Clinical Research Quality Control Associate Jobs in Ohio

Maintain compliance with applicable ICH, GLP, GMP and safety regulations. Notify management of unexpected results, procedural deviations and equipment problems.

Record data per GxP requirements. Provide peer review of documentation as needed.

At least 1 year of experience in GMP pharmaceutical environment.

Senior Manager Quality Control, Biologics CMC

Perform sampling, testing and release of raw materials and in process testing.

Perform testing as per current approved test method and maintain accurate laboratory records and adhere to cGMP/GDP expectations.