The QA Compliance Associate I supports product release by reviewing manufacturing batch records to ensure compliance with SOPs, cGMPs, FDA, and global regulations.
They compile, review, and maintain batch records, perform QA reviews, investigate deviations, and collaborate with departments to correct errors. The role involves managing record documentation, supporting timely product release, and prioritizing workload.
Required skills include knowledge of cGMPs, attention to detail, strong communication, troubleshooting, and proficiency with MS Office.
Qualifications include a high school diploma, three or more years of QA experience in pharma or medical devices, and the ability to work independently.
This temporary position offers $25/hour, Monday-Friday, 6:00am-2:30pm, with benefits limited due to its duration. The role emphasizes core values like integrity, accountability, continuous improvement, and a people-centered approach.