Description

1. Responsible for analysis of development, routine and stability samples of transdermal system.
2. Responsible for execution of Method validation activities (Assay, Dissolution, Related substances, IVRT, etc.)
3. Responsible for execution of activities such as Method verification, Method equivalency, deformulation study, Regulatory query and qualification of working standards.
4. Responsible for maintaining cleanliness and compliance for analytical activities.
5. Responsible for ensuring laboratory safety, Good laboratory practices and good manufacturing practices in the lab.
6. Responsible for Valuable document practices in the lab.
7. Responsible for performing periodic calibration, daily calibration of instruments/equipment and daily temperature monitoring in the lab.
8. Responsible for preparation of report of protocol bound studies.
9. Responsible for execution of Method transfer at respective location.
10. Responsible for investigational analysis in the lab.

Qualifications

1. Very good knowledge in ICH guidelines,

2. Very good knowledge in USP General chapters,

3. Very good understanding about regulatory expectations.

4. Qualified in M. pharm with first class.

📌 Research Scientist (Hyderabad)
🏢 Aveva Drug Delivery Systems
📍 Hyderabad