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Supplier Quality Engineer

Job in Athens, Henderson County, Texas, 75751, USA
Listing for: Biomerics
Full Time position
Listed on 2025-12-02
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering
Job Description & How to Apply Below

Company Overview

Biomerics is a world-class manufacturer and innovative polymer solutions provider for the medical device and biotech industries. As a vertically integrated company, we specialize in designing, developing, and producing medical devices for diagnostic and interventional procedures. We are focused on next-generation solutions for vascular access, electrophysiology, cardiac rhythm management, neurovascular, structural heart and cardiovascular markets.

Job Description

At Biomerics, we are dedicated to our diverse employee base. We understand that a strong, skilled, and engaged workforce is the foundation of our continued success as a business. We strive to live up to the Biomerics values in all our interactions. It is an exciting time to be part of our collective team, and there is no limit to the impact that can be achieved here  improve and advance the lives of our employees and patients who depend on our products.

At Biomerics, we believe in integrity, partnership, empowerment and accountability, trust, agility, teamwork, and excellence, and we care. Our team-oriented, customer-focused corporate culture prioritizes building strategic, mutually beneficial partnerships with customers and our team members.

A Supplier Quality Engineer is responsible for ensuring the quality of products received from external suppliers by conducting thorough audits, identifying and resolving quality issues, working closely with procurement and engineering teams to implement corrective actions, and maintaining strong relationships with suppliers to continuously improve product quality and compliance with company standards. You will serve as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional, and corporate quality goals and priorities.

You may support new product development (NPD) as needed. As the Supplier Quality Engineer, you will lead Quality Assurance (QA) in support of manufacturing activities in accordance with the requirements of USFDA CFR 820, ISO 13485, and MHLW Ministerial Ordinance 169.

Job Responsibilities
  • Supplier evaluation and selection:
    Assess potential suppliers through audits and reviews to ensure they meet quality requirements and capabilities.
  • Quality system oversight:
    Monitor supplier quality management systems to verify compliance with company standards and industry regulations.
  • Supplier audits:
    Conduct on-site audits at supplier facilities to evaluate manufacturing processes, quality control procedures, and documentation.
  • Quality issue identification and resolution:
    Analyze incoming materials and products to detect defects, perform root cause analysis, and work with suppliers to implement corrective actions.
  • Process improvement:
    Collaborate with suppliers to identify opportunities for process improvements and implement solutions to enhance product quality.
  • Technical support:
    Provide technical expertise to suppliers regarding product specifications, quality standards, and testing methods.
  • Advise and support Quality Inspectors on day-to-day issues with incoming materials.
  • Documentation and reporting:
    Maintain detailed records of supplier performance, quality issues, corrective actions, and audit findings. Create, issue, and complete Supplier Corrective Action requests.
  • New product introduction support:
    Work with the engineering team to ensure new suppliers and components meet quality requirements during product development.
  • Supplier performance monitoring:
    Track key performance indicators (KPIs) to evaluate supplier quality and identify areas for improvement.
Requirements Education / Certifications
  • High School Diploma or GED required
  • ASQ / CQE certifications
  • Six Sigma Certified Green or Black Belt
Job Requirements
  • Strong understanding of quality management systems (QMS) and industry standards.
  • Working knowledge of FDA QSR (21 CFR Part 820), ISO 13485, MDD/AIMDD, CMDR, JPAL medical device regulations;
    Ability to understand other medical device regulations and standards.
  • Experience with statistical analysis tools (e.g., SPC) to identify trends and root causes.
  • Excellent communication and interpersonal…
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