Job
Description
Role Overview: You will be responsible for maintaining up-to-date launch trackers for OSD, Injectable, Ophthalmic, and CMO projects. Your role will involve coordinating with Cross-functional teams (CFTs), driving NPL meetings, and sharing minutes of the meeting. Additionally, you will prepare presentations for tracking and reporting purposes, follow up on all action items from meetings, and ensure timely closure. Material management and real-time tracking of all inputs required for the manufacturing process will be part of your responsibilities. You will track manufacturing, packaging, and release status for NPLs and collaborate with Regulatory Affairs on ANDA approval progress and post-approval supplement filing. Effective communication across all stakeholders and upper management will be essential to inform them about project status, critical path items, risks, and delays if timelines are not met. Key Responsibilities: - Maintain up-to-date launch trackers for OSD, Injectable, Ophthalmic, and CMO projects - Coordinate with Cross-functional teams (CFTs) - Drive NPL meetings and share minutes of the meeting - Prepare presentations for tracking and reporting purposes - Follow up on all action items from meetings and ensure timely closure - Manage material and real-time tracking of all inputs required for the manufacturing process - Track manufacturing, packaging, and release status for NPLs - Collaborate with Regulatory Affairs on ANDA approval progress and post-approval supplement filing - Communicate project status, critical path items, risks, and delays to all stakeholders and upper management if timelines are not met Qualifications: - B-Pharm or Graduate in another stream with relevant experience (Note: No additional details about the company were provided in the job description.) Role Overview: You will be responsible for maintaining up-to-date launch trackers for OSD, Injectable, Ophthalmic, and CMO projects. Your role will involve coordinating with Cross-functional teams (CFTs), driving NPL meetings, and sharing minutes of the meeting. Additionally, you will prepare presentations for tracking and reporting purposes, follow up on all action items from meetings, and ensure timely closure. Material management and real-time tracking of all inputs required for the manufacturing process will be part of your responsibilities. You will track manufacturing, packaging, and release status for NPLs and collaborate with Regulatory Affairs on ANDA approval progress and post-approval supplement filing. Effective communication across all stakeholders and upper management will be essential to inform them about project status, critical path items, risks, and delays if timelines are not met. Key Responsibilities: - Maintain up-to-date launch trackers for OSD, Injectable, Ophthalmic, and CMO projects - Coordinate with Cross-functional teams (CFTs) - Drive NPL meetings and share minutes of the meeting - Prepare presentations for tracking and reporting purposes - Follow up on all action items from meetings and ensure timely closure - Manage material and real-time tracking of all inputs required for the manufacturing process - Track manufacturing, packaging, and release status for NPLs - Collaborate with Regulatory Affairs on ANDA approval progress and post-approval supplement filing - Communicate project status, critical path items, risks, and delays to all stakeholders and upper management if timelines are not met Qualifications: - B-Pharm or Graduate in another stream with relevant experience (Note: No additional details about the company were provided in the job description.)
