- Abbott (Sylmar, CA)
- …Lead data generation, validation protocols, and submission strategies for new FDA 510(k) AI-based SaMD modules. Support international regulatory submissions. + ... least 5 years in healthcare or medical devices. + Proven track record of FDA -cleared AI tools and SaMD development. + Strong understanding of regulatory pathways and… more
- Owens & Minor (Sacramento, CA)
- …**Valid driver's license.** + **Must meet job-related requirements to comply with DOT, FDA and standards of accrediting body.** + **Current MVR must meet company ... **PREFERRED QUALIFICATIONS** **Education and/or Experience** + Knowledge of DOT and FDA regulations + Knowledge of Home Healthcare industry + Two years… more
- Kelly Services (San Marcos, CA)
- …products, finished goods, and environmental samples using compendial methods (USP, AOAC, FDA -BAM) as well as validated in-house protocols + Executing testing for ... year's related experience + Experience with compendial methods (USP, AOAC, FDA -BAM) and in-house validation + Demonstrable proficiency in SOPs, documentation tools,… more
- Stanford Health Care (Palo Alto, CA)
- …Furnishing or Prescribing of Drugs; Formulary Protocol] Medications that are not FDA -approved or are used for a non- FDA -approved indication (off-label use) ... require a patient-specific order in advance from the supervising physician. + After appropriate training, assists the supervising physician in the operating room. The RN First Assistant directly assists the surgeon and practices under the supervision of the… more
- Stryker (San Jose, CA)
- …software lifecycle by implementing software industry best practices and regulatory standards ( FDA , TGA, EUMDR, IT). + Engage in design and development activities for ... or similar, demonstrating strong technical skills + Experience with regulatory agencies ( FDA , MoH, TUV) and medical device regulations (820, IEC 62304/82304, 60601),… more
- PeopleReady (Chatsworth, CA)
- …statement, cooking instructions and regulatory information in compliance with CFR, USDA, FDA and other related laws and regulations + Create product specifications ... market research principles + Must be familiar with CFR 9 and 21, USDA, FDA and other related laws and regulations + Knowledge of organic certifiers, Kosher, gluten… more
- Sutter Health (Sunnyvale, CA)
- …Drug Enforcement Administration (DEA), and the Food and Drug Administration ( FDA ) by monitoring nursing unit inspections; maintaining records for controlled ... Security (DHS), Drug Enforcement Administration (DEA), Food and Drug Administration ( FDA ) and United States Pharmacopeia (USP). **Job Shift:** Days **Schedule:**… more
- Cedars-Sinai (Los Angeles, CA)
- …all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board (IRB). **Primary Duties and Responsibilities** + ... with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. + Maintains research practices using Good… more
- University of Southern California (San Diego, CA)
- …clinical trials + In-depth knowledge of Good Clinical Practices (GCP), ICH, IRB, FDA , & HIPAA guidelines + Experience leading successful teams + Ability to train, ... experience with Good Clinical Practices (GCP), ICH guidelines, and pertinent FDA regulations. Proven ability to interpret and apply all relevant federal,… more
- UCLA Health (Los Angeles, CA)
- …study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). ... to assist with the preparation of clinical trial budgets. + Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for… more