Nivagen Pharmaceuticals, Inc. Benefits Overview

Perform aseptic, cGMP-compliant sterile drug manufacturing in ISO cleanrooms: operate and maintain formulation, filtration, filling, autoclave and sterilization equipment; perform visual/AQL inspection, documentation, environmental monitoring, gowning, and cleaning; assist investigations, batch records, and quality activities; follow SOPs and regulatory guidelines.

Perform routine and specialized cleaning/sanitization of Grade A-D cleanrooms per SOPs and cGMP. Prepare disinfectants, maintain cleaning logs and Master Cleaning Schedule, don proper gowning/PPE, report anomalies, support audits, and collaborate with QA, Facilities, and Manufacturing to maintain aseptic conditions and regulatory compliance.

As a Microbiologist, you will ensure pharmaceutical products meet quality standards by conducting tests, developing methods, and maintaining compliance with regulations.