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Medical Device Labeling Jobs in Indiana (NOW HIRING)

Synkriom

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Medical Device Regulatory Affairs Specialist

Warsaw, IN · On-site

$45 - $55/hr

... proposed labeling for compliance with applicable global regulations · Writes and manages the ... A minimum of one year of experience in orthopaedic or medical device industry preferred * A minimum ...

New

Actalent

Regulatory Affairs Specialist

Warsaw, IN

$50 - $55/hr

Review proposed product labeling to ensure compliance with applicable global regulations. * Write ... Experience with EU Medical Device Regulation (EU MDR) is beneficial. * Background in Quality ...

New

Red Star

Sterile Packaging Manager

IN · On-site

Oversee the design, evaluation, and approval of packaging components and sterile packaging systems for medical device products. * Review, approve, and maintain packaging, labeling, and related ...

Red Star

Sterile Packaging Manager

Larwill, IN · On-site

Oversee the design, evaluation, and approval of packaging components and sterile packaging systems for medical device products.Review, approve, and maintain packaging, labeling, and related technical ...

Red Star

Senior Sterile Packaging Engineer

Larwill, IN · On-site

$85 - $110/hr

Design, evaluate, and approve packaging components and sterile packaging systems for medical device products. * Develop, review, approve, and maintain packaging, labeling, and related technical ...

Red Star

Senior Sterile Packaging Engineer

IN · On-site

Design, evaluate, and approve packaging components and sterile packaging systems for medical device products. * Develop, review, approve, and maintain packaging, labeling, and related technical ...

avalign

Sr. Design Quality Engineer

Fort Wayne, IN

Support processes for Medical Device Reporting and Complaints for Avalign as specification ... Advise project teams on subjects such as premarket regulatory requirements, export and labeling ...

Viant

Silkscreen Operator

Indianapolis, IN · On-site

$16.25 - $19.25/hr

About the company: Viant is a global medical device partner providing design, development ... Equipment, Incident/Injury Reporting, Hazard Communication and Labeling. * Notifies supervisor of ...

medplast

Silkscreen Operator

Indianapolis, IN

$16.25 - $19.25/hr

About the company: Viant is a global medical device partner providing design, development ... Equipment, Incident/Injury Reporting, Hazard Communication and Labeling. * Notifies supervisor of ...

medplast

Silkscreen Operator

Indianapolis, IN · On-site

$16.25 - $19.25/hr

About the company: Viant is a global medical device partner providing design, development ... Equipment, Incident/Injury Reporting, Hazard Communication and Labeling. * Notifies supervisor of ...

medplast

Silkscreen Operator

Indianapolis, IN

$16.25 - $19.25/hr

About the company: Viant is a global medical device partner providing design, development ... Equipment, Incident/Injury Reporting, Hazard Communication and Labeling. * Notifies supervisor of ...

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All JobsMedical Device Labeling JobsMedical Device Labeling Jobs in Indiana

Medical Device Labeling information

See Indiana salary details

$12

$29

$90

How much do medical device labeling jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for medical device labeling in Indiana is $29.05, according to ZipRecruiter salary data. Most workers in this role earn between $16.49 and $37.31 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 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 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 are popular job titles related to Medical Device Labeling jobs in Indiana?

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

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

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

Medical Device Labeling jobs near you
Infographic showing various Medical Device Labeling job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $60,418 per year, or $29 per hour.

Medical Device Regulatory Affairs Specialist

Synkriom

Warsaw, IN • On-site

$45 - $55/hr

Contractor

Medical, Dental, Vision, Life

Posted 2 days ago

New

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Job description

JOB DESCRIPTION:

Responsible for assisting the team with regulatory filings as necessary to market Zimmer Biomet products. This position requires an intermediate understanding of medical devices and their use as well as an understanding of the regulatory submission process. 

·        Assist with assembly, distribution, storage and tracking and retrieval of information pertinent to the regulatory process, including the regulatory submissions process. May author and publish electronic submissions.

·        Respond to requests from foreign government and/or distributors as needed

·        Assist with the research, analysis and communication of information pertaining to the appropriate regulatory pathway for new or modified products

·        Provides regulatory direction to development project teams as a core team member; develops regulatory strategy for new products

·        Evaluate risk of proposed regulatory strategies; may offer solutions

·        Reviews proposed labeling for compliance with applicable global regulations

·        Writes and manages the development of package inserts

·        Reviews and evaluations promotion and advertising material for compliance with applicable regulations

·        Reviews proposed product changes for impact on regulatory status of the product

·        Communicates with regulatory and governmental agencies with supervision

·        Applies FDA regulations to business practices and provides regulatory input, advice and guidance to design teams

Skills:

  • Strong writing, communication, and interpersonal skills
  • Strong attention to detail; ability to multi-task and balance competing priorities
  • Knowledge of overall business environment, the orthopaedic industry, and the marketplace
  • Ability to learn and stay abreast of regulations pertinent to medical devices, biologics, drugs and combination products as needed, based on functional area
  • Ability to building relationships between Regulatory Affairs and other areas of the organization; ability to communicate effectively at all levels
  • Knowledge of FDA, EU, and other regulatory body regulations
  • Ability to identify risk in Regulatory strategies
  • Strong problem solving skills
  • Effective negotiating skills

Basic computer skills, including Microsoft Office Suite

Education:

  • Bachelor’s degree (or non-US equivalent) required; concentration in life sciences, technical/engineering or related field, preferred
  • A minimum of one year of experience in orthopaedic or medical device industry preferred
  • A minimum of 3 years of experience in Regulatory Affairs, Engineering, Quality, or related field required
  • Regulatory Affairs Certification (US or EU) preferred
  • A combination of education and experience may be considered

Company Description

Founded in 2015 and backed by two decades of hands-on experience, our strong insight on the enterprise ecosystem and its dynamics helps to offer a complete end-to-end solution. We automate recruitment processes with intelligent solutions to save time and money. Synkriom leads the industry with experience authentication of candidates.