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This client is a growing international full-service CDMO/CRO within the biotechnology space looking to aggressively expand its footprint in the US. The company has a strong base of API/Small Molecule, Biologics, Clinical Research, Bioanalytical Sciences, DMPK, Cell and Gene Therapy and other capability centers across the US. This business has developed a fantastic brand in the US through exceptional service which drives repeat business.
$200,000 a yearRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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In this vital role you will support Formulation & Drug Product Development at Amgen's site in Rockville, MD. This group is responsible for drug product formulation and process development for biologics in Amgens Rare Disease Business Unit. Working closely with a team of scientists and engineers, the successful candidate will apply scientific and engineering principles to advance the technical aspects of Amgens drug product and process development.
$129,162 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Qualifications & Experience: - in Chemical/Biochemical Engineering, Biotechnology, Biochemistry, or related biologics fields with - years of industry experience is required - Prior hands-on experience with downstream process development, including preparative chromatography, ultrafiltration/diafiltration, viral inactivation, viral filtration and high throughput robotic platforms is desired.
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BS, MS, or PhD in Biology, Biotechnology, Biopharmaceutical sciences or similar life science discipline, along with significant industry experience leading Tech Transfer projects for Biopharmaceutical or Cell Therapy manufacturing processes.
$200,000 a yearFull-timeExpandUpdated 22 days ago - UpvoteDownvoteShare Job
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Proven practical experience using chromatography HPLC methods (including RP, SEC, IEX for biologics process development, electrophoresis, sensor-based technologies other related techniques. Key Words Innovation, Research, Biopharma, Biotechnology, NIIMBL, University of Delaware, Entrepreneurial, Bioprocess, Biopharmaceuticals Share this job on your Social Network.
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BS or MS degreein biology, bioengineering, or related scientific field with relevant experience of 4+ years for BS & 2+ years for MS in a biotechnology, cell therapy or pharmaceutical industry.
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Senior Account Executive-CDMO Large Molecule (Antibodies, Proteins, Gene Therapy, Biologics, etc) As a Large Molecule Senior Account Executive, you will be responsible for driving revenue growth for large molecule products (e.g. antibodies, proteins, gene therapy, biologics) within the life sciences industry.
Full-timeRemoteExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Sr. Director - Executive Director, Biologics CMC Project Management & Operations coordinates phase appropriate biopharmaceutical development and clinical manufacturing activities for the Biologics portfolio.
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Bachelor's Degree in Sciences or related field and 8+ years', MS with 6+ years, PhD with 3+ years, or HS with 10+ years' experience in Quality Assurance, Quality Control, or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility or an AA Degree and 9+ years' experience in Quality Assurance, Quality Control, or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility.
$140,079 a yearFull-timeExpandUpdated 29 days ago - UpvoteDownvoteShare Job
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The ideal candidate should have a strong background in Regulatory Affairs CMC in a global pharmaceutical and/or biotechnology company with expertise in biologics, deep experience in product development and understanding of US, international regulations, and ICH guidelines related to biologics and cell therapy development.
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Experience in technical development of cell and gene therapy or biologics in early and late-stage developmentHands-on experience in cell and gene therapy, specifically in T cells is highly desirable.
$157,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Bachelor’s Degree and 5+ years’ experience in Quality Assurance or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility. Bachelor’s Degree and 5+ years’ experience in Quality Assurance or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility.
$55 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Lilly’s Biotechnology Discovery Research (BioTDR) organization has a track record for delivering novel biotherapeutic medicines to advance into clinical research in key areas of unmet medical need including diabetes, oncology, immunology, neuroscience, and others.
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Bachelor’s or master’s degree in biotechnology, biology, biomedical engineering, or equivalent. Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity for a top performing operational professional looking to join and contribute to a commercial stage company with an established portfolio of unique advanced cell therapies and specialty biologics.
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10+ years of experience in the pharmaceutical/biotechnology industry, 7 of which are in CMC Regulatory Affairs. Responsible for the development of US and global CMC regulatory strategy, identifying key regulatory issues, deliverables, and remediation activities needed throughout the product/project lifecycle for Drug and Biologics products.
$275,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
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