Location : Coyol, Alajuela (CR-A), Costa Rica (CR)
Additional Locations :
Hiring Manager : Andrea Esquivel Viquez
Recruiter : Raquel Alvarado Munoz
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.
Your Responsibilities Include :
May execute the following responsibilities :
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 & Training Materials by gaining knowledge of prevalent tools used and by reviewing & 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 We’re Looking For :
Bachelor's degree in Industrial, Electromechanical or Electric Engineering.
English Level desired : B2 : (70% - 79%).
Desired knowledge : Statistical skills, ASQ Certified, Knowledge of Six Sigma, Knowledge of Lean, APQP or similar.
Or an equivalent combination of education and experience
Requisition ID : 488964
As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most united by a deep caring for human life.
Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate.
Now more than ever, we have a responsibility to apply those values to everything we do as a global business and as a global corporate citizen.
So, choosing a career with Boston Scientific (NYSE : BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!