Staff Quality Engineer

BD • Durham, NC

76d

About The Position

We are the makers of possible 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. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.

Requirements

• Bachelor’s degree in Electrical, Mechanical, or Systems Engineering (or related field)
• 10 years of experience in hardware quality engineering, with a strong focus on compliance and safety certification in regulated environments.
• Experience leading teams through hardware safety certification processes (UL, IEC, ISO, etc.).
• Experience with regulatory and international standards, including EU MDR 2017/745, ISO 9001, ISO 14971, and relevant hardware safety standards.

Nice To Haves

• Experience with lean or six sigma methodologies applied to hardware quality processes.
• Prior success in achieving safety certifications for large-scale automation or central fill systems.
• ASQ Certified Quality Engineer (CQE) or equivalent certification.
• Experience supporting hardware/software integrated systems and working with central fill or automation technologies.

Responsibilities

• Serve as the core team quality lead for hardware design and development projects, including new product introductions and sustaining engineering efforts.
• Oversee all quality aspects of the hardware design control process: quality planning, verification and validation (V&V), risk management, and regulatory compliance.
• Provide expert guidance on compliance engineering standards (e.g., UL, IEC, ISO 60601, ISO 14971, and EU MDR 2017/745) and safety certification requirements for central fill automation.
• Lead the preparation and maintenance of technical files, Design History Files (DHFs), and documentation required for regulatory submissions and audits.
• Collaborate closely with cross-functional teams (R&D, Regulatory, Manufacturing, and Program Management) to ensure hardware deliverables meet internal and external standards.
• Drive root cause analysis and structured problem-solving for hardware failures and nonconformities.
• Mentor and coach team members, fostering a culture of quality, safety, and continuous improvement.
• Actively participate in product risk assessments, hazard analyses, and design reviews.
• Ensure traceability and completeness of all hardware design artifacts and safety documentation.
• Stay current with evolving global safety and compliance standards relevant to central fill pharmacy automation.

What This Job Offers

• Job Type: Full-time
• Education Level: Bachelor's degree