Sr Packaging Associate
Read straight from Par Health's careers page, verified 2d ago.Seekless can tailor your résumé to it.
Seekless can write your résumé for this posting first.
Before you apply
LocationIndia - Pudupakkam
Work modeon-site
SenioritySenior
Company size1,001–5,000 people
PostedSep 11, 2025 · 1y ago
Verified live2d ago
May no longer be actively hiring
Posted by the company on Sep 11, 2025
At a glanceSummarised by Seekless from the posting.
Verification of dispensed materials before start of the operation
Environmental monitoring as per the product specifications
Execute production activities in a shift by managing available resources to achieve production target
Maintain standard process parameters as per BPRs and other supporting documents
Prepare manufacturing records and update online documentation to meet production and cGMP requirements
Initiation of Type A and Type B cleaning line clearances
Handle granulation, compression, coating, capsule filling, imprinting, tablet inspection activities
Minimize documentation error on shop floor
Gap analysis of existing SOPs for further improvement
Develop multi skilled personnel in the department for operations of equipment as well documentation
Provide training to the operator daily for any update, observations, incidents etc.
Coordinate with CFT
Ensure maintenance & cleanliness of critical utilities as per procedures
Ensure all manufacturing operations and related documentation updation as per BPR, SOP and cGMP
Responsible for Validation, Qualification and Calibration of process or equipment
Handling of all QMS documentation
Responsible for training for new joining, schedule and unscheduled department training
Work with production teams to ensure cost-effective, high quality and timely delivery of products
Carry out activities assigned by supervisor, shift in charge and management based on company requirement
Monitoring and minimizing of spillage and in process rejection shift wise
Involved in yield improvement program
In process check in manufacturing operation
Swab sample request submission to QC
BPR reconciliation, batch review and closing
Executed document retrieval to QA
Ensure and complete equipment and instruments calibration as per schedule
Ensure area fumigation activity within timeline
Job Description Summary
Supervisor required for packing operation
Job Description
Key Responsibility:
Verification of dispensed materials before start of the operation. Environmental monitoring as per the product specifications. Execute production activities in a shift by managing available resources to achieve production target. Maintain standard process parameters as per BPRs and other supporting documents for achieving production target and maintaining quality. Prepare manufacturing records and update online documentation to meet production and cGMP requirements. Initiation of Type A and Type B cleaning line clearances. Supervisor shall handle granulation, compression, coating, capsule filling, imprinting, tablet inspection activities and all non-process area maintenance on requirement basis. Minimize documentation error on shop floor. Gap analysis of existing SOPs for further improvement. To develop multi skilled personnel in the department for operations of equipment as well documentation. To provide training to the operator daily for any update, observations, incidents etc., for the smooth functioning of department with 100% compliance. To maintain the area anytime presentable. To coordinate with CFT. To ensure maintenance & cleanliness of critical utilities (if applicable) as per procedures Ensure All manufacturing operations and related documentation updation as per BPR, SOP and cGMP, review of BPR. Responsible for Validation, Qualification and Calibration of process or equipment’s. Handling of all QMS documentation. Responsible for training for new joining, schedule and unscheduled department training. Work with production teams to ensure cost-effective, high quality and timely delivery of products. To carry out the activities whenever assigning by supervisor, shift in charge and management based on the company requirement. By Monitoring and minimizing of spillage and In process rejection shift wise and involved in yield improvement program. In process check in manufacturing operation. Swab sample request submission to QC. BPR reconciliation, batch review and closing. Executed document retrieval to QA. Ensure and complete the equipment and instruments calibration as per the schedule. Ensure the area fumigation activity within the timeline.