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Pharmaceutical Manufacturing Technician II (DPI) Hardware
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- Durham, North Carolina, United States
- Durham, North Carolina, United States
Über
Location: Durham, North Carolina (on‑site 100% of the time).
Job Tags: Hardware
About The Role 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 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.
You’re a pharmaceutical manufacturing professional with experience working in upstream processes in a GMP environment. You’re skilled at handling raw materials, preparing and moving large‑scale suspensions, and operating equipment like tanks, mixers, and filtration systems. Accuracy and compliance come naturally to you, whether weighing and dispensing materials, and completing batch records. You’re quick to troubleshoot issues and collaborate with others to find solutions, always keeping efficiency, quality, and safety in mind. Above all, you take pride in process ownership — ensuring upstream operations run seamlessly and contribute to the production of life‑changing therapies.
Minimum Requirements
H.S. Diploma or General Education Degree (GED) and 2+ years of relevant hands‑on experience in a regulated production environment
Strong cGMP documentation practices
Experience with production equipment within a regulated industry
Ability to navigate sophisticated HMI control systems on automated equipment
Demonstrated ability to work effectively in a team
Ability to work shifts to cover a 3 shift 5 day or 24/7 operation
Strong verbal and written skills with the ability to understand and clearly communicate both orally and in writing in English
Basic computer skills
Preferred Qualifications
Associate's Degree in a scientific discipline or a related field and 2+ years of relevant hands‑on experience in a regulated production environment
Knowledge with production equipment, such as spray dryers, product transfer equipment, isolator technology, and filtration systems
Experience with process deviation investigations, CAPA, etc.
Experience with the use of test equipment such as scales, balances, solids percentage testers, filter integrity testers
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Sprachkenntnisse
- English
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