Conmed
Healthcare & Life SciencesDirect Workday career site

Supplier Quality Engineer I

Pay
$69,900 – $108,300 per year
Location
Utica, NY · On-site
Job type
Full-time
Level
Entry level
Education
Bachelor's degree
Listed
30 days ago

Skills & highlights for this role

  • ASQ CQE
  • FDA 21 CFR Part 820
  • ISO 13485
  • CAPA
  • root cause analysis

Also useful

  • SPC
  • IQ/OQ/PQ validation
  • ISO 14971

About the role

The Supplier Quality Engineer I is responsible for ensuring that suppliers and externally provided processes, products, and services meet applicable regulatory requirements and company quality standards. This role supports supplier qualification, monitoring, and improvement activities to ensure compliance with FDA regulations, ISO 13485, and other applicable medical device standards.

Pay and benefits

Supplier Qualification & Management * Support supplier selection, evaluation, and qualification activities (e.g., audits, capability assessments). * Assist in onboarding new suppliers, including quality agreements and documentation review. * Maintain Approved Supplier List (ASL) and related supplier records. * Monitor supplier performance using metrics (defects, on-time delivery, responsiveness).

Supplier Quality Assurance * Review and approve supplier-related documentation including: First Article Inspection (FAI) PPAP (Production Part Approval Process), if applicable Certificates of Conformance (CoC) and material certifications * Ensure suppliers comply with regulatory requirements (FDA 21 CFR Part 820, ISO 13485, ISO 14971 as applicable).

Incoming Quality & Nonconformance Management * Support incoming inspection processes and sampling plans. * Investigate supplier-related nonconformances and defects. * Initiate and manage Supplier Corrective Action Requests (SCARs). * Verify effectiveness of corrective and preventive actions (CAPA support).

Auditing & Compliance * Participate in supplier audits (on-site, remote, or desk audits). * Ensure suppliers adhere to Good Manufacturing Practices (GMP) and internal procedures. * Support internal and external audits (FDA, notified bodies, customers). Risk Management * Contribute to supplier risk assessments (criticality, risk ranking). * Support risk mitigation strategies for high-risk suppliers or materials.

Continuous Improvement * Drive supplier quality improvement initiatives. * Analyze trend data and identify opportunities for defect reduction and process improvements. Cross-Functional Collaboration * Work closely with Purchasing, R&D, Manufacturing, and Regulatory teams. * Support product transfers, validations, and design changes involving suppliers.

Qualifications * Bachelor's degree in Engineering or related scientific/technical discipline * 0-3 years of experience in supplier quality, quality engineering, or manufacturing engineering in a regulated industry (medical device preferred) Required Skills & Knowledge Strong working knowledge of: FDA 21 CFR Part 820 ISO 13485 quality systems Risk management (ISO 14971) Expertise in root cause analysis and structured problem-solving methodologies Experience with CAPA systems and regulatory compliance expectations Hands-on experience with supplier audits and performance management Knowledge of validation methodologies (IQ/OQ/PQ) and statistical tools (SPC preferred) Ability to interpret engineering drawings, specifications, and technical documentation Strong analytical, communication, and decision-making skills Preferred Qualifications ASQ Certified Quality Engineer (CQE) or equivalent certification Lead Auditor certification (ISO 13485) This position is not open to employer based sponsorship.

Travel 0-20% Disclosure as required by applicable law, the annual salary range for this position is $69,900 to $108,300. The actual compensation may vary based on geographic location, work experience, education, and skill level. The salary range is CONMED's good faith belief at the time of this posting. This job posting is anticipated to close on November 7, 2026.

We may, however, extend this time period, in which case the posting will remain available on careers.conmed.com. Please submit your application as soon as possible as we will be reviewing applications on a rolling basis as we receive them.

Benefits

CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information.

Competitive compensation Excellent healthcare including medical, dental, vision and prescription coverage Short & long term disability plus life insurance -- cost paid fully by CONMED Retirement Savings Plan (401K) -- CONMED matches your contributions dollar for dollar, with the potential for up to 7% per pay period Employee Stock Purchase Plan -- allows stock purchases at discounted price Tuition assistance for undergraduate and graduate level courses Know someone at CONMED?

Have them submit you as a referral before applying for this position to be eligible for our Employee Referral Program incentives! The Know Your Rights: Workplace Discrimination is Illegal Poster reaffirms this commitment. Colorado Residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation.

You will not be penalized for redacting or removing this information.

Read the original posting

From Conmed's careers page, first listed on Rolev.ai on October 11, 2026. Rolev.ai is not the employer.

How Rolev.ai helps with this application

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Common questions

What is the salary for the Supplier Quality Engineer I role at Conmed?

The Supplier Quality Engineer I posting at Conmed states compensation of $69,900 – $108,300 per year. It is listed as a full-time position. Final pay may depend on location, experience, and interview evaluation on Conmed's official career site.

Where is the Supplier Quality Engineer I job at Conmed located?

This Supplier Quality Engineer I position at Conmed is located in Utica, NY (On-site). Always check Conmed's application page for specific state eligibility or relocation policies.

What qualifications are required for Supplier Quality Engineer I at Conmed?

For the Supplier Quality Engineer I role, Conmed highlights a bachelor's degree; experience with FDA 21 CFR Part 820, ISO 13485, CAPA, root cause analysis. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.

How do I apply for the Supplier Quality Engineer I position at Conmed?

This listing links directly to Conmed's Workday application page. You can apply directly on Conmed's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.