1

Medical Device Compliance Jobs in Indiana (NOW HIRING)

Medical Device Assembler

Westfield, IN ยท On-site

$21.50 - $23/hr

Under close supervision, the Medical Device Assembler performs assembly, repair, and test ... Maintain compliance with safety guidelines and utilize appropriate safety devices during all ...

Medical Device Assembler

Westfield, IN ยท On-site

$20 - $23/hr

Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ... Prior experience as a Medical Device Assembler or Production Assembler is required * Ability to ...

Medical Device Assembler

Carmel, IN ยท On-site

$20 - $23/hr

Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ... Prior experience as a Medical Device Assembler or Production Assembler is required * Ability to ...

Medical Device Coder

Carmel, IN ยท On-site

$18.50 - $24.75/hr

Maintains compliance with data privacy, company security policies, ethical coding standards, and ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Medical Device Coder

Indianapolis, IN ยท On-site

$18 - $24/hr

Maintains compliance with data privacy, company security policies, ethical coding standards, and ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Medical Device Coder

Carmel, IN ยท On-site

$18.50 - $24.75/hr

Maintains compliance with data privacy, company security policies, ethical coding standards, and ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Be Seen First

Machinist / Inspector - Medical Device Manufacturing Company Overview Flotec is an Indianapolis ... Inspect machined components to ensure compliance with engineering drawings, tolerances ...

Medical Device In The Quality Department In Some Jobs You Take Orders. In This One, You Write ... Maintains compliance with data privacy, company security policies, ethical coding standards, and ...

Medical Device In The Quality Department Join the healthcare information technology team that ... Maintains compliance with data privacy, company security policies, ethical coding standards, and ...

Medical Device In The Quality Department Join the healthcare information technology team that ... Maintains compliance with data privacy, company security policies, ethical coding standards, and ...

next page

Showing results 1-20

Medical Device Compliance information

See Indiana salary details

$30K

$94.2K

$197.4K

How much do medical device compliance jobs pay per year?

As of Sep 1, 2026, the average yearly pay for medical device compliance in Indiana is $94,157.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,500.00 and $109,400.00 per year, depending on experience, location, and employer.

What is medical device compliance?

Medical device compliance refers to the process of ensuring that medical devices meet all regulatory requirements and standards before they are marketed or used. This includes adhering to laws and regulations set by agencies such as the FDA in the United States or the European Medicines Agency in Europe. Compliance covers the entire product lifecycle, including design, manufacturing, labeling, and post-market surveillance, to ensure that devices are safe and effective for patients. Companies must maintain thorough documentation and undergo regular audits to demonstrate ongoing compliance.

What are some common challenges faced in a medical device compliance role, and how can they be addressed?

Professionals in Medical Device Compliance often encounter the challenge of keeping up with rapidly evolving global regulations and standards, such as FDA, ISO 13485, and MDR. This requires continuous education and close collaboration with regulatory affairs, quality assurance, and product development teams to ensure all documentation and processes meet compliance requirements. Effective communication and attention to detail are key, as is proactively participating in internal audits and training sessions. By fostering a culture of compliance and staying current with industry updates, these challenges can be managed successfully.

What are the key skills and qualifications needed to thrive in medical device compliance, and why are they important?

To excel in Medical Device Compliance, you need a comprehensive understanding of regulatory requirements (such as FDA, ISO 13485), risk management, and quality assurance processes, usually supported by a science or engineering degree. Familiarity with quality management systems (QMS), regulatory submission tools, and certifications like RAC (Regulatory Affairs Certification) are highly valuable. Attention to detail, strong problem-solving abilities, and effective communication skills set top professionals apart in this field. These competencies are crucial for ensuring that medical devices meet legal standards, protecting patient safety, and facilitating successful product approvals.

What is the difference between Medical Device Compliance vs Medical Device Quality Assurance?

AspectMedical Device ComplianceMedical Device Quality Assurance
CertificationsRegulatory knowledge, such as FDA, ISO 13485Quality management system standards, audits, and inspections
Work EnvironmentRegulatory agencies, compliance departmentsManufacturing facilities, quality departments
Employer & Industry UsageMedical device companies, regulatory bodiesMedical device manufacturers, quality assurance teams

While both roles focus on ensuring medical device safety and effectiveness, Medical Device Compliance primarily involves adhering to regulatory requirements and standards, whereas Medical Device Quality Assurance emphasizes maintaining and improving product quality through testing, audits, and process controls. Both are essential for bringing safe, compliant medical devices to market.

Is healthcare compliance a good career?

Medical device compliance is a growing field that involves ensuring products meet regulatory standards such as FDA and ISO requirements. It offers opportunities for professionals with knowledge of regulations, quality systems, and documentation, often requiring certifications like RAC or ISO auditor training. The role provides stability and the chance to contribute to patient safety and product effectiveness.

Is medical device regulatory affairs a good career?

Medical device regulatory affairs is a growing field that involves ensuring compliance with industry standards and regulations such as FDA and ISO. It requires knowledge of regulatory processes, documentation, and often a background in healthcare, engineering, or science. The role offers opportunities for specialization, career advancement, and work in a highly regulated industry focused on patient safety.

What are popular job titles related to Medical Device Compliance jobs in Indiana?

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

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

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

Infographic showing various Medical Device Compliance job openings in Indiana as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $94,157 per year, or $45.3 per hour.

Medical Device Assembler

Westfield, IN โ€ข On-site

$21.50 - $23/hr

Contractor

Medical, Dental, Vision

This job post hasย expired today.ย Applications are no longer accepted.


Job description

This position is responsible for the production of high-quality medical devices within a manufacturing cell. Under close supervision, the Medical Device Assembler performs assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies. The role requires following specified procedures, maintaining accurate documentation, adhering to safety protocols, and participating in continuous improvement initiatives to enhance quality and productivity. This position supports divisional initiatives and complies with Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. The ability to communicate effectively, manage small components, and prioritize work efficiently is essential. No travel is required, and day or evening shifts are typical. On-the-job training is provided for skill development.

Responsibilities

  • Perform precise assembly, repair, and testing of medical devices following standardized procedures.
  • Handle equipment and small components with care to ensure product integrity.
  • Maintain compliance with safety guidelines and utilize appropriate safety devices during all operations.
  • Accurately document work activities to ensure traceability and quality control.
  • Participate in Lean Manufacturing and continuous improvement initiatives to optimize production processes.
  • Communicate effectively with manufacturing management and internal/external customers.
  • Support adherence to Quality Management Systems (QMS), Environmental Management Systems (EMS), and regulatory standards.
  • Follow strict dress code and contamination control policies relevant to the production environment.

Preferred Qualifications

  • 1+ years of experience in medical device assembly.
  • High school diploma or equivalent.
  • Knowledge of assembly techniques and quality assurance processes.
  • Understanding of Lean Manufacturing principles.
  • Computer literacy and proficiency with electronic data collection systems.
  • Strong communication skills.
  • Familiarity with safety procedures in manufacturing environments.

Company Description

ATR International is a staffing and workforce solutions firm providing high‐quality talent across a wide range of industries, including technology, operations, and professional services.