Job Description: CMC Regulatory Affairs Program Manager Chemistry Manufacturing and Controls, CMC The Company - Syner-G Pharma Consulting, LLC: � A dynamic, entrepreneurial and g…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s , and . Job Description Are you loo…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s , and . Job Description Are you loo…
Sr. Manager, Regulatory Affairs, CMC Overview Founded in 2002, Alnylam was built upon a bold vision of turning scientific possibility into reality by harnessing the power of RN…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s , and . Job Description Are you loo…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s , and . Job Description Are you loo…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s , and . Job Description Are you loo…
Reporting to the Director of Regulatory Affairs, CMC, this position will be primarily responsible for the implementation of regulatory CMC strategy in support of overall regulatory…
Job Description The Senior Director is responsible for overseeing the development and implementation of global regulatory CMC strategies for all cell and gene therapy product dev…
By clicking the Apply button, I understand that my employment applic process with Takeda will commence and that I agree with Takeda s Privacy Notice, Privacy Policy and Terms of Us…
Reporting to the Senior Director, Regulatory CMC, you will support CMC regulatory affairs activities for the company’s products. You will drive the development of innovative CMC re…
Assignment Detail Industry: Biotech/Pharma Job Description US - Regulatory & Medical Affairs Expert Job Number: 20-09412 Be a part of a company that supports life-changing …
What will you be doing? Lead the planning, preparation, and tracking of clinical trial applications (CTAs) Maintain active INDs/CTAs (amendments and annual reports) Develop and…
Title: Regulatory & Medical Affairs Expert Location: Billerica MA Duration:6months Job responsibilities: Roles responsible for ensuring Client's compliance with pharmaceuti…
By clicking the Apply button, I understand that my employment applic process with Takeda will commence and that I agree with Takeda s Privacy Notice, Privacy Policy and Terms of Us…
Opportunity Our Client is currently seeking a Regulatory Medical Affairs Expert to join their team in Billerica, MA. The selected candidate will be responsible for ensuring complia…
Opportunity Our Client is currently seeking a Regulatory Medical Affairs Expert to join their team in Billerica, MA. The selected candidate will be responsible for ensuring complia…
CASSS Job Search Keywords Submit Search Director of Medical Affairs O Director of Medical Affairs Oncopeptides Waltham, Massachusetts, United States 1 day ago D…
POSITION OVERVIEW Regulatory Site Officer External Supply QA Core Responsibilities Acts as a focal regulatory interface between the external and internal manufacturing sites…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s , and . Job Description Are you loo…