QIAGEN

Quality Control Development Scientist 1

$80K–$90KFull-time · Germantown
✓ Verified live on the employer's own system · added 11 days ago
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Mid-level · 4+ yrs exp

Requirements

Education: Master's degree or related field

Experience: 4+ years

Skills & tools

Quality AssuranceTest MethodsProcess ImprovementOperationsTroubleshootingTeam LeadershipRegulatory ComplianceManufacturing Methods

Benefits — mentioned in this posting

Bonus / commissionHealth, dental & visionRemote / flexible
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Full job description

About the opportunity 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.

Your tasks include 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. Your profile 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.

The estimated base salary range for this position is $80,000-$90,000.

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 bonus plan 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

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This posting was published by QIAGEN on their own careers system and is shown here with a direct link to apply there. Employers: for corrections or removal, contact jobs@veritahire.com.