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The Associate Director, CMC Development leads CMC projects, ensures operational excellence, manages risks, and oversees cross-functional teams in pharmaceutical development.

The Site Project Engineer will lead project execution for capital projects in a healthcare setting, ensuring safety, compliance, and coordination with stakeholders throughout all project phases.

The Lead Technician in QC-AESG provides technical support, manages equipment maintenance, performs laboratory testing, and leads continuous improvement initiatives. Responsibilities include troubleshooting, training, and ensuring compliance with GMP standards.

The Scientist role involves technical support for manufacturing systems, ensuring compliant production, leading design changes, and providing cross-functional collaboration.

The role focuses on technical transfer and process validation in parenteral operations, requiring expertise in manufacturing processes, support, and leadership in investigations and improvements.

The Lead Operator for API manufacturing is responsible for the production process, compliance, safety, and equipment maintenance while supporting a new manufacturing site.

Lead U.S. trade compliance efforts, manage control systems, mitigate risks, influence cross-functional teams, and represent the company externally.

The Engineer - Quality - FUME ensures GMP compliance in Facilities, Utilities, Maintenance, and Equipment, providing quality oversight, mentoring staff, and supporting site expansion and improvements.

The Advisor Federated Learning Data Scientist leads the development of federated learning algorithms and models to leverage distributed datasets in drug discovery, ensuring data privacy.

The Principal Reliability Engineer supports facility start-up by providing reliability engineering, coaching local teams, and utilizing root cause analysis for equipment issues.