Intern - Specification Creator
QIAGEN•Beverly, MA
•Hybrid
About The Position
Support a document control project focused on creating and standardizing raw material specifications. Under the guidance of the Document Control team, review supplier documentation and develop internal specifications that support quality and manufacturing processes.
Requirements
- Currently pursuing or recently completed a degree in Biochemistry, Chemical Engineering, Biology, Biomedical Engineering, or a related STEM field.
- Basic chemistry and biology knowledge, including understanding purity levels, chemical grades (e.g., USP, ACS, EP), and biological properties (e.g., endotoxin levels, sterility).
- Ability 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.
- Effective written communication and technical writing skills.
Responsibilities
- Review supplier documentation, including Certificates of Analysis (CoA), Technical Data Sheets (TDS), and Safety Data Sheets (SDS).
- 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.
Benefits
- Bonus/Commission
- Local benefits
- Referral Program
- Volunteer Day
- Internal Academy (QIALearn)
- Employee Assistance Program
- Hybrid work (conditional to your role)
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What This Job Offers
Career Level
Intern
Education Level
No Education Listed
