E0

Job Description
Department: Production
Designation: Jr. Officer - Production (E0)
Working Section: Granulation / Compression / Coating
 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 or Biochemistry
Competencies
Customer Centricity
Developing Talent
Collaboration
Strategic Agility
Process Excellence
Stakeholder Management
Innovation & Creativity
Result Orientation

Work arrangement
No