Sr. Supplier Quality Engineer

Job Description Summary
Develop, implement, and manage the components and materials Supplier Management Program.
Establish an effective communication and interaction, with suppliers focused on solving quality issues.
Participate on the identification, selection, evaluation, approval and certification of supplier components and materials.
Coordinate the Materials Review Board (MRB).
Participate in the problem solving of raw material components with the plant manufacturing areas.
Work development on Lean Manufacturing environment. Job Description

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For more than 125 years, we’ve pursued our Purpose of advancing the world of health™. We relentlessly commit to a promising future by developing innovative technologies, services and solutions, helping the healthcare community improve safety and increase efficiency. It takes the imagination and passion of all of us at BD, from the manufacturing to marketing of our products, to look at the impossible and find transformative solutions to turn dreams into possibilities – For people today, tomorrow and beyond. Become a maker of possible with us!

• Design, implementation and management of the Supplier Quality Development Program.
• Update and issue the “Approved Supplier List”.
• Manage and maintain the audit files and the supplier corrective action.
• Participate with Buyers and General Supervisors of Inspection of Raw Materials and Quality Engineering on the evaluation of performance and the elaboration of supplier’s trend graphs.
• Analyze the inspection and test results, investigates the causes of the external failures and propose and/or take corrective actions.
• Participate and/or lead failure investigation of the process rejects, applicable to the suppliers.
• Train suppliers in the use of problem solving tools and statistics techniques.
• Propose and recommend continuous improvement changes for product material.
• Generation, follow up, and closing, of the generated corrective actions requisitions (SCAR).
• Elaborate periodical reports and schedule information meetings about the certification activities.
• Perform evaluations and statistical analysis of new materials or components.
• Lead the Material Review Board.
• Trace, identify trends, and prepares reports for the rejects applicable to the suppliers (DMNs and/or NCs).
• Coordinate meetings for the Supplier Certification Board.
• Perform certification audits for components and materials.
• Evaluate and approve the corrective action plans for the suppliers.
• Establish and implement, personal, departmental, and plant goals, (reachable and measurable), that help the continuous improvement and support the divisional and corporative goals.
• Participate as an internal auditor in the verification of the quality system to assure the maintenance of the ISO-13485-2003 record, compliance with the current Good Manufacturing Practices (GMP’s) and the adherence to regulations and internal, divisional, corporative policies and regulatory organisms.
• Effective use of the Documentation Electronic System.

  Industrial Engineer Professional Career preferably.

  2 years of experience in similar position preferably.

  Certified Lead Auditor (ASQ, IRCA, Exemplar Global or similar) preferably.

  Experience in (FDA) Food and Drug Administration Regulated Industry.

  Computer and MS-Office application skills.
• Language skills : Upper Intermediate
• “BD values equity in the workplace without discrimination for any disability, class, ethnicity, age, religion, gender identity or sexual orientation.”

Primary Work Location
MEX Nogales South – Parque Industrial El Cid Additional Locations
Work Shift