| Resume alert | Resumes 31 - 40 of 748 |
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
SAP Systems Architect and EDI Team Lead focusing on SAP SD OTC PI
Tustin, CA
... Ensured global Quality Systems and compliance within FDA regulatory requirements. Managed EDI related projects and maintenance activities in SAP R3 ECC and EDI IBM Sterling Integrator, Gentran for Windows and Gentran for UNIX to establish new ... - Jan 13
... Ensured global Quality Systems and compliance within FDA regulatory requirements. Managed EDI related projects and maintenance activities in SAP R3 ECC and EDI IBM Sterling Integrator, Gentran for Windows and Gentran for UNIX to establish new ... - Jan 13
Quality Assurance Systems
Glendora, CA
... Assists in preparation activities for third party audits including FDA, Notified Body, corporate and international regulatory authorities audits. . •Quality System Metrics - Assists in preparation and improvement of quality system metrics, and ... - Jan 11
... Assists in preparation activities for third party audits including FDA, Notified Body, corporate and international regulatory authorities audits. . •Quality System Metrics - Assists in preparation and improvement of quality system metrics, and ... - Jan 11
Project Management Machine Tool
Irvine, CA
... Validation, risk-based CSV/SDLC per FDA 21 CFR Part 11, ISO 14971, IEC 62304, -62366, ISPE GAMP, ICH Q9, ASTM E2500, IVDR. Data Integrity compliance, GxP assessment, create policy/SOP/template per 2018 FDA, UK-MHRA, EU Annex 11, ISPE, and ALCOA+. ... - Jan 06
... Validation, risk-based CSV/SDLC per FDA 21 CFR Part 11, ISO 14971, IEC 62304, -62366, ISPE GAMP, ICH Q9, ASTM E2500, IVDR. Data Integrity compliance, GxP assessment, create policy/SOP/template per 2018 FDA, UK-MHRA, EU Annex 11, ISPE, and ALCOA+. ... - Jan 06
Technical Writer
Huntington Beach, CA
... Lead Writer/Project Manager for business priority projects: o700 Series pumps, Guardian sensor and transmitters, and Synergy/Simplera/Instinct sensor o670G Hybrid Closed Loop – received FDA approval in record time of 102 days o630G Canada – reduced ... - Jan 05
... Lead Writer/Project Manager for business priority projects: o700 Series pumps, Guardian sensor and transmitters, and Synergy/Simplera/Instinct sensor o670G Hybrid Closed Loop – received FDA approval in record time of 102 days o630G Canada – reduced ... - Jan 05
Research Associate Product Development
Irvine, CA
... •Proficiency in MS Word, Excel, and experience in cGMP, GLP and FDA regulations for biotech and pharmaceuticals. SKILLS •Experienced in HPLC, GC, AA, FTIR and Dissolution •Report technical writing, training •Proficiency in MS Word, Excel, Powerpoint ... - Jan 03
... •Proficiency in MS Word, Excel, and experience in cGMP, GLP and FDA regulations for biotech and pharmaceuticals. SKILLS •Experienced in HPLC, GC, AA, FTIR and Dissolution •Report technical writing, training •Proficiency in MS Word, Excel, Powerpoint ... - Jan 03
Los Angeles Mechanical Designer
Los Angeles, CA
... Mechanical Engineering, SolidWorks, FDA regulations. Fenestration product manufacturing/design experience - Jan 02
... Mechanical Engineering, SolidWorks, FDA regulations. Fenestration product manufacturing/design experience - Jan 02