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The Process Engineer for MS&T supports technology transfer and ensures successful execution of biologic processes, authoring documentation and improving processes for manufacturing operations.

The Project Manager leads CDMO client projects throughout the product lifecycle, ensuring customer satisfaction and compliance with quality standards while managing relationships and project timelines.

The Manager of QA Operations leads a team ensuring compliance with cGMP and QMS requirements, manages client relationships, and drives continuous improvement initiatives.

The Director of Human Resources will manage HR strategy, employee relations, talent development, compensation, and HR operations across multiple sites.

The Senior EHS Specialist ensures regulatory compliance and oversees EHS programs, including audits and investigations to promote employee health and safety.

The Procurement Manager will lead indirect and capital procurement, negotiating contracts, managing supplier performance, and implementing savings strategies to optimize costs.

The Statistician will support biologics process and analytical method development through statistical analysis, study designs, and communicating data-driven decisions to improve manufacturing processes.

The role focuses on ensuring the compliance and effectiveness of Supplier and Material Quality Assurance programs, conducting audits, managing documentation, and collaborating on quality agreements. Training and oversight of quality systems are also involved.

The Supervisor of Quality Control in Data Review oversees performance tracking, implements action plans, ensures compliance, and collaborates with departments to support product release and employee development.

The Senior Director of Manufacturing leads cGMP production, ensuring quality and cost-effectiveness while managing staff and compliance with regulations. This role oversees manufacturing operations and develops strategies aligned with site objectives.