{"schemaVersion":"jobsearcher.job.v1","id":"cf6571049669b85188f242a2","url":"https://jobsearcher.com/jobs/cf6571049669b85188f242a2","canonicalUrl":"https://jobsearcher.com/jobs/cf6571049669b85188f242a2","title":"Stability Program Specialist: Data-Driven Lab Operations","description":"A pharmaceutical company in Durham, NC is seeking a Stability Coordinator to manage the Stability program for QC and R&D laboratories. Responsibilities include authoring stability protocols, tracking stability samples, compiling analytical data, and collaborating across departments. Candidates should have a B.S/M.S in a relevant field with experience in a GMP lab setting. Strong documentation and communication skills are essential, along with knowledge of FDA regulations. This role is crucial for ensuring product quality and safety, with opportunities for career growth.\r\nJ-18808-Ljbffr","company":"Medpharm","rawCompany":"medpharm","city":"Durham","state":"NC","isRemote":false,"isActive":false,"createdAt":"2026-04-24T04:36:25.752Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-9121.00","title":"Natural Sciences Managers","slug":"natural-sciences-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Stability Program Specialist: Data-Driven Lab Operations","description":"A pharmaceutical company in Durham, NC is seeking a Stability Coordinator to manage the Stability program for QC and R&D laboratories. Responsibilities include authoring stability protocols, tracking stability samples, compiling analytical data, and collaborating across departments. Candidates should have a B.S/M.S in a relevant field with experience in a GMP lab setting. Strong documentation and communication skills are essential, along with knowledge of FDA regulations. This role is crucial for ensuring product quality and safety, with opportunities for career growth.\r\nJ-18808-Ljbffr","datePosted":"2026-04-24T04:36:25.752Z","dateModified":"2026-04-24T04:36:25.752Z","hiringOrganization":{"@type":"Organization","name":"Medpharm","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Durham","addressRegion":"NC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"cf6571049669b85188f242a2"},"url":"https://jobsearcher.com/jobs/cf6571049669b85188f242a2"}}