Quality Control Associate

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.

Download the full job description here.

Quality Control Associate/Scientist

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.

Download the full job description here.