EA

Lupin; Goa; Sur place; INR 320 000 - 520 000; Plein temps

Résumé du poste

Lupin Ltd. in Goa is seeking an Associate- Production to operate Granulation, Compression, Coating and Encapsulation processes in a cGMP environment.

You will ensure adherence to SOPs and BMR, handle RM/PM, perform in-process checks, maintain area cleanliness, and coordinate with QA Head for quality and yield improvements.

Training on SOPs, EH&S compliance, and ongoing skill development will be provided to support cost effectiveness and production yield goals.

Qualifications

• Diploma in Pharmacy is required.
• Graduation in Science is preferred.
• 2-5 years of relevant experience in pharmaceutical production is desirable.

Responsabilités

• Manufacture/batch processing under supervision as per BMR and SOPs.
• Handle raw materials, in-process, and finished goods with proper documentation.
• Perform line clearances during batch changes and ensure GMP compliance.

Connaissances

Result Orientation

Customer Centricity

Developing Talent

Stakeholder Management

Strategic Agility

Process Excellence

Formation

Diploma in Pharmacy

Graduation in Science

Description du poste

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

2-5 years

Education

Diploma in Pharmacy

Graduation in Science

Result Orientation

Customer Centricity

Developing Talent

Stakeholder Management

Strategic Agility

Process Excellence