The Project Manager will lead capital projects in the Life Sciences industry, ensuring compliance and effective collaboration with cross-functional teams and vendors.

Provide advanced engineering principles for system modifications and maintenance, supervise engineers, and develop policies for engineering projects.

The MES Specialist will design and optimize PAS-X systems, oversee administration, manage projects, provide end-user training, and ensure compliance in manufacturing environments.

The Validation Specialist will provide validation services for equipment and systems in the life sciences sector, ensuring compliance and executing protocols.

Provide technical support for purification and fermentation, engage in daily operations, and collaborate with various departments for system improvements.

Provide technical support and troubleshooting for equipment issues in drug substance/API operations, ensuring compliance and operational performance.

The CSV Specialist will develop and execute validation deliverables, ensure compliance, support change controls, collaborate with stakeholders, and participate in audits.

Perform various Quality Assurance duties including validation, document review, and NPI processes with minimal supervision while supporting facilities programs.

Provide technical support and troubleshooting for equipment issues in daily operations. Involves auditing performance and compliance, assisting in design engineering projects.