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50 Watson Pharmaceuticals Jobs
Supv Production
Watson Pharmaceuticals
posted 30d ago
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Fixed timing
Key skills for the job
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: 60664
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.
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.
Responsible to perform Glorya EDMS related activities.
Performing batch manufacturing activities as per BMR instruction.
Documentation of all activities in areas worked.
Daily production planning and execution.
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.
Responsible for maintaining disciplined work culture in manufacturing area.
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
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Teva s Equal Employment Opportunity Commitment
Employment Type: Full Time, Permanent
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Strict timing
Monday to Friday
No travel
Day Shift
Watson Pharmaceuticals Benefits
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