Cencora (via PharmaLex India Pvt Ltd) is actively hiring across multiple high-impact roles in Pharmacovigilance (PV), Drug Safety, Risk Management, and Regulatory Affairs in India. These roles are based primarily in Noida, Mumbai, and Thane, offering excellent opportunities for professionals with experience in ICSR processing, aggregate reporting, PV QMS, signal detection, and regulatory submissions.
If you are looking to advance your career in drug safety, pharmacovigilance operations, or regulatory affairs, this is a strong opportunity to work with a globally recognized healthcare organization.
🔥 Open Positions at Cencora (India)
1. Senior Specialist – Pharmacovigilance (Literature & ICSR)
📍 Location: Noida
🧪 Experience: ~2+ years
Key Responsibilities:
- Literature screening & Medical Literature Monitoring (MLM – EMA)
- ICSR data entry and case processing
- Preparation of CIOMS / MedWatch / XML reports
- Duplicate search and case validation
- Client communication & project coordination
2. Assistant Manager – PV Quality & QMS
📍 Location: Noida
Key Responsibilities:
- CAPA management (5 Whys, Fishbone, RCA)
- PV QMS compliance (ICH, EU GVP, FDA, MHRA)
- Audit readiness & inspection preparation
- PV compliance dashboards (ICSR timelines, RFT, CAPA metrics)
- Trend analysis & risk mitigation
3. Manager – Drug Safety Physician
📍 Location: Noida
🧑⚕️ Qualification: MBBS / MD
🧪 Experience: 5–7+ years
Key Responsibilities:
- PSUR, PBRER, RMP, DSUR authoring
- Benefit-risk evaluation & safety strategy
- Medical review of safety data & ICSRs
- Health Authority responses
- Mentoring PV teams
4. Senior Specialist – PV Epidemiology & Risk Management
📍 Location: Noida / Mumbai
Key Responsibilities:
- Signal detection & EVDAS screening
- PSUR, DSUR, PADER, ACO writing
- Risk Management Plans (RMPs)
- Signal assessment reports (SARs)
- Regulatory authority communication
5. Senior Manager – Regulatory Affairs
📍 Location: Thane
🧪 Experience: 12+ years
Key Responsibilities:
- Regulatory submissions (India market)
- Marketing authorization lifecycle (renewals, variations)
- Regulatory strategy & client consulting
- Health Authority interactions
- Project leadership & team management
6. Medical Reviewer – Case Processing
📍 Location: Noida
🧑⚕️ Qualification: MBBS
🧪 Experience: 8+ years
Key Responsibilities:
- Medical review of ICSRs
- Causality assessment & narrative review
- MedDRA coding validation
- Signal identification support
- Mentoring PV associates
🎓 Qualifications Required
- Life Sciences (B.Pharm, M.Pharm, MSc, PharmD)
- MBBS / MD (for physician roles)
- Strong knowledge of:
- Pharmacovigilance workflows (ICSR, MLM, signal detection)
- MedDRA & safety databases
- ICH-GCP, EU GVP, FDA guidelines
💼 Key Skills
- Pharmacovigilance case processing & medical review
- Aggregate safety report writing (PSUR, RMP, DSUR)
- CAPA, RCA, QMS compliance
- Regulatory submissions & strategy
- Strong communication & stakeholder management
💰 Salary Range (Estimated INR)
- Senior Specialist (PV): ₹6 – ₹12 LPA
- Assistant Manager (PV QA): ₹10 – ₹18 LPA
- Drug Safety Physician: ₹18 – ₹35 LPA
- PV Risk Management Specialist: ₹12 – ₹22 LPA
- Regulatory Affairs Senior Manager: ₹25 – ₹45 LPA
- Medical Reviewer: ₹20 – ₹40 LPA
🎁 Benefits of Working at Cencora
- Global exposure in pharmacovigilance & regulatory domains
- Work with top pharmaceutical clients
- Strong career progression in PV & RA
- Competitive compensation & benefits
- Learning & development opportunities
📩 How to Apply
Application Link For Senior Specialist – Pharmacovigilance (Literature & ICSR)
Application Link For Assistant Manager – PV Quality & QMS
Application Link For Manager – Drug Safety Physician
Application Link For Senior Specialist – PV Epidemiology & Risk Management
Application Link For Senior Manager – Regulatory Affairs
Application Link For Medical Reviewer – Case Processing
