Teams at The Ritedose Corporation

Leads technical and commercial execution of sterile BFS pharmaceutical programs from feasibility and technology transfer through validation, launch, and commercial supply. Serves as the primary client contact, directs cross-functional teams, manages schedules, risks, scope, change orders, regulatory deliverables, budgets, and audits. Mentors project managers, supports PMO governance, and improves project standards, dashboards, and stage-gate processes. The role is on-site in Columbia, South Carolina, with access to manufacturing and laboratory areas.

Performs pharmaceutical QC microbiology testing, environmental and personnel monitoring, microbial enumeration and identification, utility and product testing, data review, equipment maintenance, investigations, audit support, SOP training, and laboratory inventory and housekeeping. Ensures accurate documentation and compliance with cGMP requirements while supporting special projects and microbial culture collection maintenance.

Lead QA oversight for manufacturing process monitoring, process control, and investigations to ensure cGMP and regulatory compliance. Manage and mentor QA staff, lead complex investigations and root cause analyses, approve GMP system changes, participate in audits, drive continuous improvement, and maintain effective quality systems across pharmaceutical manufacturing and distribution.