
This on-site Validation Engineer role is based in Tucson, AZ, within a leading biotechnology and life sciences organization. The position involves developing, executing, and reviewing process validation protocols and reports to ensure compliance with FDA, ISO, and cGMP standards. Key responsibilities include conducting risk assessments for manufacturing processes, analyzing validation data, and collaborating with cross-functional teams to resolve issues and drive continuous improvement. The role appeals to candidates seeking a long-term contract with potential for full-time conversion, offering a collaborative environment focused on operational excellence and regulatory adherence. The company provides comprehensive benefits including health insurance and retirement planning.
