About this role
Join a leading biotechnology company in Juncos, Puerto Rico, creating the defect standards used to qualify and train visual inspection of parenteral products. What you'll do Prepare syringes and vials with cosmetic, particle and solution defects for development studies, equipment characterization, training and commercial equipment setup. Develop, introduce and improve defect-creation methods for laboratory use.
Evaluate defects and container conditions in primary containers. Design, run and interpret experiments, and write scientific reports. Coordinate small projects with other departments in a fast-paced environment.
Doctorate, or Master's + 2 years, or Bachelor's + 4 years of scientific experience. Hands-on use of calipers, microscopes and analytical balances. Excellent manual dexterity and fine motor skills to cut, shape and craft miniature items and particles. Aseptic technique, 5S, Lean and manual visual inspection. Strong cGMP knowledge; fully bilingual (English/Spanish). Comfortable using AI tools for research and workflow organization (a plus).
Contract: 6 months, with possible extension Shift: Administrative, 9:00 AM – 6:00 PM