Executive Production

Abbott

Solan

On-site

INR 420,000 - 640,000

Full time

19 hours ago
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Job summary

Abbott in Solan, Himachal Pradesh, India, seeks a manufacturing specialist to execute SAP transactions, drive monthly production targets, and train subordinates on GxP practices on the shop floor. You will manage QMS documentation, perform line clearances, and ensure in-process checks against BMR and PLC/SCADA parameters before machine runs, while upholding cGMP and Good Documentation Practices.

Additionally, you will identify and troubleshoot equipment issues, review PV protocols, and support

Qualifications

  • Handle SAP transactions and ensure data accuracy.
  • Maintain QMS documentation and ensure GxP compliance.
  • Provide training on shop floor GxP activities.
  • Identify alarms and manage per SOP.
  • Review machine operation per equipment SOP.

Responsibilities

  • 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 knowledge
QMS documentation
Alarms management
Training subordinates
Safety & COBC

Tools

PLC/SCADA
Darius
ISOtrain
BMR

Job description

Job Description
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.
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