• Manager, Regulatory Affairs - Advertising…

    Regeneron Pharmaceuticals (Sleepy Hollow, NY)
    …to conference exhibit activities, disease awareness and speaker programs + Provide review of US and Global (if applicable) product and disease state ... company policies. + Ability to identify process improvement for promotional review activities that would enable the establishment of portfolio wide standardization… more
    Regeneron Pharmaceuticals (09/06/25)
    - Related Jobs
  • Senior Manager, Regulatory Affairs Advertising…

    Regeneron Pharmaceuticals (Sleepy Hollow, NY)
    …to conference exhibit activities, disease awareness and speaker programs + Provide review of US and Global (if applicable) product and disease state ... input to direct management with respect to process improvement for promotional review activities and establishment of portfolio wide standardization of policies +… more
    Regeneron Pharmaceuticals (07/03/25)
    - Related Jobs
  • Vice President, Regulatory Affairs - Oncology

    Sumitomo Pharma (Lansing, MI)
    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 ... + Oversee the regulatory activities at CROs, providing document review in order to ensure the quality and scientific...by law. Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in… more
    Sumitomo Pharma (09/23/25)
    - Related Jobs
  • QA Specialist

    Actalent (San Diego, CA)
    …in ensuring quality and compliance across multiple functions, including record review , document control activities, line clearance, API label creation, and more. ... reviews and update Standard Operating Procedures (SOPs). + Manage material review reports and control logbooks/notebooks. + Collaborate regularly with OPS team… more
    Actalent (09/23/25)
    - Related Jobs
  • Microbiologist II

    The Ritedose Corporation (Columbia, SC)
    …in-process product testing. Other responsibilities include data entry, data review , ensuring calibration of equipment, maintaining inventory of laboratory supplies, ... VITEK MS - Raw Material Testing including APIs - Review - Growth Promotion Level 2 - Minimum 2...Growth Promotion Level 2 - Minimum 2 years of Pharmaceutical EM and Microbiology laboratory - Endotoxin Testing -… more
    The Ritedose Corporation (09/23/25)
    - Related Jobs
  • Conventions Manager

    Bausch + Lomb (Bridgewater, NJ)
    …meetings and lead management. Administrative functions included such as contract review , purchase orders and invoicing. + Create and obtain Medical, Legal ... of convention content and final exhibit plans/renderings through our Promotional Review Committee (PRC). + Responsible to produce, track and maintain current,… more
    Bausch + Lomb (09/10/25)
    - Related Jobs
  • Quality Assurance Specialist IV - Therapeutics

    LGC Group (Petaluma, CA)
    …and inspection readiness within organization. + Investigations: Performance and review for investigations associated with Complaints, Deviations, CAPA, OOS, Out ... Atypical Results, Environmental Discrepancy Reports and Alert Level Reports. + Batch Review : Perform technical review of the manufacturing batch records and… more
    LGC Group (09/07/25)
    - Related Jobs
  • Associate Director, Corporate Counsel

    Amneal Pharmaceuticals (Bridgewater, NJ)
    …The incumbent will serve as a member of Amneal's promotional assets review committee (PARC), draft/ review /negotiate general commercial and other types of ... Advise on a broad array of issues relating to the marketing and promotion of pharmaceutical products and actively represent Legal on the company PARC to review more
    Amneal Pharmaceuticals (07/30/25)
    - Related Jobs
  • Executive Medical Director, Oncology Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …Sciences in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. ... to our inspiring, bold mission. **OBJECTIVES** **:** Responsible for ensuring ongoing review and agreement of the Therapy Area Strategy and associated documents… more
    Takeda Pharmaceuticals (07/28/25)
    - Related Jobs
  • QMS Investigator

    Astrix Technology (New Brunswick, NJ)
    …+ Develop and manage weekly schedules for QC analysts. + Author, review , and revise technical documents (protocols, specifications, reports, SOPs, test methods, ... reports with scientific justification and root cause analysis. + Review /perform equipment calibration, validation, and maintenance records to ensure timely… more
    Astrix Technology (07/28/25)
    - Related Jobs