Alvotech Hiring for PV Associate Role: PV Jobs 2026

Alvotech, a globally recognized biopharmaceutical company focused on biosimilar development and manufacturing, is hiring for a Pharmacovigilance (PV) role in Bangalore, with partial remote work options. This opportunity is suitable for professionals looking to build or advance their career in pharmacovigilance, drug safety, and clinical research operations.

This hiring is part of Alvotech’s Integrated Clinical and Medical Research (iCMR) expansion, supporting activities across safety data management, benefit‑risk assessment, and the clinical data lifecycle. The role offers strong exposure to global R&D practices within a regulated biopharmaceutical environment.

For candidates targeting a long‑term career in drug safety and pharmacovigilance, this is a high‑value opportunity within an international research‑driven organization.

🏢 About the Organization

Alvotech is a global biopharmaceutical company focused on the development and commercialization of biosimilars and complex biologic medicines. The organization operates across multiple regions and follows robust global pharmacovigilance, regulatory, and quality frameworks. Working at Alvotech provides exposure to international safety regulations, global products, and advanced PV systems, making it a strong environment for experienced drug safety professionals.

📊 Position Overview

• Position: PV Associate,Safety data management
• Department: PV
• Location: Banglore, India(Partially Remote)
• Experience: 2+ Years
• Qualification: M.Pharm
• Job Type: Full-Time
• Last Date to apply: 31 March 2026

📋 Main Responsibilities– PV Associate

• Perform assigned clinical safety and post‑marketing pharmacovigilance activities, including ICSR/SAE management, regulatory submissions, literature monitoring, digital platform monitoring, reconciliations, EudraVigilance (EV), and XEVMPD activities.
• Support pharmacovigilance safety systems setup, configuration, validation, and ongoing system lifecycle management activities.
• Contribute to the maintenance and optimization of global pharmacovigilance processes, ensuring compliance with international regulations such as FDA, EMA, and ICH guidelines.
• Work closely with PV teams such as Benefit‑Risk Management, Clinical Trials, and Partner Compliance to support timely delivery and regulatory compliance.
• Collaborate cross‑functionally with internal departments including Quality, Regulatory, IT, and Clinical Product Development (CPD).
• Coordinate with external PV service providers and business partners to support pharmacovigilance activities and compliance expectations.
• Deliver pharmacovigilance training sessions on PV processes and standards to internal teams and external stakeholders as required.
• Support and participate in audits and regulatory inspections related to safety data management and pharmacovigilance system compliance.

🎓 Required Qualification

Candidates applying for this role must meet the following requirements:

• Educational Background:
  • Master’s degree in:
    • Pharmaceutical Sciences
    • Medicine
    • Pharmacy
    • Life Sciences
    • Or a related scientific discipline
• Experience:
  • Minimum 2+ years of experience in Pharmacovigilance / Drug Safety
  • Hands‑on involvement in:
    • Safety data management
    • Clinical trial safety
    • Post‑marketing pharmacovigilance activities

🧠 Essential Skills

• Practical experience working with PV safety databases such as:
  • Argus
  • ARISg
  • Or similar pharmacovigilance platforms
• Prior exposure to Veeva Safety Vault is a strong advantage
• Proven experience supporting global products
• Exposure to international clinical trials and multi‑region PV activities
• Experience working with:
  • Biologic products
  • Combination products (preferred)

⭐ Role Summary

The PV Associate role at Alvotech offers advanced exposure to global drug safety operations for biologic and complex products. Professionals in this role contribute directly to patient safety, regulatory compliance, and global risk management strategies. With hands‑on safety system usage and regulatory interaction, this role is well‑suited for PV professionals aiming to move into senior safety or leadership positions.

🎯 Suitable Candidates

This opportunity is suitable for:

• Pharmacovigilance professionals with 2+ years of experience
• Drug safety specialists with hands‑on ICSR and safety database exposure
• Professionals experienced in global PV operations
• Candidates seeking growth in biologics and complex product safety

📈 Career Opportunities

With experience and performance, professionals can grow into roles such as:

• Senior Pharmacovigilance Associate
• Global Safety Specialist
• PV Lead or Safety Scientist
• Drug Safety Manager / PV Operations Manager

Alvotech supports long‑term career development within global PV structures.

💰 Compensation Details

• Expected Salary: As per Alvotech company standards for experienced PV roles
• Compensation varies based on expertise, system exposure, and product experience.

💡 Preparation Tips

• Highlight global trial exposure and system expertise in your resume
• Revise global PV regulations (ICH, GVP, CIOMS, 21 CFR)
• Strengthen hands‑on knowledge of Argus / ARISg workflows
• Be prepared to discuss biologic or combination product safety scenarios

🔗 Application Process

Interested candidates should apply only through the official company career website using the link provided below.

Important Disclaimer: This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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FAQ-PV Associate

1. Who can apply for this Pharmacovigilance role at Alvotech?

Candidates with a Master’s degree in Pharmaceutical Sciences, Pharmacy, Medicine, or Life Sciences and 2+ years of experience in pharmacovigilance or drug safety.

2. What type of pharmacovigilance activities will I handle?

You will work on clinical safety and post‑marketing PV activities, including ICSR/SAE management, regulatory submissions, literature monitoring, reconciliations, EV/XEVMPD, and safety system lifecycle activities.

3. Is this role focused on global projects?

Yes. You will support global products and international clinical trials, working within Alvotech’s global pharmacovigilance and iCMR framework.

4. Which safety systems will I work with?

You will primarily work with Argus, ARISg, or similar safety systems. Experience with Veeva Safety Vault is an added advantage.

5. Will I collaborate with other teams?

Yes. The role requires close collaboration with Clinical Trials, Benefit‑Risk Management, Quality, Regulatory, IT, and external PV service providers.

About Vaibhav

Vaibhav is the founder of Pharma Hiring Hub, a platform focused on Pharmacovigilance, Regulatory Affairs, Clinical Research, pharma careers, interview preparation and industry updates for life science professionals and freshers across India.

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