Team member MSAT injectable

Role Overview: You will be responsible for preparing, reviewing, and approving technical protocols, reports, and product impact assessments related to product lifecycle management (LCM). Additionally, you will initiate change controls, incidents, and risk assessments related to technology transfer activities. Supporting technology transfer activities for new products, scale-ups, line transfers, and site-to-site commercial batches for injectable products will also be part of your responsibilities. You will coordinate with cross-functional teams for the execution and documentation of new products, scale-ups, and line or site transfers. Furthermore, you will support investigations for non-conformances through root cause analysis and impact assessments and provide technical support for process changes and improvements along with addressing regulatory deficiencies and support audits to ensure timely product approvals. Collaborating with cross-functional teams to improve manufacturing processes, conducting data analysis to identify trends and opportunities for process improvement, assisting in the implementation of process improvements and new technologies, and ensuring compliance with Good Manufacturing Practices (GMP) and regulatory requirements are key aspects of this role. Key Responsibilities: - Prepare, review, and approve technical protocols, reports, and product impact assessments related to product lifecycle management (LCM) - Initiate change controls, incidents, and risk assessments related to technology transfer activities - Support technology transfer activities for new products, scale-ups, line transfers, and site-to-site commercial batches for injectable products - Coordinate with cross-functional teams for the execution and documentation of new products, scale-ups, and line or site transfers - Support investigations for non-conformances through root cause analysis and impact assessments - Provide technical support for process changes and improvements, address regulatory deficiencies, and support audits to ensure timely product approvals - Collaborate with cross-functional teams to improve manufacturing processes - Conduct data analysis to identify trends and opportunities for process improvement - Assist in the implementation of process improvements and new technologies - Ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements Qualifications: - Bachelor of Technology or Bachelor of Engineering (Chemical engineer) - Bachelor of Pharmacy/Master of Pharmacy,