Latest pharma jobs for freshers and experienced candidates in RIM IDMP XEVMPD roles apply online now with eligibility and salary details
Introduction
The intersection of life sciences and regulatory technology is creating high-value career opportunities in data-driven compliance roles. The TCS RIM IDMP XEVMPD Jobs are ideal for professionals experienced in regulatory information systems and pharmaceutical data standards. With global exposure and enterprise-level projects, this opportunity allows candidates to work on advanced regulatory transformation initiatives in leading pharma IT environments.
Job Overview
| Job Title | RIM / IDMP / XEVMPD Specialist |
|---|---|
| Company Name | Tata Consultancy Services (TCS) |
| Location | Pune & Mumbai |
| Employment Type | Full-Time |
| Department | Regulatory Affairs / Life Sciences IT |
| Experience Required | 3–10 Years |
| Education | Pharmacy, Life Sciences, IT or related field |
| Salary | As per company norms |
Company Overview
Tata Consultancy Services is one of the world’s leading IT services, consulting, and business solutions organizations. With a strong presence in life sciences and healthcare domains, TCS delivers advanced regulatory technology solutions to global pharmaceutical companies. Working at TCS provides professionals with exposure to large-scale digital transformation projects and international regulatory frameworks.
Job Location & Employment Type
- Locations:
- Pune
- Mumbai
- Employment Type: Full-Time
- Work Mode: Hybrid / Project-based
Open Positions / Department Details
Regulatory Information Management (RIM)
- Data management and regulatory systems handling
IDMP (Identification of Medicinal Products)
- Implementation and compliance with global standards
XEVMPD
- Regulatory data submission and updates for European markets
Key Roles & Responsibilities
- Manage Regulatory Information Management (RIM) systems and ensure data accuracy
- Support IDMP implementation and compliance processes
- Handle XEVMPD submissions and lifecycle updates
- Collaborate with global regulatory teams for product data standardization
- Ensure compliance with international regulatory authorities (EMA, FDA, etc.)
- Support digital transformation initiatives in regulatory operations
- Troubleshoot issues in regulatory databases and systems
- Maintain consistency and integrity of pharmaceutical product data
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in:
- Pharmacy
- Life Sciences
- Information Technology
- Or related fields
Experience
- Minimum 3 to 10 years of experience in:
- RIM systems
- IDMP implementation
- XEVMPD submissions
Skills Required
- Strong knowledge of regulatory affairs and pharma product lifecycle data
- Understanding of EMA IDMP standards and XEVMPD requirements
- Experience with regulatory platforms (e.g., Veeva Vault RIM)
- Analytical thinking and problem-solving skills
- Good communication and stakeholder management abilities
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with a global IT leader
- Exposure to international regulatory projects
- Career growth in specialized regulatory domains
- Hybrid work flexibility (depending on project)
- Professional development and learning opportunities
Selection Process
The hiring process typically includes:
- Resume screening
- Technical interview (domain-specific)
- Managerial/HR discussion
- Final selection
How to Apply
Interested candidates can apply via email:
Subject Line: Application for RIM / IDMP / XEVMPD Role – Experience (Years)
Important Dates
- Application Start Date: April 2026
- Last Date: Not specified (Apply immediately as shortlisting is ongoing)
Why Apply for This Job?
The TCS RIM IDMP XEVMPD Jobs offer exceptional career advantages:
- Work with a globally recognized IT and consulting company
- Gain experience in high-demand regulatory data domains
- Exposure to international pharma regulatory standards
- Opportunity to work on digital transformation projects
- Strong career growth in regulatory IT and data management
This role is ideal for professionals aiming to specialize in regulatory systems and global pharmaceutical compliance.
FAQs
1. What is the experience required for this role?
Candidates need 3–10 years of experience in RIM, IDMP, or XEVMPD domains.
2. What qualifications are required?
A degree in Pharmacy, Life Sciences, IT, or related fields is required.
3. What are the job locations?
The roles are available in Pune and Mumbai.
4. Is prior experience with regulatory systems required?
Yes, experience with RIM platforms and regulatory data systems is preferred.
5. How can I apply for this job?
You can apply by sending your resume to the official email mentioned in the job post.
Conclusion
The TCS RIM IDMP XEVMPD Jobs provide a high-growth opportunity for experienced professionals in regulatory affairs and life sciences IT. With global exposure, advanced technologies, and strong career progression, this role is ideal for candidates looking to excel in regulatory data management. Apply as soon as possible to be considered.
Disclaimer
LatestPharmaJobs.in is an independent job information platform. We do not provide jobs or recruitment and are not affiliated with any company.