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Director, Reagent Operations

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San Carlos
Posted 5 days ago
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Job Description

At Nautilus, we have a big and important mission: improve the health of millions by unleashing the potential of the proteome to accelerate drug development and enable a new world of precision and personalized medicine. We are developing a single-molecule protein analysis platform of unprecedented sensitivity, scale, and ease of use that we believe will democratize access to the proteome – one of the most dynamic and valuable sources of biological insight. To accomplish this, we are pursuing hard scientific problems with an entrepreneurial mindset and creating a world-class team of builders, innovators, and dreamers across a wide range of disciplines.

The Director of Reagent Operations will lead the end-to-end strategy and execution for reagent manufacturing, process transfer, and supply chain readiness to support commercial scale. This role sits at the critical interface of R&D, Quality, Supply Chain, and Manufacturing, ensuring robust, scalable, and cost-effective reagent production.

This leader will drive process industrialization, establish high-performing supplier networks, and implement operational rigor through quality systems and in-process controls to enable consistent product performance and reliable supply.

Responsibilities

  • Partner with R&D to transition reagent formulations and processes from development into robust, repeatable manufacturing processes

  • Lead process characterization, scale-up, and transfer to internal pilot manufacturing and external CMOs

  • Define critical process parameters (CPPs) and critical quality attributes (CQAs)

  • Establish Design for Manufacturability (DFM) and Design for Supply Chain (DFSC) principles early in development

  • Own process validation strategy (IQ/OQ/PQ where applicable, RUO-appropriate rigor)

  • Build and optimize reagent manufacturing workflows for; yield improvement, cycle time reduction, cost of goods (COGS) reduction, throughput scalability

  • Implement lean manufacturing and continuous improvement (CI) methodologies

  • Drive electronic batch record (EBR) adoption and standardized work instructions

  • Define and monitor KPIs: yield, scrap, batch success rate, OTIF, cycle time

  • Develop and manage a network of strategic suppliers and contract manufacturers (CMOs)

  • Lead supplier selection, qualification, and performance management

  • Drive suppliers to meet targets for; cost, quality, and lead time/responsiveness

  • Implement supplier scorecards, business reviews, and continuous improvement plans

  • Partner with Quality on supplier audits and qualification (ISO-aligned where applicable)

  • Ensure full compliance with Quality Management System (QMS) requirements including; document control, change control, non-conformance (NCR), CAPA, and supplier quality

  • Embed quality at the source through; in-process QC checks, incoming inspection strategies, final release criteria

  • Drive strong linkage between quality metrics and operational performance

  • Lead root cause analysis (RCA) and implement sustainable corrective actions

  • Establish traceability frameworks (lot tracking, genealogy, cold chain integrity)

  • Serve as the operational bridge between, R&D, quality and regulatory, supply chain, manufacturing, and service/field support

  • Lead reagent readiness for product launches and scale-up phases

  • Provide executive-level visibility into risks, bottlenecks, and mitigation plans

Requirements

  • Deep experience in reagent/process development and scale-up (NGS, proteomics, antibodies, or similar life science products preferred)

  • Strong understanding of process transfer methodologies, DOE / process characterization, manufacturing workflows for biological/chemical reagents

  • Proven experience with contract manufacturing and supplier development

  • Strong working knowledge of quality systems (QMS, CAPA, change control, validation) and GMP-lite / RUO environments (with ability to scale toward regulated environments)

  • Experience implementing in-process controls, QC strategies tied to product performance, traceability systems

  • 10+ years of experience in biotech/diagnostics/manufacturing operations

  • Demonstrated success scaling products from R&D → pilot → commercial manufacturing

  • Strong analytical and data-driven decision-making skills

  • Proven ability to lead cross-functional teams and influence without authority


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