Sudeep Pharma Hiring Senior Executive – Regulatory Affairs in Vadodara

Sudeep Nutrition Recruitment Notification
    • Full Time
    • Anywhere
    • 60000 USD / Year

    Embark on a rewarding journey with Sudeep Pharma Private Limited, a trailblazer in the pharmaceutical industry. Established in 1989, Sudeep Pharma has evolved into a powerhouse, specializing in excipient and mineral actives manufacturing. As we expand our horizons into specialty pharmaceutical ingredients and the Food and Nutrition Segments, we’re on the lookout for a Senior Executive in Regulatory Affairs to join our dynamic team.

    About Sudeep Pharma Private Limited

    Founded with a vision of innovation, Sudeep Pharma Private Limited has been a driving force since 1989. Specializing in excipient and mineral actives manufacturing, we have successfully ventured into specialty pharmaceutical ingredients and the Food and Nutrition Segments. Our commitment to cutting-edge solutions and advanced technologies sets us apart, making Sudeep Pharma a versatile and influential player across multiple sectors.

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    Sudeep Pharma Vacancies

    Explore exciting career opportunities at Sudeep Pharma. We are currently seeking a qualified candidate for the following position:

    • Position Title: Senior Executive – Regulatory Affairs
    • Company Name: Sudeep Pharma Private Limited
    • Salary: Competitive
    • Company Address: Nandesari, Vadodara

    Qualifications and Requirements:

    • Educational Background: B. Pharm / M. Pharm / M.sc
    • Experience: Minimum 4 years

    Job Description

    Role: Senior Executive – Regulatory Affairs

    Industry Type: Pharmaceutical

    Department: Regulatory Affairs

    Employment Type: Full-time

    Role Category: Regulatory Compliance

    Key Skills: Regulatory affairs, Documentation, Drug Master File, CEP, Tech-Pack, Dossier Preparation, Customer Communication

    Responsibilities:

    • Prepare documents for applying new certificates and updating existing ones.
    • Maintain the annual update of Drug Master File and CEP of Calcium Carbonate.
    • Prepare dossiers as per guidelines and regulatory requirements.
    • Update tech-pack and dossiers as per customer and country guidelines.
    • Coordinate with customers and provide necessary documents for product registration.
    • Issue and keep records of LOA issued to various customers.
    • Communicate with customers regarding ongoing dossier filing in various countries.

    How to Apply

    Be part of a team that truly makes a difference. Forward your resume to jobs@sudeepgroup.com or contact us at +91 90161 34609.

    To apply for this job email your details to jobs@sudeepgroup.com


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