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    Executive Regulatory Affairs Jobs at Sun Pharma | M Pharm Graduates Apply Now

    Executive Regulatory Affairs Jobs at Sun Pharma Baroda

    Sun Pharmaceutical Industries Ltd is hiring an Executive – Regulatory Affairs for its R&D Regulatory Affairs division in Baroda. This Executive Job role is ideal for M. Pharm professionals with 3–6 years of regulatory experience, offering hands-on exposure to global dossier submissions, lifecycle management, and regulatory coordination across the US, EU, Canada, Australia, and Israel markets. Graduates seeking M Pharma jobs or Pharma jobs can apply now.

    • Job Title: Executive – Regulatory Affairs
    • Location: Baroda (Tandalja – R&D)

    About the Company

    Sun Pharmaceutical Industries Ltd is India’s largest pharmaceutical company and a global leader in specialty generics. At Sun Pharma, employees are encouraged to “Create Your Own Sunshine” by growing continuously, taking ownership, and thriving together in a collaborative, innovation-driven environment. This Executive Job role plays a significant role in the company.

    Educational Requirements

    • M. Pharm

    Relevant Work Experience

    • 3–6 years of experience in Regulatory Affairs
    • Hands-on experience with global regulatory submissions

    Key Responsibilities

    • Compile and review regulatory dossiers for the US, EU, Australia, Canada, and Israel markets
    • Handle submissions for solid oral and non-oral dosage forms
    • Review query responses prepared by regulatory associates
    • Manage end-to-end dossier submission activities for assigned markets
    • Ensure adherence to submission and response timelines
    • Review documents received from stakeholders for:

      • Dossier compilation

      • Query responses

      • Lifecycle management

    • Allocate projects to regulatory associates and manage submission teams
    • Handle lifecycle management activities for the US, EU, Canada, and Israel markets
    • Act as a single point of contact for regulatory activities for the Israel and Palestine markets

    Skills Required

    • Strong knowledge of global regulatory requirements
    • Experience in CTD / eCTD dossier compilation
    • Regulatory submission and lifecycle management expertise
    • Team coordination and project management skills
    • Ability to meet strict regulatory timelines
    • Strong communication and stakeholder management skills

    Behavioral & Professional Competencies

    • Self-driven with an ownership mindset
    • Collaborative team player
    • Strong attention to detail
    • Ability to manage multiple regulatory projects simultaneously
    • Graduates seeking M Pharma jobs or Pharma jobs can apply now.

    CLICK HERE TO APPLY ONLINE

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