The incumbent will be responsible for Analytical Development Department (ANDA) , validation and transfer of method to sites Regulatory queries and QA reviews. .
Effective in communicating status, progress and challenges
Create SOPs, test dosage forms like tablets, capsules, syrups, suspensions and injections.
Designing of master validation protocols for various analytical methods.
Analytical development report generation for generic products (EU/ ANDA)
Troubleshooting problems for various analytical methods.
Validation of analytical methods.
M.Sc. / M.Pharma / Ph.H. with similar experience in a reputed pharma R&D.