Padagis LLC Benefits Overview

Lead customer-facing CDMO/CMO projects across pharmaceutical manufacturing programs, coordinating operations and site teams in Minnesota and Israel. Manage project plans, milestones, risks, customer communications, commercial handoffs, invoicing coordination, and internal projects that improve CDMO processes, governance, tools, and cross-functional execution.

The Associate Director develops and executes pricing strategies, analyzing market dynamics, leading pricing initiatives, and ensuring compliance in the pharmaceutical industry.

Lead a team of five QA professionals to oversee site quality and compliance activities including audits, deviations, validation, data review, change control, investigations, CAPA, and continuous improvement. Manage internal and external (FDA) audit responses, deliver training, provide performance feedback, and support HR matters to maintain cGMP compliance.