New

Quality Control Scientist 1

QIAGEN
$60,000-$80,000
United States, Maryland, Frederick
May 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 opportunity In this role, you contribute directly to the quality and reliability of QIAGEN products by performing quality control testing across raw materials, components, bulks, and finished kits. Working in a regulated laboratory environment, you execute essential laboratory activities in compliance with QSR, ISO, OSHA, and IVDR requirements, while following established Standard Operating Procedures. You play an active role in data review, investigations, and continuous improvement, supporting both day-to-day operations and the ongoing development of robust, compliant QC processes. Your tasks include Perform quality control testing for assigned QIAGEN product lines, including qPCR- and sequencing-based assays Prepare, review, and document test data; enter results into batch records and perform initial reviews of peer data Initiate and support Out of Specification (OOS) investigations, contributing to root cause analysis and conclusions Maintain laboratory readiness by managing reagents, consumables, and equipment calibration status Troubleshoot routine assay issues independently and support more complex investigations with the Supervisor or Manager Train and mentor Associate Scientists and new team members as assigned Create, review, and update Standard Operating Procedures, validations, and technical documentation Your profile Bachelor's degree in a scientific discipline with 2-3 years of relevant industry experience, or a Master's degree with 1-2 years of equivalent experience Hands-on experience with qPCR and sequencing techniques in a laboratory setting Working knowledge of regulated environments; cGMP experience is an advantage Ability to analyze data, apply basic experimental design, and interpret statistical concepts (e.g., standard deviation, % variation) Proficiency in MS Office applications, particularly Word and Excel Strong communication skills with the ability to clearly document results and collaborate across teams Comfortable working in a fast-paced laboratory environment with biohazardous and/or chemically hazardous materials The estimated base salary range for this position is $60,000-$80,000. Compensation will be based on the candidate's experience, skills, geographic location, and other job-related factors. In addition to base salary, we offer a total compensation package that includes a commission plan, annual bonus, and generous benefits. 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.