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The Business Affairs HR team seeks an experienced and talented individual to join our team as an Associate Director of Human Resources for our Financial Management Services (FMS) organization.
$165,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Vaxcyte is looking for an energetic and talented individual to join our Quality Control team as an Associate Director. Reports to: Director, Method Transfer and Quality Control.
$197,000 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Associate Director, R&D Quality Business PartnersUnited States – Remote, United States - California - Foster City Clinical Development & Clinical Operations RegularJob DescriptionAt Gilead, we’re creating a healthier world for all people.
$230,230 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Associate Director/Director, Clinical Operations Job Overview We are looking for a talented and highly motivated Clinical Operations professional to join our client's fast-paced biotech startup.
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The Associate Director for Drug Substance (DS) Commercialization of Polysaccharides will lead and facilitate launch readiness and commercial supply of the polysaccharides used in glycoconjugate vaccines.
$197,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The primary reporting relationship for this position is to the Senior Director of HR for Business Affairs (BA), with a matrixed reporting relationship to the Manager of Finance and Administration (FMS.
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Protein Characterization Associate Scientist III will report to Director-level personnel in Assay Development to support Quality Control, Process Development, and other CMC departments.
$138,000 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The capital project director will manage project safety, schedule, quality, cost control, risk, suppliers, and client relations on a day-to-day basis. Windfall’s proprietary microbes are capable of consuming dilute methane from various sources such as landfill gas, coal mine vent gas as well as low-quality concentrated methane streams such as raw biogas from anaerobic digester, vented gas and flared gas from upstream oil well operations, etc.
$215,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Report all concerns of test quality and/or safety to the Laboratory Supervisor, Laboratory Director or Safety Officer. In the case of qualitative and semi-quantitative tests, the unlicensed personnel may add the test reagent to the specimen or vice versa, but the results must be read by the laboratory director or appropriately licensed personnel.
$44.13 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Associate Director of CMC Process Development and Characterization will play a pivotal role in developing and managing process development principles and practices of early- and late-stage cell therapy programs at Orca-Bio. Work will focus on activities to ensure all appropriate process design, process characterization, key quality elements, qualifications and validations are completed for Orcabio’s cell therapy drug products.
$235,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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We are looking for a Senior Manager/Associate Director of Process Engineering (PE) to lead and strategically guide our high-performing Process Engineering team, driving the next level of clinical patient testing within our high-throughput CLIA lab for our groundbreaking oncology tests (level commensurate with experience and strategic acumen.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Associate Director, Regulatory Affairs is expected to bring knowledge of the clinical development process and regulatory requirements, strong project management and vendor management skills, and excellent communication and writing skills to ensure that company submissions meet regulatory and company standards with high quality and within stated timelines.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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The Associate Director of Scientific Communications will play a crucial role in providing expert scientific and medical writing support to Clinical Development and cross-functional teams, including support for NDA/MAA submissions and launch planning.
$212,900 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Cytokinetics is seeking a highly motivated individual to join our team as Associate Director, Quality Systems. Bachelor's degree in a scientific field, with 10+ years experience in a biopharmaceutical, pharmaceutical, biologics, or related life sciences area and relevant Quality Systems experience.
$231,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Significant experience advising business functions in the biopharma industry on GCP quality and compliance requirements, evolving regulations, risk minimization and mitigation, and continuous improvement.
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quality director jobs Title: associate in Foster City, CA
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