Sr Design Assurance Engineer (Software Medical Devices)

Lead quality and compliance activities for the development of innovative medical devices with embedded and standalone software. Serve as a subject matter expert in Design Controls, Risk Management, Human Factors, Software Lifecycle Processes, and Cybersecurity, ensuring products meet regulatory, quality, and customer requirements from concept through commercialization., * Provide Quality Engineering support for new product development, design changes, and OEM projects.

• Lead Design Control, Verification & Validation, and Risk Management activities.
• Develop and review quality plans, validation plans, design documentation, traceability matrices, and risk assessments.
• Ensure compliance with IEC 62304, IEC 60601, IEC 62366, ISO 14971, FDA, and ISO 13485 requirements.
• Analyze quality metrics, identify trends, and drive continuous improvement initiatives.
• Lead root cause investigations, CAPA activities, and problem-solving efforts.
• Partner with R&D, Regulatory Affairs, Manufacturing, and external stakeholders to achieve project and quality objectives.
• Present quality and compliance updates to leadership and project teams.

• Bachelor’s degree in Engineering or related technical discipline.
• 6+ years related experience required.
• Experience with Design Controls, Verification & Validation, and Risk Management within a regulated industry.
• Strong knowledge of medical device software and quality regulations.
• Proven experience with root cause analysis, CAPA, and continuous improvement methodologies.
• Excellent communication, collaboration, and leadership skills.

Preferred Skills

• Expertise in medical device software development and cybersecurity.
• Hands-on experience with IEC 62304, IEC 60601, IEC 62366, and ISO 14971.
• ASQ CQE, CSQE, or other relevant quality certifications.
• Experience supporting global product development teams and regulatory submissions.
• Strong project leadership and cross-functional influencing skills.

• Collaborative, cross-functional environment working with Quality, R&D, Manufacturing, and Regulatory teams.
• Primarily office-based with occasional time spent in laboratory and manufacturing settings.
• Opportunity to influence product quality, patient safety, and innovation in healthcare. Salary Range: $92,215 - $115,300

B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap® and CAPS®., Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise® philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit [click to reveal website link]www.bbraunusa.com, B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at [click to reveal website link]www.bbraunusa.com.

Through its “Sharing Expertise®” initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.