Executive Production

abbott; Mauza Ka Nagla; On-site; INR 400,000 - 700,000; Full time

Job summary

Abbott in India seeks a manufacturing professional for handling SAP transactions and ensuring GMP/compliance in production. The role focuses on QMS documentation, training shop-floor teams on GxP practices, and optimizing manpower use across production lines.

Key tasks include monitoring process parameters (PLC/SCADA), ensuring cGMP adherence, and maintaining batch documentation per SOPs, with ongoing line clearance and in-process checks.

Qualifications

• Experience handling SAP transactions on manufacturing line.

Responsibilities

• Followings will be the Core Job Responsibilities of the position holder:
• To handle various transaction 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.

Skills

SAP transactions

GxP compliance

QMS documentation

Training subordinates

Line clearance

Tools

PLC/SCADA

ISOtrain

Darius

Job description

JOB DESCRIPTION:

Job Description

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.

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Manufacturing

DIVISION:

EPD Established Pharma

LOCATION:

India > Village Mauza : Baddi

WORK SHIFT:

Standard

TRAVEL:

Not specified

MEDICAL SURVEILLANCE:

Not Applicable

SIGNIFICANT WORK ACTIVITIES:

Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)