ASSISTANT MANAGER

Biocon

ProductionProduction Supervisor

Responsible for manufacturing of Solid oral dosage forms in Generic formulation facility BPL.
To prepare standard procedures for different activities.
To impart training to the team members as per the requirement.
To follow and implement GMP and GMP norms in daily production activities.
To follow the GDP during documentation.
To act towards the organizational goals assigned from time to time.
To follow the standard operating procedures, good documentation practices and good documentation practices all the time.
Follow the safety practices and company policies in factory premises.
Responsible for preparation and execution of Qualification of documents.
To handle the Quality Management System (QMS).
To maintain the minimum inventory of change parts.
To co-ordinate with internal stake holders like Warehouse, QA, QC, Maintenance to meet daily production plans.
To coordinate with maintenance persons for on the time maintenance for equipment.
To execute Process Validation, exhibit batches and preprocess optimization batches.
To prepare Batch Manufacturing records for different products.
To update reporting manager about availability of change parts and consumables on shopfloor.
To facilitate R&D for product scale up, product validation as per production plan.
To coordinate for execution of exhibit batch.
To ensure the implementation of CAPA.
To work upon Operational Excellence projects.

Responsible for Manufacturing of solid oral dosage forms in Generic formulation facility

Responsible for manufacturing of Solid oral dosage forms in Generic formulation facility BPL.
To prepare standard procedures for different activities.
To impart training to the team members as per the requirement.
To follow and implement GMP and GMP norms in daily production activities.
To follow the GDP during documentation.
To act towards the organizational goals assigned from time to time.
To follow the standard operating procedures, good documentation practices and good documentation practices all the time.
Follow the safety practices and company policies in factory premises.
Responsible for preparation and execution of Qualification of documents.
To handle the Quality Management System (QMS).
To maintain the minimum inventory of change parts.
To co-ordinate with internal stake holders like Warehouse, QA, QC, Maintenance to meet daily production plans.
To coordinate with maintenance persons for on the time maintenance for equipment.
To execute Process Validation, exhibit batches and preprocess optimization batches.
To prepare Batch Manufacturing records for different products.
To update reporting manager about availability of change parts and consumables on shopfloor.
To facilitate R&D for product scale up, product validation as per production plan.
To coordinate for execution of exhibit batch.
To ensure the implementation of CAPA.
To work upon Operational Excellence projects.

B.Pharm, M.PharmRequired Education Qualification: B.pharma
Required Experience: 6 - 10 years