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Medical Device Reporting Jobs in Indiana (NOW HIRING)

Post Market Quality Engineer

Warsaw, IN · On-site

$69K - $89K/yr

The Post Market Quality Engineer is responsible for medical device complaint investigations and write-ups as part of the Complaint Handling, Medical Device Reporting and Vigilance Reporting process.

Perform medical record review to assist with FDA Medical Device Reporting and complaint investigation. * Respond to questions that complaint handling personnel may have and provide medical insight ...

... medical device regulations. Key Responsibilities: * Maintenance Oversight: * Plan, schedule, and ... Reporting & Communication: * Prepare and present maintenance performance reports, metrics, and ...

... sterile medical device experience to impact patient safety and help determine which new products go to market. Technical Specialist Responsibilities: Responsible for planning, reporting and ...

... sterile medical device experience to impact patient safety and help determine which new products go to market. Technical Specialist Responsibilities: Responsible for planning, reporting and ...

Assembler

Plainfield, IN · On-site

$15.75 - $19.50/hr

Medical Device Manufacturing Company Duration : 12 Months Location : Plainfield, IN 46168 Shift ... Report production or equipment issues when identified • Assist with inventory, shipping ...

Assembler

Plainfield, IN · On-site

$18 - $20/hr

Medical Device Manufacturing Company Duration : 12 Months Location : Plainfield, IN 46168 Shift ... Report production or equipment issues when identified • Assist with inventory, shipping ...

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Medical Device Reporting information

See Indiana salary details

$12

$18

$24

How much do medical device reporting jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for medical device reporting in Indiana is $18.67, according to ZipRecruiter salary data. Most workers in this role earn between $16.49 and $20.14 per hour, depending on experience, location, and employer.

What is the difference between Medical Device Reporting vs Medical Device Technician?

AspectMedical Device ReportingMedical Device Technician
Required CredentialsRegulatory knowledge, often a background in healthcare or regulatory affairsTechnical skills, certifications in medical equipment maintenance or biomedical technology
Work EnvironmentRegulatory agencies, healthcare compliance departmentsHospitals, clinics, biomedical equipment service centers
Employer & Industry UsageUsed by medical device manufacturers, healthcare providers, and regulatory bodiesEmployers include hospitals and biomedical service companies
Common Search & Comparison IntentUnderstanding regulatory roles in medical device safetyTechnical maintenance and repair of medical devices

Medical Device Reporting focuses on regulatory compliance and reporting adverse events, while Medical Device Technicians handle the maintenance and repair of medical equipment. Both roles are essential in the medical device industry but serve different functions within healthcare and regulatory environments.

What are the key skills and qualifications needed to thrive in Medical Device Reporting, and why are they important?

To excel in Medical Device Reporting, you need a solid understanding of regulatory requirements, data analysis, and healthcare compliance, often supported by a degree in life sciences or a related field. Familiarity with regulatory databases such as FDA’s MAUDE, electronic reporting systems, and quality management software is typically required. Strong attention to detail, analytical thinking, and effective written communication help ensure accurate and timely reporting. These skills are critical for maintaining regulatory compliance, protecting patient safety, and supporting product quality in the medical device industry.

What are some typical challenges faced by professionals in Medical Device Reporting, and how can they be managed?

Professionals working in Medical Device Reporting often encounter challenges such as managing tight regulatory deadlines, ensuring complete and accurate documentation, and staying current with evolving global reporting requirements. Effective time management, attention to detail, and regular training on regulatory updates are essential for success in this role. Collaboration with quality assurance, regulatory affairs, and clinical teams also helps ensure timely and compliant submissions, minimizing the risk of non-compliance.

What is medical device reporting?

Medical device reporting is the process by which manufacturers, importers, and device user facilities notify regulatory authorities, such as the FDA, about certain adverse events and product problems involving medical devices. This reporting system helps monitor the safety and effectiveness of medical devices once they are on the market. The information collected can lead to recalls, safety alerts, or other actions to protect public health.
What are popular job titles related to Medical Device Reporting jobs in Indiana? For Medical Device Reporting jobs in Indiana, the most frequently searched job titles are:
Infographic showing various Medical Device Reporting job openings in Indiana as of June 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% In-person job distribution, with an average salary of $38,836 per year, or $18.7 per hour.
Post Market Quality Engineer

