We are seeking an experienced Principal Scientist to support technology transfer activities and provide scientific, technical, and compliance expertise to sterile manufacturing operations. This role will support the Site Subject Matter Expert (SME) and Process Owner for liquid and lyophilized parenteral manufacturing processes, ensuring operations remain in a validated state and compliant with cGMP regulations, site procedures, and regulatory requirements.
The incumbent must comply with all Environmental Health & Safety (EHS), security, and Good Manufacturing Practice (GMP) requirements.