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Quality Engineer Fulltime Jobs in Indiana (NOW HIRING)

Quality Engineer

Noblesville, IN ยท On-site

$67K - $87K/yr

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 ...

Quality Engineer

Bluffton, IN ยท On-site

$65K - $84K/yr

Job Type Full-time Description Company Overview Founded in 1961, WEG has grown into a global ... Position Overview The Quality Engineer is responsible for acting in the interest of quality ...

Quality Engineer

Lafayette, IN ยท On-site

$69K - $89K/yr

... Foundational|Quality Engineering|Quality Engineering Strategy Design Technical Skills 2 ... Benefits Along with competitive pay, as a full-time Infosys employee you are also eligible for the ...

Quality Engineer

Seymour, IN ยท On-site

$65K - $85K/yr

Quality Engineer Location: Seymour, IN (Relocation Assistance Available) Salary Range: $65K - 85K ... Employment Type: Full-Time, 1st Shift Job Summary This role is responsible for ensuring product ...

Quality Engineer

Lafayette, IN ยท On-site

$69K - $89K/yr

... Foundational|Quality Engineering|Quality Engineering Strategy Design Technical Skills 2 ... Benefits Along with competitive pay, as a full-time Infosys employee you are also eligible for the ...

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Quality Engineer

Indianapolis, IN ยท On-site

$85K - $110K/yr

Direct Hire / Full-Time Compensation: Competitive base salary + benefits package (details shared ... Quality Engineer - Indianapolis, IN (Confidential) Company Description OPPORTUNITY OVERVIEW ...

Quality Engineer

Michigan City, IN

$70K - $90K/yr

Engineering & Science Job Schedule: Full time Remote: No Hitachi Global Air Power: We build the ... The Quality Engineer serves as the primary liaison between the organization and the quality ...

Quality Engineer

Terre Haute, IN ยท On-site

$68K - $88K/yr

Job Purpose The Quality Engineer is responsible for ensuring the highest quality standards in the ... full-time, exempt position that works primarily Monday-Friday, supporting all shifts as needed.

Quality Engineer

Elkhart, IN ยท On-site

$69K - $89K/yr

Production Quality Manager Employment Type: Full-time Visa Sponsorship: Available Position Summary The Quality Assurance Engineer plays a key role in ensuring the highest standards of quality ...

Quality Engineer

Elkhart, IN ยท On-site

$69K - $89K/yr

Production Quality Manager Employment Type: Full-time Visa Sponsorship: Available Position Summary The Quality Assurance Engineer plays a key role in ensuring the highest standards of quality ...

Quality Engineer

Elkhart, IN

$69K - $89K/yr

Production Quality Manager Employment Type: Full-time Visa Sponsorship: Available Position Summary The Quality Assurance Engineer plays a key role in ensuring the highest standards of quality ...

Quality Engineer

Argos, IN ยท On-site

$63K - $81K/yr

Job Type Full-time Description About Sequel Wire and Cable LLC: At Sequel Wire and Cable, we're not ... The Quality Engineer is responsible for maintaining and improving Sequel's quality management ...

Quality Engineer

New Paris, IN ยท On-site

$62K - $81K/yr

The Quality Engineer is responsible for ensuring that products are designed and manufactured to ... UNAVAILABLEEmployment Type: FULL_TIME

Quality Engineer

New Paris, IN ยท On-site

$62K - $81K/yr

The Quality Engineer is responsible for ensuring that products are designed and manufactured to ... This is a full-time salary position, and hours/days of work are decided by production schedules and ...

Quality Engineer

New Paris, IN

$62K - $81K/yr

The Quality Engineer is responsible for ensuring that products are designed and manufactured to ... UNAVAILABLEEmployment Type: FULL_TIME

Quality Engineer

Indianapolis, IN ยท On-site

$68K - $88K/yr

Applicants must be currently authorized to work in the United States on a full-time basis ... Support the Quality Techs in CMM Programming with Calypso Software and inspecting parts on the CMM.

Quality Engineer

Indianapolis, IN ยท On-site

$68K - $88K/yr

Applicants must be currently authorized to work in the United States on a full-time basis ... Support the Quality Techs in CMM Programming with Calypso Software and inspecting parts on the CMM.

Quality Engineer

Indianapolis, IN

$68K - $88K/yr

Applicants must be currently authorized to work in the United States on a full-time basis ... Support the Quality Techs in CMM Programming with Calypso Software and inspecting parts on the CMM.

Quality Engineer

Indianapolis, IN

$68K - $88K/yr

Summary/Objectives The Quality Engineer maintains quality control processes, systems and ... Employment Type: FULL_TIME

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Showing results 1-20

Quality Engineer Fulltime information

Is there a demand for a quality engineer?

There is consistent demand for quality engineers across various industries such as manufacturing, technology, and healthcare, as companies prioritize product quality and compliance. Skilled quality engineers with knowledge of quality management systems, testing tools, and certifications like Six Sigma are especially sought after in the job market.

What engineers make $300,000 a year?

Senior engineers in specialized fields such as software engineering, petroleum engineering, and aerospace engineering can earn $300,000 or more annually, especially with extensive experience, advanced skills, and in high-demand industries. Executive-level engineering roles or those with significant managerial responsibilities may also reach or exceed this salary level.

What is the difference between Quality Engineer Fulltime vs Quality Technician?

AspectQuality Engineer FulltimeQuality Technician
CredentialsBachelor's in Engineering or related field, certifications like CQEHigh school diploma or associate degree, certifications like CQTA
Work EnvironmentDesign, development, process improvement in manufacturing or tech industriesInspection, testing, and data collection on production lines
ResponsibilitiesProcess analysis, quality planning, root cause analysisProduct inspection, testing, data recording

Quality Engineer Fulltime roles focus on process improvement, analysis, and quality planning, often requiring a bachelor's degree. Quality Technicians primarily perform inspections and testing, typically with less formal education. Both roles are essential in manufacturing and industry settings, but differ in scope and responsibilities.

What is the average salary of a QA engineer?

The average salary of a QA engineer varies by location and experience but typically ranges from $60,000 to $90,000 annually. Senior QA engineers with specialized skills or certifications can earn over $100,000 per year, especially in competitive markets or with extensive expertise in automation tools and testing frameworks.

What engineer makes $500,000 a year?

While most engineering roles do not reach a $500,000 annual salary, some senior-level engineers in specialized fields such as petroleum, aerospace, or software engineering with executive responsibilities can earn this level through base pay, bonuses, and stock options. High compensation typically requires extensive experience, advanced skills, and often leadership or managerial roles within large organizations.
What cities in Indiana are hiring for Quality Engineer Fulltime jobs? Cities in Indiana with the most Quality Engineer Fulltime job openings:

Quality Engineer

Ambu

Noblesville, IN โ€ข On-site

$67K - $87K/yr

Full-time

Posted 27 days ago


Job description

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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.

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