Supply Chain Associate (Boston or Philadelphia) Job at Tandym Group, Philadelphia, PA

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  • Tandym Group
  • Philadelphia, PA

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

Job Tags

Internship, Work at office, 3 days per week, Monday to Friday,

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