- Perform environmental monitoring in cleanroom environments to support GMP production of clinical-grade products.
- Operate EM equipment (e.g., Solairs, ApexZ50, active counters) and document results per GMP standards.
- Prepare buffers, components, and operate autoclaves.
- Assist with cleanroom setup, stocking, and aseptic processing support.
- Maintain accurate batch records and EM documentation.
- Bachelor’s in Life Sciences preferred, or HS diploma with relevant cGMP lab experience.
- 1–3 years of laboratory or GMP manufacturing experience; strong aseptic technique required.