Department of Biology at New Mexico State University is seeking to fill a college-track Assistant Professor position that will contribute to undergraduate instruction and advising.

This role is a Scientist in the Digital Engineering Strategy (W-DES) group at LANL, supporting five nuclear weapon systems (B61, W76, W78, W88, W93). You’d develop, document, and maintain system requirements, manage changes to those requirements, and work closely with weapon system engineers, production realization team leads, design physicists, and external agencies like DoD and NNSA. The job calls for a STEM bachelor’s + ~2 years of related experience (or equivalent), basic R&D/technical problem-solving skills, solid written communication, and the ability to work both independently and on teams. Experience with nondestructive analysis, project reporting/presentations, and an active DOE Q clearance are pluses. The position is onsite at Los Alamos, requires the ability to get a Q clearance, and comes with full LANL benefits (health, PTO, 401(k), tuition assistance, etc.).

This is a Materials Scientist (Scientist 2 or 3) position at Los Alamos National Lab on the W93 nuclear warhead program, focused on materials compatibility and aging qualification. You’d plan, run, and analyze tests that show how materials in the new W93 warhead and test bodies perform over time, then use that data to help qualify the system for the Navy’s new submarine-launched missile. At the Scientist 2 level, you manage planning, execution, and reporting for a subset of tests and coordinate with internal LANL teams; at the Scientist 3 level, you also lead larger test portfolios, work more directly with external partners (NNSA, Navy, Sandia, Lockheed), and mentor junior staff. The job requires at least a STEM bachelor’s + 4 years (Sci 2) or STEM master’s + 6 years (Sci 3), strong materials/chemical science and testing experience, and, at the higher level, proven leadership, cross-org collaboration, project management, and interface with DoD/NNSA-type stakeholders. It’s an onsite role in Los Alamos, requires the ability to get and hold a Q clearance, US citizenship, and passing a federal background check and drug test. The salary ranges are $104,100–$172,200 (Sci 2) and $125,200–$211,300 (Sci 3), with strong benefits (medical, PTO, 401(k) match, relocation, etc.).

This Manager, Microbiology role at Curia in Albuquerque leads the daily operations and long-term strategy of the microbiology lab that supports sterile pharmaceutical manufacturing. You’d serve as the site’s microbiology and contamination-control expert, oversee environmental and product testing, manage investigations and CAPAs, maintain and write SOPs, support audits and regulatory inspections, and supervise, train, and schedule a team of microbiology staff. The job requires at least a bachelor’s degree in microbiology or a related field, 5+ years of cGMP pharmaceutical experience, and 2+ years in a leadership role, with strong knowledge of USP microbiology chapters, FDA cGMPs, and cleanroom operations. Curia offers day-one benefits, paid training and vacation, 401(k) with match, education reimbursement, and growth opportunities.

This role is a Manager of Analytical Chemistry at Curia in Albuquerque, overseeing all operations in the analytical chemistry lab. You’d manage and mentor a team of analysts, handle scheduling and performance reviews, ensure the lab stays GMP/GLP audit-ready, lead investigations (like OOS), manage equipment qualifications and calibrations, and represent the lab in audits and cross-functional meetings. The job requires at least a bachelor’s degree in a science field, around 5+ years of experience in analytical chemistry/QA/regulatory roles (with sterile/aseptic experience preferred), 2+ years of leadership experience, and the ability to work in a highly regulated pharmaceutical environment.

The University of New Mexico School of Medicine, Department of Cell Biology and Physiology is currently recruiting for a HS Research Technician 1. The Vascular Physiology Group investigates the mechanisms that regulate vascular function in both health and disease. Our research spans cellular, molecular, and systemic processes to understand how vascular cells, signaling pathways, and hemodynamic forces work together to maintain cardiovascular and metabolic health and how disruptions in these processes contribute to age- and disease-related vascular dysfunction. Duties include: - Animal care and husbandry, including genotyping - Routine cell culture - Laboratory organization, ordering, and equipment maintenance - Safety and compliance management - Support Training

The Department of Chemistry & Chemical Biology is seeking several instructional assistants for undergraduate chemistry Atomic Start Programs and Parachute. The Instructional Assistants will work under supervision of faculty in charge of the courses duties. Possible Duties include: 1. Supervise student work and provide guidance 2. Attend mandatory training and preparatory meetings 3. Hold review sessions for students with questions related to the course 4. Facilitate student coursework discussion and problem solving 5. Assist program coordinator prepare program materials 6. Other duties assigned by the program coordinator

You’d work closely with faculty to grade weekly homework, quizzes, projects, and exams, keep the course gradebook, hold weekly office hours, help run in-class activities, and assist with moving course materials into Canvas. They prefer students who’ve earned at least a B in Biochemistry and who are self-motivated with strong verbal and written communication skills. To apply, you need to submit an application through UNMJobs with your resume and unofficial transcript.

The Production Supervisor supports the timely manufacturing of parenteral products in an aseptic environment according to Current Good Manufacturing Practice (cGMP). The supervisor responsibilities include supervising the setup of sterile filling equipment, operating dehydrogenation equipment, managing filling and capping processes, and overseeing formulation tasks. Additionally, the supervisor ensures compliance with all relevant regulations and procedures, maintains current good documentation practices (cGDP) for all activities, and participates in training and continuous improvement initiatives to enhance production processes and efficiency. The role also requires supervising the sanitation of aseptic and controlled areas with specialized solutions and equipment, adhering to sanitization protocols for sterile equipment processing, and following Standard Operating Procedures (SOPs) for all sanitation and documentation activities.

