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Experience must include 6 months in each of the following: mechanical engineering; MES; 5S; Kaizen; Six Sigma; Quality Tools; Lean manufacturing; VSM; PFMEA; and Computer-Aided Design (CAD) software.
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ProSidian clients represent a broad spectrum of industries to include but are not limited to Energy, Manufacturing, Chemical, Retail, Healthcare, Telecommunications, Hospitality, Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government Agencies.
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Lead early stage pipeline programs, including process development, scale-up, toxicology material production, technology transfer, clinical material manufacturing support, analytics, formulations and IND submissions, to support development of molecules leading to commercialization.
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Serve as bioprocess SME that provides technical oversight in support of IND filling and to ensure that clinical manufacturing is successfully executed per schedule. Independently author technical reports of studies, protocols, SOP and risk assessments to enable technology transfer, manufacturing and IND activities.
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Standard Solar, a Brookfield Renewable Company, is a leading independent power producer focused on acquiring, developing, funding and operating DG-scale solar energy and storage projects throughout the US. We are looking to expand our in-house legal department with an attorney who has direct experience with preparing and negotiating agreements for the acquisition and development of DG-scale solar energy and storage projects.
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Our research groups focus on human genomic medicine, infectious disease, plant, microbial and environmental genomics, synthetic biology and biological energy, bioinformatics, and software engineering.
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5 years of work experience in private equity, investment banking, management consulting, or the power/energy/infrastructure sectors. Contribute and develop to team's views on deep decarbonization, energy markets & public policy debates, capital allocation, and strategic partnerships.
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JOB OVERVIEW Provide services and support as a Cost Reimbursement (eLearning Developer) in the Energy, Resources, And Industrials Industry Sector focusing on Human Capital Solutions for clients such as The Department of Energy ( DOE | OC - EHSS) | Office of Classification (OC) | Office of Environment, Health, Safety, and Security (EHSS) Located In Washington, DC and across the Mid Atlantic Region.
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Proficiency in multiple technical disciplines, including DevOps, DevSecOps, cloud services, IT infrastructure, cyber security, networking, data management, storage, and XaaS. GDIT is seeking a Technical Program Manager to support the National Institute of Health (NIH) National Institutes of Allergies and Infectious Diseases (NIAID) program.
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Serves on team projects (i.e. qualifications, investigation) in the role of testing support and initiation of investigationResponsible for completing laboratory housekeeping to ensure safety and complianceIdentifies areas for improvement or gaps in both safety and compliance (ZAPs/ZIPs)Effectively communicates issues/hurdles to supervisor and/or managerSupports GSK site initiatives and departmental goalsJob requires gowning into GMP manufacturing spaces to collect samples.
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Familiarity with cloud computing services (AWS, Azure, Google Cloud) for data storage, processing, and analytics solutions. Knowledge of natural language processing (NLP) techniques for mining insights from scientific literature, patents, and lab notes.
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This position is responsible for directing all aspects of CMC (Chemistry, Manufacturing and Controls) for pharmaceutical drugs and agents as well as the analytical work associated with that CMC across all of the small molecule projects within Pharma Cinq and, potentially, gene therapy projects.
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The work will entail: The candidate will join a multi-disciplinary team of scientists working to advance the current state-of-the-art in nanocalorimetry-based measurements and expand the technique's applicability to monitoring of semiconductor manufacturing processes.
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Strong understanding of quality systems, validation processes, and risk management in a pharmaceutical manufacturing environment. Ensure effective Document Control and Change Control processes, including review and approval of all relevant documents such as manufacturing batch records, SOPs, protocols, and quality policies.
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Strong technical knowledge of the following: mechanical, electrical, plumbing, HVAC, safety systems, civil, low voltage, demolition, architectural and energy management; Certified Healthcare Facilities Manager (CHFM) is a plus; and.
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