3rd Shift Production Operator

We’re a company that takes on the toughest health challenges. But we do more than treat diseases—we aim to make a remarkable impact on people’s lives. We are AbbVie, a highly focused research-driven biopharmaceutical company.

Here at AbbVie we are looking for a Production Operator to join our organization. This role will be based at the AbbVie Park location. You will support pharmaceutical product finishing / packaging operations including inspecting, cartoning, kitting and packaging finished pharmaceutical and consumer products AbbVie operates 13 state-of-the-art manufacturing facilities located in North America, Puerto Rico and Europe that offer a high degree of flexibility, scale and wide-ranging manufacturing capabilities. These include some of the world’s most technically advanced facilities for their respective specialties – supported by an extensive team of scientific and technical experts.

* Perform manual assembly and inspection of commodities and components to final product and GMP specifications. * Operate semi-automated manufacturing equipment to produce finished product. * Perform and document in-process quality checks on product and equipment in order to assure that batch record specifications are attained * Move material to and from production lines as required to support efficient work flow * Adhere to safety guidelines and follow proper PPE gowning practices * Implementing and maintaining the effectiveness of the quality system. * Manual finishing of pharmaceuticals utilizing semi-automated and automated equipment. * Understand and perform basic line changeover activities. * Verification of components and testing equipment necessary to assure that pharmaceuticals are labeled and packaged per specifications. * Assists with the set up and close out of work orders on production lines including beginning and end of lot line clearances. * Review and audit in process and completed work order packets for accurate and complete data entry, and proper documentation practices.

**Basic:** • High School Diploma or GED **Preferred:** * Knowledge of applicable regulations and standards affecting Pharmaceutical Products (e.g. CFR 210/211, cGMP) specifically. * Previous related work experience in a pharmaceutical production environment, including knowledge of related cGMP requirements and procedures is preferred. * Position will be hired based on level of experience