Industry

Post market quality engineer

POST MARKET QUALITY ENGINEER.

warsaw, indiana

Posted 1 day ago

Closes 9/30/2026 Job details Summary Spherion

$90,000 - $95,000 per year

Permanent

8:00 AM - 5:00 PM

Industry

industry (Production Occupations)

Reference number

S_180390 We are seeking a Post Market Quality Engineer to manage medical device complaint investigations.

This role ensures timely failure investigations, root cause analyses, and risk assessments for product field failures while maintaining compliance with medical device regulations. What's in it for You? Competitive salary and comprehensive benefits package Opportunity to work in a collaborative, innovative environment Professional growth and skill development in medical device quality systems

Responsibilities:

Investigate device field complaints with cross-functional teams and perform failure analysis using test equipment and software. Conduct root cause analyses, complete post-market risk assessments, and maintain complaint documentation. Review internal and external records (e.g., device history records, inspection reports) for compliance. Maintain and update investigation Job Aids, Work Instructions, and risk management documentation. Support quality leadership and interface with external auditors as needed.

Working hours:

8:00 AM - 5:00

PM Skills:

5+ years of Medical Device Quality experience. ...

ISO 13485

Audit Certification. ASQ Certification.

Education:

High School Experience:

1-4 years

Qualifications:

Bachelor?s degree in an Engineering discipline (or equivalent quality role experience). Strong working knowledge of medical device regulations and standards (e.g., 21 CFR 820, ISO 13485, ISO 14971). Proficiency with GD&T, statistical process control (SPC), non-destructive testing, and measuring methods. Excellent written/verbal communication skills and analytical problem-solving abilities. Proficiency in Microsoft Office (Excel, Word, Outlook, PowerPoint).Valid driver's license. Send your resume to emmaemmert@spherion.com for immediate consideration! #PROFDIV Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.

Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). Show more

key responsibilities Investigate device field complaints with cross-functional teams and perform failure analysis using test equipment and software. Conduct root cause analyses, complete post-market risk assessments, and maintain complaint documentation. Review internal and external records (e.g., device history records, inspection reports) for compliance. Maintain and update investigation Job Aids, Work Instructions, and risk management documentation. Support quality leadership and interface with external auditors as needed. experience 1-4 years skills 5+ years of Medical Device Quality experience.

ISO 13485

Audit Certification. ASQ Certification. qualifications Bachelor?s degree in an Engineering discipline (or equivalent quality role experience).Strong working knowledge of medical device regulations and standards (e.g., 21 CFR 820, ISO 13485, ISO 14971). Proficiency with GD&T, statistical process control (SPC), non-destructive testing, and measuring methods. Excellent written/verbal communication skills and analytical problem-solving abilities. Proficiency in Microsoft Office (Excel, Word, Outlook, PowerPoint).Valid driver's license. education High School share this job.

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Get in touch. We are here to help you with your questions. EA

Ewing, Ashly

ashlyewing@spherion.com