Immediate opening for Quality Control Associate with hands on, industry experience in running and validating analytical assays such as HPLC, capillary isoelectric focusing, or capillary electrophoresis, preferably in a cGMP or QC environment.
The Quality Control Associate will have a proven ability to troubleshoot and solve problems with assays both during development and routine work. They should have experience in areas such as writing technical reports, stability testing, environmental monitoring, aseptic environment, and instrument calibration.
The successful candidate will have a Master’s degree in Chemistry, Biology, Biomedical, Pharmaceutical Sciences or related field with 1 – 3 years of work experience, or a Bachelor’s degree with 2 – 4 years of work experience, in pharmaceutical or biotech industry analytical laboratories. Quality Control Laboratory experience in support of GMP/GLP strongly preferred.
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