- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , GRA CMC Small Molecules where you will oversee ... CMC team, you will report to the Senior Director Global Regulatory Affairs CMC . **How you...ability to liaise with Regulatory Agencies, having served as lead in successful Agency Interactions related to CMC… more
- AbbVie (Worcester, MA)
- …. Job Description The primary goal of this position is to lead the digital transformation effort for PDS&T Biologics. The selected individual will ... and digital strategy, influencing and driving end-to-end digital integration within Biologics CMC . This leader will collaborate closely with IT partners to evaluate… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... drug product at CDMOs + Design and lead method validation and implementation activities for drug substance and drug product ensuring compliance with relevant ICH and… more
- Takeda Pharmaceuticals (Lexington, MA)
- …application is true to the best of my knowledge. **Job Description** ** Associate Director , Clinical Research, Value & Evidence Generation, US Medical** ... objectives include: + Partners with Head of US Medical Clinical Science Lead to translate strategy into efficiently executable research plan; predicting and planning… more
- Takeda Pharmaceuticals (Lexington, MA)
- …Health and a Brighter Future to people worldwide. As an Associate Director in Analytical Development, you will lead efforts to develop advanced analytical ... separation-based techniques (eg, U/HPLC, CE-SDS, icIEF, glycan profiling, etc), you will lead a team to ensure analytical methods and strategies meet scientific,… more
- AbbVie (Cambridge, MA)
- …to ensure an in-depth understanding of the science behind each of these opportunities. The Associate Director , Search & Evaluation will be a key member of the ... the Company. Review external opportunities for scientific merit and feasibility. + Lead the assessment of opportunities (in conjunction with the R&D Therapeutic Area… more
- AbbVie (Worcester, MA)
- …Drug Master files/Certificate if suitability of monographs of the Ph. Eur. Documents. Lead QA contact with AbbVie Affiliates and Regulatory to prepare submissions. + ... obtained, with no delays to market entries. + Core team member or lead of strategic programs; including Brand Teams, New Product Introductions, Product Transfers, … more