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Responsibilities
Job Description Summary
Supplier QA Engineer will be responsible for providing leadership and guidance to the supplier to ensure compliance to established corporate standards and to regulated agencies for industry (ISO, FDA and others as applicable). Responsible for the execution, planning, development and/or implementation of quality systems that support the organization in the successful management of suppliers.Job Description
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Performs any combination of tasks involved in the manufacture and assembly of medical devices. We are the makers of possible.
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Provide a timely follow up and communication on all supplier related quality issues (NCs / SCARs) reported in production / incoming areas, following applicable procedures.
Provide proper analysis, follow up and communication all supplier related customer complaints, following applicable procedures.
Asure the completion of Supplier Audits and/or Supplier Surveys/Assessments, following Supplier Annual Monitoring Plan and applicable procedures.
Participate during supplier selection-qualification and approval to provide required quality-related input/output, following applicable procedures.
Provide support and/or actively participate in internal and/or external audits (FDA, ISO, Corporate).
Work with project teams to coordinate or implement supplier quality initiatives in the plant.
Provide guidance on documentation associated with supplier qualification/approval and supplier-driven changes including supplier validations, supplier quality agreements, process controls, audits, and compliance to regulations and company procedures.
Work with suppliers to improve processes and Quality Systems.
Strong understanding of Root Cause Analysis, Corrective Action, Preventive Action, Efficiency Verification.
Strong Microsoft Office skills (Word and Excel).
Strong working knowledge of statistical quality tools and statistical process control (SPC).
Process Validation Activities skills (IQ/OQ/PQ), preferred.
Strong working knowledge of Quality System Regulations, ISO regulations (ISO13485 preferable), Risk Management, GMPs / GDPs.
Preferred Knowledge on Foreign country (Japan, Brazil, Canadian, China, Europe) Medical Device regulations.
Demonstrate effective communication, presentation and influencing skills, fluidly bilingual English and Spanish required.
Bachelor’s degree in engineering or equivalent.
2 years of experience on industry; quality experience on medical devices preferred.
Required Skills
Optional Skills
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Primary Work Location
MEX ReynosaAdditional Locations
Work Shift
Success Profile
What makes a successful Quality Professional at BD? Check out the top traits we’re looking for and see if you have the right mix.
- Ambitious
- Collaborative
- Goal-oriented
- Persuasive
- Results-driven
- Self-starter
Advancing the world of health™
BD is one of the largest global medical technology companies in the world and is advancing the world of health™ by improving medical discovery, diagnostics and the delivery of care. BD helps customers enhance outcomes, lower costs, increase efficiencies, improve safety and expand access to health care.