Leben Life Sciences Walk-In for Regulatory Affairs – Trainee Positions

Leben Life Sciences recruitment notification
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    • Full Time
    • Anywhere
    • Applications have closed

    Leben Life Sciences Pvt. Ltd., an established pharmaceutical formulation company with over four decades of experience, is inviting applications for Trainee positions in the Regulatory Affairs department. The walk-in interview will be held at their EU-GMP approved manufacturing site located in Akola, Maharashtra.

    This is an excellent opportunity for aspiring pharma professionals to join a company known for its global quality standards and responsible healthcare practices.

    About Leben Life Sciences Pvt. Ltd.

    Leben Life Sciences (LLS) is a well-reputed pharmaceutical company known for manufacturing high-quality formulations that meet stringent global standards. Headquartered in Maharashtra, LLS has been a consistent supplier to both domestic and international markets, with a focus on innovation, quality, and compliance.

    With its EU-GMP-certified facility, LLS provides a professional environment that promotes growth and hands-on experience in highly regulated pharmaceutical operations.

    Job Overview

    Position: Regulatory Affairs – Trainee

    Department: Regulatory Affairs

    Qualification Required: M.Pharm (Master of Pharmacy)

    Experience: Freshers (0 Years)

    Job Location: Akola, Maharashtra

    Employment Type: Full-time, On-site

    This position is ideal for fresh M.Pharm graduates who are enthusiastic about starting a career in the regulatory field within the pharmaceutical industry.

    Key Responsibilities

    As a Regulatory Affairs Trainee, you will:

    • Assist in the preparation and submission of regulatory documents for domestic and international markets.
    • Maintain and update regulatory files and databases.
    • Ensure compliance with current regulations and guidelines from various global health authorities.
    • Coordinate with the Quality Assurance, Quality Control, and Production teams to gather and compile regulatory data.
    • Learn the intricacies of dossier compilation and regulatory strategy under the guidance of experienced professionals.

    Skills & Attributes Required

    • Strong academic background in pharmaceutical sciences.
    • Good communication and documentation skills.
    • Willingness to learn and adapt in a fast-paced regulatory environment.
    • Basic knowledge of regulatory guidelines (like ICH, WHO, EU) is an advantage.

    Walk-In Interview Details

    Interview Date: Wednesday, 07th May 2025

    Reporting Time: Between 09:30 AM and 10:30 AM

    Venue:

    Leben Life Sciences Pvt. Ltd.

    Plot No. C-20/1 & C-21, Phase III, MIDC,

    Akola, Shivar, Maharashtra – 444104

    Documents to Carry:

    • Updated resume (hard copy)
    • Color passport-size photograph
    • Photocopies of educational qualifications


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