QC Environmental Monitoring (EM) Officer

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 is looking for a QC Environmental Monitoring (EM) Officer to join our site in Liège. In this role, you’ll support the quality and compliance of our classified areas by reviewing environmental monitoring documentation and results, analysing trends, and helping ensure that EM activities are completed on schedule. Working closely with the QC Lead and QC EM Subject Matter Expert (SME), you’ll contribute to reliable laboratory operations and continuous improvement in a GMP-regulated environment. Key Responsibilities Review EM records and results within your authorised scope, ensuring documentation is complete, traceable and compliant with applicable procedures. Work with the QC EM SME to monitor EM schedules and sampling frequencies. Maintain EM control charts, analyse trends and prepare EM reports. Support the follow-up of excursions, investigations and related actions under the coordination of the QC Lead, with appropriate technical support. Draft and update operational EM documents, including instructions, forms and training materials, for review and approval through the established process. Contribute to the review and maintenance of procedures, methods, forms and training documentation. Support day-to-day QC laboratory activities, such as sample and reagent receipt, laboratory organisation and maintaining appropriate laboratory conditions. Help maintain training in line with role requirements and deliver operational training when authorised. Support continuous improvement and participate in relevant EM meetings and follow-up actions as requested by the QC Lead. Follow applicable safety, environmental and hygiene requirements. Bachelor’s or Master’s degree in a scientific discipline, or equivalent experience with GMP laboratory. Good knowledge of environmental monitoring activities and working practices in classified areas. Practical experience with EM sampling, result follow-up and documentation review used to produce report, trend analysis. Good knowledge or experience in Microbiology is an asset. Knowledge of GMP, good documentation practices, data integrity principles. Good working knowledge of laboratory systems and tools, such as Microsoft Office, LIMS and SAP. Proficiency in French. English communication skills at B2 level, written and spoken. A rigorous and organised approach, initiative and the ability to coordinate and follow up on actions. Strong communication and relationship-building skills, with the ability to work collaboratively and adapt to changing priorities. Critical thinking, a continuous-improvement mindset and the ability to manage work effectively in a regulated environment. 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.  US & Puerto Rico only - to learn more, visit  https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html