Packaging Associate

Paladin Labs Inc.; India; On-site; INR 600,000 - 900,000; Full time

Job summary

Paladin Labs Inc. seeks a Supervisor for packing operations to oversee segregation, storage and movement of dispensed materials, and verification of materials before start of production. The role emphasizes adherence to BMR/BPR, cGMP, GDP and accurate online documentation against PLC data.

The candidate will lead shift activity, train multi-skilled operators, drive CAPA discussions, and ensure safe, compliant operations with emphasis on quality and efficiency.

Qualifications

• Experience in pharmaceutical packing or manufacturing preferred.
• Strong emphasis on document control and GMP compliance.
• Ability to supervise shifts and manage resources effectively.
• Familiarity with BMR/BPR and SOP documentation.
• Capable of training operators on CAPA and continuous improvement.

Responsibilities

• Oversee segregation, storage and movement of dispensed materials.
• Verify dispensed materials before start of production.
• Monitor environmental conditions per product specifications.
• Execute production activities and manage resources to meet targets.
• Validate online documentation against PLC data (events/alarms).
• Initiate cleaning line clearances (Type A/B) and supervise non-process areas.
• Minimize documentation errors on the shop floor and drive process improvements.
• Coordinate with cross-functional teams and ensure cGMP compliance.

Skills

PLC data monitoring

Quality compliance (cGMP)

CAPA training

Documentation accuracy

Team supervision

Process validation awareness

Tools

PLC

BMR

BPR

SOPs

Job description

Job Description SummarySupervisor required for packing operationJob Description1. To ensure the Segregation, storage and movement of dispensed materials.2. Verification of dispensed materials before start of the operation.3. Environmental monitoring as per the product specifications.4. Execute production activities in a shift by managing available resources to achieve production target.5. Maintain standard process parameters as per BMRs,BPRs and other supporting documents for achieving production target and maintaining quality.6. Responsible for verifying online documentation against the electronic data available in the PLC, including events and alarms during the process. Ensure to verify specified vs actual data recording practices.7. Initiation of Type A and Type B cleaning line clearances.8. Responsible to perform the supervisor activities and all non-process area maintenance on requirement basis.9. Minimize documentation error on shop floor.10. Gap analysis of existing SOPs for further improvement.11. To develop multi skilled personnel in the department for operations of equipment as well documentation.12. Ensures that key points and decisions are regularly summarized, and it emphasizes the understanding of critical steps by technical staff throughout the meeting.13. Ensure to prepare and distribute a detailed agenda before the meeting, outlining key topics and objectives and provide training to the operators daily for CAPA, recent events, DI,GDP and other relevant topics which will boost the awareness on DI for the smooth functioning of department with 100% compliance.14. To maintain the area anytime presentable.15. To coordinate with CFT.16. To ensure maintenance & cleanliness of critical utilities (if applicable) as per procedures.17. Ensure All manufacturing operations and related documentation updation as per BMR,BPR, SOP and cGMP & review of BMR, BPR.18. Responsible for Validation, Qualification and Calibration of process or equipment's. Handling of all QMS documentation.19. Responsible for training for new joining, schedule and unscheduled department training.20. Work with production teams to ensure cost-effective, high quality and timely delivery of products.21. To carry out the activities whenever assigning by supervisor, shift in charge and management based on the company requirement.22. By Monitoring and minimizing of spillage and In process rejection shift wise and involved in yield improvement program.23. In process check in manufacturing and packing operation.24. Swab sample request submission to QC.25. BMR & BPR reconciliation, batch review and closing.26. Executed documents retrieval to QA.27. Ensure and complete the equipment and instruments calibration, MP as per the schedule.28. Ensure the area fumigation activity within the timeline.29. Responsible for handling critical processes must oversee and guide activities such as recipe loading, binder addition, kneading, loading, AWC, and gun validation etc.30. Responsible for being especially vigilant during manual operations where electronic data is unavailable and ensuring to witness critical activities such as granulation and sampling.31. Review and approve all master documents.32. Responsible for operational excellence include analyzing current operational processes,identifying inefficiencies and implementing changes to improve productivity and reduce costs.