Arroyo, Puerto Rico
Full time
What You Will Do:
Support the design and testing of new products.
Ensure that everything functions well and meets quality standards.
Identify and prevent potential problems (especially risks, defects, and inspection issues).
Ensure the product can be manufactured efficiently and safely.
Support validations (process, tool, and equipment testing)
What You Will Need:
Required:
University degree in engineering (or similar).
Experience in regulated industries, such as medical devices or pharmaceuticals.
Understanding of manufacturing processes and quality tools such as FMEA (Failure Mode and Effects Analysis), CAPA (Corrective and Preventive Actions), PPAP (Production Part Approval Process), validations, and inspections.
Knowledge of standards such as ISO 13485 (quality standard for medical devices).
Advanced English communication skills.
Desirable:
Experience with Process Flow Mapping (PFM) or process risk assessment.
Experience with non-conformity management.
Travel Percentage: 20% Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.