88 Quality Assurance And Engineering jobs in Anaheim.

Lake Forest

• Skills: Optical Engineering, Opto-Mechanical Design, Imaging Systems, Optics, Creative Solutions, Material Science, Quality Control, Risk Assessment, Regulatory Requirements, Medical Devices
• Level: senior
• Type: full_time

Irvine

• Skills: Regulatory Affairs, medical devices, FDA regulations, ISO standards, clinical trials, implantable devices, submission strategy, compliance, technical writing, product development
• Level: senior
• Type: full_time

Irvine

• Skills: quality assurance, medical devices, regulatory compliance, inspections, lab techniques, QA methodologies, documentation, safety standards, process improvement, team collaboration
• Level: mid
• Type: full_time

Lake Forest

• Skills: optical engineering, surgical microscopes, optical metrology, quality control, cross-functional collaboration, optical components, light behavior, high-precision designs, GxP regulations, continuous improvement
• Level: senior
• Type: full_time

Irvine

• Skills: Quality Control, cGMP, LIMS, Sterility Test, Bioburden, Growth Promotion, Bacterial Endotoxins, Environmental Monitoring, Laboratory Maintenance, Analytical Techniques
• Level: mid
• Type: full_time

Irvine

• Skills: Quality Engineering, Compliance, ISO 9001, Root Cause Analysis, Manufacturing Processes, Quality Standards, Production, Efficiency, Defect Prevention, Cross Functional Teams
• Level: mid
• Type: full_time

Irvine

• Skills: regulatory affairs, dietary supplements, formulation review, ingredient safety, claims and labeling, compliance culture, cross-functional leadership, risk management, marketing compliance, nutraceuticals
• Level: senior
• Type: full_time

Irvine

• Skills: quality assurance, GMP, ISO 13485, FDA regulations, audit management, root cause analysis, corrective actions, medical devices, audit program, data analysis
• Level: mid
• Type: full_time

Irvine

• Skills: Regulatory Affairs, Medical Devices, Global regulatory submissions, Healthcare innovation, Product registration, Microsoft Office, Project team collaboration, Data management, Life Sciences, Engineering
• Level: entry
• Type: internship

Aliso Viejo

• Skills: next-generation sequencing, clinical diagnostics, NGS experiments, cancer genomics, assay development, design control, validation, regulatory submissions, minimal residual disease, technical reports
• Level: senior
• Type: full_time

Irvine

• Skills: New Product Introduction, Class II medical device, regulatory clearance, project management, design control principles, project approval pitches, cross-functional teams, product lifecycle management, schedules, resource allocation
• Level: mid
• Type: full_time

Aliso Viejo

• Skills: NGS assay development, hematological assays, regulatory submissions, design control, validation packages, clinical diagnostics, minimal residual disease, cross-functional, whole genome sequencing, technical reports
• Level: senior
• Type: full_time

Irvine

• Skills: Aseptic processing, Pharmaceutical manufacturing, Quality specifications, Good Documentation Practices, Active Pharmaceutical Ingredients, Mechanical troubleshooting, Production efficiency, cGMP, ISO standards, Production records
• Level: mid
• Type: full_time

Loma Linda

• Skills: quality assurance, patient safety, data analysis, statistical analysis, regulatory standards, process mapping, root cause analysis, leadership skills, healthcare quality, collaborative team
• Level: mid
• Type: full_time

Irvine

• Skills: Regulatory Affairs, Medical Devices, Global Regulatory Submissions, Quality Databases, Healthcare Solutions, Life Sciences, Engineering, Microsoft Office, Clinical Trials, Strategic Discussions
• Level: entry
• Type: internship

Irvine

• Skills: Quality Systems, Regulatory Compliance, Medical Device, Project Management, Audit Readiness, Continuous Improvement, Document Control, SOPs, Process Improvements, Training
• Level: senior
• Type: full_time

Irvine

• Skills: Quality Engineering, medical technology, new product development, design control, FMEA, regulatory documentation, risk management, cross-functional collaboration, clinical strategies, talent management
• Level: senior
• Type: full_time

Brea

• Skills: product development, design controls, ISO 13485, risk management, stakeholder management, project deliverables, technical strategies, team leadership, data analytics, medical devices
• Level: senior
• Type: full_time

Irvine

• Skills: process validation, Six Sigma, supplier qualification, regulatory compliance, statistical analysis, fda, iso 13485, lean manufacturing, quality engineering, technical writing
• Level: senior
• Type: full_time

Irvine

• Skills: Regulatory Affairs, IVDR, technical files, labeling conversion, quality assurance, compliance, project management, biomedical, FDA, CE marking
• Level: mid
• Type: temporary