Pharmacovigilance Jobs – Alvotech, a global specialty biopharmaceutical company focused on high-quality biosimilars, is hiring a Pharmacovigilance Associate (Safety Data Management) in Bangalore, India (partially remote).
This is an exciting opportunity for professionals with 2+ years of hands-on experience in clinical trial safety and post-marketing PV to join a lean, efficient Global Safety Data Management team supporting biosimilar development and commercialization.
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About the Company
Alvotech is a fully integrated specialty biopharmaceutical company dedicated exclusively to the development and manufacturing of high-quality biosimilar medicines.
Headquartered in Reykjavik, Iceland, with a global footprint including R&D and commercial operations in Europe, North America, and Asia, Alvotech focuses on complex biologics across immunology, oncology, ophthalmology, and other therapeutic areas.
The company emphasizes scientific excellence, regulatory compliance (FDA, EMA, and global agencies), operational efficiency, and patient access through cost-effective biosimilars.
Alvotech’s integrated Clinical and Medical Research (iCMR) team drives innovative strategies aligned with biosimilar guidelines, making it a trusted partner for sustainable biosimilar development.
Job Details
- Company Name: Alvotech
- Position: Pharmacovigilance Associate – Safety Data Management
- Experience: 2+ years in Pharmacovigilance / Drug Safety (hands-on in clinical trial safety and post-marketing PV)
- Qualification: Master’s degree in pharmaceutical sciences, medicine, pharmacy, life sciences, or related field
- Location: Bangalore Office / India Home Office (partially remote)
- Work Type: Full-time, Partially Remote
- Job ID: JR100088
- Application Deadline: March 31, 2026
Job Description
The Pharmacovigilance Associate will join Alvotech’s newly formed, lean Global Safety Data Management team reporting to the Safety Data Management Director.
The role focuses on end-to-end safety data management for clinical trials and post-marketing programs, including ICSR/SAE processing, regulatory submissions, literature monitoring, reconciliations, EV, XEVMPD, and support for PV system lifecycle management.
Pharmacovigilance Associate – Safety Data Management
- Department: Pharmacovigilance / Safety Data Management
- Market: Biopharmaceuticals – Biosimilars & Clinical Development
- Role: Pharmacovigilance Associate
- Experience: 2+ Years
- Education/Qualification: Master’s degree in pharmaceutical sciences, medicine, pharmacy, life sciences, or related field
Skills/Qualifications
- 2+ years hands-on experience in pharmacovigilance/drug safety, covering clinical trial safety and post-marketing PV activities
- Proven expertise in safety systems (Argus, ARISg preferred; Veeva Safety Vault experience is a strong advantage)
- Detailed knowledge of global PV regulations and guidelines (FDA, EMA, ICH, GVP, GCP, CIOMS, 21 CFR, etc.)
- Experience with ICSR/SAE management, regulatory submissions, literature/digital monitoring, reconciliations, EV, XEVMPD
- Strong understanding of safety database lifecycle management, CSV, and data integrity (ALCOA+)
- Excellent organizational, time-management, and interpersonal skills
- Ability to work independently in a multicultural, cross-functional team
- Willingness to travel internationally as required
Key Responsibilities
- Manage assigned clinical safety and post-marketing PV tasks (ICSR/SAE processing, submissions, reconciliations, literature/digital monitoring, EV, XEVMPD)
- Support safety system setup, configuration, validation, and lifecycle management
- Maintain and optimize global pharmacovigilance processes in line with international regulations
- Collaborate cross-functionally with PV teams, clinical operations, regulatory, quality, IT, and external partners/service providers
- Deliver pharmacovigilance training to internal staff and external parties
- Participate in audits and inspections related to safety data management
- Ensure data integrity, compliance, and timely delivery of all assigned activities
Benefits/Perks
- Career growth in a fast-expanding global biosimilar company
- Opportunity to shape a modern, efficient PV operating model
- Exposure to end-to-end safety data management for biosimilars
- Partially remote flexibility with international collaboration
- Competitive compensation and benefits package
- Inclusive, innovative culture focused on patient impact
How to Apply
Apply directly through the Alvotech careers portal: https://careers.alvotech.com (search for Job ID JR100088 or “Pharmacovigilance Associate Safety Data Management Bangalore”).
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Alvotech Career page.
Submit your updated resume highlighting 2+ years of PV experience, safety database expertise (Argus/ARISg/Veeva), and regulatory knowledge. For more pharmacovigilance jobs, biosimilar careers, safety data management roles, and pharma opportunities in Bangalore, visit Pharma Recruiter.
Apply before March 31, 2026, and join Alvotech in accelerating access to high-quality biosimilars worldwide!
Why You Should Join
Alvotech offers a unique chance to be part of a newly formed, efficient Global Safety Data Management team at the forefront of biosimilar development.
With a lean structure, focus on modern PV processes, and exposure to global clinical trials and post-marketing safety for complex biologics, the role provides significant learning, cross-functional collaboration, and career growth.
Joining Alvotech means contributing to affordable, innovative therapies while working in an inclusive, agile organization committed to transforming healthcare access worldwide.
FAQs
What is the minimum experience required for the Pharmacovigilance Associate role?
2+ years of hands-on experience in pharmacovigilance/drug safety, including clinical trial safety and post-marketing PV activities.
Is prior experience with specific safety systems mandatory?
Expertise in safety databases like Argus or ARISg is required; Veeva Safety Vault experience is a strong advantage.
Where is the job located?
Bangalore Office / India Home Office (partially remote with some on-site requirements).
What makes this role unique at Alvotech?
You’ll help build and optimize a modern, lean Global Safety Data Management function for biosimilars, working cross-functionally in a fast-growing, innovative company focused on global patient access.
