Regulatory Manager
Saint Paul, MN · On-site
Summary The Regulatory Manager is a key member of the Company Global Research & Development team, responsible for ensuring that new and existing products are designed, tested, and documented to meet ...
Saint Paul, MN · On-site
Summary The Regulatory Manager is a key member of the Company Global Research & Development team, responsible for ensuring that new and existing products are designed, tested, and documented to meet ...
Saint Paul, MN · On-site
Summary The Regulatory Manager is a key member of the Company Global Research & Development team, responsible for ensuring that new and existing products are designed, tested, and documented to meet ...
Hibbing, MN · On-site
We're looking for a Regulatory Compliance Coordinator who is passionate about healthcare excellence and thrives on keeping organizations survey-ready, compliant, and continuously improving. If you're ...
Hibbing, MN · On-site
We're looking for a Regulatory Compliance Coordinator who is passionate about healthcare excellence and thrives on keeping organizations survey-ready, compliant, and continuously improving. If you're ...
Minneapolis, MN · Remote
$85K - $95K/yr
The Regulatory and Clinical Specialist will support the clinical evaluation activities, review promotional materials and support regulatory submissions for the active implantable medical devices for ...
Minneapolis, MN · Remote
$85K - $95K/yr
The Regulatory and Clinical Specialist will support the clinical evaluation activities, review promotional materials and support regulatory submissions for the active implantable medical devices for ...
Maplewood, MN · On-site
$22 - $25/hr
Support regulatory compliance by obtaining documentation to maintain product level data in all Systems * Prepare Chemical Hazard Summaries and Biological Evaluation Generate and review hazard ...
Maplewood, MN · On-site
$22 - $25/hr
Support regulatory compliance by obtaining documentation to maintain product level data in all Systems * Prepare Chemical Hazard Summaries and Biological Evaluation Generate and review hazard ...
$22 - $25/hr
Support regulatory compliance by obtaining documentation to maintain product level data in all Systems * Prepare Chemical Hazard Summaries and Biological Evaluation Generate and review hazard ...
$22 - $25/hr
Support regulatory compliance by obtaining documentation to maintain product level data in all Systems * Prepare Chemical Hazard Summaries and Biological Evaluation Generate and review hazard ...
Maplewood, MN · On-site
$22 - $25/hr
Support regulatory compliance by obtaining documentation to maintain product level data in all Systems * Prepare Chemical Hazard Summaries and Biological Evaluation Generate and review hazard ...
Maplewood, MN · On-site
$22 - $25/hr
Support regulatory compliance by obtaining documentation to maintain product level data in all Systems * Prepare Chemical Hazard Summaries and Biological Evaluation Generate and review hazard ...
Providingexpert advice on regulatory requirements * Preparing submissions * Supporting approval activities * Assistingwith license maintenance, including annual reports, renewals, design ...
Providingexpert advice on regulatory requirements * Preparing submissions * Supporting approval activities * Assistingwith license maintenance, including annual reports, renewals, design ...
Blaine, MN · On-site
$120K - $150K/yr
Description Summary The Regulatory & Compliance Manager is responsible for leading, developing, implementing, and sustaining Arrow Finishing's regulatory compliance, environmental stewardship, safety ...
Blaine, MN · On-site
$120K - $150K/yr
Description Summary The Regulatory & Compliance Manager is responsible for leading, developing, implementing, and sustaining Arrow Finishing's regulatory compliance, environmental stewardship, safety ...
As a Regulatory Affairs Specialist in the Access and Instruments Operating Unit, you will play an important role in supporting innovative medical technologies throughout the product lifecycle. You ...
As a Regulatory Affairs Specialist in the Access and Instruments Operating Unit, you will play an important role in supporting innovative medical technologies throughout the product lifecycle. You ...
The Regulatory Affairs Specialist will assist in maintaining market authorizations for Scanlan products, including design files, technical documentation, product registrations and listings. They will ...
The Regulatory Affairs Specialist will assist in maintaining market authorizations for Scanlan products, including design files, technical documentation, product registrations and listings. They will ...
Providingexpert advice on regulatory requirements * Preparing submissions * Supporting approval activities * Assistingwith license maintenance, including annual reports, renewals, design ...
Providingexpert advice on regulatory requirements * Preparing submissions * Supporting approval activities * Assistingwith license maintenance, including annual reports, renewals, design ...
The role supports the Regulatory Affairs team by communicating regulatory strategies and preparing essential documentation for market authorizations. Additionally, the position involves maintaining ...
The role supports the Regulatory Affairs team by communicating regulatory strategies and preparing essential documentation for market authorizations. Additionally, the position involves maintaining ...
The role supports the Regulatory Affairs team by communicating regulatory strategies and preparing essential documentation for market authorizations. Additionally, the position involves maintaining ...
The role supports the Regulatory Affairs team by communicating regulatory strategies and preparing essential documentation for market authorizations. Additionally, the position involves maintaining ...
he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast's quality system and applicable regulatory requirements. This ...
he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast's quality system and applicable regulatory requirements. This ...
As a Regulatory Affairs Specialist in the Access and Instruments Operating Unit, you will play an important role in supporting innovative medical technologies throughout the product lifecycle. You ...
As a Regulatory Affairs Specialist in the Access and Instruments Operating Unit, you will play an important role in supporting innovative medical technologies throughout the product lifecycle. You ...
Regulatory support will focus on sustaining globalization, international submissions, commercial support, manufacturing support, systems improvement, and other responsibilities aligned with global ...
Regulatory support will focus on sustaining globalization, international submissions, commercial support, manufacturing support, systems improvement, and other responsibilities aligned with global ...
