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Regulatory Program Manager Jobs in Minnesota (NOW HIRING)

Regulatory Affairs Program Manager Location: Maple Grove, MN 55311 Duration: 12 Months Work Arrangement: Onsite Position Overview The Regulatory Affairs Program Manager will support the Global ...

MN

$64 - $68/hr

Regulatory Affairs Program Manager Location: Maple Grove, MN 55311 Duration: 12 Months Work Arrangement: Onsite Position Overview The Regulatory Affairs Program Manager will support the Global ...

Knowledge of industry-specific regulations and compliance standards relevant to the organization ... Nice to have: Certification in project and program management. Please note that this is not ...

Knowledge of industry-specific regulations and compliance standards relevant to the organization ... Nice to have: Certification in project and program management. Please note that this is not ...

Program Manager Job Location: Minneapolis, MN Job Category: Residential Counselor Job. Description ... federal and state regulations and the organization's policies and procedures. REQUIRED ...

Program Manager

Saint Paul, MN · On-site

$100K - $180K/yr

Summary North Wind is seeking Program Management candidates that are responsible for the overall ... Persons" as defined by the International Traffic in Arms Regulations (ITAR) Preferred ...

Job ID: MNSITE-3830-PrgM Hybrid/Local Govt Program Manager (15+) with BA, product/service/change ... adherence to laws, regulations, policies, and procedures.. Sample Tasks Plan and manage ...

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Regulatory Program Manager information

See Minnesota salary details

$37.7K

$105.2K

$153.8K

How much do regulatory program manager jobs pay per year?

As of Aug 9, 2026, the average yearly pay for regulatory program manager in Minnesota is $105,248.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,900.00 and $129,800.00 per year, depending on experience, location, and employer.

What are some common challenges faced by regulatory program managers, and how can they be addressed in day-to-day work?

Regulatory Program Managers often encounter challenges such as navigating evolving regulatory requirements, coordinating across multiple departments, and ensuring timely submissions to regulatory bodies. Staying updated on changes in regulations and fostering strong communication with cross-functional teams are key to overcoming these hurdles. Leveraging project management tools and establishing clear processes can also help maintain compliance and keep projects on track. Building relationships with regulatory agencies and internal stakeholders further facilitates smoother approvals and minimizes delays.

What is the difference between Regulatory Program Manager vs Regulatory Affairs Specialist?

AspectRegulatory Program ManagerRegulatory Affairs Specialist
Required CredentialsBachelor's degree, certifications like RAC often preferredBachelor's degree, certifications like RAC often preferred
Work EnvironmentOversees multiple projects, manages teams, strategic planningFocuses on specific regulatory submissions, documentation, compliance
Employer & Industry UsageUsed in healthcare, pharmaceuticals, medical devicesCommon in similar industries, often collaborates with managers
Search & Comparison IntentUnderstanding managerial roles, project scopeDetailing compliance tasks, submission processes

The Regulatory Program Manager typically oversees multiple regulatory projects, manages teams, and develops strategic compliance plans. In contrast, the Regulatory Affairs Specialist focuses on preparing documentation, ensuring regulatory compliance for specific products, and supporting submissions. Both roles require similar credentials and are vital in regulated industries like healthcare and pharmaceuticals, but they differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a regulatory program manager?

To excel as a Regulatory Program Manager, you need expertise in regulatory compliance, project management, and industry-specific regulations, often supported by a relevant degree and certifications like PMP or RAC. Familiarity with regulatory submission systems, document management tools, and compliance tracking software is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing complex projects and diverse stakeholders. These abilities ensure regulatory objectives are met efficiently, reducing risks and supporting organizational success in a highly regulated environment.

What does a regulatory program manager do?

A Regulatory Program Manager oversees and coordinates regulatory compliance activities within an organization, often in industries such as pharmaceuticals, healthcare, finance, or energy. They ensure that the company meets all applicable laws, regulations, and industry standards by managing projects related to regulatory submissions, audits, and communications with regulatory agencies. Their role often includes developing strategies for regulatory approvals, monitoring changes in regulations, and working cross-functionally with other departments to maintain compliance. Effective Regulatory Program Managers help minimize compliance risks and support the organization's business objectives.
What are popular job titles related to Regulatory Program Manager jobs in Minnesota? For Regulatory Program Manager jobs in Minnesota, the most frequently searched job titles are:
What cities in Minnesota are hiring for Regulatory Program Manager jobs? Cities in Minnesota with the most Regulatory Program Manager job openings:
Infographic showing various Regulatory Program Manager job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 1% Temporary, and 4% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $105,248 per year, or $50.6 per hour.

Regulatory Affairs Program Manager

Abbott

Maple Grove, MN • On-site

$110 - $160/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 16 days ago


Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 137 frontline employees who took The Breakroom Quiz

179th of 537 rated manufacturers


Job description

Job Title: Regulatory Affairs Program Manager

Location: Maple Grove, MN 55311

Duration: 12 Months

Work Arrangement: Onsite

Position Overview

The Regulatory Affairs Program Manager will support the Global Regulatory Services team and be responsible for managing large-scale regulatory programs across multiple medical device businesses. This role requires strong program and project management experience, cross-functional leadership, and the ability to drive complex initiatives from planning through execution.

Key Responsibilities

  • Lead large-scale regulatory programs spanning multiple functional areas and business units.
  • Manage the execution of projects and programs in accordance with the organization's program management methodology.
  • Develop, prioritize, and manage project plans, budgets, timelines, and methodologies.
  • Define project resources, milestones, deliverables, and lead cross-functional teams to achieve program goals.
  • Take ownership of multiple related projects that collectively comprise a program.
  • Lead complex and/or critical programs, including Extended Producer Responsibility (EPR) initiatives.
  • Establish, review, and own program charters while partnering with program sponsors for approvals.
  • Monitor program progress, performance, budgets, timelines, and overall program health.
  • Re-evaluate program direction based on project status and business objectives.
  • Identify risks, resolve program issues, and minimize project delays.
  • Build and manage relationships across business units and project teams.
  • Support and mentor local Program Managers in implementing standardized processes.
  • Coordinate with the Corporate PMO to manage implementation schedules and budgets.
  • Develop sustainable processes and best practices across business locations.
  • Lead meetings, prepare presentations, and provide regular status updates to senior leadership.
  • Provide training, implementation planning, and ongoing support to program participants.
  • Evaluate external consultants to optimize project costs and business value.

Required Experience

  • Minimum 5 years of Program/Project Management experience.
  • Experience managing large-scale cross-functional programs.
  • Experience developing project plans, budgets, timelines, and resource allocation.
  • Experience leading cross-functional teams and managing multiple projects simultaneously.

Preferred Qualifications

  • Background in Program/Project Management.
  • Experience within Regulatory Affairs, Medical Device, or other regulated industries preferred.
  • Strong leadership, communication, and stakeholder management skills.
  • Experience working with Project Management Office (PMO) methodologies.

Education

  • Bachelor of Science required.

Consultants Eligible Benefits Upon Waiting Period

  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account (for High Deductible Health Plans)
  • Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
  • Supplemental Life Insurance
  • Short Term Disability (coverage varies by state)
  • Long Term Disability
  • Critical Illness, Hospital coverage, Accident Insurance
  • MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
  • 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.

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