About the role#
This internship supports a document control project focused on creating and standardizing raw material specifications. You will work under the guidance of the Document Control team to review supplier documentation and develop internal specifications that support quality and manufacturing processes.
What you'll do#
- Review supplier documentation, including Certificates of Analysis, Technical Data Sheets, and Safety Data Sheets.
- Create material specifications using company templates.
- Organize and track specification data in Excel.
- Collaborate with cross-functional teams to verify specification content.
- Support document review and implementation within the document management system.
- Identify opportunities to standardize requirements across similar materials.
What you'll need#
- Current pursuit or recent completion of a degree in Biochemistry, Chemical Engineering, Biology, Biomedical Engineering, or a related STEM field.
- Basic knowledge of chemistry and biology, including understanding of purity levels, chemical grades, and biological properties.
- Research skills to cross-reference supplier documentation, internal manufacturing needs, and regulatory standards.
- Strong attention to detail and organizational skills.
- Proficiency with Microsoft Excel and Word.
- Ability to interpret technical documentation and communicate effectively in writing.
Location & details#
- Location: Beverly, Massachusetts.
- Schedule: Full-time, 40 hours per week, 5 days per week on-site.
- Duration: 6 months.
- Compensation: $20 per hour.
- Note: This position does not offer visa sponsorship.
About QIAGEN
QIAGEN is a biotechnology company founded in 1984. Based in Venlo, Netherlands, the firm provides tools to isolate and process DNA, RNA, and proteins for molecular analysis. It serves customers in clinical healthcare, pharmaceutical research, and forensics. The company employs over 5,000 people across 25 countries.
How to get in at QIAGEN
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