifications

    • Knowledge of controlled substances and diversion trends is preferred.
    • Working knowledge of Federal and State government laws and regulations related to controlled substances.
    • Knowledge or experience monitoring controlled substances and diversion trends.
    • Experience conducting due diligence or investigations.
    • Experience with SAP or other reporting and analytics tools.
    • Ability to analyze data and draw conclusions.

    What's In It For You:

    We provide competitive benefits, unique incentive programs and rewards for our eligible employees:

    • Full Medical, Dental, and Vision benefits and an integrated Wellness Program.

    • 401(k) Match Retirement Savings Plan.

    • Employee Stock Purchase Plan (ESPP).

    • Paid Time Off (PTO).

    • Holiday Pay & Floating Holidays.

    • Volunteer Time Off (VTO).

    • Educational Assistance Program (Tuition Reimbursement).

    • Full Paid Parental and Adoption Leave.

    • LifeWorks (Employee Assistance Program).

    • Patterson Perks Program.

    EEO Statement

    As a people-first company, Patterson promotes a culture that embodies and celebrates diversity and inclusivity. We believe our employees’ unique experiences and differences is what strengthens us and drives our success. We consider all qualified applicants without regard to race, religion, color, sex, national origin, age, sexual orientation, gender identity, disability or veteran status.

    We are Patterson. We welcome you.

  • 17 Days Ago

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Regulatory Specialist
  • infinite Computing solutions
  • Saint Paul, MN FULL_TIME
  • Required: · Regulatory operations team · SAP and windchill experience are must. · Other PLM systems experience is good to have. · Work cross-functionally with other teams. · Data analysis and running ...
  • 18 Days Ago

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Regulatory Specialist
  • Electromed Inc.
  • Prague, MN FULL_TIME
  • People Purpose: Beyond CompetitiveIt is no longer ok to just be competitive regarding how we treat our people in everything we do. Our leadership team believes wholeheartedly we need to be beyond comp...
  • 1 Month Ago

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Senior Regulatory Affairs Specialist
  • ICONMA, LLC
  • Saint Paul, MN FULL_TIME
  • This position will be working with multiple business units to develop, update, and improve regulatory affair processes. Assist the strategy implementation and operations for regulatory affairs activit...
  • 16 Days Ago

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Sr. Regulatory Affairs Specialist
  • Medtronic
  • Minneapolis, MN FULL_TIME
  • Position Description: Sr. Regulatory Affairs Specialist for Medtronic, Inc. Minneapolis, MN. Multiple positions available. Responsible for developing regulatory strategies, preparing U.S. and internat...
  • 1 Day Ago

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Regulatory Affairs Specialist
  • PMT Corporation
  • Chanhassen, MN FULL_TIME
  • Find Fulfillment in Work Every Day! We Offer Careers that Make a Difference.PMT Corporation, located in Chanhassen, Minnesota, is known for manufacturing and distributing high end, innovative products...
  • 5 Days Ago

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0 Regulatory Relations Specialist jobs found in Minneapolis, MN area

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Principal Regulatory Affairs Specialist
  • Philips
  • Minneapolis, MN
  • Philips Principal Regulatory Affairs Specialist Plymouth , Minnesota Apply Now Principal Regulatory Affairs Specialist- ...
  • 4/23/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Insight Global
  • Saint Paul, MN
  • Location: St. Paul, MN - remote to start, but will transition to a hybrid model in the coming months Contract: 12 month ...
  • 4/22/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • PMT Corporation
  • Chanhassen, MN
  • Find Fulfillment in Work Every Day! We Offer Careers that Make a Difference. PMT Corporation, located in Chanhassen, Min...
  • 4/22/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Insight Global
  • Saint Paul, MN
  • Insight Global is seeking a Regulatory Affairs Specialist to join one of our largest chemical and water clients in Minne...
  • 4/21/2024 12:00:00 AM

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Regulatory Affairs Specialist II - Electrophysiology
  • Abbott
  • Minneapolis, MN
  • Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-chan...
  • 4/21/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Insight Global
  • Eagan, MN
  • Location: St. Paul, MN - remote to start, but will transition to a hybrid model in the coming months Contract: 12 month ...
  • 4/20/2024 12:00:00 AM

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Senior Regulatory Affairs Specialist - Electrophysiology
  • Abbott Laboratories
  • Plymouth, MN
  • Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-chan...
  • 3/4/2024 12:00:00 AM

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Regulatory Affairs Specialist II - Electrophysiology
  • Abbott Laboratories
  • Plymouth, MN
  • Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-chan...
  • 2/22/2024 12:00:00 AM

Minneapolis (/ˌmɪniˈæpəlɪs/ (listen)) is the county seat of Hennepin County and the larger of the Twin Cities, the 16th-largest metropolitan area in the United States. As of 2017, Minneapolis is the largest city in the state of Minnesota and 45th-largest in the United States, with an estimated population of 422,331. The Twin Cities metropolitan area consists of Minneapolis, its neighbor Saint Paul, and suburbs which altogether contain about 3.6 million people, and is the third-largest economic center in the Midwest. Minneapolis lies on both banks of the Mississippi River, just north of the riv...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Relations Specialist jobs
$78,758 to $108,121
Minneapolis, Minnesota area prices
were up 1.4% from a year ago

Regulatory Relations Specialist in Albany, GA
The Regulatory Relations Specialist is responsible for the execution of the overall strategy for regulatory engagement and enterprise-wide standards.  This includes assisting with the management of regulatory examinations, inquiries and meetings.  Additional responsibilities include.
December 09, 2019
Regulatory Relations Specialist in Monroe, LA
We are looking for a Marketing Specialist to plan, coordinate and manage marketing campaigns and activities across marketing channels.
February 06, 2020