Consultant | SAP DMS (Document Management System) | Noida | SAP | DSA LS&HC • Job requisition ID : 109255 • Location: Noida • Entity: Deloitte Touche Tohmatsu India LLP Consultant | SAP DMS (Document Management System) | SAP | DSA LS&HC Location : Noida Key responsibility: • Core Functions: Manages document info records (DIR), controls document versions/revisions, and automates the distribution of documents to modules like PP (Production Planning) or QM (Quality Management). • Business Benefits: Minimizes data redundancy, centralizes storage, and streamlines role-based access to vital corporate information. • Consultant Role: A DMS consultant maps document types, configures storage categories, manages KPro (Knowledge Provider) and ArchiveLink, and establishes virtual copies of documents. • Core Functions: Ensures data integrity, accurate audit trails, and secure electronic signatures. • Business Benefits: Mitigates the risk of non-compliance, prevents costly regulatory penalties, and guarantees patient safety in life sciences. • Consultant Role: A CSV consultant authors and reviews critical validation deliverables, including User Requirements Specifications (URS), Functional Specifications (FS), Installation/Operational/Performance Qualification (IQ/OQ/PQ) protocols, and Traceability Matrices. • Shift Time : 11 AM to 8 PM Key Skills Required: • Education: Bachelor’s or master’s degree in computer science, Engineering, Applied Mathematics, or a related quantitative discipline. • Strong knowledge of SAP DMS configuration, including Document Info Records (DIR), document types, version and revision management. • Experience in configuring storage categories, KPro (Knowledge Provider), ArchiveLink, and content repositories. • Understanding of document distribution and integration with SAP modules such as PP (Production Planning), QM (Quality Management), PM, and MM. • Familiarity with document lifecycle management, engineering change management, and virtual document structures. • Knowledge of authorization concepts, role-based access control, and document security. • Ability to analyze business requirements and design efficient document management solutions. • Strong troubleshooting, testing, and user support skills. • In-depth understanding of GxP regulations, FDA 21 CFR Part 11, EU Annex 11, and data integrity principles. • Experience in preparing and reviewing validation documentation, including User Requirements Specifications (URS), Functional Specifications (FS), IQ/OQ/PQ protocols, Validation Plans, and Traceability Matrices. • Knowledge of risk-based validation methodologies and validation lifecycle management. • Familiarity with electronic records, electronic signatures, audit trails, and compliance requirements. • Strong documentation, analytical, and quality assurance skills. • Experience collaborating with business, IT, quality, and regulatory stakeholders during validation activities. • Ability to identify compliance gaps, support audits, and ensure validated system maintenance through change control and periodic review.