Life Science Jobs | Genpact is Hiring a Senior Manager | Apply Now
Ready to elevate your professional journey in Regulatory Affairs Jobs? This senior-level Genpact Career opportunity is designed for experienced life science professionals who want to lead regulatory transformation at a global scale. If you are targeting impactful Life Science Jobs that blend regulatory expertise, digital systems, and leadership, this role places you at the forefront of pharma innovation and compliance.
Job Details
- Job Title: Senior Manager – Regulatory Affairs
- Location: Delhi, India
- Job Type: On-site, Full-time
About the Company
Genpact is a global advanced technology services and solutions company driving large-scale digital transformation for leading enterprises. With deep expertise in data, AI, and operations, Genpact helps organizations work smarter and faster. Operating across industries and geographies, Genpact is known for its innovation-driven culture and strong regulatory and compliance capabilities. The company empowers professionals to shape the future of work through technology, governance, and intelligent operation through Genpact Careers.
Responsibilities
- Project Management & Coordination
- Manage all process-related tasks in Veeva RIMS projects, including planning, tracking, and reporting.
- Ensure timely delivery of process deliverables by coordinating across cross-functional teams and stakeholders.
- Stakeholder Engagement
- Facilitate workshops and working sessions with Regulatory SMEs, Affiliates, and other business units to gather input and validate process designs.
- Act as a central point of contact for process-related discussions and decisions.
- Governance & Alignment
- Ensure process designs are aligned with regulatory requirements, internal governance standards, and Veeva RIMS configuration constraints.
- Support the development and enforcement of data governance frameworks within the regulatory domain.
- Support decision-making and escalation processes related to business process changes.
- Documentation & Communication
- Maintain comprehensive documentation of current-state and future-state processes, including process maps, SOPs, and decision logs.
- Communicate process changes and impacts effectively to all relevant stakeholders.
- Change Management Support & Training
- Collaborate with Change Management teams to support training, communication, and adoption of redesigned processes.
- Monitor and address user feedback during process rollout and stabilization phases.
- Migration Strategy & Planning
- Define migration scope, timelines, resources, and success metrics.
- Develop detailed migration plans and risk mitigation strategies.
- Manage migration activities across multiple workstreams and ensure compliance with GxP, 21 CFR Part 11, and validation protocols (IQ, OQ, PQ).
- Support Data Migration Activities
- Collaborate with IT and business teams to support data extraction, transformation, and loading (ETL) processes into Veeva RIMS.
- Validate migrated data to ensure accuracy, completeness, and compliance with business and regulatory requirements.
- Data Mapping & Transformation
- Lead mapping of legacy data structures to Veeva Vault RIM.
- Oversee ETL (Extract, Transform, Load) processes ensuring accuracy and completeness.
- System Configuration & Governance
- Support configuration of Veeva Vault RIM modules.
- Establish governance frameworks for data quality, access control, and audit readiness.
- Testing & Validation
- Lead testing to validate migrated data and system functionality.
- Document validation results and support regulatory audits.
- Continuous Improvement & Reporting
- Track regulatory updates and adapt processes accordingly.
- Drive automation and digital transformation initiatives for regulatory data management.
- Data Quality & Standardization
- Oversee data mapping, cleansing, and enrichment for IDMP and XEVMPD.
- Ensure controlled terminology alignment across regulatory systems.
Qualifications
Bachelor’s degree, preferably in related Life Science discipline required with relevant experience in the pharmaceutical industry.
Skills
- Enthusiasm & confidence
- Adhere to our principles and values.
- Time Management skills.
This role is an outstanding opportunity for experienced professionals aiming to advance their Genpact Career in leadership-level Regulatory Affairs Jobs. For candidates seeking senior Life Science Jobs that combine regulatory excellence, digital innovation, and global exposure, this position offers strong career acceleration and industry influence.
