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3 or more years industry experience in Laboratory Operations or related function in clinical / commercial biologics, cellular therapy, or gene therapy biotech companies. 3 or more years industry experience in Laboratory Operations or related function in clinical / commercial biologics, cellular therapy, or gene therapy biotech companies.
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Work closely with Global Product Quality, External Manufacturing, and Supply Chain to understand forecasts and deadlines to ensure timely CoA/CoT (Certificate of Analysis/Certificate of Testing) generation for Cell Therapy vector products.
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Assistant QC Scientist is responsible for supporting lab management related activities within the New Brunswick (primary) and Summit (secondary) Biologics Development (Client) methods development department in direct support of clinical method development activities.
$41 - $42 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Expertise in GCP/ICH, drug development process, study design, statistics, clinical operations. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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Partners with Clinical Scientist VP/Head to plan, lead, and advance programs and talent. The Clinical Scientist Program Lead reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs.
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Experience in blood collection, therapeutic and cellular therapies, and infusion. Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the development of clinical strategy and the design of study protocols.
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The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products.
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The Operations Specialist, Scheduling and Cell Logistics will be responsible for monitoring patient treatment schedules for the manufacturing of BMS’s clinical and commercial autologous cellular immunotherapy products.
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Work cross functionally to provide single point of contact for CTL sample management to internal teams and external manufacturing partners, as needed. Conduct weekly meetings with Contract Test Labs (CTL) to provide testing forecast, generate sample submission, provide shipping details to CMO, tract testing status and be point of contact for any test status question in collaboration with ERMs.
$36.75Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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E Excel, QuickBase, Outlook etc.) Required Bachelor's degree in biochemistry, cell biology, microbiology, chemistry, engineering or related areas. This role is accountable for generating CTL sample submission forms, sample shipment tracking, test status oversight and maintaining related daily updates to our internal sample tracker in a timely manner.
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Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP.
$32 - $35.99 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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3+ years of experience in Laboratory Operations or related function in clinical / commercial biologics, cellular therapy, or gene therapy biotech companies. 3+ years of experience in Laboratory Operations or related function in clinical / commercial biologics, cellular therapy, or gene therapy biotech companies.
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