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Immediate opening for Quality Control Associate/Scientist with strong proficiency in developing, optimizing, and validating analytical assays, such as ELISAs, qRT-PCR, or microbiological assays, preferably in a cGMP or QC environment.

The Quality Control Associate/Scientist will have a proven ability to troubleshoot and solve problems with assays both during development and routine work, and extensive experience in several of the following: writing technical reports, validation reports and SOPs, release and stability testing for pharmaceutical products, environmental monitoring, aseptic environment, analytical instrument IQ/OQ/PQ and calibration. The successful candidate will have a PhD in Chemistry, Biology, Biomedical, Pharmaceutical Sciences or related field with 1 – 3 years of work experience, or a Master’s degree with 3+ 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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