QUALITY CONTROL ANALYST Argos Therapeutics
ARGOS IS GROWING!
After having met several important milestones including exciting clinical data, we are poised for new strategic objectives which will require significant new resources. Those new resources include well-qualified Quality Control Analysts.
The individual will conduct routine and non-routine analysis of raw materials, in process, and finished formulations according to standard test methods. The individual may also assist in the qualification or validation of in-process and release assays utilized in Quality Control and assist in preparing necessary documentation. All activities will be performed in a cGMP compliant environment.
? Responsible for conducting routine and non-routine analysis of raw materials, in process, and finished formulations according to standard test methods. Test methods include gel electrophoresis, spectrophotometry, immunophenotyping, and Northern blot analysis.
? Compiles data for technical reports.
? Writes and updates standard test methods as needed.
? Participate in assay validation/qualification.
? Strive to improve assays for better efficiency and consistent results.
? Report any lab result that is out of specification
? Apply knowledge of cGMP on a daily basis.
? Perform other duties as required.
? BS degree in Molecular Biology, Cell Biology, or Biochemistry with 2 - 5 years- experience in biotech/pharmaceutical industry with experience in Quality Control and/or Quality Assurance preferred.
? Prefer experience in molecular biology.
? Must have strong computer skills.
? Must be able to communicate effectively with co-workers.
? Must have initiative, high attention to detail, and the ability to multi-task.
? Ability and willingness to be regularly, predictably, and reliably at work.
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