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Freelance Medical Device Labeling Jobs (NOW HIRING)

Collabera

Labeling Specialist

Moundsview, MN · On-site

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 ...

Collabera

Labeling Specialist

Moundsview, MN

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 ...

Teleflex

Labeling Specialist

Maple Grove, MN · On-site

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 ...

Teleflex

Labeling Specialist

Maple Grove, MN · On-site

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 ...

Saransh Inc

Labelling Change Manager

Irving, TX · On-site

Execute Medical device Labeling and packaging re-design and test methods to improve label readability, barcode placement, and manufacturing efficiency * Participate in investigations related to ...

AllSTEM Connections

Medical Device Assembler

Poway, CA · On-site

$45K - $47K/yr

... medical device manufacturing environment. The team operates under cGMP and ISO 13485 standards ... Key Responsibilities - Perform repetitive assembly line filling, packaging, and labeling of ...

Three Point Solutions

Graphic Designer

Lafayette, CO · On-site

$40 - $45/hr

Medical Device Labeling * IFU (Instructions for Use) Documentation * Technical Documentation * Regulated Industry Documentation * Packaging Artwork Support * Quality Review & Compliance Documentation

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How much do freelance medical device labeling jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for freelance medical device labeling in the United States is $47.71, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $61.78 per hour, depending on experience, location, and employer.

What is freelance medical device labeling?

Freelance medical device labeling involves independent professionals who create, review, and manage the labels and instructions that accompany medical devices. These labels must meet strict regulatory requirements to ensure patient safety and regulatory compliance. Freelance specialists may work with manufacturers to develop compliant packaging, user manuals, and product inserts for various markets. They need to be knowledgeable about international regulations and guidelines, such as those from the FDA or the European MDR. This role often requires attention to detail, regulatory expertise, and clear communication skills.

What are the key skills and qualifications needed to thrive as a freelance medical device labeling specialist?

To thrive as a Freelance Medical Device Labeling Specialist, you need expertise in regulatory requirements, medical terminology, and technical writing, often supported by a background in life sciences or regulatory affairs. Familiarity with labeling management systems, document control software, and knowledge of FDA, EU MDR, or ISO standards is typically required. Attention to detail, strong organizational skills, and clear communication are essential soft skills to ensure accuracy and compliance. These skills are critical for producing precise, regulation-compliant labeling that ensures patient safety and successful product approval.

What are some common challenges freelance medical device labeling specialists face when collaborating with multiple clients?

Freelance medical device labeling specialists often navigate varying regulatory requirements and documentation standards from different clients, which can be challenging. Each client may use different systems for document management and have unique internal review processes, requiring adaptability and strong organizational skills. Additionally, balancing multiple projects with tight deadlines demands effective time management to ensure all labeling materials remain compliant and up to date. Proactive communication and a thorough understanding of regional regulations are crucial for successful collaboration and project delivery.
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Freelance Medical Device Labeling jobs near you
Infographic showing various Freelance Medical Device Labeling job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

Associate Director, Global Labeling Lead

Scorpion Therapeutics

Cambridge, MA • On-site

$150 - $190/hr

Other

Posted 8 days ago

Job description

Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies Business Unit (PDT BU)Responsibilities:
  • Provide regulatory expertise and strategic guidance to internal stakeholders to develop and maintain pharmaceutical drug/device labeling.
  • Contribute labeling strategy to regulatory strategies; liaise on evolving submission/negotiation plans.
  • Formulate labeling strategies for new/revised prescribing information and packaging; interpret scientific/medical/regulatory data.
  • Advise on labeling requirements, templates/tools, and Health Authority guidance.
  • Drive CCDS/US/EU labeling strategy and lifecycle management; lead development and maintenance of CCDS, US, and EU labels.
  • Prepare labeling vision for early programs; align stakeholders.
  • Lead global labeling teams and cross-functional projects; resolve conflicts/issues with minimal escalation.
  • Support combination product/drug-device labeling; prepare backup strategies for labeling negotiations.
  • Manage labeling processes/tools/systems, project-manage labeling updates to meet timelines, ensure version control/QC, maintain labeling decision records, and deliver labeling training.
Qualifications & Required/Preferred Skills:
  • 7–10 years biopharmaceutical industry experience; 5–7 years direct global US/EU labeling experience desired.
  • Knowledge of EU/US labeling requirements/guidance; combination product/drug-device labeling preferred.
  • Expertise maintaining Core Data Sheet (CCDS), USPI, and EU SmPC; understanding of SPL format for legacy/PLR labels.
  • Proficiency with Electronic Document Management Systems and end-to-end (E2E) labeling tracking systems.
  • Bachelor’s or Master’s required (advanced scientific/health sciences preferred); leadership/management of direct reports preferred.
Location:

Cambridge, MA (Hybrid)

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