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projects to expand and maintain the system. Collaborating with the Infrastructure lead on strategy, methodologies, master planning and documentation of the PI data historian to align with industry best
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or master's level education Previous experience in managed markets analytics or a job function supporting the promotion of pharmaceuticals. Other Job Details: Last Date to Apply for Job: April 19th, 2024
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work in a GMP environment. Comprehensive knowledge of analytical techniques in Chemistry, Bioanalytical, or Microbiology. Relevant pharmaceutical experience. Nice-to-Have Master ' s degree in
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of project planning and resource forecasting tools and systems (e.g. Microsoft Project, Planisware)) Rapidly mastering new software tools Nice-to-Have Project Management for Professionals (PMP) Certification
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/verification protocols Supervision and direction of others performing this work Perform routine periodic review activities Provide/maintain Site Validation Master Plan information Support regulatory audits
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working to the overall plan, including management of and reporting. Support development of the Site Master Plan and Site Space Plan to ensure effective and strategic use of assets and capital investment
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recommendations Demonstrated ability to manage vendors to ensure effective project delivery Nice-to-Have Master's degree Experience in quality control and/or quality assurance within the pharmaceutical industry
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-to-Have Master's degree Experience engaging in the external regulatory and pharmaceutical environment 2+ years of hands-on CMC authoring experience (investigational, initial registrations or post-approval
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Will Achieve It Responsibilities include the following: Leading process validation activities: Defining PV strategies in a process validation master plan Generating protocols, evaluating data, and
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(min. 10 years experience preferred) Master's degree or Ph.D. in Chemistry, Material Science or similar with focus on construction materials (dry mix mortars and/or water-based products) Fluent English