Scientist 1, Microbiology Development

MillenniumSoft Inc

  • San Diego, CA
  • 4 days ago

    Highlights

    Teams of hardworking scientists are responsible for initiating and driving the reagent and assay development projects and integrating assays and flow cytometry instruments to create the next generation of research and clinical Flow Cytometry platforms. We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions.

    Numbers & Facts

    LocationSan Diego, CA

    Description

    Bill Rate ? On site

    We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!

    Our people make all the difference in our success.

    Scientist II, Reagent and Assay Development

    The Reagent & Assay Development Group focuses on providing differentiated reagent solutions that uncover truths in biology and medicine. Teams of hardworking scientists are responsible for initiating and driving the reagent and assay development projects and integrating assays and flow cytometry instruments to create the next generation of research and clinical Flow Cytometry platforms. Products include cell analyzers, cell sorters, reagents, assays and software. The Scientist II is responsible for supporting the sustainment and continuous improvement of reagent and assay products throughout their lifecycle.


    Primary responsibilities:

    Support reagent and assay sustainment projects for marketed products

    Review and approve technical documentation to support reagent and assay products

    Review design history files, validation reports, risk assessments, technical files, and product specifications to ensure completeness and compliance

    Ensure documentation aligns with applicable quality system requirements and regulatory expectations

    Support change control activities and assess the impact of proposed product, process, or documentation changes

    Provide technical support during internal and external audits

    Support preparation of audit readiness activities and ensure technical documentation is inspection-ready

    Partner with Regulatory Affairs, Quality, Marketing, Manufacturing, Medical Affairs and Operation teams to support business objectives

    Minimum Qualifications:

    Minimum of bachelor's degree in Life Science

    Minimum 2 years of related experience in a research setting, clinical/diagnostic laboratory, or pharmaceutical/biotechnology R&D environment

    Strong understanding of immunology, flow cytometry, assay development or related cell-based research technologies

    Experience authoring and reviewing technical documentation

    Demonstrated ability to collaborate effectively across functions

    Excellent written and verbal communication skills

    Desired Qualifications:

    Experience with flow cytometry-based diagnostic products

    Experience supporting regulatory inspections and quality audits

    Familiarity with design controls, risk management, verification/validation, and change control processes

    Strong immunology, cancer biology and cell biology knowledge

    Experience in reagent and assay development

    Experience with product lifecycle management



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