Alvotech Pharmacovigilance Specialist Bangalore Hiring
- Alvotech Hiring Pharmacovigilance Specialist in Bangalore | Safety Data Management Role (3+ Years)
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Background:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Why This Role Matters in Healthcare
- Frequently Asked Questions (FAQs)
- 1. Is this role suitable for freshers?
- 2. What safety systems are used in this role?
- 3. Is this a remote job?
- 4. What career growth can I expect?
- Summary
Alvotech Hiring Pharmacovigilance Specialist in Bangalore | Safety Data Management Role (3+ Years)
Looking to advance your career in pharmacovigilance and drug safety? Alvotech is hiring Pharmacovigilance Specialists for its Safety Data Management team in Bangalore with partial remote flexibility. This is a high-impact opportunity for professionals with 3+ years of experience in clinical safety, ICSR management, and global pharmacovigilance operations.
The role sits within the Clinical and Medical Research (iCMR) function and focuses on safety data management across clinical trials and post-marketing programs, making it a strong career move for professionals targeting global drug safety and regulatory compliance roles.
Company Overview
Alvotech is a global biopharmaceutical company focused on the development and manufacturing of high-quality biosimilars. The organization operates with a strong R&D backbone and is committed to expanding access to affordable biologic therapies worldwide.
Its integrated Clinical and Medical Research (iCMR) division plays a key role in clinical strategy, regulatory compliance, and post-marketing surveillance, ensuring that biosimilar products meet global safety and efficacy standards.
Job Role & Responsibilities
As a Pharmacovigilance Specialist, you will manage safety data activities across clinical trials and post-marketing programs while ensuring compliance with global pharmacovigilance regulations.
Key Responsibilities:
- Manage clinical safety and post-marketing pharmacovigilance activities including ICSR and SAE processing
- Perform literature monitoring, digital safety surveillance, and reconciliation activities
- Handle regulatory submissions including EudraVigilance (EV) and XEVMPD reporting
- Participate in safety database setup, validation, and lifecycle management
- Develop and optimize pharmacovigilance processes aligned with global regulatory requirements
- Collaborate with cross-functional teams including regulatory, quality, and clinical operations
- Coordinate with external vendors and pharmacovigilance service providers
- Conduct training sessions on PV processes and compliance standards
- Support audits and regulatory inspections related to safety data management
Eligibility / Qualifications
Educational Background:
M.Pharmacy, Pharm.D, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Medicine, Pharmacy, Life Sciences
Experience Required:
- Minimum 3 years of experience in pharmacovigilance or drug safety
- Hands-on experience in safety data management and clinical trial safety
- Experience with global pharmacovigilance systems and processes
- Experience in biologics or combination products preferred
Skills Required:
- Strong knowledge of global PV regulations (ICH, GCP, GVP, CIOMS, FDA, EMA)
- Experience with safety databases such as Argus, ARISg, or Veeva Safety Vault
- Strong analytical and documentation skills
- Excellent communication and cross-functional collaboration abilities
- Ability to work independently in a global environment
Location & Salary
- Location: Bangalore, India (Partial Remote)
- Job Type: Full-time
- Salary: Competitive salary package based on experience
This role offers strong growth opportunities in pharmacovigilance, drug safety, and global regulatory compliance, which are among the most in-demand and high-paying domains in the pharmaceutical and biotech industry.
Application Process
Interested candidates can apply through the official Alvotech careers portal:
Application Deadline: March 31, 2026
Candidates are advised to apply early due to limited openings and high competition.
Why This Role Matters in Healthcare
Pharmacovigilance Specialists play a critical role in ensuring the safety of medicines throughout their lifecycle. By managing safety data, monitoring adverse events, and ensuring regulatory compliance, this role directly impacts patient safety and the success of biosimilar drug programs.
Working in this position provides exposure to global safety systems and contributes to improving healthcare outcomes worldwide.
Frequently Asked Questions (FAQs)
1. Is this role suitable for freshers?
No, this position requires a minimum of 3 years of experience in pharmacovigilance or drug safety.
2. What safety systems are used in this role?
Common systems include Argus, ARISg, and Veeva Safety Vault.
3. Is this a remote job?
This is a partially remote role based in Bangalore.
4. What career growth can I expect?
You can grow into roles such as Senior PV Specialist, Drug Safety Manager, or Global Safety Lead.
Summary
| Category | Details |
|---|---|
| Company | Alvotech |
| Vacancies | Pharmacovigilance Specialist |
| Required Education | M.Pharmacy, Pharm.D, MSc, Life Sciences |
| Experience | 3+ years |
To apply for this job please visit alvotech.wd103.myworkdayjobs.com.
