Quality Control Specialist

To support a biopharmaceutical client, the remote Quality Control Specialist will write, review, and execute documentation for validation procedures, conduct quality control analyses, and ensure compliance with regulatory standards over a 12-month contract period. Key responsibilities Write and approve documentation for validation procedures and technical reports Conduct quality control analyses of testing results and process anomalies Verify calibration and maintenance of instruments to support the Quality Systems validation program Required qualifications Bachelor's Degree in Sciences or Engineering or equivalent experience 0-3 years of related quality/validation experience in pharmaceutical manufacturing In-depth knowledge of cGMP principles and applications Demonstrated ability to write and approve technical documents ASQ Certification preferred