Role & responsibilities Preferred candidate profile 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 current products /Site transfer products. 4. Preparation and review of scale up batches documents for new 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 (Ahmedabad)
🏢 Intas
📍 Ahmedabad
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