Job Description
Job Description
To ensure charging and withdrawal of stability samples as per approved protocols.
Analysis of Stability / Finished product samples, and compile the report as per ALCOA procedure, other miscellaneous samples, and compile their report.
Regular participation in internal and external training programs.
To maintain the instrument usage and maintenance of instrument 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.
To maintain the Stability chamber and tracker.
To follow all SOP compliance exp. CQA, QA and QC etc.
To prepare Quality documents like Stability protocol and summary reports etc.
Work Experience
4-6 years in analysis of tablets and capsules.
Education
Graduation in Pharmacy
Competencies
Innovation & Creativity
Result Orientation
Collaboration
Customer Centricity
Developing Talent
Stakeholder Management
Strategic Agility
Process Excellence
