Product Manager – Global NGS Diagnostic Applications

3T Biosciences

. Support the development, launch, global commercialization, and lifecycle management of NGS-based diagnostic and companion diagnostic products .

Posted 10/5/2026full-timeRemote • United StatesMid-LevelSenior💰 $135,000 - $185,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in product management and commercialization of NGS-based diagnostic products, with a strong focus on regulatory submissions, market analysis, and cross-functional collaboration. Proficient in managing product lifecycle, pricing strategies, and customer engagement within the molecular diagnostics and biotechnology sectors.

Highest-signal resume keywords

Product Management ExperienceNGS Technologies ExpertiseRegulatory Submissions KnowledgeCompanion Diagnostics ExperienceMarket Analysis Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Product Strategy DevelopmentMarket AnalysisRegulatory ComplianceFinancial ModelingNGS Workflow UnderstandingLibrary PreparationTargeted SequencingBioinformatics AnalysisCompanion DiagnosticsGlobal Product Launches

Soft Skills

Excellent CommunicationPresentation SkillsOrganizational SkillsAnalytical MindsetCustomer-Focused Approach

Tools & Technologies

Illumina Sequencing PlatformsNextSeqDxMiSeqDxThermo Fisher PlatformsElement Biosciences

Industry Keywords

Molecular DiagnosticsGenomicsBiotechnologyPharmaceutical IndustryPrecision MedicineMarket AccessReimbursement StrategiesCROsLaboratory NetworksDecentralized Testing Models

About the role

Key responsibilities & impact

Support the development, launch, global commercialization, and lifecycle management of NGS-based diagnostic and companion diagnostic products
Define product strategy and align cross-functional and external stakeholders around molecular diagnostic solutions
Conduct market analysis, competitive assessments, and customer research across oncology diagnostics and NGS technologies
Define and maintain product requirements, target product profiles, application roadmaps, intended use, product claims, product naming, and value propositions
Prioritize features and manage trade-offs across technical, clinical, regulatory, operational, and commercial considerations
Partner with Regulatory Affairs and external regulatory partners on CDx classification strategy, submission planning, vendor/contract review, and consultation strategy
Partner with pharmaceutical collaborators and Alliance Management teams on product plans, clinical evidence strategies, regulatory pathways, and commercialization objectives
Lead market-by-market and global commercialization strategy and execution, including launch plans, readiness milestones, and lifecycle management
Support pricing strategy, reimbursement rate analysis, and financial/market-sizing modeling
Represent Product Management across project teams, governance forums, and partner committees
Monitor commercialization performance using KPIs and recommend corrective or growth actions
Lead customer-facing product discussions, scientific presentations, advisory boards, conferences, payer discussions, and advocacy engagement
Identify, evaluate, and govern contract laboratories, Centers of Excellence, reference laboratories, CROs, and other strategic testing partners
Partner with Marketing, Sales, and Scientific Affairs to develop positioning, messaging, sales enablement tools, and training content

Requirements

What you’ll need

Bachelor's degree in molecular biology, genetics, biomedical engineering, bioinformatics, life sciences, or a related field required
5+ years of product management or commercialization experience in molecular diagnostics, genomics, biotechnology, or pharmaceutical industry, supporting NGS or molecular diagnostic applications
3+ years of direct experience with companion diagnostics, precision medicine applications, and pharmaceutical partnership programs
3+ years of experience supporting global product launches or regulatory submissions across multiple jurisdictions, including FDA and at least one ex-US authority such as PMDA or EMA, in regulated diagnostic environments
3+ years of experience working with laboratory networks, CROs, Centers of Excellence, or decentralized testing models, including subcontractor governance and oversight
Strong understanding of NGS technologies and workflows, including library preparation, targeted sequencing, liquid biopsy, variant detection, and bioinformatics analysis
Familiarity with major sequencing platforms, including Illumina, Thermo Fisher, and Element Biosciences
Excellent communication, presentation, and organizational skills
Strategic, analytical, and customer-focused mindset with ability to influence cross-functional teams and external partners
Working knowledge of market access, reimbursement, pricing/transfer-pricing negotiation, demand forecasting, and financial or market-sizing analysis
Hands-on experience specifically with Illumina sequencing platforms, such as NextSeqDx and MiSeqDx
Ability to travel globally up to 25% as required
Pillar Biosciences is unable to provide sponsorship for this role

Benefits

Comp & perks

Equal Opportunity employment commitment
Global travel opportunity of up to 25% (may be required)