Facilitate and coordinate inventory, documentation and perform record-related activities for manufacturing. Maintain and coordinate inventory, scheduling, sampling, and documentation requirements for manufacturing.
Essential Duties and Responsibilities include, but are not limited to, the following:
* Coordinating, reviewing and cataloguing various types of manufacturing documentation
* Preparing routine progress reports and tracking on various KPIs.
* Managing lifecycle management of documentation
* Maintaining inventory systems through investigations, weekly reviews, reconciliations, and other related activities to ensure accuracy
* Serving as a liaison between manufacturing and other functional areas as needed
* Performing analysis of GMP and GxP data
* Coordinating appropriate material needs using varying systems and forms to ensure production continuity
* Ensuring systematic bill of materials are created and maintained for production needs
* Evaluating, initiating, and monitoring deviations and other compliance events
* Creating and reviewing sampling intake for all manufacturing unit operations and protocols per the appropriate documentation prior to operators going on the floor
This role might be for you if:
* You have the ability to decipher and navigate a variety of different systems, data, calculations, and documentation
* You have experience within a GMP environment and have good GDP knowledge
* You possess excellent verbal and written communication skills
* You enjoy problem solving
* You demonstrate a can-do attitude
* You are proficient in Microsoft Word, Excel, PowerPoint, and Outlook
To be considered for this opportunity you should have a BS/BA in Life Sciences or a related field and 0-2+ years of related experience or equivalent combination of education and experience. Experience in a cGMP environment, quality assurance, project management, or inventory management is desired.
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