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Freelance Medical Device Labeling Jobs in Kentucky

$102 - $133/hr

... 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 ...

$85 - $120/hr

... medical device company focused on improving the quality of life for patients undergoing spine ... Assess the regulatory impact of design, labeling, materials, and manufacturing changes, and ...

$121 - $205/hr

Previous experience in medical device industry * Cross functional leadership and collaboration across highly matrixed organization * Experience with labeling systems and printer * PMP or equivalent ...

$145 - $205/hr

... labeling and training issues. You will also follow standard practices and procedures in analyzing ... Reviews complaint codes and FDA Medical Device Reports, reviews and assists with reporting ...

New

Ensure full compliance with cGMP, labeling requirements, and all applicable medical device regulations.2. **Risk Management & Continuous Improvement** * Lead and support risk management activities ...

$60 - $100/hr

... medical device programs. This is a part-time/fractional opportunity, expected to require up to 25 ... In this role, you'll evaluate product and labeling changes, support audit activities, and help ...

Posted today

$140 - $190/hr

Coordinates preparation, review and submission of product applications (510(k), BLA, Medical Device ... Reviews and approves significant changes (e.g. facility, product, process and labeling changes) for ...

Posted today

$90 - $130/hr

... device and pharmaceutical organizations of all sizes to confidently advance scientific ... related to label changes for assigned brands. * Stay up to date with relevant clinical data ...

$130 - $150/hr

... with FDA medical device regulations, ISO 13485 and other regional requirements as applicable ... labelling, change control, complaints, CAPA, record retention, reporting and recall readiness ...

$80 - $95/hr

Coordinates and supports Medical Device Reporting (MDR), vigilance, recall, and other applicable ... Reviews labeling, including Instructions for Use (IFUs), product labels, and promotional materials ...

$75.53/hr

Quality Documentation and Labeling Associate Full Time Clerical Plymouth, MN, US 2 days ago ... medical application. We treat every component and finished device as though it will be used by a ...

$110 - $150/hr

Saluda Medical is a commercial‑stage medical device company focused on developing treatments for ... Prior experience with labelling would be an advantage What You'll Bring: * Bachelor's degree in ...

Office Associate

Newport, KY · On-site

$16.50 - $22/hr

... medical device receipt, ordering, storage, label printing, labeling activities, inventory management, distribution, return drug accountability and destruction • Ensure all activities executed by ...

New

$85 - $110/hr

The key responsibility of this position is to exercise medical device packaging subject matter ... Assisting in creating and editing labeling templates, and implementation of those changes to ...

$105 - $110/hr

... medical device products. This role serves as a critical bridge between Product Development ... labeling, and in-process quality checks following approved batch records and SOPs. * Manage ...

Posted today

$75 - $90/hr

Experience with medical device standards (ISO 13485 & 21 CFR 820) * Strong problem-solving skills ... Review labeling, design controls, and sterilization documentation * Participate in audits and ...

$70 - $90/hr

Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device ... Assesses product, manufacturing, and labeling changes for regulatory reporting impact and ...

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Freelance Medical Device Labeling information

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.

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

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

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

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

What cities in Kentucky are hiring for Freelance Medical Device Labeling jobs?

Cities in Kentucky with the most Freelance Medical Device Labeling job openings:

Infographic showing various Freelance Medical Device Labeling job openings in Kentucky as of June 2026, with employment types broken down into 38% Full Time, 13% Part Time, 4% Temporary, and 45% Contract. Highlights an 73% Physical, 3% Hybrid, and 24% Remote job distribution.

Human Factors Engineer 3, Device Development

AstraZeneca GmbH

On-site

$102 - $133/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago


Job description

This is what you will do:

This position will serve the role of Engineer III for device development / human factors engineering within the Alexion Device Development organization. The role will support the human factors workstreams for pipeline products as well as lifecycle management. This role will interact with multiple functional teams including Device Development, Clinical, Commercial/Marketing, Quality, and Regulatory, clinical development through registration and commercial product support.

You will be responsible for:
  • Lead and support activities under the human factors and usability engineering process for combination product design and development from feasibility, clinical development through registration and post-market.

  • Support core teams to develop and support the strategy for human factors/ usability engineering activities from formative studies to final HF validation for combination products.

  • Support design validation activities including summative human factors study (i.e. human factors validation) from protocol development, study execution, and reporting.

  • Provide feedback and/or author for user need identification and user interface specifications development.

  • Provide feedback to use-related risk management activities such as known use problem analysis, hazard analysis, and use-related risks analysis

  • Draw findings from competitive analysis, market sensing, complaint handling to inform new product design (inclusive of device, labeling and secondary packaging)

  • Collaborate with human factors firms (vendors) and manage their activities for a formative or summative human factors study.

  • Communicate effectively, both verbally and in writing, internally across departments and with external suppliers.

  • Ensure all human factors engineering activities as required and comply with the Company’s quality assurance requirements as well as applicable regulatory requirements.

  • Support feasibility activity of device assessment (e.g., testing, fixturing, protocol, report).

You will need to have:
  • Experience in human factors engineering and exposure to design and development of medical device and combination products.

  • Experience in design control activities.

  • Ability to manage external human factors firms (vendors).

  • Strong communication and collaboration skills; ability to connect with all levels of the organization. Proficient in writing internal reports, project summaries, and internal/external presentations.

  • Knowledge of human factor/usability engineering, safety, performance and regulatory compliance requirements of medical device and combination products (e.g. IEC 62366, FDA HF guidances, EU Regulation 2017/745 (MDR)).

  • [For office-based positions:]As is typical of an office-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.

We would prefer for you to have:
  • Bachelor’s or Master’s degree in Engineering (Biomedical, Chemical, Mechanical, Electrical Engineering or Human Factors) plus 3-6 years experience in medical device Human Factors development and design control.

  • Experience with injection based combination product development and risk management preferred.

  • Experience with graphics design a plus.

Joining Alexion means embracing an opportunity where work isn’t ordinary. We are a beacon in the global Biopharmaceutical landscape. Our closeness to patients brings us closer to our work and each other. Combined with our brave, pioneering spirit – we are truly unique in R&D and healthcare. At Alexion, grow and innovate in a business with a rapidly expanding portfolio. Enjoy the entrepreneurial spirit of a leading biotech while meeting the needs of some of the most under-served patients in the world. You will be empowered with tailored development programs designed not just for skill enhancement but for fostering a deep understanding of our patient's journeys. Supported by outstanding leaders and peers ready to lift you in marketing, compliance, and beyond.

The annual base pay (or hourly rate of compensation) for this position ranges from $101,643.20 to $133,406.70. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

27-Aug-2026

Closing Date

29-Sept-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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