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Working with the Senior Director, Global Data Science, and in close partnership with GCSO partner teams, you will use your deep technical expertise and pharmaceutical industry knowledge to advance the application of leading data science analytical methodologies to domain-specific data assets in order to drive insights and decisions that optimize the patient benefit and commercial value of Janssen’s pharmaceutical pipeline.
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Minimum of 5 years’ experience in the biotech/pharmaceutical industry or health authoritySolid understanding of the drug development and commercialization process, globally (US, JP and EU at a minimum.
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A background of pharmaceutical manufacturing or quality control/quality assurance is a plus. The candidate must have at least 5 years' experience in the pharmaceutical industry. Knowledge of US pharmaceutical Regulations is essential.
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Job Title: Senior Research Associate Location: Bridgewater, NJ Hours /Schedule: 8:30am - 5:30pm Type: Contract Overview Leading Pharmaceutical Company in NJ is seeking a Research Scientist with at least 2 years of experience in performing in-vitro assays.
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We are a global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes. Prior Pharmaceutical or manufacturer industry experience is a plus.
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With a strong financial position and employee centric focus, the company strive to be a pacesetter in the specialty pharmaceutical market. Solaris Pharma Corporation is a leading specialty pharmaceutical company committed to the development and commercialization of high-quality, specialty pharmaceutical products.
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Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Ability to use software applications daily such as Photoshop, Premiere, Captivate, Illustrator, InDesign, Dreamweaver, Articulate and RISE.
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Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expandingLooking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization.
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Minimum of 7 years’ experience in a GxP role; Pharmaceutical experience is preferred. Experience with Veeva (Quality Docs, QMS and Training modules) a plus. Intermediate knowledge of Microsoft Word, Microsoft Excel and Adobe AcrobatKnowledge of cGMP/GDP regulations, ICH Guidelines, and CMC (Chemistry and Manufacturing Controls) recommendedExcellent communication, organizational, interpersonal and computer skillsExcellent Oral/Written Communication SkillsDemonstrated ability to manage multiple competing prioritiesSolid organizational skills and attention to detail.
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Knowledge and understanding of the various laws, regulations and industry including, but not limited to, OIG Compliance Program Guidance for Pharmaceutical Manufacturers, PhRMA Code on Interactions with Healthcare Providers, Anti-Kickback Statute, FCPA, FDA rules and regulations, and other industry guidance, and other issues affecting the development, sales, promotion and marketing of pharmaceutical and biological products.
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Create, route and track controlled records within documents management system, Veeva. This includes documentation control, change control, deviation management, and CAPA (Corrective and Preventive Action) systems.
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10+ years of professional experience with at least 2+ years in a direct or matrix management position of a CMC-related function in the pharmaceutical/biopharmaceutical industry (preferably in a global company.
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IQVIA has the world’s largest Commercial Sales & Medical Solutions (CSMS) organization dedicated to the launch and marketing of pharmaceutical and medical products. We are excited to announce that currently we are looking for a 100% remote (work from home—WFH) contract Technical Support Representative – Optos to join our team.
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Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with capabilities in product development, manufacturing, and commercial operations. Knowledge of the AMA, ACCME, PhRMA and FDA regulations associated with promotion and industry-supported scientific education activities.
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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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pharmaceutical job in Far Hills, NJ
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