Description
Quality Consulting Group is hiring a Specialist Manufacturing professional in Juncos, Puerto Rico to support biopharmaceutical manufacturing operations. The role covers process validation, change controls, root-cause investigations, CAPA, microbial and risk assessments, commercial campaign readiness, troubleshooting, functional and water testing, technical documentation, and process improvement. It requires a bachelor's degree in life sciences, biology, chemistry, or engineering, bioprocessing experience, root-cause analysis knowledge, Lean Manufacturing familiarity, GDP proficiency, and proficiency with manufacturing systems and tools. The schedule is Monday through Friday from 8:00 a.m. to 5:00 p.m., with overtime possibly requested.
