Senior Regulatory Affairs Associate
Parexel International Corporation, King of Prussia, PA, United States
Senior Regulatory Affairs Associate
Experience: Biologic CMC
5+ years of experience
Supported the CMC activities related to Vaccine/Biologic manufacturing and control including authoring of submission dossiers related to:
- new application, post approval variations
- Understanding of EU/CA/WHO/US regulations & guidance allowing appropriate review and compilation of data to appropriate standards & requirements
- Experienced in CTD update/authoring ( CTD Module 1, 2&3)
- Handled and responded Health Authorities Request
- US & CA Annual reports, Renewals, PQVAR, APR
- Assessment of the Change Controls and associated technical dossiers
- Excellent individual project management and communication skills
- Veeva tool experience
Education:
Bachelors/Masters in Pharmacy OR Bachelors/ Masters in any of Life