JOB RESPONSIBILITIES :
1. To perform analysis of routine FRD samples, market complaint samples & Stability samples, analytical method development and validation by different spectroscopic methods as per ICH guidelines.
2. To perform Drug-Excipient comparability studies of different projects and Analysis of Reference Listed Drug samples to generate data for dossier submission.
3. Literature search on Internet regarding analytical methods i.e journals, pharmacopoeia.
4. Preparation of Standard Testing Procedures, Analytical method validation protocol & Analytical method validation Report.
5. HPLC trouble shooting.
6. Calibration of all analytical instruments like Analytical Balance, UV Spectrophotometer,Karl Fischer, Dissolution Apparatus, HPLC, Gas Chromatography.
7. To review internal and external calibration reports and submit to DQA.
GMP Aspects:
1. To adhere to cGMP as per ICH Q7 guidelines relevant to the job.
2. To maintain Good Documentation Practices and Good Laboratory Practices.
Safety Aspects:
1. Follow all safety instructions and practices.
2. Responsible to maintain the cleanliness and hygiene.
3. Responsible to maintain and use Personal Protective Equipment, wherever applicable.
Pay: Up to ₹50,000.00 per month
Benefits:
- Food provided
- Paid sick time
- Provident Fund
Work Location: In person
