- BeOne Medicines (San Mateo, CA)
- …packages throughout the world and ensures timelines are met including the review global submission documents in support of clinical trials and marketing ... 7+ years or PhD/MD/PharmD with 5+ years of experience in the biotechnical or pharmaceutical industry, and 5+ years of experience in a Regulatory capacity with broad… more
- BeOne Medicines (Emeryville, CA)
- …and documents. + Designs and conducts quality issue trending, analysis and review activities to proactively identify broader issues and/or patterns within GCO ... and to relevant leadership. + Ensures provision of actionable data and insights regarding the state of quality and...Degree with minimum of 10 years of experience in pharmaceutical or biotechnology drug development, preferably in a relevant… more
- GRAIL (Menlo Park, CA)
- …sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine's greatest challenges. GRAIL ... United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com… more
- Cordis (Santa Clara, CA)
- …and production teams to establish and maintain quality control procedures. Analyze data to identify areas for improvement and implement corrective actions to enhance ... quality standards and regulations. + Collaborate with cross-functional teams to create, review and approve manufacturing documents. + Conduct root cause analysis and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …on time and follow established policies and procedures. Function as a rebate data subject matter expert to ensure proper data validation, verification of ... advantage whenever practical. * Use statistical methods to gather and analyze data , create reports and recommend potential adjustments based on variance analysis. *… more
- AbbVie (Irvine, CA)
- …launch assessments as well as associated analytics and supporting presentation materials for review with US AA Commercial and Finance as well as AbbVie leadership. ... compliance with legal and corporate guidelines. + Identify key insights from data analysis, highlighting trends, opportunities, and risks. + Develop and drive… more
- ThermoFisher Scientific (Foster City, CA)
- …full-time benefits. This role will be onsite in: Foster City, CA Key responsibilities: + Review raw data + Numerical data verification for regulatory filings ... + Transcribe SOPs + Perform administrative updates + Consolidate data for QC metrics + Author clinical and commercial stability protocols + Evaluates laboratory … more
- Abbott (Sylmar, CA)
- …compliance Review Committee meetings. Provide the tracking and trending data . + Identifies basic legal and regulatory issues and elevates as appropriate. ... remediation plans and corrective actions. + Assists in facilitating the routing for review of new and/or updated divisional policies, procedures and related forms. +… more
- Bio-Techne (San Marcos, CA)
- …Food and Drug Administration (FDA) and industry standards. . Participate in management review meetings and/or prepare information and trending data to be shared ... including new products, Supplier Corrective Action Reports, change notifications, etc. Review SCARs sent back from suppliers to assess corrective actions. Conduct… more
- US Tech Solutions (CA)
- …social media **content creation,** digital storytelling Client Company, the fourth largest pharmaceutical company in the world. We have a duty to provide training ... for collaboration with key stakeholders (AMI Programs team, Brand teams, Internal review team, etc) to **create and design educational materials** for the Medical… more