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Teva Pharmaceuticals
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Supv Production

Supv Production

Teva Pharmaceuticals

0 years

0 Lacs

goa india

Posted:4 days ago| Platform:

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Skills Required

documentation manufacturing sap reports compliance calibration maintenance storage training development management inspection

Work Mode

On-site

Job Type

Full Time

Job Description

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.

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Teva Pharmaceuticals

Pharmaceutical Manufacturing

Teva Pharmaceuticals

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Supv Production