N

Nautilus Biotechnology

Proteomics platform for drug target prioritization

Manager, Reagent Manufacturing

Bioprocess & BiomanufacturingPosted on Nov 9
Full-timeSan Carlos, CA, USA$111k - $162k /yr

About the Job

Requirements

  • A BS or MS in Biochemistry, Molecular Biology, Chemistry, or a related field is required.
  • At least 5–7 years of hands-on experience in reagent production or life science reagent manufacturing, or at least 4 years with an MS, including experience leading or training others as a team lead, shift lead, or supervisor.
  • Experience training and coaching technical staff, with an interest in growing as a people manager.
  • Hands-on experience with bioconjugation chemistries and protein purification and characterization, including HPLC, TFF, SEC, PAGE, or ELISA.
  • A proven track record authoring and reviewing batch records, SOPs, and test procedures in a regulated or quality-driven environment.
  • Experience leading troubleshooting, root cause analysis, quality investigations, and CAPA.
  • Experience scheduling production and managing team workload against shifting priorities.
  • Strong data analysis skills and proficiency with Excel and statistical tools such as JMP, R, or similar.
  • Ability to use data and judgment to make decisions, recognize when to escalate ambiguous or complex situations, and manage multiple priorities as business needs change.
  • Written and verbal communication skills to give clear, specific feedback and present technical information to peers and cross-functional groups clearly.

Responsibilities

  • Supervise reagent manufacturing associates and specialists by setting expectations, holding the team accountable, giving regular feedback and coaching, supporting development, and partnering with the manager on hiring and performance reviews.
  • Translate department and company goals into team goals with the manager and regularly track progress against them.
  • Plan and assign daily and weekly production work across the team, balancing build schedules, staffing, and equipment availability to meet commercial and internal demand.
  • Train team members on bioconjugation processes, SOPs, equipment, and good manufacturing practices; maintain training records and ensure staff are qualified on the processes they run.
  • Foster a safe, quality-first team culture and ensure the team follows EHS requirements, good documentation practices, and clean room procedures.
  • Plan and execute manufacturing builds for antibody and protein bioconjugated complex formulations and buffers used on the platform, and handle the most complex or time-critical builds hands-on in the lab.
  • Own reagent processes from technology transfer out of R&D through pilot lots, scale-up, and routine production.
  • Lead scale-up and process optimization projects, break complex problems into manageable workstreams, delegate across the team, and drive projects to completion on schedule.
  • Set up, run, and troubleshoot bioconjugation reactions and associated purification steps, including HPLC, TFF, and filtration, and coach team members through troubleshooting.
  • Author Master Batch Records, SOPs, Standard Test Procedures, and work instructions; review and approve team documentation and executed batch records for accuracy and completeness.
  • Partner with R&D and QC to define and refine in-process and release specifications, analytical and functional tests, and acceptance criteria for raw materials and finished reagents.
  • Lead investigations of failed or out-of-specification builds, perform root cause analysis, assign corrective and preventive actions, and track them to closure.
  • Ensure production equipment, including liquid handlers and other automation, is qualified, validated, maintained, and troubleshot.
  • Drive continuous improvement using lean and 5S principles, and maintain records and the clean room environment in compliance with good manufacturing practices.
  • Oversee reagent inventory, material planning, and ordering using ERP/LIMS systems to prevent supply interruptions.
  • Use production data and metrics such as on-time delivery, right-first-time builds, and deviations to drive team decisions; report status and recommendations to the manager, R&D, and Applications teams; recommend changes to team procedures and processes.

Desired Qualifications

  • Experience with proteins, antibodies, DNA, and/or bioconjugates.
  • Working knowledge of ISO 13485 and good manufacturing practice standards.
  • Prior experience as a formal people manager or supervisor in a manufacturing environment.
  • Experience with ERP, PLM, and LIMS systems.
  • Experience supporting technology transfer to contract manufacturers.
  • Strong understanding of lean manufacturing and 5S principles.

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

Recently Posted Jobs

Explore more opportunities at Nautilus Biotechnology

See more jobs