Teams at Nephron Pharmaceuticals Corporation

Manages DEA compliance and controlled-substance programs, including procedures, inventories, reporting, registrations, records, inspections, investigations, corrective actions, and staff training. Serves as the organization’s controlled-substance subject matter expert and power of attorney. Coordinates DEA and state regulatory requirements, supports FDA inspections, maintains inspection readiness, and improves tracking and reconciliation systems. The role requires pharmaceutical and controlled-substance experience, regulatory knowledge, technical writing, and root-cause analysis skills.

Manages document control operations in a regulated pharmaceutical environment, including document lifecycle management, batch records, media fill documentation, records retention, audit readiness, and quality-system support. Leads and develops the Document Control team, ensures compliance with cGMP, FDA, 21 CFR Part 11, and ALCOA+ principles, and coordinates with Quality, Manufacturing, and Product Development teams.

Manages procurement categories by analyzing costs and market trends, negotiating vendor contracts, placing and tracking orders, forecasting demand, managing inventory, resolving pricing issues, and developing category strategies. Collaborates with marketing, buyers, and merchandisers on pricing, promotions, product positioning, and category growth while managing budgets and vendor relationships.