• Senior Manager , Global…

    Otsuka America Pharmaceutical Inc. (Annapolis, MD)
    …with 5+ years' experience or Master's degree with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, ... needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC- RA , labeling,...quality assurance , etc.) in pharmaceutical or healthcare… more
    Otsuka America Pharmaceutical Inc. (04/23/25)
    - Related Jobs

  • Sr . Director, Clinical Affairs

    BD (Becton, Dickinson and Company) (Sparks, MD)
    …functions on clinical requirements related to new product development and required approvals, regulatory affairs , quality assurance , marketing, and ... global health issues. The ** Senior Director, Clinical Affairs , Diagnostic Solutions** reports directly to the Sr...in the development and submission of clinical reports to Regulatory Affairs + Provide guidance to … more
    BD (Becton, Dickinson and Company) (05/01/25)
    - Related Jobs

  • Senior Manager , Verification…

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    … Quality (ASQ) as a Certified Quality Auditor (CQA) and/or from the Regulatory Affairs Professional Society (RAPS) as a Regulatory Affairs ... tools to promote engaged, collaborative, and results-driven work environments. _The Senior Manager , Verification Programs has the following responsibilities:_ *… more
    The US Pharmacopeial Convention (USP) (04/30/25)
    - Related Jobs

  • Building Envelope Project Manager

    The Falcon Group (Rockville, MD)
    …related to construction administration and observation, with a focus on quality assurance /conformance with contract documents, building codes, and industry ... growth. The Role SUMMARY: We are seeking an energetic Building Envelope Project Manager , who is passionate about repair and rehabilitation of existing buildings, to… more
    The Falcon Group (04/22/25)
    - Related Jobs

  • Clinical Research Program Specialist

    Johns Hopkins University (Baltimore, MD)
    Under limited supervision of the Sr . Clinical Research Program Manager , we are seeking a **_Clinical Research Regulatory Specialist_** who will be ... timely submission of data, and adherence to guidelines. + Conduct internal quality assurance measures, including periodic monitoring and training sessions, to… more
    Johns Hopkins University (04/12/25)
    - Related Jobs