The Specific Pay Range For A Preferred Location

ProductDataManagement-ChangeAnalyst

₹15–25L ~AI est. Manesar, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“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.

Problems you'll solve

Analyze engineering changes; Root cause analysis

Eligibility Requirements

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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