Quality Assurance Engineer II, Heredia Turno C

hace 1 mes


San Francisco, Heredia, Costa Rica Boston Scientific Corporation A tiempo completo

About Us

Boston Scientific Corporation is a global medical technology leader. Our mission is to improve patient lives with innovative medical solutions. We are committed to advancing science for life and improving patient health. We recognize that nurturing a diverse and inclusive workplace helps us be more innovative.

Job Summary

Provide Process/Quality Engineering support to manufacturing or new product development teams, helping to ensure delivery of highest quality product or new products to the customer. Identify Manufacturing process defects by dispositioning non-conforming material, assisting in identification of primary root causes and understanding corrective and preventative actions.

Responsibilities

  1. Identify Manufacturing process defects by dispositioning non-conforming material, assisting in identification of primary root causes and understanding corrective and preventative actions.
  2. Understand product quality plans, documents and systems by reviewing product specifications, quality specifications, and working with quality systems.
  3. Become familiar with Product/Process improvement efforts by understanding current quality metric data and learning the various analysis methods used to enhance sustaining product design and new product development.
  4. Learns Quality Tools & Training Materials by gaining knowledge of prevalent tools used and by reviewing & utilizing available training materials.
  5. Check and provide support in the execution and investigation of CAPAs, NCEP, Failure Mode Investigations, etc.
  6. Evaluate new equipment and processes and participate in the transfer of new products.
  7. Get involved in various stages of equipment and processes validations: Run and / or review and / or approve reports I.Q 's, O.Q' s and P.Q 's as well as any other document relating to validation.
  8. Read and interpret technical drawings, procedures, and protocols.
  9. Assure that all laboratory equipment is in compliance to perform the analysis activities (calibration, safety, cleanness).
  10. Document investigation findings in analysis report on GCS2.
  11. Become a trainer for the Software related with complaints handling process (GCS2), as required.
  12. Work with Research and Development to efficiently qualify new components; assist suppliers in creating of statistical sampling plans, inspection methodology and quality procedures for new components.
  13. Responsible for reviewing and developing process validation protocols and reports. Support other functional areas during the validation activities.

What We're Looking For

Bachelor or Licenciature degree in Chemical, Industrial, Electronic, Biotechnology, Electromechanical Engineering or Related Field. English Level desired: 70-79%. At least 2 years of experience. ASQ certification (CQE, SSGB) desired, Problem Solving, Knowledge of QSR's, Formal training on statistical and quality techniques desirable, Networking. Please submit Resume in English.



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