Pulmovant is a Roivant-backed clinical-stage biotechnology company developing innovative therapies for patients suffering from pulmonary diseases. Pulmovant’s first program, mosliciguat is designed to provide an effective, once-daily, inhaled treatment option for patients with pulmonary hypertension (PH). Mosliciguat
Location: This position may be performed remotely but requires flexibility and a willingness to travel as needed. Position Summary The Associate Director, Regulatory CMC willbe responsible forthe planning, preparation, and execution of Chemistry, Manufacturing, and Controls (CMC) regulatory
Sabin Vaccine Institute, Inc. in the United States is seeking a Senior Manager, CMC Technical Operations to drive end-to-end CMC activities from development through regulatory readiness. You will partner with the CMC Product Champion and external partners to align
Praxis Precision Medicines, Inc. is seeking an Associate Director, Regulatory CMC to lead planning, preparation, and execution of regulatory activities for small molecule and ASO programs. You will coordinate with cross-functional teams and external vendors to support global
When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement.read on In 2015, we pioneered a “moneyball for biotech” approach, pooling
Enliven Therapeutics, a clinical-stage biopharmaceutical company, seeks a Vice President, Supply Chain to own global supply strategy across clinical and late-stage programs. You will ensure uninterrupted supply of investigational products and coordinate with CMC, Clinical Operations, Quality, and
Sabin Vaccine Institute, Inc. is seeking a Director of Technical Project Management in R&D to lead a team of technical Project Managers spanning nonclinical, clinical, regulatory, and CMC activities. You will drive strategic planning, governance, and delivery,
Generate:Biomedicines is seeking a Senior Director of Analytical Development to lead strategic direction and execution of analytical programs for biologics in a lean, virtual development model. This role partners with CMC, Quality, Regulatory, and external partners to ensure
Loyal is seeking a Principal Analytical QA Specialist, Drug Substance to oversee GMP manufacturing, release, stability, validation, and lifecycle programs across drug substance and drug product. The role collaborates with outsourcing partners to ensure cGMP compliance and
Location: This position may be performed remotely, but requires the flexibility and willingness to travel as needed.Opportunity As Director of Process Chemistry, you will take the lead on drug substance activities for one or more projects
Cogent Biosciences is seeking an Associate Director, Analytical Development for remote work in the United States. You will lead analytical activities across Cogent’s development portfolio, partnering with Regulatory CMC, Quality, and external CDMOs to ensure analytical data,
Location This position may be performed remotely, but requires the flexibility and willingness to travel as needed.The Opportunity Were seeking a Principal Scientistin Process Chemistry to lead drug substance activities for one or more projects within
Associate Director/Director Pharmaceutical Development Remote - USA Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement.read on In
Praxis Precision Medicines, Inc. seeks a Director of Process Chemistry to lead drug substance activities across small molecule programs, driving clinical and commercial readiness. You will design products and processes supporting clinical testing and mature them through