Job Description

The person follows Good Laboratory Practices, Safety measures and good documentation and to ensure compliance with all the existing SOPs in the routine work. The person follows Standard Operating Procedures and Standard Test Procedures while working. The person ensures charging and withdrawal of stability samples as per approved stability protocols. The person responsible for analysis of Stability / Finished product samples, and compile the report as per ALCOA procedure, other miscellaneous samples, and compile their report. Having experience in the operation of QC instruments like Dissolution Test apparatus, UV Spectrophotometer, Balance, PH meter, HPLC, GC and Sonicator etc. Ensuring data integrity policy, GDP, and its effectiveness up to compliance. The person is responsible for preparation of Stability protocol and summary reports, maintains the stability sample record and its analytical planning as per the pullout schedule. The person has an awareness of EHS Rules, Procedures, Guidelines, Policy, Practices, Requirements & Applicable Legal Compliances. Work Experience 5 to 7 years experience in QC. Education Post Graduation in Chemistry Graduation in Pharmacy Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence