Assistant General Manager

Role Overview: As a QC Team Leader at our company located in Ambernath, Maharashtra, your primary responsibility will be to lead a team of 30+ members in the QC-AMV team, including LC-MS, Nasal, and FT-NIR teams, for regular testing and method validation activities. You will also provide backup support to the QC Head of Department (HOD) by managing daily updates, commercial output, monthly sample status, training, review meetings, and coordination with stakeholders to align work requirements. Your role will involve executing and approving various types of Quality Management System (QMS) processes, identifying scientific root causes, implementing corrective and preventive actions (CAPA), and ensuring laboratory compliance. Key Responsibilities: - Lead the QC-AMV team for regular testing and method validation activities with analytical knowledge and leadership qualities to achieve company goals. - Support the QC HOD with daily updates, commercial output, monthly sample status, training, review meetings, and stakeholder coordination. - Execute and approve different QMS processes, identify root causes, implement CAPA, and maintain lab compliance. - Design and execute analysis planning, data interpretation, and presentation to the HOD. - Provide guidance to team members, monitor key performance indicators, and lead QC-AMV work in the absence of the QC HOD. - Collaborate with cross-functional teams, stay updated on industry trends, and ensure compliance with GLP and health, safety, environmental systems. - Manage work in all shifts and travel to other sites as per company policy. Qualifications Required: - Master's degree in Science or Bachelor's/Master's in Pharma. - Strong analytical knowledge and expertise in modern analytical instruments (HPLC, GC, LC-MS, NIR, Nasal performance testing). - Work experience in QC, AMV, and AD departments. - Leadership skills, problem-solving abilities, strategic mindset, organizational skills. - Knowledge of Chromeleon 7.2 and Sciex software is advantageous. - Experience in GMP, USFDA/EU audits. - Excellent communication skills. (Note: Additional details about the company were not included in the provided job description.),