Supply Chain Associate (Boston or Philadelphia) Position Available In Philadelphia, Pennsylvania
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Job Description
A recognized pharmaceutical company is currently seeking a new Supply Chain Associate to join their growing team. About the
Opportunity:
Schedule:
Monday to
Friday Hours:
Standard business
Location:
Boston or Philadelphia Setting:
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 submissions Ensure 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 information Maintain and organize document management systems to ensure timely retrieval and version control of CMC documents Participate in document review meetings and incorporate feedback from cross-functional teams Perform other duties, as needed
Qualifications:
Bachelor’s Degree or background in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related Scientific field Familiarity with Scientific terminology and concepts related to Pharmaceutical Development and Manufacturing Proficient in Microsoft Office Suite (Word, Excel, PowerPoint) Strong attention to detail Excellent written communication skills Strong attention to detail
Desired Skills:
Experience with Electronic Document Management systems (EDMS) Previous internship or academic experience in a GMP, Regulatory, or Scientific Writing setting
