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Cell Manufacturing Associate I​/II; iPSC

Job in Silver Spring, Montgomery County, Maryland, 20900, USA
Listing for: United Therapeutics Corporation
Full Time position
Listed on 2026-01-11
Job specializations:
  • Science
    Medical Science, Medical Device Industry, Data Scientist
Job Description & How to Apply Below
Cell Manufacturing Associate I/II (iPSC) page is loaded## Cell Manufacturing Associate I/II (iPSC) remote type:
On-Site locations:
Silver Spring, MDtime type:
Full time posted on:
Posted Todayjob requisition :
R04438

California, US residents .
** The job details are as follows:
**** Who We Are
** 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.

** Who You Are
** This position is responsible for executing end-to-end cell manufacturing processes in a regulated environment, while also contributing to startup activities such as drafting standard operating procedures, supporting technology transfer, and performing experiments using established protocols.
* Set up and operate cell manufacturing equipment used for cell production
* Perform cell manufacturing processes like cell culture, expansion according to established procedures
* Maintain aseptic technique and operate within a controlled, regulated manufacturing environment
* Prepare required raw materials, assemblies, solutions, tools, and samples
* Perform cleaning and sanitization of cleanroom environment and equipment
* Set up and run analytical tests and/or in-process checks to confirm compliance with quality standards
* Perform good documentation practices on batch records and logbooks
* Contribute to scaling-up, basic trouble-shooting and assisting with technical issues and problems
* Maintain and prepare production documentation (standard operating procedures)
* Maintain personal cGMP training to ensure compliance
* All other duties as required
** Minimum Requirements
*** Education and Experience Required for Cell Manufacturing Associate I  + Bachelor’s degree in biology, cell and molecular biology, biomedical sciences, biomedical engineering, biomanufacturing, or a related field  + 0+ years of relevant experience in biology, cell and molecular biology, biomedical sciences, biomedical engineering, biomanufacturing, regenerative medicine, or a related field
* Education and Experience required for Cell Manufacturing Associate II  + Bachelor’s degree in biology, cell and molecular biology, biomedical sciences, biomedical engineering, biomanufacturing, or a related field  + 2+ years of relevant experience in biology, cell and molecular biology, biomedical sciences, biomedical engineering, biomanufacturing, regenerative medicine, or a related field  + 1+ years of experience with aseptic technique and cell culture
* Knowledge of cGMP regulations and Good Documentation Practices (GDP)
* Experience operating cell manufacturing equipment like biosafety cabinets, incubators, bioreactors, centrifuges, pipettes, etc
* Ability to document work accurately in batch records and logbooks and follow standard operating procedures
* Ability to work in a regulated cleanroom environment, including extended periods in full gowning
* Capacity to learn new techniques quickly and…
Position Requirements
10+ Years work experience
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