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Purpose and Passion - Comprehensive Benefits - Life:Work Integration - Community - Career Growth
At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we're solving some of the most important healthcare industry challenges. Together, we're one global team committed to making a difference in people's lives around the world. This is a place where you can find a career with meaningful purpose-improving lives through your life's work.
About the Role:
This opportunity will make you a part of Boston Scientific internship program that offers on:the:job training or project performed by university senior students at a company. The role will include activities 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.
The internship period will be for a period of up to 12 months and the student will receive a subsidy during their period on the company.
Your 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.
: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
:Support environmental monitoring, microbiology and product testing as in approved procedures and protocols.
What Were Looking For:
:At least 60 of studies completed in Bachelor in Chemical,Industrial, Electronic, Biotechnology, Electromechanical Enginnering or Related Field.
:English Level required: B2:(70 : 79)
:Desirable knowledge in:Statical skills, ASQ Certified, Knowledge of Six Sigma, Knowledge of lean, APQP or similar.
:Avaible for a temporary position(12 months).
About us
As a global medical te
Salario:Competitive
Ciudad: coyol
