Job Summary
CMC SME
Responsibilities
Adv degree in science pharmacy chemistry or a related technical area. Overall 15+ yrs experience with at least 8+ years in CMC area implementing solutions life cycle management of products etc Broad knowledge of biologics and therapeutics
Good understanding of drug manufacturing activities and processes drug substance process development and cGMP manufacturing at external contract manufacturing and development organizations (CDMOs)
Evaluating change controls and deviations related to drug products.
Experience with late-stage development of biologic drug products
Experience with regulatory documentation including regulatory commitments and quality documentation according to Good Manufacturing Practice.
Good compliance and regulatory understanding
Ability to provide solutions for drug substance development manufacturing and CDMO management.
Understanding of other departments that influence CMC work and all phases of preclinical and clinical development.
Understanding of development and validation of analytical test methods for drug substances