Associate

Lupin Ltd

Chhatrapati Sambhajinagar District

On-site

INR 300,000 - 500,000

Full time

24 hours ago
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Job summary

Lupin Ltd in Maharashtra, India is seeking a Production Operator with 2–5 years of experience in GMP manufacturing. The role involves following SOPs, handling materials, operating equipment, and recording process data to ensure quality and compliance.

The candidate should hold a Diploma and be ready to participate in cGMP training, with a focus on process excellence and team collaboration in a fast-paced production environment.

Qualifications

  • Diploma required
  • 2–5 years of work experience in manufacturing/ pharma environments
  • Familiarity with GMP/GxP standards and SOP adherence
  • Ability to follow BMRs and SOPs accurately
  • Capable of maintaining clean and organized production areas
  • Willingness to attend cGMP/On Job training and in-house courses

Responsibilities

  • Manufacture/pack/batch production under supervision following BMR and SOPs
  • Handle raw materials, intermediates, and finished goods with proper inventory control
  • Operate, clean and maintain production equipment per SOPs
  • Record process results accurately in documentation
  • Maintain hygiene and compliance with HR and GMP requirements
  • Conduct in-process checks and participate in line clearance activities
  • Identify and report quality issues, deviations, or non-conformances
  • Assist in calibration and preventive maintenance of equipment as scheduled
  • Assist in training and development activities as needed

Skills

GMP compliance
Attention to detail
Problem solving
Team collaboration
Process excellence
Innovation
Stakeholder management
Strategic agility

Education

Diploma

Job description

Job Description
  • 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

2 to 5 years.

Education

Diploma

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