About the role

QUALITY CONSULTING GROUP, LLC is seeking a talented engineer to join its team in a pharma/biotech manufacturing context, supporting in Puerto Rico and the USA. The role focuses on process characterization, commissioning, qualification, and ongoing validation activities across GMP-compliant systems. You will lead risk assessments, develop CQ strategies, manage documentation, and collaborate with engineering, QA, and production groups to ensure compliant, traceable results.

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JOB OVERVIEW

Experience level

Senior

Location

Juncos, PR

Occupation

Validation Engineers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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