Job Description: To Prepare SOP & Other documents required in day-to-day operations To fulfill requirements of GMP and other associated codes such as GLP and GCP by conducting training. To interact with product development and manufacturing personnel for validation work. (USFDA, MCA & TGA) To Review Stability Testing for process development. To resolve Market complaints investigation received from any source. To interact with Regulatory Bodies for Technical agreement and dossier. To involve in Audit Preparation like USFDA, TGA, MCA, MCC, and WHO etc
Experiance: 2-3 years
send resumes: info@digvijaya.com