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Qpex Biopharma Inc

Oct 16, 2026
PERMANENT
Qpex Biopharma Inc San Diego, CA
Overview Qpex Biopharma is seeking an Administrative Assistant to join our innovative team in San Diego, California. This on-site role is essential in supporting daily operations, office management, streamlining processes, and fostering teamwork across the organization. The ideal candidate must be proactive and take initiative, is independent, detail-oriented, organized and skilled at making sound decisions with minimal supervision. The Administrative Assistant must also possess excellent communication, written, and multitasking skills, providing critical support to leadership and multiple departments to ensure smooth and efficient office operations. Detailed Description KEY RESPONSIBILITIES Provide proactive administrative assistance to executives and team members, including coordinating and scheduling meetings or company events. Manage day-to-day office operations, including maintaining supplies, organizing workspaces, and coordinating office equipment maintenance....
Oct 04, 2026
PERMANENT
Qpex Biopharma Inc San Diego, CA
Overview The Director of Quality provides strategic and operational leadership for Quality Assurance across Qpex's multi-therapeutic, multinational Phase 1-3 infectious disease development programs. This role is responsible for designing, implementing, and overseeing robust global quality systems that ensure compliance with FDA, ICH, GLP, GCP, and GMP requirements. Working closely with executive leadership, Regulatory Affairs, Shionogi Quality partners, CMOs, and external consultants, this role ensures quality oversight across development, manufacturing, testing, and product release activities. The position leads internal teams and external vendors, supports regulatory submissions and inspections, and drives continuous improvement of quality systems to enable successful regulatory approvals and commercialization. Detailed Description Primary Duties and Responsibilities include: Direct multi-therapeutic, multi-national quality assurance oversight in Phase 1-3 drug development...