Supplier Quality Engineer

Becton Dickinson; Tempe (AZ); On-site; USD 85,000 - 110,000; Full time

Job summary

Becton, Dickinson, and Company is seeking a Supplier Quality Engineer for a fixed-term assignment in Tempe, AZ. The role focuses on supplier quality program development, audits, and process improvements to ensure regulatory compliance and cost reduction.

You will collaborate with R&D, Sourcing, Manufacturing, and Regulatory teams to define critical-to-quality characteristics, manage CAPAs, and drive continuous improvement across the supplier base.

Qualifications

• Bachelor's degree in Engineering (e.g., Mechanical, Biomedical, Electrical, Industrial) or related technical field.
• Minimum of 3-5 years of experience in supplier quality engineering, quality assurance, or similar role within a regulated industry, preferably medical devices.
• Strong understanding of quality management systems (ISO 13485, 21 CFR Part 820) and regulatory requirements.
• Proficiency in quality tools such as FMEA, SPC, MSA, 8D problem-solving, and root cause analysis.
• Experience conducting supplier audits and assessments.
• Excellent analytical, problem-solving, and decision-making skills.
• ASQ certifications (e.g., CQE, CQA) are a plus.

Responsibilities

• Develop, implement, and maintain supplier quality management systems and procedures to ensure compliance with regulations.
• Conduct supplier audits and assessments evaluating quality systems and processes.
• Lead selection and qualification of new suppliers including technical reviews and process validations.
• Monitor supplier performance metrics and implement CAPA to address issues.
• Collaborate with R&D, Sourcing, Manufacturing, and Regulatory to define critical-to-quality characteristics.
• Manage supplier-related quality issues and disposition of non-conforming materials.
• Drive continuous improvement projects with suppliers to reduce costs and enhance quality.
• Prepare and present reports on supplier quality performance and risks to management.
• Ensure supplier quality documentation is accurate and maintained.

Skills

Quality management

Audits

Root cause analysis

Regulatory compliance

Data analysis

Education

Bachelor's degree in Engineering

Tools

FMEA

SPC

MSA

8D Problem Solving

Job description

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 MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

This is a FIXED-Term assignment from start date to 10/31/27. This position is responsible for data acquisition, task management, and projects associated with the Supplier Quality function. The scope of the position encompasses, but is not limited to, supplier assessments, supplier development and the establishment of effective process controls to improve the quality of the products received, while driving the costs down, for the current supply base, new projects and product transfers activities. This job description is intended as a summary of the primary responsibilities and qualifications for this position. The job description is not intended as inclusive of all duties an individual in this position might be asked to perform or of all qualifications that may be required either now or in the future.

Responsibilities

• Develop, implement, and maintain supplier quality management systems and procedures to ensure compliance with internal and external regulations (e.g., ISO 13485, FDA QSR).
• Conduct supplier audits and assessments to evaluate their quality systems, manufacturing processes, and overall capability to meet BD's specifications and quality requirements.
• Lead and participate in the selection and qualification of new suppliers, including the review of technical specifications, quality plans, and process validations.
• Monitor supplier performance metrics, identify trends, and implement corrective and preventive actions (CAPA) to address quality non-conformances and improve supplier performance.
• Collaborate with R&D, Sourcing, Manufacturing, and Regulatory Affairs teams to define critical-to-quality characteristics for new products and ensure supplier readiness.
• Manage and resolve supplier-related quality issues, including non-conforming material disposition, root cause analysis, and effectiveness verification of corrective actions.
• Drive continuous improvement projects with suppliers to enhance product quality, reduce costs, and optimize supply chain efficiency.
• Prepare and present regular reports on supplier quality performance, risks, and improvement initiatives to management.
• Ensure all supplier quality documentation is accurate, complete, and maintained in accordance with company policies and regulatory requirements.

Job Qualifications

• Bachelor's degree in Engineering (e.g., Mechanical, Biomedical, Electrical, Industrial) or a related technical field.
• Minimum of 3-5 years of experience in supplier quality engineering, quality assurance, or a similar role within a regulated industry, preferably medical devices.
• Strong understanding of quality management systems (e.g., ISO 13485, 21 CFR Part 820) and associated regulatory requirements.
• Proficiency in quality tools and methodologies such as FMEA, SPC, MSA, 8D problem-solving, and root cause analysis.
• Experience conducting supplier audits and assessments.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong communication (written and verbal) and interpersonal skills with the ability to effectively collaborate with internal teams and external suppliers.
• ASQ certifications (e.g., CQE, CQA) are a plus.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.

Required Skills Optional Skills . Primary Work Location USA AZ - Tempe Headquarters Additional Locations Work Shift We are the #MakersofPossible Working together, we make products that patients, families and their healthcare professionals rely on. We do this because we are committed to advancing the world of health™. But it takes the imagination and passion of all of us at BD, from manufacturing to marketing, to look at the impossible and find solutions that turn dreams into possibilities with real-life health benefits for people today, tomorrow and beyond. We make this happen, together. We are the makers of possible.

This is a FIXED TERM assignment until 10/31/27.