- Gilead Sciences, Inc. (Foster City, CA)
- …Description** The Associate Director - QA Compliance , will report to the Director of Supplier Management and Auditing. This key position will conduct GMP ... excellent verbal, written, and interpersonal skills. + Demonstrates a thorough knowledge of compliance requirements, and an understanding of current… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …disciplines strongly preferred) + 4+ years of experience in promotional compliance and product labeling in the pharmaceutical industry + Advanced Degree ... Must demonstrate a high level of understanding of regulations related to promotion compliance . May... of the product labeling + Fundamental understanding of the pharmaceutical industry drug development process… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Quality deliverables for various integrations. + Develop and maintain metrics to monitor compliance of integration activities and completion of deliverables. ... Management System (QMS): 1) drive intelligence change management activities, ie implementation of new legislation to ensure proactive compliance , and 2) serve… more
- Gilead Sciences, Inc. (Foster City, CA)
- …international finance teams and business partners. The **Associate Director , SOX Compliance and Controls** key area of responsibility include: design of ... their aspirations. Join Gilead and help create possible, together. **Job Description** The SOX Compliance team is part of the Controllership group at Gilead and… more
- Stanford Health Care (Palo Alto, CA)
- …operations. **This is a Stanford Health Care job.** **A Brief Overview** The Director of Pharmacy Supply Chain, including Purchasing, Inventory Management, and ... Supply Chain Management* Provide daily leadership for all levels of pharmaceutical procurement and purchasing to ensure...departmental policies and procedures for pharmacy personnel and ensure compliance .* Knowledge of and adherence to all… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …8+ years of quality and enterprise risk management within the pharmaceutical or biopharmaceutical industry OR + Master's degree in a scientific discipline (eg, ... 10+ years of quality and enterprise risk management within the pharmaceutical or biopharmaceutical industry OR + Bachelor's degree in a scientific discipline… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …gene therapy product manufacturing. This role ensures the safety, quality, and compliance of our products and processes through the development, implementation, ... create more tomorrows. **Job Description** We are seeking a Director for Sterility Assurance role. This is a critical...of experience in a microbiology/virology role within the pharmaceutical or biotechnology industry, with a focus on sterile… more
- Gilead Sciences, Inc. (Oceanside, CA)
- …cell and gene therapy product manufacturing network. This role ensures the quality, compliance , and effectiveness of our operations through the management of ... years of progressive experience in Quality Assurance within the pharmaceutical or biotechnology industry, with a significant focus on quality systems management… more
- Charles River Laboratories (Northridge, CA)
- …SME for Technical Operations, the Director is responsible for ensuring compliance of all technical operations with applicable Standard Operating Procedures ... areas of donor operations and donor recruitment) * Establishes with the guidance of the CS Medical Director (s) the Donor Center operations best practices and… more
- University of Southern California (Los Angeles, CA)
- …and gene therapies and other biological products for internal/external users. The Associate Director of Process Development (cGMP) is responsible for all aspects ... cGMP Associate Director , Process DevelopmentApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/cGMP-Associate- Director --Process-Development\_REQ20159691-1/apply) Keck School of Medicine Los… more