Site QA Head

As the Site QA Head at Sun Pharmaceutical Industries Ltd, your role will involve managing overall quality assurance oversight and site activities related to quality systems. This includes documentation review, SOP updates, in-process quality assurance, sampling and batch release, preventive maintenance, calibration, qualification, validation, internal audits, compliance, quality oversight of electronic systems, budget management, continuous improvement of quality systems, RA support, monitoring of pest control, and retention sample management as per Good Manufacturing Practices requirements. Your key responsibilities will include: - Defining operational strategy and road map for quality assurance management at the site - Setting site quality assurance goals and strategy aligned with Sun Pharma compliance, product quality management objectives, and regulatory requirements - Managing site Quality Assurance activities and resources effectively - Identifying and implementing solutions to improve existing site quality assurance systems and processes - Coaching and developing direct and indirect reports through performance feedback, reviews, and training opportunities - Ensuring readiness for regulatory agency inspections and internal audits, and implementing corrective actions when needed - Monitoring quality assurance metrics and driving improvement in deviation, change control, OOS/OOT, CAPA effectiveness, and market complaints - Collaborating with other Sun Pharma sites and ensuring smooth coordination - Providing inputs to manufacturing, R&D, and PDL work processes to ensure Quality by Design - Designing, implementing, and ensuring compliance with quality-related SOPs, policies, standards, and QA systems - Facilitating internal and regulatory agency audits and addressing findings comprehensively - Monitoring industry trends and identifying opportunities for improving site quality assurance management and processes - Fulfilling all training requirements of quality assurance employees - Implementing and adhering to quality policies, standards, and procedures for computerized systems - Reviewing and approving documents in accordance with quality procedures - Collaborating with site cross-functional and corporate functions for the implementation of new initiatives You should possess a B.Pharm or M.Pharm degree with at least 17 to 18 years of experience, including QA experience in OSD. Please note that the above responsibilities and qualifications are essential for the position of Site QA Head at Sun Pharmaceutical Industries Ltd.,