SUNIL KUMAR PANIGRAHI

To Work in a challenging environment wherein I can make the best use of my academic knowledge and abilities. To contribute to the success of the organization and thereby enhance professional advancement inthepharmaceutical Field.

➢ To monitor shop floor activities and report non-compliance in

terms of Nonconformance along with root cause.

➢ Audit trial review of SCADA system

➢ Product related recipe review of manufacturing equipment.

➢ To ensure and perform on time sampling like Blend

Uniformity, Statified sample,Inprocess sample,Finish product

sample and monitoring of process validation, engineering batches

and commercial batches.

➢ Review of Critical Process Parameter of product.

➢ Review of executed record and release for next stage.

➢ GMP round in facility to check activities performed as per

approved instructions.

➢ Basic norms of cGMP are being followed.

➢ Line clearance during Product changeover for equipment and

area.

➢ In process control as per procedure.

➢ Checking of overprinted details and proof checking.

➢ Perform to AQL as per SOP

➢ Sampling and pack line inspection of finished product.

➢ Review of Batch records (BMR & BPR), Daily production

records

➢ Approval of Excess material consumption memo.

➢ Batch card printing (BMR & BPR).

➢ Approval of Machine setting before execution of batch.

➢ Job card number issue during Breakdown.

REVIEW:

➢ Review of BMR & BPR.

➢ Review of log books and Checklist.

➢ Review of machine alarm Log book.

➢ Review of Audit trail. (Critical and non-critical equipments)

I hereby declare that all the statements made in above are correct to the best of my knowledge and belief.