Associate

• 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.
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Work Experience

2-5 years

Education

Competencies