
This senior C&Q validation engineering role supports a major parallel manufacturing enablement project within a regulated biotechnology facility in eastern Puerto Rico. The position focuses on the commissioning, qualification, and validation of new single-use mixing systems, centrifuges, and cell collection tanks to eliminate shared-equipment dependencies. Key responsibilities include developing validation plans and reports, reviewing user requirements and risk assessments, executing factory and site acceptance testing, and ensuring full integration of new equipment into existing production workflows. The role appeals to candidates seeking to lead complex validation lifecycle management in a high-impact environment where they can drive continuous improvement and ensure audit readiness. This is a fully onsite position requiring close collaboration with cross-functional teams to maintain compliant manufacturing operations.

