EDI Engineer

Job Description Summary

We are the people who give possibilities purpose 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.

This position supports Automation and Equipment Design and Process Implementation across the MDS business. The Engineer 1 role builds foundational technical knowledge and execution experience while contributing to business, quality, safety, and regulatory objectives.

• Design and development of assembly, packaging, automation, inspection, and manufacturing equipment including mechanical, electrical, and control elements.
• Preparation, maintenance, and execution of User Requirement Specifications (URS).
• Evaluation of technical concepts considering risk, scalability, validation impact, cost, and lifecycle.
• Participation in design reviews, machine safety reviews, risk assessments, and FMEA activities.
• Support Proof of Concept (POC) evaluations and Design of Experiments (DOE).
• Verification of relationships between Key Process Input Variables (KPIVs) and Key Process Output Variables (KPOVs).
• Improvement of equipment operability, ergonomics, maintainability, reliability, and cost of ownership.
• Problem‑solving and troubleshooting of equipment systems, materials, or process issues using scientific approaches.
• Support supplier coordination, RFQs, technical evaluations, and supplier capability reviews.
• Review of supplier designs, specifications, and safety concepts.
• Participation in Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT) and tracking of deviations, corrective actions, and issue resolution.
• Execution of equipment installation plans, qualification, process verification, and validation activities.
• Support of vertical start‑up and production ramp‑up, minimizing disruption to ongoing operations.
• Continuous improvement and Lean Manufacturing initiatives.
• Documentation creation, handover, operating instructions, and training of site personnel.
• Compliance with EHS, machine safety, ISO, FDA, GMP, and BD Quality System requirements.

Minimum Education:

Bachelor’s Degree in Mechanical Engineering, Controls Engineering or related field, or relevant equivalent experience.

Minimum Experience:

1year of progressively responsible engineering and project management experience. Desired experience includes integration of equipment within complex manufacturing sites with focus on validation and vertical start‑up.

Familiarity with Solid Works or other 3D modeling software is desired. Strong organization, planning, and capital budgeting skills are required.

Ability to use a laptop/computer for extended periods of time (up to 8hours). Ability to sit for long periods of time (up to 8hours) in virtual and/or on‑site meetings. Ability to stand for long periods of time (up to 8hours) during FAT, SAT, and on‑site equipment/process troubleshooting. Ability to climb steps, squat, etc. Ability to work independently in high volume manufacturing floor.

Follow Safety and Quality/GMP requirements for medical device manufacturing site (e.g., safety shoes, safety glasses, hair net, beard net, face mask, hard hat, etc. as required).

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.