Engineering Manager, Integrated Systems, Development

Becton Dickinson Medical Devices•Louisville, KY

2d•Onsite

About The Position

BD’s Urology and Critical Care (UCC) business is seeking a dynamic and experienced engineering leader to lead our Integrated Systems Development team within R&D. This role is pivotal in driving verification testing, launch readiness, and post-launch support for complex electro-mechanical medical devices. The successful candidate will ensure product reliability, performance, and compliance with global regulatory standards. 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. Job Summary BD’s Urology and Critical Care (UCC) business is seeking a dynamic and experienced engineering leader to lead our Integrated Systems Development team within R&D. This role is pivotal in driving verification testing, launch readiness, and post-launch support for complex electro-mechanical medical devices. The successful candidate will ensure product reliability, performance, and compliance with global regulatory standards.

Requirements

Bachelor’s or Master’s degree in Electrical, Mechanical, Biomedical Engineering, or a related technical discipline.
10+ years of engineering development experience, including 5+ years in leadership or management , preferably in the medical device industry.
Proven expertise in designing and integrating complex embedded systems (hardware, software, firmware).
In-depth knowledge of medical device regulatory requirements (FDA 21 CFR Part 820, ISO 13485) and design controls.
Experience with risk management tools (e.g., FMEA) and verification/validation processes.
Exceptional leadership, communication, and interpersonal skills with the ability to inspire and motivate technical teams.
Strong analytical and problem-solving skills with a structured approach to complex challenges.
Ability to manage multiple projects and adapt to shifting priorities in a fast-paced environment.

Responsibilities

Lead and Inspire : Serve as a player-coach, managing and mentoring a growing team of engineers responsible for the downstream lifecycle of medical device systems, from design freeze through commercialization and post-launch sustenance.
Cross-Functional Collaboration : Partner with R&D, Product Management, Quality Assurance, Regulatory Affairs, and Manufacturing to deliver seamless product launches and lifecycle support.
Ensure Compliance and Quality : Establish and maintain robust engineering processes, best practices, and documentation aligned with medical device regulations (e.g., ISO 13485, FDA QSR).
Technical Leadership : Conduct design reviews, risk assessments, and verification/validation activities to guarantee system integrity and performance.
Team Development : Foster a culture of innovation, continuous improvement, and technical excellence through coaching and mentorship.
Project Ownership : Oversee schedules, budgets, and resources to ensure timely delivery of high-quality products.
Lifecycle Management : Define and implement sustenance strategies for multiple platform products in collaboration with Reliability, Service & Repair, and Quality Assurance teams.
Innovation : Identify and integrate new technologies and methodologies to enhance testing efficiency and automation across multiple sites.
Subject Matter Expertise : Act as a technical authority for multiple UCC products.

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