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. 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.

• 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 productionrelated 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, with a focus on quality, supply continuity, and cost efficiency.
• Contribute to validations and drive process improvements, including costreduction and efficiency initiatives.
• Build and manage effective relationships with internal and external stakeholders while supporting departmental and corporate goals.

• 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/ISOregulated biotechnology or diagnostics manufacturing environment.
• Handson 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 fastpaced 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.

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.