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Process Engineer II, Assay Automation - Menlo Park, United States - GRAIL, Inc.
Description
GRAIL is seeking a Process Engineer II to join the Global Development & Operations department in Menlo Park, CA to transfer a high throughput DNA processing assay for a Laboratory Developed Test.
In this position, the candidate will work closely with Assay Development, Reagent Development, Operations, Equipment, and Software teams as we develop operational and maintenance procedures and processes for a groundbreaking, high-throughput laboratory.
Candidates would ideally have hands-on experience in process development and documentation within a regulated environment.This is an on-site role and requires you to be onsite 5 days a week in Menlo Park, CA Responsibilities:Assist in building out our state-of-the-art sample processing platform and develop the necessary loading, usage, and maintenance procedures to support the system for continuous operationCollaborate with Development teams in evaluating early-stage products and processesAnalyze data from various sources to update platform capacity models and simulate system throughputHelp the team balance operator efficiency, cost of goods, and maximize system uptime while upholding safety and compliance standardsDevelop and maintain user manuals, process flow charts, Standard Operating Procedures (SOPs), and work instructions around your developed methodsGather Critical Process Parameters (CCPs) and Critical Quality Attributes (CQAs) to support the development of equipment for GRAILs new companion and pharmaceutical diagnostics productsWork within multi-functional teams to transfer processes and equipment from Research and Development into Laboratory and Operations teamsCollaborate with other departments to define GRAILs assay specifications, drive equipment requirements, and develop test methods for asset qualificationProvide technical support during integration testing and contribute to troubleshooting effortsOccasionally provide off-shift or weekend coverage to support technical team activities during development and validation phases
Preferred Qualifications:
BS (MS preferred) in an Engineering or Life Sciences Field3+ years of experience in manufacturing operational development, or supportProven track record in writing and executing SOP's, Work Instructions, and Test ProtocolsExperience in creating and interpreting process and material flow diagramsFamiliarity with transferring prototypes and concepts from R&D into operational environmentsExpertise in manufacturing or automation of clinical diagnostics, medical devices, or equivalent technologiesStrong background in liquid handling equipment such as Agilent, Hamilton, Beckman, Dynamic Devices, etc.
Knowledge of molecular biology to support equipment activities in a Next-Generation Sequencing (NGS) workflowHands-on experience in qualifying equipment within a high-throughput clinical laboratory settingApplied knowledge of root cause analysis and troubleshooting techniquesExperience supporting commercial products and working cross-functionally across departments to capture system requirements and specifications Ability to take initiative and independently drive projects to completion with detailed and efficient execution and reportingWillingness to travel up to 10% of the time to our facility in North CarolinaPhysical Demands and Working EnvironmentHours and days may vary depending on operational needs.
Standing or sitting for long periods of time may be necessary.May be exposed to hazardous materials, blood specimens and instruments with moving parts, heating or freezing elements, and high speed centrifugation.
The estimated, full-time, annual base pay scale for this position is $90,000 - $107,000. Actual base pay will consider skills, experience, and location.