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Staff Engineer - R&D

Job in Franklin Lakes, Bergen County, New Jersey, 07417, USA
Listing for: BD (Tissuemed Ltd)
Full Time position
Listed on 2025-11-10
Job specializations:
  • Engineering
    Biomedical Engineer, Manufacturing Engineer, Mechanical Engineer, Product Engineer
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below

Job Description

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 Med Tech 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.

BD has a presence in virtually every country and partners with organizations around the world to address some of the most complicated global health issues. By working in close collaboration with customers, BD can help enhance outcomes, lower costs, increase efficiencies, improve safety and expand access to health care.

Overview

We are seeking a Staff Engineer to join the R&D team within the Medication Delivery and Vascular Care Solutions (MDVC) business. The ideal candidate will demonstrate an ability to lead and teach others to assess project/program needs, formulate strategies, build support, and complete initiatives. The incumbent will display strong interpersonal and decision‑making skills and the ability to effectively manage change and ambiguity.

The ability to engage and mentor team members and to enhance diverse perspectives to achieve the best outcomes will be necessary for success.

In this exciting role, you will impact health care by driving the commercialization of products central to global healthcare that are focused on the insertion, stabilization, maintenance, and removal of Peripheral and Central IV catheters. You will apply your expertise and experience to scope, plan, and complete projects to advance the Vascular Care Solutions portfolio. As part of an integrated cross‑functional team, you will own the R&D strategy and execution of the design control deliverables inclusive of VOC, user needs, requirements, product design, risk management, design verification, design validation, human factors, and design transfer.

Responsibilities
  • Plan through all project phases with a focus on the strategy and execution of the comprehensive design control deliverables.
  • Write, edit, and communicate technical strategies, protocols, reports, work instructions, design reviews, etc.
  • Expertly apply engineering principles for design development/analysis, including use of digital engineering tools (e.g., FEA).
  • Complete statistical analysis and sample plan development.
  • Demonstrate accountability for the successful and timely achievement of goals.
  • Drive innovation and process efficiency through a growth mindset focused on continuous improvement.
Minimum Qualifications
  • Minimum 10 years of experience in medical device or other similarly regulated industry.
  • Expertise with design verification & validation strategy development and execution on medical devices (or similarly regulated products).
  • Must have a demonstrated track record of technical problem solving and effective product development through expert application of engineering principles.
  • Design controls expertise including, but not limited to, new product launches, post‑launch changes, and the governing regulations (globally).
  • Proficiency in solid mechanics/mechanics of materials and good knowledge of statistical methods/tools.
Preferred Qualifications
  • Master's Degree in Mechanical or Biomedical Engineering and 7+ years of experience
  • PhD in Mechanical or Biomedical Engineering and 5+ years of experience.
  • Experience in solid modeling (Solid Works or similar) and finite element analysis/mechanics tools (FEA)
  • Experience in high‑volume manufacturing processes (inclusive of injection molding and high‑speed assembly)
  • Experience in the development of drug delivery devices and/or combination products.
  • Exposure to Chemistry and Chemical / Materials Engineering.
  • DFSS (Design for Six Sigma) training or certifications.
Location

Primary

Work Location:

USA, NJ - Franklin Lakes

Seniority Level

Mid‑Senior…

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