Staff

Lupin Ltd

Chhatrapati Sambhajinagar District

On-site

INR 300,000 - 420,000

Full time

36 hours ago
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Job summary

Lupin Ltd in Maharashtra is seeking an Associate- Production to work in the Granulation, Compression, Coating and Encapsulation areas. You will ensure adherence to cGMP/GxP, complete SOP training, and report any deviations to supervisors. You will handle materials and perform manufacturing steps under BMR instructions.

The role requires strict hygiene, line clearance during batch changes, and active participation in QA/QMS processes, with attention to safety, health and environment guidelines.

Qualifications

  • Follow cGMP, GxP and EH&S requirements as applicable.
  • Complete training on SOPs and understand activities before task.
  • Report any difficulty or deviation to supervisor/ managers.

Responsibilities

  • Manufacture/ process batches under supervision per BMR instructions.
  • Handle and move raw materials, bulk, semi-finished and finished goods.
  • Operate, wash and clean equipment and accessories as per SOPs.

Skills

cGMP compliance
SOP training
Quality reporting

Job description

Job Description

Department: Production

Designation: Associate- Production

Working Section: Granulation, Compression, Coating and Encapsulation

  • Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements.
  • Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task.
  • Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers.
  • Report any quality concern or suggestion for improvement to supervisors/ managers.
  • Manufacturing / processing of batches of assigned products under supervision as per instructions given in the BMR.
  • Handling and movement of raw material, bulk, semi-finished and finished goods.
  • Operation, washing and cleaning of equipment’s and accessories used in related production activities as per respective SOP.
  • Up-keeping area and machines as per GMP requirements.
  • To Support Quality Management Systems and to report any discrepancy, abnormity, non-conformance or any incidence observed to the Department Head and QA Head.
  • Receipt of RM and PM from Warehouse and ensuring overall cleanliness of areas.
  • Doing operations as per the SOPs and BMR with online recording in respective documents as applicable.
  • To ensure self-hygiene before entering in the production area and follow all the other rules & regulation set by HR department.
  • Performing in-process checks as per respective BMR and recording of results of in respective documents as applicable.
  • To fulfil the training need as per current needs with respect to cGMP, Job, safety, health & Hygiene by attending the training programmes.
  • Cost effectiveness in production operation by controlling overtime, revenue expenses and achieving standard yield.
  • Critically monitoring of the environmental conditions with a view to meet the standards mentioned in BMR and SOP.
  • Ensure calibration and preventive maintenance of manufacturing equipment and instruments as per approved schedule and the results of same meeting the standards.
  • To perform line clearance activity during batch to batch and product to product change over and ensure the compliance as per SOP.
  • Issuance, retrieval and destruction of dies and punches, product dedicated bags and sieves, silicon sleeves, pipes, hose pipes and screens.
  • To ensure the audit compliance.
  • Trouble-shooting: To attend the problems of machine and process as and when necessary.
  • Any other assignment allocated by production Head.
  • To attend required cGMP/ On Job /Functional training activities as per planner.

Work Experience

Education

Competencies
  • Innovation & Creativity
  • Result Orientation
  • Collaboration
  • Customer Centricity
  • Developing Talent
  • Stakeholder Management
  • Strategic Agility
  • Process Excellence
Job Description

Department: Production

Designation: Associate- Production

Working Section: Granulation, Compression, Coating and Encapsulation

  • Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements.
  • Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task.
  • Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers.
  • Report any quality concern or suggestion for improvement to supervisors/ managers.
  • Manufacturing / processing of batches of assigned products under supervision as per instructions given in the BMR.
  • Handling and movement of raw material, bulk, semi-finished and finished goods.
  • Operation, washing and cleaning of equipment’s and accessories used in related production activities as per respective SOP.
  • Up-keeping area and machines as per GMP requirements.
  • To Support Quality Management Systems and to report any discrepancy, abnormity, non-conformance or any incidence observed to the Department Head and QA Head.
  • Receipt of RM and PM from Warehouse and ensuring overall cleanliness of areas.
  • Doing operations as per the SOPs and BMR with online recording in respective documents as applicable.
  • To ensure self-hygiene before entering in the production area and follow all the other rules & regulation set by HR department.
  • Performing in-process checks as per respective BMR and recording of results of in respective documents as applicable.
  • To fulfil the training need as per current needs with respect to cGMP, Job, safety, health & Hygiene by attending the training programmes.
  • Cost effectiveness in production operation by controlling overtime, revenue expenses and achieving standard yield.
  • Critically monitoring of the environmental conditions with a view to meet the standards mentioned in BMR and SOP.
  • Ensure calibration and preventive maintenance of manufacturing equipment and instruments as per approved schedule and the results of same meeting the standards.
  • To perform line clearance activity during batch to batch and product to product change over and ensure the compliance as per SOP.
  • Issuance, retrieval and destruction of dies and punches, product dedicated bags and sieves, silicon sleeves, pipes, hose pipes and screens.
  • To ensure the audit compliance.
  • Trouble-shooting: To attend the problems of machine and process as and when necessary.
  • Any other assignment allocated by production Head.
  • To attend required cGMP/ On Job /Functional training activities as per planner.

Work Experience

Education

Competencies
  • Innovation & Creativity
  • Result Orientation
  • Collaboration
  • Customer Centricity
  • Developing Talent
  • Stakeholder Management
  • Strategic Agility
  • Process Excellence
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