Quality Manager

Responsibilities: Lead and manage the organization's Quality Management System (QMS). Ensure compliance with FDA, cGMP, ISO 9001, ISO 13485, ICH, and applicable regulatory requirements. Oversee Quality Assurance (QA) and Quality Control (QC) operations. Develop, review, and approve SOPs, quality procedures, and controlled documents. Manage deviations, investigations, CAPA, change controls, and non-conformance reports (NCRs). Lead internal, supplier, customer, and regulatory audits and inspections. Ensure effective complaint handling, root cause analysis, and corrective/preventive actions. Monitor quality metrics and prepare management review reports. Support product development, technology transfer, process validation, and qualification activities. Manage supplier qualification and vendor audits. Collaborate with Manufacturing, Engineering, Validation, Regulatory Affairs, R&D, and Supply Chain teams. Lead risk assessments using FMEA and other quality risk management tools. Drive continuous improvement initiatives using Lean, Six Sigma, and Kaizen methodologies. Mentor and develop QA/QC personnel while fostering a quality-focused culture.

Requirements: Bachelor's or Master's degree in Pharmacy, Biotechnology, Chemistry, Microbiology, Life Sciences, Engineering, or a related field. 8–15+ years of Quality Assurance and/or Quality Control experience in a regulated industry. Previous experience in a leadership or management role. Strong understanding of Quality Management Systems and regulatory compliance.