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
2-6 yrs
Education
Graduation in Science
Diploma in Pharmacy or Engineering
Competencies
- Customer Centricity
- Developing Talent
- Collaboration
- Strategic Agility
- Process Excellence
- Stakeholder Management
- Innovation & Creativity
- Result Orientation
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
2-6 yrs
Education
Graduation in Science
Diploma in Pharmacy or Engineering
Competencies
- Customer Centricity
- Developing Talent
- Collaboration
- Strategic Agility
- Process Excellence
- Stakeholder Management
- Innovation & Creativity
- Result Orientation