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The Sr. Manager of MES Operations will lead and manage technical guidance for the IT manufacturing systems team. Responsibilities include executing digital strategy for MES solutions, adhering to GMP regulations, managing resources, ensuring compliance with system lifecycle processes, and addressing issues effectively while communicating across all levels of management.

The Supervisor/Sr. Supervisor in Manufacturing leads teams in upstream and downstream processing of biopharmaceutical products, ensuring compliance with safety and quality standards. Responsibilities include planning and monitoring production tasks, reviewing batch documentation, training staff, and driving continuous process improvements.

The Process Development Associate I supports laboratory studies, executes lab work, documents and reports results, and authors operational documents. The role requires a basic understanding of Process Development methods, technical writing skills, and the ability to perform experiments from instructions. Responsibilities include evaluating new technologies, maintaining training compliance, and participating in process development meetings.