Alvotech is hiring a Pharmacovigilance Specialist – Safety Data Management for its Bangalore Office / India Home Office. The position focuses on clinical safety and post-marketing pharmacovigilance activities, safety data management, regulatory compliance and safety system lifecycle management.
The role is suitable for candidates with a Master’s Degree in pharmaceutical sciences or a related field and 3+ years of experience in Pharmacovigilance/Drug Safety, particularly in safety data management functions.
Job Overview
| Details | Information |
|---|---|
| Company | Alvotech |
| Job Title | Pharmacovigilance Specialist, Safety Data Management |
| Department | Global Safety Data Management |
| Location | Bangalore Office / India Home Office |
| Work Type | Partially Remote |
| Job Type | Full Time |
| Qualification | Master’s Degree in Pharmaceutical Sciences or related fields |
| Experience | 3+ Years |
| Job Requisition ID | JR100100 |
| Last Date to Apply | September 29, 2026 |
Job Description
The Pharmacovigilance Specialist will be responsible for assigned Clinical Safety and post-marketing PV activities within Alvotech’s Global Safety Data Management team.
The role involves safety data management for clinical trials and post-marketing programs, development of PV processes, safety system development and lifecycle management, and ensuring compliance with applicable regulatory requirements.
Key Responsibilities
- Manage assigned clinical safety and post-marketing pharmacovigilance activities.
- Work on ICSR and SAE management and regulatory submissions.
- Perform literature monitoring and digital platform monitoring.
- Support reconciliations, EV and XEVMPD activities.
- Participate in safety system setup and lifecycle management.
- Support system configuration and validation activities.
- Create, maintain and optimize global pharmacovigilance processes.
- Ensure compliance with applicable international laws and regulations.
- Work with PV, Benefit-Risk Management, Clinical Trials and Partner Compliance teams.
- Collaborate with Quality, Regulatory, IT, CPD and other internal departments.
- Work with external PV service providers and business partners.
- Deliver training on pharmacovigilance processes and standards.
- Participate in audits and inspections related to Safety Data Management activities.
Eligibility / Qualification
- Master’s Degree in Pharmaceutical Sciences or a related field such as:
- Medicine
- Pharmacy
- Life Sciences
- Minimum 3+ years of experience in Pharmacovigilance/Drug Safety.
- Hands-on experience in Safety Data Management.
- Experience in clinical trial safety and post-marketing PV activities.
- Experience with safety systems such as Argus or ARISg.
- Experience with Veeva Safety Vault is an advantage.
- Experience working with global products and clinical trials.
- Experience with biologic and combination products is an advantage.
- Knowledge of PV processes, directives, regulations and international guidelines including:
- 21 CFR
- ICH
- GVP
- GCP
- CIOMS
Required Skills
- Strong self-organization and time-management skills.
- Good interpersonal and communication skills.
- Ability to work independently.
- Ability to plan, organize and deliver assigned activities.
- Ability to work effectively in a multicultural team.
- Willingness to travel internationally when required.
How to Apply
Interested and eligible candidates can apply online through the Alvotech careers portal.
Last Date to Apply: September 29, 2026 employer and encourages qualified candidates to apply.