Engage in quality oversight to promote compliance in manufacturing and testing operations, ensuring adherence to cGMP and regulatory guidelines. Collaborate with cross-functional teams to enhance quality systems in a fast-paced environment.

Join a team that drives cGMP manufacturing excellence, ensuring the readiness and production of biopharma products through collaborative efforts in documentation, aseptic operations, and continuous improvement in a dynamic environment.

Drive the development and assessment of single-use disposable materials in collaboration with cross-functional teams. Serve as an expert in material compatibility, lead risk assessments, and innovate process improvements in manufacturing operations.

Engage in cross-functional support for GxP activities, leading eQMS optimization and quality process improvement initiatives to ensure compliance and inspection readiness. Become a subject matter expert in Veeva Quality applications and governance.

Shape quality assurance practices by supporting GMP compliance and enhancing your expertise in a dynamic environment. Collaborate cross-functionally, manage records, and prepare for inspections to ensure product readiness and quality standards are met.