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Executive - Regulatory Affairs

Sun Pharma
2-5 years
₹6–10 LPA
Baroda, India
15 July 7, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Executive – Regulatory Affairs (US Group)

Company: Sun Pharmaceutical Industries Ltd
Location: Baroda (Tandalja – R&D)
Department: R&D – Regulatory Affairs (US Group)
Employment Type: Full-Time

Experience: 2–5 years of relevant experience in Regulatory Affairs with exposure to USFDA submissions, CTD/eCTD dossier preparation, regulatory documentation, and lifecycle management activities.
Salary Package: ₹6–10 LPA (Approx., based on current market standards; final compensation depends on candidate experience, regulatory expertise, and skills.)


Role Overview

The Executive – Regulatory Affairs (US Group) is responsible for supporting global regulatory activities, including preparation and submission of regulatory dossiers, regulatory strategy execution, compliance activities, and coordination with cross-functional teams to ensure timely approvals and successful product registrations.


Key Responsibilities

Regulatory Submission Management

  • Prepare, compile, and submit regulatory dossiers in CTD/eCTD formats.

  • Support regulatory submissions for:

    • New Drug Applications (NDAs)

    • Abbreviated New Drug Applications (ANDAs)

    • Marketing Authorization Applications (MAAs)

    • Post-approval regulatory changes

  • Ensure regulatory documents comply with applicable guidelines and submission requirements.

  • Track submission timelines, approvals, and regulatory commitments.


Regulatory Strategy & Compliance

  • Support development of regulatory strategies for new products and markets.

  • Interpret and apply regulatory requirements for US, EU, India, and other applicable regions.

  • Maintain strong understanding of:

    • USFDA guidelines

    • ICH guidelines

    • Regional regulatory requirements

  • Support lifecycle management activities and regulatory updates.


Regulatory Authority Communication

  • Prepare responses to regulatory authority queries, deficiency letters, and requests for additional information.

  • Coordinate with internal teams to collect required data and documentation.

  • Ensure timely submission of regulatory responses.


Cross-Functional Collaboration

  • Collaborate with:

    • R&D teams

    • Manufacturing teams

    • CDMO partners

    • Quality Assurance

    • Quality Control

    • Other business functions

  • Coordinate collection, review, and compilation of regulatory documents.

  • Support regulatory project timelines and deliverables.


Regulatory Documentation & Tracking

  • Maintain regulatory databases and submission trackers.

  • Monitor regulatory milestones, approvals, and commitments.

  • Ensure accuracy, completeness, and compliance of regulatory documentation.

  • Support continuous improvement initiatives within regulatory operations.


Educational Qualification

  • Master’s Degree in Pharmacy (M.Pharm) is required.

  • Specialization in Regulatory Affairs, Pharmaceutics, Pharmaceutical Chemistry, or related fields is preferred.


Required Experience

  • 2–5 years of experience in Regulatory Affairs within the pharmaceutical industry.

  • Experience with US Regulatory Affairs is preferred.

  • Hands-on experience in CTD/eCTD dossier compilation and submission activities.

  • Knowledge of regulatory submission processes and post-approval changes.


Technical Skills

  • Strong knowledge of:

    • USFDA regulations

    • ICH guidelines

    • CTD/eCTD submission formats

    • Regulatory documentation requirements

  • Experience with regulatory tracking systems and databases.

  • Good working knowledge of Microsoft Office applications.


Key Competencies

  • Strong regulatory documentation and review skills.

  • Excellent attention to detail and compliance focus.

  • Good analytical and problem-solving abilities.

  • Strong written and verbal communication skills.

  • Ability to coordinate effectively with cross-functional teams.

  • Strong organizational and time management skills.

  • Ability to manage multiple regulatory projects and timelines.