- AbbVie (Irvine, CA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. ... Operations, ensure overall timelines for programs. + Responsible for design, analysis , interpretation, and reporting of scientific content of protocols, Investigator… more
- Bristol Myers Squibb (San Diego, CA)
- …clinical development plans + This leader will supervise the development, monitoring, analysis and interpretation of clinical trials and will supervise and have ... accountability for the clinical components of regulatory filings + Will contribute to overall strategy for...documents delegated as needed **Qualifications & Experience** + MD ( PhD or other high level degree optional) **Experience Requirements:**… more
- Cytel (Sacramento, CA)
- …Affairs, including contributing to post approval study designs, study protocol and analysis plan development, reviewing and interpreting the analysis of study ... Value, Evidence & Strategy), Medical Communications and Publications, Epidemiology and Regulatory to design post approval studies. + Writes the statistical sections… more
- The Clorox Company (Pleasanton, CA)
- …chemist with knowledge and experience in analytical problem solving and chemical analysis of a variety of raw materials, intermediates and finished products related ... responsibilities include product and material characterization, method development, data analysis , and providing chemical expertise to develop new products,… more
- Ford Motor Company (Long Beach, CA)
- …management electronics for electric vehicle applications. + Perform complex circuit design analysis , magnetics design analysis , thermal analysis , and control ... circuit schematics and PCB layout. + Perform design failure analysis and support functional safety activities. + Hands-on hardware...with magnetics and filter design. + BS, MS, or PhD in EE. Even better, you may have +… more
- Gilead Sciences, Inc. (Foster City, CA)
- …CROs to assure high quality and timely delivery of written PK reports and regulatory documents (IND, IMPD, IB, BLA) for regulatory submissions. + Supervising of ... Experience OR Masters' Degree and 10 Years' Experience OR PhD and 8 Years' Experience **Preferred Qualifications:** + Requires...with latest advances in DMPK of biologics and PK analysis with a proven track record of sustained external… more
- Merck (South San Francisco, CA)
- …external vendors and partners, creating an aligned, quantitative and model-informed regulatory framework to impact strategies and decisions of drug discovery and ... and interpretation of data. + Maintain a comprehensive understanding of global regulatory expectations and shape, present and defend regulatory documents and… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …downstream process technology transfers to CDMOs, including documentation review, gap analysis , and risk assessment. + Provide expert technical oversight of ... review technical reports, protocols, risk assessments, and relevant sections of regulatory submissions (IND, BLA, MAA, etc.) related to downstream processing. +… more
- J&J Family of Companies (Santa Clara, CA)
- …optimize tools, software, and other technologies to support acoustic testing and analysis + Simulate acoustic propagation field and energy distribution + Prototype ... hydrophones, high speed cameras, and other equipment + Perform data processing and analysis to generate reports and presentations for all levels of management +… more
- General Atomics (Poway, CA)
- …Such methods should be based on standards and on rigorous statistical analysis , ideally involving UQ (uncertainty quantification) methods. + Help develop tools for ... **Job Qualifications:** + Typically requires a bachelors degree, masters degree or PhD in engineering or a related technical discipline from an accredited… more