Quality engineer ii - medical devices

Descripción general

Apply knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports.
Develop moderately complex experiments and tests (including writing and executing protocols) to create, validate, and improve products (including evaluation of source materials and suppliers) and manufacturing processes/methods based on engineering principles; analyze results, make recommendations, and develop reports.

Requisitos para aplicar

• Bachelor's Degree in Engineering or Scientific field
• Minimum of 3 years of experience as Quality Process Engineer within Medical Devices Industry
• CQE (Certified Quality Engineer) preferred (if applicable)
• Basic understanding of statistical techniques
• Availability to travel to Cartago
• Advanced English