Supv Production - Compression jobs at Teva in India

• 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.

• B.Pharm / M.Pharm
• 4-7 Years of experience

• 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.

• B. Pharm / M. Pharm
• 6+ years of experience

• 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.

• B.Pharm / M.Pharm
• 7-10 Years of experience

• Qualified in Production Tech and Senior Production Technician duties: Assigning daily tasks to production technicians pertaining to manufacturing of encapsulated products, while completing manufacturing documentation per approved procedures. Includes reviewing documentation for completeness and accuracy per established timelines
• Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team.
• Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision
• Extensive equipment knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives.
• Work is performed without appreciable direction while exercising considerable latitude in determining objectives and approaches to assignment
• Good organizational skills, basic first-line management skills for daily operation, situational Leadership and decision-making skills.
• Contributes to the development of new concepts, techniques, and standards including expert knowledge of cGMP standards, and the current Code of Federal Regulations (CFR)
• Coordination of production tasks to meet assigned schedule

• Requires a B.Tech Chemical / Msc -Chemistry. or equivalent

• Requires a minimum of 3 - 5 years of relevant experience in a regulated industry

• Prefer previous experience in a leadership role

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

1. Responsible for upkeep of Granulation area in Production.

2. Responsible for supervising the Granulation area in Production.

3. Preparation and review of SOP’s and other documentation in manufacturing areas.

4. Handling of SAP R/3 system (Manufacturing related transactions).

5. To prepare and review the investigations related to Deviations, OOS, OOT, Market complaints, Exception reports etc.

6. Signing of equipment qualification related documents as a business owner.

7. To review and ensure compliance, calibration, preventive maintenance of all machines in manufacturing areas.

8. Responsible to perform Glorya EDMS related activities.

9. Performing batch manufacturing activities as per BMR instruction.

10. Review of executed batch manufacturing records.

11. Material storage areas management.

12. Ensure Standard Operating Procedure compliance.

13. To comply with the cGMP practices.

14. Undergoing the training as per the identified training needs.

15. Training and utilization of the manpower allotted.

16. Training and development of the manpower allotted in the area to meet the business need.

17. To execute all the tasks assigned by immediate Supervisor/ HOD/ Designee.

18. Responsible for maintaining disciplined work culture in manufacturing area.

19. Management of inspection readiness Program in the Production Department.

20. Participate in the regulatory inspections and internal and external audits.

21. Identification of Shop floor related Improvement Project and implement best Practices in the Production Department.

B.Pharm / M.Pharm

4-7 Years of experience

• Responsible for upkeep of Compression and Coating 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.
  

• Minimum 4 to 7 years of experience in compression and coating (OSD Tablets).
• Should have experience in team handling.
• Qualification B.pharm or M.Pharm is must

Shift Manager

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Qualified in Production Tech and Senior Production Technician duties: Assigning daily tasks to production technicians pertaining to manufacturing of encapsulated products, while completing manufacturing documentation per approved procedures. Includes reviewing documentation for completeness and accuracy per established timelines

•Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team.

•Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision

•Extensive equipment knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives.

•Work is performed without appreciable direction while exercising considerable latitude in determining objectives and approaches to assignment

•Good organizational skills, basic first-line management skills for daily operation, situational Leadership and decision-making skills.

•Contributes to the development of new concepts, techniques, and standards including expert knowledge of cGMP standards, and the current Code of Federal Regulations (CFR)

•Coordination of production tasks to meet assigned schedule

• Requires a B.Tech Chemical / Msc -Chemistry. or equivalent

• Requires a minimum of 3 - 5 years of relevant experience in a regulated industry

• Prefer previous experience in a leadership role

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.