Tata Consultancy Services (TCS) is inviting applications from qualified B.Pharm, M.Pharm, BHMS, BAMS, BDS, and MSc graduates for full-time roles in Pharmacovigilance and PV Case Processing. If you have 1–4 years of experience in Argus, global submissions, coding, and case handling, this is an excellent opportunity to advance your career with India’s leading IT & Life Sciences employer.
Pharmacovigilance professionals play a key role in ensuring drug safety, regulatory compliance, and patient protection — and TCS offers a strong platform to grow in this field.
🔍 Job Overview
- Company: Tata Consultancy Services (TCS)
- Role: Pharmacovigilance / PV Submission Specialist
- Locations: Mumbai & Pune
- Experience: 1–4 years
- Employment Type: Full-Time, Permanent
- Department: Healthcare & Life Sciences / Business Process Services
🧪 Key Responsibilities
For Mumbai – PV Submission Specialist
- Process Individual Case Safety Reports (ICSRs) in Argus Safety.
- Perform global safety report submissions to Health Authorities.
- Ensure compliance with global & local PV guidelines.
- Maintain high-quality documentation and follow-up activities.
- Support process improvements and adopt new safety systems.
For Pune – Pharmacovigilance Executive
- Review and analyze complex safety data.
- Perform Argus case entry, coding, narrative writing, and QC.
- Conduct end-to-end case handling as per global SOPs.
- Implement patient safety procedures and PV policies.
- Contribute to continuous improvement initiatives.
🎓 Required Qualifications
Candidates with any of the following degrees may apply:
- B.Pharm / M.Pharm
- BHMS / BAMS / BDS
- B.Sc / M.Sc (Biotechnology, Zoology, Chemistry)
- Life Sciences graduates
⭐ Desired Skills
- 1–4 years of experience in Pharmacovigilance
- Hands-on Argus Safety experience
- Strong analytical and data interpretation skills
- Familiarity with global PV guidelines (FDA, EMA, MHRA)
- Good communication and documentation skills
💼 Why Join TCS?
- Work with a global leader in IT, clinical data, and life sciences.
- Exposure to global regulatory submissions.
- Strong learning and career development programs.
- Stable long-term career with excellent growth potential.
- Employee-centric benefits and supportive work culture.
📨 How to Apply
