B

Becton Dickinson

Global medical devices, lab equipment supplier

Manufacturing Equipment Engineer

Manufacturing EngineeringConfirmed live in the last 24 hours
Full-timeCanaan, CT, USA$105.5k - $168.8k /yr

About the Job

Requirements

  • A bachelor's degree in Mechanical Engineering, Controls Engineering, or a related field, or relevant equivalent experience.
  • At least 3 years of experience in automation, procurement, assembly, and packaging.
  • Experience leading projects end to end.
  • Willingness and ability to travel domestically and internationally up to 25%.
  • Experience with SolidWorks or other 3D modeling software is preferred.
  • Previous experience with Good Manufacturing Practice (GMP), ISO standards, and Lean Manufacturing concepts is preferred.
  • Experience in an FDA-regulated quality environment is preferred.
  • Technical skills in project management, organization, planning, and capital budgets.
  • Ability to apply problem-solving and data-analysis methods.
  • Risk analysis and Failure Mode and Effects Analysis (FMEA).

Responsibilities

  • Partner with cross-functional teams to ensure equipment, processes, and products are designed, delivered, and operated to high standards of quality, efficiency, safety, and compliance.
  • Ensure products are designed for efficient manufacturing, target cost of goods, and required quality standards.
  • Ensure equipment design and manufacturing comply with regulatory requirements and industry standards.
  • Design equipment that supports efficient manufacturing, is easy to operate and maintain, and consistently achieves production targets.
  • Maximize equipment uptime through reliable, maintainable designs and preventive maintenance practices.
  • Ensure components meet quality and safety standards while remaining cost-effective and readily available.
  • Monitor equipment performance to ensure products consistently meet quality and regulatory requirements.
  • Deliver projects on time, within budget, and aligned with business requirements.
  • Support capital planning, forecasting, budgeting, and reporting activities.
  • Lead the design and development of assembly, packaging, automation, inspection, and manufacturing equipment, including mechanical, electrical, controls, robotics, vision, and software systems.
  • Convert product, process, quality, and capacity requirements into scalable equipment and automation solutions.
  • Create, review, and maintain User Requirement Specifications aligned with manufacturing, quality, regulatory, safety, and business needs.
  • Evaluate design concepts by balancing risk, reliability, scalability, standardization, cost, and lifecycle impact.
  • Develop automation and mechanical system concepts incorporating industry trends and company standards.
  • Create, review, and approve equipment layouts, system architectures, 3D models, and engineering drawings.
  • Perform engineering analyses and simulations to validate and optimize designs.
  • Lead design reviews, risk assessments, machine safety evaluations, and FMEA activities.
  • Establish and verify relationships between Key Process Input Variables and Key Process Output Variables.
  • Support Proof of Concept and Design of Experiments activities to define process capability and operating windows.
  • Optimize equipment for manufacturability, ergonomics, maintainability, reliability, and overall cost of ownership.
  • Use production data to drive equipment designs and continuous improvement initiatives.
  • Provide technical and financial input for capital investment justifications and business cases.
  • Lead equipment suppliers, system integrators, and external vendors throughout the project lifecycle.
  • Partner with Procurement on supplier selection, requests for quotation, technical evaluations, and risk assessments.
  • Define and manage supplier scope, costs, timelines, deliverables, and technical requirements.
  • Review and approve supplier-generated designs, schematics, software architecture, and safety systems.
  • Plan, witness, and approve Factory Acceptance Testing.
  • Drive corrective actions, engineering changes, and supplier performance improvements.
  • Support contract execution, change management, and claims resolution.
  • Build and maintain relationships with equipment manufacturers and technology partners.
  • Lead the integration of new equipment and processes into existing manufacturing operations.
  • Develop installation and integration plans covering site readiness, utilities, logistics, safety, and resource requirements.
  • Support Site Acceptance Testing, commissioning, and handover activities.
  • Execute equipment qualification, process verification, and validation in compliance with quality and regulatory requirements.
  • Ensure validation protocols, reports, and documentation are completed and approved.
  • Manage start-up execution to ensure readiness of equipment, documentation, processes, materials, and personnel.
  • Develop training programs, standard work, and operational procedures before production handoff.
  • Minimize operational disruptions during equipment installation, upgrades, and software implementations.
  • Troubleshoot and resolve equipment, automation, and process issues using structured problem-solving methodologies.
  • Provide technical leadership during production ramp-up to achieve performance, quality, and capacity targets.
  • Lead centerlining activities to stabilize and optimize manufacturing processes.
  • Measure and analyze performance gaps against expected outcomes.
  • Develop and implement corrective actions to improve long-term equipment performance and reliability.
  • Identify and implement opportunities to improve equipment design, validation strategies, and integration methods.
  • Support Lean Manufacturing, process optimization, and continuous improvement initiatives.
  • Ensure complete and accurate documentation for equipment, validation, maintenance, controls, and operating systems.
  • Support creation of operating procedures, troubleshooting guides, maintenance plans, and standard work instructions.
  • Deliver training programs for operators, engineers, maintenance personnel, and quality teams.
  • Execute formal handover to Operations, Maintenance, Engineering, and Quality teams for long-term production support.
  • Ensure equipment, installations, and modifications comply with EHS requirements, machine safety standards, and company policies.
  • Maintain compliance with GMP, ISO, FDA, and Quality System requirements throughout design, validation, and production.
  • Support internal and external audits, regulatory inspections, and compliance reviews.
  • Promote safety, quality, and regulatory compliance across project phases.
  • Provide technical guidance, coaching, and mentorship to engineers and project team members.
  • Lead technical decision-making and collaboration across global, cross-functional teams.
  • Support global standardization initiatives, best-practice sharing, and knowledge transfer across manufacturing sites.

Desired Qualifications

  • Experience with SolidWorks or other 3D modeling software.
  • Previous experience with Good Manufacturing Practice (GMP), ISO standards, and Lean Manufacturing concepts.
  • Experience in an FDA-regulated quality environment.

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

Recently Posted Jobs

Explore more opportunities at Becton Dickinson

See more jobs