The Specific Pay Range For A Preferred Location
ProductDataManagement-ChangeAnalyst
Neural analysis suggests this role is
optimal for Senior candidates.
“Product Data Management- Change Analyst at The Specific Pay Range For A Preferred Location. Skills: Product Data Management, Change Management, Master Data, QMS Compliance. Manage Engineering Change Management process. Manage master data”
Industry & Context.
Analyze engineering changes; Root cause analysis
Occasional travel
What They're Looking For.
Must Have
8+ years relevant experience, Bachelor's degree in Engineering /B. Tech (Mechanical Engineering, Biotechnology, Industrial Management, or a related field), Relevant experience on medical equipment's / pathology
Nice to Have
Post-graduate, certification and/or license may be required
What You'll Do.
Manage Engineering Change Management process
Manage document control
Lead Engineering Change Orders
Release Bills of Materials
Maintain Bills of Materials
Maintain documentation
Standardize master data
Communicate product attributes
Support line of business initiatives
Support global SAP rollout programs
Define master data updates
Implement master data updates
Govern master data updates
Ensure change control adherence
Ensure documentation standards adherence
Ensure traceability adherence
Ensure audit readiness
Apply knowledge of product lifecycle processes
Execute master data activities
Execute BOM activities
Execute change activities
Coordinate cross-functional collaboration
Ensure timely change implementation
Ensure accurate change implementation
Ensure compliant change implementation
Support documentation aligned with GMP
Support documentation aligned with GLP
Support documentation aligned with GCP
Manage procedure manuals
Manage controlled records
Manage formal change authorizations
Analyze engineering changes
Gather required inputs
Validate required inputs
Configure BOM structures
Maintain BOM structures
Ensure accurate system data setup
Ensure controlled document maintenance
Collaborate with manufacturing teams
Ensure seamless implementation of changes
Update routing alignment
Ensure data integrity between PLM and ERP
Ensure document integrity between PLM and ERP
Assign internal part numbers
Manage internal part numbers
Load material master records
Maintain material master records
Ensure completeness of ERP master data
Update product information
Update product descriptions
Drive process improvements
Drive system improvements
How You'll Work.
Team & Collaboration
Cross-functional collaboration; Partner with business teams; Partner with SAP teams; Collaborate with manufacturing teams
Full Job Description
## **Job Description** **Role Summary** Responsible for managing and executing Product Data Management (PDM) and Engineering Change processes for regulated pathology and medical equipment. Ensures compliant master data, documentation, and change implementation across the product lifecycle within ERP and PLM systems, in alignment with Quality Management System (QMS) and regulatory requirements. **Key Responsibilities** * Implement, manage, and sustain the **Engineering Change Management (ECN/ECO) process** , including master data and document control across the complete product lifecycle within **PLM and ERP systems (Agile & SAP)**. Lead and coordinate **Engineering Change Orders (ECOs)** for the release and maintenance of **sales and production Bills of Materials (BOMs)**. * Author, review, and maintain documentation related to **product improvements, repairs, deviations, and new product development** , covering parts, assemblies, tools, and finished medical devices. * **Owns the documentation, governance, and global standardization of Pathology, Reagent Partner, and CDx master data** , ensuring compliant creation, maintenance, and communication of regulated product attributes across **Agile PLM, SAP, and POMS** , in alignment with **QMS, change control, and medical device regulatory requirements** throughout the product lifecycle. * Supports line of business initiatives and global SAP rollout programs by partnering with business and SAP teams to define, implement, and govern master data updates and changes in strict adherence to GMD processes. * Ensure strict adherence to **Quality Management System (QMS)** requirements, including **change control, documentation standards, traceability, and audit readiness** for regulated medical products. * Apply strong knowledge of **medical and regulated product lifecycle processes** , ensuring compliant execution of master data, BOMs, and change activities for pathology and medical equipment. * Coordinate cross‑functional colla
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