Engineer Ii, Quality

hace 1 día

Heredia, Costa Rica Boston Scientific Corporation A tiempo completo

**Engineer II, Quality**:

- Remote Eligible: Onsite- Onsite Location(s): Heredia, H, CR**Additional Locations**: N/A

**Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance**

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing - whatever your ambitions.

**About the role**
- Provide Process/Quality Engineering support to manufacturing and 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 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.
- 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).
- 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 we are looking for**:

- Background: Bachelor’s degree in, Electrical, Electronic, Mechanical or related field.
- English level: B2 (70%-79%)
- Experience: 2+ years working with CAPA, manufacturing engineering, post market complaints, risk management, validations, and process engineering.
- Preferred qualifications: technical writting, SAP, Statistical skills, ASQ Certified, Knowledge of Six Sigma, Knowledge of Lean, APQP or similar.
- Formal studies in process & product validation is desired as well as thorough understanding of inspection techniques and statistical methods.
- Skills: teamwork, proactivity, goals oriented.

**Requisition ID**:558399

**Job Segment**:R&D Engineer, Quality Engineer, Six Sigma, Lean Six Sigma, Manufacturing Engineer, Engineering, Management

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