Hiring for GM ( R&D formaultion of Solid & injectables)
Location - Hyderabad
Years of experience - 15 Years
Role
1. To lead development teams (FD & AD) responsible for the sterile drug product development.
2. Responsible for the identification and development of New drug as per company requirement.
3. Review and approval of necessary technical documents required for submission.
4. Coordination with cross functional teams of regulatory submission.
5. Responsible for supporting regulatory affairs department and ANDA submission and responding CMC query.
6. Responsible for review and approval of technical documents related to drug product development for ANDA submission.
7.Responsible for FD and AD SOP approval and implementation.
8. Follow all SOPs and safety guidelines to ensure compliance with a cGmp environment and par safety practices.
9. Activities other than those defined in the job responsibilities are to be done, as per the requirement of management by following management instructions and guidance.
For more details reach us to neelima@aegisconsultants.in/ 7045502901
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