Quality Engineer Ii Job

Quality Engineer Ii Job
Empresa:

(Confidencial)


Lugar:

Heredia


Área:

Otros

Quality Engineer Ii Job

Detalles de la oferta

Location: Heredia, Heredia (CR:H), Costa Rica (CR) Additional Locations:
Hiring Manager: Adriana Nanne Garcia
Recruiter: Maria Gabriela Campos Mora

About the role:

: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.

Youre Responsibilities Include

:May execute the following resposibilities:
:Identify Manufacturing process defects (scrap, nonconforming material, customer complaints) by dispositioning non:conforming material, assisting in identification of primary root causes and understanding corrective and preventative actions. May be responsible for working with process owner to bound product stops and document release criteria.
:Understanding of product quality plans, documents and systems by reviewing product specifications, quality specifications, and working with quality systems. May be responsible for learning risk analyses and FMEAs.
:Monitoring Systems by becoming familiar with systems applications and critical process steps; and through familiarization with methods used to reduce process variation.
:Becomes 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
:Learns Quality Tools and Training Materials by gaining knowledge of prevalent tools used and by reviewing and utilizing available training materials.
:Checks and provides support in the execution and investigation of CAPAs, NCEP, Failure Mode Investigations, etc.
:Evaluates new equipment and processes and participates in the transfer of new products.
:Evaluates new equipment and processes and participates in the transfer of new products.
:Get involve 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.
:Read and interpret technical drawings, procedures, and protocols
:Assure that all laboratory equipment is in compliance to perform the analysis activities (calibration, safety, cleanness).
:Document investigation findings in analysis report on GCS2
:Become a trainer for the Software related with complaints handling process (GCS2), as required.
: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
:Responsible for reviewing and developing process validation protocols and reports. Support other functional areas during the validation activities

What were looking for:

:Experience: At least 2 years
:English level: 70:79
:Bachelor: Licenciature:Chemical, Industrial, Electronic, Biotechnology, Electromechanical Engineering or related field
:ASQ Certification (CQE, SSGB)
:Knowledge of QSRs
:Scientific tools (Gage, R and D, DOE, process capability SPC)
:Formal studies in process and product validation in desired as well as through understanding of inspection techniques and statistical methods
:knowledge of Six Sigma, Lean APQP or similar tools

About us

As a global medical technology leader for more than 35 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you're looking to truly make a difference to people both around the world and around the corner, there's no better place to make it happen.

Requisition ID:431505

:ul


Fuente: Tiptopjob2_Xml


Área:

  • Otros / Otros

Requisitos

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