Regulatory support will focus on sustaining globalization, international submissions, commercial support, manufacturing support, systems improvement, and other responsibilities aligned with global ...
Regulatory support will focus on sustaining globalization, international submissions, commercial support, manufacturing support, systems improvement, and other responsibilities aligned with global ...
he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast's quality system and applicable regulatory requirements. This ...
he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast's quality system and applicable regulatory requirements. This ...
Our Clinical and Regulatory Affairs teams play a critical role in supporting clinical research, physician engagement, global regulatory strategy, and the advancement of breakthrough therapies through ...
Our Clinical and Regulatory Affairs teams play a critical role in supporting clinical research, physician engagement, global regulatory strategy, and the advancement of breakthrough therapies through ...
Minneapolis, MN · On-site +1
$295K/yr
Our Energy & Regulatory Team Stoel Rives is a nationally recognized leader in the energy and natural resources industries, advising clients across the full lifecycle of project development-from ...
Minneapolis, MN · On-site +1
$295K/yr
Our Energy & Regulatory Team Stoel Rives is a nationally recognized leader in the energy and natural resources industries, advising clients across the full lifecycle of project development-from ...
$18.60 - $22.47
3% of jobs
$22.47 - $26.35
6% of jobs
$26.35 - $30.22
13% of jobs
$30.73 is the 25th percentile. Wages below this are outliers.
$30.22 - $34.10
20% of jobs
The median wage is $35.60 / hr.
$34.10 - $37.97
19% of jobs
$37.97 - $41.84
9% of jobs
$43.78 is the 75th percentile. Wages above this are outliers.
$41.84 - $45.72
10% of jobs
$45.72 - $49.59
6% of jobs
$49.59 - $53.47
5% of jobs
$53.47 - $57.34
5% of jobs
$57.34 - $61.21
3% of jobs
$18
$38
$61
| Aspect | Regulatory | Compliance Officer |
|---|---|---|
| Required Credentials | Regulatory certifications, industry-specific licenses | Compliance certifications, such as CCEP or CRCM |
| Work Environment | Regulatory agencies, government bodies, legal teams | Corporate offices, compliance departments, financial institutions |
| Employer & Industry Usage | Used in industries like healthcare, finance, manufacturing | Common in banking, insurance, healthcare sectors |
| Search & Comparison Intent | Understanding regulatory roles, legal compliance | Ensuring company adherence to policies, internal audits |
While both roles focus on adherence to rules, Regulatory professionals primarily interpret and implement government regulations, often working with legal and government entities. Compliance Officers focus on internal policies and procedures to ensure their organization meets legal and ethical standards. Both roles are essential for risk management but differ in scope and focus.
The most popular types of Regulatory jobs in Minnesota are:
For Regulatory jobs in Minnesota, the most frequently searched job titles are:
The top searched job categories for Regulatory jobs in Minnesota are:
Cities in Minnesota with the most Regulatory job openings:

Summary
The Regulatory Manager is a key member of the Company Global Research & Development team, responsible for ensuring that new and existing products are designed, tested, and documented to meet applicable regulatory and certification requirements. This role focuses on achieving maintaining compliance with Factory Mutual (FM), ATEX, and CE certification standards and works cross-functionally with engineering, manufacturing, and external certification bodies to support successful product launches and lifecycle compliance.
Essential Functions
• Serve as the regulatory and certification subject matter expert for Factory Mutual (FM), ATEX, and CE requirements throughout product development lifecycle.
• Partner with product development, mechanical, electrical, and software engineering teams to integrate regulatory requirements product designs from concept through release.
• Interpret applicable standards, directives, and codes (e.g., ATEX Directive, CE marking requirements, FM Approval Standards) and translate them into actionable design and testing requirements.
• Develop and maintain regulatory compliance plans, certification strategies, and risk assessments for new and modified products.
• Act as the primary technical interface with external certification bodies, notified bodies, and test laboratories.
• Documentation Preparation: Prepare and submit regulatory documentation to relevant authorities, ensuring accuracy and completeness.
• Cross-Functional Collaboration: Work closely with team in research & development, quality, manufacturing, and supply chain to integrate compliance measures early in the new product development process.
• Regulatory Reviews: Conduct regulatory reviews and risk assessments to identify potential compliance issues and recommend solutions.
• Monitoring Regulations: Stay updated on changes in regulations and industry standards, advising the organization on necessary adjustments to maintain compliance.
• Training and Guidance: Provide training to staff on regulatory requirements and best practices, fostering a culture of compliance within the organization.
• Audit Participation: Facilitate regulatory inspections and audits, ensuring that all processes adhere to established standards.
• Due to the Global Sales and Distribution of our products, the regulatory standards may include, but are not limited to the following: ATEX, Class 1 - Div 1, UL, CE, UKCA (UK Conformity Assessed), CSA, FM, Machinery Directive and Safety Compliances.
Qualifications
• Bachelor’s degree in engineering or related field is required
• 5 + years of experience in a regulatory role for engineered products or systems, with a strong understanding of industry regulations and standards.
• Working knowledge of Factory Mutual (FM), ATEX, and CE certification processes and requirements.
• Strong analytical and problem-solving abilities.
• Excellent communication and collaboration skills.
• Proficiency in regulatory software tools and electronic submission processes.
•Detail-oriented with strong technical writing skills
• Willingness to travel occasionally, including international travel if required.
Applicants may be subject to a background check and pre-employment drug screen.*
*A conviction does not automatically disqualify you from employment. We will consider factors such as your age at the time, the timing and nature of the offense, its seriousness, and any rehabilitation efforts when determining your suitability for the role.
Sparrow Company Executive Search & Staffing is an Equal Opportunity Employer.