• Senior Director, Global Quality Strategy…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …ensuring the effectiveness of global systems. This role will also encompass document management , learning and development, risk management , data integrity ... ideal candidate will have a strong background in quality management within the pharmaceutical industry and a...to monitor Quality performance and drive data-driven decision-making. Maintain risk management toolkit and best practices. +… more
    Otsuka America Pharmaceutical Inc. (09/03/25)
    - Related Jobs
  • Regional Manager of Southeast CQV Services

    VTI Life Sciences (Raleigh, NC)
    …preferred). The ideal candidate will have proven people and project management experience in a highly customer-centric consulting setting. Their hands-on ... minimum of 8+ years of previous Commissioning and Qualification (C&Q) and Project Management experience. It is preferred that this candidate have experience as a… more
    VTI Life Sciences (06/11/25)
    - Related Jobs
  • Associate Director, Channel Strategy and Patient…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …external pressures (eg, 340B, patient leakage) and internal shifts (eg, LOE management , innovative distribution models), this role will be critical in anticipating ... Responsibilities:** + **Proactive Program Optimization:** Own the end-to-end performance management process for affordability and channel programs across in-line… more
    Otsuka America Pharmaceutical Inc. (08/19/25)
    - Related Jobs
  • Senior Solution Consultant

    Norstella (Raleigh, NC)
    …our customers come from over 3000 of the world's leading pharmaceutical , contract research organizations (CROs), medical technology, biotechnology and healthcare ... and development to regulatory approval, and from product launch to lifecycle management , we provide the intelligence and insight to help our customers seize… more
    Norstella (08/08/25)
    - Related Jobs
  • Manager, PVRM

    Sumitomo Pharma (Raleigh, NC)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and Biostatistics is essential. **Job Duties and Responsibilities**… more
    Sumitomo Pharma (08/01/25)
    - Related Jobs
  • Quality Systems Specialist

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …Change Controls, Quality Events, Deviations, Corrective and Preventative actions, QMR, Risk Management . This individual works closely with cross-functional teams ... in terms of their impact to CGMP and using Risk Management tools. + Prepares and compiles...(BS) / Bachelor of Arts (BA) on Science, Engineering, Pharmaceutical Sciences, or equivalent Experience: + Minimum 3 years… more
    Glenmark Pharmaceuticals Inc., USA (07/16/25)
    - Related Jobs
  • Commissioning & Qualification Program Lead

    Genentech (Holly Springs, NC)
    …in the project. + Develop C&Q execution strategies in alignment with Pharmaceutical Quality Management System, global standards and processes and regulations. ... or related discipline with 20 or more years of experience preferable in pharmaceutical /biopharmaceutical industry. + Experience in management of C&Q scope in… more
    Genentech (09/06/25)
    - Related Jobs
  • Sr/Lead DeltaV Automation Engineer(remote)

    Cognizant (Raleigh, NC)
    …especially with MES, digital, and process engineering teams. . Advanced problem-solving and risk management skills. . Demonstrated ability to define and enforce ... for client stakeholders and senior leadership regarding automation scope, progress, and risk mitigation . Collaborate with Program technical offices to ensure the… more
    Cognizant (09/05/25)
    - Related Jobs
  • Sterility Assurance Manager

    ThermoFisher Scientific (Greenville, NC)
    …Comportment/Training/Oversight + Oversee sterilization processes + Implement and Lead risk assessments and improvement programs against current and future ... updated Annex 1 - leading the transition and any risk assessments we need + Represent site on the...or Environmental Monitoring experience, and ideally within a sterile pharmaceutical manufacturing facility). + 5 years of leadership experience… more
    ThermoFisher Scientific (07/19/25)
    - Related Jobs
  • Senior Staff Quality Specialist - QMS, Labeling

    GRAIL (Durham, NC)
    …ensuring effective implementation of change. Evaluate and identify areas of noncompliance, risk and/or potential improvement to management and develop plans for ... equivalent experience. + 10 + years of experience working within a medical device, pharmaceutical , or biotech quality management system, with at least 5 years… more
    GRAIL (07/26/25)
    - Related Jobs