- Takeda Pharmaceuticals (Boston, MA)
- …or managing components of regulatory submissions. + Expert knowledge of drug development process and regulatory requirements. Knowledge of FDA, EU, Canada, ... By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application… more
- AbbVie (Worcester, MA)
- … development and planning skills coupled with necessary knowledge of pharmaceutical development , manufacturing and supply activities. + Issue identification ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Third Party Manufacturing (TPM) Manager will be the main supplier… more
- Sanofi Group (Cambridge, MA)
- …Drug Development & Regulatory: Broad understanding of the drug development process , regulatory requirements, risk management, health authority interactions, ... **Job Title:** SPC Global Medical Director - Ophthalmology **Location:** Cambridge, MA / Morristown, NJ **About the Job** Join the team transforming care for people… more
- Takeda Pharmaceuticals (Boston, MA)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... analytics, digital tools, and AI to accelerate the discovery, development , and delivery of innovative therapies to patients. The..., and delivery of innovative therapies to patients. The Director , R&D DD&T Strategy Lead will report into the… more
- Evident Scientific (Needham, MA)
- Director of Creative Services & Marketing Communications (Evident MIS) Job ID #: 2237 Company: Evident Posting Date: Jan 16, 2026 Are you looking for a company that ... digital pathology platforms. With customers spanning hospitals, academic research, pharmaceutical and biotech organizations, semiconductor and electronics manufacturers, and… more
- Takeda Pharmaceuticals (Boston, MA)
- …of regulatory and/or related experience. + Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA, EU, Canada, ... the "Apply" button, I understand that my employment application process with Takeda will commence and that the information...lasting impact on patients worldwide. Join Takeda as Associate Director , Global Regulatory Lead Oncology where you will be… more
- Takeda Pharmaceuticals (Cambridge, MA)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... Description** **About the role:** Join Takeda as the Senior Director , US Medical Affairs - Head of Dermatology in...the PM to track progress against strategic plans, including development + communication of periodic reports. **Develop US Product… more
- IQVIA (Boston, MA)
- **Associate Technology Solution Sales Director -eQMS (SmartSolve) & Quality Consulting** The Associate Technology Solution Sales Director will focus on promoting ... to prospective clients. + Key responsibilities include new business development through prospecting and relationship-building with key decision-makers, managing… more
- Lilly (Boston, MA)
- …manufacturing and development activities by partnering with Technical Operations, Process Development , Analytical Development , Quality, and other ... to single-course gene editing medicines. **Position Summary:** The Associate Director , Regulatory CMC will work closely with cross-functional subject matter… more
- Takeda Pharmaceuticals (Boston, MA)
- …submissions including for Late-Stage assets. + Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA, EU, Canada, ... the "Apply" button, I understand that my employment application process with Takeda will commence and that the information...impact on patients worldwide. Join Takeda as a Senior Director , Global Regulatory Lead - Oncology, where you will… more
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