Quality Engineer Consultant

3 weeks ago


Los Angeles, United States Katalyst Healthcares and Life Sciences Full time

Responsibilities: Perform problem identification & resolution Participate in internal and external quality audits Support/approve design verification, validation activities & inspection Collaborate with cross-functional teams to provide quality guidance Prepare and maintain documentation and records Requirements: Bachelor's degree or equivalent in Mechanical, Electrical, or Manufacturing Engineering Must have 3-5 years of recent experience in the Medical Device industry Knowledge of ISO 13485, FDA QSR, MDR, ICH Quality Systems & Regulatory requirements Strong problem-solving, communication, and teamwork skills bility to work independently and manage multiple tasks and priorities


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