Qualification - B. Pharm / M.Sc. (First Division only)
Department - Quality Control (Sterile / Ophthalmic only)
Role & Responsibilities (USFDA / EU GMP exposure mandatory)
- Analysis of ophthalmic finished products using parameters such as Assay, Related Substances (RS), Dissolution, PSD by Malvern, and various physical tests in compliance with quality standards.
- Operation and calibration of analytical instruments including HPLC and GC (Chromeleon software), UV-Visible Spectrophotometer, IR, Dissolution Apparatus, Malvern Particle Size Analyzer, Analytical Balance, and pH Meter.
- Ensure compliance with GMP, data integrity principles, and 21 CFR Part 11 regulations,
maintaining accurate and reliable QC documentation.
Note: Apply only if you have minim 2 years of on roll experience and willing to work as Officer - E1 grade.
- Based on your application and screening responses, profiles will be shortlisted for the next stage of the selection process.
- Shortlisted candidates will receive an email communication containing the virtual interview details and meeting link for their selected time slot.
- Please ensure that the email ID and contact details provided in your application are accurate and active.