Jobs at Beeline Medicines

Manages GMP quality assurance oversight for external manufacturing and testing partners. Reviews batch records, deviations, CAPAs, and change controls; supports product release, audits, quality agreements, and health authority inspections. Applies GMP regulations and quality risk-management judgment across biologic and small-molecule manufacturing networks.

Leads global clinical supply chain strategy and execution across clinical programs, including forecasting, inventory planning, packaging, labeling, distribution, cold-chain integrity, trade compliance, and returns. Manages CDMOs, 3PLs, depots, and logistics partners while ensuring GMP, GDP, GCP, and regulatory compliance. Partners cross-functionally with Clinical Operations, CMC, Quality, Regulatory, and Finance; develops SOPs, manages deviations and CAPAs, supports inspections, and builds scalable supply infrastructure in a pre-commercial biotech environment.

Field-based senior clinical development professional responsible for building and managing investigator and site relationships, supporting site identification and activation, driving enrollment and retention, providing field intelligence to Clinical Development and Medical Affairs, and representing the company at scientific meetings across a multi-state territory.