Senior Regulatory Compliance Job at EY in Kochi for Veeva Vault RIM PV professionals with pharma experience apply now online quickly
Fresh Opportunity in Pharma Regulatory & Digital Compliance
If you are an experienced pharma professional with expertise in Regulatory Affairs, Pharmacovigilance, and Veeva Vault, this opportunity could be a strong career move. A leading global consulting firm is hiring skilled professionals to contribute to high-impact regulatory and compliance projects. This role combines technical configuration, client consulting, and leadership responsibilities within a fast-growing digital pharma ecosystem.
Company Overview
Ernst & Young (EY) is one of the world’s leading consulting and professional services organizations, operating across more than 150 countries. Known for delivering innovative solutions in consulting, assurance, tax, and strategy, EY plays a key role in transforming businesses through technology and compliance frameworks. Its Global Delivery Services (GDS) division focuses on delivering high-quality consulting and risk management solutions across industries, including pharmaceuticals and life sciences.
Job Overview (Quick Details)
| Field | Details |
|---|---|
| Job Title | Senior – Regulatory Compliance (Veeva Vault RIM/PV) |
| Company | Ernst & Young (EY) |
| Location | Kochi, India |
| Department | Enterprise Risk – Regulatory Compliance |
| Experience Required | 6–9 Years |
| Employment Type | Full-Time |
| Industry | Pharma / Life Sciences / Consulting |
| Qualification | Bachelor’s in IT / Computer Science / Related Field |
| Salary | As per company norms |
| Job Mode | Client-Facing / Consulting Role |
Open Positions / Department Details
The opening is within EY’s Enterprise Risk (ER) Consulting division, focusing on Regulatory Compliance solutions for pharmaceutical clients. The role is designed for professionals experienced in Veeva Vault RIM (Regulatory Information Management) and Pharmacovigilance (PV) systems.
Candidates will work on enterprise-level digital transformation initiatives, helping global pharma companies streamline regulatory processes, ensure compliance, and improve operational efficiency.
Key Roles & Responsibilities
As a Senior Regulatory Compliance Specialist, you will take ownership of both technical and strategic aspects of regulatory systems:
- Lead configuration and implementation of Veeva Vault RIM modules such as submissions, registrations, and archival systems
- Design workflows, security frameworks, object lifecycles, and system architecture for scalable solutions
- Manage pharmacovigilance operations including case processing, safety reporting, and signal detection
- Ensure compliance with global regulatory authorities including US FDA, EMA, and ICH guidelines
- Drive integration between Veeva Vault and external systems like safety databases and clinical platforms
- Oversee data migration, validation, and system documentation aligned with GxP standards
- Support validation processes including IQ, OQ, and PQ documentation
- Collaborate with cross-functional teams including Regulatory Affairs, Quality, IT, and business stakeholders
- Provide consulting insights to improve regulatory processes and digital transformation initiatives
- Handle release management, testing cycles, and production deployments
- Mentor junior team members and lead internal capability-building initiatives
- Act as a key client interface, understanding requirements and delivering tailored solutions
Eligibility Criteria
Education
- Bachelor’s degree in Computer Science, Information Technology, or a related discipline
- Additional certifications in quality or compliance (preferred but not mandatory)
Experience
- Total experience: 6–9 years in regulatory or pharma IT domain
- Minimum 3–5 years hands-on experience in Veeva Vault RIM and Pharmacovigilance systems
- Experience in client-facing consulting roles is highly desirable
Skills Required
Technical Skills:
- Strong expertise in Veeva Vault configuration (objects, workflows, lifecycles)
- Knowledge of Vault APIs, data migration tools, and integration frameworks
- Familiarity with regulatory submission formats such as eCTD and NeeS
- Understanding of global data standards like IDMP and xEVMPD
Regulatory Knowledge:
- Strong understanding of FDA, EMA, and ICH guidelines (E2B, E2C, E2D)
- Knowledge of Pharmacovigilance processes and safety reporting
- Experience with GxP, CSV/CSA, and 21 CFR Part 11 compliance
Soft Skills:
- Excellent communication and stakeholder management abilities
- Analytical thinking and problem-solving skills
- Leadership capabilities and team mentoring experience
- Ability to work in Agile/Scrum environments
Salary & Benefits
- Compensation: As per company norms
- Additional benefits include career growth opportunities, learning programs, and global exposure
Selection Process
The hiring process typically includes:
- Application screening
- Technical interview (Veeva Vault / Regulatory domain)
- Managerial or client-facing round
- HR discussion and final offer
How to Apply
Candidates must apply through the official EY careers portal or the job listing platform where this vacancy is published. Ensure your resume highlights relevant experience in Veeva Vault, regulatory compliance, and pharmacovigilance systems.
Important Dates
- Application Deadline: Not specifically mentioned (apply as early as possible)
Why Apply for This Pharma Job?
This role offers a unique opportunity to work at the intersection of technology and regulatory compliance in the pharmaceutical industry. You will gain exposure to global regulatory frameworks and work with international clients on large-scale digital transformation projects.
Key benefits include:
- Opportunity to work with a globally recognized consulting firm
- Exposure to cutting-edge pharma technologies like Veeva Vault
- Strong career progression with leadership responsibilities
- Hands-on experience with international regulatory standards
- Collaborative and knowledge-driven work environment
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We are not directly affiliated with any company mentioned in this job post. Candidates are advised to verify all details and apply through official company channels only. We do not charge any fee for job information or applications.
Final Call-to-Action
Interested candidates with relevant experience in regulatory compliance and Veeva Vault systems should apply promptly to secure this opportunity. Enhance your pharma career by joining a globally respected organization and contributing to impactful regulatory transformation projects.
