This position will support the organization of the QC Biochemistry laboratory at the Flu Cell Culture facility in Holly Springs, NC.
Primary responsibilities for this position include method development and validation for biochemistry assays (protein content determination by BCA, SDS-PAGE, ELISA, and UV/Vis spectrometry).
Perform and assist in the method development and validation Author SOPs, protocols and technical reports
Perform laboratory testing associated with development studies
Conduct data analysis and troubleshooting
Maintain accurate and traceable laboratory notebooks
Complete documentation in compliance with cGMPs
Complete training as required.
Support training of other analysts as necessary.
3+ years of related experience in a pharmaceutical or biotechnology
Experience working in a cGMP environment preferred but not required
Self-starter, results-oriented individual with the ability to organize and analyze data
Experienced with method development and validation
Strong technical knowledge of analytical / bio analytical methods and related instrumentation (BCA, SDS-PAGE, ELISA and UV/Vis spectrometry, microplate reader)
Strong technical writing skills Strong computer skills (MS Word, Excel, Powerpoint,)
BS Degree is sciences, preferably biology or chemistry, or other related scientific field
NO sponsorship, NO relocation. US based candidates only, please
Qualified candidates, please send current Word resume to: email@example.com for immediate consideration
- 15 months ago - save job