Job Description:
Relevant exp (2-3) yrs in QA.
2. Well versed in CR Phases of-(III & III).
3. Faced Audits like-USFDA, DCGI, MHRA.
4. Released SOP Delegations.
5. Involved in Protocol Inputs.
6. Involved in Documentation.
7. Developed Quality Manuals/Policy/Certification in CR.
8. Involved in monitoring.
9. Immediate Joining.
Send Resume to: hr@g7infotech.in