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Senior Executive, Regulatory Affairs - Injectable

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 Executive – Regulatory Affairs (US Injectable Products)

Location: Ahmedabad, Gujarat, India
Job Type: Full-Time | Regulatory Affairs
Job ID: 6242
Application Deadline: 30/01/2026

About Amneal

Amneal Pharmaceuticals is a global leader in pharmaceutical innovation, delivering high-quality medicines across multiple therapeutic areas. The company emphasizes regulatory excellence, compliance, and patient safety, providing opportunities for professionals to develop and lead complex regulatory submissions in a dynamic global environment.

Role Overview

Amneal is seeking a Senior Executive – Regulatory Affairs with expertise in US sterile products, including injectables, ophthalmic, otic, and IV bags. The role focuses on ANDA preparation, submission, and review, ensuring regulatory compliance and timely approvals with minimal deficiencies.

Key Responsibilities

  • Compile, prepare, review, and submit ANDA submissions and amendments to the FDA, aiming to achieve fast-track approvals.

  • Maintain full awareness of all regulatory activities for assigned projects, ensuring deadlines and performance standards are met.

  • Review and prepare documents that meet FDA requirements, minimizing queries or reject-to-file (RTR) scenarios.

  • Evaluate change controls and determine appropriate filing categories; escalate critical issues to management when necessary.

  • Submit post-approval supplements, including CBE, CBE-30, and PAS, ensuring accuracy and compliance.

  • Collaborate closely with cross-functional teams during product development, R&D, ANDA execution, and stability phases.

  • Prepare controlled correspondences and pre-submission meeting packages (Pre-ANDA, Pre-IND, Pre-NDA) for FDA.

  • Assess FDA deficiency letters, perform gap analysis, and define response strategies in consultation with management.

  • Evaluate final compositions for IIG and proportionality criteria, developing regulatory strategies to avoid filing issues.

  • Review API DMFs, share review comments with the purchase department, and follow up for compliance.

  • Maintain systematic archival of submissions and ensure ongoing regulatory compliance.

  • Stay updated on FDA, ICH, and 21 CFR regulations, providing regulatory guidance to project teams.

Required Skills

  • Regulatory Submission & Dossier Filing | Advanced

  • Regulatory Guidelines Knowledge | Advanced

  • CMC Documentation | Advanced

  • Regulatory Strategy Development | Advanced

  • Health Authority Query Response | Advanced

  • Product Lifecycle Management | Advanced

  • Change Control & Regulatory Impact Assessment | Advanced

  • Cross-Functional Communication | Intermediate

  • Problem Solving & Risk Mitigation | Intermediate

  • Change Management & Documentation | Intermediate

Qualifications

  • Master’s Degree (M. Pharm) in Pharmacy or Life Sciences.

  • Strong experience with US ANDAs, INDs, NDAs, and FDA correspondence.

  • Expertise in sterile dosage forms, including injectables, ophthalmic, otic, or IV bags, using aseptic or terminal sterilization.

  • Excellent technical writing, analytical, and problem-solving skills.

  • Strong time management, organization, and multi-tasking abilities in fast-paced environments.

  • Ability to work independently, interface with global teams, and maintain high accuracy under deadlines.

  • Proficient in MS Word, Excel, PowerPoint, Outlook, and Adobe Professional.

Why Join Amneal

  • Take ownership of critical regulatory submissions for US sterile products.

  • Collaborate with cross-functional and global teams in a fast-paced, professional environment.

  • Implement regulatory strategies and mentor junior team members.

  • Grow your career in a global pharmaceutical organization that values compliance, innovation, and professional development.

Location: Shapath-V, Near Hotel Crown Plaza, Ahmedabad, Gujarat, 380015, India
Job Schedule: Full-Time
Category: Regulatory Affairs | Master’s Degree