Quality Associate II – QA Ops

Job description

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description: About the role: As a Quality Associate II at the Takeda Round Lake aseptic pharmaceutical manufacturing facility, you will work to perform review and approval of released raw material documentation. You will focus on product quality and compliance through Documentation review (Batch records, electronic batch records, etc.), Investigation/Change control approvals and Quality oversight of manufacturing processes. How you will contribute: Responsible for raw material and bulk container receipts, release, and investigation if any issues are found. Follow-up with appropriate Takeda facilities for documentation correction in timely manner. Manufacturing support activities including batch record documentation, issuance of Batch record, approval of OSI PI Reports, scanner card management, management and delivery of test and stabi...