Executive Production

Abbott Laboratories; Solan; On-site; INR 700,000 - 1,000,000; Full time

Job summary

Abbott Laboratories in India (Baddi) seeks a Senior Executive to supervise production activities, ensure GMP/GxP compliance, and train shop floor staff. The role emphasizes SAP-based transactions, line clearances, and adherence to BMR and SOPs.

Safety and COBC practices are required as part of daily operations. The position covers monitoring of process parameters, troubleshooting manufacturing issues, and maintaining documentation per cGMP guidelines while supporting continuous improvement

Responsibilities

• To handle various transactions in SAP.
• Responsible for achieving monthly target of production department.
• Handling of QMS documents, impart training to subordinates in manufacturing area on shop floor for GxP activities.
• Work distribution and optimum utilization of manpower. Alarm Identification and management as per SOP.
• To ensure all in-process checks and monitoring of all intermediate processes, to check set process parameters in PLC/SCADA as per BMR before machine run in manufacturing area.
• Ensure compliance of all procedure, practices and system to cGMP with respect to Abbott Quality guideline, other applicable regulatory guidelines and standard operating procedures at site. Ensure that Good Documentation Practices shall comply during the production process.
• To check/ review/verify operation of manufacturing machine as per respective equipment operation SOP.
• Provide input and guidance to improve the right first time of the production batch/ batch documents. Preparation, review of protocol and report (Technical/ Study/ Non-routine) on need basis.
• To identify the problems with the machine and undertake trouble shooting activity where required, upkeep the change parts, to ensure work is carried in the Manufacturing section according to the SOPs, to coordinate with departmental colleagues, HOD & QA in cases of any discrepancies in manufacturing Section.
• Responsible for investigation of exception/ non-compliance in the manufacturing area, preparation and review of investigation report. Review of standard operating procedure, master documents of production and batch document etc.
• Preparation, review and execution of commercial batch, PV protocol/ BMR.
• Dispensing and manufacturing process compliance in accordance with approved BMR.
• To carry out line clearance, In-Process checks at the different stages of manufacturing.
• SOP training in ISOtrain of self-train within stipulated times and to ensure no past due training.
• SOP preparation and upload in Darius as per need.
• To follow all the practices related to safety and COBC.
• To support the team on additional responsibilities assigned time to time.

Job description

Location India > Village Mauza : Baddi Category Operations

Followings will be the Core Job Responsibilities of the position holder:

1.To handle various transaction in SAP.

2.Responsible for achieving monthly target of production department.

3.Handling of QMS documents, impart training to subordinates in manufacturing area on shop floor for GxP activities.

4.Work distribution and optimum utilization of manpower. Alarm Identification and management as per SOP.

5. To ensure all in-process checks and monitoring of all intermediate processes, to check set process parameters in PLC/SCADA as per BMR before machine run in manufacturing area.

6.Ensure compliance of all procedure, practices and system to cGMP with respect to Abbott Quality guideline, other applicable regulatory guidelines and standard operating procedures at site. Ensure that Good Documentation Practices shall comply during the production process.

7.To check/ review/verify operation of manufacturing machine as per respective equipment operation SOP.

8.Provide input and guidance to improve the right first time of the production batch/ batch documents. Preparation, review of protocol and report (Technical/ Study/ Non-routine) on need basis.

9. To identify the problems with the machine and undertake trouble shooting activity where required, upkeep the change parts, to ensure work is carried in the Manufacturing section according to the SOPs, to coordinate with departmental colleagues, HOD & QA in cases of any discrepancies in manufacturing Section.

10. Responsible for investigation of exception/ non-compliance in the manufacturing area, preparation and review of investigation report. Review of standard operating procedure, master documents of production and batch document etc.

11. Preparation, review and execution of commercial batch, PV protocol/ BMR.

12. Dispensing and manufacturing process compliance in accordance with approved BMR.

13. To carry out line clearance, In-Process checks at the different stages of manufacturing.

14. SOP training in ISOtrain of self-train within stipulated times and to ensure no past due training.

15. SOP preparation and upload in Darius as per need.

16. To follow all the practices related to safety and COBC.

17. To support the team on additional responsibilities assigned time to time.

Location India > Village Mauza : Baddi Category Operations

MAIN PURPOSE OF THE ROLEPlan, direct, and monitor all production activities within an assigned area or unit to maximize the use of the organization's resources and meet established production specific

Location India > Village Mauza : Baddi Category Operations

Department . Engineering (Plant Maintenance.)Designation . Senior Executive 1C Qualification . B Tach (Electrical/Instrumentation

Location India > Village Mauza : Baddi Category Operations

Division-Location : EPD-Baddi Department: Operational ExcellenceDesignation Senior Manager Grade/Band: 3BReporting to

Job Id 31163415 LocationIndia > Village Mauza : Baddi Medical surveillance Not Applicable Division EPD Established Pharma Travel Not specified Additional Location Significant work activities Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

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