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  • ID
    #7260378
  • Job type
    Contract
  • Salary
    USD $Based on Experience Based on Experience
  • Source
    Stellar Consulting Solutions
  • Date
    2020-12-23
  • Deadline
    2021-02-21

Stellar Consulting Solutions is a boutique business & technology consulting company headquartered in Atlanta, GA. We deliver high quality, agile, and experienced workforce for niche technology projects of any scale. We help forward thinking clients to solve specific problems by understanding their needs and align talent that can move fluidly to match skill supply and demand on a real-time basis. Stellar Consulting has a unique combination of technical and digital skills to recruit, engage, and retain qualified talent. We have a stellar reputation for striving to achieve high ethical standards. Our use of Innovative techniques and industry best practices has made us one of the fastest growing boutique firms delivering to enterprise business. Role: Validation Engineer Location: San Jose, CA Description: Responsible for performing process, equipment, and software validation activities including, but not limited to, gathering historical data for product manufacture, analyzing data using statistical principles, writing validation protocols and reports, GDP review of data and reports, and final approval of validation protocols, reports, and deviations. May interact in cross-functional teams including Reagent Manufacturing Engineers and Chemists, Research and Development, and Quality Assurance Validation Engineers. May be responsible for leading teams to perform validation activities or perform as a member of the team. Will simultaneously work on multiple projects. Knowledge of general reagent manufacturing processes, antibody purification and conjugation, and flow cytometry, is preferred. Process, Test Method, Equipment, and Software Validations used in IVD product manufacture (IQ, OQ, PQ) Acts as Quality Assurance reviewer/approver or author for validation protocols, reports, and deviations. Provides and applies quality engineering direction to projects using quality engineering and statistical principles

  • Root Cause Analysis
  • FMEA
  • Risk Management and Mitigation
  • DOE
  • Measurement Systems Analysis
  • Sampling and Control Plans
  • Post Market Surveillance Trend Review
  • Process Capability
  • Provides and applies scientific technical principles/concepts Follows company procedures Demonstrates working knowledge and application of applicable regulatory requirements Other duties as assigned. Requirements: Education: bachelor's degree Experience (preferred): Experience in a quality related function in a medical device or other FDA regulated environment. Previous work with IVD reagent products under GMP conditions Process validation (IQ, OQ, PQ) and test method validation experience Software validation experience Knowledge of general reagent manufacturing processes, antibody purification and conjugation, flow cytometry Certified Quality Engineer Six Sigma Certification Knowledge of applicable regulatory requirements including ISO13485, ISO14971, ISO9001, quality systems regulations (21 CFR: 820) Training in statistics. Experience with Minitab or other statistical software, MS Excel, and MS Word required Regards Vineet Tripathi

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