Associate

Lupin Ltd; Nagpur District; On-site; INR 200,000 - 340,000; Full time

Job summary

Lupin Ltd in India is seeking a Production/Manufacturing operator to execute batch manufacturing activities under supervision in accordance with approved SOPs and BMRs.

The role requires 2–6 years' experience in pharmaceutical manufacturing, a science degree or diploma in engineering/pharmacy, and diligent adherence to cGMP, EH&S and safety standards in a fast-paced production environment.

Qualifications

• 2-6 years of pharmaceutical manufacturing experience.
• Graduation in Science or Diploma in Engineering/Pharmacy.
• Knowledge of cGMP and safety guidelines.

Responsibilities

• Manufacturing and processing of batches under supervision.
• Follow SOPs and record results in BMR.
• Maintain GMP compliance and workplace hygiene.

Skills

Innovation & Creativity

Result Orientation

Collaboration

Customer Centricity

Developing Talent

Stakeholder Management

Strategic Agility

Process Excellence

Education

Graduation in Science

Diploma in Engineering or Pharmacy

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 - 6 yrs

Education

Graduation in Science

Diploma in Engineering or Pharmacy

Competencies

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