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Associate Medical Device Labeling Jobs in Minnesota

Labeling Specialist

Maple Grove, MN · On-site

$40 - $60/hr

Design, update, and maintain medical device labels using BarTender. * Manage label changes through the full lifecycle, including creation, review, approval, and retirement. * Develop labeling content ...

This position will be a subject matter expert in Medical Device labeling regulations and standards. They will be responsible for planning, development and execution of product labeling for Structural ...

This position will be a subject matter expert in Medical Device labeling regulations and standards. They will be responsible for planning, development and execution of product labeling for Medtronic ...

Principal Responsibilities Leads development of medical device labels from concept through release. Changes are managed in the Agile Quality Management System (QMS). Partners with R&D sustaining and ...

Principal Responsibilities • Leads development of medical device labels from concept through release. Changes are managed in the Agile Quality Management System (QMS). • Partners with R&D ...

This includes labeling for both clinicians and patients that accompany medical device products that conform to the Medtronic documentation and quality assurance standards. Projects include new ...

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Associate Medical Device Labeling information

What is an associate medical device labeling?

Associate Medical Device Labeling professionals are responsible for creating, reviewing, and maintaining the labeling and packaging materials for medical devices. Their work ensures that all product information, instructions, and regulatory warnings are accurate, clear, and compliant with industry regulations. They collaborate closely with regulatory affairs, quality assurance, and product development teams to make sure that labels meet local and international standards. This role is critical in helping ensure patient safety and regulatory approval of medical devices.

What are the key skills and qualifications needed to thrive as an associate medical device labeling?

To thrive as an Associate Medical Device Labeling Specialist, you need a strong understanding of regulatory requirements, attention to detail, and experience in technical writing, often supported by a degree in life sciences or a related field. Familiarity with labeling software, document management systems, and knowledge of FDA or EU MDR regulations are typically required. Excellent communication, collaboration, and organizational skills set top performers apart in this position. These skills are crucial to ensure label accuracy, regulatory compliance, and patient safety in a highly regulated industry.

What are some common challenges faced by associate medical device labeling, and how can they be addressed?

Associate Medical Device Labeling professionals often encounter challenges such as keeping up with evolving regulatory requirements across different countries, ensuring accuracy and clarity in complex technical information, and coordinating input from multiple departments like regulatory affairs, engineering, and marketing. Addressing these challenges involves staying updated on global labeling standards, developing strong attention to detail, and building effective communication and collaboration skills. Leveraging project management tools and regularly participating in training can also help manage these complexities and ensure timely, compliant labeling deliverables.

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

The most popular types of Medical Device Labeling jobs in Minnesota are:

Labeling Specialist

Actalent

Maple Grove, MN • On-site

$40 - $60/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago


Key responsibilities

  • Design, update, and maintain medical device labels using BarTender.

  • Manage label changes through the full lifecycle, including creation, review, approval, and retirement.

  • Partner with Packaging, Regulatory, Quality, and Manufacturing teams to ensure labeling compliance and accuracy.


Job description

Position Summary

Support the creation, maintenance, and management of medical device labeling using BarTender software. This role ensures labels meet regulatory, quality, and packaging requirements while partnering with cross-functional teams in a regulated medical device environment.

Key Responsibilities
  • Design, update, and maintain medical device labels using BarTender.
  • Manage label changes through the full lifecycle, including creation, review, approval, and retirement.
  • Develop labeling content and associated documentation.
  • Partner with Packaging, Regulatory, Quality, and Manufacturing teams to ensure labeling compliance and accuracy.
  • Manage labeling records and approvals within PLM/QMS systems.
  • Troubleshoot labeling issues and support audits, inspections, and continuous improvement initiatives.
  • Ensure compliance with FDA, ISO 13485, and other applicable regulations.
Required Qualifications
  • 4+ years of medical device labeling experience.
  • Hands-on experience with BarTender labeling software.
  • Knowledge of ISO 13485, 21 CFR 820, and medical device labeling requirements.
  • Experience with technical documentation, label lifecycle management, and change control processes.
  • Familiarity with PLM and QMS systems.
  • Strong attention to detail, technical writing, and organizational skills.
  • Ability to work independently and collaborate across functions.
Preferred Qualifications
  • Experience with Agile PLM, Windchill, or similar systems.
  • Knowledge of UDI, FDA labeling regulations, and EU MDR requirements.
  • Experience in document control and fast-paced medical device environments.
  • Strong cross-functional communication and project management skills.
Job Type & Location

This is a Contract to Hire position based out of Maple Grove, MN.

Pay and Benefits

The pay range for this position is $40.00 - $60.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Maple Grove,MN.

Application Deadline

This position is anticipated to close on Sep 9, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Industry

Business management consulting

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

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