Specialist - Regulatory Affairs - Operations 4B

BrightClaim; Gurugram District; On-site; INR 900,000 - 1,400,000; Full time

Job summary

Genpact is hiring a Specialist - Regulatory Affairs - Operations to manage regulatory reporting and SME support across IFRS-17 and Solvency II. You will collect, map, validate, and reconcile data from multiple systems, translating business needs into technical requirements for IT teams.

The role focuses on coordinating reporting processes, ensuring accuracy, and updating templates as regulatory frameworks evolve.

Qualifications

• Bachelor's degrees in health administration, healthcare, pharmacy, or related field may be required.
• Master's degree in public health or regulatory affairs is advantageous.
• Experience with regulatory reporting and compliance processes is preferred.
• Familiarity with IFRS-17 and Solvency II reporting concepts is beneficial.
• Strong data management and data dictionary understanding is desirable.

Responsibilities

• Execute day-to-day tasks relating to regulatory reporting across IFRS-17 and Solvency II.
• As an SME, support data collection by reconciling data from multiple source systems.
• Translate business requirements into detailed technical requirements for tech teams.
• Coordinate gathering, estimation and planning for projects or work streams.
• Support data and systems analysis activities and define acceptance criteria.
• Perform data mapping based on the reporting templates' data dictionary.
• Conduct first-level validation checks for reporting data fidelity.
• Identify data exceptions and escalate issues with documentation.
• Prepare draft regulatory and management reports monthly, quarterly and annually.
• Maintain version control by tracking updates and timestamps for drafts.
• Coordinate with data owners, IT, and risk/compliance stakeholders to resolve issues.
• Monitor updates to regulatory frameworks and adapt reporting templates accordingly.

Skills

Client relations

Collaboration tools

Data analytics

Generative AI

Lean Six Sigma

People leadership

Personal effectiveness

Storytelling

Education

Bachelors - Health Administration

Bachelors - Healthcare

Bachelors - Pharmacy

Masters - Public Health

Masters - Regulatory Affairs

Job description

Specialist - Regulatory Affairs - Operations

Ready to turn bold ideas into real-world impact? At Genpact, we don’t just adapt to change, we lead it. AI and digital innovation are transforming the way businesses work, and we’re at the forefront of it. Genpact’s AI Gigafactory, our industry-first accelerator, exemplifies how we scale advanced technology solutions to help global enterprises work smarter, grow faster, and transform at scale. Whether tackling complex challenges through large-scale models or agentic AI, our breakthrough solutions tackle companies’ most complex challenges. If you thrive in a fast-moving, innovation-driven environment, love building and deploying cutting-edge AI solutions, and want to push the boundaries of what’s possible, this is your moment. Genpact (NYSE: G) is an agentic and advanced technology solutions company. We leverage process intelligence and artificial intelligence to deliver measurable outcomes. With a strong partner ecosystem and decades of client trust, we provide innovative solutions that transform how businesses run. Powered by a team with an active learning mindset and client centricity at its core, we deliver lasting value for the world’s leading enterprises. Get to know us at genpact.com and on LinkedIn, YouTube, X, and Facebook.

Job Description

Responsibilities

• Execute day-to-day tasks relating to regulatory (IFRS-17, Solvency II) and internal (KRI delivery, sustainability reports) reporting activities across reporting frameworks.
• As an SME, Support data collection for regulatory and internal reports by compiling and reconciling data from multiple source systems and reporting tools within organization.
• Support business teams in the definition of business requirements and translate these into more detailed technical requirements for use by the technology teams where required
• Help co‑ordinate the technical requirements gathering, estimating and planning for single or multiple projects or work streams
• Support the data and systems analysis activities within the project, identifying the business and technical requirements and acceptance criteria
• Perform data mapping to ensure data is appropriately mapped based on data dictionary of reporting templates.
• Perform first‑level validation checks on reporting data to ensure completeness, accuracy, and consistency.
• Identify data exceptions during report preparation and elevate issues with appropriate documentation.
• Assist in preparing draft regulatory and management reports (quantitative and qualitative) as per reporting requirements - monthly, quarterly and annually.
• Support version control by tracking updates, changes, and timestamps for report drafts.
• Coordinate with upstream data owners, IT teams, and risk/compliance stakeholders to resolve data or reporting issues
• Regulatory Change & Impact Control: Monitor updates (such as IFRS 17, Solvency II, and sustainability frameworks) to perform gap analyses, adapt compliance reporting templates, and maintain an auditable log of reporting methodology changes

Qualifications

• Bachelors - Health Administration
• Bachelors - Healthcare
• Bachelors - Pharmacy
• Masters - Public Health
• Masters - Regulatory Affairs

Certifications

• Certified Compliance Officer (CCO) - VskillsVskills
• Certified Public Accountant (CPA) - Perfekt SzolnokPerfekt Szolnok
• Certified Regulatory and Compliance Professional (CRCP) - JSS UniversityJSS University
• Certified Regulatory Compliance Manager (CRCM) - The International Association of Risk and Compliance Professionals (IARCP)The International Association of Risk and Compliance Professionals (IARCP)

Required Skills

• Client Relations
• Collaboration Tools
• Data Analytics
• Generative AI
• Lean Six Sigma (LSS)
• People Leadership
• Personal Effectiveness
• Storytelling

Language

English (Required)

Language Proficiency -

Advanced - C1

Job Type

Regular

Master Skill List -

Regulatory Affairs - Operations

Remote Type -

Office

Work Shift -

Flex Time (India)

Why join Genpact?

• Lead AI-powered transformation – Drive innovation and solve real-world business challenges that matter
• Make an impact – Help global enterprises solve business challenges that matter
• Accelerate your career – Gain hands‑on experience, mentorship, and world‑class learning opportunities to stay ahead
• Work with the best – Join 140,000+ bold thinkers and problem‑solvers who push boundaries every day
• Thrive in a values‑driven culture – Our courage, curiosity, and incisiveness - built on a foundation of integrity and inclusion - allow your ideas to fuel progress

Come join the 140,000+ coders, tech shapers, and growth makers at Genpact and take your career in the only direction that matters: Up.

Let’s build tomorrow together.

Genpact is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, religion or belief, sex, age, national origin, citizenship status, marital status, military/veteran status, genetic information, sexual orientation, gender identity, physical or mental disability or any other characteristic protected by applicable laws. Genpact is committed to creating a dynamic work environment that values respect and integrity, customer focus, and innovation.