Tecomet logo

Quality Engineer I - Warsaw

Tecomet

Warsaw, INFull-time$70–80K/yrTracked 1mo ago

Most applications go out cold — see where you stand first. No sign-up to start.

At a glance

Compensation
$70–80K/yr
Location
Warsaw, IN
Schedule
Full-time
Work Authorization
Not specified

Requirements

Credentials this posting asks for.

ASQ CQE Or CMQ/QE CertificationBachelor's degree

Job overview

Tecomet is hiring a Quality Engineer I - Warsaw. The Quality Engineer I ensures compliance with internal and external customer requirements, focusing on quality engineering. This role operates within Tecomet's principles of continuous improvement, customer-driven innovation, and a win-first culture, while meeting company financial and performance metrics.

Key focus areas include Maintain applicable quality system, environmental, and FDA requirements/certifications, Facilitate operator owned quality program, and Support MRB and RMA processes.

Successful candidates bring Bachelor's Degree In Engineering Or Related Field, 4 Years Experience Within Medical Device Industry, and ASQ CQE Or CMQ/QE Certification. Important skills include QE, Continuous Improvement, Customer Driven Innovation, Win First Culture, Maintaining Quality System, and Facilitate Operator Owned Quality Program. Preferred (not required): Forging, Metalworking, Measuring Devices, and Quality Systems.

Skills & qualifications

RequiredNice to have

Skills

QEContinuous ImprovementCustomer Driven InnovationWin First CultureMaintaining Quality SystemFacilitate Operator Owned Quality ProgramSupporting MRB ProcessesSupporting RMA ProcessesSolve Quality IssuesSolve Cost IssuesSolve Schedule IssuesPrepare FMEA'sPrepare Controls PlansPrepare Quality PlansPrepare PPAPCoordinate Process ValidationsReduce Dependence on InspectionGenerating Quality Metric ReportsCost of QualityManagement by FactsInvestigate Customer ComplaintsCAPADeviationsComplaint ResponsesStandard Manufacturing OperationsFDA RegulationsISO RegulationsGood Manufacturing PracticesGood Documentation PracticesStandard Problem-Solving TechniquesStatistical ConceptsSix Sigma ConceptsWorks With Internal CustomersWorks With External CustomersParticipates in AuditsParticipates in InspectionsForgingMetalworkingMeasuring DevicesQuality SystemsGMPBlueprint ReadingGD&TMetrology8DAlgebraTrigonometryMicrosoft WordMicrosoft Outlook

Qualifications

Bachelor's Degree in Engineering or Related Field4 Years Experience Within Medical Device IndustryASQ CQE or CMQ/QE CertificationISO 13485 ExperienceFDA 820 ExperienceCustomer Interaction Experience

Full job description

#585

Warsaw, IN, USA

Position Type

Full-time

Salaried/Hourly

Salaried

Travel Requirements

5%

Job Description

Quality Engineer I

Position Summary

The Quality Engineer I will interact with team members to ensure compliance and internal and external customer requirements are met, with focus on quality engineering. This will be accomplished within Tecomet’s principles of continuous improvement, customer driven innovation and a win first culture, while meeting company financial and other performance metrics.

Principle Responsibilities

  • Maintaining applicable quality system, environmental, and FDA requirements/certifications.

  • Facilitate operator owned quality program.

  • Supporting the MRB and RMA processes.

  • Work with team members and support manufacturing/operations to solve quality, cost and schedule issues.

  • Prepare FMEA’s, controls plans, quality plans, PPAP.

  • Coordinate process validations and reduce dependence on inspection.

  • Generating applicable quality metric reports; cost of quality, management by facts.

  • Investigate customer complaints including associated actions including CAPA, deviations, and complaint responses.

  • Special projects as assigned by quality management.

  • Must demonstrate a working knowledge of standard manufacturing operations, FDA and ISO regulations.

  • Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) requirements.

  • Standard problem-solving techniques.

  • Applies statistical and Six Sigma concepts and techniques.

  • Works with Internal and External Customers.

  • Participates in audits and inspections.

Qualification Requirements

Credentials/Experience:

  • Bachelor’s Degree in Engineer or related field. Or a minimum of 4 years’ experience within the Medical Device Industry, and Certification (ASQ CQE or CMQ/QE)

Experience/Educational/Training Preferred:

  • ASQ CQE or CMQ/QE preferred

  • 2 years’ experience in quality within medical device manufacturing industry preferred

  • ISO 13485, FDA 820 and customer interaction experience preferred

Knowledge, Skills, and Abilities:

  • Manufacturing operations – forging and/or machining.

  • Measuring devices.

  • Quality Systems.

  • Regulations – FDA, GMP and ISO.

  • Blueprint reading.

  • GD&T.

  • Metrology.

  • Problem solving and 8D.

  • Math skills (algebra, trigonometry) skills.

  • Microsoft office (Word, Excel, Outlook, PowerPoint).

  • Minitab.

Other Requirements

Work Environment

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Physical Requirements

The employee could frequently be required to walk; use hand to finger, handle, or feel; reach with hands and arms and talk or hear. The employee could be required to sit; climb or balance and stoop, kneel, crouch, or crawl. The employee could occasionally lift and or move up to 50 pounds. Specific vision abilities required by the job could include close vision, distance vision, peripheral vision and ability to adjust focus.

Travel Requirements

Up to 10%

Americans with Disabilities Act (ADA): Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

The statements herein are intended to describe the general nature and level of work being performed by employees and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the Company.

Pay Range

$70,000.00 - $80,000.00 / year

Pay Transparency

In order to support the Fair Compensation Strategy by the US Govt., HR Dept., clients are required to adhere to "Pay Transparency Law"; in the impacted states; that have mandated the employers to list the salary ranges in Job advertisements or postings for job opportunities and Job promotions.

You've read the whole posting — now see how you match it.