The Validations Department is responsible for formulating, reviewing, and approving all validation protocols related to manufacturing or support operations. The Validation Analyst II is responsible for executing and supporting validation activities for equipment, processes, utilities, systems, and components in alignment with cGMP regulations, internal procedures, and applicable regulatory expectations. This intermediate-level role involves authoring, reviewing, and executing validation protocols; analyzing test results; and compiling final reports to support qualification and ongoing validation efforts. The Validation Analyst II collaborates with cross-functional teams to ensure validation work is efficiently integrated into production and quality timelines. This role may also support investigations related to validation deviations, participate in risk assessments, and contribute to the development and continuous improvement of validation practices.

The Quality Operations Specialist III is an essential part of the Quality Operations team and is responsible for QA oversight, review, and quality approval of large-scale expansion project deliverables. This role supports QA activities related to equipment, facilities, processes, computerized systems, and manufacturing projects, including facility expansion and new line installations, as well as commercial manufacturing operations. The role provides clear guidance on quality requirements consistent with cGMPs, regulatory expectations, and industry best practices, ensuring objectives are met within timeline constraints. Additionally, this position helps establish and maintain cross-departmental relationships to enhance overall compliance and efficiency. The Specialist III supports facilities, validation, manufacturing, and engineering activities while providing QA input and guidance for the review and approval of regulated, controlled documents, including but not limited to SOPs, validation protocols, commissioning documents, deviations, change controls, work orders, and Validation Master Plans.

The Process Engineer III is responsible for facilitating the technology transfer of multiple client processes and executing engineering functions including design and scale-up document controls. This role functions as a program lead. The Process Engineer III provides guidance and instruction to supporting team members on tasks directly related to their project, in addition to providing guidance and instruction on site-driven projects.

The Clinical Lab Assistant Phlebotomist is able to work independently and with minimal supervision and/or oversight. Successful candidates have the experience and skillset to perform one or more identified modalities. Compensation is dependent on the number of modalities performed. Candidates without experience may be considered for a paid apprenticeship level. Regular in-person attendance during scheduled work hours is essential.

The Clinical Lab Assistant Phlebotomist is able to work independently and with minimal supervision and/or oversight. Successful candidates have the experience and skillset to perform one or more identified modalities. Compensation is dependent on the number of modalities performed. Candidates without experience may be considered for a paid apprenticeship level. Regular in-person attendance during scheduled work hours is essential.

The Clinical Lab Assistant is able to work independently and with minimal supervision and/or oversight. Successful candidates have the experience and skillset to perform one or more identified modalities. Compensation is dependent on the number of modalities performed. Candidates without experience may be considered for a paid apprenticeship level. Regular in-person attendance during scheduled work hours is essential.

The Clinical Lab Assistant is able to work independently and with minimal supervision and/or oversight. Successful candidates have the experience and skillset to perform one or more identified modalities. Compensation is dependent on the number of modalities performed. Candidates without experience may be considered for a paid apprenticeship level. Regular in-person attendance during scheduled work hours is essential.

We seek a highly talented and motivated Post Baccalaureate researcher with a strong background in chemical synthesis, especially nanomaterials synthesis, to join our cutting-edge team focused on the discovery, synthesis, and application of functional nanomaterials. This position offers a unique opportunity to contribute to innovative research at the forefront of chemical synthesis and nanotechnology.

The New Mexico HPV Prevention Center is a complex clinical and public health research center. The Center has been supported by industry, state and federal grant dollars. The Program Manager plays a key role in overseeing the daily administrative operations for the Center and core functions of the New Mexico HPV Pap Registry. Acting as an administrative point of contact for internal informatics, clinical, laboratory and administrative functions, the position is a liaison for other UNM organizations. The position works directly with the Center Director, Faculty of the Center and the New Mexico HPV Pap Registry (NMHPVPR), Strategic Support Manager, and staff to assist with the development and implementation of NMHPVPR policies consistent with the standard operating procedures ensuring efficient, productive and safe operations of public health reporting activities, and associated laboratory and clinical research.

Under general supervision, the Buyer will be responsible for the complete cycle of procurement transactions from initiating, reviewing and coordinating purchase requests, requests for quotes, bids, proposals and orders. The Buyer will be responsible for preparing supporting procurement documentation to comply with goals and terms of Small Business Subcontracting Plans, when required. All functions to be performed in accordance with Institute policies and procedures and all procurement codes and guidelines.

A Research Technician 1 is being sought to join the laboratory of Dr. Ryoma “Puck” Ohi in the Department of Internal Medicine, Division of Molecular Medicine at the University of New Mexico Health Sciences Center, with lab space located on the 2nd floor of Cancer Research Facility (CRF). Studies in the Ohi laboratory focus on the microtubule cytoskeleton with an emphasis on tubulin post-translational modifications (PTMs) and tubulin PTM “readers”. The laboratory uses a wide range of techniques, which includes biochemistry, cell culture, and quantitative optical microscopy. The successful applicant will be expected to carry out administrative and organizational tasks, which include ordering and upkeep of standard laboratory reagents. The role will also include molecular cloning, cell culture, and protein isolation from either prokaryotic or eukaryotic sources. Proficiency in the following techniques will be considered assets: PCR, DNA cloning, immunoblotting, protein purification, microbiology, microscopy and cell culture.