Posted:1 week ago|
Platform:
Work from Office
Full Time
A. To handling and Leading the production team.
B. Handling of all activities in the production of API and intermediate complying with safety, GMP and Statutory requirements.
C. Production planning based on target set by the management and arranging manpower and raw material.
D. Trouble shooting and critical situation handling during the manufacturing at plant.
E. To focus and work towards achieving cost reduction, reduction in Batch time cycle, improvement in production capacity.
F. To be done technology transfer of new product in co-operation with R & D dept.
G. To be scale up from kilo lab / pilot plant to commercial scale.
H. Review the documents prepared by the Executive/designee production.
I. Review of BMR /ECR after Batch / Cleaning completion.
J. Execute the production planning with the coordination of production team.
K. Conduct training of staff on cGMP etc.
L. Coordinate with other department like Quality control, Quality assurance, ware House, HR and engineering, and R & D for smooth functioning of production activity.
M. To ensure that all policy and procedures are followed in the department during the manufacturing activity.
N. Handling of deviation/ Incident and prepare CAPA for any deviation/OOS occurred during the manufacturing activity.
O. To ensure good housekeeping in the production area.
P. Ensure that all production related documents are filled online and submitted in the Quality Assurance department on time.
Q. Review Qualification documents and Monitor Qualification for All new Equipment, and generate its Qualification report and submit to QA.
R. To ensure that validation activities are carried out as per respective protocol.
S. To ensure compliance of SOP in their respective areas.
BDR Pharmaceuticals
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