Technical Consultant / Analyst (Data & Systems Migration)

Role Overview We are seeking a highly skilled and efficient Systems & Data Migration Specialist with 5 to 10 years of experience to join our team for a high-scale, time-critical migration project. The ideal candidate will possess a strong background in Computer Systems Validation (CSV) and must have deep, hands-on expertise with regulatory and compliance platforms. Veeva is an absolute, non-negotiable prerequisite for this role. Because this project operates on a highly accelerated timeline, we need a self-starter who can immediately drive value without a learning curve. Key Information - Experience Level: 5 10 years - Location: Noida/Remote (100%) - Working Shift- EST working hours - Employment Type: Contract - Duration : 6 months - Urgency: Immediate Joining Required Key Responsibilities - Migration Execution: Support and execute data/document migration strategies, ensuring data integrity, mapping accuracy, and seamless transition across regulatory systems. - Validation & Compliance: Author, review, and execute Computer Systems Validation (CSV) deliverables, including Validation Plans, Risk Assessments, Requirements Traceability Matrices (RTM), and Validation Summary Reports. - Platform Management: Navigate, configure, and manage data extraction and loading within enterprise Life Sciences platforms, prioritizing Veeva. - Timeline Management: Work efficiently under tight deadlines to meet critical migration milestones without compromising quality or compliance standards. - Cross-Functional Collaboration: Partner with business stakeholders and technical teams to resolve data discrepancies and system bottlenecks rapidly. Requirements & Qualifications Critical / Must-Have Skill Set: - Veeva Systems: 100% Mandatory. Extensive, hands-on experience with Veeva platforms (e.g., Veeva Vault RIM, Veeva QualityDocs, or Veeva PromoMats) is required. You must be comfortable hitting the ground running on day one. - Computer Systems Validation (CSV): Strong foundational knowledge of GxP, GAMP5, 21 CFR Part 11, and Annex 11 regulations. Proven track record of validating software in a regulated environment. Preferred Platform Familiarity: - Experience or familiarity with Regulatory Information Management systems like Rimsys . - Familiarity with training and learning management platforms such as Educare . - Experience with other industry-standard QMS, RIM, or LMS platforms is a major plus. Professional Attributes: - Thrives Under Pressure: Proven ability to deliver high-quality work in a fast-paced, time-sensitive project environment. - Strong Analytical Skills: Exceptional data mapping, data profiling, and troubleshooting capabilities. - Communication: Excellent verbal and written communication skills for cross-functional alignment.