<p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.</p> <p>Job Description</p> <p>The QC Data Reviewer I reviews data from laboratory testing within a fast-paced GMP environment to support one or more of the following areas: raw materials, in-process product, final bulk, stability, environmental monitoring, microbiology and or validation. Reviews data for compliance to SOP, protocol and GMP requirements. Works under the guidance of a supervisor but can manage time efficiently in achieving timely completion of assigned duties. Assists in review of data to support investigations.</p> <p>Responsibilities</p> <ul> <li>Reviews data from laboratory testing to support product/material release </li><li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements </li><li>Understand, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements </li><li>Accepts responsibility to complete assigned tasks as committed. Works with other to maintain a positive atmosphere to accomplish business objectives </li><li>Able to interpret and perform data review on results from complex lab tests with minimal error. </li><li>Able to guide lab analysts on mitigation of documentation errors </li><li>Participatory in continuous improvement projects, and change request </li><li>Basic leadership of small projects and change management (i.e. annual logbook reconciliation/issuance, archive process maintenance…) </li><li>Review of raw data for non-routine studies where protocols are already written and approved. </li></ul> <p>Qualifications</p> <ul> <li>BA/BS in Chemistry, Biochemistry, Medical technology, Biology, or equivalent Science degree </li><li>2+ years of related work experience </li><li>Previous experience preferred with LIMS, EMPOWER, HPLC, ELISA </li></ul> <p>Additional Information</p> <p>Applicable only to applicants</p>