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PhD in Organic Chemistry and a minimum of 7 years of experience in process chemistry in a pharmaceutical, biotechnology, CMO or related environment OR equivalent experience and/or education. The Research Fellow, Chemical Process Development coordinates activities in Active Pharmaceutical Ingredients (API) process scale-up, process improvement and process optimization studies.
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10+ years of experience in a GMP environment in pharmaceutical, biologics, vaccines, cell or gene therapy operations, including solid experience in Quality Systems and Regulatory CMC. 10+ years of experience in a GMP environment in pharmaceutical, biologics, vaccines, cell or gene therapy operations, including solid experience in Quality Systems and Regulatory CMC.
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Clinical trial data analysis in the pharmaceutical industry. Seeking an R Shiny Programmer to join the growing R Programming Team. In this role, you will design, develop, test, and maintain R programs which support the development of state-of-the-art reports and, at times, shiny applications, used by biostatisticians and statistical programmers worldwide.
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Bachelor's in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field with 10+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry.
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Good knowledge of PL/SQL and MS OfficeMinimum 10 years of pharmaceutical industry experience with a focus on pharmacovigilance. Knowledge of IT systems in the pharmaceutical industry with an emphasis on PV systems.
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Our client, a world-leading Pharmaceutical Company in Spring House, PA is currently looking for a Bioprocess Manufacturing Associate to join their expanding team. Responsible for maintaining lab notebook in compliance with Pharmaceutical policy.
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Job Title: Associate Director, Biostatistics Client - Global Pharmaceutical Company Location: Remote, US Based only - must reside in EST or CST time zones Type: Direct Hire - Full time salaried direct with the client Base Salary: $180k - $195K Must Haves: Oncology lead experience.
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Evonik's Health Care Business Line includes a fast-growing portfolio of products, services and technologies for the pharmaceutical, medical device, nutraceutical and biopharmaceutical industries.
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Experience with ELISA, SDS-PAGE, and electrophoresis. QA Scientist I: A Bachelor's degree in Medical Technology/Medical Laboratory Scientist, Biology, Chemistry or related field and a minimum of 1-3 years.
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7 or More Years 8+ years in pharmaceutical/biopharmaceutical industry experience with a focus on small molecules and monoclonal antibodies/monoclonal antibody drug conjugates. Coordinates with regional/global RACMC, Quality Assurance, Pharmaceutical Technology, and other functional areas to secure approval of CMC changes and assess regulatory implications.
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Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology.
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The Analytical Chemist will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity, dissolution, residual solvents testing, Particle size distribution of active pharmaceutical ingredients, excipients and finished dosage forms.
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The Analytical Chemist will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity and dissolution testing of pharmaceutical finished dosage forms.
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Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017.
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Author product statements and documentation in compliance with international and country specific legislation (e.g. product dossiers, registration certificates) with the support of the SDS authoring specialist for label data, GHS classifications, Dangerous Goods classifications, worker safety or environmental risk assessments and with the support of the Regulatory affairs team for site specifics and environmental regulation.
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