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Quality Assurance Coordinator - Life sciences - biotechnology

Company: BioIVT
Location: Santa Clara
Posted on: January 10, 2022

Job Description:

This position supports work completed in our Santa Clara, California location. The preferred candidate will work out of the Santa Clara, California office. We will consider candidates working remotely from one of BioIVT's offices across the US.BioIVT, formerly BioreclamationIVT, is a leading global provider of high-quality biological specimens and value-added services. We specialize in control and disease state samples including human and animal tissues, cell products, blood, and other biofluids. Our unmatched portfolio of clinical specimens directly supports precision medicine research and the effort to improve patient outcomes by coupling comprehensive clinical data with donor samples.Our Research Services team works collaboratively with clients to provide in vitro hepatic modeling solutions. And as the world's premier supplier of ADME-Tox model systems, including hepatocytes and subcellular fractions, BioIVT enables scientists to better understand the pharmacokinetics and drug metabolism of newly discovered compounds and their effects on disease processes. By combining our technical expertise, exceptional customer service, and unparalleled access to biological specimens, BioIVT serves the research community as a trusted partner in ELEVATING SCIENCE -ResponsibilitiesWe are currently looking for a talented, detail-oriented, associate to fill an opening in our transporter assay service group.

  • Perform QC reviews on multiple customer studies, of study proposals, study protocols, data analyses, study summaries, and reports
  • Train and understand in vitro cell-based studies and assays
  • Check, compare, and analyze data generated in Excel and GraphPad Prism
  • Quickly and timely communicate feedback to team members
  • Ability to manage the QC review of multiple projects simultaneously to meet internal and external deadlines
  • Meticulous attention to detail in finding errors, correcting, and defining solutions
  • QC documents for clients that will comply with regulatory guidelines
  • Perform general lab responsibilities as needed, logging of client compounds, compound preparation, creating buffers and solutions, performing serial dilutions, monitoring equipment, and maintaining inventories of lab supplies
  • Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, following and modifying SOPs
  • Ideally, the candidate will demonstrate high proficiency across a wide range of in vitro ADME-Tox technologies and be capable of keeping current with emerging literature in the transporter, ADME, and DMPK fields
  • Working knowledge of drug Toxicity or transporter sciences, and being capable of performing or reviewing assays in cell lines or hepatocytes is desirable Attributes
    • Excellent written and verbal communication skills
    • Ability to effectively present information to internal staff members
    • Self-motivated,
    • Collaborative in a fast-paced team environment
    • Able to cope with the pressure and meet the needs of a dynamic and rapidly growing companyPosition Requirements
      • Bachelor's in Biochemistry, Pharmacology, or related field or and at least 2 years industry experience or equivalent combination of advanced degree and experience
      • Related experience in the contract research or pharmaceutical industry
      • Oral and written communication skills
      • Meticulous attention to detail, able to troubleshoot
      • Strong organizational skills, ability to manage numerous projects simultaneously
      • Capable of organizing and presenting scientific data analysis, formulating conclusions and executing experiments.
      • Experience in a biotech/pharmaceutical and/or academic research setting, with strong experience in facilitating research program development and management of research resources is preferred
      • Experience using purchasing software a plus (ERP, SAP, Oracle, Sage, Infor) PHYSICAL DEMANDS:
        • The role will require extended periods of computer work for data analysis and reporting
        • Ability to work in a fast-paced environment and meet time and quality-based objectives WORKING CONDITIONS:
          • Able to occasionally work outside of normal business hours when required for client calls
            The Company is an AA/EEO/Veterans/Disabled Employer

Keywords: BioIVT, Santa Clara , Quality Assurance Coordinator - Life sciences - biotechnology, Other , Santa Clara, California

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