CORONA Remedies Job Openings for Regulatory Affairs – AM Position

Corona remedies pvt ltd recruitment notification
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    • Full Time
    • Anywhere

    CORONA Remedies, one of India’s fastest-growing pharmaceutical companies, is currently hiring for the Assistant Manager – Regulatory Affairs position at its Ahmedabad, Gujarat location. This is an excellent opportunity for qualified candidates with a strong background in EU regulatory submissions to join a leading organization making a mark in women’s healthcare and specialty pharma.

    About CORONA Remedies

    CORONA Remedies is a ₹1200+ crore pharmaceutical company growing at an impressive CAGR of 18%. With 11 dynamic divisions and over 4500 employees, CORONA has positioned itself as a market leader, especially in Women’s Healthcare. The company has successfully acquired 7 renowned brands from multinational companies (MNCs) and continues to expand its global footprint.

    With innovation at its core and a commitment to delivering high-quality healthcare, CORONA provides a nurturing and performance-driven environment for professionals to thrive.

    Position Details: Regulatory Affairs – Assistant Manager (Europe Market)

    Location: Ahmedabad, Gujarat

    Qualification: B Pharm / M.Pharm

    Experience: 7 to 10 years in Regulatory Affairs (EU Market)

    Department: Regulatory Affairs

    Role: Assistant Manager – Regulatory Affairs (EU Submissions)

    Key Responsibilities

    As an Assistant Manager – Regulatory Affairs for the EU Market, you will:

    • Lead a team of RA professionals and manage day-to-day regulatory operations.
    • Handle end-to-end dossier preparation and submission for European countries.
    • Conduct literature searches during the development phase of drug products.
    • Liaise with internal departments and clients to ensure timely and complete dossier submissions.
    • Compile EU eCTD dossiers and manage regulatory pathways for the European market.
    • Maintain regulatory databases, manage product life cycles, and review commercial documentation.
    • Ensure compliance with European labelling requirements and documentation standards.

    Desired Skills and Expertise

    • To succeed in this role, the candidate should possess:
    • Proven experience in the EU market regulatory processes.
    • Strong capabilities in dossier compilation, review, and submission as per EU standards.
    • Excellent communication skills to coordinate with cross-functional teams and international clients.
    • A proactive attitude towards compliance, accuracy, and timely documentation.

    How to Apply?

    Interested and qualified candidates can send their updated resumes to:

    👉 Email: yashb@coronaremedies.com

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