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
