Select how often (in days) to receive an alert: Supv Production
Date: Feb 7, 2025
Location:
Goa, India, 403722
Company: Teva Pharmaceuticals
Job Id: 60666
Who we are
How you ll spend your day
Responsible for upkeep of Granulation area in Production.
Responsible for supervising the Granulation area in Production.
Preparation and review of SOP s and other documentation in manufacturing areas.
Handling of SAP R/3 system (Manufacturing related transactions).
To prepare and review the investigations related to Deviations, OOS, OOT, Market complaints, Exception reports etc.
To initiate, review and impact assessment of Quality management systems as part of investigation such as Change controls, CAPAs, Risk assessment etc.
Signing of equipment qualification related documents as a business owner.
Responsible to perform Glorya EDMS related activities.
Performing batch manufacturing activities as per BMR instruction.
Coordination with cross functional departments for smooth functioning of production activities.
Review of executed batch manufacturing records.
Material storage areas management.
Ensure Standard Operating Procedure compliance.
To comply with the cGMP practices.
Undergoing the training as per the identified training needs.
Training and utilization of the manpower allotted.
Training and development of the manpower allotted in the area to meet the business need.
To execute all the tasks assigned by immediate Supervisor/ HOD/ Designee.
To follow the normal safety precautions in production department.
To ensure readiness of the department for regulatory inspections and ensure their compliance.
Management of inspection readiness Program in the Production Department.
Participate in the regulatory inspections and internal and external audits.
Your experience and qualifications
B.Pharm/M.Pharm
4-7 Years of experience
Reports To
In process of validation
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