10x Genomics is seeking a detail-oriented individual to join our Quality Control team. This role will bridge the gap between traditional laboratory quality control and modern data automation. As a QC Associate, you will be responsible for testing and inspection, as well as supporting automation of data workflows and analysis. If you have strong laboratory fundamentals and practical background in python or other scripting experience, you would be a great fit for the team.

Key Responsibilities

• Laboratory Execution: Follow ISO standard to conduct QC testing on raw materials, intermediates, and finished products using metrology check, PCR, NGS, and HPLC.
• Process Automation: Use Python and AI tools (Claude) to help write and maintain scripts that streamline QC inspections, data collection, and analysis.
• Quality Assurance: Initiate and follow up on nonconformance, support new product launches and investigations.
• Data Management Work with the team to identify metrics, and help build and maintain real-time data visualizations using Streamlit and Retool. 

Minimum Qualifications

• Major/Education: B.S. or M.S. in Biological Engineering, Bioinformatics, Data Science, or a related Life Science discipline. 
• Laboratory Experience: 1 year of experience in a manufacturing or QC environment (NGS or PCR experience preferred). 
• Python: Essential  for building Streamlit apps, managing Claude/AI API integrations.

Preferred Skills

• Experience with Git/GitHub for version control of scripts.
• SQL: Useful for manipulating and extracting data in Snowflake
• Snowflake: Knowledge and experience with cloud data warehousing and data architecture.
• Experience building dashboards for data automation/monitoring.
• Basic knowledge of Statistics for quality control. 
• Prompt Engineering: Capability to use Claude for complex reasoning and workflow automation.
• Prior experience in a manufacturing setting utilizing production control tools like ERP or LIMS.

#LI-onsite #LI-ES1

10x Genomics is looking for a Production Technician to join its consumable manufacturing team. In this role, the individual will be responsible for 10x consumables product – handling of automated equipment and manual packaging of finished goods. This individual will also work with the manufacturing engineering team on the maintenance and simple troubleshooting of some of the manufacturing equipment.  This position may require extended periods of sitting or standing and extensive work using laboratory and packaging equipment.

This will be a temp/contract position in the 10x manufacturing team. Individuals applying to this position should have a basic understanding of good manufacturing practices. This individual must be a self-starter, quick learner and detail oriented, work well in a team atmosphere, have good communication skills, ability to adapt and thrive in working at a fast-paced environment.

What you will be doing:

• Execute production operations according to defined procedures and ensure the integrity and quality of our products
• Ability to operate and maintain laboratory to clean room standards required in the production of Life Science products
• Process work orders accurately using an ERP system in a timely manner
• Maintenance of production batch records and good documentation under ISO requirement
• Accurate tracking of production data, test data and inventory
• Assembly of 10x consumables and finished goods both manually and using semi-automated packaging equipment
• Ability to set up and operate packaging equipment and handle simple troubleshooting
• Perform preventive maintenance on some lab equipment
• Provide feedback to improve process quality and efficiency
• Identify issues occurring in production labs and escalate issues to supervisor’s or MSE’s attention

Minimum Requirements:

• High school education / Associate Degree or above
• Strong team player and detail oriented
• Good communication skills
• Ability to read and understand SOPs and equipment user manual
• Ability to enter data into electronic tracking systems like Excel
• Ability to multi-task and prioritize work load to meet strict deadlines under supervision
• Good documentation skills and ability to write procedures and reports
• Desire to be part of a rapidly evolving organization and taking products and processes to the next level
• Ability to lift up to 15 pounds and potentially stand or sit for up to 3 hour increments

Preferred Skills and Experience:

• Experience in automation and packaging of Life Science products, Food Packaging products or related field preferred
• Relevant experience in a production environment working with standard production control tools – ERP, inventory control, and work orders
• Experience training employees on production processes defined in production batch records and work instructions
• Experience writing and revising work instructions and production batch records
• Experienced in communicating and collaborating with production departments

#LI-MH1 #on-site

About the role: 

10x Genomics is looking for a Temporary Production Planner to join the Planning team. The ideal candidate is expected to Plan, schedule, and coordinate products through the production cycle. Manages production plans to ensure material availability. Interfaces with procurement, logistics, manufacturing, and quality control to review supply vs demand, prioritize production orders, and manage potential schedule interruptions or rescheduling. Works to resolve labor and material shortages.

What you will be doing:

• Plan and create production orders for components and assemblies considering demand and lead times to optimize stock levels across the global network.
• Generate MRP and coordinate with Procurement to secure materials for production orders, plus manage inventory including safety stock and shelf life.
• Interface with Logistics regarding material receipt and movement, with Manufacturing concerning scheduling and capacity, and with Quality for Quality Control coordination.
• Communicate regularly with cross functional partners, such as Commercial and Finance to make inventory decisions based on trends, inventory targets, and customer order fill rates.
• Plan and coordinate balanced inventory levels by Distribution Center.
• Establish and track KPIs such as Backorder, On Time Request, WO Shortage.
• MRP master data maintenance including lead time, lot size, stocking levels.

