| Resume alert | Resumes 31 - 40 of 757 |
Software Engineer C C++
Los Angeles, CA
... · Complete FDA documentation implementation. · Complete project life cycle. · Architecture design and optimization · Certified Agile Scrum Master Languages / Protocols: Q/QML, C/C++, Python, Assembly, Java, Javascript, HTML, Pascal, Basic, Fortran, ... - Jan 30
... · Complete FDA documentation implementation. · Complete project life cycle. · Architecture design and optimization · Certified Agile Scrum Master Languages / Protocols: Q/QML, C/C++, Python, Assembly, Java, Javascript, HTML, Pascal, Basic, Fortran, ... - Jan 30
Supply Chain Operations Planning
Anaheim, CA
... Inventory • Contract Manufacturing • Master Scheduling • Root Cause Analysis • Total Quality Management • GMP • ISO-9001 • FDA Compliance • Demand Solutions Forecasting • JDEdwards ERP • MS Word, Excel & PowerPoint PROFESSIONAL EXPERIENCE FULL TIME ... - Jan 28
... Inventory • Contract Manufacturing • Master Scheduling • Root Cause Analysis • Total Quality Management • GMP • ISO-9001 • FDA Compliance • Demand Solutions Forecasting • JDEdwards ERP • MS Word, Excel & PowerPoint PROFESSIONAL EXPERIENCE FULL TIME ... - Jan 28
Production Manager Quality Assurance
Buena Park, CA
... • Fully involved on third party inspections from different agencies (FDA, County Health, OSHA, Private Customers). • Fully involved on monthly raw materials inventory. Preventing over stock of unnecessary materials and reducing any possible waste of ... - Jan 22
... • Fully involved on third party inspections from different agencies (FDA, County Health, OSHA, Private Customers). • Fully involved on monthly raw materials inventory. Preventing over stock of unnecessary materials and reducing any possible waste of ... - Jan 22
Clinical Research Associate
Long Beach, CA, 90808
... -Primary responsibility is site management and performance (including documentation) according to ICH guidelines (and country specific guidelines and government regulations), as well as FDA regulations (state and local laws), GCPs, and SOPs. ... - Jan 22
... -Primary responsibility is site management and performance (including documentation) according to ICH guidelines (and country specific guidelines and government regulations), as well as FDA regulations (state and local laws), GCPs, and SOPs. ... - Jan 22
Manufacturing Manager Injection Molding
Lake Forest, CA, 92630
... leadership experience Quality & Regulatory Compliance: ISO 9001, ISO 13485, 21 CFR (Parts 11, 210, 211, & 820), Audits ( FDA, EU, PAI, and Customer), Quality Risk Management, Change Control, cGMP, Document Control, and CAPA Plastics Processing: ... - Jan 21
... leadership experience Quality & Regulatory Compliance: ISO 9001, ISO 13485, 21 CFR (Parts 11, 210, 211, & 820), Audits ( FDA, EU, PAI, and Customer), Quality Risk Management, Change Control, cGMP, Document Control, and CAPA Plastics Processing: ... - Jan 21
Patient Care Level 1
Newport Coast, CA
... Supervisor Participated in a research study for the management of chronic urinary incontinence Responsible for reviewing data, overseeing patient care and supervising clinical monitors as it relates to the study for inspection for FDA approval. ... - Jan 19
... Supervisor Participated in a research study for the management of chronic urinary incontinence Responsible for reviewing data, overseeing patient care and supervising clinical monitors as it relates to the study for inspection for FDA approval. ... - Jan 19
Personal Care Raw Materials
Orange, CA
... training • Related to regulations regarding cosmetics, personal care, OTC, pharmaceutical, and dietary manufacturing o 21 CFR 820 – FDA’s cGMP Medical Device Training o 9 CFR 417 – USDA HACCP Training o 21 CFR 210 & 211 – FDA’s cGMP For Finished ... - Jan 18
... training • Related to regulations regarding cosmetics, personal care, OTC, pharmaceutical, and dietary manufacturing o 21 CFR 820 – FDA’s cGMP Medical Device Training o 9 CFR 417 – USDA HACCP Training o 21 CFR 210 & 211 – FDA’s cGMP For Finished ... - Jan 18
System design and test Engineer
Irvine, CA
... safety), biocompatibility, ICD, regulations (ISOs ASTM, CFR, or FDA) Supported system requirements management using DOORS, design, test and MFG life cycles from characterization, clinical verification, MFG, commercial validation for user need market ... - Jan 18
... safety), biocompatibility, ICD, regulations (ISOs ASTM, CFR, or FDA) Supported system requirements management using DOORS, design, test and MFG life cycles from characterization, clinical verification, MFG, commercial validation for user need market ... - Jan 18
Process Improvement Project Engineering
El Monte, CA
... Fostered compliance with government regulations (i.e., EPA, FDA, HACCP, FQP, GMP, AIB, and OSHA). NESTLE WATER NORTH AMERICA, Los Angeles, California Site Operations Manager (Arrowhead Spring Water Plant), 2007-2017 Managed Cap-X and expense ... - Jan 18
... Fostered compliance with government regulations (i.e., EPA, FDA, HACCP, FQP, GMP, AIB, and OSHA). NESTLE WATER NORTH AMERICA, Los Angeles, California Site Operations Manager (Arrowhead Spring Water Plant), 2007-2017 Managed Cap-X and expense ... - Jan 18
M D Molecular Biology
Irvine, CA
... Passed all sequencing runs independently in a project two months earlier than FDA deadline Familiar with basic bioinformatic tools for NGS analysis, designing, conducting and troubleshooting of experiments; well-interpret results and draw ... - Jan 16
... Passed all sequencing runs independently in a project two months earlier than FDA deadline Familiar with basic bioinformatic tools for NGS analysis, designing, conducting and troubleshooting of experiments; well-interpret results and draw ... - Jan 16