The Senior Process Specialist supports pharmaceutical manufacturing by standardizing processes, leading continuous improvements, coaching teams, and ensuring adherence to cGMP standards.

Responsible for QA activities supporting operations and external quality systems, including document approval, batch release, and regulatory compliance. Collaborate with teams for continuous improvement and training of junior QA members.

The Senior Manager of Infrastructure oversees the architecture, implementation, and maintenance of operational IT infrastructure, ensuring regulatory compliance and continuity.

The L3 Systems Engineer is responsible for designing, implementing, and managing identity and endpoint systems, ensuring security and compliance while collaborating with multiple teams on platform enhancements.

The Manufacturing Systems Engineer will lead manufacturing systems implementation, focusing on design, configuration, automation, and integration within the biomanufacturing environment.

The Specialist II in Supply Chain manages logistics for temperature-controlled shipments, oversees export compliance, and improves delivery performance. Responsibilities include scheduling, monitoring, and SOP development for shipping operations.

The Quality Control Systems Engineer oversees LabVantage LIMS, leading enhancements and validations, ensuring compliance and effective system operations in a regulated environment.

The Automation Specialist will provide technical automation support for manufacturing operations, oversee automation systems, manage projects, and ensure compliance with cGMP.

The Specialist II, QC Systems coordinates sample management, lab instrument maintenance, and supports QC Chemistry and Microbiology, ensuring compliance and improving processes.

The Process Engineer II is responsible for executing technical aspects of technology transfer, process validation, continuous improvement, and supporting manufacturing operations in a biomanufacturing environment.