Minimum Requirements:

• Bachelor’s degree in Supply Chain, Industrial Engineering, or a related field
• 5+ years of Planning experience
• Proficient in using MRP for supply chain and inventory planning
• Experience with Production Planning, Item Master Data (Bills of Material, Routing, lead time, lot size, safety stock), and Capacity Planning
• Effective team player with strong interpersonal and collaboration skills
• Sense of urgency regarding objectives and timelines, while maintaining flexibility to shifting priorities
• Must have the ability to prepare and deliver effective presentations. Strong organizational, communication and reporting skills

Preferred Skills and Qualifications:

• Experience in ERP systems, Oracle Cloud preferred
• APICS certification desirable

#LI-MH1 #On-Site 

About the Role

10x Genomics is establishing its first CLIA/CAP-certified laboratory to bring cutting-edge single-cell and spatial genomic technologies into clinical practice. Reporting to the Head of Quality and Regulatory, the Quality Assurance Manager will play a pivotal role in defining, developing and implementing the lab’s quality infrastructure, ensuring compliance with CLIA, CAP, and state (including California and New York) requirements. This is a hands-on leadership role suited for a quality professional who can independently execute quality assurance (QA) responsibilities during the lab’s early buildout phase and later lead a small QA team as clinical operations scale. The ideal candidate combines deep knowledge of clinical laboratory quality systems with practical, solution-oriented execution in a fast-paced and collaborative environment.

What you will be Doing:

Clinical Quality Framework Establishment and Oversight

• Implement document control, deviation/CAPA systems, training programs, and internal audit processes compliant with CLIA, CAP, and applicable state and federal regulations.
• Collaborate closely with CLIA and assay development teams to develop and manage SOPs and work instructions
• Partner with the broader Quality/Regulatory team to  integrate the CLIA lab’s quality infrastructure into 10x’s enterprise-wide quality management system (QMS).
• Establish and track key quality metrics for laboratory operations (e.g., deviations, nonconformances, complaint handling, audit findings, proficiency testing).
• In partnership with CLIA Lab Director, ensure inspection readiness and execute regulatory submissions (CLIA, CAP, and state licensure).

Operational Quality Support

• Provide day-to-day quality oversight of clinical laboratory operations, including review and approval of validation plans, QC data, and reports.
• Serve as QA reviewer/approver for method validation, verification, and change control documentation for both laboratory methods and assay software components
• Ensure effective management of reagents, instruments, and workflow changes per CLIA/CAP requirements.
• Support onboarding and verification of LDTs transferred from Diagnostic Assay Development teams
• Act as quality liaison with external auditors and partners.

Team Leadership and Growth

• Initially serve as an individual contributor responsible for implementing and maintaining quality processes.
• As sample volume and operations expand, recruit, train, and manage a small team of QA specialists or analysts supporting lab quality activities.
• Foster a culture of compliance, continuous improvement, and scientific rigor.

Cross-Functional Collaboration

• Partner closely with Laboratory Operations, Diagnostic Assay Development, Clinical Bioinformatics, and IT teams to ensure compliant workflows and data integrity.
• Work with Quality and Regulatory leadership to align CLIA/CAP quality practices with 10x’s broader corporate systems and standards.
• Contribute to strategic planning for quality-related resources, tools, and training across diagnostic programs.

To be successful, you will Need:

• Bachelor’s or Master’s degree in Life Sciences, Medical Laboratory Science, Quality Management, or related field.
• 10+ years of experience in quality assurance within a regulated clinical laboratory (CLIA/CAP environment).
• Demonstrated experience building or expanding quality systems in a CLIA lab setting.
• Strong working knowledge of CLIA / CAP quality and documentation requirements
• Additional knowledge of  FDA 21 CFR Part 820 and ISO 13485 strongly preferred.
• Experience preparing for and leading CAP inspections and CLIA audits.
• Excellent written and verbal communication skills, with an ability to collaborate across scientific, operational, and regulatory functions.
• Hands-on, proactive, and adaptable, capable of working effectively in an early-stage, fast-growing diagnostic environment.
• Experience with LIMS, electronic QMS tools, and training management systems is required.

It would be advantageous if you Have:

• A Builder mentality – motivated by creating compliant, fit-for-purpose systems from the ground up.
• Hands-on and detail-oriented, with strong follow-through and accountability.
• Collaborative and pragmatic, balancing regulatory rigor with operational needs.
• Leadership-ready, with the ability to grow into managing a small, high-performing team.
• Mission-driven, passionate about enabling genomic technologies to transform patient care.

Impact:

The Quality Assurance Manager - CLIA/CAP Laboratory, will be instrumental in establishing 10x Genomics’ diagnostic quality foundation. This role ensures that every assay and clinical result produced under the CLIA/CAP framework meets the highest standards of accuracy, reliability, and compliance—paving the way for 10x to deliver transformative precision medicine insights.