Scientific Product Owner

🔥 18 hours ago

🌐 United States, Germany – Remote

infoinfo

💵 $120k - $165k / year

⏰ Full Time

🟢 Junior

✅ Product Manager

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Logo of QIAGEN

QIAGEN

5001 - 10000 employees

🧬 Biotechnology

🏥 Healthcare

💰 $750M Post-IPO Debt - Qiagen on 2025-08

Biotechnology • Healthcare

QIAGEN is a global provider of sample and assay technologies and related systems for molecular diagnostics, applied testing, academic and pharmaceutical research. The company supplies instruments, consumable kits and assays (including PCR and nucleic-acid–based workflows), as well as software and bioinformatics solutions that support clinical laboratories, life-science research, and drug development. QIAGEN’s offerings focus on enabling detection, extraction, and analysis of biological samples for diagnostics, research and applied molecular testing.

📋 Description

• Own the product backlog for assigned releases • Write and refine user stories and acceptance criteria for development • Translate scientific needs from product managers, content scientists, key opinion leaders, and customers into software requirements • Lead refinement sessions and resolve domain questions for engineering • Shape scientific design for hereditary and somatic workflows • Collaborate with engineers on scientific content, variant annotation, and classification logic • Test new features from a scientific user’s perspective • Prioritize customer-reported issues and enhancement requests by clinical impact • Assess issues for severity, patient safety, and usability risk in the IVD clinical decision-support product • Maintain design control documentation and support release readiness within an ISO 13485 quality system • Prepare release notes, user guides, and training for field application scientists and support teams • Act as scientific subject-matter expert and contribute to roadmap planning

🎯 Requirements

• MS or PhD in genetics, molecular biology, genomics, or a related life science • Expertise in cancer and/or hereditary disease • Preferred: 2+ years interpreting clinical next-generation sequencing (NGS) data in a clinical lab, research, or testing environment • Working knowledge of variant classification guidelines (e.g. ACMG/AMP) • Knowledge of common genomic data formats and databases • 1+ year in a product owner, business analyst, or requirements role on a software or bioinformatics product, or equivalent hands-on experience writing specifications for developers • Familiarity with agile development (Scrum or Kanban) • Familiarity with Jira, Confluence, and requirements-management systems • Preferred: comfort discussing APIs, data models, and system behaviour with engineers • Excellent written and spoken English, including scientific and technical writing • Ability to coordinate work across US and European time zones • Attentive to detail, curious, and comfortable with complex scientific, technical, and regulatory topics

🏖️ Benefits

• Bonus/Commission • Local benefits • Referral Program • Volunteer Day • Internal Academy (QIALearn) • Employee Assistance Program • Hybrid work (conditional to your role) • Generous benefits • Total compensation package including a bonus plan

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