Quality Eng

Job Title:  Quality Eng - P1

Hiring Manager:  Stephanie Whyte

Recruiter: James Porter

Requisition ID:  588270

Closing Date: 16th August 2024 

Reminder: 

We are committed to providing access to opportunities at Boston Scientific for all applicants. If you have a disability and require supported assistance and you would like to talk about potential accommodations related to applying for employment at Boston Scientific Cork, please contact us directly for a confidential discussion .

Purpose:

Provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products.

Key Responsibilities:

Learns to 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. Gains 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. Learns Process 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. Responsible for the final Process Monitor Release for products prior to distribution.

Education & Experience:

Minimum of Bachelor of Science Degree in Engineering/Technology. 2/3 years’ experience in a manufacturing environment or equivalent with direct experience in a QA environment (preferably GMP regulated). Experience in the medical device industry is an advantage. Experience on an automated/high volume line an advantage.

BSCI

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