Engineer I, Quality at Boston Scientific Corporation Malaysia

La Asunción, Cantón de Belén, Costa Rica -

Full Time

Start Date

Immediate

Expiry Date

08 Jan, 26

Salary

0.0

Posted On

10 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, Root Cause Analysis, Process Improvement, Statistical Sampling, Technical Drawing Interpretation, CAPA, FMEA, Validation Protocols, Minitab, Office, Power BI

Industry

Medical Equipment Manufacturing

Description

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. Manage and disposition non-conforming material, adhering to internal and external requirements. Assess process changes, by evaluating the impact to the current process, product or builder behavior and also ensuring adherence to system requirements. 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 Provides support in the execution and investigation of CAPAs, NCEP, Failure Mode Investigations, etc. 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 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 Education: Engineer Degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering or similar. English Level desired: B2 Experience: At least one year in a similar position. Or an equivalent combination of education and experience. Desired knowledge: Minitab, Office, Power BI.

Responsibilities

The Engineer I, Quality will identify manufacturing process defects and manage non-conforming materials while ensuring adherence to internal and external requirements. They will also support process validation activities and assist in product and process improvement efforts.