Lizette Carrillo

Senior Quality Engineer @ Imperative Care

About

At Imperative Care, my role as Senior Quality Engineer is anchored in over 8 years of experience in the medical device industry. Our team leverages my expertise in manufacturing process improvement and quality risk management to enhance product safety and efficacy. With a Six Sigma Green Belt certification, I've been pivotal in refining processes that ensure regulatory compliance and operational excellence. My competencies extend to process validation and implementing rigorous failure mode and effects analysis (FMEA), which has significantly contributed to advancing Imperative Care's product quality. My bilingual proficiency in English and Spanish facilitates effective communication across diverse teams, supporting our mission to deliver innovative healthcare solutions.

Country

United States

City

San Jose

Industry

Medical Device

Skill

Quality Auditing, Manufacturing Process Improvement, Process Validation, Quality Risk Management, Quality System, Leadership, Six Sigma Green Belt, Public Speaking, Presentation Skills, Organization Skills, Time Management, Root Cause Analysis, MDR Reporting, Technical Writing, Complaint Investigations, Quality Assurance, Metrics Reporting, Corrective and Preventive Action (CAPA), NCR, Good Manufacturing Practice (GMP)

Experience

Senior Quality Engineer

Imperative Care

2022-4 - Present · 4 yrs 6 mos

Campbell, California, United States

In my role as a Senior Quality Engineer at Imperative Care, I led process improvements for Non-Conformance (NC) issues, ensuring enhanced efficiency and quality compliance. I provided quality oversight for manufacturing operations, ensuring adherence to quality standards and supporting bioburden monitoring. Additionally, I collaborated cross-functionally to define validation requirements for process changes on commercially launched products.

Quality Assurance Engineer

Johnson & Johnson MedTech

2018-5 - 2022-3 · 3 yrs 11 mos

Fremont, CA

• Led validation and integration of new inspection systems, including IQC processes and equipment qualifications. • Supported manufacturing transfer projects by creating quality plans and validating processes for new and relocated production lines.