SQA Process Engineering

Description du poste:

Supplier Quality Engineer

About the Role
We're looking for people who embody our values, aren't afraid to challenge, innovate, experiment, and move at a fast pace. We're always looking for ways to improve our products and ourselves. If this is you, we'd love to talk.

What You Will Do
* 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

Who You Are
* Bachelor's degree in engineering or equivalent.
* 2 years of experience on industry; quality experience on medical devices preferred.
* Experience in similar position (SQA)
* Visa Laser
* Demonstrate effective communication, presentation and influencing skills, fluidly bilingual English and Spanish required.
* Strong experience with supplier quality
* 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.

What We Can Offer You
Our purpose, Breaking Barriers to Well-Being, provides meaning to everything we do. Join us to improve well-being for people and drive positive change for society and the environment. At Essity, you'll feel valued, empowered to grow, and challenged to achieve business results in a collaborative and open atmosphere. Innovate for Good | Excel Together | Be You with Us

Ubicación: Planta Reynosa
Innovate for Good | Excel Together | Be You with Us
#EstamosContratando #OfertaDeTrabajo #Empleo #Reclutamiento #Talento #SQA#QC #Manufactura #TrabajoEnEquipo #DesarrolloProfesional #BienestarLaboral #Innovación #Sostenibilidad

Reynosa Villa Florida

Application End Date:

30 ene 2026

Job Requisition ID:
Essity258677