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Medical Device Labeling Jobs in Massachusetts (NOW HIRING)

Ensure compliance with medical device labeling requirements, including UDI (Unique Device Identification) * Implement and validate barcode systems in alignment with GS1 standards * Support regulatory ...

... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...

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Medical Device Labeling information

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$14

$33

$104

How much do medical device labeling jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for medical device labeling in Massachusetts is $33.34, according to ZipRecruiter salary data. Most workers in this role earn between $18.89 and $42.79 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 Massachusetts? The most popular types of Medical Device Labeling jobs in Massachusetts are:
What job categories do people searching Medical Device Labeling jobs in Massachusetts look for? The top searched job categories for Medical Device Labeling jobs in Massachusetts are:
Infographic showing various Medical Device Labeling job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $69,342 per year, or $33.3 per hour.

Packaging Engineer

Intellectt INC

Boston, MA • On-site

Contractor

Re-posted 14 days ago


Job description

Job Title: Senior Packaging Engineer 

Location: Boston, MA

Duration: 12+ Months

Experience: 5 Years

Job Summary:

We are seeking an experienced Senior Packaging Engineer with a strong background in medical device packaging to support design, validation, and compliance activities. The ideal candidate will bring hands-on expertise in sterile packaging systems, labeling, and regulatory standards, along with the ability to drive packaging improvements and compliance initiatives.

Key Responsibilities:

  • Design and develop medical device packaging systems, including material selection and sterile barrier systems
  • Lead and execute packaging validation activities including IQ/OQ/PQ, transit testing, and aging studies
  • Ensure compliance with medical device labeling requirements, including UDI (Unique Device Identification)
  • Implement and validate barcode systems in alignment with GS1 standards
  • Support regulatory compliance efforts with FDA and ISO standards (ISO 13485, ISO 11607)
  • Collaborate with cross-functional teams including Quality, Regulatory, Manufacturing, and Supply Chain
  • Participate in packaging remediation projects and continuous improvement initiatives
  • Assist in post-acquisition integration activities related to packaging and labeling
  • Manage label conversions, barcode updates, and compliance gap assessments

Required Qualifications:

  • Bachelor’s degree in Engineering or a related field
  • 5–10 years of experience in medical device packaging engineering
  • Strong expertise in packaging design and sterile barrier systems
  • Hands-on experience with packaging validation (IQ/OQ/PQ, transit testing, aging studies)
  • Experience with UDI, labeling compliance, and barcode implementation
  • Working knowledge of GS1 standards
  • Familiarity with FDA regulations and ISO standards (ISO 13485, ISO 11607)

Preferred Qualifications:

  • Experience with post-acquisition integration projects
  • Background in packaging remediation and compliance gap closure
  • Experience with label conversions and barcode updates
  • Ability to work in fast-paced, cross-functional environments