Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Quality Engineer I

Job

Tecomet

Warsaw, IN (In Person)

Full-Time

Posted 5 days ago (Updated 10 hours ago) • Actively hiring

Expires 7/4/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
68
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

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. #QA2
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. Equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities Americans with Disabilities Americans with Disabilities Act (ADA): Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 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.