12 Quality Assurance And Engineering jobs in Los Angeles.

Los Angeles

• Skills: Biomanufacturing, Project Management, Validation, Pharmaceuticals, Cell and Gene Therapy, Quality Compliance, Technical Delivery, Life Cycle, Engineering Automation, Patient Focused
• Experience: 0-3 years of consulting and/or project engineer experience

Irvine

• Skills: Quality Assurance, Software Development Lifecycle, Regulatory Compliance, ISO 13485, FDA QSR, Risk Management, Agile, IEC 62304, Embedded Software Development, Cybersecurity
• Experience: Minimum eight (8) years of experience in quality engineering in the FDA QSR/ISO 13485 medical device industry.

Irvine

• Skills: manufacturing engineering, medical devices, lean manufacturing, process improvements, FDA regulations, ISO 13485, work instructions, standard operating procedures, collaboration, workflow planning
• Type: full_time

Glendale

• Skills: Quality Management, Clinical Trials, Project Management, Regulatory Compliance, Biopharmaceutical, Process Improvement, Risk Management, Team Leadership, Data Analysis, Stakeholder Engagement

Lake Forest

• Skills: Regulatory Affairs, GxP, compliance, medical devices, pharmaceuticals, Standard Operating Procedures, quality control, product submissions, project goals, continuous improvement
• Type: full_time

Irvine

• Skills: quality inspection procedures, sacral neuromodulation, nonconformance investigations, medical device manufacturing, ethylen oxide sterilization, process and equipment qualification, statistical methods, cross-functional teams, continuous improvement, project management
• Type: full_time

Irvine

• Skills: process engineering, supply chain, healthcare innovation, vision treatments, design specifications, project management, technical risks, quality compliance, data analysis, engineering techniques
• Type: full_time

Brea

• Skills: Quality Management Systems, Regulatory Inspections, Compliance Audits, Corrective Actions, Standard Operating Procedures, New Product Development, Quality System Controls, ISO 14971, FDA cGMP, Continuous Improvement
• Type: full_time

Irvine

• Skills: drug delivery systems, device development, Design Controls, risk management, mechanical design, electromechanical systems, 3D CAD modeling, feasibility assessment, cross-functional collaboration, quality management systems
• Type: full_time

Santa Monica

• Skills: GMP manufacturing, cell therapy, operational excellence, cross-functional integration, capacity planning, tech transfer, Lean principles, continuous improvement, regulatory affairs, quality culture
• Type: other

Los Angeles

• Skills: Manufacturing Execution Systems, electronic batch records, data integrity, validation documents, operational SOPs, MES technology, drug product, collaboration, biological manufacturing, leadership
• Type: full_time

Irvine

• Skills: Complaint Investigation, Quality Assurance, Medical Devices, Regulatory Compliance, Product Testing, Calibration, Preventive Maintenance, Project Management, Data Analysis, Root Cause Analysis
• Type: full_time