Medical Device Quality Assurance Jobs in Santa Ana, CA

Concentra Career Choice - Santa Ana, California (+1 location)

in accordance with state regulations Complete quality assurance activities on equipment and medical devices as well as testing processes used in the center Maintain supplies, clean rooms and equipment, and stock

from: resume-library.com - 6 days ago

Fujifilm - Santa Ana, California

Service and/or Quality Assurance/Regulatory Affairs/Compliance, technical and customer support in a medical device discipline. Two (2) or more years of direct supervisory or management experience. GMPs

from: resume-library.com - 2 days ago

Medasource - Irvine, CA, United States (+1 location)

program for medical devices, including medical device hazard investigations, to assure compliance with patient safety goals, SMDA, and TJC requirements; ability to conduct capital asset and infrastructure

from: linkedin.com - 10 days ago

Compunnel Inc. - Irvine, CA, United States

functions (e.g., Manufacturing, Quality Assurance, Suppliers, etc.) to identify assignable root cause, resolve open action items, and gather additional technical information to resolve complaint. Additional

from: linkedin.com - 18 days ago

Katalyst Healthcares & Life Sciences - Irvine, California

Responsibilities: A minimum of 2-4 years of experience in Quality Engineering or Quality Assurance, including data analysis, risk assessment and risk mitigation is required. Working experience

from: resume-library.com - 4 days ago

MicroVention-Terumo - Aliso Viejo, CA, United States

and manufacture of medical devices and resolve product quality issues. What You'll Be Doing Provide the quality/independent review at design reviews. Review and provide guidance for project design plans, risk

from: linkedin.com - 8 days ago

Sunrise Systems Inc - Brea, California

Our client a leading medical devices manufacturing company is looking for Quality Assurance Analyst in Brea, CA location. This position is for 6 months of contract to start Position title: Quality

from: resume-library.com - 6 days ago

Applied Medical - Rancho Santa Margarita, California

devices meet regulatory requirements and quality standards. This position involves inspecting, testing, and documenting various stages of the manufacturing process to guarantee product integrity

from: resume-library.com - 5 days ago

Johnson and Johnson - Irvine, CA

and risk mitigation. * Working knowledge of regulatory compliance requirements (Quality System Regulations (QSRs), Medical Device Regulation (MDR), ISO 9001, ISO 13485, ISO 14971 or other international

from: Johnson and Johnson - 4 days ago

Diverse Lynx - Irvine, California

), Medical Device Directive (MDD), ISO 9001, ISO 13485, ISO 14971. 1. Provides overall quality assurance leadership in the management of Direct, Indirect Suppliers and/or External Manufacturers. 2. Leads

from: resume-library.com - 13 days ago