Associate

Lupin Ltd

Goa

On-site

INR 167,000 - 391,000

Full time

9 hours ago

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Job summary

Lupin Ltd in Goa seeks a pharma production operator with 2–5 years of hands-on experience in manufacturing. You will work under BMR instructions, ensure GMP compliance and maintain equipment in a clean, safe production area.

The role requires a Diploma in Pharmacy (Pharm D) and HSC, with strong adherence to SOPs and quality guidelines. On-site work with standard QA practices and collaboration with production teams.

Qualifications

2–5 years of experience in pharmaceutical manufacturing.
Diploma in Pharmacy (Pharm D) required.
HSC (10th) or equivalent education.

Responsibilities

Comply with cGMP, GxP and EH&S requirements.
Complete SOP training and follow procedures precisely.
Operate and monitor manufacturing processes under BMR instructions.
Handle raw materials, intermediates and finished goods.
Maintain cleanliness, calibrate and maintain equipment as per SOP.

Skills

Compliance & SOP adherence

Quality awareness

Team collaboration

Problem solving

Attention to detail

Education

Diploma in Pharm D Degree

HSC

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.