ASSISTANT MANAGER

Department Details

Role Summary

Generic Formulations - Supervisor Manufacturing

Key Responsibilities

• Responsible for Manufacturing of solid oral dosage forms. • Candidate must have faced major regulatory audits (like USFDA, MHRA etc.) • Preparation and updatation standard procedures (SOP/EOP/IOP/SCP) for different activities, as per regulatory requirements. • Team Development through technical and procedural training. • To ensure the compliance of standard procedures by the team. • Implementation of GMP norms in daily production activities. • Assure the real time data capturing and other GDP principles by the team at production. • To ensure online up-date of manufacturing records. • Execution of Equipment Qualification. • Equipment upkeeping through on time completion of machine maintenance in co-ordination with Engineering persons. • Candidate shall be responsible to maintain change part inventory at minimum level. • Person shall have responsibility to handle the Quality management system (QMS) activities in Trackwise. • Candidate should have SAP knowledge and shall be responsible to update the production related activities in SAP. • Responsible for execution and completion of daily production plan. • Should have good communication skill to co-ordinate with internal stake holders like Warehouse, QA, QC, Maintenance to meet daily production plans. • Work with FR&D and TT persons from smooth execution of Process optimization activity. • Candidate shall be responsible for deliverance of exhibit/process validation batches as per committed timeline. • Preparation and updatation of Batch Manufacturing records considering the regulatory requirements. • To update reporting manager about availability of spares and consumables on shop floor. • To prioritize and practice the safety principles and company policies in factory premises. • To work upon Operational Excellence projects.

Educational Qualifications

Required Education Qualification: B.pharma
Required Experience: 4 - 10 years