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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. 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 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.
Job Responsibility:
Reviews change records to evaluate impact of the change with respect to reportability and product restrictions
Defines and documents the reporting and product distribution restriction requirements
Liaise with other functions to ensure alignment of regulatory strategies
Provides expertise and guidance to interdepartmental and cross-functional teams
Identifies and implements process improvements for the change management process
Requirements:
Master’s degree
Bachelor’s degree and 2 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry
Associate’s degree and 6 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry
Nice to have:
Degree in Life Science discipline
Regulatory CMC specific knowledge & experience
Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry
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