Teams at Nephron Pharmaceuticals Corporation

Lead continuous improvement for change control and document revision, optimize eQMS (Dot Compliance), analyze KPIs and quality data, implement process and system improvements, develop training, support audits, and mentor document control staff across cross-functional teams in a regulated pharmaceutical environment.

Perform USP-based microbiological testing of raw materials, in-process, and finished products (sterility, bioburden, ID, environmental monitoring). Document and report OOS/OOT, assist investigations and sample management, train QC staff, perform method validation when requested, and maintain cGMP-compliant laboratory practices and aseptic technique.

Provide engineering support for MS&T: maintain and control CAD drawings, support cleanroom construction and capital projects, assist equipment procurement/commissioning, troubleshoot facility systems, manage engineering documentation, ensure cGMP compliance, and oversee stability chamber qualification, calibration, and inventory.