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Fmea Engineer Jobs in Indiana (NOW HIRING)

Thermo Fisher Scientific

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

The Quality Engineer is responsible for providing oversight for commissioning and qualification ... Duties also include participating in internal and external audits, conducting FMEA assessments, and ...

Carrier

Staff Electronics Engineer

Fort Wayne, IN · On-site

$96K - $192K/yr

Apply knowledge of FMEA, tolerance stack up analysis, simulation, statistical methods and Design ... Mentor junior engineers to facilitate robust design. * Review technical documentation including ...

Thermo Fisher Scientific

Quality Engineer

Indianapolis, IN

$68K - $88K/yr

The Quality Engineer is responsible for providing oversight for commissioning and qualification ... Duties also include participating in internal and external audits, conducting FMEA assessments, and ...

Integrity Trade Services

Quality Engineer

La Porte, IN · On-site

$66K - $86K/yr

{Quality Engineer} Pay : Pay: Competitive Shift : To be discussed Location : La Porte, IN Integrity ... Experience with ISO 9001, PPAP, FMEA, CAPA, and industry standards. * Excellent analytical ...

Nishikawa Cooper LLC

QUALITY ENGINEER I

Topeka, IN · On-site

$75K - $100K/yr

Interfaces with all other engineering components within the company and with customers and ... Prepare PPAP's, FMEA's, Control plans, 5P's or 8 D's (Responsible during launch, mass production ...

Nishikawa Cooper LLC

ENGINEER I

Fort Wayne, IN · On-site

$44K - $90K/yr

A Process Engineer, or Manufacturing Process Engineer, designs and implements systems and equipment ... such as FMEA). * All personnelare responsible forconformity to product requirements andthe ...

Fitesa Simpsonville Inc.

Sr. Process Engineer

Terre Haute, IN · On-site

$99K - $128K/yr

Maintaining FMEA * Troubleshooting Industrial Machinery for the nonwoven industry. * Leading the ... Engineering and technical support for manufacturing non-woven/Film and elastic products * Executing ...

Fitesa Simpsonville, Inc.

Sr. Process Engineer

Terre Haute, IN · On-site

$99K - $128K/yr

Maintaining FMEA * Troubleshooting Industrial Machinery for the nonwoven industry. * Leading the ... Engineering and technical support for manufacturing non-woven/Film and elastic products * Executing ...

Fitesa Simpsonville Inc

Sr. Process Engineer

Terre Haute, IN

$99K - $128K/yr

Maintaining FMEA * Troubleshooting Industrial Machinery for the nonwoven industry. * Leading the ... Engineering and technical support for manufacturing non-woven/Film and elastic products * Executing ...

Valeo

Quality Projects Engineer

Seymour, IN · On-site

$62K - $80K/yr

Verify LLCs have been used in the D/P FMEA to reduce RPN and respected * After design freeze ... Bachelor's Degree in Engineering * Minimum of 4 years experience in Quality Join us! Thanks to its ...

Valeo

Quality Projects Engineer

Seymour, IN · On-site

$62K - $80K/yr

Verify LLCs have been used in the D/P FMEA to reduce RPN and respected * After design freeze ... Bachelor's Degree in Engineering * Minimum of 4 years experience in Quality Join us! Thanks to its ...

MS Companies

Quality Engineer

Seymour, IN

$65K - $85K/yr

... APQP, FMEA, Control Plans, Check Sheets, Capability Studies, and SPC charts ● Ability to ... in Engineering ● Six Sigma experience ● CMM operation and/or programming experience ● ...

NSG Group

PROCESS ENGINEER III

Shelbyville, IN · On-site

Develops/maintains equipment FMEA's to ensure that critical failure modes are identified and ... Ensure that the spare parts meet the engineering standards, updating engineering standards as ...

Trojan Battery Company

Engineer, Quality (CDT)

Attica, IN · On-site

$61K - $78K/yr

Root Cause and Corrective Action (RCCA), Process Mapping, Failure Mode & Effects Analysis (FMEA ... Areas of Focus Quality Engineer is responsible for development and implementation of product and ...

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Fmea Engineer information

How does an FMEA engineer typically collaborate with cross-functional teams during the risk assessment process?

As an FMEA Engineer, you will work closely with teams from design, manufacturing, quality, and sometimes suppliers to systematically identify and evaluate potential failure modes in products or processes. Effective collaboration is essential, as you’ll facilitate FMEA sessions, gather input from subject matter experts, and ensure that all relevant perspectives are considered. This teamwork helps to create robust mitigation strategies and action plans, making communication and coordination core parts of your daily responsibilities.

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

To thrive as an FMEA Engineer, you need a strong background in engineering principles, risk analysis, and quality management, often supported by a relevant engineering degree and experience in process improvement. Familiarity with technical tools like FMEA software (such as APIS IQ-FMEA or PTC Windchill), statistical analysis programs, and quality standards like ISO 9001 or IATF 16949 is typically required. Excellent attention to detail, analytical thinking, and strong communication skills help you collaborate effectively with cross-functional teams and present findings clearly. These skills and qualifications are essential for proactively identifying and mitigating risks, ensuring product reliability, and maintaining high quality standards in manufacturing or design processes.

What is the difference between Fmea Engineer vs Quality Engineer?

