Piramal Pharma Hiring Senior Executive Pharmacovigilance in Mumbai
Pharmacovigilance has become one of the most critical functions within the pharmaceutical industry. As global regulatory authorities continue to strengthen drug safety requirements, organizations are investing heavily in professionals who can manage adverse event reporting, aggregate safety reporting, regulatory compliance, and risk management activities.
For professionals who already possess experience in Individual Case Safety Report (ICSR) processing and drug safety operations, Piramal Critical Care (PCC) has announced an exciting opportunity in Mumbai. The company is currently hiring a Senior Executive – Pharmacovigilance to support global safety operations, aggregate reporting activities, literature monitoring, and regulatory compliance functions.
This position is ideal for Pharmacovigilance professionals looking to move beyond basic case processing and gain exposure to advanced safety activities such as PADER preparation, PBRER authoring, regulatory submissions, audit support, and global pharmacovigilance operations.
📌 Job Overview
| Particulars | Details |
|---|---|
| Company | Piramal Critical Care |
| Position | Senior Executive – Pharmacovigilance |
| Job ID | R00002203 |
| Location | Kurla, Mumbai |
| Work Mode | Hybrid |
| Department | Pharmacovigilance |
| Experience | 2–3 Years |
| Application Deadline | 30 June 2026 |
| Application Mode | Online Application |
🏢 About Piramal Critical Care
Piramal Critical Care is a business unit of Piramal Pharma and is known for its focus on critical care products and healthcare innovation. The organization operates globally and works closely with healthcare professionals, regulatory authorities, and pharmaceutical partners to ensure patient safety and product quality.
Working within the Pharmacovigilance function at Piramal provides exposure to global safety reporting standards, regulatory requirements, risk management practices, and advanced drug safety operations.
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Join WhatsApp Channel💊 Why Pharmacovigilance Remains a High-Growth Career
Every medicine available in the market must be continuously monitored for safety throughout its lifecycle. Pharmacovigilance professionals help identify, assess, and report adverse events while ensuring compliance with global regulatory requirements.
As pharmaceutical companies expand globally and launch new therapies, demand for experienced drug safety professionals continues to rise. Skills such as ICSR processing, literature screening, aggregate reporting, signal detection, and risk management are increasingly valuable across pharmaceutical companies and CROs.
Professionals interested in long-term growth can also explore resources such as: Best Career Options After B.Pharm and Top Pharmacovigilance Interview Questions to strengthen their career preparation.
💼 Key Responsibilities
The selected candidate will support end-to-end Pharmacovigilance operations while ensuring compliance with global regulatory requirements.
- Perform end-to-end ICSR case management activities.
- Handle case receipt, follow-up, review, and regulatory submissions.
- Manage Pharmacovigilance mailbox and case tracking activities.
- Perform reconciliation of Individual Case Safety Reports.
- Submit safety cases to regulatory authority databases.
- Conduct literature screening and monitoring activities.
- Maintain safety logs, files, and compliance documentation.
- Prepare compliance reports and safety metrics.
- Support product complaint reconciliation activities.
- Assist during audits and regulatory inspections.
- Prepare aggregate reports such as PADERs and PBRERs.
- Coordinate with internal and external stakeholders.
🎓 Eligibility Criteria
Educational Qualifications
- B.Pharm
- M.Pharm
Experience Requirements
- 2–3 Years Overall Pharmacovigilance Experience
- Minimum 1 Year Experience in ICSR Processing
- Literature Screening Experience
- PADER / PBRER Authoring Experience
- Aggregate Safety Reporting Knowledge
🧠 Required Skills
- ICSR Processing
- Pharmacovigilance Case Management
- Literature Screening
- PADER Authoring
- PBRER Preparation
- Regulatory Compliance
- Safety Database Management
- Audit & Inspection Readiness
- Communication Skills
- Stakeholder Management
- Microsoft Word, Excel & PowerPoint
💰 Salary & Benefits
Based on current industry benchmarks for professionals with aggregate reporting and ICSR processing experience, the estimated compensation range is:
Estimated Salary: ₹5.5 LPA – ₹9.5 LPA
Actual compensation may vary depending on candidate experience, technical expertise, aggregate reporting exposure, and interview performance.
Employee Benefits
- Competitive Compensation Package
- Hybrid Working Model
- Global Pharmacovigilance Exposure
- Learning & Development Programs
- Professional Training Opportunities
- Work-Life Balance Initiatives
- Health & Wellness Benefits
- Long-Term Career Growth
🌟 Why Join Piramal Critical Care?
- Part of a Leading Global Pharmaceutical Organization.
- Exposure to Global Drug Safety Operations.
- Hands-On Aggregate Reporting Experience.
- Opportunity to work on Regulatory Compliance Activities.
- Strong Learning & Development Culture.
- Interaction with Global Stakeholders.
- Career Advancement in Pharmacovigilance.
- Long-Term Professional Development.
📈 Career Growth Opportunities
Professionals entering aggregate reporting and advanced pharmacovigilance functions often progress into specialized leadership roles.
- Pharmacovigilance Specialist
- Senior Drug Safety Associate
- Aggregate Reporting Specialist
- Safety Scientist
- Risk Management Specialist
- Pharmacovigilance Manager
- Global Safety Lead
- Drug Safety Team Lead
📑 Resume Tips for Pharmacovigilance Professionals
A strong resume can significantly improve interview opportunities. Candidates should:
- Highlight ICSR Processing Experience.
- Mention Aggregate Reports (PADER, PBRER, PSUR).
- Include Literature Screening Activities.
- Showcase Regulatory Submission Experience.
- Mention Safety Database Knowledge.
- Highlight Audit & Inspection Readiness Activities.
Before applying, candidates may also find it useful to review: Common Pharma Interview Mistakes.
