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56 Watson Pharama Jobs
Supv Production
Watson Pharama
posted 4hr ago
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Job Description
Find a Career With Purpose at Teva
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Select how often (in days) to receive an alert: Supv Production Date: Feb 7, 2025
Location:
Goa, India, 403722
Company: Teva Pharmaceuticals
Job Id: 60662
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.
Signing of equipment qualification related documents as a business owner.
To review and ensure compliance, calibration, preventive maintenance of all machines in manufacturing areas.
Responsible to perform Glorya EDMS related activities.
Performing batch manufacturing activities as per BMR instruction.
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.
Responsible for maintaining disciplined work culture in manufacturing area.
Management of inspection readiness Program in the Production Department.
Participate in the regulatory inspections and internal and external audits.
Identification of Shop floor related Improvement Project and implement best Practices in the Production Department.
Your experience and qualifications
B.Pharm / M.Pharm
4-7 Years of experience
Teva s Equal Employment Opportunity Commitment
Employment Type: Full Time, Permanent
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based on 8 employees
Strict timing
Monday to Friday
Within city
Day Shift
Watson Pharama Benefits
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