GIE - EDE Engineer 3

We are the people who give possibilities purposeBD 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. Job DescriptionResponsibilities:Product Design Team: to ensure product is designed to enable a mfg. process which can produce product efficiently (target COGS) and to required quality standards.Unit Quality Team: to ensure that equip. is designed/manufactured in compliance with regulatory requirements/industry standards.Production Team: to ensure that equipment is designed for efficient production, and to support mfg. process. To ensure that the integrated equipment / processes are easy to operate, maintain, reliable and that equipment is operating efficiently / effectively from handover / hyper care to meet production targets.Maintenance/Engineering Team: to ensure max. equip. uptime, and that equip. is designed for easy maintenance/repair. To ensure that equipment is maintained and serviced according to recommended schedules and procedures.Procurement & Vendors: to ensure that components meet standards/safety and can be sourced timely/cost-effective.Plant Quality Team: to ensure that equip. is operating within specified tolerances and products meet required quality & regulatory standards.Program Management Team: to ensure that project meets specified requirements that equipment is delivered on time within budget.Finance team: Support CapEx planning, forecasting, and reporting.1. Process & Equipment Design and DevelopmentLead the design and development of assembly, packaging, automation, inspection, and manufacturing equipment, including mechanical, electrical, controls, vision, robotics, and software elements.Translate product, process, quality, and capacity requirements into robust equipment and automation concepts.Define, create, review, and maintain User Requirement Specifications (URS) aligned with manufacturing, quality, regulatory, safety, and business needs.Develop and evaluate multiple technical solutions and concepts, considering risk, robustness, scalability, standardization, cost, and lifecycle impact.Develop innovative concepts for mechanical systems and automation based on project requirements, industry trends, and BD standards.Create, review, or approve 3D models, 2D drawings, layouts, and system architectures generated internally or by suppliers.Perform or review engineering analyses and simulations (e.g., stress, strain, thermal, airflow, cycle time) to validate and optimize designs.Lead and participate in design reviews, risk assessments, machine safety reviews, and FMEA activities to ensure compliance, safety, reliability, and performance.Verify relationships between Key Process Input Variables (KPIVs) and Key Process Output Variables (KPOVs).Support Proof of Concept (POC) activities and Design of Experiments (DOE) to establish process windows, baselines, and capability metrics.Optimize equipment designs to improve manufacturability, operability, ergonomics, maintainability, changeover time, reliability, and total cost of ownership.Capture, analyze, and leverage process and equipment performance data from existing production lines to inform new designs and improvements.Provide detailed technical and cost input for capital justification activities (e.g., CB-2), including equipment cost, engineering effort, validation scope, risk, and implementation timeline.2. Supplier & Capital Project LeadershipLead and coordinate external suppliers, system integrators, and equipment vendors throughout the full project lifecycle.Support and lead vendor selection in partnership with Procurement, including RFQs, technical evaluations, supplier capability and risk assessments.Define and manage supplier technical scope, cost, lead time, risks, deliverables, and interfaces.Review and approve supplier designs, specifications, software architecture, electrical and mechanical schematics, and safety concepts.Plan, witness, and approve Factory Acceptance Tests (FAT), including definition of test plans, acceptance criteria, deviation management, and re-tests.Manage supplier corrective actions, technical changes, and continuous improvement actions.Support contract execution, change control, and claims management in collaboration with Procurement and Legal.Establish and maintain strong technical relationships with key equipment manufacturers and technology partners.3. Equipment Integration, Installation, Validation & Start-UpDrive the end-to-end integration of new equipment and processes into existing manufacturing environments.Prepare and execute detailed equipment installation and integration plans, including site readiness, utilities, layout, logistics, EHS compliance, and resource planning.Coordinate and support Site Acceptance Tests (SAT), commissioning, and handover readiness.Execute and/or support equipment qualification, process verification, and process validation in alignment with Quality and Regulatory requirements.Ensure validation strategies, protocols, and reports are completed, reviewed, and approved.Manage and execute vertical start-up activities, ensuring equipment, process, documentation, materials, and people readiness.Ensure training plans, operating instructions, standard work, and competence assessments are completed prior to formal handover.Ensure minimal disruption to ongoing operations during installation, integration, or software changes.Lead or support troubleshooting, diagnosis, and resolution of equipment, automation, process, or integration issues using structured problem-solving and root cause analysis methodologies.4. Ramp-Up, Performance Management & Continuous ImprovementProvide sustained technical support during production ramp-up to achieve OEE, yield, throughput, scrap, reliability, and capacity targets.Perform and support center lining activities to stabilize and optimize equipment and process performance.Measure, analyze, and track gaps between expected and actual performance during ramp-up and early production.Lead and support corrective actions and recovery plans to close performance gaps and ensure long-term capability.Identify, consolidate, and implement improvement opportunities related to equipment design, integration approach, validation strategy, tools, and methodologies.Support and lead Continuous Improvement (CI) initiatives, including Lean Manufacturing, data-driven optimization, and standardization efforts.5. Documentation, Training & HandoverEnsure creation, completion, review, and formal handover of comprehensive equipment documentation, including URS, specifications, architecture diagrams, FAT/SAT reports, validation documentation, maintenance plans, control plans, spare parts lists, and software backups.Support the documentation of equipment operating instructions, process parameters, standard work, troubleshooting guides, and maintenance procedures.Support and deliver training to site personnel on new equipment, automation systems, and manufacturing processes.Coordinate and execute formal handover to Operations, Maintenance, Engineering, and Quality teams to ensure sustainable steady-state production.6. Compliance, Safety & QualityEnsure all equipment, installations, and modifications comply with EHS requirements, international standards, and BD policies, including machine safety, LOTO, guarding, controls, and ergonomics.Ensure compliance with GMP, ISO, FDA, and BD Quality System requirements throughout design, integration, validation, ramp-up, and sustained production phases.Support internal and external audits, inspections, and regulatory interactions related to equipment and process changes.Promote and demonstrate a strong safety, quality, and compliance culture across all project phases.7. Leadership, Mentoring & CollaborationProvide technical guidance, coaching, and informal mentoring to engineers and cross-functional project team members.Lead technical discussions and decision-making across global, cross-functional teams.Support global standardization, harmonization, and knowledge sharing across GIE and BD manufacturing sites.Required Qualifications:Bachelor’s Degree in Mechanical Engineering, Controls Engineering or related field, or relevant equivalent experience.3+ years in automation / procurement and assembly and packaging experienceExperience leading projects end to end.Willingness and ability to travel domestically and internationally up to 25%.Preferred Qualifications:Experience in SolidWorks or other 3d modeling softwarePrevious experience with Good Manufacturing Practice (GMP), ISO standards and Lean Manufacturing concepts.Experience in an FDA regulated quality environmentKnowledge and Skills:Excellent technical skills including project management, organization, planning, and capital budgets.Demonstrated ability to apply problem solving and data analysis methods.Strong communication skillsRisk analysis / FMEAAt BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.Why Join Us?To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success. To learn more about BD visit.Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.Required SkillsOptional Skills.Primary Work LocationUSA CT - CanaanAdditional LocationsWork ShiftSummaryLocation: USA CT - CanaanType: Full time