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PharmD or PhD in the STEM disciplines: bioinformatics, Public Health, Pharmacology, Toxicology, Biology, Biomedical Engineer, biology, biostatistics, epidemiology, health informatics, or pharmaceutical science.
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Performs duties as assigned by Pharmacy Manager, Staff Pharmacist and Store Manager including utilizing pharmacy systems to enter patient and drug information, ensuring information is entered correctly, filling prescriptions by retrieving, counting and pouring pharmaceutical drugs, verifying medicine is correct, and checking for possible interactions.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Office of Testing and Research (OTR) conducts laboratory research on manufacturing, formulation, and characterization of drugs, and provides advice/consults, collaborative research opportunities, and scientific training to FDA staff on pharmaceutical quality, pharmaceutical equivalency, and bioavailability/bioequivalence issues including manufacturing, formulation, analytical testing, and modeling.
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This early stage health tech SaaS startup has proven their product's value to improve efficient work between healthcare providers, insurance providers, pharmaceutical providers, and clinical quality assurance.
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Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:BSc in Scientific Discipline Minimum 5 years' demonstrated experience in the Pharmaceutical Industry in leading the technical aspects of the product lifecycle, including technical risk assessments, product control strategies, bench, pilot & commercial scale validation studies, QbD, PPQ, CPV and change control.
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A minimum of 5 years' recent experience in publishing/Regulatory Operations in the biotechnology or pharmaceutical industries. Under this Task Order, the Contractor(s) shall provide services in support of the overall functions of the Office of Regulatory Support (ORS), Vaccine Research Center (VRC), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Department of Health and Human Services (DHHS.
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QC Microbiologist needed for a contract opportunity with Yoh Scientific’s client located in Rockville, MD. This position is for a pharmaceutical company and is seeking an Expert Scientist in Quality Control Microbiology with experience or specialty in endotoxin detection methods.
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A minimum of 10 years of experience in a GMP-related industry with at least 7 years of experience in GMP quality assurance in the pharmaceutical or medical device industry. Demonstrate a solid understanding of pharmaceutical and medical device manufacturing - process, analytical operations, quality systems, and regulations.
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Master’s degree preferred (2) Minimum of 5 years of experience in the pharmaceutical, vaccine, biologics, or similar industry (3) Minimum of 3 years of experience in R&D, product development, or GMP manufacturing.
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We provide biomanufacturing strategy and execution to start up and established gene and cell therapy, pharmaceutical, and biotechnology companies. Experience with Smartsheet's, Microsoft Projects, and/or Primavera highly preferred.
$61,000 - $65,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Minimum of 1 year experience, preferably in the pharmaceutical industry, graduate degree strongly preferred (PhD, MS, MPH) in health economics, epidemiology, outcomes research and/or related fields.
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Expand the Mid Atlantic (D.C., DE, MD, NJ, PA, VA) client base, including pharmaceutical, biotech, healthcare, higher education institutions, manufacturing, and/or construction industry sectors.
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PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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The scope of required regulatory knowledge includes pharmacy, drug distribution, pharmaceutical manufacturing, and 340B. This position will be engaged in various compliance efforts, acting as a subject matter expert to support business partners and will need to work with a high degree of independence.
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Experience with pharmaceutical drug development and Medical/Scientific Affairs. Detailed understanding of drug development and pharmaceutical market support and in-depth knowledge of Hematology/Oncology (clinical evidence and real-world patient management.
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pharmaceutical job in Rockville, MD
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