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
  

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