Job description
1. Having exposure in Pharmaceutical manufacturing in Tab/Liq/cap formulation
2. Receiving and cross verification of dispensed Raw material from stores
3. Supervising the daily manufacturing process and activity as per written SOP
4. Daily documentation entries (BMR/Machine Log/ Temp log/ humidity logs/ cleaning logs and other formats)
5. Shift management & section manpower allocation
6. Should be ready to work in shift.
7. Should be aware of c-GMP guidelines
Desired Candidate Profile
- Please refer to the Job description above
Education-
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