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Drug Master File Role

3-6 years
Not Disclosed
10 Nov. 11, 2025
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

Primary Responsibility

The Drug Master File (DMF) Specialist is responsible for the preparation, submission, and maintenance of DMFs in compliance with global regulatory requirements. The role involves managing technical documentation, ensuring data integrity, and supporting submissions such as Type V DMFs, INDs, NDAs, and ANDAs in eCTD format.


Key Responsibilities

Regulatory Submissions

  • Prepare, review, and submit Type V DMFs to the U.S. FDA, ensuring compliance with all applicable regulations and guidance documents.

  • Manage pre-approval processes for Type V submissions and coordinate with regulatory authorities as needed.

  • Support and contribute to submissions related to IND (Investigational New Drug), NDA (New Drug Application), and ANDA (Abbreviated New Drug Application) filings.

  • Ensure all submissions meet eCTD (Electronic Common Technical Document) formatting and structure requirements.

Technical Documentation

  • Compile, review, and maintain proprietary technical content, including:

    • Validation reports

    • Manufacturing process details

    • Product and material specifications

    • Analytical method validations and testing methodologies

  • Provide detailed descriptions of manufacturing facilities, including specialized or sterile processing areas when required.

  • Ensure all documentation is accurate, complete, and compliant with regulatory expectations.

Compliance and Coordination

  • Liaise with internal departments such as Quality, R&D, and Manufacturing to gather required technical information.

  • Maintain up-to-date knowledge of regulatory guidelines and best practices related to DMF submissions.

  • Support audits and regulatory inspections by providing relevant documentation and technical input.


Mandatory Requirements

Candidates must possess the following:

  • Hands-on experience with Type V DMF submissions and prior FDA pre-approval interaction.

  • Strong working knowledge of IND, NDA, and ANDA regulatory frameworks.

  • Proven experience handling technical proprietary data and preparing complex regulatory dossiers.

  • Proficiency in compiling and submitting applications in eCTD format.


Qualifications and Skills

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

  • 3–6 years of experience in Regulatory Affairs with specific expertise in DMF management.

  • Excellent understanding of FDA guidelines, ICH standards, and GMP documentation.

  • Strong attention to detail and ability to work under tight regulatory timelines.

  • Effective communication and collaboration skills across cross-functional teams.


Work Environment

  • Location: Hyderabad / Office-based 

  • Fast-paced, collaborative regulatory environment with opportunities for professional development.