Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. Amgen's Regulatory Compliance team is seeking to expand its capacity in India. The Regulatory Compliance team performs assessment of operational changes for regulatory reportability for Amgen products across phases of development, modality, and countries. The Change Assessor will report into the Regulatory Compliance Team lead. The Regulatory Compliance Change Assessor will interface with the Amgen Global, Site, Biosimilars, and / or Device RA CMC teams, as well as Amgen Operations, Quality, and / or Supply Chain for specific strategies or activities that impact a product. The Change Assessor will be responsible for varying levels of product support, including global reportability assessment of single or cross-product changes, based upon their experience level.
Key responsibilities of the Regulatory Sr Associate include :
What We Expect Of You
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a type of person with these qualifications.
Basic Qualifications :
Preferred Qualifications :
Skills Required
Process Development, Change Management, Manufacturing, Supply Chain
Compliance Associate • Hyderabad / Secunderabad, Telangana, India