We are the people who give possibilities purpose BD is one of the largest integral 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 Description
Function and Responsibilities
- Create and maintain high-quality documentation that covers various aspects of Device Master Records (DMR) for existing and new product introductions.
- Initiate and submit manufacturing documentation to comply BD Reynosa QMS and Division Design Center Quality System.
- Initiate and submit Change Requests (CR) in Master Control or applicable EDMS.
- Supports Engineering activities for Sustaining and New Product Introduction.
- Supports Validation Activities for any new /or existing product/processes.
- Develop product DMR (Assembly drawings, BOMs, Routing, Manufacturing Procedures,
Component/Assembly Item Master & Inspection Procedures, etc.) as require per the project deliverable.
- Initiate change requests (CR) pertaining to the QMS documentation and Project Deliverables.
- Develop, execute and report results of:
- Special Production Orders (SPO) for new and/or existing products.
- Installation Qualification (IQ) for new or existing processes as required by the project owner.
- Supports on developing Operational Qualification (OQ) protocols, execute and report results as required by the project owner.
- Develop and creating new tooling design.
- Provide support on Engineering Study and reporting Lab Book Results.
- Perform other tasks as required.
Requirements
- Bachelor’s degree in Engineering or equivalent preferred, or Highschool diploma plus 3 years of experience in Manufacturing environment.
- 1 year of experience in Manufacturing environment.
- Customer service oriented