AspectFmea EngineerQuality Engineer
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 9001, Six Sigma, ASQ certifications
Work EnvironmentManufacturing, automotive, aerospaceManufacturing, software, healthcare
Primary FocusFailure Mode and Effects Analysis (FMEA)Overall quality management and process improvement

Fmea Engineers specialize in conducting FMEA to identify potential failures and improve product reliability, often working closely with design and manufacturing teams. Quality Engineers have a broader role in overseeing quality systems, audits, and continuous improvement initiatives. While both roles require similar certifications and often operate within manufacturing industries, Fmea Engineers focus specifically on failure analysis, whereas Quality Engineers manage overall quality assurance processes.

What is an FMEA engineer?

An FMEA Engineer is a professional who specializes in conducting Failure Mode and Effects Analysis (FMEA) within manufacturing, engineering, or product design teams. Their main responsibility is to systematically evaluate processes or products to identify potential failure modes, assess their impact, and prioritize corrective actions to mitigate risks. FMEA Engineers work closely with cross-functional teams to improve reliability, safety, and quality standards by proactively addressing weaknesses before issues arise. Their work is crucial in industries such as automotive, aerospace, electronics, and healthcare, where product safety and reliability are critical.
What are popular job titles related to Fmea Engineer jobs in Indiana? For Fmea Engineer jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Fmea Engineer jobs in Indiana look for? The top searched job categories for Fmea Engineer jobs in Indiana are:
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Fmea Engineer jobs near you
Infographic showing various Fmea Engineer job openings in Indiana as of August 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 97% In-person, and 3% Remote job distribution.

Quality Engineer

Thermo Fisher Scientific

Indianapolis, IN • On-site

$68K - $88K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 5 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 423 frontline employees who took The Breakroom Quiz

198th of 538 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
Location/Division Specific Information
1223 West Morris Street, Indianapolis, IN - Pharma Services Group
Discover Impactful Work:
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 ongoing quality initiatives and projects in alignment with Thermo Fisher values. Duties also include participating in internal and external audits, conducting FMEA assessments, and driving process improvement. Candidate must be an established quality system leader, strong communicator, and able to work with minimal direct oversight.
Day in the Life:
  • Applies Good Manufacturing Principles in all areas of responsibility.
  • Demonstrates and drives the Thermo Fisher values- Integrity, Intensity, Involvement and Innovation (The Four l's).
  • Responsible for ensuring GMP compliance and improving quality systems by leading or participating in projects, policy/procedure revisions.
  • Review and approve Engineering and Maintenance documents inclusive of engineering studies, FAT/SAT, IQ, 00, and PO.
  • Provide Quality support in the identification/development/qualification of new processes, featuring/tooling, and technologies into packaging operations.
  • Support the development of test plans to ensure risk mitigation and quality requirements are met.
  • Initiate and/or support in the development and/or update of Risk Management FMEA documentation in collaboration with multi-functional engineering teams per project requirements.
  • Play an integral role in Practical Process Improvement (PPI) program.
  • Works with FCS sites to assure consistency in validation strategy/approach for local and global projects.
  • Conduct periodic self-inspections and participate in or internal. client and Regulatory inspections to assure cGMP requirements.
  • Ensure that the Packaging facility and equipment are maintained in compliance with cGMPs.
  • Conducts all activities in a safe and efficient manner.
  • Able to partner with contacts at all levels of the organization. Additionally, periodic contact is required with the client in support of the FCS Validation Program, projects, presentations, tours, and capabilities.
  • Strong attention to detail, collaboration, partnership, influencing, prioritization, decision-making, analytical problem solving, and verbal and written communication skills are required.
  • Able to travel between sites, including international travel.
  • Other duties may be assigned to meet business needs.

Keys to Success:
  • Minimum Bachelor's degree in Engineering field
  • Minimum of 4 years total experience required with equipment/process validation experience.
  • Equivalent combinations of education, training, and relevant work experience may be considered.
  • Advanced experience with Microsoft Office Suite {Excel, Word, etc.) required.
  • Ability to work with a variety of functional areas.
  • Must be a self-starter, have excellent time management and organization skills, a high degree of work quality, attention to detail, and strong communication skills.
  • Knowledge and experience with external standards: ISO 9000/9001, ISO 13485, 21 CFR, and EU MDR especially pertaining to quality management systems, good manufacturing practices, medical devices, and auditing.
  • Vision requirements for this position: Near Vision Acuity with minimum 20/40 corrected vision (clear vision at 20 inches or fewer), color vision, and the ability to adjust focus.
  • Proficiency with the English language.
  • Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 5-25 pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.

Preferred Qualifications:
  • Experience with computer system validation is preferred.
  • Experience with quality system investigations, root cause analysis. and risk assessment tools preferred.

Excellent Benefits
  • Benefits & Total Rewards | Thermo Fisher Scientific
  • Medical, Dental, & Vision benefits-effective Day 1
  • Paid Time Off & Designated Paid Holidays
  • Retirement Savings Plan
  • Tuition Reimbursement

OTHER
  • Relocation assistance is NOT provided
  • Must be legally authorized to work in the United States now and in the future, without sponsorship.
  • Must be able to pass a comprehensive background check, which includes a drug screening

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