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Supplier Quality Engineer

Job in El Paso, El Paso County, Texas, 88568, USA
Listing for: Regulatory Jobs
Full Time position
Listed on 2026-10-09
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 90000 - 125000 USD Yearly USD 90000.00 125000.00 YEAR
Job Description & How to Apply Below

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Job Responsibilities

  • Collaborate with suppliers and business partners to ensure robust materials, products, processes, and systems.

  • Support internal and supplier root cause investigations and CAPA. Drive corrective actions for supplier process by driving suppliers to true root cause analysis and corrective and Preventive actions

  • Manage and escape supplier issues when intervention or a change at a supplier is necessary.
    Plan, execute, report and follow-up on supplier quality system audits

  • Partner with Procurement, R&D,Engineering/Technical Operations, Quality, Operations, and Suppliers in the timely investigation,resolution/prevention of supplier-related issues to minimize/prevent business disruptions.

  • Monitor and analyze supplier performance metrics, identify areas of opportunity, communicate supplier risks, and drive the resolution of supplier quality issues and risk control processes.

  • Implement supplier change management process including change notification, dissemination of information, impact assessment, approval of changes, and supports material/supplier qualifications.

  • Own, drive, and lead the assigned Supplier Quality related projects, activities, initiatives with limited supervision.

  • Utilize Project Management methodologies to plan, organize, connect, shape, lead, and deliver results for SQM projects.

  • Utilize analytical and problem-solving skills to develop and optimize supplier performance working in conjunction with the Worldwide Supplier Quality Management Team.

  • Analyze quality data and identify trends impacting risk benefits requirements of product and quality systems for external suppliers. Lead discussions to drive resolution.

  • Collaborate with operations and franchise operations development on process/product improvement projects.

  • Prepare Supplier Quality Agreements and drives discussion with supplier while consulting Supplier Quality Manager.

  • Develop/execute Quality Risk Management process for supplier-related matters with partnerships of subject-matter experts

  • Lead component qualification change projects in collaboration with key business partners and the supplier’s applicable functional groups.

  • Apply appropriate Quality Engineering and PEx tools (e.g. PM/VSM, Kaizen, DMAIC, FMEA/FTA, RCA, MSA, SPC, Cp/Cpk/Cpm/Ppk, Hypothesis Testing, ANOVA/DOE/EVOP, etc.) to support innovations and continuous improvements

  • Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO
    14001 & OSHAS
    18001).

  • Responsible for communicating business related issues or opportunities to next management level

  • Other duties as assigned

Required Qualifications

  • Bachelor’s degree in Engineering or a related field

  • 5years Supplier Quality and/or Supplier Development

  • Understanding of 21 CFR 820, ISO 13485, and ISO 14971 requirements

  • Prior Supplier Quality experience in a manufacturing plant or technical background

  • Working experience in good manufacturing practice regulated environment is preferred (medical device, pharmaceutical, etc.)

  • Demonstrated knowledge of manufacturing principles and practices, and procedures

  • Direct experience in plant and/or supplier GMP auditing

  • Broad experience with quality systems, including but not limited to validation, non-conformance, CAPA/SCAR systems…

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