2 - 7 years
4 - 6 Lacs
Posted:13 hours ago|
Platform:
Work from Office
Full Time
Greetings of the day !
Our reputed MNC Client is hiring for:
Designation: Regulatory Affairs- EU Market- Pre & Post Approval
Location: Hyderabad
Shift: General
Work Mode: WFO (5 days working)
Interview Mode: F2F interview
1. Component with EU-Filing requirements with respect to Module 2 & 3 ability to independently and correctly review technical documents related to Quality Module
2. Well versed with EU- Regulatory guidance and Processes (i.e. Ability to understand and interpret technical expectations as per applicable ICH & EMEA guidelines)
3. Clear Knowledge of basic aspects of a formulation (primarily pharmaceutical development along with general analytical aspects) for effective review of R&;D documents
4. Should be aware of post approval variation requirements in EU markets. Should have basic QA knowledge to enable correct review of plant related documents
Warm Regards,
Gayatri Kumari
V3 Staffing Solutions
V3 Staffing
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