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Nautilus Biotechnology

Proteomics platform for drug target prioritization

New Product Introduction Staff Scientist

Bioprocess & BiomanufacturingPosted on Nov 10
Full-timeSan Carlos, CA, USA$145k - $196k /yr

About the Job

Requirements

  • A PhD in chemistry, biochemistry, molecular biology, or a related field with 10 or more years of relevant industry experience, or an MS with 15 or more years of relevant industry experience.
  • A proven record leading cross-functional projects through new product introduction, scale-up, process validation, and technology transfer into manufacturing, ideally involving life science reagents, antibodies, or diagnostic consumables.
  • Deep knowledge of protein biochemistry, protein purification, reagent formulation, or analytical chemistry, including HPLC, MS, or FPLC; expertise in antibody conjugation and protein expression and purification.
  • Experience building project plans, managing timelines, risks, and resources, and holding cross-functional team members accountable without direct authority.
  • Experience mentoring and guiding scientists and associates, and delegating and reviewing their work.
  • Experience setting up bills of materials using Arena or Agile software, conducting costing analysis, setting up supply chains, and managing vendors.
  • Hands-on experience in controlled development or manufacturing environments under ISO 9001 and ISO 13485, including design control, process validation, and corrective and preventive action.
  • Proficiency in Excel and statistical tools such as JMP, Minitab, or R; experience with project tracking tools such as Smartsheet, Microsoft Project, or similar.
  • Willingness to work hands-on in the laboratory and production environment.

Responsibilities

  • Lead new product introduction projects end to end by defining scope, deliverables, milestones, and resource needs, and driving cross-functional teams to transfer new reagents, proteins, antibodies, and assays from R&D to commercial production on time and within budget.
  • Serve as the technical lead and primary contact for assigned products across R&D, Reagent Manufacturing, Quality, Supply Chain, and Program Management; track progress and communicate status, risks, and mitigation plans to stakeholders and leadership.
  • Set technical strategy for scale-up, process characterization, and process validation; design and oversee studies to improve yield, stability, and robustness of complex formulations and processes.
  • Make and defend data-driven decisions at project gates, including design transfer, pilot readiness, validation, and launch; escalate schedule, cost, and quality trade-offs as needed.
  • Partner with R&D to establish QC release criteria and product specifications, and conduct guard-band and robustness studies for manufactured reagents; lead specification-setting discussions across teams.
  • Lead root-cause investigations of complex production and transfer issues during pilot and production phases, and drive corrective and preventive actions to closure.
  • Own technical documentation for transferred products, including SOPs, batch records, bills of materials, technical reports, and transfer packages; ensure compliance with quality standards and review documents authored by others.
  • Develop and improve new product introduction processes, templates, and best practices, including stage-gate checklists, transfer plans, and risk assessments.
  • Mentor and provide technical guidance to scientists and research and manufacturing associates; delegate and review work on project teams and contribute to hiring and onboarding.
  • Work hands-on in the laboratory and production environment as needed, including reagent formulation, conjugation, and analytical sample preparation, particularly for new or high-risk processes.
  • Support supplier and contract manufacturer selection and technology transfer, including vendor qualification, costing analysis, and supply-chain setup for new products.

Desired Qualifications

  • Experience leading new product introduction, scale-up, process validation, and technology transfer into manufacturing for life science reagents, antibodies, or diagnostic consumables is ideally suited to the role.

About the Company

Nautilus Biotechnology

Proteomics platform for drug target prioritization

Nautilus Biotechnology develops a proteomics platform that maps the human proteome to speed up drug discovery. The platform analyzes thousands of proteins across biological samples to reveal which drug targets are most likely to succeed in clinical trials, helping researchers prioritize targets with higher potential. The company sells the platform and related services to pharmaceutical companies, research institutions, and biotech firms, operating on a B2B model. Unlike tools that focus only on genes or small-molecule data, Nautilus provides direct protein-level insights at large scale, combining deep proteome coverage with analytics to reduce time and costs in target discovery. Its goal is to unlock the proteome to enable breakthroughs in biology and medicine and to improve global health outcomes by accelerating and improving drug development.

Company size
51-200
Company stage
IPO
Headquarters
Seattle, WA
Founded
2016

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