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The Associate Director of Clinical Quality Assurance will be responsible for building the clinical quality assurance processes and providing quality oversight for the clinical programs and CRO throughout the development stages of antibody-based radiopharmaceuticals.
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PRIMARY DUTIES AND RESPONSIBILITIES: Work closely with the Associate Director of Behavioral Health, and the Administrative Assistant/Quality Assurance Specialist to reach all Medi-Cal billing goals and outcomes.
$90,693.72Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Kelly Science & Clinical is looking for an Associate Clinical Supplies Director to work at an innovative biotech company in Alameda, CA. Let us help you grow at work and discover the next step in your career, all while being a vital part of your community.
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The Area Manager works collaboratively with the CMO, Clinic Managers, Associate Medical Directors, staff, leaders and support departments to ensure the successful operation of high quality, efficient clinic administration.
$113,597 - $131,738Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Sr. Manager/Associate Director of Quality Operations is critical in providing Quality oversight of the cell and gene therapy manufacturing facility and ultimately ensuring successful execution and maintenance of the established process and procedures.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Kyverna is recruiting an Associate Director, Quality Assurance in its Technical Operations organization to help advance its mission to free patients from the siege of autoimmune disease.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Associate Director may represent RAMS at multi-agency meetings related to BEST Neighborhoods and will collaborate with DPH-BHS and RAMS leadership to build in successful strategies and frameworks to ensure the goals of the programs are met at the highest quality and level reflective of RAMS standards.
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Nurix Therapeutics seeks an experienced Senior Manager/Associate Director to join the CMC Analytical Development and Quality Control group. The Senior Manager/Associate Director will oversee and execute analytical development, tech transfer, and testing operations internally and at external CDMO/CRO partners, evaluate and implement new analytical and data management technologies, and author relevant sections of regulatory filings.
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The Associate Director will work closely with the Shelter Director regarding operations, supplies, and making sure the shelter is meeting all expectations. The Associate Director will also be responsible for aspects of contract management, scheduling, budgets creation, monitoring, and modifications and support in data tracking and programmatic evaluation.
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The Associate Director, DP Commercial Small Molecule in External Supply Quality organization is responsible for ensuring the commercial small molecule products are manufactured, packed, labelled, stored and transported in a controlled way at CMOs that is in accordance with the regulatory expectations and applicable GMP/GDP quality standards.
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The Associate Director, California Central Valley River Restoration, will help American Rivers develop and implement projects to protect and restore critical rivers and floodplains in the Central Valley to increase resiliency to climate change, support natural biodiversity, increase nature access and flood safety among vulnerable communities, and promote a river stewardship ethic among California decision makers.
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Reporting to the our CMC Executive Director, the Associate Director/Director, CMC Regulatory Technical Writer will be responsible for CMC technical document review and writing, authoring and compiling the CMC sections for global regulatory filings by working closely with the cross-functional teams including CMC, Quality, Clinical and Regulatory Affairs to ensure all CMC technical writing objectives are met.
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This Associate Director Regulatory Affairs – US New Product Introduction and On-Market Changes will work on-site out of our Alameda, CA location in the Diabetes Care Division. 5-7 years’ experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area.
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Works with Chief Dental Officer and Associate Chief Dental Officer to develop a quality assurance program for residency and student externship programs, to insure the quality of care and clinical experiences meet CODA standards.
$179,406.75 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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PNC is looking for an experienced leader ready to help us continue to build our Quality team as an Associate Director of Co-Manufacturing Quality. Strong understanding of Quality and Food Safety principles, process control and statistical analysis.
Full-timeExpandApply NowActive JobUpdated 11 days ago
quality director associate jobs in Oakland, CA
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