• Director Site CMC

    Takeda Pharmaceuticals (Boston, MA)
    …what is possible in order to bring life-changing therapies to patients worldwide. The Director Site CMC ensures efficient and compliant management of ... on risk and scientific rationale. + Facilitate alignment between site teams and global Regulatory CMC on...alignment between site teams and global Regulatory CMC on post-approval strategies and activities and represent global… more
    Takeda Pharmaceuticals (06/04/25)
    - Save Job - Related Jobs - Block Source
  • Associate Director , Clinical Research,…

    Takeda Pharmaceuticals (Lexington, MA)
    …is true to the best of my knowledge. **Job Description** **Associate Director , Clinical Research, Value & Evidence Generation, US Medical** **Lexington, MA** ... action items and deliverables, distribution of minutes, and maintenance of relevant SharePoint site (or equivalent). + Partners with the Head of US Medical Clinical… more
    Takeda Pharmaceuticals (05/03/25)
    - Save Job - Related Jobs - Block Source
  • Executive Director , Cell Therapy Global…

    Bristol Myers Squibb (Devens, MA)
    …lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Executive Director , Cell Therapy Global Product Quality (CTGPQ) is responsible for ... Development, Analytical Development, Global Manufacturing Sciences and Technology Operations, Portfolio Management, site and above site QA and QC, Internal and… more
    Bristol Myers Squibb (05/25/25)
    - Save Job - Related Jobs - Block Source
  • Senior Manager - Associate Director

    Sumitomo Pharma (Boston, MA)
    …are currently seeking a versatile and experienced Senior Manager - Associate Director level scientist with strengths in clinical pharmacology, and a working ... drug metabolism and bioanalytic chemistry. This position will report to Senior Director of Clinical Pharmacology and Drug Metabolism. S/he will work across… more
    Sumitomo Pharma (05/14/25)
    - Save Job - Related Jobs - Block Source
  • PharmSci PM

    ManpowerGroup (Andover, MA)
    …in the Biotherapeutics Pharmaceutical Sciences Department. The position will report to Director of BPS Project Management. The successful applicant will join a cross ... site group to provide project management expertise to the...early and late stage product development teams inclusive of CMC regulatory submission support. Early phase support will include… more
    ManpowerGroup (06/19/25)
    - Save Job - Related Jobs - Block Source
  • FSP - Sr. Scientist - Stability

    ThermoFisher Scientific (Devens, MA)
    …and external manufacturing sites. The principal scientist reports to the Associate Director of GBS and is responsible for stability product strategy and oversight ... of stability protocols, and preparation, review and approval of CMC elements of regulatory filings to support the activities...work and ensure that stability activities are completed per site and brand timelines. + Perform change control impact… more
    ThermoFisher Scientific (06/06/25)
    - Save Job - Related Jobs - Block Source