Not specified; pyy ranges determined by role, leve...
Not specified (potentially hybrid or onsite based on typical roles in manufacturing and compliance).
Engineering change order (eco/ecn) management
Agile plm and sap erp systems expertise
Regulated medical device lifecycle processes
Agilent is seeking a Product Data Management - Change Analyst to manage and execute Engineering Change processes for regulated medical equipment, ensuring compliance with quality and regulatory standards. The role involves cross-functional collaboration and oversight of documentation related to product changes, with a strong emphasis on adherence to QMS and master data management
Job Summary
The role is responsible for managing and executing Product Data Management and Engineering Change processes for regulated pathology and medical equipment.
Candidates must ensure compliant master data, documentation, and change implementation across the product lifecycle within Agile PLM and SAP ERP systems.
The position requires strict adherence to Quality Management System requirements including GMP, GLP, and GCP standards for audit readiness.
Matching Summary
Match Score: 85
Agilent is seeking a Product Data Management - Change Analyst to manage and execute Engineering Change processes for regulated medical equipment, ensuring compliance with quality and regulatory standards. The role involves cross-functional collaboration and oversight of documentation related to product changes, with a strong emphasis on adherence to QMS and master data management.
Salary
Not specified; Pay ranges determined by role, level, and location; Individual pay determined by work location and additional factors
Skills & Requirements
Must-have
Engineering Change Order (ECO/ECN) management
Agile PLM and SAP ERP systems expertise
Regulated medical device lifecycle processes
Quality Management System (QMS) compliance
Master data governance and BOM maintenance
Nice-to-have
Cross-functional stakeholder collaboration
Process improvement and optimization skills
Global standardization of product attributes
Technical feasibility analysis capabilities
Key Requirements
Bachelor's or Master's Degree in relevant field
8+ years of experience in medical equipment or pathology
Post-graduate certification or license may be required