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Experience working with common clinical systems critical to the pharmaceutical industry, such as Electronic Health Records (EHRs), Clinical Trial Management Systems (CTMS), Electronic Data Capture Systems (EDC), and Laboratory Information Management Systems (LIMS.
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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.
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PhD in Biochemistry, Chemistry, Chemical Engineering, Pharmaceutical Sciences, life sciences or equivalent amount of experience and a minimum of 15 years of biotech industrial experience working with cell culture, purification, analytical, and/or formulation development.
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We are seeking a Facilities Engineer to support the Pilot Bioproduction Facility (PBF) at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland. Support the operation of key facility utilities, such as WFI and Pure Steam Generation Systems, Water Distribution Systems, Process Gas Distribution, and other supporting utilities.
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Communicate frequently with other Virtual Respiratory Specialists, Virtual Respiratory Representatives, the Associate Director, Virtual Sales, and Respiratory Sales Specialists across the country to create alignment of business plans, focus on strategic drivers, and share best practices.
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Experience with pharmaceutical drug development and Medical/Scientific Affairs. Thorough 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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Job Title: QA/QC Analyst Company : AstraZeneca Overview : The QA/QC Analyst at AstraZeneca is likely responsible for ensuring the quality and compliance of products and processes within the company's pharmaceutical manufacturing or research facilities.
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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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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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Previous exposure to and understanding of the tenets of qualitative and mixed methods research Strong knowledge of HEOR, pharmaceutical industry, health policy, and payer value assessment and HTA evidence requirements in the US and globally.
$192,000 - $270,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Pharmaceutical, Biotech, Nutraceutical, or Life Science industry experience. At IPS, youll apply your knowledge, skills, and passion to make a difference in the lives of people, solving complex challenges related to pharmaceutical, biotech, and animal health research and manufacturing facilities.
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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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Our client, a world-leading Pharmaceutical Company in Rockville, MD is currently looking for a Senior Associate Scientist / Cancer Research / Pharma Industry to join their expanding team.
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6+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation. 6+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation.
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Detailed understanding of drug development and pharmaceutical market support and in-depth knowledge of Hematology/Oncology (clinical evidence and real-world patient management) Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be.
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pharmaceutical job Title: associate director Company: Amerisourcebergen in Rockville, MD
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