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Medical Device Reporting Jobs in Indiana (NOW HIRING)

Nexxt Spine

CNC Mill Setup/Operator

Noblesville, IN · On-site

$20.75 - $27.50/hr

... in the medical device industry, dedicated to designing, manufacturing, and distributing an ... Position Summary: Reporting to the Mill Program Engineer, the CNC Mill Setup/Operator will be ...

Red Star

Sterile Packaging Manager

IN · On-site

... medical device experience strongly preferred. * Previous experience leading projects, initiatives, teams, or direct reports preferred. OTHER SKILLS and ABILITIES: * Strong leadership, project ...

Red Star

Sterile Packaging Manager

Larwill, IN · On-site

... medical device experience strongly preferred. * Previous experience leading projects, initiatives, teams, or direct reports preferred. OTHER SKILLS and ABILITIES: * Strong leadership, project ...

Stevanato Group S.p.A.

Production Manager

Fishers, IN · On-site

Reporting & Communication: * Prepare and present production and compliance performance reports ... Experience with ISO 13485, FDA, GMP, and other medical device regulatory standards. * Experience ...

INCOG

Senior QA Risk Management Engineer

Fishers, IN · On-site

... medical device and combination product operations, manufacturing processes, and continuous improvement initiatives. The QA Risk Management Sr Engineer will prepare risk management reports and metrics ...

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 ...

Red Star

Senior Sterile Packaging Engineer

Larwill, IN · On-site

Design, evaluate, and approve packaging components and sterile packaging systems for medical device ... Prepare and provide technical oversight for protocols, reports, technical justifications, and ...

Red Star

Senior Sterile Packaging Engineer

IN · On-site

Design, evaluate, and approve packaging components and sterile packaging systems for medical device ... Prepare and provide technical oversight for protocols, reports, technical justifications, and ...

CTE Solutions

CMM Technician

Plymouth, IN · On-site

Generate CMM reports * Assess potential non-conforming results to root cause * Replace broken probe ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements. * Other work ...

Three Point Solutions

Machine Operator

Warsaw, IN · On-site

$19 - $21/hr

Medical Device Manufacturing Company Duration : 1 Year (Possible Extension) Location : Warsaw, IN ... Report machine malfunctions and assist in troubleshooting * Support production, packaging ...

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Showing results 41-60

All JobsMedical Device Reporting JobsMedical Device Reporting Jobs in Indiana

Medical Device Reporting information

See Indiana salary details

$12

$18

$24

How much do medical device reporting jobs pay per hour?

As of Aug 6, 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:
What job categories do people searching Medical Device Reporting jobs in Indiana look for? The top searched job categories for Medical Device Reporting jobs in Indiana are:
Medical Device Reporting jobs near you
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.

Senior Quality Engineer

Culver Tool & Engineering Solutions

Plymouth, IN • On-site

$80K - $109K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Job description

Build More Than a Job-Build a Career at SpiTrex CTE

At SpiTrex CTE, we invest in our people. You'll find opportunities to grow, real flexibility, and a culture that values balance, development, and teamwork.


Why join CTE?

  • Career Growth:Ongoing training and development through Bamboo Path Track & WorkForge
  • Flexibility:Flextime options that support real life
  • Culture:Team events, Donut Fridays, food trucks, and more
  • Rewards:Referral bonuses, quarterly bonuses, and a 401(k) with 50% company match (up to 10%)
  • Benefits:No-cost vision, life, and short-term disability; dental & medical with HSA or PPO options


Ready to grow with a company that values you?Join SpiTrex CTE.


1st Shift: Monday to Thursday, 6AM - 3PM; Friday, 6AM - 10AM


Essential Functions:

  • Assisting with Customer Audits, Internal Audits, Notified Body Audits, and FDA Inspections
  • Assisting with Supplier Management (including but not limited to supplier performance review, and supplier audits)
  • Managing Direct Reports
  • Developing and implementing quality control procedures and guidelines
  • Monitoring and analyzing data to identify areas for improvement
  • Initiate quality improvement projects
  • Collaborate with cross-functional teams to resolve quality issues
  • Conducting audits on products and processes
  • Providing guidance to other team members
  • Investigating and resolving customer complaints
  • Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements
  • Reviewing and approving product and process changes
  • Developing procedures and work instructions as needed
  • Other work-related tasks as assigned


Competency:

  • Strong background in quality control and quality engineering functions
  • Understanding GD&T
  • Experience with Statistical Software
  • Experience with Gage Repeatability and Reproducibility
  • Excellent communication skills
  • Excellent leadership skills
  • Detail-oriented
  • Strong analytical and problem-solving skills
  • Ability to manage multiple projects simultaneously
  • Strong understanding of medical device regulations


Educational Requirements:

B.S. in Engineering field preferred or minimum of 5 years in Quality Engineering role


Experience:

5-7 years of Medical Device experience in Quality setting preferred


Benefits Include:

  • Medical, Vision and Dental Insurance
  • Short-Term Disability
  • Life Insurance
  • 401(k) - 50% company match (up to 10% contribution)
  • Paid vacation days
  • Paid holidays

Apply