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Based near Washington DC, our client is dedicated to producing high-quality pharmaceutical and bioscience products. 1-3 years of Pharmaceutical/Bioscience or regulated manufacturing environment experience.
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BS in a bioscience, pharmaceutical science, engineering (mechanical, biomedical, chemical) discipline with 15 years of experience or MS with 12 years. BS in a bioscience, pharmaceutical science, engineering (mechanical, biomedical, chemical) discipline with 15 years of experience or MS with 12 years.
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The Senior Director of Pharmaceutical Manufacturing supervises the manufacture of Heparin Sodium Active Pharmaceutical Ingredients (API) and other pharmaceutical products at our Smithfield BioScience manufacturing site in Cincinnati, Ohio. The successful candidate will provide overall technical leadership to the manufacturing team, while promoting operational excellence, employee development and continuous process improvement.
$152,000 - $228,125 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience: 2-4 years in the Pharmaceutical or Biotechnology with emphasis in aseptic processing, QC microbiology, environmental monitoring, water system, quality control, validation and manufacturing processes.
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Synergy Bioscience is a CRO providing pharmaceutical product development support, analytical chemistry, and microbiology testing services to different industry sectors. Previous experience in pharmaceutical quality systems functions.
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Experience in a pharmaceutical, medical device, bioscience, or other FDregulated environment required." Quality Inspector reports into the Quality Inspection team within the broader Quality Operations department.
$24 - $28 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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At least four (4) years work experience required in Production/Supply Planning/Inventory management preferably in a Biological or Pharmaceutical Environment. Our four divisions Bioscience, Diagnostic, Hospital and Bio Supplies develop, produce and market innovative medicines, solutions and services in more than 100 countries and regions.
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Bachelor's degree in a scientific discipline such as life sciences, pharmacy, bioscience; advanced degree preferred. 5+ years of experience in regulatory affairs within the pharmaceutical or biotech industry, with a focus on quality-of-life products preferred.
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Join our bioscience client's team in Millburn, NJ, as a Life Sciences Account Coordinator, where you'll support both large and small pharmaceutical and biotech clients in developing targeted therapeutics.
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Please be aware this is not a remote position and QA Software/Tech experience is not applicable to this position* We are seeking a dynamic and experienced Quality Assurance Specialist to join our team at our Dallas, Texas facility.
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Develop a detailed understanding and strong application knowledge of the Thermo Fisher Scientific Nicolet FTIR product line, including the theory and operation of FTIR spectrometer and IR Microscope and their applications in material science research, industrial, pharmaceutical, environmental and bioscience.
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Bachelor's degree in a relevant scientific or engineering discipline (e.g., biotechnology, life sciences, chemical engineering) from an accredited four-year college or university and 5+ plus years of relevant experience in quality management in biotech or pharmaceutical industry.
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R&D Partners is seeking to hire aScientist Bioscience in Gaithersburg, MD.Your main responsibilities as a Scientist Bioscience:As a Scientist you will have a unique opportunity to contribute to the success of Bioscience Immunology drug discovery pipeline.
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FTIR Spectroscopy instruments provide scientific insights across a wide variety of applications including pharmaceutical and industrial QA/QC, contaminant analysis, forensic investigation of toxicological substances and trace materials and industrial chemical/polymer analysis.
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Ability to lift, tug, pull up to fifteen (15) pounds. The Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior Director in overseeing regulatory activities related to QOL initiatives.
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