Quality Control Planner

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.

The Quality Control Planner is responsible for the oversight of QC Laboratory Planning and Scheduling within the Plant QC Group. Additional responsibilities may include short-term forecasting for enablement of efficient and effective laboratory scheduling, maintenance of laboratory planning and scheduling applications, evaluation and presentation of laboratory KPI's, and cross site harmonization of planning/scheduling processes.

Responsibilities

Maintains/manages laboratory planning/scheduling application, ensuring accurate configuration for laboratory workflows and timely prioritization of laboratory samples.; Monitors, maintains, evaluates, and reports out laboratory KPI's.; Collaborates with Laboratory Management to identify and implement process changes that enable continuous improvement.; Coordinates batch release activities and Quality Control checks, ensuring testing, documentation, review, and approvals are completed accurately and within established timelines and cGMP requirements.; Participates in cross-site harmonization of laboratory planning and scheduling process.; Maintains short-term forecasts to ensure effective and efficient laboratory scheduling to reduce overall testing cycle times.; Performs other duties as assigned; Incumbent has full authority to make decisions and/or take action that is required to carry out job duties. Internal requirements include compliance with ethics, environmental health and safety, financial, human resources, cGMP procedures, general business policies, requirements and objectives. The incumbent must be willing to take temporary assignments as required.

Requirements

Bachelor’s Degree required. Life sciences, engineering, or related field preferred.; Three (3) to five (5) years of experience in a laboratory or quality role with preferred experience in program/ project/ product management.; Advanced use of MS Office applications required, experience with planning and scheduling software preferred.; Experience in a regulated environment preferred.