Employment Type : Full-Time
Takeda Development Center Americas, Inc. is seeking a Global CMC Regulatory Affairs Manager based in Boston, MA. Responsibilities include: Developing regulatory submission strategies for products in commercial and development phases...
Employment Type : Full-Time
Job Title: Regulatory Affairs Manager ICareer Level - DIntroduction to role:Join our dynamic Biopharmaceuticals R&D team as a Regulatory Affairs Manager I. This role is a unique opportunity for a regulatory specialist with project management...
Employment Type : Full-Time
A Regulatory Affairs Documentation Specialist utilizes strong written communication skills to enhance the level of documentation maintained within the Department. The Documentation Specialist is primarily responsible for attending all regulatory...
Employment Type : Full-Time
The Senior Director - Regulatory Affairs is responsible for managing Regulatory Affairs activities (nonclinical and clinical) for assigned investigational and/or marketed products. This individual manages the development of regulatory strategies...
Employment Type : Full-Time
Job Details The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the...