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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 -
Responsibilities We 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 company
Position 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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