• Director - Engineering - Synthetic Molecule Design…

    Lilly (Indianapolis, IN)
    …candidates to lead unit operation development and process optimization of synthetic drug candidates to support clinical trials, regulatory submission, and ... synthetic active pharmaceutical ingredients from pre-clinical phases through commercialization of drug substances and drug products. Our scientists and engineers… more
    Lilly (08/20/25)
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  • Clinical Pharmacist

    HCA Healthcare (Pasadena, TX)
    …and dispense pharmaceuticals + Complies with facility policy and procedures and regulatory requirements. + Monitor drug therapy regimens for contraindications, ... cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free...drug - drug interactions, drug -food interactions, allergies and appropriateness of … more
    HCA Healthcare (08/10/25)
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  • Advanced Clinical Pharmacist

    HCA Healthcare (Webster, TX)
    …and dispense pharmaceuticals. + Complies with facility policy and procedures and regulatory requirements. + Monitor drug therapy regimens for contraindications, ... cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free...drug - drug interactions, drug -food interactions, allergies and appropriateness of drug more
    HCA Healthcare (07/18/25)
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  • Sr. Quality Engineer

    Abbott (Temecula, CA)
    …other regulatory requirements. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating ... customers, contractors, and vendors. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies,… more
    Abbott (08/14/25)
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  • Medical Director, Clinical Development - Job: MDCD

    Ascendis Pharma (Palo Alto, CA)
    …Analyze, evaluate, interpret, and report clinical data + Anticipate and solve complex drug development problems + Contribute to regulatory strategy + Contribute ... our core values of Patients, Science, and Passion, we use our TransCon(R) drug development platform to fulfill our mission of developing new and potentially… more
    Ascendis Pharma (07/04/25)
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  • Contractor - Global Drug Safety & PV…

    System One (Plainsboro, NJ)
    Title: Global Drug Safety and PV Compliance Associate Location: Must be local for hybrid schedule in Princeton area Rate: Up to $42/hour (dependent on experience) ... detail-driven Associate to support the Compliance Team within the Global Drug Safety and Pharmacovigilance (GDS&PV) Department. The ideal candidate will possess… more
    System One (09/03/25)
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  • Manager, Clinical Drug Supply & Logistics

    Regeneron Pharmaceuticals (Armonk, NY)
    The Manager, Clinical Drug Supply & Logistics is responsible for forecasting Investigational Product (IP) supply requirements for multiple clinical trials and for ... within budget and with good quality, in compliance with Regulatory Authorities' regulations / guidelines and Regeneron SOPs /...stability). **A Typical Day Includes:** + Serves as lead drug supply manager of multiple small and/or less complex… more
    Regeneron Pharmaceuticals (09/02/25)
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  • Project Engineer- Drug Delivery

    PCI Pharma Services (Rockford, IL)
    …and shape the future of PCI. **Position Summary** As a Project Engineer - Drug Delivery, you'll play a hands-on, critical role in the design, development, and ... for diabetes management-giving you the opportunity to work on cutting-edge drug delivery technology. You'll collaborate with both internal stakeholders and external… more
    PCI Pharma Services (07/18/25)
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  • Sr. Quality Associate I/II

    Grifols Shared Services North America, Inc (Clayton, NC)
    …skills (written and verbal). Demonstrated use of domestic (ie Food and Drug Administration) and applicable foreign regulatory agency requirements/guidelines. Be ... * Interacts regularly with members of management and as needed with regulatory officials. * Lead multi-disciplined project teams with highly technical objectives.… more
    Grifols Shared Services North America, Inc (08/29/25)
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  • Director R&D Program Management

    Abbott (Pleasanton, CA)
    …other regulatory requirements. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating ... closely with cross-functional peers in quality, operation, marketing, clinical and regulatory , medical affairs, commercials to define an aligned and predictable NPD… more
    Abbott (08/13/25)
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