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Medical Device Labeling Jobs in Wisconsin (NOW HIRING)

Abbott

Ops Label & Kit Design Associate IV

Madison, WI

$61K - $122K/yr

... labeling and kitting for reagents to be used in In Vitro Diagnostic (IVD) or Research Use Only (RUO) medical device manufacturing processes and procedures in accordance with cGMP, ISO13485, and FDA ...

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Medical Device Labeling information

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$13

$30

$96

How much do medical device labeling jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for medical device labeling in Wisconsin is $30.81, according to ZipRecruiter salary data. Most workers in this role earn between $17.45 and $39.57 per hour, depending on experience, location, and employer.

What is a medical device labeling?

A Medical Device Labeling job involves creating, reviewing, and managing labeling content for medical devices to ensure compliance with regulatory requirements. This includes instructions for use, packaging labels, and safety information for healthcare professionals and patients. Professionals in this role collaborate with regulatory, quality, and engineering teams to meet industry standards and country-specific regulations. Their work ensures that medical devices are used safely and effectively, reducing risks associated with improper usage.

What are the key skills and qualifications needed to thrive in medical device labeling?

To thrive in Medical Device Labeling, you need a strong understanding of regulatory requirements (such as FDA and EU MDR), attention to detail, and experience with technical writing or documentation, often supported by a degree in life sciences or a related field. Familiarity with labeling management systems, document control tools, and knowledge of ISO standards are key technical qualifications, and certifications like RAC can be advantageous. Strong communication, collaboration, and organizational skills set candidates apart, as these roles often involve coordinating with cross-functional teams such as regulatory, engineering, and quality assurance. These capabilities ensure labeling materials meet strict compliance standards, avoid costly errors or recalls, and support timely product launch and patient safety.

What does a medical device labeling do?

Professionals in Medical Device Labeling are responsible for creating, reviewing, and updating product labels, instructions for use, and packaging materials to ensure compliance with regulatory standards. They often collaborate closely with regulatory affairs, engineering, and quality assurance teams to gather technical product information and incorporate feedback. Daily activities may also include managing document control processes, implementing labeling changes driven by new regulations or product updates, and preparing submissions for global markets. Attention to detail and the ability to manage multiple projects simultaneously are crucial for success in this role.

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

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

What are popular job titles related to Medical Device Labeling jobs in Wisconsin?

For Medical Device Labeling jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Medical Device Labeling jobs in Wisconsin look for?

The top searched job categories for Medical Device Labeling jobs in Wisconsin are:

Medical Device Labeling jobs near you
Infographic showing various Medical Device Labeling job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $64,087 per year, or $30.8 per hour.

Medical Device Quality Inspector

Kellton Tech

Madison, WI • On-site

$30/hr

Contractor

Re-posted 22 days ago

Job description

Job Title: Medical Device Quality Inspector
Location: Madison, WI (Onsite)
Pay Rate: $30/hr (W2)
 

Job Summary

The Medical Device Quality Inspector is responsible for ensuring that materials, processes, and conditions related to the daily manufacturing, processing, and packaging of medical devices meet cGMP standards and comply with internal quality procedures and regulatory standards. This position plays a critical role in ensuring product quality and integrity in a regulated environment.

Essential Functions

  • Perform one of the following Quality department functions:
    • Inspect raw materials to ensure they meet production requirements.
    • Conduct in-process inspections of products and manufacturing processes.
    • Review final documentation and inspect packaging for medical devices, subassemblies, and kits.
  • Assist in documentation control activities within the manufacturing facility.
  • Complete activity documentation and attach appropriate quality status labeling.
  • Ensure proper storage and secure handling of products and labels.
  • Support the Quality team by occasionally conducting nonconformance investigations and assisting with preventive actions.
  • Perform quality reviews for quarantine releases on specific non-reportable, non-complaint materials.

Minimum Requirements

Education & Experience:

  • High School diploma or equivalent required.
  • Minimum 1 year of experience in a regulated work environment preferred.
  • Familiarity with FDA Quality System Regulations and ISO 13485 standards for medical device manufacturing.

Skills & Competencies:

  • Self-motivated and able to work independently.
  • Strong attention to detail.
  • Proficient in using computer-based systems daily.
  • Strong teamwork and collaboration skills.
  • Effective verbal and written communication abilities.

Organizational Relationship / Scope

  • Reports to the Quality Control Manager.
  • Interfaces primarily with manufacturing, engineering, and quality departments to assess nonconforming products and support supplier quality issues.

Working Conditions

  • Work is performed in a controlled environment within a medical device manufacturing facility.
  • Adherence to safety and hygiene protocols is required.