Product Data Management- Change Analyst

Agilent Technologies UK

Not specified; pyy ranges determined by role, leve...
Not specified
Engineering change order (eco/ecn) management
Agile plm and sap erp systems expertise
Qms, gmp, glp, and gcp regulatory compliance
Agilent Technologies UK is seeking a Product Data Management Change Analyst to oversee the management and execution of Product Data Management and Engineering Change processes for regulated pathology and medical equipment. The role emphasizes compliance with quality management systems and regulatory requirements while coordinating cross-functional collaboration to ensure effective change implementation

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 audit readiness and traceability for regulated medical products.

Matching Summary

Match Score: 85

Agilent Technologies UK is seeking a Product Data Management Change Analyst to oversee the management and execution of Product Data Management and Engineering Change processes for regulated pathology and medical equipment. The role emphasizes compliance with quality management systems and regulatory requirements while coordinating cross-functional collaboration to ensure effective change implementation.

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
  • QMS, GMP, GLP, and GCP regulatory compliance
  • Master data governance for medical products
  • BOM structure configuration and maintenance

Nice-to-have

  • Cross-functional stakeholder collaboration
  • Process improvement and optimization skills
  • Global standardization of product attributes
  • Technical feasibility analysis experience

Key Requirements

  • Bachelor's or Master's Degree
  • 8+ years relevant experience in medical equipment or pathology
  • Experience with regulated product lifecycle processes

Work Rights

Not specified

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