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This position requires technical expertise in upstream and downstream process of biologics (Cytokines, monoclonal antibodies manufacturing). Documentation includes reviewing executed batch records (both Upstream department and Downstream batch record.
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Protein Biologics Development experience with proteins refolded from E. coli and proteins expressed in CHO cells with oversight of process development for both upstream and downstream. Experience with Tech transfer to CDMO for non-GMP and GMP manufacturing, including cell line development, process development, analytical method development and manufacturing scale up.
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To help us meet our mission LOTTE BIOLOGICS is in need of a Scientist, Manufacturing Technology to support upstream cell culture and downstream purification commercial manufacture of biopharmaceutical drug substance produced at the LOTTE BIOLOGICS Syracuse facility.
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BPR&D includes three lab-facing technical functional areas: Process Cell Sciences (PCS), Upstream and Downstream Process Development & Engineering. Biologics Process R&D Associate Scientist.
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Leading biologics downstream process development to design and conduct studies to deliver high process yield, robust, and scalable processes to support GMP manufacturing of biotherapeutics.
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As Manufacturing Engineer, you will support operational activities in Downstream of Antibody Drug Conjugate manufacturing, e.g., tech transfer support, material planning, document and batch record preparation, training and troubleshooting, deviation handling.
$76,000 - $113,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Subject Matter Expert of biopharmaceutical manufacturing practices, as well as a high technical knowledge of biologics principles required. Executes and coordinates unit operations in Downstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility.
$58,000 - $107,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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10+ years experience in biologics process development and a strong working knowledge of antibody processing, including upstream and downstream processes. Ensure development of phase-appropriate drug substance processes for portfolio of bispecific antibodies and cytokine fusion molecules, including cell banking, upstream cell culture, and downstream purification.
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The successful candidate will have strong technical, scientific, management and leadership skills, experience in process development through commercialization of biologics, process technology transfer, project management and the ability to influence across functions.
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1-5 years of experience with biologics and/or cell & gene therapy downstream process development. Experience in viral vector purification is a plus but not a requirement since purification techniques from biologics are transferrable.
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Since integrating into Lundbeck in October 2019, Lu-SBP has supported commercial launch of Lundbeck's first biologic product (Vyepti) and advancement of a growing biologics pipeline in collaboration with our Copenhagen-based Process Science & Validation Team. The Lu-SBP team leads and supports the development of new product candidates from cell line development through commercial validation of Drug Substance and Drug Product manufacturing processes.
$20 - $22 an hourInternExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Responsible for manufacture of biologics products performing activities within production facilities to support the manufacture of downstream operations according to current Good Manufacturing Practices.
$20 - $27 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Just - Evotec Biologics' Bioreactor Process Development group is seeking an enthusiastic and hardworking team member who is passionate about expanding worldwide access to biotherapeutics through the advancement of continuous bioprocessing technology and mammalian cell culture processes.
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The Senior Biologics Engineer II (Drug Substance) role is focused on commercial manufacture technical oversight. The individual will serve as a key subject matter expert (downstream) for commercial manufacture oversight, process monitoring, capital improvements, risk assessments, and process validation where applicable.
$154,020 - $199,320Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API.
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