Sr Packaging Associate

Role Overview: As a Supervisor for the packing operation, your main responsibility will be to manage the production activities in a shift by effectively utilizing available resources to achieve production targets. You will be required to maintain standard process parameters, update manufacturing records, and ensure compliance with cGMP requirements. Additionally, you will be responsible for handling granulation, compression, coating, capsule filling, tablet inspection activities, as well as non-process area maintenance as needed. Key Responsibility: - Verify dispensed materials before the start of the operation - Conduct environmental monitoring as per product specifications - Execute production activities to achieve production targets - Maintain standard process parameters and update documentation - Initiate Type A and Type B cleaning line clearances - Handle granulation, compression, coating, capsule filling, tablet inspection activities, and non-process area maintenance - Minimize documentation errors on the shop floor - Conduct gap analysis of existing SOPs for improvement - Develop multi-skilled personnel for equipment operations and documentation - Provide daily training to operators for smooth department functioning - Maintain the area presentable and coordinate with cross-functional teams - Ensure maintenance and cleanliness of critical utilities as per procedures - Update manufacturing operations documentation as per BPR, SOP, and cGMP - Validate, qualify, and calibrate processes and equipment - Manage all Quality Management System (QMS) documentation - Provide training for new and existing department personnel - Work with production teams to ensure cost-effective and timely delivery of products - Perform assigned activities based on company requirements - Monitor and minimize spillage and in-process rejection - Conduct in-process checks during manufacturing operations - Submit swab sample requests to QC - Reconcile BPRs, review batches, and execute document retrieval to QA - Complete equipment and instrument calibrations as per schedule - Ensure fumigation activity within the timeline Qualification Required: - Degree in Pharmacy or relevant field - Previous experience in a supervisory role within a manufacturing environment - Knowledge of cGMP regulations and quality systems - Strong communication and leadership skills - Ability to work effectively in a team environment - Attention to detail and problem-solving skills (Note: The additional details of the company were not included in the provided job description.),