1. To handling of QMS activities (CRF/Deviation/OOS/OOT)
2. To review and technical input for tech transfer documents.
3. Preparation and review of scale up batches documents for new products /Site transfer products.
4. Preparation and review of scale up batches documents for current products /Site transfer products.
5. Preparation & review of relevant documents (MPCR, PVP, PVR, hold time study protocol / report).
6. To manage the department documentation activities (TTD Distribution/Maintain logbook and other documents.
7. Tech transfer activities for CMO products.
Experience: 3 To 6 Years
Education: B.Pharma/M.Pharma
Designation: Executive/Sr. Executive
Department: PDL
📌 Urgent opening For PDL -Doc cell Department @ SEZ Plant- Ahmedabad
🏢 Intas
📍 Ahmedabad
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