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Resume alert |
Resumes 81 - 90 of 553 |
Long Beach, CA
... HIPPA, PHI, FDA, local, state, and federal regulatory compliant MAB infusion (CDPH) Los Angeles- Pharmacist, EMSA Liaison September 2021- 2023 Administered monoclonal antibodies (MABs) for patients diagnosed with Coronavirus Disease 2019 (COVID-19) ...
- 2023 Feb 16
Rancho Santa Margarita, CA
... Completed remediation as requested by FDA. Worked with the design team for new Mfg. Processes and Design for manufacturability (SOW, DFM). Completed DFMEA, PFMEA and, APQP for new products with the project team. Worked with our suppliers to optimize ...
- 2023 Feb 07
Long Beach, CA
... Negotiate freight rates and contracts Overweight: Frozen/Refrigerated/Fresh: 2010-06 - 2022-05 Education Seafood/Beef/Pork DRY FCL, LTL, CY/SDD, OTR, CROSS-DOCK, DROP/PICK, IN-BOND FTZ, CBP MET/CET EXAMS AIR FDA Coordinator, CCS-Entry Writer, ...
- 2023 Feb 02
Irvine, CA
... • Managed large size FDA regulated database projects for Amgen’s critical patient safety system with Active/Passive Design using Veritas Clustering. • Architected, designed and implemented disaster recovery procedures using Netapp tools for critical ...
- 2023 Jan 27
Anaheim, CA
... • Familiar with FDA regulations, Good Manufacturing Practices (GMP’s) • High degree of mechanical aptitude and aseptic techniques. • Qualified in Gowning Procedures – ISO Class 5 • Receive, review, respond, perform and corrective actions. Huntington ...
- 2023 Jan 27
Anaheim, CA
... In-depth knowledge of FDA and USDA guidelines as well as AIB, GSFI(SQF&BRC), and FSA audit protocols. Areas of Expertise: Process/Program Improvement Staff Training & Supervision Food Packaging Updating Formulas Allergen Control Systems Cost ...
- 2023 Jan 23
Anaheim, CA, 92804
... Understand of a variety of FDA regulatory standards (Label/Document Review, DHF, CAPA, System Validation, 21 CFR 820, 510K submission, ISO 9000's/13485 regulations, specially EU MDR, FDA, GSDM, SDLC, SQA, SOX, PUC) relative to document design ...
- 2023 Jan 09
Fullerton, CA
... revises drawing, design, and assembly to support the build plan while maintaining compliance with ISO 9001, ISO 13485 and FDA Standards for part manufacturing with regulatory requirements, reliability, and support for design compliance. ...
- 2023 Jan 05
Irvine, CA
... QA Remediations Specialist/ Technical Write SOP Revisions - Worked as Author for writing and formatting SOPs for CAPA Remediation’s on change control and engineering design controls, projects to ensure quality meet all FDA regulations/Compliance. ...
- 2022 Dec 09
Santa Ana, CA
... Followed safety rules, manufacturing procedures, company policies and procedures, QSR and FDA regulations. Mechanical Assembler, Rockwell Collins; Irvine, CA - 2005 - Aug. 2011 Built mechanical components by following blueprints and wiring ...
- 2022 Dec 08