Within this role you will facilitate and coordinate inventory, documentation and perform record- related activities for manufacturing. Maintain and coordinate inventory, scheduling, sampling, and documentation requirements for manufacturing.
As a Biotech Production Coordinator, a typical day 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
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, initiate, and monitor deviations and other compliance events
Creating and review sampling intake for all manufacturing unit
operations and protocols per the appropriate documentation prior to operators going on the floor
This role might for you if:
You have the ability to decipher and navigate a variety of different systems, data, calculations, and documentation
You have experience within and 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 Degree with 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 desired.