Macleods Pharmaceuticals Hiring PBRER Reviewer & RMP Drafter | Pharmacovigilance Jobs in Mumbai 2026 (Macleods Pharmaceuticals Hiring PBRER Reviewer & RMP Drafter) Introduction Professionals looking for Pharmacovigilance jobs in Mumbai have an excellent opportunity to join Macleods Pharmaceuticals, one of India's leading pharmaceutical companies. The organization is currently recruiting experienced candidates for PBRER Reviewer and RMP Drafter positions within its Pharmacovigilance Department. This recruitment drive is ideal for M.Pharm graduates who have experience in aggregate safety reporting, PSUR preparation, PBRER review, Risk Management Plans (RMP), and global regulatory compliance activities. Selected candidates will gain exposure to international pharmacovigilance projects covering Europe, the UK, India, and other global markets. About the Company Macleods Pharmaceuticals is a well-established pharmaceutical company known for its presence in multiple the...
Get link
Facebook
X
Pinterest
Email
Other Apps
Pharma Duniya is a trusted platform providing the latest pharma job updates, walk-in interviews, clinical research openings, and pharmacy career guidance.
All job information is collected from official company websites and public sources.
We do not charge any fees and are not official recruiters.
TCS Pharmacovigilance Associate Jobs in Hyderabad 2026 | Argus Safety & Drug Safety Careers
Get link
Facebook
X
Pinterest
Email
Other Apps
TCS Pharmacovigilance Associate Jobs in Hyderabad 2026 | Apply Now
(TCS Pharmacovigilance Associate Jobs in Hyderabad 2026)
Introduction
The pharmacovigilance and drug safety industry in India is growing rapidly due to increasing global clinical trials, regulatory monitoring, and patient safety requirements. Tata Consultancy Services (TCS) is currently hiring Pharmacovigilance Associates in Hyderabad for professionals with experience in Argus Safety, adverse event reporting, and ICSR case processing.
This opportunity is highly suitable for candidates looking for Pharmacovigilance jobs in Hyderabad, Drug Safety Associate roles, and healthcare IT careers in India. Professionals with experience in medical coding, global safety compliance, and drug safety operations can build a strong, long-term career through this opening at TCS.
About Tata Consultancy Services (TCS)
Tata Consultancy Services (TCS) is one of the world’s leading IT services, consulting, and business solutions companies. Founded in 1968, TCS is part of the Tata Group and operates in more than 50 countries globally.
Headquartered in Mumbai, Maharashtra, India, TCS employs over 600,000 professionals worldwide and provides services across healthcare, pharmaceuticals, banking, engineering, artificial intelligence, cloud computing, and digital transformation sectors.
TCS has established a strong presence in healthcare and life sciences by supporting pharmaceutical companies, clinical research organizations (CROs), and drug safety operations through advanced technology and regulatory solutions.
The company is widely recognized for offering stable career growth, global project exposure, professional learning programs, and long-term employment opportunities.
Job Overview Summary
TCS is recruiting experienced Pharmacovigilance Associates for its Healthcare & Life Sciences division in Hyderabad. The selected professionals will handle drug safety case processing, adverse event review, Argus database management, and pharmacovigilance operations while ensuring compliance with global safety regulations.
Candidates with experience in ICSR processing, medical coding, and safety reporting systems will have an advantage during the selection process.
Vacancy Details
Particulars
Details
Job Title
Pharmacovigilance Associate
Company
Tata Consultancy Services (TCS)
Location
Hyderabad
Experience Required
2–6 Years
Employment Type
Full Time, Permanent
Department
Healthcare & Life Sciences
Industry
IT Services & Consulting
Salary Estimate
₹4.5 LPA – ₹8.5 LPA
Job Role Explanation
The Pharmacovigilance Associate role at TCS involves managing and reviewing adverse drug reaction reports, maintaining drug safety databases, and supporting global pharmacovigilance activities. Professionals will work closely with healthcare and life sciences teams to ensure patient safety and regulatory compliance.
The role also includes handling end-to-end case processing activities, reviewing medical information, and ensuring timely submission of safety reports according to international pharmacovigilance standards.
Candidates will gain exposure to global drug safety projects, regulatory frameworks, and healthcare technologies.
Key Responsibilities of a Pharmacovigilance Associate
Adverse Event Case Processing
Selected candidates will review, process, and assess adverse event cases within the Argus Safety database while ensuring data accuracy and compliance.
Medical Coding & Documentation
Professionals will perform medical coding, safety data entry, and documentation review activities related to drug safety operations.
Regulatory Compliance
The role requires compliance with global pharmacovigilance guidelines, SOPs, and local safety reporting regulations.
Safety Follow-Up Activities
Candidates will coordinate follow-up activities for incomplete or pending safety cases and maintain appropriate documentation.
Collaboration & Reporting
Employees will collaborate with cross-functional teams and contribute to process improvement initiatives while meeting strict project timelines.
