CMC & Manufacturing, Science and Technology Drug Substance Lead job opportunity at Sobi.

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Date2026-02-27T17:56:12.956Z bot
Sobi CMC & Manufacturing, Science and Technology Drug Substance Lead
Experience: General
Pattern: Full-time
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Science and Technology Drug Substance Lead

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degreeGeneral
loacation San Diego, California, United States Of America
loacation San Diego, Cal..........United States Of America
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Job DescriptionLocation Requirement: This position may be based on either the U.S. West Coast (ideally near San Diego, CA) or the East Coast (ideally near Raleigh, NC or Boston, MA). The role requires periodic travel between both locations to support cross‑site collaboration and business needs.The CMC & Manufacturing, Science and Technology Drug Substance Lead will be responsible for:Experienced subject matter expert (SME) and process owner for Drug Substance (DS) synthesis of a small molecule used in oral dosage forms.  Lead the technical workstreams of a manufacturing process transfers from development to commercial site and between commercial sites, scale-up activities, process validations and oversees manufacturing of Drug Substance small molecules at external manufacturers for projects in clinical and commercial phase. Experience in collaborating effectively with external manufacturing partners and to oversee all technical drug substance synthesis aspects (GMP and non-GMP steps).    Lead internal activities related to external manufacturing such as process change assessments, major/critical deviations, risk assessments and CAPAs  Review and supervise design, set up, execution and documentation of DS related technical studies (CMC development as well as commercial operations), process and equipment qualifications and validations.  Write and review applicable sections in registration files, variations and market expansion  Issue, review and approve applicable internal and external SOP's and fully oversee correctness and compliance of external manufacturer manufacturing instructions.  Contribute during set up of new analytical specifications and stability programs and review changes thereof  Support in sourcing evaluation of new Drug Substance small molecules, oral dosage forms alternative contract manufacturers and participation in developing supply and quality agreements. Be aware of modern synthetic organic chemistry methodologies, advancements, understand and introduce new technologies and how they may be applicable to process innovation, cost or yield improvement 

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