We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs. United Therapeutics (Nasdaq: UTHR) seeks to travel down the corridors of indifference to develop treatments for rare, deadly diseases. We were founded in 1996 by a family seeking a cure for their daughter’s pulmonary arterial hypertension (PAH). Today, we have six FDA-approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF). The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need. For this reason, we are working to create manufactured organs to address the shortage of kidneys, hearts, lungs, and livers available for transplant. We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option. Are you a validation professional looking to apply your expertise in a dynamic biotech and pharmaceutical environment? As a Senior Validation Engineer or Specialist, Equipment, you’ll be a subject matter expert in equipment validation, playing a key role in ensuring the compliance and performance of critical manufacturing systems—including QC lab equipment, and upstream, downstream, and aseptic fill/finish manufacturing equipment. You’ll leverage your experience in developing sterilization cycles and writing validation protocols from scratch to support a fast-paced, highly regulated environment. This role offers the opportunity to lead complex validation projects, troubleshoot unique challenges, and collaborate across teams to uphold the highest industry standards. If you’re passionate about driving validation excellence and contributing to life-changing manufacturing for a rare disease population, we want to hear from you!