Eligibility Criteria
Candidates applying for the TCS Pharmacovigilance Associate job should possess:
2–6 years of experience in Pharmacovigilance or Drug Safety
Hands-on experience with Argus Safety database
Knowledge of ICSR case processing and adverse event reporting
Understanding of global safety regulations and compliance procedures
Strong analytical and communication skills
Ability to work effectively in team environments
Skills Required
Technical Skills
Argus Safety case processing
Adverse event assessment
Medical coding knowledge
Drug safety database handling
ICSR workflow management
Regulatory documentation review
Soft Skills
Attention to detail
Communication skills
Analytical thinking
Time management
Problem-solving ability
Team coordination
Salary Estimate
Based on current pharmacovigilance industry standards in India, the estimated salary for the Pharmacovigilance Associate role at TCS ranges between:
Estimated Salary Range:
₹4.5 LPA – ₹8.5 LPA
The final salary package may vary depending on experience, technical expertise, Argus Safety exposure, and interview performance.
Why Join Tata Consultancy Services?
Working at TCS provides excellent career opportunities for professionals interested in healthcare IT and pharmacovigilance operations.
Benefits of Joining TCS
Competitive salary packages
Stable long-term employment
Exposure to global healthcare projects
Professional learning programs
Career growth in drug safety operations
Collaborative work culture
Experience with international pharmacovigilance standards
Interview Details
Selection Process May Include:
Resume Shortlisting
HR Interview
Technical Pharmacovigilance Round
Argus Safety Knowledge Assessment
Final Managerial Discussion
Candidates should prepare topics related to:
ICSR processing
Adverse event reporting
Pharmacovigilance workflows
Argus Safety database
Medical terminology
Regulatory compliance
Required Documents
Candidates should keep the following documents ready before applying:
Updated Resume/CV
Educational Certificates
Government ID Proof
Experience Certificates
Salary Slips (if applicable)
Pharmacovigilance Training Certificates
Passport-size Photograph
Job Location
Hyderabad, Telangana, India
Hyderabad is one of India’s fastest-growing pharmaceutical and healthcare technology hubs with multiple opportunities in clinical research, pharmacovigilance, regulatory affairs, and drug safety operations.
How to Apply
Interested and eligible candidates can apply through the official application link below:
Q1. What is the role offered by TCS in this hiring?
TCS is hiring for the position of Pharmacovigilance Associate in Hyderabad.
Q2. What experience is required for this pharmacovigilance job?
Candidates should have 2–6 years of experience in Pharmacovigilance or Drug Safety operations.
Q3. Is Argus Safety experience mandatory?
Yes, hands-on experience with the Argus Safety database is preferred for this role.
Q4. What is the estimated salary for this TCS Pharmacovigilance role?
The estimated salary ranges between ₹4.5 LPA and ₹8.5 LPA.
Q5. Who can apply for this Pharmacovigilance Associate job?
Candidates with relevant pharmacovigilance, drug safety, and ICSR case processing experience can apply.
Q6. What skills are important for this role?
Important skills include adverse event reporting, medical coding, Argus Safety handling, regulatory compliance, and analytical abilities.
Final Conclusion
The TCS Pharmacovigilance Associate job in Hyderabad is an excellent opportunity for professionals looking to build a stable and rewarding career in drug safety and healthcare operations. With growing demand for pharmacovigilance professionals globally, this role offers strong exposure to adverse event reporting, regulatory compliance, and patient safety systems.
Candidates with experience in Argus Safety, ICSR case processing, and medical coding can significantly enhance their careers by joining Tata Consultancy Services. Interested applicants are advised to apply as early as possible before the recruitment process closes.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
🚨 Not Getting Interview Calls in Pharma?
Even after applying to multiple companies, still no response.
👉 The real problem is NOT your qualification — it’s your resume + wrong job strategy
Most pharma candidates: ❌ Use non-ATS resumes ❌ Apply randomly without direction ❌ Don’t match recruiter expectations
That’s why they don’t get shortlisted.
✅ Here’s How Pharma Duniya Can Help You
We don’t just “make resumes” — We help you get results 👇
✔ ATS-Friendly Resume (PV / QA / QC / Clinical – role-based) ✔ Proper Job Direction (which domain is best for you) ✔ Daily Apply Strategy (where & how to apply) ✔ Interview Preparation (real pharma questions) ✔ Personal Guidance (step-by-step support)
🎯 Choose What You Need
👉 Resume Only (ATS Optimised) 👉 Resume + Basic Guidance 👉 Complete Career Guidance 👉 Premium Mentorship (for serious candidates)
Recommended Pharma Career & Job Updates (Must Read)
If you are preparing for pharma job interviews or actively searching for the latest QA, QC, Pharmacovigilance jobs and walk-in interviews, don’t miss these important and student-friendly career resources from Pharma Duniya 👇
📢 Stay Updated with Latest Pharma Jobs & Walk-In Interviews
If you want daily verified updates on QA, QC, Pharmacovigilance, Clinical Research, and Pharma Walk-In Interviews, join Pharma Duniya’s official channels and never miss an opportunity.
