To be responsible for managing technology in complex projects ,providing technical guidance and ensuring successful delivery of solutions.
Polarion ArchitectRole OverviewWe are looking for a highly experienced Polarion Architect with 10–15 years of IT experience and strong expertise in Siemens Polarion ALM . The candidate should have deep experience in customization, data migration, macro development, and Risk Management (Risk Sheets) and be capable of working in regulated and fast-paced environments.Primary Skills (Must-Have)Strong hands-on experience in Polarion ALM customization & configurationExpertise in Velocity scripting, macro development, and LiveDocsExperience in Risk Management implementation (Risk Sheets) within PolarionProven track record in Data Migration (legacy systems → Polarion)Strong understanding of ALM processes (Requirements, Test Management, Defect tracking, Traceability)Workflow design, configuration, and automationExperience in Live Reports & dashboard configurationSecondary Skills (Good-to-Have)Experience with integrations (REST APIs, SAP, Windchill, Teamcenter, Jira, etc.)Knowledge of Java, scripting, or extension developmentExposure to Agile / SAFe methodologiesExperience in CSV (Computer System Validation)Performance optimization and troubleshootingBasic understanding of PLM ecosystemsKey ResponsibilitiesLead end-to-end Polarion customization and implementation activitiesDevelop macros, scripts, workflows, and reports as per business needsImplement and configure Risk Management solutions (Risk Sheets)Execute data migration ensuring data integrity, traceability, and validationCollaborate with stakeholders to translate requirements into scalable ALM solutionsEnsure compliance with regulatory standards and validation processesProvide technical leadership and mentor team membersSupport production issues, enhancements, and continuous improvementsDomain Experience (Mandatory / Preferred)Medical Devices / Life Sciences (Primary domain)Exposure to Semiconductor (Semi) domain is an added advantageRegulatory & Compliance Knowledge (Preferred)ISO 13485, ISO 14971 (Risk Management)FDA 21 CFR Part 11CSV / Validation lifecycle (IQ, OQ, PQ)
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