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Manager Quality Management System QMS

Agio Pharmaceuticals Ltd.
Pune
Experience2-5 Years
Salary Not Disclosed
LocationPune
Job Typefull time
Skills: SAP QM Capa Change Control QMS Strategy and Maintenance QMS Deviation
Job Description
This is a Manager Quality Management System QMS position at Agio Pharmaceuticals Ltd.. This is a great opportunity to build a career in the SAP QM domain. Interested candidates looking to grow in SAP QM are encouraged to apply. This role offers hands-on exposure to real-world SAP QM projects.
Requirements
Key Responsibilities. For both Sterile & non-sterile plants. QMS Strategy and Maintenance:. Lead the development, implementation, and maintenance of the site's Quality Management System in accordance with ICH guidelines, cGMP regulations and relevant ISO standards. Ensure the QMS is comprehensive, well documented, and effectively deployed across all functions in the plant. Deviation, CAPA, and Change Control Management:. Own and manage the overall Deviation and Non-Conformance process, ensuring timely investigation, root cause analysis (using tools like 5 Whys/Fishbone), and effective documentation. Oversee the Corrective and Preventive Action (CAPA) system, ensuring actions are relevant, effectively implemented, and verification of effectiveness (VoE) is performed. Manage the Change Control process, assessing the impact of proposed changes on product quality and regulatory status. Audits and Inspections Readiness:. Plan and execute the Internal Audit (Self-Inspection) program to monitor system compliance. Serve as a key resource during external regulatory inspections and customer audits, providing requested QMS documentation and leading follow-up on corrective actions. Quality Metrics and Review:. Define, monitor, and report Key Performance Indicators (KPIs) for all QMS processes (e.g., CAPA closure rate, deviation trends, training compliance) for management review. Prepare and lead the Management Review of the PQS to evaluate system effectiveness, align quality policies, and drive organizational quality objectives. Documentation and Training:. Oversee the Document Control system, ensuring all documents (SOPs, protocols, policies, batch records) are controlled, current, and accessible. Develop and manage the quality Training Program, ensuring all personnel are adequately trained on cGMP, SOPs, and QMS principles. Risk Management:. Facilitate the application of Quality Risk Management (QRM) principles across the organization to proactively identify, assess, and mitigate quality risks. Candidates with strong communication skills and a willingness to learn are encouraged to apply. Freshers and experienced professionals meeting the above criteria are welcome to apply. Only candidates matching the required skill set and experience level will be considered.
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