Executive

1

Should have knowledge of Ophthalmic Dosage Forms manufacturing process – Solutions, Suspensions and Emulsions

2

Should be well versed with Process Development, Process Design and Process validation.

3

Should have awareness of regulatory guidance for USA/EU and other regulatory markets. 

4

Execution of Development, Scale up, exhibit and validation batches.

5

Review of scale up / exhibit documents – Scale up protocols, Reports, BMRs etc.

6

Should have good communication and writing skills and aware of Good Documentation Practices. 

7

Should have well versed with SAP handling and Quality system software.