Within this role you will be responsible for facilitating and coordinating inventory, documentation and performing record-related activities for manufacturing. You will also be maintaining and coordinating inventory, scheduling, sampling, and documentation requirements for manufacturing.
As a Biotech Production Coordinator, a typical shift might include, but is not limited to, the following:
* Coordinating, reviewing, and cataloguing various types of manufacturing documentation
* Preparing routine progress reports and tracking on various KPIs
* 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
* Navigating a variety of different systems, data, calculations, and documentation
* 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 thrive in a multifaceted and fast-paced environment
* You possess excellent verbal and written communication skills
* You demonstrate an ability to work within a successful team
* You have experience in a cGMP environment along with experience in quality assurance, project management, or inventory management
To be considered for this opportunity you should have a BS/BA Degree with 0-2+ years of related experience or equivalent combination of education and experience. #J-18808-Ljbffr