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    M Pharm Job Alert: Apply for a Data Review Specialist Role at Eurofins, Bangalore

    M Pharm Job at Eurofins | Apply Now

    M Pharm job opportunities are expanding rapidly in the pharmaceutical and life sciences sector, and this exciting opening at Eurofins Scientific is a perfect example. If you’re looking for Eurofins careers or exploring jobs in Bangalore, this Data Review Specialist role offers a great chance to work in a global organization known for its excellence in analytical testing and regulatory compliance.

    • Job Position: Data Review Specialist – Extractables and Leachable
    • Location: Bengaluru, Karnataka, India

    About the Company

    M Pharm job seekers looking into Eurofins careers will find Eurofins Scientific to be a global leader in analytical testing services. The company supports industries such as pharmaceuticals, food, environmental, and cosmetics by ensuring safety, authenticity, and accuracy. With more than 900 laboratories worldwide, Eurofins is highly recognized for its expertise in genomics, clinical studies, and specialized diagnostics, making it a top choice for jobs in Bangalore.

    Job Description

    M Pharm job role focused on ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations. This role is ideal for candidates exploring Eurofins careers with strong analytical and regulatory knowledge.

    Qualifications

    M Pharm job eligibility criteria include:

    Education/Experience

    • Master’s degree in a pharma / science-related field with 2-6 years of experience in Bio/Pharmaceutical or Medical Device Analysis testing
    • Knowledge of regulatory requirements

    Technical Skills

    • Experience with chromatography and mass spectrometry techniques (HPLC, GC, LC/MS, GC/MS)
    • Knowledge of USP/EP compendia
    • Familiarity with laboratory software such as Waters Empower, LIMS, Electronic Notebook

    Key Responsibilities

    M Pharm job responsibilities in this role include:

    • Applies GMP/GLP in all areas of responsibility, as appropriate
    • Demonstrate and promote the company vision
    • Regular attendance and punctuality
    • Read and understand analytical procedures
    • Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs
    • Gain a technical understanding of the techniques in which review is being performed
    • Use MS Windows applications such as EXCEL, Word, Access, Outlook email
    • Conducts all activities in a safe and efficient manner
    • Performs other duties as assigned

    APPLY ONLINE HERE

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