Analytical Development Scientist, QC & Assay Expert

Aspect Biosystems

Fremont (CA)

On-site

USD 86,000 - 102,000

Full time

14 days+
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Job summary

Aspect Biosystems, a biotechnology company in Fremont, CA, is seeking an enthusiastic Scientist for the Quality Control & Analytical Development team. You will be a subject matter expert in cell-based analytical methods and support the development, optimization, and qualification of assays for bioprinted tissue therapeutics.

You will lead end-to-end development of ddPCR, qPCR, and flow cytometry assays, perform ELISAs and cell-based tests, and ensure regulatory compliance and data integrity

Qualifications

  • Bachelor's or Master's degree in a relevant scientific discipline with 3+ years of analytical development experience in biotech/pharma.
  • Hands-on experience with flow cytometry, ELISA, and cell-based assays.
  • Familiarity with GLP/GMP and regulatory expectations for biologics/advanced therapies.
  • Strong problem-solving and data interpretation skills.
  • Willingness to learn and improve analytical processes.

Responsibilities

  • Lead end-to-end development and optimization of analytical methods (ddPCR, qPCR, flow cytometry).
  • Perform cell-based assays and ELISAs ensuring precision, scalability, and regulatory compliance.
  • Design experiments to support product characterization and process understanding.
  • Qualify and validate analytical methods with documentation and SOPs.
  • Maintain and calibrate analytical instruments and ensure data integrity.

Skills

Flow cytometry
ELISA
Cell-based assays
Analytical development
GxP familiarity

Education

Bachelor's or Master's in a relevant scientific discipline

Tools

ddPCR
qPCR

Job description

Aspect Biosystems, a biotechnology company in Fremont, CA, is seeking an enthusiastic Scientist for the Quality Control & Analytical Development team. You will be a subject matter expert in cell-based analytical methods and support the development, optimization, and qualification of assays for bioprinted tissue therapeutics.

You will lead end-to-end development of ddPCR, qPCR, and flow cytometry assays, perform ELISAs and cell-based tests, and ensure regulatory compliance and data integrity

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