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Case Processing: Oversees intake activities (i.e. mailbox management, LP recon, post marketing follow up), and interacts with the DSI Case Management team / global case management team and partners on a daily and as-needed basis.
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Submit a verity of sales reports as required including activities, opportunities, deals pending and adherence to goals. Responsible for all sales activities, from lead generation through quote and close.
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Reporting to the Executive Director of Development Quality Assurance, the Senior Director of Pharmacovigilance QA serves as a strategic partner managing quality and regulatory compliance related to Good Pharmacovigilance Practices (GVP) and other related activities performed by Drug Safety & Pharmacovigilance and Medical/Clinical Departments.
$200,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Handling day-to-day activities inclusive of project execution and management, vendor management, data management, life cycle management, issues, deviations, corrections, remediation and improvement efforts within the plant of all computerized systems such as SAP, MES, manufacturing and laboratory equipment, BAS, EDS and other software, systems and associated interfaces.
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The ideal candidate has expertise developing and managing S&OP/IBP processes, with solid understanding of End-to-End Commercialization / Manufacturing activities including product life cycle management.
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Lead pre-sales activities, including solution envisioning, proof of concept development, and client presentations. Design and deploy RPA solutions using industry-leading automation platforms such as UiPath, Blue Prism, or Automation Anywhere, tailored to the unique processes of our pharmaceutical clients.
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Manage and oversee all the CMO activities from apheresis delivery till timely DP shipment. Manage the CMO tech transfer and clinical/commercial manufacture: trouble shooting problems, conducting investigations, track timeline and KPIs, overseeing capacity expansion, monitoring budget, driving cost reduction and quality improvement and serve as Person in Plant.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Sourcing Support: Collaborate with the Indirect Procurement, Finance, and business teams to provide critical support for sourcing activities, including sourcing strategy development, supplier relationship management, and negotiations.
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Performs required procedures and data collection activities at necessary in observational settings such as, ED, Cath Lab, EP Lab, ICU/Step down area, physician office, OR, and other required areas.
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Performs all activities as directed by the Care Manager or BOM. Assists with "Independent Activities of daily living" which may include light housekeeping, shopping, laundry and meal preparation, per the Plan of.
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Featuring 78,000 square feet of action-packed sports and activities BSC is one of the area's largest and most exciting indoor recreation destinations! At BSC, our goal is to provide quality sports instruction, exciting family-friendly activities, memorable parties, corporate outings and special events in a clean and safe environment.
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Presales Solution Architect - Digital Workplace is responsible for driving and co owning digital workplace solution sales, business development and marketing activities across North America. Digital Workplace Solutions includes a focus on technologies inclusive of Service Desk, End User Computing, Desktop Engineering, Field Services, Microsoft Cloud; Business Productivity Applications, Unified Communications and Collaboration (UCC), windows 10 migration, O365 & Skype for Business migration.
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We are seeking a highly motivated collaborative Director, Quality Control & Bioanalytics who will be responsible for supporting the launch, ramp-up, and production activities within a state-of-the-art multi-product cell therapy manufacturing facility that will be utilized to manufacture autologous and allogeneic cell therapy products.
$170,000 - $220,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Working knowledge of medical concepts and familiarity with safety activities in drug development and post marketing and global safety health authority requirements is required. · Support SMT activities (e.g.preparing and presenting data, compiling meeting minutes, updating signal tracking information.
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Experience: Significant experience in clinical development/ real world evidence, launches and post-marketing medical activities on a global level. The Medical Head assures the delivery of the medical strategy plan and scientific activities, sharing medical expertise of functional areas such as marketing, clinical development, pharmacovigilance and regulatory in compliance with law, ethical/scientific principles, and Group products strategy.
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activities job in Warren, NJ
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