Public biotech commercializing inhaled therapies for pulmonary hypertension
Liquidia is a public biopharmaceutical company with an FDA-approved inhaled treprostinil powder (YUTREPIA) for pulmonary arterial hypertension and related lung disease, now scaling sales and regulatory infrastructure. The hiring mix—dominated by sales (22 roles) with secondary focus on healthcare, legal, and manufacturing—reflects a commercial-stage company ramping field teams and navigating complex drug-device combination product compliance across global markets.
Notable leadership hires: Regulatory Affairs Director
Liquidia develops and commercializes inhalation therapies for rare cardiopulmonary diseases, anchored by YUTREPIA (treprostinil inhalation powder) for pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD). The company also operates Liquidia PAH, a subsidiary handling commercialization of generic treprostinil formulations. A second-generation candidate, L606, is in development as a twice-daily liposomal treprostinil with a next-generation nebulizer for North American markets. Core operations span drug formulation, device integration, regulatory affairs, specialty pharmacy support, and direct sales across U.S. markets.
YUTREPIA (treprostinil inhalation powder), FDA-approved for pulmonary arterial hypertension and pulmonary hypertension associated with interstitial lung disease. The company also commercializes generic treprostinil injection via subsidiary Liquidia PAH.
Veeva (CRM and PromoMats), Microsoft Office suite (Excel, PowerPoint), HPLC for analytical work, and Steam. The stack reflects clinical trial management and field sales infrastructure typical of commercial-stage biotech.
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