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Deputy Manager, Pharmacovigilance Safety System (Argus) Administrator

Amneal
Amneal
0-2 years
Not Disclosed
10 Jan. 1, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Deputy Manager, Pharmacovigilance Safety System (ARGUS) Administrator

Location: Ahmedabad, Gujarat, India
Job Type: Full-Time | Pharmacovigilance & Drug Safety
Job ID: 6995
Application Deadline: 06/01/2026

About Amneal

Amneal Pharmaceuticals is a global, patient-focused pharmaceutical company committed to delivering high-quality, safe, and affordable medicines. We foster a workplace culture that emphasizes diversity, inclusion, and continuous professional growth, empowering employees to excel while advancing patient safety.

Role Overview

Amneal is seeking a Deputy Manager – Pharmacovigilance Safety System (ARGUS) Administrator to manage and optimize the company’s ARGUS safety database system. The ideal candidate will ensure compliance, efficiency, and accuracy in safety case processing while supporting global pharmacovigilance operations.

Key Responsibilities

  • Configure and maintain the ARGUS safety system, including workflow setup, user management, and system validations.

  • Monitor system compliance with pharmacovigilance regulations (ICH, GVP) and internal SOPs.

  • Generate reports, dashboards, and analytics to support safety monitoring and risk assessment.

  • Provide training and support to pharmacovigilance teams on ARGUS functionalities.

  • Assist in troubleshooting technical and operational issues within the safety system.

  • Maintain documentation related to system administration, validations, and SOPs.

  • Collaborate with cross-functional teams to ensure accurate and timely data entry and PV operations.

Qualifications & Experience

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related field.

  • Strong understanding of pharmacovigilance regulations (ICH, GVP) and PV processes.

  • Experience in database administration, workflow management, and system validation.

  • Analytical skills with attention to detail, problem-solving, and effective communication.

  • Ability to train, support, and guide PV staff in system-related tasks.

  • Knowledge of safety signal management, ADR reporting, and regulatory compliance is a plus.

Why Join Amneal

  • Contribute to global pharmacovigilance operations and patient safety.

  • Work in a collaborative, growth-oriented environment with learning opportunities.

  • Be part of a diverse and inclusive workplace that values innovation and professional development.

Location: 2nd Floor, W-1, Behind Old Big Bazaar, Ahmedabad, Gujarat, 380058, India
Job Schedule: Full-time
Category: Pharmacovigilance & Drug Safety | Master’s Degree Preferred