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.
Candidates must knowledge on all areas of production activities. Like handling of GLR, SSR, Centrifuge, Driers, Blender, Shifter, Miler, Documentation review, and regulatory knowledge.
B.Pharma, M.Sc., M.Pharma, in sterile manufacturing plant. Proactively assess quality issues and ensure compliance to QA/QC as per regulatory requirements