QA Review Support Specialist

Responsibilities:Review cleaning verification and validation protocols, reports, and analytical data for accuracy, completeness, and compliance with SOPs and cGMP requirementsEnsure acceptance criteria, limits, and test methods meet validation requirementsVerify calculations, data integrity, and consistency across documentationEnsure cleaning validation documentation complies with internal and regulatory standardsIdentify, document, and support the investigation of deviations and nonconformancesCollaborate closely with Validation, QA, and Manufacturing teams to ensure timely review and approval of documentationContribute to continuous improvement initiatives for cleaning verification and validation processesQualifications:Bachelor’s degree in a scientific discipline (e.g., Chemistry, Microbiology, Engineering, or related field)2+ years of experience in a GMP-regulated environment (pharmaceutical, biotech, or medical device industry preferred)Experience with cleaning verification/validation or QA documentation review required