**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
**Reynosa Villa Florida**
**Application End Date**:
16 mar 2025
**Job Requisition ID**:Essity

📌 Supplier Quality Engineer (Reynosa)
🏢 Essity
📍 Reynosa