Senior Technical Associate, Production NGS

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 The Senior Technical Associate, Production NGS is responsible for performing routine manufacturing activities associated with the Next Generation Sequencing (NGS) diagnostic kits and Molecular diagnostics products in a GMP compliant environment. The individual will execute production processes, maintain accurate documentation, perform troubleshooting with appropriate support, and operate, and maintain laboratory equipment to ensure the consistent production of high-quality products. The position also supports continuous improvement initiatives, investigations, and the implementation of new products and processes. Your tasks include Prepare buffers, oligonucleotide libraries, enzyme mixes, and complete kit components for NGS products according to production schedules, ensuring accurate batch record and compliance with applicable regulatory requirements. Perform manual and automated manufacturing and assembly activities in accordance with established procedures and regulatory standards. Execute batch records and accurately complete all production related documentation in a timely manner. Operate, maintain and calibrate standard laboratory equipment to support production activities. Initiate and support investigations of product, process, equipment nonconformities, and assist with corrective actions as needed. Ensuring ongoing compliance to applicable quality, regulatory and EHS requirements, including ISO, FDA, MDD, IVDD, OSHA. Contribute and support departmental and corporate goals. Contribute to new product implementation. Your profile Bachelor’s degree in a scientific or engineering discipline with 1-3 years of relevant experience in manufacturing environment. Previous experience working in a GMP and/or ISO-regulated manufacturing environment is highly preferred. Hands-on experience with magnetic beads (suspension material), and oligonucleotide quantification is preferred. Knowledge of current QSR, ISO, OSHA, IVDD, MDD regulations are desirable. Basic mathematical skills, including the ability to accurately perform calculations and work with metric units, volumes and measurements. Ability to thrive in a fast-paced manufacturing environment, effectively managing changing priorities and multi-task while maintaining a professional demeanor. Able to work safely and effectively in a team environment. Strong organization skills with exceptional attention to detail and accuracy. Minimum travel between the Germantown and Frederick sites may be required. The estimated base salary range for this position is $50,000-$60,000. 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. At QIAGEN, our vision is clear: Making improvements in life possible. This is reflected in our daily actions to help scientists, clinicians and professionals tackle some of the world’s greatest challenges – unlocking insights that advance science, improve healthcare and enhance lives. To achieve this, we stay focused on one mission: to offer Sample to Insight solutions. Our products and services turn complex biological samples into valuable answers. Whether it’s enabling a breakthrough discovery or improving patient outcomes, we help our customers move from data to insight, faster and with greater confidence. Applying for your dream job is exciting - below you can find more information on the recruitment process and other relevant topics to guide you in your path to QIAGEN. Find out more here. Privacy Policy and contacts