Post Market Quality Engineer

OrthoPediatrics

Warsaw, IN • On-site

$69K - $89K/yr

Full-time

Posted 11 days ago


Job description

Founded in 2006, OrthoPediatrics is an orthopedic company focused exclusively on advancing the field of pediatric orthopedics. As such it has developed the most comprehensive product offering to the pediatric orthopedic market to improve the lives of children with orthopedic conditions. OrthoPediatrics currently markets 53 products that serve three of the largest categories within the pediatric orthopedic market. This product offering spans trauma and deformity, scoliosis, and sports medicine/other procedures. OrthoPediatrics' global sales organization is focused exclusively on pediatric orthopedics and distributes its products in the United States and over 70 countries outside the United States. For more information, please visit www.orthopediatrics.com.
GENERAL SUMMARY: The Post Market Quality Engineer is responsible for medical device complaint investigations and write-ups as part of the Complaint Handling, Medical Device Reporting and Vigilance Reporting process. This position will ensure timely, accurate, and complete failure investigations, root cause analyses, risk analyses, and other complaint-related tasks are performed and documented for product field failures.
ESSENTIAL FUNCTIONS:
  • Work within cross-functional internal and external teams to investigate device field complaints and provide solutions to resolve complaints in a timely manner.
  • Perform failure analysis of medical devices using various types of test equipment, fixtures, and software tools.
  • Utilize applicable quality tools (Root cause analyses) to ensure timely, accurate, and complete failure investigations of product complaints leading to the root cause and ensure that all activities are documented in the complaint management system.
  • Review internal and external documentation such as device history records, material certifications, inspection reports, and any additional supporting documentation for conformance for complaint investigations.
  • Comply with Quality Management's guidance and instruction and provide complaint status updates.
  • Work with Product Line Engineers to complete post market risk assessments and drive periodic updates to risk management documentation and potentially other documents.
  • Develop, update, and maintain Job Aids and Work Instructions to facilitate and standardize investigation activities.
  • Ability to interface with external auditors.

SUPERVISORY RESPONSIBILITIES:
There are no supervisor responsibilities with this position.
QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. (The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
  • Thorough knowledge of specifications, dimensions, tolerances, and GD&T.
  • Ability to work in a strong team environment and/or independently while being self-motivated and having self-direction.
  • Proficient in the use of statistical applications; must be familiar with the use of SPC.
  • Knowledge on non-destructive testing and measuring techniques.
  • Must have excellent verbal and technical writing skills.
  • Must be analytical and can interpret data.
  • Ability to solve problems.
  • Strong working knowledge of medical device quality system regulations and standards (e.g. 21CFR820, ISO 13485, ISO 14971)
  • ISO 13485 Audit Certification preferred
  • 5 years of Medical Device Quality experience preferred.

EDUCATION AND/OR EXPERIENCE: Requires a bachelor's degree in an Engineering discipline, or equivalent experience in a related quality role. ASQ certification preferred. Must have computer skills; (MS-Excel). Knowledgeable in gauging methods and their applications.
LANGUAGE SKILLS: Ability to read and comprehend instructions, correspondence, and memos. Ability to prepare routine reports and correspondence. Ability to communicate effectively with customers, vendors and other employees of the organization. Requires excellent grammar and spelling.
Mathematical Skills: Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
Reasoning Ability: Ability to carry out instructions furnished in written, oral, or diagram form. Ability to use critical thinking to deal with problems involving multiple variables in a variety of situations.
Certificates, Licenses, Registrations: Requires a valid driver's license. ISO 13485 Audit Certification
Other Skills and Abilities: Requires the ability to operate a variety of standard office equipment, such as a computer and keyboard, calculator, fax, photocopier, telephone, cell phone, etc. Requires proficiency with Microsoft Word, Excel, Outlook and PowerPoint.
physical demands: (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
While performing the duties of this job, the employee is regularly required to sit and use hands to finger, handle or feel. The employee is frequently required to climb stairs, talk and hear. The employee is occasionally required to stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, and ability to adjust focus.
Work Environment: (The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
The noise level in the work environment is that found in a "normal office environment; noise levels during visits to other locations in the building may be moderate and occasionally loud. The employee will be required to travel 5% of the time.
The above statement reflects the general details necessary to describe the principle functions of the occupation described and shall not be construed as a detailed description of all the work requirements that may be inherent in the occupation.