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3 Nov 2021

Full-Time QC Analyst

Stealth Mode Startup Company – Posted by stealthmodestartup Newark, California, United States

Job Description

High growth, pre-IPO company in stealth mode

Join a rapidly growing company that is developing ground-breaking genomics technologies that will push the boundaries in the clinical, life sciences research and therapeutic fields. We are well-funded by global top-tier investors, including venture capital firms and growth equity investors. Our team brings together unique and diverse expertise across multiple disciplines, from healthcare and life sciences, to engineering, to technology and software and beyond.  We are a collaborative group of more than 200 employees, including successful entrepreneurs, hardware and software engineers, genomics and biotechnology experts, molecular and computational biologists, software and algorithm experts, and operations and commercial leaders. Play an important role in the development and commercialization of technology and products that will accelerate our understanding of life, biology and disease and transform large industries.


We are looking for a highly motivated QC Analyst to join our team!


How You’ll Contribute

  • Follow lab protocols and procedures, and assist in optimizing workflows
    • Manage shared laboratory equipment, perform required instrument calibrations as needed and support instrument maintenance
    • Maintain accurate and thorough batch records and ensure quality control data is accounted for manufactured goods and materials
    • Perform quality control assays of buffers, reagents and finished goods
    • Ensure quality control testing performed by internal or external vendors is on track to meet production deadlines
    • Assist in defining specifications for quality control testing performed
    • Track and trend quality control data to assess changes in products
    • Monitor, track and maintain inventory of raw materials and lab consumables
    • Work closely with Chemistry and Biochemistry R&D to develop necessary quality control assays to ensure production of quality finished goods 


Qualifications, Skills, Knowledge & Abilities

  • BS in chemistry, biochemistry, biology, bioengineering, or closely related field
  • 1-2 years experience working in a laboratory environment, preferably in a quality control environment
  • Exceptional micro-pipetting required
  • Familiarity with GDP, GMP and GLP
  • Working knowledge of UV Spectrophotometers, plate readers, pH and Conductivity meters
  • Basic wet lab skills – weighing, measuring, pH, mixing, using balances, serological pipettes
  • Meticulous and detail-oriented, ability to follow complex operating procedures (SOPs) with reproducible results and thorough documentation of work
  • Excellent organizational, communication and time management skills
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint) required, inventory management software and LIMS familiarity a plus
  • Motivated and willing to work in a fast-paced environment as part of a hard-working and multidisciplinary team

Job Categories: Equal Opportunities. Job Types: Full-Time.

Job expires in 14 days.

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