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TCS RIM IDMP XEVMPD Jobs 2026 | Regulatory Affairs Jobs in Pune & Mumbai
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TCS RIM IDMP XEVMPD Jobs 2026 | Regulatory Affairs Jobs in Pune & Mumbai
(TCS RIM IDMP XEVMPD Jobs 2026)
🧪 Introduction
The pharmaceutical regulatory domain is evolving rapidly, especially with the rise of structured data standards like IDMP and XEVMPD. In 2026, professionals with expertise in Regulatory Information Management (RIM) are in high demand across global pharma and IT companies.
This opportunity at Tata Consultancy Services (TCS) is ideal for candidates looking to build or advance their careers in pharma regulatory IT, data management, and compliance systems. With roles available in Pune and Mumbai, this job offers exposure to global regulatory frameworks and cutting-edge life sciences technology.
🏢 About The Company
Tata Consultancy Services (TCS) is one of the world’s leading IT services, consulting, and business solutions organizations. Headquartered in Mumbai, India, TCS was established in 1968 and is part of the Tata Group.
The company operates in over 50 countries and employs more than 600,000 professionals globally. TCS has a strong presence in life sciences and healthcare IT, offering solutions in regulatory affairs, pharmacovigilance, and clinical data management.
📊 Job Overview Summary
Company: TCS
Role: RIM / IDMP / XEVMPD Specialist
Location: Pune / Mumbai
Experience: 3–10 Years
Industry: Pharma Regulatory IT / Life Sciences
Job Type: Full-Time
This role focuses on managing regulatory data systems, ensuring compliance, and supporting global pharmaceutical submissions.
📋 Vacancy Details (Official)
Position: RIM / IDMP / XEVMPD Specialist Experience: 3–10 Years Location: Pune / Mumbai Joining: Immediate / Short Notice Industry: Life Sciences / Pharma Regulatory IT
🧾 Responsibility Explanation
In this role, professionals will handle complex regulatory data systems and ensure that pharmaceutical product data is maintained accurately across global platforms. You will be responsible for managing structured data required for regulatory submissions and compliance.
The job involves working closely with international regulatory teams, ensuring that product information meets standards set by global authorities. You will also support digital transformation initiatives in regulatory operations, making processes more efficient and compliant.
🎓 Eligibility (Official)
Bachelor’s / Master’s degree in:
Pharmacy
Life Sciences
IT or related field
Experience Required:
3–10 years in RIM / IDMP / XEVMPD
Knowledge of:
EMA IDMP guidelines
XEVMPD reporting
🧠 Skills Required
To succeed in this role, candidates must have strong technical and regulatory knowledge. Understanding how pharmaceutical data is structured and submitted globally is key.
Important skills include:
Regulatory data management expertise
Knowledge of IDMP standards
Familiarity with RIM platforms like Veeva Vault
Analytical and problem-solving skills
Strong communication and teamwork
Understanding of global regulatory compliance
💰 Salary Estimate
Expected Salary: ₹8 LPA – ₹20 LPA
Senior professionals can earn ₹25 LPA+
Salary depends on experience, domain expertise, and technical skills.
🗓️ Interview Details (Official)
Mode: Virtual / In-person
Rounds:
HR Round
Technical Round (RIM / IDMP concepts)
Final Managerial Round
Candidates may be asked scenario-based regulatory questions.
📄 Required Documents
Updated Resume
Educational Certificates
Experience Letters
ID Proof (Aadhaar / PAN)
Latest Payslips
❓ FAQs Section
Q1. What is RIM in pharma?
RIM stands for Regulatory Information Management, which involves managing regulatory data and submissions.
Q2. What is IDMP?
IDMP is a global standard for identifying medicinal products and managing their data.
Q3. What is XEVMPD?
XEVMPD is a European database used for reporting medicinal product information.
Q4. Is this job good for pharma professionals?
Yes, it offers high growth, global exposure, and strong salary potential.
Q5. What tools are used in RIM jobs?
Tools like Veeva Vault RIM and other regulatory databases are commonly used.
✅ Final Conclusion
The demand for RIM, IDMP, and XEVMPD professionals is rapidly increasing as pharmaceutical companies move toward structured regulatory data systems. This opportunity at TCS provides a strong platform for working on global regulatory projects and building expertise in high-demand domains.
If you have experience in regulatory affairs and want to transition into pharma IT or advanced regulatory systems, this role can significantly boost your career in 2026 and beyond.
📥 Apply Method
Interested candidates can apply by sending their updated resume to:
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