EA

Job Description

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

1-4 YEARS

Education

Diploma in Pharmacy

Others in Industrial Chemistry

Competencies

Innovation & Creativity

Result Orientation

Collaboration

Customer Centricity

Developing Talent

Stakeholder Management

Strategic Agility

Process Excellence