Search the 12 jobs at Nature's Toolbox (NTx)

The Director of Strategy will be responsible for leading and executing operational strategic initiatives. They will provide strategic guidance and financial analysis to help identify and evaluate potential sales, investment, and development projects/opportunities.

The QA Technical Process Specialist will provide support for the Quality Management System, including technical writing, manufacturing oversight, and adherence to cGMP standards. Responsibilities include equipment qualification, change control, issuance of controlled documents, review of production batch records, oversight of investigations, and batch release. Additional duties include audits, regulatory inspections, and data analysis. The ideal candidate has 10+ years of experience in a biopharma or pharmaceutical environment, knowledge of Good Documentation Practices (GDP), and proficiency in Microsoft Office Suite.

The QA Document Control Associate (QADCA) will provide administrative support for the organization, including technical writing of controlled documents and administration of the Quality Management System (QMS). They will work with Subject Matter Experts (SMEs) to formalize controlled documents within the approved format.

The Engineer/Scientist, Protein Development is responsible for research and process development in our enzyme program using conventional fermentation and purification methods. This position will support producing and isolating enzymes for the NTxscribe and NTxpress platforms. The position also will support the eventual recovery of products produced by NTx platforms.

The Research Technician (Tech Ops) will be responsible for supporting projects related to the NTxscribe RNA manufacturing platform. The candidate will be involved in manufacturing RUO RNA products for external partners and contribute to internal and external tech transfers.

The Manufacturing Operator (Tech Ops) will be responsible for operating the NTxscribe RNA manufacturing platform to manufacture RUO RNA products for external partners. The candidate will be expected to work closely across various teams and communicate important results to members and management.

The Xpress Technician position is available at NTx for a highly motivated postbaccalaureate technician to engage in research and development on the in vitro translation team. The technician will perform molecular biology and biochemical techniques, be involved in continuous improvement of protocols, and communicate across teams.

Contribute to the development and optimization of mRNA production processes. Focus on manufacturing and purification of modified nucleoside/nucleotide building blocks and evaluating them in in vitro transcription reactions.

Nature’s Toolbox (NTx) in Rio Rancho, NM, is establishing a Manufacturing Technology (MT) team within Commercial Operations to oversee the production of enzymes for use in NTx’ innovative cell-free platforms for the manufacture of mRNA, saRNA, proteins, and other biologics. NTx technology will transform how biologic therapeutics are manufactured and replace the status quo.

Your Impact

The Project Engineer will re...

The Manufacturing Technology Scientist/Engineer is responsible for overseeing late-stage process development and commercial enzyme manufacturing at external partners. They will manage technology transfer, process optimization, and quality management, while collaborating with R&D and Business Development on new product introductions. Additionally, they will lead the scale-up and manufacture of pharmaceutical grade materials and provide technical and regulatory support.

The Manufacturing Technology Director is responsible for overseeing the late-stage process development and commercial enzyme manufacturing at contract development and manufacturing organization (CDMO) partners. They will manage a team of engineers and scientists, collaborate with R&D and Business Development, and provide technical and regulatory support to external partners. The director should have a minimum of 12 years of experience in pharmaceutical or industrial protein process development and a master's or Ph.D. in a related discipline.

Seeking a Facility Manager responsible for overseeing day-to-day operations, maintenance, safety compliance, budget management, vendor management, space management, sustainability initiatives, security, and software platforms. Requirements include a Bachelor's degree in engineering or 10+ years of facility and/or operations experience, certification in Facilities Management and Emergency Management, familiarity with GMP and R&D facilities, strong communication skills, and ability to work independently.