10x Genomics is looking for an outstanding individual to join its Quality Control team. In this role, the individual will be responsible in the inspection of raw material, intermediate, and finished good parts mainly for reagent and consumable but also for instrument parts. A variety of lab techniques will be used to ensure the integrity and quality of our products. This position may require extended periods of sitting or standing and extensive work using laboratory equipment.

This will be a non-exempt position in 10x’s quality control team in Pleasanton, California. Individuals applying to this position should have a basic understanding of industry manufacturing workflow and ERP systems.
Ideal candidates would have the following traits: self-starter, quick learner, team player, and the ability to adapt and thrive in a fast-paced environment.
Title commensurate with educational and prior experience.

What you will be doing:

• 85% of the time shall be performing inspection on raw material, intermediate and finished goods reagent and consumables using standard molecular biology techniques such as Next Generation Sequencing, microscopy, PCR/qPCR and HPLC
• 15% of the time shall be performing inspections on both metal components and electromechanical assemblies, visually and dimensionally, based upon internal and customer supplied workmanship standards and drawing specifications. Areas of inspection will include primarily machining, sheet metal fabrication, paint and welding, but may extend to clean room and final assembly inspection
• Execute QC workflows from submission to batch closure. Follow work instructions and standard operating procedures with the ability to identify discrepancies. Complete QC batch records and Receiving Inspection Reports using Good Documentation Practices
• Assist in root cause investigation and managing non-conforming material
• Identify and communicate any complications that arise from QC testing. Work with engineers/scientists to establish and maintain a solution
• Assist in the development of processes and products. This includes performing product and process optimization, stability studies and validation
• Maintain laboratory to clean room standards required in the production of Life Science products and laboratory management

Minimum Qualifications:

• B.S. in one of the following disciplines: Biological Engineering, Molecular Biology, Analytical Chemistry or Chemical Engineering.
• 2 years relevant laboratory experience in manufacturing, QC or R&D
• Detail oriented, organized, quality focused and self-motivated
• Good communication and observation skills
• Able to multitask and prioritize workload to meet strict deadlines in an evolving environment. Is cool under the pressure and enjoys a challenge
• Strong critical and logical thinking with ability to analyze problems
• Must be flexible as priorities shift with new developments
• Must be flexible in regards to overtime availability and work with minimal supervision.
• Desire to be part of a rapidly evolving organization and taking products and processes to the next level
• Can lift up to 25 lbs

Preferred Skills & Experience:

• Advanced degree preferred
• Experience in Spatial and In Situ technology
• Experience in Next Generation Sequencing technology
• Experience working in GMP environment with LIMS
• Experience with ISO9001,ISO13485, and FDA 21 CFR part 820 Standards