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Minimum of 5 years of experience in a Pharmacovigilance/Drug Safety environment with substantial experience in managing adverse event and SAE processing, medical surveillance and risk management, signal detection, on a global basis within the pharmaceutical industry.
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Calliditas is led by an experienced and dedicated management team with an average of more than 15 years of prior experience in the pharmaceutical industry, including at leading companies such as GlaxoSmithKline, Pfizer and AstraZeneca.
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PhD Degree in Pharmaceutical Science or related scientific field WITH minimum 3 years experience in pharmaceutical formulation and product development. BS Degree in Pharmaceutical Science or related scientific field WITH Minimum 10 years experience in pharmaceutical formulation and product development.
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B.A./B.S degree in Chemical Engineering, Biology, or similar relevant field with at least 6 years of direct GMP manufacturing experience in a biotechnology manufacturing facility or Pilot Plant OR a High School Diploma with 10 years of experience in protein purification in Biotech/Pharmaceutical industry.
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As our US National Sales Director, you will lead the development of new business for our full-service thermal packaging company focused on food, beverage and pharmaceutical industries with an emphasis on pharma and biomedical.
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Deep experience & optimization in sales enablement, sales training, sales automation systems, CRM/CRS tool development in global Pharmaceutical/Healthcare related field across product portfolios.
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Operations Manager, HCP Events and FMV Processes - Pharmaceutical Job ID: 943677 Lawrence Township , New Jersey Job Type: Contract Added - 03/01/24. BA/BS Degree Required; 2-4 years of pharmaceutical industry experience with understanding of KOL/Thought Leader Engagements; Project Management and/or Advertising Agency experience preferred; Travel may be required up to 25.
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Job Description Innova Solutions is immediately hiring for an Validation Specialist
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Background in the pharmaceutical packaging marketplace and/or regulated environment requiring serialization: customer requirements, applications, regulations, packaging plant locations, decision makers, and key players.
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A minimum of 10 years of relevant data management experience in the biotech or pharmaceutical sector, with a strong emphasis on cell therapy and CAR-T therapy. The ideal candidate will have in-depth experience in cell therapy, with specialized expertise in CAR-T therapy, solid tumors, leading a data management function, and expertise using Medidata Rave. This role encompasses the management of external Contract Research Organizations (CROs), acting as a Subject Matter Expert (SME) for all data management activities, and ensuring the highest data quality and integrity across the clinical operations organization.
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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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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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Intermediate knowledge of pharmaceutical manufacturing and utilities that support cell therapy clinical manufacturing. Intermediate knowledge of cGMP pertaining pharmaceutical facilities, utilities, and equipment.
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Fresh PhD with 3+ years experience or MS with 5+ yearsexperience in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience.
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Board Certified in therapeutic area and US fellowship training, or MD with 2-4 years' experience in within the pharmaceutical industry including 2 years in-house Medical Affairs role, or PhD or PharmD with 5 years' experience within the pharmaceutical industry, including experience in the therapeutic area and 3 years in an in-house Medical Affairs role; MD preferred.
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labeling pharmaceutical jobs in Trenton, NJ
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