New

Intern - Specification Creator

QIAGEN
United States, Massachusetts, Beverly
100 Cummings Center (Show on map)
Oct 22, 2026
Overview At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible. We're dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We're always striving to identify talented individuals to join our exceptional teams. We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. At QIAGEN, every day is an opportunity to make a real-life impact. Join us, grow with us, and together, let's shape the future of biological discovery. About the Role Support a document control project focused on creating and standardizing raw material specifications. Working under the guidance of the Document Control team, you will review supplier documentation and develop internal specifications to support quality and manufacturing processes. Your Tasks 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. Your profile Currently pursuing or recently completed a degree in Biochemistry, Chemical Engineering, Biology, Biomedical Engineering, or a related STEM field. Basic Chemistry/Biology Knowledge: Understanding of purity levels, chemical grades (e.g., USP, ACS, EP), and biological properties (e.g., endotoxin levels, sterility). Research Skills: 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. The typical hourly rate for this position is $20/hour. Compensation will be based on the candidate's experience, skills, geographic location, and other job-related factors. What we offer Bonus/Commission Local benefits Referral Program Volunteer Day Internal Academy (QIALearn) Employee Assistance Program Hybrid work (conditional to your role) Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve.We inspire with our leadership and make an impact with our actions.We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking. QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.