Quality engineer 1 page is loaded quality engineer 1remote type: onsitelocations: reynosa, tamps, mextime type: full timeposted on: posted todaytime left to apply: end date: november 21, 2025 (30 days left to apply)job requisition id: r0221286quality engineerresponsibilities: completes projects as assigned by the department manager. Must be able to prioritize responsibilities and establish time lines in order to maintain a balance of support in all projects and execute projects with clear objectives. Communicates project deliverables, objectives, and timelines to team members.* utilize established procedures to perform routine assigned tasks under close supervision.* support the evaluation of customer complaints along with the development of corrective/preventive actions/corrections (capa/nc).* monitor internal nonconformance (nc) and assist developing corrective and preventive actions as part of the quality team.* responsible for making regular walkthroughs throughout the manufacturing area in order to develop and/or participate in projects for process improvement and the overall quality of the product.* knowledge of sampling distributions, binomial, poisson, normal and exponential distributions and be able to apply statistical inference in each.* responsible for the development and implementation of test methods for medical devices and equipment.* assist the different departments in validations of product, processes as well as on the writing of the validation protocol when needed.* analyze data with statistical software and quality tools such as risk analysis, flow charts, control charts, scatter diagrams and histograms.* conducts correlation and regression analysis, experimental design (doe) and acceptance sampling; as well as conducting and interpreting gage r&r studies.* ensure regulatory compliance to cgmp’s of all medical device regulatory agencies (i. e fda, iso and mdd) providing proper documentation corporate regulatory on evaluation and analysis on customer complaint samples as well as fir’s when required.* participate in conference calls, presentation and meetings with internal departments, cross site teams and upper management when required.* maintain constant communication with corporate qe/pss, canada or other fmc sites in relation to capas, overall quality improvement projects and customer complaints when required.* this position will be required to support and respond to internal/external audit observations and corrective actions.* support new design transfer activities, engineering changes and savings projects.* apply and incorporate risk management techniques throughout the product life cycle.* initiate and participate in change control activities. Qualifications: bachelor’s degree required, preferably in mechanical, industrial, electrical, electromechanical, biomedical or any other equivalent engineering degree.* two years of experience in quality engineering or related field (medical devices preferred).* excellent interpersonal, verbal and written communication skills.* must have good technical and analytical skills.* ability to understand and employ mathematics at an engineering or scientific level.* strong computer skills.* ability to effectively present information to upper management and other groups.* problem solving and root cause analysis.* knowledge of six sigma methodology.* responsible of providing the necessary engineering support and developing process/product/quality improvements and controls to assure a high confidence on the final finished product.* ability to develop and implement new methods as well as the usage of statistical tools to solve quality problems and detect process behaviors.* should practice a customer-focused quality approach.* perform process capability studies.* bilingual english / spanish.* u.s.a visa required.1 top workplace in the area. J-18808-ljbffr