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Medical Device Reporting Jobs in Indiana (NOW HIRING)

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... reports, filing, and other customer service functions as needed. Required Qualifications * Prior ... Experience in medical device, healthcare, manufacturing, distribution, or regulated industries.

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 ...

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.

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Quality Engineer

Avon, IN · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Manufacturing Company Overview Flotec is an Indianapolis-based ... reports, material review board activities, and disposition documentation. * Review and approve ...

... medical device environment. * Hands-on experience with validation activities including URS, FAT, SAT, IQ, OQ, and PQ. * Ability to prepare, complete, and interpret complex validation reports and ...

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

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Showing results 1-20

Medical Device Reporting information

See Indiana salary details

$12

$18

$24

How much do medical device reporting jobs pay per hour?

As of Jul 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 July 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.
Machinist / Inspector - Medical Device Manufacturing

Machinist / Inspector - Medical Device Manufacturing

Flotec

Avon, IN • On-site

$40K - $55K/yr

Full-time

Medical, Dental, Vision

Posted 8 days ago


Job description

Machinist / Inspector – Medical Device Manufacturing

Company Overview

Flotec is an Indianapolis-based medical device manufacturer specializing in respiratory and oxygen delivery equipment. We manufacture precision medical products including oxygen regulators, flowmeters, fittings, valves, and related components used by hospitals, EMS providers, fire departments, military organizations, and medical device OEMs.

We are seeking a skilled and detail-oriented Machinist / Inspector to join our manufacturing team. This position supports both precision machining and inspection activities in a regulated medical device environment.

Position Summary

The Machinist / Inspector will be responsible for producing, inspecting, and verifying precision machined components used in medical device manufacturing. This role involves working with CNC machines, CNC Swiss machines, CNC mills, and mills with robotic automation.

The ideal candidate will have strong machining knowledge, excellent attention to detail, and the ability to inspect parts accurately using measuring instruments, drawings, specifications, and quality requirements. This is a hands-on position for someone who takes pride in producing high-quality parts and understands the importance of precision, documentation, and consistency in medical device manufacturing.

Key Responsibilities

  • Set up, operate, and monitor CNC machines, CNC Swiss machines, CNC mills, and robotic milling systems.
  • Inspect machined components to ensure compliance with engineering drawings, tolerances, specifications, and quality standards.
  • Use precision measuring equipment such as micrometers, calipers, thread gauges, plug gauges, pin gauges, height gauges, indicators, comparators, and other inspection tools.
  • Perform first-piece, in-process, and final inspections.
  • Read and interpret engineering drawings, work instructions, inspection plans, routings, and manufacturing documentation.
  • Verify dimensional accuracy, surface finish, threads, features, and critical characteristics.
  • Document inspection results accurately and completely.
  • Identify and report nonconforming parts, tooling issues, machine issues, or process concerns.
  • Make machine offsets and basic adjustments as needed to maintain part quality.
  • Work with production, quality, and engineering personnel to resolve machining or inspection issues.
  • Maintain clean, organized, and safe work areas.
  • Follow company procedures, quality system requirements, and medical device manufacturing standards.
  • Support continuous improvement efforts related to quality, productivity, setup reduction, and scrap reduction.
  • Assist with maintaining traceability and proper documentation for regulated medical device production.

Required Qualifications

  • Prior experience as a CNC machinist, CNC Swiss machinist, machine operator, inspector, or machinist/inspector.
  • Ability to read and understand engineering drawings and dimensional tolerances.
  • Experience using precision measuring instruments.
  • Strong attention to detail and commitment to quality.
  • Ability to work in a manufacturing environment and follow documented procedures.
  • Basic math skills, including decimals, fractions, and measurement conversions.
  • Ability to document work accurately and communicate issues clearly.
  • Dependable attendance and a strong work ethic.
  • Willingness to work in a regulated medical device manufacturing environment.

Preferred Qualifications

  • Experience with CNC Swiss machines.
  • Experience with CNC mills, lathes, or mills with robotic automation.
  • Experience inspecting small precision machined components.
  • Experience in medical device, aerospace, defense, automotive, or other regulated manufacturing industries.
  • Familiarity with ISO 13485, FDA-regulated manufacturing, or quality system documentation.
  • Experience with first article inspection, in-process inspection, final inspection, and nonconforming material processes.
  • Experience with oxygen equipment, brass, aluminum, stainless steel, or precision valve and regulator components.
  • Ability to perform basic machine setup, tooling changes, offsets, and troubleshooting.

Ideal Candidate

The ideal candidate is a hands-on machinist who also understands inspection and quality requirements. This person should be comfortable working around CNC equipment, checking their own work, identifying problems early, and helping ensure that every part meets the required specifications before moving to the next operation.

This position is well suited for someone who takes pride in precision work, enjoys manufacturing high-quality components, and wants to be part of a company producing products used in critical medical and emergency response applications.

Compensation and Benefits

Flotec offers competitive compensation based on experience and qualifications. Benefits may include paid time off, paid holidays, health insurance options, retirement plan participation, and opportunities for professional growth.

Schedule

Full-time position. Day shift. On-site position in Indianapolis, Indiana.

Work Location

Indianapolis, Indiana

Equal Opportunity Employer

Flotec is an Equal Opportunity Employer. We consider qualified applicants without regard to race, color, religion, sex, national origin, age, disability, veteran status, or any other legally protected status.

How to Apply

Qualified candidates are encouraged to submit a resume or work history outlining their CNC machining, Swiss machining, inspection, and manufacturing experience.

Company Description

Flotec is a Medical Device manufacturing company that makes Respiratory Equipment. Flotec is located off Rockville Rd east of Avon.
Flotec is an “Essential Business” as per Indiana Executive Order 20-08. Flotec is classified as a “Healthcare & Public Health Operation” and is EXEMPT from the Stay at Home Order.