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The Zone Operations Manager oversees the manufacturing team to ensure quality and timely production of pharmaceutical products. They manage technician allocation, ensure compliance with cGMP standards, troubleshoot operational issues, and coordinate with other departments. The role requires effective leadership, performance evaluation, and training execution.

The Senior Project Engineer will manage engineering projects in a regulated FDA environment, overseeing project scheduling, documentation, and communication between departments. Responsibilities include preparing project reports, managing invoices, coordinating timelines, and ensuring project scopes are adhered to. The role involves collaboration with engineering SMEs and stakeholders to meet business goals while maintaining project governance standards.

The Sr. Specialist, QA OTF is responsible for providing quality assurance support for GMP manufacturing operations, ensuring compliance with regulatory standards and quality improvements. Primary duties include on-floor oversight, documentation review, AQL inspection, audits, and guiding personnel in cGMP operations.