Senior Manager, Manufacturing Injectables

The role involves ensuring CGMP compliance and supervising overall production activities of the manufacturing area of multiple assigned manufacturing lines. Additionally, the position requires reviewing and maintaining online documents. You will be responsible for the preparation, review, revision, control, and implementation of standard operating procedures. You will also handle the preparation and review of master production documents, protocols, reports, and various document management tasks such as BMRs and BPRs. Your duties will include managing Change Control, Deviations, CAPA, Investigations, and ensuring line clearance activities are conducted before operations like manufacturing, filling, capping, and packing. Generating general purchase indents, preparing production planning, and daily production reports based on achieved goals will be part of your responsibilities. It is crucial to ensure that all equipment and lines are in validated and calibrated status and to uphold cGMP, GDP, and discipline standards within the department. Additionally, you will be responsible for providing training to subordinates, technicians, and operators, and following any additional activities as required by the Head of Department. Attending training sessions as per the schedule and ensuring compliance will be important aspects of the role. To qualify for this position, you must have a Bachelor's Degree in B. Pharm, with a Master's Degree in M. Pharm or M. Sc. being preferred. A minimum of 12 years of experience in the field is required. Your specialized knowledge, skills, and licenses will further enhance your ability to succeed in this role.,