We Are The People Who Give Possibilities PurposeBD is one of the largest integral medical technology companies in the world.
Advancing the world of healthTM 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 DescriptionJob Responsibilities: (Primary Duties, Roles, and/or Authorities)Develops new manufacturing procedures, sort/rework procedures, visual aids; updates and improves the existing ones, ensuring that the documents of productive processes are friendly and reflect properly the actual practice.Provides training to the operative personnel in the process documents.Participates in the elaboration of tools of assessment of risks in the process (for example: Risk Assessment, Fault Tree Analysis and FMEA).
Participates actively in the quality improvement teams (CAPA) to respond to Clients Complaints, Rejections, and defects in the Business Unit.Participates in the determination of the monitoring plan in the critic machines of the unit.Brings technical support to the Business Units in activities related to a validation and manufacturing.Proposes and recommend changes to the continuous improvement of processes, products, procedures, and methods focused on the problem prevention.Participates in the process of design of manufacturing and assemble tools, as well as errorproof devices (poka-yokes, etc.).
Coordinates and runs capital investment projects for the productive process improvement.Uses the Infinity QS software to control the CTQs and the CTPs (Critical to Process).
Performs Process Develop Studies to identify the critical variables of the processes,



and to determinate the parameter window of the process to validate.Plans and runs validation studies to analyze the capability of the production process to provide product that meets consistently and reproducibly with the quality specifications and attributes.Conducts validation studies to determinate if the software involved in the quality production/systems processes is capable of perform its functions consistently and reproducibly to bring support to the processes related to product manufacturing.Education And ExperienceFinished Professional Career at the Bachelor's level in Electronic, Mechatronic, and/or Industrial Engineering.Two Years Of Experience In a Similar Job Preferred.Management of statistics concepts and lean manufacturing tools preferred.Knowledge of standards and regulations related to medical industry preferred.Language SkillsElementaryWhy Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do.
We welcome people with the imagination and drive to help us reinvent the future of healthcare.
At BD, you'll discover a culture in which you can learn, grow and thrive.We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture.
Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.Becton, Dickinson, and Company is an Equal Opportunity Employer.
We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.Primary Work LocationMEX Nogales South – Parque Industrial El Cid
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📌 Ingeniero De Procesos De Unidad De Manufactura (Heroica Nogales)
🏢 Bd
📍 Heroica Nogales