Nature's Toolbox, Inc. (NTx)
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The Project Engineer will oversee the build-out of internal capacity and capability for manufacturing biopharmaceutical materials. They will be responsible for equipment specification and design, project management, manufacturing and procurement, quality assurance and compliance, equipment qualification and validation, and technical leadership and support.
The QA Technical Process Specialist will provide technical support for the Quality Management System and ensure adherence to cGMP standards. Responsibilities include technical writing, manufacturing oversight, and qualification of equipment/processes.
The QA Document Control Associate will support the quality management system by providing administrative support, technical writing of controlled documents, and administration of the document control system. They will work with Subject Matter Experts to formalize controlled documents and ensure compliance with standards.
The Facility Manager will oversee the operations and maintenance of facilities, ensure safety and compliance, manage budgets, vendor contracts, space allocation, and sustainability initiatives. They will need a Bachelor's degree in engineering or related field with 10+ years of experience, as well as certifications in facilities and emergency management preferred. Additional requirements include familiarity with GMP facilities, strong communication skills, and the ability to work independently.