Supply Chain Associate (Boston or Philadelphia)
Tandym Group - Philadelphia, PA
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A recognized pharmaceutical company is currently seeking a new Supply Chain Associate to join their growing team.About the Opportunity:Schedule: Monday to FridayHours: Standard businessLocation: Boston or PhiladelphiaSetting: Hybrid (3 days a week in-office)Responsibilities:Assist in drafting, editing, and formatting scientific documents such as batch records, specifications, validation reports, and CMC sections of regulatory submissionsEnsure that documentation complies with internal quality standards, regulatory guidelines, and good documentation practices (GDP)Collaborate with subject matter experts in manufacturing, quality control, and regulatory affairs to gather and verify technical informationMaintain and organize document management systems to ensure timely retrieval and version control of CMC documentsParticipate in document review meetings and incorporate feedback from cross-functional teamsPerform other duties, as neededQualifications:Bachelor's Degree or background in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related Scientific fieldFamiliarity with Scientific terminology and concepts related to Pharmaceutical Development and ManufacturingProficient in Microsoft Office Suite (Word, Excel, PowerPoint)Strong attention to detailExcellent written communication skillsStrong attention to detailDesired Skills:Experience with Electronic Document Management systems (EDMS)Previous internship or academic experience in a GMP, Regulatory, or Scientific Writing setting
Created: 2025-06-19