Identification de l’offre d’emploi R-508044 Date d’affichage 29 de gener 2025

Faites partie de quelque chose de plus grand chez BD. Ici, vous nous aiderez à améliorer continuellement la façon dont nous faisons les choses chaque jour ; pour être plus efficace, plus performant et mieux servir nos clients. Vous ferez cela au sein d'une équipe exceptionnelle qui s'efforce de s'assurer que tout ce que nous faisons est conforme aux réglementations et aux normes, non seulement parce que c'est la bonne chose à faire, mais aussi parce que nos produits ont un impact sur la qualité de vie des gens. Ici, vous mettrez votre expérience en matière de conformité, vos attentes élevées et votre souci du détail au service du meilleur : faire progresser le monde de la santé™. Chez BD, vous pouvez faire une véritable différence d'une personne.

  • Job Type:
    Full-Time
  • Job Level:
    Entry to Senior
  • Travel:
    Varies
  • Salary:
    Competitive
  • Glassdoor Reviews and Company Rating

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

Excited to grow your career?

We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!

Our people make all the difference in our success.

Performs any combination of tasks involved in the manufacture and assembly of medical devices. We are the makers of possible.

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.

We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.

  • 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 Reynosa

Additional Locations

Work Shift

Postuler

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.

BD is unique in how fully dedicated it is to a specific disease state. It makes it clear how the work we do directly impacts the daily lives of the patients we serve.


Eric Rainis
Senior Director Quality Management

To know that our products touch 30 million people with diabetes around the globe is powerful and fuels our teams to deliver best in class products to them each and every day.


Bridget Bagnato
VPGM Injection

It is inspiring to see BD products to be used globally to advance human healthcare.


Yang Zeng
Manager Medical Laboratory

BENEFITS

Healthcare

401(k)/
Retirement Plans

Professional Development

Paid Time Off

Awards &
Recognition

Travaillant dans

Ciudad Reynosa

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