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

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 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 role involves ensuring quality assurance for drug development processes, focusing on compliance and product safety in a fast-paced environment.

The Quality Control Auditor reviews GMP documents for compliance, participates in audits, trains analysts, conducts testing, and supports quality processes.

The role involves managing Quality Control resources, ensuring employee training, monitoring KPIs, driving continuous improvement, maintaining a safe environment, and overseeing quality standards and project timelines.

The Program Manager I leads client projects in Process Development and GMP Manufacturing, managing communication, schedule, scope, and budget while coordinating cross-functional teams.

The Manager - Process Development, Downstream oversees late-stage process development for protein biologics, ensuring compliance and effective execution, while leading and mentoring team members.

The Reliability Engineer will support capital projects, improve processes, ensure compliance in maintenance systems, and manage equipment documentation.