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The QA Document Control Lead role is an exempt level position with responsibilities for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
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The QC Supervisor is an exempt level position with responsibilities for supervising the operation and workflow of the quality control laboratories in support of cell therapy manufacturing. 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 candidate will collaboratively deliver multidisciplinary new application and product development under applied research and development projects in Pharmaceutical and Nutraceutical Excipient segments, executing the defined scope with some level of autonomy.
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4-6 years of experience in an operations coordination role, within a pharmaceutical marketing environment. Constantly work with the Creative Director (CD) and Studio Lead to identify talent or level gaps in our talent pool and actively search for additional freelancers to add to our roster.
$55 an hourRemoteExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience in a food, dairy, pharmaceutical, nutraceutical etc., manufacturing plant environment. We are committed to establishing and enhancing site safety competency and capability, fostering a culture of continuous improvement and maintaining a consistently high level of safety performance.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Comprehension of the Health Care or Pharmaceutical industry and knowledge of using various 3rd party data sources, such as IQVIA Exponent and/or Longitudinal Patient Level Data are necessary.
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Less than one year in Pharmaceutical Packaging/Manufacturing - Preferred. Packaging Operator I is an entry-level position in the packaging department. High school level math and mechanical skills.
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At least 5 years of experience in pharmaceutical clinical trial data management or at least 2 year of experience as a Clinical Data Manager II, with demonstrated knowledge, experience and ability to perform to meet high quality standards and high level of customer satisfaction.
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Minimum of a relevant masters or doctorate level advanced scientific/medical degree (e.g. MD, PhD, PharmD), with experience in oncology required. Minimum of 10 years of experience in the pharmaceutical or biotechnology industry within medical affairs strategy.
$271,400 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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As required by law, Bausch Health provides a reasonable range of compensation for roles that may be hired in the US. Actual compensation is influenced by a wide array of factors including but not limited to skill set, level of experience, and specific office location.
$225,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our pharmaceutical specialists support drug development and products through contract laboratory services, regulatory guidance, and supply chain assurance. Intertek's Chemical & Pharmaceuticals team brings quality and safety to life through regulatory guidance and supply chain assurance to support your unique pharmaceutical or biopharmaceutical outsourcing requirements.
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As required by law, Bausch Health provides a reasonable range of compensation for roles that may be hired in the US. Actual compensation is influenced by many factors including skill set, level of experience, and specific office location.
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