Supplier Quality Engineer
hace 2 semanas
**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 (ISO***** 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 ******Job Requisition ID**:Essity******
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