About this opportunity
Croda Singapore lists this QA Lead - GMP, CAPA & Document Control opportunity in alabaster, Alabama. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.