Pharmaceutical Product Quality Specialist

Document receipt of stability samples and complete inventories. Appropriately handle documentation. Understand stability requirements – protocols, LIMS, storage chamber conditions, labeling of samples and storage positions. Provide support for project managers and laboratory staff. Compose business appropriate communication (i.e. e-mail, document) for client or internal use.Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrates and promotes the company vision  Regular attendance and punctuality Applies quality to all areas of responsibility, understands and promotes quality culture. Understand and update LIMS appropriately for protocol and sample activities. Manage inventory for incoming project samples; set up stability studies, label samples, and place into chambers. Verify sample chamber placement, labeling, container counts, and LIMS entry Pull samples from chambers at appropriate intervals; perform periodic chamber inventories Maintain contents of stability chambers in an organized manner, monitor and change charts; clean inside of chambers Follow all department procedures and SOPs; understand and apply GMP/GLP regulations to daily work; document data according to regulatory requirements Attend department meetings Independently evaluate and/or provide shipment paperwork, package samples for shipment as needed with additional training. Effectively use word, tone, body language to share and receive information. Accept and implement process change to support business goals. Conducts all activities in a safe and efficient manner Performs other duties as assigned