Manufacturing Engineer

hace 15 horas


Alajuela, Alajuela, Costa Rica Abbott Laboratories A tiempo completo

About Abbott Laboratories

Abbott Laboratories is a pioneering healthcare company committed to revolutionizing the treatment of heart disease through cutting-edge medical technologies.

Working at Abbott Laboratories

As a global leader in healthcare, we offer our employees the opportunity to work on groundbreaking projects that make a tangible impact on people's lives. Our team is dedicated to creating an inclusive and dynamic work environment where everyone can grow professionally and personally.

The Opportunity

This position plays a critical role in developing and implementing optimal manufacturing processes and methods for our Electrophysiology business. You will work closely with cross-functional teams to drive process improvements, ensure quality standards are met, and identify opportunities for cost reduction.

Your Key Responsibilities:

  • Develop and implement efficient manufacturing processes and methods aligned with product specifications and quality standards.
  • Support daily manufacturing activities to meet established goals for safety, quality, cost, and production.
  • Analyze key performance indicators (KPIs) such as yield, nonconforming material, and lead time to inform improvement initiatives.
  • Prepare product and process reports by collecting, analyzing, and summarizing data and trends.
  • Apply statistical techniques to facilitate decision-making and draw conclusions from available data.
  • Collaborate with vendors to select and purchase equipment/fixtures considering production requirements, redundancy, or line capacity expansion.
  • Maintain knowledge and expertise on product requirements and specifications, understanding potential risks related to product malfunctions.
  • Ensure production lines output meets product specifications and maintains clear criteria for conforming and non-conforming products.
  • Navigate and execute activities on manufacturing systems, update routers, BOMs, generate new part numbers, and ZFINs, and coordinate new ZFINs implementation.
  • Participate in identifying and investigating non-conforming products, applying root cause problem-solving techniques to identify and eliminate causes, implement controls, and define corrections and corrective actions.
  • Identify and implement continuous improvement projects for safety, quality, production, and cost using project management tools.

Requirements:

  • Bachelor's degree in Technical Engineering fields such as Electronic, Electrical, Mechatronics, Electromechanical, Chemical.
  • 7+ years of manufacturing/process development experience, at least 5 years prior experience in medical devices manufacturing.
  • Statistical techniques knowledge (DOE, SPC) required. PE license a plus.
  • Computer software knowledge (Microsoft Word, Excel, Power Point).
  • Willingness to travel.
  • Experience with continuous improvement methodologies, such as Lean Manufacturing.


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