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Employer Job Description
From BioPharma Consulting JAD Group's posting. “We” and “our” refer to the employer.
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.
Requirements
- 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).
Benefits
- Contract: 6 months, with possible extension
- Shift: Administrative, 9:00 AM – 6:00 PM
About this listing
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