About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved
About the Role The Senior Director, Technical Operations provides strategic leadership and oversight of drug product manufacturing and external CDMO operations from late-stage development through commercialization. This role is accountable for defining manufacturing strategy, managing increasing
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Department:106800 Technical Operations Location:San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease. At Travere Therapeutics, we recognize that
Department:106800 Technical Operations Location:San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease. At Travere Therapeutics, we recognize that
The Director, Drug Product Development will lead late‑stage development and NDA‑enabling activities for oral solid dosage form (OSD) drug products. This role is responsible for execution of formulation, process development, scale‑up, validation, and regulatory deliverables to support NDA submission, regulatory
The Associate Director, Drug Product & Process Development, will provide technical and strategic leadership for late‑stage drug product development programs, including process characterization, control strategy development, regulatory filings (IND amendments, NDA/MAA), and post‑approval lifecycle management (LCM).
Position Summary: The Associate Director, Materials Science will lead scientific strategic leadership for small molecule drug development programs, with accountability for material understanding, solid-state control, and material-related risk management from IND through NDA and commercialization. This role
We are a sterile pharmaceutical compounding company building a new, state-of-the-art manufacturing facility in Houston, Texas . The facility is being developed from a Class A shell into a dual-license operation that includes both a 503B
We are a sterile pharmaceutical compounding company building a new, state-of-the-art manufacturing facility in Houston, Texas . The facility is being developed from a Class A shell into a dual-license operation that includes both a 503B
We are a sterile pharmaceutical compounding company building a new, state-of-the-art manufacturing facility in Houston, Texas . The facility is being developed from a Class A shell into a dual-license operation that includes both a 503B