Quality Control Development Scientist 1

QIAGEN•Germantown, TN

21d•$80,000 - $90,000•Hybrid

About The Position

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. Join QIAGEN and play a key role in advancing Quality Control capabilities within a regulated diagnostics environment. As a Quality Control Development Scientist I, you will support the development, optimization, transfer, and validation of QC test methods while driving continuous improvement across laboratory operations. Working closely with Quality Control, Manufacturing, and R&D teams, you will provide technical expertise, lead troubleshooting investigations, analyze complex datasets, and contribute to ensuring the highest quality standards for QIAGEN products. This role offers the opportunity to independently manage scientific projects while mentoring colleagues and supporting the successful transfer of innovative technologies into routine Quality Control processes.

Requirements

Master's degree in Molecular Biology, Biochemistry, Biotechnology, Life Sciences, or a related scientific discipline with 4+ years of relevant industry experience.
Demonstrated technical expertise in molecular biology methods and Quality Control testing within a regulated environment; experience in the diagnostics industry preferred.
Proven knowledge of test method development, transfer, validation, statistical analysis, and data interpretation.
Experience working within GMP-regulated environments; familiarity with QSR, ISO, OSHA, IVD, and MDD regulations is advantageous.
Hands-on experience using advanced laboratory instrumentation such as HPLC, FTIR, ion exchange chromatography, or similar analytical technologies.
Proficiency with Microsoft Office applications and statistical software such as Minitab, JMP, or equivalent tools.
Strong communication, leadership, organizational, and problem-solving skills with the ability to work independently and collaboratively in a fast-paced environment.

Responsibilities

Develop, optimize, and validate Quality Control test methods to support product quality, regulatory compliance, and laboratory efficiency.
Lead the transfer of products and test methods from acquisitions, R&D, or other QIAGEN sites into Quality Control operations.
Analyze, trend, interpret, and present data generated through routine QC testing, investigations, and validation activities.
Lead troubleshooting investigations related to manufacturing processes, Quality Control testing, and customer complaints through to effective resolution.
Author, review, and maintain technical documentation, including SOPs, validation protocols, reports, and technical assessments.
Train, mentor, and provide technical leadership to Scientific Associates, Scientists, and Quality Control team members on laboratory methods and best practices.
Manage multiple projects simultaneously, prioritize activities effectively, and collaborate across functions to meet business objectives without compromising quality.