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Quality Engineer Jobs in Anderson, IN (NOW HIRING)

Danaher

Supplier Quality Engineer

Indianapolis, IN · On-site

The Supplier Quality Engineer is responsible for driving supplier quality performance, leading continuous improvement initiatives, monitoring and supporting our suppliers to be the best Cytiva ...

Danaher

Supplier Quality Engineer

Indianapolis, IN · On-site

The Supplier Quality Engineer is responsible for driving supplier quality performance, leading continuous improvement initiatives, monitoring and supporting our suppliers to be the best Cytiva ...

Hansoninc

Air Quality Engineer

Indianapolis, IN

$100K - $150K/yr

A Day in the Life of an Air Quality Engineer at Hanson Here's a snapshot of what you would do in this role: * Lead and manage air quality permitting projects to ensure successful project execution ...

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All JobsQuality Engineer JobsQuality Engineer Jobs in Anderson, IN

Quality Engineer information

See Anderson, IN salary details

$39K

$72.8K

$103.1K

How much do quality engineer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for quality engineer in Anderson, IN is $72,822.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,400.00 and $80,600.00 per year, depending on experience, location, and employer.

What is a quality engineer?

A quality engineer ensures that the products manufactured by a company are meeting company and government quality control standards. As a quality engineer, your responsibilities include assessing and developing quality assurance protocols, examining products for compliance, and training teams to follow your policies. You also record data regarding production to track quality and produce the documentation need to communicate concerns throughout the company. The American Society for Quality (ASQ) regulates the profession and offers a path to become a certified quality engineer (CQE).

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

To thrive as a Quality Engineer, you need a solid grounding in engineering principles, quality assurance methodologies, and a relevant degree such as in engineering or a related field. Familiarity with tools like Six Sigma, ISO standards, statistical process control (SPC), and quality management systems (QMS) is typically required, and certifications like CQE (Certified Quality Engineer) are highly valued. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues, collaborate with teams, and drive continuous improvement. These skills ensure that products and processes consistently meet standards, minimize defects, and enhance overall operational efficiency.

How does a quality engineer typically collaborate with other departments to ensure product quality?

Quality Engineers work closely with cross-functional teams such as manufacturing, design, and supply chain to uphold product standards. They often participate in team meetings, review process documentation, and coordinate root cause analyses with engineers and operators. Effective communication and proactive problem-solving are key, as they must ensure that quality requirements are clearly understood and implemented throughout each stage of production. This collaborative approach not only helps resolve issues quickly but also fosters a culture of continuous improvement across the organization.

What is the difference between Quality Engineer vs Quality Technician?

AspectQuality EngineerQuality Technician
ResponsibilitiesDesigning quality systems, process improvements, root cause analysisInspecting products, conducting tests, recording quality data
Required SkillsAnalytical skills, problem-solving, knowledge of quality standardsAttention to detail, testing procedures, data collection
CertificationsASQ CQE, Six SigmaASQ CQPA, basic quality certifications
Work EnvironmentOffice, manufacturing plants, cross-functional teamsManufacturing floors, labs, inspection stations

Quality Engineers focus on developing and improving quality systems and processes, while Quality Technicians primarily perform inspections and tests to ensure product quality. Both roles are essential in maintaining standards, but they differ in scope and responsibilities.

How much does a quality engineer earn?

The average salary for a quality engineer varies by location and experience but typically ranges from $60,000 to $90,000 annually. Entry-level positions may start lower, while experienced engineers with certifications like Six Sigma or ISO may earn higher salaries. Salaries can also be influenced by industry, company size, and specific skills such as proficiency with quality management tools.

What degree do you need for a quality engineer?

A quality engineer typically needs at least a bachelor's degree in engineering, manufacturing, or a related field. Relevant skills include knowledge of quality management systems and tools like Six Sigma or ISO standards, and some roles may prefer or require professional certifications such as ASQ Certified Quality Engineer (CQE).
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What are the most commonly searched types of Quality Engineer jobs in Anderson, IN?

The most popular types of Quality Engineer jobs in Anderson, IN are:

What job categories do people searching Quality Engineer jobs in Anderson, IN look for?

The top searched job categories for Quality Engineer jobs in Anderson, IN are:

What cities near Anderson, IN are hiring for Quality Engineer jobs?

Cities near Anderson, IN with the most Quality Engineer job openings:

Quality Engineer jobs near you
Infographic showing various Quality Engineer job openings in Anderson, IN as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 14% Part Time, 6% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $72,822 per year, or $35 per hour.

Design Quality Engineer

Prophecy Technologies

Indianapolis, IN • On-site

Full-time

Re-posted 8 days ago

Job description

Design Quality Engineer
Technical/Functional
Skills • Strong understanding of Medical Device Product Development Process and Design Control requirements. • Knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, and applicable regulatory standards. • Strong knowledge of Design Controls and medical device product development. • Experience with Design History File (DHF) development, review, and remediation.
• Hands-on experience with Risk Management activities including: o dFMEA o uFMEA o Preliminary Hazard Analysis (PHA) o Hazard Analysis • Knowledge of FDA 21 CFR Part 820, ISO 13485, and ISO 14971. • Experience with Design Verification and Validation (V&V). • Understanding of User Needs, Design Inputs, Design Outputs, and Traceability requirements. • Experience preparing and reviewing: o Product Specification Documents (PSD) o Product Characterization documents o CTQ (Critical-to-Quality) documents • Experience with CAPA, Nonconformance, and root cause investigations. • Familiarity with PLM systems such as Windchill, or Teamcenter. • Experience with Cockpit Cognition DHF Build and DHF traceability management. • Strong documentation, technical writing, and audit support skills.
Roles & Responsibilities • Support quality activities throughout the product development lifecycle. • Review and maintain Design History File (DHF) documentation for compliance with regulatory and quality requirements. • Lead and support risk management activities including dFMEA, uFMEA, and PHA updates. • Ensure traceability between User Needs, Design Inputs, Risk Controls, Verification, Validation, and Design Outputs. • Support Design Verification and Validation planning, execution, and documentation reviews. • Review Product Characterization, Product Specification (PSD), and CTQ documents. • Participate in design reviews and ensure compliance with
Design Control processes. • Support Cockpit Cognition DHF Build activities, including documentation organization and traceability linkages. • Conduct DHF gap assessments and support remediation activities. • Collaborate with R&D, Manufacturing, Regulatory Affairs, and Supplier Quality teams. • Support CAPA investigations, root cause analysis, and implementation of corrective actions. • Ensure compliance with FDA, ISO 13485, ISO 14971, and internal quality procedures. • Support internal audits, customer audits, and regulatory inspections. • Drive continuous improvement initiatives related to design quality and risk management processes.

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