Croda, a global life sciences company based in Alabama, is seeking a Lead QA Specialist to own document control for GMP and QA activities at the Alabaster site. You will manage batch records, SOPs, CAPA investigations, data analysis and prepare for customer and FDA audits, collaborating across QA, manufacturing and quality systems.
The role requires knowledge of cGMP and FDA regulations, strong communication, project leadership, and attention to detail to ensure compliance and continuous
#J-18808-LjbffrQA Lead - GMP, CAPA & Document Control in alabaster at Unknown Company
This position is listed as full time and onsite.