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A minimum of 5 years of experience in project management, preferably gained at a life sciences company focused on novel excipient, drug substance and/or drug product development.
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Experience with PAS X (Korber) software for electronic batch records with detailed understanding of editing and validationStrong knowledge of PAS-X integration with external programs (SAP, PI, and DeltaV)Strong operations knowledge of drug substance manufacturing and a broad understanding of related disciplinary areas in bioprocessingDemonstrated ability to work in a teamDegree in Chemical Engineering, Biochemistry, Chemistry or Biology or Computer Science with experience in biotechnology.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Trusted products that accelerate drug discovery, development, and delivery to save lives. Health and well-being benefits include medical, dental, vision, paid parental leave, mental health/substance use, fitness, and disease management programs.
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The Downstream (purification) Process Science team is a group of Scientists and Subject Matter Experts who specialize in the development, optimization, remediation, and transfer of the production processes used in cGMP commercial manufacturing of drug substance.
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The primary roles of this position are to lead drug substance Upstream process development and optimization studies for natural and recombinant proteins (including neurotoxins) from bacterial cultures during discovery and process development.
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We maintain a drug-free workplace and perform pre-employment substance abuse testing. Eight-ten years' design and programming experience in Oracle, SQL, Forms/Reports, and Linux, Unix, and Web development environments.
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Kelly Scientific is working with an established producer of high quality and revolutionary lipid products used in pharma drug delivery. Degree/MSc qualified in a technical discipline (Chemistry, Biology, Chemical Engineering etc.
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Designing, performing, and/or overseeing the execution of stability studies of critical materials, intermediates, drug substance and drug product related to the company’s AAV gene therapy and RNA PMO product pipelines.
$180,000 - $225,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our Thousand Oaks facility. The Engineer will apply purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using single-use technology.
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In this vital role you will lead a Downstream Process engineering team at our Rhode Island Site. The Senior Manager will lead a team focused on bioprocess purification processes, drug substance manufacturing support and technology transfer of new products into the facilities.
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Ensure that CRO/CMO activities and other process development activities address drug substance needs for pharmaceutical formulation development, toxicology testing, clinical trials, and commercial launch.
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The Process Development Associate will help design and perform experiments at the bench scale that span the end-to-end Drug Substance process, covering cell culture and/or purification operations.
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The Senior Director of Addictions Services will provide operational leadership, direction, and development of clinical functions, programs, and services in the areas of substance use and addictions while advancing and supporting Aspire’s Mission, vision, values, and strategic priorities.
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Drug Enforcement Agency Controlled Substance Registration including schedules: 2, 2N, 3, 3N, 4, 5. The Psychiatrist assists the Director of Behavioral Health in the development of strategic plans and initiatives related to the residency program.
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Direct the planning and implementation of process development, scale-up, technology transfer, and validation efforts in drug substance manufacturing, ensuring strategic alignment and operational excellence.
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