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Quality Engineer Medical Devices Jobs in Indiana

Quality Engineer

Greenwood, IN ยท On-site

$40.87 - $45.67/hr

Up to $95,000 base + Quarterly Bonus , Medical, Dental, Vision & 401(k) Contribution Role Overview The Quality Engineer ensures the highest level of product quality and compliance within a regulated ...

Be Seen First

Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred Company Description Founded in 2015 and backed by two decades of hands-on experience, our ...

Quality Engineer

Fishers, IN ยท On-site

$64K - $83K/yr

The Quality Engineer is responsible for supporting the development, implementation, and continuous improvement of the company's Quality Management System (QMS). Reporting to the Quality Manager, this ...

Quality Engineer

Noblesville, IN ยท On-site

$60 - $80/hr

We are seeking a Quality Engineer with experience in medical device design quality and risk management to support product development from concept through commercialization. This role will primarily ...

Quality Engineer

Evansville, IN ยท On-site

$65 - $90/hr

Quality Engineer****Evansville, IN | Silgan Closures**We're seeking a Quality Engineer to join our ... Comprehensive benefits package including medical, dental, vision, life insurance, disability, and ...

Quality Engineer

Evansville, IN ยท On-site

$68K - $88K/yr

Quality Engineer Evansville, IN | Silgan Closures We're seeking a Quality Engineer to join our ... Comprehensive benefits package including medical, dental, vision, life insurance, disability, and ...

Quality Engineer

Evansville, IN ยท On-site

$65 - $90/hr

Quality Engineer Evansville, IN | Silgan Closures We're seeking a Quality Engineer to join our ... Comprehensive benefits package including medical, dental, vision, life insurance, disability, and ...

Quality Engineer

Evansville, IN ยท On-site

$68K - $88K/yr

Quality Engineer Evansville, IN | Silgan Closures We're seeking a Quality Engineer to join our ... Comprehensive benefits package including medical, dental, vision, life insurance, disability, and ...

Quality Engineer

Indianapolis, IN ยท On-site

$68K - $88K/yr

The Quality Engineer tackles critical Quality department functions and responsibilities such as ... Medical, Dental, Vision, 401k, Life Insurance * Paid Vacation and Holidays * STD and LTD * Much ...

Quality Engineer

Indianapolis, IN

$68K - $88K/yr

The Quality Engineer tackles critical Quality department functions and responsibilities such as ... Medical, Dental, Vision, 401k, Life Insurance * Paid Vacation and Holidays * STD and LTD * Much ...

Quality Engineer

Indianapolis, IN ยท On-site

$68K - $88K/yr

The Quality Engineer is responsible for improving the quality of products by working with Design, Manufacturing, and other functions to identify sources of variation and defects and develop ...

Quality Engineer

Madison, IN ยท On-site

$66K - $85K/yr

Job Summary The Quality Engineer is responsible for ensuring product quality and process ... medical, dental, vision, basic life insurance, paid time off (sick/vacation), and Paid Parental ...

Quality Engineer

Bluffton, IN ยท On-site

$65K - $84K/yr

Position Overview The Quality Engineer is responsible for acting in the interest of quality assurance of our products and processes, performing problem-solving project coordination involving multi ...

Showing results 21-40

Quality Engineer Medical Devices information

See Indiana salary details

$42.8K

$80K

$113.2K

How much do quality engineer medical devices jobs pay per year?

As of Sep 6, 2026, the average yearly pay for quality engineer medical devices in Indiana is $79,968.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,500.00 and $88,500.00 per year, depending on experience, location, and employer.

What does a quality engineer do in the medical device industry?

A Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory standards and quality requirements throughout their lifecycle. They develop and implement quality control processes, conduct risk assessments, lead investigations into product defects, and work closely with cross-functional teams to ensure compliance with regulations such as FDA and ISO 13485. Their work helps to guarantee the safety, reliability, and effectiveness of medical devices before they reach patients.

How does a quality engineer collaborate with cross-functional teams in the medical device industry?

Quality Engineers in the medical device field work closely with design, manufacturing, and regulatory teams to ensure products meet stringent quality and compliance standards. They participate in design reviews, help develop verification and validation protocols, and support the implementation of corrective actions. Regular communication with production and R&D teams is essential to identify potential risks early and to ensure that quality is built into every stage of product development. This collaborative approach not only improves product safety and efficacy but also streamlines regulatory submissions and audits.

What are the key skills and qualifications needed to thrive as a quality engineer in medical devices, and why are they important?

