TCS Hiring for Pharmacovigilance Associate – BPharm, MSc, BDS, BAMS
- Tata Consultancy Services (TCS) Hiring Pharmacovigilance Professionals | Mumbai & Pune Drug Safety Jobs
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Drug Safety & Compliance Activities
- Process Improvement & Team Collaboration
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Skills Required
- Location & Salary
- Application Process
- Why This Role Matters in Healthcare
- Frequently Asked Questions (FAQs)
- 1. What experience is required for this role?
- 2. What qualifications are required?
- 3. What are the main responsibilities?
- 4. Is this an urgent hiring?
- 5. What skills are important for selection?
- Summary Table
Tata Consultancy Services (TCS) Hiring Pharmacovigilance Professionals | Mumbai & Pune Drug Safety Jobs
Tata Consultancy Services (TCS) is hiring Pharmacovigilance professionals for multiple vacancies in Mumbai and Pune locations. This is a full-time, on-site opportunity for candidates with 2 to 5 years of experience in drug safety, ICSR case processing, and pharmacovigilance operations. Immediate joiners are preferred, making this an urgent hiring opportunity for experienced professionals in clinical research and safety data management.
Company Overview
Tata Consultancy Services (TCS) is a global leader in IT services, consulting, and business solutions, with a strong presence in healthcare, life sciences, and pharmacovigilance services. As part of its healthcare and life sciences division, TCS supports pharmaceutical companies with drug safety monitoring, regulatory compliance, and clinical data management.
With decades of expertise and a global client base, TCS provides advanced pharmacovigilance solutions including safety database management, adverse event reporting, and regulatory support. The company is known for its strong compliance framework, technology-driven processes, and commitment to delivering high-quality healthcare solutions.
Job Role & Responsibilities
As a Pharmacovigilance Associate at TCS, you will be responsible for end-to-end case processing and drug safety activities, ensuring compliance with global pharmacovigilance regulations and timelines.
Core Responsibilities
- Perform Individual Case Safety Report (ICSR) processing using safety databases such as Argus
- Access, review, and analyze safety cases with accuracy and attention to detail
- Enter and code data using MedDRA terminology in pharmacovigilance systems
- Complete all steps in the case-handling process including data entry, validation, and submission
Drug Safety & Compliance Activities
- Ensure compliance with global and local pharmacovigilance procedures and SOPs
- Perform follow-up activities for incomplete or missing safety data
- Maintain adherence to patient safety policies and regulatory requirements
- Meet strict reporting timelines and quality standards
Process Improvement & Team Collaboration
- Contribute to development and implementation of safety systems and workflows
- Support a performance-driven culture within the pharmacovigilance team
- Collaborate with team members and stakeholders to ensure smooth operations
Eligibility / Qualifications
Educational Qualification
Candidates must have a degree in healthcare or life sciences disciplines.
Required courses include:
B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Nursing, Biomedical Sciences
Experience
- 2 to 5 years of experience in pharmacovigilance or drug safety
- Strong experience in ICSR case processing and safety databases (Argus preferred)
Skills Required
- Strong knowledge of pharmacovigilance processes and ICSR workflows
- Experience in MedDRA coding and safety data entry
- Good analytical and problem-solving skills
- Excellent written and verbal communication skills
- Ability to work under strict timelines and handle multiple cases
Location & Salary
- Job Locations: Mumbai & Pune, India
- Employment Type: Full-time, On-site
- Salary: Competitive salary based on experience in pharmacovigilance and clinical research domain
Application Process
Interested candidates can apply by sharing their updated CV with required details to the official email ID:
Email ID: babeeta.shahi@tcs.com
Or apply through the job posting link below:
Apply Here: https://www.linkedin.com/jobs/view/4392884344/
Why This Role Matters in Healthcare
Pharmacovigilance professionals are responsible for ensuring the safety of medicines by monitoring adverse events and maintaining regulatory compliance. This role plays a critical part in protecting patient health, improving drug safety profiles, and supporting global healthcare systems.
Frequently Asked Questions (FAQs)
1. What experience is required for this role?
Candidates must have 2 to 5 years of experience in pharmacovigilance or drug safety.
2. What qualifications are required?
A degree in Pharmacy, Life Sciences, Nursing, or related healthcare fields is required.
3. What are the main responsibilities?
The role involves ICSR processing, data entry, MedDRA coding, and regulatory compliance.
4. Is this an urgent hiring?
Yes. Immediate joiners are preferred for this position.
5. What skills are important for selection?
Strong PV knowledge, attention to detail, communication skills, and ability to meet deadlines.
Summary Table
| Category | Details |
|---|---|
| Company | Tata Consultancy Services (TCS) |
| Vacancies | Pharmacovigilance Associate |
| Required Education | B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Nursing, Biomedical Sciences |
| Experience | 2–5 Years Pharmacovigilance Experience |
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