Summary
Location
Beverly
Type
internship
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About this role
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.
Responsibilities include:
- Working both individually and in a team environment, this project requires much computer work looking at vendor COA’s and specifications as well as company documents and templates.
- Possible opportunity to use advanced computing skills like AI.
- Working under supervision of Document Control and using company template, project requires gathering vendor information and QIAGEN material requirements to create internal specification documents for raw materials (~400 of them).
- Individual will look at grouping similar materials to ensure comparable requirements/specifications, create a specification for each material while also working with department users to verify content of specification upon writing them. The finish line is to have a part specific document for each purchased material identified by it’s part number, verified by its primary user, and effective in the document management system so that upon ordering new material, receiving new material, or testing new material; staff will know what a passing material should be and what a failing material should be. This can further be expanded to include testing forms to go with each specification that would require such place to record data and have disposition and signature.
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.
Other facts
About QIAGEN
QIAGEN is the leading global provider of Sample to Insight solutions that enable customers to gain valuable molecular insights from samples containing the building blocks of life.
Our sample technologies isolate and process DNA, RNA and proteins from blood, tissue and other materials. Assay technologies make these biomolecules visible and ready for analysis. Bioinformatics software and knowledge bases interpret data to report relevant, actionable insights. Automation solutions tie these together in seamless and cost-effective workflows.
QIAGEN provides solutions to more than 500,000 customers around the world in Molecular Diagnostics (human healthcare) and Life Sciences (academia, pharma R&D and industrial applications, primarily forensics).
As of December 31 2021 QIAGEN employed more than 6,000 people in over 35 locations worldwide. Further information can be found at www.qiagen.com.
What you'll do
- The intern will work on creating internal specification documents for raw materials by gathering vendor information and company requirements. This involves both individual and team efforts, with a focus on ensuring specifications are accurate and verified.
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