Primary responsibilities include Issuing production batch records, labels, and other controlled documents to support manufacturing operations Responsible for the organization of cGXP controlled document files within the Document Center and ensure that records are readily retrievable and sent off to final archive facility as needed. Assist with managing the Document Center

Review executed batch records to ensure compliance with approved procedures and communicate and resolve discrepancies with manufacturing operators or supervisors. Provide Quality on the floor oversight including quality walk throughs of the production, testing and warehouse locations to ensure practices fully adhere to cGMP. Provides technical knowledge and guidance towar

Job Title Sr. Validation Engineer Job ID 24 01974 Location Seattle, WA About the Role In this position, the Sr. Validation Engineer will be a contributor to both the Electrical and Platform level validation of server platforms. The Sr. Validation Engineer will be working with cross functional teams to aid in developing as well as executing test plans which will verify pro

Job Title QA Associate Specialist – Document Control Job ID 24 02003 Location Seattle, WA, 98109 Duration 12 Months contract on W2 Job Description Top Skills 2+ years of Document Control & Reporting Experience, Veeva experience preferred Technical troubleshooting Self motivated, independent, great communication Experience working cross functionally Position Summary

and Scope of Position This job is part of an organization established to manage our rapidly evolving Cell Therapy business. The Business System Analyst Operational Support will work alongside the Global Business Process Owner (BPO) for Cell Therapy Warehouse & Inventory Management, to support cross site material transfers management, facilitate & drive troubleshooting/issu

The hourly rate for this position is between $76.00 $84.00 per hour.  

Job Title QA Associate Specialist – Document Control Job ID 24 01634 Location Seattle, WA, 98109 Duration 12 Months contract on W2 Top Skills 2+ years of Document Control & Reporting Experience, Veeva experience preferred Technical troubleshooting Self motivated, independent, great communication Experience working cross functionally Position Summary The Quality Assu

The Assistant/Associate Scientist/Engineer to join our Vector and Gene Delivery MS&T group in GDPAD. The successful candidate will design and execute experiments related to supporting commercial vector manufacturing processes. This person will collaborate across all CMC functional areas to insure project advancement, rapid and best in class execution, and communication of

The hourly rate for this position is between $71.00 - $78.00 per hour.