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Biopharma-Consulting-Jad-Group seeks an experienced Quality oversight professional to supervise drug product manufacturing, packaging and inspection operations in Juncos, PR. You will review master production records, approve change controls, and participate in incident triage and product introductions.
The role requires GMP QA experience, documentation discipline, and bilingual English/Spanish. Administrative shift, 40 hours per week, with a 5-month contract and potential extension.
Biopharma-Consulting-Jad-Group seeks an experienced Quality oversight professional to supervise drug product manufacturing, packaging and inspection operations in Juncos, PR. You will review master production records, approve change controls, and participate in incident triage and product introductions.
The role requires GMP QA experience, documentation discipline, and bilingual English/Spanish. Administrative shift, 40 hours per week, with a 5-month contract and potential extension.