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Manager – Pharmacovigilance Operations | Icsr Operations Location: Ahmedabad, Gujarat, India Employment Type: Full-Time Category: Pharmacovigilance | Drug Safety | Icsr Operations Experience Required

Amneal
Amneal
8-12 years
preferred by company
10 Jan. 2, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Manager – Pharmacovigilance Operations | ICSR Operations

Location: Ahmedabad, Gujarat, India
Employment Type: Full-Time
Category: Pharmacovigilance | Drug Safety | ICSR Operations
Experience Required: 8–12 years (Minimum 5 years in a people management role)
Education Required: Doctor of Pharmacy (Pharm.D)
Industry: Pharmaceuticals | Global Drug Safety
Job Type: Onsite / Hybrid (as applicable)
Job Status: Hot & Trending Role


Job Overview

Amneal is seeking an experienced Manager – Pharmacovigilance Operations (ICSR Operations) to lead global case processing activities and ensure end-to-end compliance with international pharmacovigilance regulations. This leadership role is ideal for seasoned pharmacovigilance professionals with deep expertise in ICSR operations, audit readiness, regulatory compliance, and people management within a global drug safety environment.


Key Responsibilities

  • Lead, mentor, and develop a global ICSR case processing team, fostering a high-performance and compliance-driven culture.

  • Oversee day-to-day pharmacovigilance operations, ensuring timely and accurate processing of adverse event reports.

  • Manage intake, triage, and medical assessment of ICSRs, including seriousness, causality, and expectedness evaluations.

  • Conduct regular performance reviews, provide constructive feedback, and support professional development of team members.

  • Ensure full compliance with ICH, FDA, EMA, and global regulatory requirements.

  • Collaborate with cross-functional stakeholders to resolve complex safety cases and support benefit–risk assessments.

  • Develop, implement, and monitor Corrective and Preventive Action (CAPA) plans in response to audits, inspections, deviations, and findings.

  • Lead internal and external audits and regulatory inspections, ensuring inspection readiness at all times.

  • Monitor key performance indicators (KPIs) and prepare operational and compliance reports for senior management.

  • Drive process optimization initiatives and implement best practices to improve efficiency, quality, and compliance.

  • Develop and deliver training programs on pharmacovigilance procedures, regulatory standards, and ICSR best practices.

  • Support the creation, review, and maintenance of SOPs, work instructions, templates, and training materials.

  • Provide inputs for medical information responses related to safety inquiries from regulatory authorities and healthcare professionals (MIRF).

  • Support pharmacovigilance-related projects and ad hoc initiatives as assigned by senior leadership.


Required Skills & Expertise

  • Advanced knowledge of Pharmacovigilance Regulations (ICH, FDA, EMA).

  • Expert-level experience in ICSR Processing and Case Management.

  • Strong medical assessment and benefit–risk evaluation capabilities.

  • Advanced proficiency in MedDRA and WHO Drug coding standards.

  • Hands-on expertise with safety databases such as Argus, ArisG, and Veeva Vault Safety.

  • Strong understanding of global reporting requirements and regulatory timelines.

  • Expertise in data integrity principles (ALCOA+) and quality management systems.

  • Advanced experience in CAPA management, root cause analysis, and FMEA.

  • Proven capability in audit and inspection readiness, deviation management, and compliance monitoring.

  • Strong leadership, stakeholder management, and operational excellence skills.


Qualifications & Experience

  • Doctor of Pharmacy (Pharm.D) is mandatory.

  • Minimum 8 years of experience in pharmacovigilance operations.

  • At least 5 years of experience in a managerial or team leadership role within ICSR or drug safety operations.

  • Demonstrated experience managing global pharmacovigilance teams and regulatory inspections.


About the Company

Amneal is an equal opportunity employer committed to fostering a diverse, inclusive, and respectful workplace. Employment decisions are based on merit, qualifications, and business needs without discrimination of any kind.


Why Join Amneal

  • Opportunity to lead large-scale global pharmacovigilance operations.

  • Work in a compliance-driven, quality-focused pharmaceutical environment.

  • Career growth through leadership, innovation, and continuous improvement.

  • Collaborative culture that values expertise, integrity, and accountability.