The role will be test record reviews, supporting this function will help to take that load off the team so they can focus on the extra assay work with their Lead being out.
This person will go in the lab to verify data entry, go into the system to verify GMP records. Analysts would submit records to this person to review.
Required:
Bachelor's degree in biology, Chemistry, Life Science, or Engineering is preferred
Must have GMP QC experience within the biotech or pharma industry