About this role
Conduct chemical and physical laboratory tests and analyze excipients, cleaning samples, raw materials, intermediates, and final products including protocol testing in a timely manner to ensure compliance with standards and production targets.Recognize and report to immediate supervisor any issues or deviations from accepted standards.Provide status updates on own activities and productivity challenges according to defined proceduresMaintain data integrity and ensure compliance with FDA, GLP, QSR and cGMP regulations, as well as with company SOPs and specifications.Complete and conform to all training requirements for job role, including company-required and job role-specific training.Observe all safety and compliance procedures and actively highlighting any safety concerns to help drive the reduction of accidents or near misses.Conforming to the safety culture on site on Zero, Believe it, Achieve it.Participate in the 6S activities within the QC Laboratory.Positively contribute to departmental goals and programs such as Right First Time A third level qualification in Chemistry or related Science, preferably a Bachelor’s DegreeGraduate with a third level qualification in Chemistry or related Science.Demonstrate knowledge of cGMP requirements and practices including knowledge of the USP and FDAGuidance Documents relating to the pharmaceutical Quality Control Laboratory.Demonstrate knowledge of common analytical instrumentation e.g. HPLC, Dissolution, GC, FTIR, Electro Chemistry (DME), UV/Vis and other USP instrumental and Wet chemistry technologies used in pharmaceutical Quality Control Laboratory. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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