Avantika Medex Hiring for Regulatory Affairs – Executive Position

Avantika Medex Recruitment Alert
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    • Full Time
    • Anywhere

    Explore an exciting career opportunity in Regulatory Affairs at Avantika Medex Pvt. Ltd. If you are a qualified B Pharm or M.Pharm graduate with 4 to 6 years of hands-on experience in international regulatory submissions, this position at the Head Office (HO) could be your next big move.

    Avantika Medex, committed to advancing healthcare through quality pharmaceutical products, is expanding its regulatory team. This role is an excellent opportunity to work on dossiers, re-registrations, variations, and regulatory communications across multiple global markets including Uzbekistan, Kazakhstan, and Azerbaijan.

    Job Overview

    Position Title: Executive – Regulatory Affairs

    Department: Regulatory Affairs

    Location: Avantika Medex Head Office

    Qualification Required: B Pharm / M.Pharm

    Experience Required: 4–6 Years

    Industry: Pharmaceuticals – Solid Dosage, Injectables, Topicals

    Key Responsibilities

    As a Regulatory Affairs Executive at Avantika Medex, you will:

    • Prepare and compile dossiers in CTD, ACTD, and country-specific formats
    • Handle re-registration, renewal, and variation applications across different regulatory authorities
    • Coordinate responses to regulatory queries from global agencies
    • Manage Drug Master File (DMF) activities and associated documentation
    • Conduct detailed artwork reviews – including carton, foil, label, shipper, and inserts
    • Create pack inserts following specific country guidelines
    • Collect registration-related samples and documents from F&D, QA, QC, and Stores

    Review technical documents such as:

    • Pharmaceutical Development Reports
    • Process Validation Protocols & Reports
    • Specifications/MOA for excipients and packaging materials
    • Stability protocols, MFRs, BMRs, BPRs
    • Clinical and non-clinical literature review
    • BE Study data and Analytical Method Validation (AMV)

    Region-Specific Regulatory Experience

    Candidates with exposure to regulatory submissions for the following countries will be preferred:

    Uzbekistan

    Kazakhstan

    Azerbaijan

    Dosage Forms You’ll Work With

    Experience with the following dosage forms will be advantageous:

    • Tablets
    • Capsules
    • Sachets
    • Ointments
    • Injections

    📍 Job Location

    Workplace: Avantika Medex Pvt. Ltd.

    Location: Head Office

    Contact Email: hr@avantikamedex.com

    Phone Contact: +91 96248 49118

    How to Apply

    Qualified and interested candidates can send their CVs directly to hr@avantikamedex.com.

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