Job Description

Department DetailsRole Summary1 To monitor the compliance with the requirements of Good Manufacturing Practice
2 Ensure that the batches are manufactured as per production plan without any delays
3 Adherence to the standard operating procedures and ensure the team is following the defined procedures
4 Production planning and inventory control : Responsible for ensuring the availability of Raw material prior to start of batch
5 DS dispensing in coordination with team and ensure timely release of batches
6 Ensure the GMP documents are reviewed and submitted to QA as per the SLA
7 Investigation of non-conforming/Deviations/OOS/OOT and implementation of CAPA. To ensure these documents are closed on time as per SLA
8 Ensuring to maintain the qualified status of all the production equipment in coordination with CFT
9 Regular maintenance of production equipment in coordination with engineering and maintenance department
10 Planning for CAPEX and OPEX requirements
11 To initiate, coordinate and verify the CAPA taken against the nonconformance observed during the audit
12 Guiding the team members in the preparation, hazard and risk assessment register, aspect/impact register and reviewing the adequacy
13 To follow the established procedures and policies of the company pertaining to EHS and ensuring effective implementation of EHS management system .Reviewing the progress/status of EHS objectives & targets periodically
14 Responsible for giving objectives and proper utilization production personnel
15 Training and evaluation of production personnel and there by minimise the manual errorsKey Responsibilities1 To monitor the compliance with the requirements of Good Manufacturing Practice
2 Ensure that the batches are manufactured as per production plan without any delays
3 Adherence to the standard operating procedures and ensure the team is following the defined procedures
4 Production planning and inventory control : Responsible for ensuring the availability of Raw material prior to start of batch
5 DS dispensing in coordination with team and ensure timely release of batches
6 Ensure the GMP documents are reviewed and submitted to QA as per the SLA
7 Investigation of non-conforming/Deviations/OOS/OOT and implementation of CAPA. To ensure these documents are closed on time as per SLA
8 Ensuring to maintain the qualified status of all the production equipment in coordination with CFT
9 Regular maintenance of production equipment in coordination with engineering and maintenance department
10 Planning for CAPEX and OPEX requirements
11 To initiate, coordinate and verify the CAPA taken against the nonconformance observed during the audit
12 Guiding the team members in the preparation, hazard and risk assessment register, aspect/impact register and reviewing the adequacy
13 To follow the established procedures and policies of the company pertaining to EHS and ensuring effective implementation of EHS management system .Reviewing the progress/status of EHS objectives & targets periodically
14 Responsible for giving objectives and proper utilization production personnel
15 Training and evaluation of production personnel and there by minimise the manual errorsEducational QualificationsRequired Education Qualification: B.Pharma
Required Experience: 1 - 5 years

Biocon