- Takeda Pharmaceuticals (Cambridge, MA)
- …to patients worldwide. Join Takeda as an Associate Director, Global Reg Affairs Device , PDT in our Global Regulatory Affairs CMC & Device organization ... Affairs CMC & Device organization is responsible for global device regulatory strategies and activities for the PDT BU product portfolio through clinical… more
- Bristol Myers Squibb (Cambridge, MA)
- …medical device , and/or translational development processes, with ability to lead supportive project management processes + Strong understanding of global ... the patients and health care providers we serve. The Associate Director, Technical Management, reports to the Technical Management...regulatory requirements for companion diagnostic device development… more
- Takeda Pharmaceuticals (Boston, MA)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Programming in Cambridge, MA, where you will oversee and direct ... applicable to the design, analysis of clinical trials and regulatory submissions. + Work with ICH-GCP guidelines for clinical...quality execution of the deliverables by assisting Programming CoE lead . + A SME in the special data types… more
- Johnson Controls (Canton, MA)
- …to all safety standards. How you will do it . Interprets applicable regulatory requirements and ensures that project deliverables meet these as well as specific ... whenever possible. . May manage and complete the loading, device verification, and commissioning of all system controllers as.... Effectively communicates the status of projects to Project Lead and management as required and assists in preparing… more
- embecta (Andover, MA)
- …in Engineering or related field + 10+ years of post-educational experience in Medical Device Design highly desired + Experience as lead in the development of ... **The Staff Engineer, R&D - Verification and Validation, is the technical lead in the design verification or design validation of electromechanical medical devices… more
- embecta (Andover, MA)
- …in Engineering or related field. + 10+ years of post-educational experience in Medical Device Design highly desired. + Experience as lead in the development of ... Engineer, R&D - Verification and Validation, is the technical lead in the design verification or design validation of...medical devices developed by embecta. Reporting up to the Associate Director, R&D - Verification and Validation, the successful… more