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Quality Engineer 1

Fresenius Medical Care North America

Reynosa

Presencial

MXN 920,000 - 1,290,000

Jornada completa

Hoy
Sé de los primeros/as/es en solicitar esta vacante

Descripción de la vacante

A leading medical devices company in Reynosa is looking for a Quality Engineer to manage projects related to quality assurance and regulatory compliance. The ideal candidate holds a Bachelor's degree in engineering and has two years of experience, preferably in medical devices. Bilingual English/Spanish is required. Strong analytical skills and a knowledge of Six Sigma methodology are essential for this role. The position involves collaboration across departments and participation in quality improvement projects.

Formación

  • Two years of experience in quality engineering or related field required.
  • Good technical and analytical skills needed.
  • Ability to understand mathematics at an engineering level required.

Responsabilidades

  • Complete projects assigned by the department manager.
  • Support the evaluation of customer complaints and CAPA development.
  • Analyze data with statistical software and quality tools.

Conocimientos

Interpersonal skills
Analytical skills
Problem solving
Knowledge of Six Sigma
Bilingual English / Spanish

Educación

Bachelor's degree in engineering

Herramientas

Statistical software
Descripción del empleo
Quality Engineer
Responsibilities
  • 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.
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