Key Responsibilities Lead the operation, maintenance, and reliability of HVAC, Water Systems, Utilities, and Process Equipment. Plan, execute, and monitor preventive, predictive, and breakdown maintenance activities. Ensure compliance with cGMP, GEP, GDP, and regulatory requirements across
Role Job Title AVP , Principal Engineer - AI Agent Engineering (L11) Company Overview : Synchrony (NYSE: SYF) is a premier consumer financial services company delivering one of the industry’s most complete digitally enabled product suites. Our
Job Purpose To manage end-to-end project completion for Injectable and Ophthalmic products, ensuring timely development, technology transfer, regulatory filings, validation, and commercial launches through effective cross-functional coordination to meet client expectations. Key Responsibilities Lead project planning,
Key Responsibilities Execute and review Equipment Qualification (DQ/IQ/OQ/PQ) for manufacturing, packing, utilities, and laboratory equipment. Plan, execute, and review Process Validation, Cleaning Validation, Hold Time Validation, and Revalidation activities. Prepare and maintain Validation Master Plan (VMP),
Role Title: AVP, Collections Specialized Strategy (L10) Company Overview: Synchrony (NYSE: SYF) is a leading consumer financing company that has been at the heart of American commerce and opportunity for nearly a century. Synchrony delivers credit
Baddi - Himachal Key Responsibilities: 1. Product Demonstration Conduct product demonstrations for customers and internal teams. Explain technical features and benefits effectively. 2. Project Management (Customer-wise) Manage customer-specific projects from initiation to completion. Coordinate required actions
Qualification - B Pharma / M Pharma Responsibilities Plan, execute, and monitor monthly manufacturing and packing plans across multiple units (Unit I, II & III) to meet market requirements. Ensure strict compliance with cGMP, international regulatory
Key Responsibilities Lead overall Quality Assurance and Quality Management System (QMS) activities in compliance with cGMP and regulatory requirements. Review and approve SOPs, BMR/BPR, specifications, validation/qualification documents, SMF, VMP and other quality documents. Manage OOS/OOT, deviations,
Job Purpose To manage end-to-end project completion for Injectable and Ophthalmic products, ensuring timely development, technology transfer, regulatory filings, validation, and commercial launches through effective cross-functional coordination to meet client expectations. Key Responsibilities Lead project planning,