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Alvotech Hiring for PV Associate Role: PV Jobs 2026

ByPharma Hiring Hub

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.

Alvotech PV associate role

Job 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

Key Responsibilities – PV Associate

  • Clinical Safety & PV Operations: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.
  • Safety Systems & Lifecycle Management: Support pharmacovigilance safety systems setup, configuration, validation, and ongoing system lifecycle management activities.
  • Global PV Process Compliance: Contribute to the maintenance and optimization of global pharmacovigilance processes, ensuring compliance with international regulations such as FDA, EMA, and ICH guidelines.
  • Cross‑Functional Collaboration: 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).
  • External Partner Engagement: Coordinate with external PV service providers and business partners to support pharmacovigilance activities and compliance expectations.
  • Training & Knowledge Sharing: Deliver pharmacovigilance training sessions on PV processes and standards to internal teams and external stakeholders as required.
  • Audit & Inspection Support: Support and participate in audits and regulatory inspections related to safety data management and pharmacovigilance system compliance.

Required Skills & Qualifications

  • Educational Background: Master’s degree in Pharmaceutical Sciences or related fields such as Medicine, Pharmacy, or Life Sciences.
  • Experience: 2+ years of experience in Pharmacovigilance / Drug Safety, with hands‑on involvement in safety data management, including clinical trial safety and post‑marketing PV activities.
  • Safety Systems Expertise
    • Practical experience working with pharmacovigilance safety systems such as Argus, ARISg, or similar platforms.
    • Prior exposure to Veeva Safety Vault is a strong advantage.
  • Global Exposure: Proven experience supporting global products and international clinical trials.
  • Product Knowledge: Experience with biologic and combination products is preferred.
  • Regulatory Knowledge: Strong understanding of PV processes, directives, and international regulations, including 21 CFR, ICH, GVP, GCP, and CIOMS guidelines.
  • Professional Skills
    • Strong self‑organization, time‑management, and interpersonal skills.
    • Excellent communication abilities with a positive, results‑oriented approach.
  • Work Style & Collaboration:Ability to work independently, plan and deliver tasks efficiently, and collaborate comfortably within a multicultural global team.
  • Travel Requirement:Willingness to travel internationally as required.

Why Join Alvotech?

  • Global Biopharmaceutical Environment
  • Join a rapidly growing global biopharmaceutical company dedicated to biosimilar development and manufacturing, with strong presence in international markets.
  • Strong Pharmacovigilance Exposure
  • Work on end‑to‑end clinical and post‑marketing pharmacovigilance activities, including safety data management, benefit‑risk evaluation, and global regulatory compliance.
  • Integrated Clinical & Medical Research (iCMR)
  • Be part of Alvotech’s iCMR expansion, supporting safety operations across the clinical data lifecycle within a globally regulated R&D environment.
  • Advanced Safety Systems & Global Compliance
  • Gain hands‑on experience with global PV systems, international safety regulations (FDA, EMA, ICH), and audit‑ready pharmacovigilance operations.
  • Cross‑Functional Collaboration
  • Collaborate with teams across Clinical Trials, Benefit‑Risk Management, Quality, Regulatory, IT, and external PV partners, fostering broad operational exposure.

How to Apply

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

Apply Here

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 IQVIA 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.

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