Senior Operations Specialist

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, and with thousands of employees across six continents, collaboration is our greatest strength. We are always striving to identify talented individuals to join our exceptional teams. Every day is an opportunity to make a real‑life impact, and we invite you to grow with us and help shape the future of biological discovery. About the opportunity In this role, you will contribute directly to the production of Next Generation Sequencing (NGS) diagnostic kits and Molecular Diagnostics products within a GMP‑compliant manufacturing environment at QIAGEN. You will ensure that manufacturing activities meet applicable regulatory requirements while driving process robustness, operational excellence, and continuous improvement. Working cross‑functionally, you will support technology transfers, troubleshoot complex manufacturing issues, and help maintain a high‑performing laboratory environment that enables reliable, high‑quality diagnostic solutions. Your tasks include Prepare buffers, oligonucleotide libraries, enzyme mixes, and complete kit components for NGS products according to production schedules, ensuring accurate and compliant batch record documentation. Execute, review, and accurately complete batch records and all production‑related documentation in line with GMP and quality requirements. Maintain laboratories and ensure proper operation, monitoring, and maintenance of lab environments and instrumentation. Initiate and support investigations related to product, process, or equipment nonconformities. Support new product introductions and technology transfers from development to manufacturing and between sites, focusing on quality, supply continuity, and cost efficiency. Contribute to validations and drive process improvements, including cost‑reduction and efficiency initiatives. Build and manage effective relationships with internal and external stakeholders while supporting departmental and corporate goals. Your profile Bachelor’s degree in a scientific or engineering discipline with 6 years of relevant manufacturing operations experience, or a Master’s degree with 2–4 years of relevant experience. Proven experience in a GMP/ISO‑regulated biotechnology or diagnostics manufacturing environment. Hands‑on expertise with magnetic beads, oligonucleotide quantification, and NGS library preparation. Solid understanding of applicable regulations such as QSR, ISO, OSHA, IVDD, and MDD. Strong analytical and mathematical skills, including confident handling of metric volumes and measures. Proficiency with general laboratory equipment and intermediate to advanced Microsoft Office skills (Word, Excel, Access, PowerPoint); Lean and SAP knowledge is an advantage. Ability to work in a fast‑paced environment, manage changing priorities, troubleshoot complex issues, and safely handle potentially biohazardous or chemically hazardous materials, including lifting up to 25 lbs and sitting for extended periods. The estimated base salary range for this position is $68,000-$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) 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. #J-18808-Ljbffr