מציאת משרת הייטק בחברות הטובות ביותר מעולם לא הייתה קלה יותר
Teva Supv Production - Compression India, Goa 792897160
26.08.2025
How you’ll spend your day
- Responsible for upkeep of Compression area in Production.
- Responsible for supervising the Compression 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.
- 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.
- Documentation of all activities in areas worked.
- Daily production planning and execution.
- 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.
- 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.
- Identification of Shop floor related Improvement Project and implement best Practices in the Production Department.
- To ensure compliance to data integrity as per laid down system and procedure.
Your experience and qualifications
- B. Pharm / M. Pharm
- 6+ years of experience
משרות נוספות שיכולות לעניין אותך
