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Regulatory Labeling Manager Jobs in Minnesota (NOW HIRING)

Teleflex

Labeling Specialist

Maple Grove, MN

Partners with Regulatory Affairs, Quality, R&D, Packaging, Clinical, and Marketing teams to maintain real-time data in database/spreadsheet. Manages timelines for new and revised labeling projects.

Teleflex

Labeling Specialist

Maple Grove, MN · On-site

Additionally, they will apply advanced project management expertise, deliver labeling process training, and collaborate across internal functions and external agencies to ensure regulatory compliance ...

Collabera

Labeling Specialist

Moundsview, MN · On-site

Plans projects and manages scope, deliverables and timelines using project management tools ... Experience with medical device regulations and standards BS or BA in related fields. Additional ...

Collabera

Labeling Specialist

Moundsview, MN · On-site

Plans projects and manages scope, deliverables and timelines using project management tools ... Experience with medical device regulations and standards BS or BA in related fields. Additional ...

Actalent

Labeling Specialist

Maple Grove, MN

$40 - $60/hr

Partner with Packaging, Regulatory, Quality, and Manufacturing teams to ensure labeling compliance and accuracy. * Manage labeling records and approvals within PLM/QMS systems. * Troubleshoot ...

Abbott

Labeling Specialist I

Plymouth, MN · On-site

$50K - $101K/yr

Main Purpose of the Role Responsible for overseeing and managing the change control packages for ... Documentation associated with the labeling change control process must meet Quality, Regulatory and ...

New

Abbott

Labeling Specialist I

Plymouth, MN · On-site

$50K - $101K/yr

Main Purpose of the Role Responsible for overseeing and managing the change control packages for ... Documentation associated with the labeling change control process must meet Quality, Regulatory and ...

New

Abbott

Labeling Specialist I

Plymouth, MN · On-site

$50K - $101K/yr

Main Purpose of the Role Responsible for overseeing and managing the change control packages for ... Regulatory and GMP requirements, as they are official records for audits and legal actions Required ...

VDyne

Regulatory Affairs Specialist

Maple Grove, MN · On-site

... design, labeling, manufacturing, and process changes and prepare supporting regulatory ... used to manage regulatory deliverables and documentation · Support audits, inspections, and ...

Medtronic

Labeling Program Lead - Onsite

Minneapolis, MN · On-site

... manages labeling activities across product lifecycle initiatives, ensuring labeling deliverables are planned, coordinated, and executed in alignment with program objectives, timelines, and regulatory ...

Medtronic

Labeling Program Lead - Onsite

Minneapolis, MN · On-site

... manages labeling activities across product lifecycle initiatives, ensuring labeling deliverables are planned, coordinated, and executed in alignment with program objectives, timelines, and regulatory ...

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Regulatory Labeling Manager information

See Minnesota salary details

$28

$55

$84

How much do regulatory labeling manager jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for regulatory labeling manager in Minnesota is $55.79, according to ZipRecruiter salary data. Most workers in this role earn between $41.20 and $65.19 per hour, depending on experience, location, and employer.

What does a Regulatory Labeling Manager do?

A Regulatory Labeling Manager oversees the development, review, and approval of product labels and packaging to ensure compliance with all relevant regulations and guidelines. They coordinate with various departments, such as regulatory affairs, legal, marketing, and product development, to ensure that all labeling information is accurate and aligns with local and international laws. Their responsibilities often include managing labeling submissions to regulatory authorities, monitoring regulatory changes, and updating labels accordingly to maintain compliance.

How does a Regulatory Labeling Manager typically collaborate with cross-functional teams during the product development process?

As a Regulatory Labeling Manager, you will regularly collaborate with cross-functional teams including regulatory affairs, medical, legal, marketing, and product development. Your role involves ensuring that product labels meet both regulatory requirements and company standards by gathering input from these teams and facilitating consensus on label content. You’ll often lead meetings to align stakeholders, review draft labeling, and coordinate responses to regulatory authority feedback, making strong communication and project management skills essential. This collaborative environment also provides opportunities to broaden your expertise and visibility within the company, supporting long-term career growth.

What are the key skills and qualifications needed to thrive as a Regulatory Labeling Manager, and why are they important?

To thrive as a Regulatory Labeling Manager, you need expertise in regulatory compliance, labeling requirements, and scientific documentation, often supported by a degree in life sciences or a related field. Familiarity with regulatory submission systems, document management tools, and global labeling databases is typically required. Strong attention to detail, project management, and effective cross-functional communication skills set top performers apart in this role. These skills are crucial for ensuring accurate, compliant labeling that meets health authority standards and supports product success in global markets.

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

AspectRegulatory Labeling ManagerRegulatory Affairs Specialist
CertificationsRegulatory Affairs Certification (RAC), FDA certificationsRAC, FDA certifications
Work EnvironmentLeading labeling projects, cross-functional teamsSupporting regulatory submissions, research
Employer & Industry UsagePharmaceuticals, medical devices, biotechPharmaceuticals, medical devices, biotech

The Regulatory Labeling Manager focuses on developing, reviewing, and maintaining product labeling to ensure compliance with regulations. In contrast, the Regulatory Affairs Specialist handles broader regulatory submissions and compliance tasks. Both roles require similar certifications and are common in the same industries, but the Labeling Manager has a more specialized focus on labeling strategies and documentation.

What are the most commonly searched types of Regulatory Labeling jobs in Minnesota?

The most popular types of Regulatory Labeling jobs in Minnesota are:

What are popular job titles related to Regulatory Labeling Manager jobs in Minnesota?

For Regulatory Labeling Manager jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Regulatory Labeling Manager jobs in Minnesota look for?

The top searched job categories for Regulatory Labeling Manager jobs in Minnesota are:

What cities in Minnesota are hiring for Regulatory Labeling Manager jobs?

Cities in Minnesota with the most Regulatory Labeling Manager job openings:

Regulatory Labeling Manager jobs near you
Infographic showing various Regulatory Labeling Manager job openings in Minnesota as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $116,053 per year, or $55.8 per hour.

Labeling Specialist

Stark Pharma Solutions Inc

Moundsview, MN • On-site

Contractor

Re-posted 25 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Labeling Specialist right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: Labeling Specialist

Location: Mounds View, MN (Hybrid – 3 Days Onsite)
Duration: 12+ Month Contract
 

Job Overview

We are seeking a Labeling Specialist to support medical device labeling activities, ensuring product labeling complies with regulatory, quality, and design requirements. The ideal candidate will have experience with medical device packaging labels, PLM systems, and artwork management.

Key Responsibilities

  • Create, review, and maintain medical device product labeling and packaging artwork.
  • Ensure labels, specifications, drawings, and artwork comply with regulatory and quality standards.
  • Release and manage labeling specifications and drawings using PLM systems (Enovia or Windchill).
  • Develop and edit labeling artwork using Adobe Illustrator.
  • Review labeling updates and implement changes based on regulatory requirements.
  • Support review of promotional and commercial materials to ensure consistency with approved labeling.
  • Recommend process improvements to enhance labeling quality, accuracy, and efficiency.
  • Collaborate with Regulatory Affairs, Quality, Engineering, and Marketing teams to support labeling activities.

Required Qualifications

  • Bachelor's degree in a related field.
  • Experience with medical device package labeling.
  • Hands-on experience with PLM systems such as Enovia or Windchill.
  • Proficiency with Adobe Illustrator.
  • Strong attention to detail and document control skills.
  • Excellent communication and cross-functional collaboration abilities.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com