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Senior Officer, Regulatory Publishing

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

Senior Officer, Regulatory Publishing – US Market

Location: Ahmedabad, Gujarat, India
Job Type: Full-Time | Regulatory Affairs
Job ID: 6895
Application Deadline: 30/01/2026

About Amneal

Amneal Pharmaceuticals is a global, patient-focused pharmaceutical company committed to delivering high-quality medicines across multiple therapeutic areas. We emphasize an inclusive, collaborative, and growth-oriented work culture, empowering employees to excel in regulatory excellence and contribute to life-saving therapies.

Role Overview

Amneal is seeking a Senior Officer – Regulatory Publishing to manage CTD/e-CTD submission preparation and publishing for the US market. The role ensures high-quality document compilation, lifecycle management, and compliance with regulatory standards while supporting cross-functional regulatory teams.

Key Responsibilities

  • Process PDF documents, conduct quality control (QC) checks, and compile CTD/e-CTD modules for US regulatory submissions.

  • Perform submission-level publishing for ANDAs, NDAs, and other US regulatory dossiers.

  • Manage archival and lifecycle management of CTD/e-CTD submissions.

  • Prioritize tasks effectively, identifying critical items and discussing issues with Team Lead or Group Lead.

  • Support document version control, organization, and standardization to maintain regulatory compliance.

  • Perform additional duties as assigned by Team Lead or Group Lead to support the Regulatory Affairs team.

Qualifications & Experience

  • B. Pharm / M. Pharm or equivalent degree.

  • Strong understanding of US regulatory submission requirements, including CTD/e-CTD structures.

  • Experience in regulatory publishing, QC, and document management.

  • Excellent attention to detail, organizational skills, and ability to meet deadlines.

  • Strong communication skills and ability to collaborate with cross-functional teams.

Why Join Amneal

  • Gain hands-on experience in US regulatory publishing for complex submissions.

  • Collaborate with global regulatory and cross-functional teams.

  • Work in a growth-oriented, inclusive environment with opportunities to advance your regulatory career.

Location: Shapath-V, Near Hotel Crown Plaza, Ahmedabad, Gujarat, 380015, India
Job Schedule: Full-Time
Category: Regulatory Affairs | B. Pharm / M. Pharm