New

Contract Technical Associate Kit Assembly 1st Shift

QIAGEN
United States, Maryland, Germantown
Feb 19, 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 handson role, you contribute directly to the reliable production of QIAGEN kits that empower scientists and healthcare professionals worldwide. You thrive in a fastpaced manufacturing environment, enjoy working with your hands, and take pride in delivering highquality products that make a real impact. As part of our Kit Assembly team, you follow established procedures, operate production equipment, and help drive continuous improvement. Your tasks include Perform manual assembly and production tasks according to established SOPs. Complete all productionrelated documentation accurately and on time. Set up, operate, and troubleshoot equipment used in the assembly area. Maintain product quality by following defined processes and quality standards. Prepare and verify required materials before production starts. Contribute to crossfunctional process improvement activities. Ensure ongoing compliance with applicable quality and EHS regulations (ISO, FDA, OSHA, etc.). Your profile High School Diploma or equivalent and ideally 1-3 years of related experience (or an AA degree). Understand FDA and cGMP production practices or are eager to learn them. Work independently with minimal supervision and have strong attention to detail. Comfortable using general and automated laboratory/production equipment and basic computer systems. Manage your time, materials, and equipment efficiently and complete documentation accurately. Communicate issues clearly, adapt quickly to changing priorities, and collaborate well in a team. Are able to lift up to 50 lbs repeatedly and work standing for extended periods. The typical pay rate for this role is $20/hour. This temporary and/or contract position is not eligible for QIAGEN's company benefits. The position includes only those benefits mandated by applicable state and federal law, if any, which are provided by the agency employer. 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.