About AbbVie
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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.
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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.
Responsibilities
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 procedures; Maintain 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 TimeRequirements
A third level qualification in Chemistry or related Science, preferably a Bachelor’s Degree; Graduate with a third level qualification in Chemistry or related Science.; Demonstrate knowledge of cGMP requirements and practices including knowledge of the USP and FDA; Guidance 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.Jak aplikować
Aplikuj online: https://www.jobs.pl/oferta/100096999/aplikuj
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