- Organizing, maintaining, and filing regulatory documents globally, ensuring compliance with regulatory guidelines.
- Prompt regulatory support to the customers.
- Collaboration & engaging in periodic customer teleconferences to resolve queries
- Change control evaluation and plant support
- Scheduling the life cycle management activities globally for all the regulatory submissions complying with region specific requirements
- Ensure the Drug Master File (DMF) deficiency letters received from various regulatory agencies globally are responded in time with adequacy and accuracy.
Note : Synthesis R&D; experience (2 to 5 years) can be consider for 1 position - FEMALE
📌 Walk-in || Jr. Executive (Hyderabad)
🏢 Biophore
📍 Hyderabad
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