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Becton Dickinson

Global medical devices, lab equipment supplier

Associate Principal R&D Engineer

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeCovington, GA, USANo salary listed

About the Job

Requirements

  • A BS or MS in Mechanical Engineering, Electrical Engineering, Systems Engineering, Biomedical Engineering, or a related technical discipline is required.
  • At least 10 years of experience in electromechanical medical devices, portable pump systems, fluid management systems, regulated product development, or platform-based product development with reuse across releases is required.
  • Demonstrated success leading cross-functional technical strategy, beyond subsystem design or program execution, is required.
  • A strong background in systems thinking, platform architecture, trade studies, risk management, design controls, verification strategy, reliability engineering, and supplier and technology evaluation is required.
  • Ability to influence without direct authority across systems, mechanical, electrical, software, quality, regulatory, marketing, operations, human factors, service, supply chain, and program teams is required.

Responsibilities

  • Own the UCC pump and fluid platform capability roadmap across pump and fluid evacuation, battery, power and charging, patient, device and canister interfaces, liquid level detection, leak and fault detection, odor mitigation, acoustic performance, reliability, serviceability, and platform test methods.
  • Define crawl, walk, and run maturity steps for each pump and fluid platform domain and align them to product release trains across the urine evacuation portfolio.
  • Integrate inputs from voice of customer, complaints, service data, usability findings, manufacturing yield, reliability trends, cost targets, supplier constraints, component obsolescence, regulatory needs, and technological advancements into the roadmap.
  • Lead periodic pump and fluid platform strategy reviews and publish the roadmap with deliverables, decision points, investment needs, and success metrics.
  • Establish system-level architecture principles, modularity strategy, interface expectations, performance guardrails, and reuse models so improvements can be leveraged across multiple products.
  • Serve as the Pump and Fluid Platform technical authority for technology-impacting changes, including participation in change control board meetings, architecture reviews, and pre-product governance reviews technical assessments.
  • Create and maintain reference architectures, design decision records, platform standards, preferred technologies, supplier strategy recommendations, reusable design patterns, and test method expectations.
  • Provide go/no-go guidance on major platform architecture choices, including pump mechanism strategy, motor and control architecture, fluid path design, battery and power approach, charging strategy, connection interfaces, sensing architecture, and acoustic and odor mitigation approaches.
  • Establish expectations for pump and fluid evacuation performance, including vacuum, pressure, and flow targets; canister and tubing compatibility; filtration considerations; dry and wet operating conditions; and consumable interface requirements.
  • Define power and charging architecture principles that support runtime, charge time, battery life, safety, reliability, serviceability, regulatory expectations, and user experience across product releases.
  • Guide sensing and detection architecture, including liquid level detection, occlusion detection, leak and fault detection, robustness in wet and dirty environments, alarm behavior, and nuisance alarm reduction.
  • Establish odor mitigation and acoustic performance principles, including design guardrails, measurement methods, capability targets, and release-over-release improvement scorecards.
  • Partner with manufacturing, supplier quality, operations, and supply chain to align platform choices with manufacturability, scalability, yield, cost, reliability, component availability, and supply continuity.
  • Influence verification, validation, and reliability strategy, including representative use conditions, accelerated life testing, environmental stress considerations, cleaning and service assumptions, and release readiness criteria.
  • Drive platform-level decisions that improve performance, robustness, serviceability, maintainability, user experience, sustaining efficiency, and long-term platform evolution.
  • Translate the pump and fluid platform roadmap for product design teams and ensure clear ownership by systems, mechanical, electrical, software, verification, operations, service, supplier, and program teams.
  • Partner with product development leaders, clinical technology leaders, technical leads, marketing, innovation, quality, regulatory, human factors, operations, service, and supply chain to bring technical solutions to governance forums and product programs.
  • Support risk posture, verification approach, design control expectations, human factors considerations, manufacturing readiness, and regulatory submission readiness.
  • Promote reuse by ensuring teams adopt platform modules, interface standards, reference architectures, test methods, supplier strategies, and common design patterns unless a program-specific exception is justified and documented.
  • Use field data, complaints, service returns, user feedback, manufacturing trends, supplier performance, and reliability data to prioritize platform improvements.

Desired Qualifications

  • Experience with portable pumps and fluid management, battery-powered consumer or clinical devices, vacuum, pressure, and flow systems, sensors in wet and dirty environments, acoustics and odor control, and consumables ecosystems is preferred.
  • Experience with pump mechanism selection, motor and control strategy, power management, battery and charging systems, liquid level sensing, occlusion detection, leak detection, fault detection, alarm behavior, and nuisance alarm reduction is preferred.
  • Experience with FDA-regulated medical devices, design controls, risk management, verification and validation, usability and human factors, complaint trending, sustaining engineering, and regulated product release processes is preferred.
  • Experience establishing platform governance, architecture review boards, capability scorecards, reusable modules, interface standards, reference architectures, and technology roadmaps across multiple product releases is preferred.
  • Experience with manufacturing scale-up, supplier strategy, component technology evaluation, reliability engineering, serviceability, cost reduction, and lifecycle management for electromechanical platforms is preferred.

About the Company

Becton Dickinson

Global medical devices, lab equipment supplier

BD (Becton, Dickinson and Company) is a global medical technology company that designs, manufactures, and sells medical devices, laboratory equipment, and related services for hospitals, labs, clinicians, and biopharma partners. It operates in four segments: Medical Essentials (medication delivery and specimen management devices), Connected Care (medication management and advanced patient monitoring systems), BioPharma Systems (drug delivery systems for pharmaceutical partners), and Interventional (surgical, endovascular, urological, and critical care products). In addition to devices, BD offers connected software, analytics, clinical education, customer portals, and service programs to support its products. The company’s goal is to help healthcare providers improve patient outcomes by enabling safer and more efficient delivery of care through integrated devices, data, and services across the health ecosystem.

Company size
10,001+
Company stage
IPO
Headquarters
Franklin Lakes, NJ
Founded
1961

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