To thrive as a Quality Engineer in Medical Devices, you typically need a degree in engineering or a related field, combined with knowledge of quality assurance principles and regulatory requirements (such as ISO 13485 and FDA regulations). Familiarity with risk management tools, validation protocols, and quality management systems (QMS), as well as certifications like CQE (Certified Quality Engineer), are highly valuable. Strong analytical thinking, attention to detail, and effective communication skills enable you to identify issues, collaborate with cross-functional teams, and ensure compliance. These competencies are crucial for maintaining product safety, meeting regulatory standards, and supporting a culture of continuous improvement in the medical device industry.

What is the difference between Quality Engineer Medical Devices vs Quality Technician Medical Devices?

AspectQuality Engineer Medical DevicesQuality Technician Medical Devices
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, basic quality certifications
ResponsibilitiesDesigning quality systems, process improvements, root cause analysisInspecting products, conducting tests, recording quality data
Work EnvironmentDesign and development labs, manufacturing plantsManufacturing floors, quality control labs
Employer & Industry UsageMedical device companies, OEMs, suppliersManufacturers, contract labs, quality departments

In summary, Quality Engineer Medical Devices focus on developing quality systems, process improvements, and ensuring compliance, while Quality Technicians primarily perform product inspections and testing. Both roles are essential in maintaining high standards in the medical device industry but differ in scope and responsibilities.

What are popular job titles related to Quality Engineer Medical Devices jobs in Indiana?

For Quality Engineer Medical Devices jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Quality Engineer Medical Devices jobs in Indiana look for?

The top searched job categories for Quality Engineer Medical Devices jobs in Indiana are:

Infographic showing various Quality Engineer Medical Devices 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 $79,968 per year, or $38.4 per hour.

Quality Engineer

Anonymous Employer

Greenwood, IN โ€ข On-site

$40.87 - $45.67/hr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 10 days ago


Job description

Quality Engineer – Manufacturing

Compensation:Up to$95,000base +Quarterly Bonus, Medical, Dental, Vision & 401(k) Contribution

Role Overview

The Quality Engineer ensures the highest level of product quality and compliance within a regulated manufacturing environment. This role supports quality management systems, regulatory requirements, customer specifications, and internal standards. The Quality Engineer drives disciplined execution of quality processes, supports audits, leads root-cause investigations, and contributes to a zero-defect culture across all production operations.

This position is hands-on, detail-focused, and essential to maintaining product integrity, documentation accuracy, and customer satisfaction.

Key Responsibilities

Quality Systems & Compliance

  • Actively supports and promotes safety at all times — safety is always first
  • Ensures products meet all internal, regulatory, and customer quality standards
  • Supports internal and external audits, including regulatory, customer, and third-party audits
  • Supports Quality Manuals, procedures, and required training
  • Ensures compliance with all applicable regulatory requirements
  • Promotes and supports a zero-defect culture

Inspection, Testing & Documentation

  • Supports methods to inspect, test, and evaluate products and production equipment
  • Performs dimensional inspections using micrometers, calipers, bore gages, height gages, and optical comparators
  • Interprets drawings, certifications, and industry specifications
  • Creates APQP/PPAP documentation and First Article Inspection reports
  • Supports MRB activities and optimal disposition of non-conforming material
  • Maintains and communicates monthly quality metrics

Root Cause, Corrective Action & Continuous Improvement

  • Investigates customer concerns and warranty returns through structured corrective action
  • Conducts root-cause analysis and drives continuous improvement initiatives
  • Collects and analyzes data to support quality improvements and process stability
  • Audits internal processes for compliance to procedures and customer requirements
  • Audits supplier quality and manufacturing processes for compliance to purchase orders and specifications

Cross-Functional Collaboration

  • Works closely with production, engineering, supply chain, and leadership teams
  • Builds strong working relationships across all levels of the organization and with customers
  • Communicates effectively, adapts quickly, and demonstrates initiative in a fast-paced environment

Qualifications & Experience

Required

  • 5+ years of quality engineering experience
  • Bachelor’s degree in engineering (industrial, mechanical, manufacturing, electrical) or related technical field; equivalent experience considered
  • Proficiency with Microsoft Office and advanced Excel (including pivot tables)
  • Strong statistics and data-analysis capability
  • Ability to read and interpret blueprints
  • Strong organizational skills with the ability to manage priorities in a fast-paced environment

You should be proficient in:

  • Aerospace Manufacturing
  • PPAP Process Experience
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