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Quality Engineer Jobs in Anderson, IN (NOW HIRING)

Ambu

Quality Engineer

Noblesville, IN · On-site

$67K - $87K/yr

Quality Engineer City: Noblesville Country/Region: United States State: Indiana Business Area: Quality Assurance Department: QA, Noblesville Employment Type: Full-time Req ID: 9887 We are seeking a ...

PIVOT Workforce

Quality Engineer

Indianapolis, IN

$75K - $85K/yr

Quality Engineer We are looking for a highly skilled Quality Engineer to develop, implement, and enforce quality control procedures and protocols, ensuring our products and services meet the highest ...

Myhr

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

The Quality Engineer tackles critical Quality department functions and responsibilities such as return investigations, corrective action requests, system improvements, calibration management, and ...

Plansee Group

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

The Quality Engineer tackles critical Quality department functions and responsibilities such as return investigations, corrective action requests, system improvements, calibration management, and ...

EnPower, Inc.

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

The Quality Engineer will, under the general direction of the Quality Manager, have the vital responsibility of handling day-to-day product and process quality assurance support. Working with the ...

EnPower, Inc.

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

The Quality Engineer will, under the general direction of the Quality Manager, have the vital responsibility of handling day-to-day product and process quality assurance support. Working with the ...

EnPower, Inc.

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

The Quality Engineer will, under the general direction of the Quality Manager, have the vital responsibility of handling day-to-day product and process quality assurance support. Working with the ...

Rolls-Royce

Quality Engineer

Indianapolis, IN · Hybrid

$84K - $137K/yr

Quality Engineer Working Pattern: Hybrid/Onsite in office 3 days/week Working location:Indianapolis, IN Relocation is available for this position if appropriate Why Rolls-Royce? At Rolls-Royce we are ...

New

smcnorthamerica

Quality Engineer

Noblesville, IN · On-site

$67K - $87K/yr

PURPOSE This role is to provide quality engineering, continuous improvement, and documentation support within the organization. This position requires creativity, innovation, mechanical systems ...

smcnorthamerica

Quality Engineer

Noblesville, IN · On-site

$67K - $87K/yr

PURPOSE This role is to provide quality engineering, continuous improvement, and documentation support within the organization. This position requires creativity, innovation, mechanical systems ...

SMC Corporation of America

Quality Engineer

Noblesville, IN · On-site

$67K - $87K/yr

PURPOSE This role is to provide quality engineering, continuous improvement, and documentation support within the organization. This position requires creativity, innovation, mechanical systems ...

Thermo Fisher Scientific

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

The Quality Engineer is responsible for providing oversight for commissioning and qualification activities at the site, as well as supporting equipment maintenance. In addition, this role supports ...

Prophecy Technologies

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

Review engineering documents for completeness, accuracy, and compliance with quality system requirements. * Identify gaps in documentation and recommend corrective actions. * Support audits ...

Abbott

Quality Engineer II

Westfield, IN · On-site

$61K - $122K/yr

Quality Engineer II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:

Abbott

Quality Engineer I

Westfield, IN

$50K - $101K/yr

Quality Engineer I Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:

Abbott

Quality Engineer II

Westfield, IN

$61K - $122K/yr

Quality Engineer II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:

Allegion

Manufacturing Quality Engineer

Greenfield, IN · On-site

$71K - $92K/yr

Manufacturing Quality Engineer - Greenfield, IN Due to current and expected growth in volume and product offerings, as well as investment in new technologies, we are expanding our staff. The quality ...

Allegion

Manufacturing Quality Engineer

Greenfield, IN · On-site

$71K - $92K/yr

Manufacturing Quality Engineer - Greenfield, IN Due to current and expected growth in volume and product offerings, as well as investment in new technologies, we are expanding our staff. The quality ...

Allegion

Manufacturing Quality Engineer

Greenfield, IN

$71K - $92K/yr

Manufacturing Quality Engineer - Greenfield, IN Due to current and expected growth in volume and product offerings, as well as investment in new technologies, we are expanding our staff. The quality ...

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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 Aug 7, 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 the work of a quality engineer?

A quality engineer is responsible for developing and implementing quality control processes to ensure products or services meet specified standards. They analyze data, perform inspections, and collaborate with production teams to identify and resolve quality issues, often using tools like Six Sigma or ISO standards. Their work helps improve product reliability, safety, and customer satisfaction.

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 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 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.

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 much do quality engineers earn?

Quality engineers typically earn a median annual salary ranging from $60,000 to $90,000, depending on experience, location, and industry. Salaries can increase with certifications like ASQ CQE or Six Sigma, and those working in manufacturing or technology sectors often have higher compensation.
More about Quality Engineer jobs
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 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, 76% Full Time, 17% Part Time, 5% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $72,822 per year, or $35 per hour.

