Job Description

Department DetailsRole Summary1 To monitor the compliance with the requirements of Good Manufacturing Practice
2 To ensure the instructions relating to production operations are strictly followed
3 To update the real time data entry in BMR'S,CKL,LS ,ECC and other documents in
DSP2
4 To execute equipment qualification protocols and validation protocols.
5 To perform and document operations in accordance with cGMP.
6 Maintenance of Production equipment in coordination with maintenance department
7 To comply with EHS policies and procedures
8 Responsible for OTIF execution of all the activities related to Downstream Purification2
9 Data owner for process equipment used in day-today activityKey Responsibilities1 To monitor the compliance with the requirements of Good Manufacturing Practice
2 To ensure the instructions relating to production operations are strictly followed
3 To update the real time data entry in BMR'S,CKL,LS ,ECC and other documents in
DSP2
4 To execute equipment qualification protocols and validation protocols.
5 To perform and document operations in accordance with cGMP.
6 Maintenance of Production equipment in coordination with maintenance department
7 To comply with EHS policies and procedures
8 Responsible for OTIF execution of all the activities related to Downstream Purification2
9 Data owner for process equipment used in day-today activityEducational QualificationsRequired Education Qualification: B.Pharma
Required Experience: 2 - 4 years

Biocon