Pharma job at Lupin Careers | B Pharm Graduates Apply Now
Looking for a growth-driven Pharma Job with a reputed pharmaceutical company? Here’s an excellent opportunity through Lupin Careers for the Trainee Officer position in Jammu. This Pharma Job at Lupin offers hands-on experience in cGMP compliance, production operations, SAP transactions, documentation, and Quality Management Systems. If you are a Pharmacy graduate with 2–5 years of experience, this role under Lupin Careers can help you build a strong foundation in pharmaceutical manufacturing.
About the Company
Lupin is a globally-renowned pharmaceutical company committed to innovation and excellence. We are dedicated to improving patient outcomes and delivering high-quality healthcare solutions. Join our team and contribute to a brighter future for healthcare.
- Position: Trainee Officer
- Location: Jammu, JK, IN
Key Responsibilities
- Comply with all cGMP, GxP, and any other applicable regulatory requirements, including EH&S requirements.
- Complete training on relevant SOPs and develop an understanding of the activities to be conducted before undertaking any task.
- Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to the immediate supervisor/managers.
- Report any quality concerns or suggestions for improvement to supervisors/managers.
- Daily planning, job allocation of departmental activities to fulfill the market requirements, and commitment.
- Monitoring of IMS, Blister, Strip, Bulk, powder, and batch split-up activity.
- Responsible for shipper labeling as per EMO & all the transactions in SAP for finished products.
- Packing and documentation of assigned products as per instructions given in the BPR, SOP, and cGMP.
- Ensuring the movement of bulk, packing material, semi-finished, and finished goods as per SOP.
- Updating and monitoring of Overall Equipment Efficiency (OEE).
- To upkeep cleanliness of the area and the machine as per GMP requirements.
- Operation, washing, and cleaning of equipment and accessories used in related production activities as per SOP.
- Performing in-process checks as per the respective BPR and recording of results of in-process checks in the BPR.
- Monitoring of differential pressure, temperature, and relative humidity as per SOP.
- Ensure calibration and preventive maintenance of equipment and instruments as per the approved schedule, and the results of the same meet the standards.
- To initiate and review the request, such as additional material requisition, material return note, packing material carry forward stereo request, and screen request, etc.
- Area and equipment usage documented as per SOP.
- Procurement, receipt, nomenclature, issuance, retrieval, and destruction of change parts for packing.
- Online reconciliation and review of batch packing record.
- Preparation and review of Standard Operating Procedures and batch packing records.
- Preparation and review of validation and qualification of process and equipment.
- To organize and implement on-the-job training of employees and contractual workmen in the department.
- Handling of change controls, deviations, and CAPA through QAMS.
- To perform the investigation related to market complaints, deviations, nonconformities, and implementation of suitable corrective and preventive actions (outcomes of the investigations) within the proposed timelines.
- Coordination between PPC, PM, Engineering, and the QC department to ensure smooth functioning of production activity.
- To ensure proper self-hygiene before entering the production area, and follow all the rules and regulations set by the HR department.
- Plan for dispensing activities in accordance with the plan and to coordinate with the production planning and control department for the timely availability of P.M.
- To ensure effective control on usage of manpower, machines, and material in the department, and maintain proper inventory of operating supplies in the department.
- To support the Quality Management System and to report any discrepancy, abnormality, non-conformance, or any incident observed to the department head and the QA head.
- Checking of label, insert/outsert with batch packing record, and also retention of all required packing material proof with batch packing record for the packing section.
- Troubleshooting: Handling, ensuring, verifying, and troubleshooting of software like bar-coding (1D, 2D), ACG Inspection System for label, blister inspection system, inkjet coding, Data Acquisition System (DAS), and Caliber QAMS.
- Any additional responsibility delegated by the department head.
Qualification
- Graduation in Pharmacy
Work Experience:
- 2 to 5 Years
Competencies
- Collaboration
- Customer Centricity
- Developing Talent
- Innovation & Creativity
- Process Excellence
- Result Orientation
- Stakeholder Management
- Strategic Agility
