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    Senior Manager Regulatory Affairs Job at Genpact – Lead Global Regulatory Transformation

    Regulatory Affairs Jobs at Genpact Careers | Senior Manager Role | Apply Now

    Genpact Careers is hiring for one of the most impactful Regulatory Affairs jobs in the pharmaceutical and life sciences domain. The Senior Manager – Regulatory Affairs role at Genpact Careers focuses on regulatory transformation, Veeva RIMS implementation, data governance, and global compliance. This opportunity is ideal for experienced professionals looking to grow their career through high-impact Regulatory Affairs jobs at a global organization driven by AI and digital innovation.

    Job Details

    • Job Title:Senior Manager – Regulatory Affairs
    • Location: Delhi, India.

    About the Company

    Genpact Careers offers global opportunities across technology, life sciences, and regulatory domains. Genpact (NYSE: G) is an advanced technology services and solutions company delivering long-term value to leading enterprises worldwide. Known for driving digital transformation through AI, automation, and deep domain expertise, Genpact Careers enables professionals to work on large-scale global programs while shaping the future of regulated industries.

    Job Description | Regulatory Affairs Jobs at Genpact Careers

    Among the senior-level Regulatory Affairs jobs at Genpact Careers, this role focuses on regulatory process design, Veeva RIMS implementation, data migration, governance frameworks, and compliance with global regulatory standards. The position involves close collaboration with regulatory SMEs, affiliates, IT teams, and business stakeholders to ensure successful execution of regulatory transformation initiatives.

    Key Responsibilities

    1. Project Management & Coordination

    • Manage process-related tasks in Veeva RIMS projects
    • Ensure timely delivery across cross-functional teams

    2. Stakeholder Engagement

    • Facilitate workshops with Regulatory SMEs and Affiliates
    • Act as central contact for process decisions

    3. Governance & Alignment

    • Align processes with regulatory requirements and governance standards
    • Support data governance within Regulatory Affairs jobs

    4. Documentation & Communication

    • Maintain SOPs, process maps, and decision logs
    • Communicate regulatory process changes effectively

    5. Change Management Support

    • Support training, adoption, and stabilization activities

    6. Migration Strategy & Planning

    • Define migration scope, timelines, and success metrics
    • Ensure compliance with GxP and 21 CFR Part 11

    7. Data Migration & Validation

    • Support ETL activities in Veeva RIMS
    • Validate regulatory data accuracy and completeness

    8. Data Mapping & Transformation

    • Lead legacy-to-Veeva Vault RIM data mapping

    9. System Configuration & Governance

    • Support configuration of Veeva Vault RIM modules

    10. Testing & Validation

    • Lead testing and support regulatory audits

    11. Continuous Improvement

    • Track regulatory updates and drive automation

    12. Data Quality & Standardization

    • Support IDMP and XEVMPD data standardization

    Qualifications Required for Regulatory Affairs Jobs

    • Bachelor’s degree, preferably in Pharmacy, or related discipline, required with relevant experience in the pharmaceutical industry.

    Skills

    • Enthusiasm & confidence
    • Adhere to principles and values.
    • Time Management skills.

    Why join this Company?

    • Work on AI-driven regulatory transformation
    • Contribute to global regulatory compliance programs
    • Accelerate career growth through continuous learning
    • Be part of a values-driven, inclusive workplace
    • Collaborate with global experts across Genpact Careers

    CLICK HERE TO APPLY ONLINE

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