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Quality Engineer II

Work mode:  Onsite
Onsite Location(s): 

Clonmel, IE

Additional Locations: Ireland-Clonmel; Ireland-Cork; Ireland-Galway

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.

 

Purpose Statement

Provide Quality Engineering support to Printed Circuit Boards (PCB) Manufacturing Unit, helping to ensure delivery of the highest quality product to the customer. Provide Quality Engineering support to product development teams to ensure development of highest new quality product.

 

Key responsibilities

  • Develop an in-dept knowledge of the PCB manufacturing process including all aspects of production and process controls in-place on these manufacturing lines.
  • Owner of projects requiring problem solving or process improvement roadmaps and tools.
  • Coordinates and conducts technical investigations and documentation of non-conforming events and trends and develop technical investigation plans using eCAPA and Engineering Essentials.
  • May be responsible for querying & bounding data to support implementation of complex product containment & documenting release criteria.
  • Leads process improvement efforts by identifying methods to capture quality metric data and by performing appropriate analysis methods to enhance sustaining product design and new product development.
  • Supports new product development teams on the transition of new products into PCB Manufacturing.
  • Supports Supplier Quality Engineering on incoming component related issues.
  • Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
  • Be part of a strong team culture around high expectations & high performance.
  • Provide clear communication to stakeholders at key technical updates
  • Leads/Supports investigations on customer internal & external complaints.
  • May be responsible for Preventive Quality initiatives in the value stream.
  • Ensure Regulatory compliance in projects of responsibility by utilising quality tools and processes.
  • Provide clear communication to stakeholders at key technical updates.
  • Plans, organizes, and prioritizes own daily work routine to meet established schedule.

 

Qualification/Experience: 

  • Bachelor’s degree in Engineering/Quality/Science with a minimum of 3 years’ experience in a Medical Device environment or related industry.
  • Demonstrate strong leadership skills, communication skills and promote quality at source.

 

Closing Date: 2nd June

 

Requisition ID: 583626

 

 

 

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!


Job Segment: Quality Engineer, Medical Device Engineer, Manufacturing Engineer, Medical Device, Compliance, Engineering, Healthcare, Legal

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