|
Resume alert |
Resumes 41 - 50 of 723 |
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
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
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
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
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
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
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