To ascertain each batch manufacturing with high standard of quality, within established stage wise yield criteria as well as final batch yield. Timely coordination/collaborate with other functions, department to ensure seamless operation.
Masters degree or higher in Chemistry, Pharmacy; experience in a pharmaceutical quality control laboratory with a significant focus on analytical method validation.
Ensure documentation, compliance, and regulatory readiness in various section like IPQA, QMS, Qualification related activities. Design, develop, and optimize new drug formulations of OSD, Ointment and Injectable.
Product Development of Topical Dosages forms, Parenteral, Injectable forms, Tablet Dosages forms. Basic knowledge about different pharmaceutical dosage forms.
Sr. Quality Specialist, Clinical Quality responsible for managing clinical quality function, ensuring compliance with local clinical trial regulatory requirements and Takeda Quality Management Systems. Works in collaboration with local clinical operation team ensuring adherence to Good Clinical Practice Guidance.