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Resume alert |
Resumes 11 - 20 of 416 |
Westminster, CA
... ● Knowledgeable in Quality Control Procedures and standards including GMP, ISO 9000, 9001 and ISO 13485-2003 and FDA regulation. ● Well trained in auditing the schedule of Quality Control. WORK EXPERIENCE Quality Tech. Inspector Aug 21,2023 To ...
- Feb 26
Lake Forest, CA
... DEVELOPMENT National Student Leadership Conference in Biotechnology Washington, DC Student Mentee Jun - Jul 2022 • Participate in biotech sessions with direct insight from top FDA, industry, and academic leaders • Study DNA labs with global peers; ...
- Feb 18
Chino Hills, CA, 91709
... In depth experience with Verification and Validation per FDA policies and Regulatory adherence that govern IT Detailed Operating Procedure (DOP) and Standard Operating Procedures (SOP). Dynamic leadership experience in people and system assurance ...
- Feb 18
Anaheim, CA
... Oracle, SAP, QCS, Pick-to-Light, Q-Track, Connect Ship) Ensure that Distribution Centers are following all OSHA requirements and facilities operate in compliance with all governmental agency includes FDA, OCFA, OC Health Modernized and improved ...
- Feb 05
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
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
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
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
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
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