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Resume alert |
Resumes 11 - 20 of 544 |
Oakland, CA
... As a Software Verification Tester, I performed 100+ software verification protocols and detailed data analysis to provide data for FDA premarket approval submission and enable use of Class II endometrial ablation device in the clinic. Worked cross ...
- Feb 17
San Francisco, CA
... • Worked in conjunction with the FDA to have a massive mobile device management project get approved for government clinical trials with success. • Saved the company hundreds of thousands of dollars a year by keeping a keen eye on asset management, ...
- Feb 15
San Francisco, CA, 94114
... Extensive experience with managing effective Electronic Quality Management System (eQMS) fulfilling responsibilities based on Quality System Regulation (QSR), ISO 13485:2016, ISO 9001:2015 and FDA Regulations within Medical Device and Pharmaceutical ...
- Feb 09
San Francisco, CA
... • Implemented a chatbot powered by OpenAI and trained on FDA drug data, shaped by insights from user surveys, to provide safe drug suggestions, boosting customer engagement. Graduate Assistant - School of Nursing, SFSU Sep 2023 – Present • ...
- Feb 08
Hayward, CA
... Experience in administrating data rules and applications governed under regulatory compliance such as HIPAA, ISO, FDA, SOX, ITAR, EAR, DFAR, and FAR regulations. PROFESSIONAL EXPERIENCE: Data Governance Lead Solo Workforce Consulting 6-2023 -10-2023 ...
- Feb 08
Oakland, CA
... *QI: Verify material's are labled according to build of materials and component formulation (FDA Approved). * Collect and delivery all product at the component level * Complete Documentaion of product that is placed into inventory for back-fill for ...
- Jan 25
Hayward, CA
Arnold Blanco ad2wjc@r.postjobfree.com • 510-***-**** Senior Technician Technician with 20+ years’ experience in a manufacturing environment with 4 years in Quality Assurance and an extensive background in cGMP, FDA, ISO, Clean Room, and ITAR ...
- Jan 18
San Francisco, CA, 94102
... ●Understanding of Drug Safety Surveillance and the FDA Adverse Event Reporting System (FAERS). ●Experienced in adverse event reporting using the voluntary MedWatch 3500 (for HCP and consumer) and MedWatch 3500 B (consumer-friendly version of 3500) ...
- 2023 Dec 30
Redwood City, CA
... ●Performed Peptide Mapping, Carbohydrate testing with the FDA-approved products. ●Reviewed the testing records in the QC lab for the release of products including small and large molecules. ●Expert in QC investigation for OOS testing. Expert in QC ...
- 2023 Dec 27
San Rafael, CA
... I have a proven track record with FDA and International Regulatory agencies and excellent knowledge of FDA, ICH, GCP Guidelines; Expert at clinical research design and methodology --- Blue Water Counseling Port Huron, MI 48060, 5/2023 -current ...
- 2023 Dec 22