The Senior Associate in Upstream MSAT will act as a technical expert in upstream process manufacturing for biopharmaceuticals, focusing on process design, GMP documentation, and equipment qualification. Responsibilities include leading manufacturing projects, troubleshooting processes, and supporting continuous improvement initiatives while ensuring compliance with industry standards.

The Senior Specialist II, QA Operations focuses on sterility assurance, microbial control, and ensuring GMP compliance. Responsibilities include managing contamination control strategies, supporting microbiology deviations, leading risk assessments, auditing production activities, and training staff on quality programs. The role serves as the microbial control technical leader and interfaces with clients to uphold regulatory standards.