- Gilead Sciences, Inc. (Foster City, CA)
- …these. + Thorough knowledge of Food & Drug Administration (FDA), European Medicines Agency (EMA), and other applicable national regulations, International Council ... for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines and Good Clinical Practice (GCP) governing the conduct of clinical studies. + Familiar with standard medical / scientific terminology. + Ability to communicate in a… more
- Warner Bros. Discovery (San Francisco, CA)
- …out globally across Latin America and the Caribbean in 2021, followed by its first European launches in the Nordics and Spain later that year. In May 2023, Warner ... Bros. Discovery introduced Max, an enhanced streaming platform, in the US HBO Max is currently available in 46 countries and there are plans for the continued global expansion of Max in 2024. **Senior MLE, Personalization, Content Discovery** Every great story… more
- J&J Family of Companies (Santa Clara, CA)
- …IEC62304), regulations (eg 21 CFR Part 820, 21 CFR Part 11, European Medical Device Regulation (MDR), and applicable guidance. + Provide Quality representation ... during software problem resolution. + Participate in technical design reviews and project phase reviews. + Function as the quality expert in software risk management processes throughout the entire software lifecycle. + Provide leadership and strategic… more
- Howmet Aerospace (Torrance, CA)
- …customers in North America, South America, Latin America, Japan, and certain European accounts. + Supervise and manage Customer Support Representative, meet with ... Customer Support Representatives to review employee and department issues, conduct Employee Performance Reviews and Goal Setting. + Support Business Process updates/changes for Howmet Business Systems relating to Customer Support. + Coordinate with Site… more
- Danaher Corporation (Sunnyvale, CA)
- …and standards including compliance with Food & Drug Administration (FDA), ISO 13485, European Union In Vitro Diagnostic Regulation (IVDR) as well as other applicable ... global regulatory requirements, including Medical Device Single Audit Program (MDSAP) participating regulatory authorities + Provide cross-functional compliance support for global QMS and Intracompany Quality Agreement requirements. Function as SME for… more
- Sysco (Irvine, CA)
- …hygiene, and SQF (Safe Quality Food) policies and procedures as described in the European Imports - Sysco Food Safety Training Manual. + Perform other duties as ... assigned. **QUALIFICATIONS** **Minimum Requirements** + Must be at least 18 years of age. + 0 - 1 Year relevant work experience. + Frequently lift product that weighs 10lb - 75lbs and up to 100lbs. + Frequently reach up to 72 inches. + Constantly bend and… more
- Sumitomo Pharma (Sacramento, CA)
- …Locally approved labels such as, United States Prescribing Information (USPI), European Summary of Product Characteristics (SmPC), and Canadian Product Monograph ... (PM) + Ensures timely and quality review and assessment of ICSRs, including seriousness, expectedness, safety narratives, adverse event coding, concomitant medication coding, and causality statements. + Contributes to Risk Management Plans (RMPs)/Risk… more
- Meta (San Francisco, CA)
- …regarding data disclosure and content moderation, including familiarity with the European General Data Protection Regulation 23. Criminal and civil litigation ... experience **Public Compensation:** $198,000/year to $266,000/year + bonus + equity + benefits **Industry:** Internet **Equal Opportunity:** Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon… more
- Gilead Sciences, Inc. (Foster City, CA)
- …priorities + Complete knowledge of Food & Drug Administration (FDA), European Medicines Agency (EMA), and other applicable national regulations, International ... Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, Good Clinical Practice (GCP) and key Clinical Operations principles, concepts, practices, standards, processes and tools. + Familiar with standard medical /… more
- NVIDIA (Santa Clara, CA)
- …create will need to follow SI constraints, EMI/RFI control and FCC, UL and European regulations, IPC specifications and NRC regulations. What We Need to See: + Hold ... a BSEE or Computer Sciences degree (or equivalent experience) with at least 12 plus years industry experience. If you have experience in high-speed PCB design, this is a plus. + Knowledge of PCB design and consideration for layout, routing, and timing… more
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