Job Description
Specialist – Quality / Incoming Material Release (IMR)
Primary Activities
The Specialist will be part of the Quality team and will be responsible for supporting Incoming Material Receipt and Release activities while contributing to broader Quality Systems, compliance and continuous improvement initiatives within the Global Quality Shared Services (GQSS).

Key responsibilities include, but are not limited to:
Perform receipt, review and release of incoming materials in accordance with approved procedures, specifications, cGMP/GxP requirements and applicable regulatory standards, ensuring Right First Time and turnaround time KPIs are consistently achieved.
Review vendor, supplier and external laboratory documentation associated with material receipt and release to ensure compliance with approved internal specifications, applicable pharmacopoeial requirements and Quality standards.
Complete and maintain all documentation and records in compliance with cGMP/GxP requirements, ensuring accuracy, completeness and data integrity.




Demonstrate proficiency in relevant Quality and business systems, including Veeva, SAP, GLIMS and other applicable electronic Quality Management Systems.
Interpret and apply company test specifications, quality standards, procedures and applicable pharmacopoeial requirements in day-to-day activities.
Collaborate with global manufacturing sites, Quality teams, suppliers, external laboratories and other stakeholders to support timely material receipt and release and resolve issues impacting business continuity.
Support Quality investigations, root cause analysis, impact assessment, CAPA development and implementation, as applicable.
Support audit and inspection readiness activities and participate in internal and external audits/inspections, as required.
Ensure adherence to applicable Quality Systems, procedures, policies and regulatory requirements within the department.
Identify and contribute to opportunities for process improvemen

📌 Specialist – Quality (Pune)
🏢 Msd
📍 Pune