Skycraper CRS Clinical Research Internship 2026 (Skycraper CRS Clinical Research Internship 2026) Introduction Candidates planning to start a career in clinical research now have an excellent opportunity to gain practical industry exposure through the latest Clinical Research Internship program announced by Skycraper CRS. This 6-month internship program is specially designed for freshers, students, and aspiring healthcare professionals who want hands-on training and real-world experience in clinical research operations. The internship provides exposure to clinical trial coordination, clinical documentation, SOP workflows, research management, and healthcare compliance systems. Candidates interested in clinical research internships in India, CRO training opportunities, and pharmaceutical industry exposure can use this internship to build strong professional skills. This latest internship opportunity is ideal for Pharmacy, Life Sciences, Biotechnology, and Healthcare students wh...
SafeVig Solutions Hiring Executive – Business Development (Pharmacovigilance) | Freshers & Experienced SafeVig Solutions Hiring Executive – Business Development Introduction The pharmacovigilance industry continues to create exciting career opportunities for life sciences professionals across India. SafeVig Solutions, a growing drug safety and pharmacovigilance services company, has announced recruitment for the position of Executive – Business Development (Pharmacovigilance) at its Hyderabad office. This opportunity is suitable for fresh graduates as well as professionals with up to 2 years of experience who are interested in business development, client relationship management, healthcare sales, pharmacovigilance services, and life sciences consulting. Candidates looking for pharmacovigilance business development jobs, drug safety careers, healthcare sales positions, and pharmaceutical business development opportunities may find this role highly rewarding. About Th...
acuLife Healthcare Pharmacovigilance Executive / Medical Writer Jobs 2026 (acuLife Healthcare Pharmacovigilance Executive Recruitment 2026) Introduction acuLife Healthcare Pvt. Ltd., a part of the reputed Nirma Group, has officially announced new hiring opportunities for the position of Pharmacovigilance Executive / Medical Writer at its corporate office in Ahmedabad, Gujarat. This latest pharmacovigilance job opening is highly suitable for Pharm.D freshers and candidates with up to 1 year of experience who want to build a professional career in drug safety, medical writing, clinical research, and regulatory compliance. Candidates interested in Pharmacovigilance jobs in Ahmedabad, Medical Writer jobs for Pharm.D graduates, Drug Safety Associate careers, or Clinical Research opportunities in India should explore this opportunity carefully. The role provides exposure to adverse event reporting, literature review, safety monitoring, and scientific documentation within a growing pharmac...
Zydus Lifesciences Hiring Apprentice – Business Strategy in Ahmedabad | Regulatory Affairs Jobs 2026 (Zydus Lifesciences Hiring Apprentice – Business Strategy in Ahmedabad) Introduction India’s pharmaceutical and regulatory affairs sector is growing rapidly, creating excellent opportunities for pharmacy graduates interested in regulatory documentation, CDSCO submissions, and pharmaceutical compliance operations. Zydus Lifesciences has announced a new opening for the position of Apprentice – Business Strategy in Ahmedabad. This opportunity is highly suitable for: B.Pharm graduates M.Pharm graduates Regulatory Affairs professionals Pharmaceutics candidates Quality Assurance professionals Candidates looking for: Regulatory Affairs jobs in Ahmedabad CDSCO documentation careers CTD/eCTD jobs Pharma compliance careers Pharmaceutical regulatory operations jobs should consider applying for this role. The position offers strong learning exposure in: CDSCO submissions CTD/eCTD documentati...
Elevatia Solutions Regulatory Affairs Executive Jobs 2026 (Elevatia Solutions Regulatory Affairs Executive Recruitment) Introduction Elevatia Solutions has officially announced a new hiring opportunity for the Regulatory Affairs Executive position at its New Delhi office. This latest pharmaceutical regulatory affairs job is an excellent career opportunity for candidates from Pharmacy and Life Sciences backgrounds who are interested in regulatory documentation, compliance operations, product registration, and pharmaceutical submission activities. Candidates searching for Regulatory Affairs jobs in Delhi, B.Pharm jobs in CRO companies, M.Pharm regulatory jobs, pharmaceutical compliance jobs, or Clinical Research opportunities in India can explore this opportunity for career growth in the pharmaceutical industry. This opening is suitable for both freshers and candidates with up to 2 years of experience who want to build long-term careers in Regulatory Affairs and pharmaceutical operat...
Acme Generics Regulatory Affairs Executive / Senior Executive Jobs 2026 (Acme Generics Regulatory Affairs Executive Recruitment 2026) Introduction Acme Generics has announced new recruitment opportunities for Regulatory Affairs Executive and Senior Executive positions at its Ahmedabad facility. This latest pharmaceutical job opening is ideal for professionals with experience in EU Regulatory Affairs, eCTD dossier preparation, lifecycle management, pharmaceutical compliance, and regulatory submissions. Candidates looking for Regulatory Affairs jobs in Ahmedabad, EU market pharmaceutical jobs, eCTD submission careers, or international regulatory affairs opportunities can explore this opening. The company is seeking qualified professionals who can support European regulatory operations and ensure compliance with global pharmaceutical standards. About Acme Generics Acme Generics is a well-established pharmaceutical company engaged in the development, manufacturing, and marketin...
Share on WhatsApp
