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Hands-on experience with method development, validation, and transfer in support of biopharmaceutical and vaccine manufacturing. The Director, Quality Control ensures that activities related to release, stability and in-process testing and method qualifications/validations are completed promptly as in-house and/or at Outside Testing Labs (OTL's) associated with the manufacture of drug substance and drug product for Vaxart's product platform technology.
$240,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Employ hands-on and deep scientific knowledge on biochemistry, biophysics, crystallography, and screening technologies to apply to designing and executing testing funnels that serve several simultaneous drug discovery projects.
$195,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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6+ years of experience in the biopharma or related industry (i.e. investment banking, management consulting, venture capital), with at least 3 years of hands-on business development experience.
$220,000 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Vendor Management Office (VMO) is a critical pillar of the Technology organization, and we are looking for a strong, hands-on leader to drive and cultivate vendor partnerships and oversee WSI’s technology procurement, contracts management, and labor management functions.
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Lead the hands-on configuration in Oracle Cloud Supply Chain, CX, and other modules as necessary working with client stakeholders to ensure configurations are in alignment with business requirements, and ensuring the system is set up for long-term success.
$186,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Technical education and hands-on-experience in some or all of the following disciplines: HVAC design and engineering, electrical design and engineering, plumbing design and engineering, and other building support systems including but not limited to fire/life safety systems and security.
$250,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Liaise with various stakeholder, clients, partners, and funders on relevant data, impact, and performance measurement Experience in data collection, program evaluation and utilizing metrics to inform practice Excellent hands-on problem solving skills & attention to detail Must have excellent verbal and written communication skills, organizational and time management skills, and analytical skills to meet program and contract objectives.
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High level of personal and professional integrity and ethics (authentic, compassionate, genuine and honest); excellent communicator; good listening skills; skilled problem solver and negotiator; hands-on practitioner and strategic thinker.
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Degree in computer science, STEM, or technical field, or hands-on experience with building software or machine learning systems. As a Director of Growth, you will lead initiatives that will power and supply our Gen AI business unit with top-tier contributors, driving millions in weekly revenue for the business.
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Establish rhythm of business (RoB) incorporating process and cadence for OKRs, all hands meetings, leadership meetings, Provide an extra set of hands to help with or lead strategic priorities or special projects as defined by the leadership team.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Hands on keyboard experience buying bidded media and extensive knowledge of auction dynamics; well versed with platforms such as Google Ads, DV360, Meta, Snap, Tik Tok, Pinterest, Yahoo, TheTradeDesk, Beeswax, Amazon Ads, Criteo.
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The Director of Clinical Quality Assurance (CQA) is a hands-on position responsible for ensuring clinical trials adhere to applicable GCP regulations (e.g., FDA, ex-US, country-specific), ICH guidelines, Standard Operating Procedures (SOPs), and current industry standards and practices.
$230,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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This will be hands-on programming for clinical studies for exploratory analyses, regulatory responses, and defense activities. Title: Associate Director of Statistical Programming. My clinical stage biopharma client is seeking an experienced SAS programmer to fill an AD of Statistical programming opening.
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Solid technical expertise in quantitative pharmacology and strong hands-on modeling and simulation experience with Pheonix WinNonlin, R, SimBiology, SimCYP, GastroPlus and/or other modeling and simulation software.
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Strong proven hands-on experiences with GLP, GCP, GPV and GMP compliance matters, and contractor management in the bio/pharma industry. As the Senior Director of Quality Assurance, reporting to the Vice President of Regulatory Affairs and Quality Assurance, you will lead all quality activities supporting Olema's pipeline.
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hands job Title: director in San Francisco, CA
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