Supervisor de Aseguranza de Calidad

Job Description Summary

Job Summary:
The Quality Assurance Supervisor is responsible for coordinating and training a team of competent QA
inspectors to provide support to the manufacturing of medical devices by performing inspections and tests
as established in the procedures/ specifications. Leads the daily efforts to ensure the medical devices
achieve the requirements established, coordinates the containment and correction of non-conforming
material in process, as well as the release of product when all acceptance criteria is fulfilled.

Job Description

How about becoming a maker of possible?

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!

Job Responsibilities: (Primary Duties, Roles, and/or Authorities)
Personnel
Training of QA Inspectors in sampling, inspection criteria, tests, parameter reading, specifications,
and all aspects required for their daily tasks.
Supports the request of electronic platforms or access for his/her personnel.
Interviews and selects personnel that fulfill the role requirements for which they are being hired.
Inspection and Tests
Ensures that inspection and testing of the QA personnel is performed according to the established
procedures and that are documented adequately.
Escalates whenever there is a deviation from the established procedures / specifications
opportunely.
Leads the Non-Conforming (MRR) whenever a Non-Planned deviation occurs at the
product/process.
Provides support for process/ product/ test methods validations.
Materials
Verifies when material is reported as discrepant , segregates, and informs when applicable to the
IQA/SQE departments.
Documentation
Reviews his/her personnel documentation and approves when necessary.
Updates visual samples and/or limit samples when necessary.
Miscellaneous
Coordinates periodic meetings to evaluate Non-Planned deviations (MRRs) trends and action plans
to reduce recurrence of failures.

Participates actively in the implementation of quality programs that encourage a prevention
environment and not a defect or problems detection.
Participates actively in the verification of the quality system to ensure the maintenance record in
ISO 13485 certification, compliance of current Good Manufacturing Practices (GMP) and adherence
to regulations and internal, divisional, corporate, and regulatory agencies policies.
Proposes or recommends changes for continuous improvement of processes, products,
procedures, and methods.
Attends training, and/or self-profesional improvement courses.
Any other task assigned by immediate Supervisor or Manager.

Education and Experience:
Professional Career Bachelor's Degree level preferably.
Computer and MS-Office application handling preferably.
Experience not necessary.
Knowledge and Skills:
Leadership, teamwork, and critical thinking skills.
Statistic Basic knowledge.
Product/ Process Inspection.
Use of testing/ measurement equipment.

Language Skills:Elementary

"BD values equity in the workplace without discrimination for any disability, class, ethnicity, age, religion, gender identity or sexual orientation."

Required Skills

Optional Skills

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Primary Work Location

MEX Nogales South - Parque Industrial El Cid

Additional Locations

Work Shift