Production Specialist

Becton Dickinson Medical Devices•San Antonio, TX
•Onsite

About The Position

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 MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Requirements

  • High School Diploma or GED

Responsibilities

  • Perform medical-device assembly, processing, inspection, testing, packaging, and/or labeling according to approved procedures and work instructions.
  • Work within an ISO-classified cleanroom while following gowning, hygiene, material-handling, and contamination-control requirements.
  • Follow applicable GMP requirements, company procedures, and the Quality Management System, including requirements established under 21 CFR Part 820 / FDA Quality Management System Regulation (QMSR) and ISO 13485 , as applicable.
  • Complete Device History Records (DHRs), travelers, batch records, inspection records, and other controlled documentation accurately and contemporaneously.
  • Verify materials, components, equipment, tooling, and documentation before beginning manufacturing operations.
  • Perform in-process inspections and measurements using approved inspection equipment and acceptance criteria.
  • Identify and promptly report nonconforming materials, products, equipment conditions, documentation discrepancies, or process deviations.
  • Maintain traceability and proper identification and segregation of materials and products throughout the manufacturing process.
  • Operate production equipment and tooling according to approved procedures and applicable safety requirements.
  • Maintain clean and organized work areas in accordance with cleanroom and 5S requirements.
  • Participate in line clearance, cleaning, environmental-control, and changeover activities as required.
  • Assist with troubleshooting manufacturing issues and communicate observations that may affect product quality or production efficiency.
  • Support process improvements, validation activities, engineering builds, training, and implementation of new or revised manufacturing processes as assigned.
  • Demonstrate proficiency in assigned manufacturing processes and, when qualified, assist with training other production personnel.
  • Meet established production and quality expectations without compromising product quality, documentation integrity, or regulatory compliance.
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