- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. The Director Regulatory Site CMC ensures efficient and compliant management of regulatory ... with global HA requirements, beyond EU/US. who has an understanding of scientific principles and regulatory CMC requirements relevant to global drug development and… more
- Takeda Pharmaceuticals (Boston, MA)
- …my knowledge. **Job Description** We are seeking a seasoned and visionary Senior Director of Medicinal Chemistry to join our leadership team. This individual will ... our strategic decisions and contribute to the advancement of our scientific and commercial endeavors. Additionally, this person will oversee external programs… more
- Amgen (Cambridge, MA)
- …Join us and transform the lives of patients while transforming your career. ** Director , Commercial Drug Products & Life Cycle Management** **What you will do** Let's ... supply of commercial drug products. We are seeking a director to lead an impactful team of DPTLs responsible...commercial drug product programs in our portfolio. + Provide scientific , technical and managerial leadership in support of commercial… more
- Takeda Pharmaceuticals (Boston, MA)
- …medicines and make a lasting impact on patients worldwide. Join Takeda as a Director , Global Regulatory Lead Oncology where you will be part of the global regulatory ... team. As Director , Global Regulatory Lead Oncology you will set global...task-forces and initiatives. **Minimum Requirements/Qualifications:** + Bachelor's Degree required, scientific discipline strongly preferred, advanced degree in a … more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. The Director Global Regulatory Affairs, Neuroscience is responsible for developing innovative global ... Teams (GRTs) and representing the regulatory function on cross-functional Global Program Teams. + Defines, develops, and leads global strategies to maximize… more
- Bristol Myers Squibb (Devens, MA)
- …The Associate Director Stability is accountable for the stability commercial program for large molecules Drug Substances and Drug Products. + Accountable for new ... in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director Stability is responsible for stability product strategy and oversight of… more
- Lilly (Boston, MA)
- …and therapeutic management of neurodegenerative diseases. In the capacity of Director , the incumbent will assume responsibility for both the strategic direction ... assays for preclinical and clinical sample analyses. + Serve as a scientific and technical expert for in-house and outsourced biomarker discovery efforts,… more
- Lilly (Boston, MA)
- …enabling the diagnosis and treatment of neurodegenerative conditions. As Executive Director (or potentially Associate Vice President) you will drive the strategic ... and mentor a skilled team of biomarker researchers, fostering innovation and scientific excellence **Key Responsibilities:** + Lead the development and validation of… more
- AbbVie (Cambridge, MA)
- …an overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, ... + Responsible for design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory… more
- Takeda Pharmaceuticals (Lexington, MA)
- …that will inspire you and empower you to shine? Join us as an Associate Director , Global Clinical Supply Chain Operations in our Cambridge, MA office. At Takeda, we ... to our inspiring, bold mission. **POSITION OBJECTIVES:** + The Associate Director , GCSC Operations is responsible for providing leadership and direction to… more