Description
The role develops, performs, reviews, and documents equipment and utilities qualification and validation activities for pharmaceutical production and laboratory operations. Responsibilities include preparing qualification plans, risk analyses, design, installation, operation, and performance qualification documentation; issuing and reviewing reports; applying GMP and GLP standards; assessing deviations; and drafting procedures. The position requires a relevant undergraduate degree, Microsoft Office knowledge, prior pharmaceutical equipment or utilities qualification experience, and intermediate English, and is based in Valinhos, São Paulo.
