• Analytical Method Validation Specialist

    Astrix Technology (Athens, GA)


    Analytical Method Validation Specialist

     

    Laboratory

     

    Athens, GA, US

    Pay Rate Low: 26 | Pay Rate High: 28

    + Added - 06/10/2025

     

    Apply for Job

     

    Astrix is seeking an **Analytical Method Validation Specialist** for a **1-year contract** on **first shift** . In this role, you’ll play a key part in developing and validating analytical methods that ensure product quality and regulatory compliance. Work alongside talented scientists in a collaborative, state-of-the-art lab environment while supporting critical projects that impact global animal health and vaccine innovation.

     

    **Pay** : $26-$28

    **Schedule** : M-F 9a-5p

    **Type of Job** : 1 year contract

    **Location** : Athens, GA

     

    At this time, Astrix cannot transfer nor sponsor a work Visa for this position.

     

    Relocation assistance is not available for this position.

    Benefits Offered:

    Medical/dental coverage!

     

    Weekly pay!

     

    401k and PTO after 6 months!

    Analytical Method Validation Specialist** **Daily Tasks: What you will do:

    Develop and author analytical method validation protocols in alignment with FDA, EU, and USDA regulations and internal guidelines.

     

    Oversee validation projects, coordinating laboratory testing and data collection activities.

     

    Analyze and summarize validation test results; prepare comprehensive validation reports for regulatory submission.

     

    Partner with area managers to manage project timelines, regulatory documentation, and submission packages for USDA review.

     

    Support quality and compliance initiatives, including change controls and impact assessments as needed.

    Analytical Method Validation Specialist** **Qualifications/Requirements:

    Bachelor’s degree in Biology, Microbiology, Chemistry, Biochemistry, or related field.

     

    Hands-on experience with analytical method validation and regulatory standards (USDA, ICH, FDA).

     

    Working knowledge of GLP/GMP and laboratory practices.

     

    Strong technical writing and communication skills.

     

    Preferred: experience with IFA testing, change controls, and impact assessments.

     

    We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

    INDBH

    \#LI-DNP

    We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.