Quality Engineer

Ambu

Noblesville, IN • On-site

$67K - $87K/yr

Full-time

Re-posted 19 days ago

Job description

Quality Engineer
City: Noblesville
Country/Region: United States
State: Indiana
Business Area: Quality Assurance
Department: QA, Noblesville
Employment Type: Full-time
Req ID: 9887
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 support R&D and Process Engineering activities to ensure compliance with design controls and risk management requirements.
The ideal candidate must have hands-on experience with design controls and risk management, including FMEA and structured problem-solving methodologies, and a solid understanding of ISO 13485, 21 CFR 820, and ISO 14971 requirements to identify and mitigate potential compliance, product and patient safety risks.
Objective:
The objective of this position is to provide the level of resource necessary to maintain, monitor and improve the Quality Management System (QMS) for Ambu USNV, to ensure compliance with regulatory requirements and established local and Corporate practices.
Responsibilities and Essential Functions (Applicable to all positions listed above):
  • Identify and implement effective quality control systems to support on-going manufacturing and product/process development activities to meet internal and customer requirements.
  • Assist in the improvement and streamlining of quality practices across the organization to effectively identify and resolve quality issues.
  • Apply sound and systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues.
  • Responsible for product and process risk management activities.
  • Support the review, investigation, resolution and prevention of product and process nonconformances (NCRs) to meet established internal requirements.
  • Develop rework procedures to support NCR activities.
  • Act as a handler for Corrective Actions/Preventive Actions (CAPA) system activities to drive proper risk evaluation, investigation, and implementation of actions.
  • Support CAPA verification of effectiveness (VOE) activities.
  • Tracking, trending, and monitoring Quality key performance indicators (KPIs).
  • Report quality KPIs to Quality Review Board (QRB).
  • Participate in CAPA Review Board (CRB) meetings, as necessary.
  • Review calibrations out of tolerance assessments (OOTAs) and support with calibration remedial actions reports (RARs).
  • Responsible for change control activities related to quality documentation, such as updates to procedures, instructions, forms, risk management documentation, etc.
  • Quality functional approver for product and process changes as a subject matter expert (SME) of assigned areas.
  • Support Document Controls activities, as necessary.
  • Develop new and/or improve quality documentation (procedures, instructions, forms, ect.).
  • Write and execute spreadsheet validation documentation, as necessary.
  • Provide quality engineering support to process improvements and product/process development projects to ensure implementation of highest quality solutions.
  • Support complaint investigations, as necessary.
  • Become part of the internal auditing team as a certified auditor.
  • Supporting backroom activities during external audits, as necessary.
  • Provide guidance to less experienced staff.
  • Perform other related duties and responsibilities, as assigned.

Responsibilities and Essential Functions - Engineer II, Quality:
  • Responsible for, at a minimum, one critical functional area of the Quality Management System (QMS) (e.g., CAPA, NCR, Deviations, etc.).
  • Identify and implement activities geared to standardize and streamline quality practices across the organization to improve QMS efficiency and maintain its effectiveness.
  • Lead and provide guidance to the rest of the organization in proper root cause investigation techniques.
  • Provide guidance on the use of statistical techniques for selection of sampling strategies and analysis of data.
  • Facilitate CRB, QRB, and Management Review meetings.
  • Responsible for data trending and preparation for Management Reviews and Corporate Management Reviews.
  • Write and execute Test Method Validation (TMV) documentation related to Quality Assurance inspection methods, as necessary.

Qualifications:
Level: Engineer
  • Bachelor's degree in Engineering or technical field equivalent experience.
  • 1 - 2 years of experience working in quality and/or quality engineering roles. Within the medical device manufacturing industry is preferred.

Level: Engineer II
  • Bachelor's degree in Engineering or technical field equivalent experience.
  • 2 - 5 years of experience working in quality and/or quality engineering roles. Within the medical device manufacturing industry is preferred.
  • Working technical knowledge and application of quality concepts, practices, and procedures.

Required skills:
  • Experience with ISO 13485 and/or 21 CFR Part 820.
  • Ability to travel nationally and internationally up to approximately 5% of a year's time.
  • Good attention to detail and organizational skills.
  • Proficient at applying analytical and problem-solving tools and methodologies.
  • Ability to work, interact, and communicate effectively with others.
  • Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
  • Effective verbal and written communication skills.
  • Great technical writing skills.
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint).
  • Must be able to read, write and understand English.

Preferred skills:
  • Auditor or Lead Auditor certification.
  • Experience with EU MDR 2017/745.
  • Experience with ISO 14971.

Work Environment:
This is a manufacturing facility and as a result, employees have the potential to be exposed to noise, chemicals, fumes, airborne particles, machinery, vibration, or other workplace hazards controlled within compliance of current safety and health standards.
About Ambu
Ambu has been bringing the solutions of the future to life since 1937. Today, millions of patients and healthcare professionals worldwide depend on the efficiency, safety and performance of our single-use endoscopy, anaesthesia, and patient monitoring solutions. We continuously look to the future with a commitment to deliver innovative quality products that have a positive impact on patient care and the work of healthcare professionals. Headquartered near Copenhagen in Denmark, Ambu employs approximately 4,500 people in Europe, North America and the Asia Pacific.
For more information, please visit ambu.com or follow us on LinkedIn.
Ambu logo

About Ambu

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Noblesville, IN, US

Year founded

1937

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