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Reporting to the Head of Process and Analytical Development – Cell Therapy, the Director of Analytical Development will be accountable for the flawless execution of the Cell Therapy Analytical Development activities (internal and client-focused); spanning technical development, method transfer, manufacturing, product release and successful preparation of regulatory submissions.
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Under supervision from Senior Engineer(s) and Engineering Manager(s), the Electrical Hardware Design Engineer is responsible for executing electrical hardware design activities for assigned product development projects.
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Lead and track analytical development commitments of project and team’s deliveries to support all CMC filing activities such as pre-INDs, INDs, IMPDs, CTAs or NDAs, and review of regulatory filings, and address RTQs.
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The Project Manager, CMC Regulatory Affairs will be responsible for the CMC regulatory activities in the investigational, late phase development and/or early commercial lifecycle management of GSK products.
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Support design, development, management, and/or implementation of strategic network configurations and integration activities as related to value based care risk deals. Provides network development/expansion, provider relationships, and refinement activities in support of cross-market network management.
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Leads collaborative customer outcomes research projects, provides input on HQ HEOR projects, and assists in the development and execution of HEOR/market access relevant activities (e.g., payer advisory boards, consultant, and HEOR projects.
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This position will be responsible for providing strategic scientific leadership in the development and execution of scientific engagement, congress planning, and coordination of activities related to the global promotion of third -generation antibody-drug conjugate, currently in late-stage development.
$235,100 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The Proposal Manager position supports one or more business lines and contributes to meeting the goals in Gannett Fleming’s strategic plan by leading key business development support efforts, which include providing: strategic proposal management for any size proposal; capture planning leadership in support of the business lines’ capture managers; and support for both Tier 1 and Tier 2 clients.
$135,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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She/he will oversee and drive a team of analytical scientists that manages the Analytical Development-related activities, for multiple projects. The successful candidate must have hands-on background in development and GMP implementation of molecular, physical-chemical, and bioassay analytics, spanning the needs of the Cell Therapy modality.
$235,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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The Associate Scientist II, Downstream Tech Transfer (PD/Tech Transfer) will report to the Associate Director of Tech Transfer and will have responsibilities supporting the downstream process development technology transfer activities for viral vector pilot and GMP manufacturing campaigns.
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Collaborates with SVP, Communications and Web Marketing Manager to develop web strategies to enhance the user experience of the website including site navigation, content development, check-out funnel and promotional campaigns.
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Our large pharmaceutical client is seeking a Lab Scientist to join their growing Bioanalytical Discovery & Development Sciences team in Spring House, PA. This Scientist will work as part of the immunogenicity assessment team to support all validation and life cycle activities of Anti-Drug Antibody (ADA) and Neutralizing Antibody (NAb) assays for the development of biological drugs.
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Monitoring of program activities including on-site visits, service verification, incident management, review of licensing results, SAMS verification, satisfaction surveys, data reporting and analysis, outcomes development and monitoring, grant monitoring, Vendor Continuous Quality Improvement (CQI), and Performance Based Metrics.
$71,960 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Lead Medical Affairs activities in the US in Uveal Melanoma (UM) and Cutaneous melanoma (CM), collaborating closely with the Head of Global Medical Affairs, the Clinical Development LCM Lead, and the Head of Medical Affairs for Europe/International.
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The Chemical Engineer II performs engineering work dealing with the daily pilot plant operations, communicating chemical process runs with operators, development of process technology for capital projects, improving pilot plant safety & reliability and/or testing new equipment concepts.
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development activities jobs in East Norriton, PA
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