Pharmacovigilance professionals with extensive drug safety experience can explore two experienced-level opportunities at Novo Nordisk India Pvt Ltd and Teva Pharmaceuticals. The openings are based in Bangalore and Navi Mumbai/Bangalore, covering local pharmacovigilance operations, individual case safety report (ICSR) management, global PV compliance, quality systems, audits, and process improvement.
1. Novo Nordisk Hiring: Associate Pharmacovigilance Manager
Job Details
| Particulars | Details |
|---|---|
| Company | Novo Nordisk India Pvt Ltd |
| Job Role | Associate Pharmacovigilance Manager |
| Department | Regulatory Affairs and Pharmacovigilance |
| Job Category | Regulatory Affairs & Safety Pharmacovigilance |
| Location | Bangalore, Karnataka |
| Experience | 7–10 years of relevant experience, including at least 7 years in pharmacovigilance, drug safety, or a related field |
| Application Deadline | 30 October 2026 |
Job Responsibilities
The selected candidate will oversee local pharmacovigilance activities across clinical development and post-marketing settings.
- Act as the local Pharmacovigilance Responsible Person and ensure compliance with local PV requirements.
- Manage end-to-end individual case safety report (ICSR) processing, including intake, assessment, case narration, quality review, submission, follow-up, and closure.
- Coordinate health authority submissions for SUSARs, SAEs, post-marketing safety cases, and Periodic Safety Update Reports (PSURs).
- Handle adverse event reports and customer complaints received through email, phone, digital applications, and internal portals.
- Oversee safety training, mailbox reconciliation, case follow-ups, and timely regulatory reporting.
- Manage external partners and vendors supporting Customer Engagement Programmes and Organised Data Collection Systems.
- Lead pharmacovigilance audits, manage findings and corrective and preventive actions (CAPAs), and maintain inspection readiness.
- Drive PV process improvements and coordinate with Global Safety, Clinical, Medical, Regulatory, and other internal and external stakeholders.
Eligibility and Qualifications
Candidates should have:
- A Bachelor’s or Master’s degree in Pharmacy, or a PharmD.
- 7–10 years of relevant experience, including at least 7 years in pharmacovigilance, drug safety, or a related field.
- Hands-on experience in post-marketing case processing and end-to-end ICSR management.
- Experience managing Customer Engagement Programmes and Organised Data Collection Systems.
Required Skills
- Knowledge of ICH E2A, E2B(R3), and E2D guidelines.
- Understanding of New Drugs and Clinical Trials Rules, 2019 (NDCT), PvPI guidelines, and applicable Good Pharmacovigilance Practices (GVP).
- Experience with Veeva Safety and Veeva Quality.
- Basic proficiency in MedDRA.
- Knowledge of PV quality systems, regulatory reporting requirements, SOP implementation, audits, and CAPA management.
- Strong communication, stakeholder management, prioritisation, and problem-solving skills.
2. Teva Hiring: Lead GPV Professional, ICSR Conventions
Job Details
| Particulars | Details |
|---|---|
| Company | Teva Pharmaceuticals |
| Job Role | Lead GPV Professional, ICSR Conventions |
| Job ID | 70315 |
| Reference ID | 563602813635027 |
| Locations | Navi Mumbai, India; Bangalore, Karnataka, India |
| Work Mode | Hybrid |
| Experience | Minimum 7 years in the biopharmaceutical or CRO industry, including experience in a large international organisation |
Job Responsibilities
The role focuses on global pharmacovigilance compliance, System Data Innovation (SDI), quality processes, and continuous improvement across Teva’s global operations.
- Contribute to SDI audits, inspections, compliance activities, and inspection readiness.
- Coordinate SDI-related risk assessments, gap assessments, deviations, remediation plans, and CAPAs.
- Support change control management for process changes and contribute to SOPs and Working Instructions.
- Deliver SDI-related training to team members, Local Safety Officers (LSOs), and regional PV functions.
- Coordinate knowledge management and contribute to the onboarding and training of new team members.
- Participate in continuous improvement initiatives involving quality, compliance, efficiency, and V-safe functionality enhancements.
- Collaborate with ICSR Global Operations, ICSR Quality & Metrics, Project Management and Innovation, and Systems and Data Solutions.
- Contribute to global GPV projects and patient safety initiatives across Teva products.
Eligibility and Qualifications
Candidates should have:
- A minimum of 7 years of experience in the biopharmaceutical or CRO industry.
- Experience working in a large international organisation.
- Experience handling health authority inspections and third-party audits.
- Project management experience.
- AI and technical expertise.
- Fluency in English.
Experience using Veeva Vault Safety is desirable.
Required Skills
- Global pharmacovigilance compliance and inspection readiness.
- Audit coordination and CAPA management.
- SOP and Working Instruction development.
- Change control and gap assessment management.
- Training coordination and knowledge management.
- Project management and continuous improvement.
- AI and technical expertise.
- Strong English communication skills.
