Description:
Primary Function of Position The role would serve as the SME and advise on any challenges /issues that arise in formulation development, process optimization, and drug product manufacturing at external CDMOs to support non-clinical and clinical activities. The consultant will ensure scientific and technical standards are robust, data packages support regulatory filings, and quality controls are implemented in partnership with Quality Assurance and Regulatory Affairs. Responsibilities Expectati
Dec 12, 2025;
from:
dice.com