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PCI is proud to serve pharmaceutical, biotechnology, medical device, and clinical research industries nationwide by providing calibration, commissioning and consulting solutions. We are seeking a Calibration Technician II that can perform calibrations onsite at our client pharmaceutical facilities in Boston, MA and other sites in the area if needed.
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Knowledge of relevant anatomy and physiology, medical terminology, microbiology and pharmacology to ensure that optimal patient care is provided. Comprised of Tufts Medical Center, Lowell General Hospital, MelroseWakefield Hospital, Lawrence Memorial Hospital of Medford, Care at Home - an expansive home care network, and large integrated physician network.
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Delivery of specimens to labs (i.e. microbiology, cytology, pathology, etc. Operating Room Assistant - 40 hour Evening - BWH Operating Room. The Operating Room Assistant works under the direct supervision of the Supervisor of PCA. The ORA is responsible for transporting patients, cleaning O.R.s, maintaining a clean environment, moving equipment, delivery of specimens, second scrubbing PRN, and other duties as assigned.
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Contribute to overall functional direction globally and represent function within CMC/Pharmaceutical Science and across the global Takeda organization. Minimum of 10 years of experience working in CMC analytical development area for active pharmaceutical ingredients and drug products under cGMP’s.
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Demonstrated knowledge in the following scientific fields: organic chemistry, synthetic chemistry, medicinal chemistry, and pharmaceutical sciences. Demonstrated knowledge in the following scientific fields: organic chemistry, synthetic chemistry, medicinal chemistry, and pharmaceutical sciences.
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Bachelor’s degree in technical discipline (Biology/Chemistry/Microbiology/Engineering or related field) with 0-2 years of experience in a GMP Quality Control microbiology lab setting. This role will help establish the microbiology function at Elevatebio, including but not limited to; laboratory/clean room start-up and qualification, development of the environmental monitoring program and contamination and control strategies, and execution of routine QC microbiology assays.
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Catalent Pharma Solutions is hiring a Product Development Engineer II is to actively participate in the development of pharmaceutical processes, technology transfers, and scale-up of spray-drying, particle size reduction, blending and capsule filling unit operations.
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A Doctoral Degree in biochemistry, molecular biology or related field with a minimum of eight years of experience in the biotechnology/pharmaceutical industry and/or an academic setting (industry experience is preferred.
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Ph. D. in Pharmaceutical Science and 15+ years of experience in the pharmaceutical industry in roles of increasing responsibility, or equivalent in Chemistry or Biological science with drug or radiopharmaceutical agent development.
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Experience with pharmaceutical data sources (e.g., IQVIA or Symphony claims, specialty pharmacy data, and Syndicated data sources); Deep understanding across various pharmaceutical data facets/processes, including data creation and acquisition, management, governance, data quality, integration, visualization and statistical modelling.
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Requirements: BS. Food Safety, Microbiology, Chemistry, Food Science degree or related degree. If you are interested or know of someone that would be a great match, please send a MS Word resume to John Marino at John@SourceRecruitmentSolutions.com Source Recruitment Solutions, LLC. Or apply now online by directly clicking the “ APPLY NOW ” link: #Quality #QualityAssurance #QualityAssuranceManager #QualityAssuranceJobs #food #HACCP #SQF #ConsumerProducts #Monster.com.
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A strong desire to increase knowledge of chemical probes and biorthogonal chemistry emerging in pharmaceutical drug discovery Hands-on experience in proteomics sample preparation and operating modern LC/MS systems.
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CQV Engineer - Downstream - Life Sciences - Contract - Massachusetts Our client, a leading partner to pharmaceutical, biotech and nutrition markets, has an exciting opening for a CQV Engineer – Downstream for their new Capex investment project.
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The team closely integrates with Alloy scientific teams and the global community of biotech and pharmaceutical companies to empower the drug discovery community to make better medicines together.
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We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally.
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