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    Sr Quality Systems Engineer - Cartago, Costa Rica - Boston Scientific

    Boston Scientific
    Boston Scientific Cartago, Costa Rica

    hace 2 meses

    Boston Scientific background
    Descripción

    About the role:

    Provide Quality Engineering and Quality Process support at early stages of BSC Cartago West Green Field site. Establish, develop, and maintain procedures related to different elements of the Quality Management system to meet regulatory requirements, corporate policies, internal policies, and business needs. Support product transfer activities. After transfer provide support as part of sustaining mode to manufacturing, helping to ensure delivery of highest quality product to the customer. This is a key role to prepare the manufacturing site to host successful inspections by competent authorities like FDA and external Audits by Notify Bodies (some products contain Material of Animal Origin and require Premarket Approval).

    Your Responsibilities Include:

  • Ensure that BSC Costa Rica is in compliance with Corporate and Regulatory Requirements at all times.
  • Develop continuous improvements initiatives of the Quality System of BSC Costa Rica.
  • Participate & support Quality System related activities for improvement projects, transfers, new processes implementations, etc.
  • When acting as the CAPA Administrator / Coordinator:
  • Assure a flawless execution of the corrective and preventive action system (CAPA) which ensures timely tracking, follow up and closure of the CAPAS in their different phases.
  • Be in compliance with all procedure duties as the CAPA Coordinator for Costa Rica site.
  • Be in compliance with Feeder System responsibilities as the "Miscellaneous" Feeder System owner.
  • Follow up of action items related to the systems is expected in order to facilitate the closure of CAPAs and NCEPs.
  • Manage the NCEP/CAPA system for Costa Rica sites.
  • Execute activities and responsibilities according to applicable procedures for NCEP, CAPA, Feeder System Processes
  • When acting as the NCMR/ MRB administrator – Coordinator:
  • Assure a flawless execution of the NCMR system which ensures on time tracking, maintenance & closure of the NCEP/NCMRs investigations.
  • Be in compliance with all procedure duties as the NCMR & MRB administrator for Costa Rica site.
  • Assure compliance with Feeder System responsibilities as the NCMR Feeder System owner.
  • Follow up of action items related to the systems is expected in order to facilitate the closure of NCEPs/NCMR .
  • Manage the NCEP/NCMR System for Costa Rica site.
  • Execute activities and responsibilities according to applicable procedures for non conforming product control and rework.
  • Authorities related to control of non-conforming product may include: Batch electronic hold removal after completing all requirements according to appropriate procedures.
  • Additional Duties:
  • Ensure that BSC Costa Rica is in compliance with Corporate and Regulatory Requirements at all times.
  • Review and update documents within their areas of responsibility in order to be in compliance with Corporate and Regulatory Requirements
  • Support other Quality System department areas when it is required.
  • Develop continuous improvements initiatives of the Quality System.
  • Coordinate logistics and preparation of Management Review meetings; assure proper update and closure of the action items generated during the meetings. Prepare, if required, meeting minutes and distribute as required.
  • Execute activities and responsibilities according to applicable procedures for Management Review Meeting
  • Provide required site information/metrics to other Management Review forums held at Boston Scientific Corporation and participate/present the information if required in those forums
  • May supervise Compliance Technician
  • May lead audit readiness activities
  • What we're looking for:

  • Bachelor or Licenciature degree in Chemical, Industrial, Electronic, Biotechnology, Electromechanical Engineering or Related Field
  • English Level desired: 80-89%.
  • Experience: At least 5 years
  • Desired knowledge: ASQ certification (CQE, SSGB) desired, Problem Solving, Knowledge of QSR's, Formal training on statistical and quality techniques desirable, Networking.
  • Desirable experience in ISO 13485, QSR/GMPs, ISO :2020, ISO :2020, ISO :2020 and Regulation EU 722/2012.
  • Willing to travel to Brazil or Canada.
  • Requisition ID: 583024

    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

    Benefits
    • Life-Work Integration
    • Community
    • Career Growth

    At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination, and a deep caring for human life, we're solving some of the most important healthcare industry challenges. Together, we're one global team committed to making a difference in people's lives around the world. This is a place where you can find a career with meaningful purpose—improving lives through your life's work.


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