Work closely with internal teams (R&D, QA, regulatory affairs) to communicate technical requirements, quality expectations, and regulatory compliance needs to suppliers.
Collaborate with suppliers on issues like material specifications, formulation improvements, scalability, and process validation to ensure consistency in drug quality and safety.
Coordinate with suppliers to ensure that documentation, such as Certificates of Analysis (CoA), Drug Master Files (DMFs), and regulatory filings, are accurate and up to date....