- Takeda Pharmaceuticals (Boston, MA)
- …Experience in reviewing, authoring, or managing components of regulatory submissions. + Expert knowledge of drug development process and regulatory requirements. ... 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
- Charles River Laboratories (Wilmington, MA)
- …imports and reconcile with demand and capacity constraints. + Recommends and develops process improvements. + Acts as backup liaison between third party suppliers: + ... development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND… 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 ... best of my knowledge. **Job Description** About the role: As a recognized expert within your business or function, you have comprehensive expertise in your… more
- Charles River Laboratories (Shrewsbury, MA)
- …this position, **a resume/CV must be uploaded and submitted during the application process .** Please make sure work history and education are added correctly. **Job ... development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND… 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 ... capability throughout the USBU E&C organization and act as a subject matter expert and internal resource for USBU E&C colleagues. Collaborate with other USBU E&C… 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 ... for internal or corporate reporting + Facilitate the Management of Change (MOC) process with Facilities, Lab Operations and other partners to capture changes within… more
- Charles River Laboratories (Shrewsbury, MA)
- …development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND ... our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic… more
- Prime Therapeutics (Boston, MA)
- …to the company policies and procedures. Upholds clinical integrity of pharmaceutical solutions by participating in on-going training programs to ensure quality ... performance in compliance with applicable standards and regulations. Expert within the organization. + Conducts Program Integrity Audits including outreach and… more
- Actalent (Worcester, MA)
- …Location: Worcester, MA Employment Type: 12 month Contract Experience Level: Expert Overview: The Biotherapeutics and Genetic Medicine Department in Worcester, MA ... a BS, or 3-5+ years with an MS in pharmaceutical or related industry. + Proven track record of...as the modification or adjustment of the job application process or interviewing due to a disability, please email… more
- Sanofi Group (Cambridge, MA)
- …into brand strategy and tactical development for Dupixent indications, serving as expert for the payer, distributor and channel perspective and ensuring economic ... + Working understanding of strategic pricing and commercial contracting strategy, process and rules **Demonstrated ability to identify and develop business… more