More

    Sun Pharma Hiring Pharma Graduates | Executive -Analytical Development Role

    Sun Pharma Hiring for Executive -Analytical Development Role – Apply Now

    Looking for a Regulatory Affairs Job in the pharmaceutical industry? Sun Pharma Careers is hiring an Executive – Analytical Development for its R&D facility in Vadodara. This opportunity is suitable for M.Pharm and M.Sc professionals. The role focuses on ensuring cGMP compliance, analytical testing, documentation, and supporting product development processes.

    • Job Title: Executive – Analytical Development
    • Location: Tandalja – R&D, Vadodara

    About The Company

    Sun Pharmaceutical Industries Ltd is a leading global pharmaceutical company based in India, specializing in the development and manufacturing of a wide range of pharmaceutical products. With a commitment to quality and innovation, Sun Pharma operates in the regulatory affairs space, ensuring compliance with global standards. The company is dedicated to improving patient outcomes through its extensive portfolio of medicines.

    Job Description

    The regulatory affairs job at Sun Pharmaceutical involves working in compliance with current Good Manufacturing Practices (cGMP) and ensuring adherence to guidelines and standard operating procedures (SOPs). The selected candidate will engage in method development and validation studies for various finished products, while also performing routine and stability studies.

    Key Responsibilities

    • Ensure compliance with cGMP and current guidelines.
    • Complete necessary training before executing assigned tasks and maintain training files.
    • Adhere to safety protocols as per laboratory procedures.
    • Report any incidents to the manager for corrective action.
    • Conduct method development and validation studies for finished products.
    • Perform routine and stability studies on various products.
    • Follow Quality Management Document procedures.
    • Prepare study protocols and reports, and maintain instruments as per SOPs.

    Eligibility Criteria

    • Education: M.Pharm / M.Sc
    • Experience: 2-5 years of relevant experience in handling non-oral dosage forms.

    Required Skills

    • Knowledge of analytical method development and validation.
    • Understanding of cGMP and regulatory guidelines.
    • Experience with stability studies.
    • Knowledge of laboratory instruments and calibration procedures.
    • Ability to prepare technical protocols and reports.
    • Strong documentation and quality compliance skills.

    Why Join Sun Pharmaceutical Industries Ltd?

    Sun Pharma Careers provides opportunities to work with one of the world’s leading pharmaceutical companies. Employees get exposure to innovative research, professional development programs, collaborative teams, and a culture focused on continuous growth. This Regulatory Affairs Job is an excellent opportunity for pharma professionals looking to advance their career in analytical development and pharmaceutical R&D.

    CLICK HERE TO APPLY ONLINE

    Pharmanika is a career information portal. Please verify all details from the original notification before applying.

    Related Articles

    LEAVE A REPLY

    Please enter your comment!
    Please enter your name here

    Stay Connected

    42,522FansLike
    21,523FollowersFollow
    32,000SubscribersSubscribe
    - Advertisement -

    Latest Articles