Research scientist jobs in Albuquerque, NM - 34 jobs

Imagine how your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes. Aortic stenosis and aortic regurgitation impact millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. How you'll make an impact: * Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements * Develop and deliver technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities. Act as a mentor to new or junior level employees * Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Boards, Contract, and Training, developing process improvements * Contribute to the development of clinical protocols, informed consent forms, and case report forms. Also contribute to team projects * Validate investigational device accountability by tracking the history of investigational devices from Edwards to the field sites and through final disposition * Verify trial/study data, including maintaining appropriate regulatory documents both internal and external, auditing to be sure the site has the appropriate regulatory documentation to conduct the trial/study, and source documentation is properly recorded * Edit/amend informed consent documents What you'll need (Required): * Bachelor's Degree and a minimum of 5 years of work experience in clinical research monitoring, with a strong focus on quality assurance, quality control, and regulatory compliance or equivalent based on Edwards criteria * Experience working in a regulated industry * Experience with electronic data capture * Ability to travel up to 75% for clinical site visits What else we look for (Preferred): * Knowledge of cardiovascular physiology and structural heart anatomy * Previous medical device Clinical Research experience in cardiology * Clinical research certification (ACRP or SOCRA, Clinical Coordinator/CRA certification) * Prior clinical research experience with Class III Medical Devices including PMA, IDE and 510(k) * Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families. For Colorado (CO), the base pay range for this position is $106,000 to $149,000 (highly experienced). The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website. Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities. COVID Vaccination Requirement Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

Seeking a highly motivated individual to serve as a Research Associate within the Laboratory Animal Sciences/Applied Sciences group. Under limited supervision, performs a variety of routine and non-routine research tasks, following established techniques and procedures. Will work extensively with computer-based programs. Will assist in study preparation (protocols), data collection and evaluation (data management), and reporting (data management and report writing). Conducts technical aspects of the position in accordance with applicable guiding documents that include but are not limited to SOPs, protocols, and regulations and assists in refining these procedures as well as implementing new procedures and perform all other related duties and tasks as required or assigned. Qualifications Requires a Master's degree in a related scientific discipline and a minimum of 2 years demonstrated research experience; or an equivalent combination of education, training and/or experience from which comparable knowledge, skills and abilities have been attained. Ability to gain and maintain access to Kirtland Air Force base (KAFB) is required. Physical Requirements Work is performed in a wet laboratory environment. Will operate standard laboratory equipment and will frequently stand, walk, sit, perform lab- and desk-based computer tasks, perform laboratory techniques requiring grasping/pipetting/hand dexterity, perform repetitive motions and occasionally lift objects that weigh up to 50 pounds. Will wear personal protective equipment which may include a respirator. May work in close proximity to an environment containing research animals and may be required to work with or be in areas where hazardous materials and/or infectious agents are present which may require vaccinations. The above is intended to describe the general requirements for the position and should not be interpreted as an exhaustive statement of physical requirements. The Institute will provide reasonable accommodation to any employee with a disability who requires an accommodation to perform the essential functions of the position. Salary Salary is commensurate with experience. Lovelace Biomedical is an Equal Opportunity Employer

We are seeking a Senior Advanced Photonics Scientist at our Broomfield, CO or Albuquerque, New Mexico Location. Key Responsibilities: * Participate in a team of physicists and optical engineers supporting the development of commercial and research systems for quantum computing * Design and develop integrated photonic components and systems in novel ways to deliver and manipulate light across the spectrum * Collaborate across disciplines (architecture, physics, photonics, fabrication, mechanical engineering) to define systems and requirements to support quantum computing and demonstrate systems meeting performance requirements * Gather technical requirements, turn them into action plans, and ensure the components and systems meet the requirements * Design novel integrated photonic components to meet challenging specifications * Layout test PICs and work closely with fabrication and test teams to validate photonic component performance * Lead and work with PIC development team and external vendors to ensure timely development and delivery of key demonstrators YOU MUST HAVE: * PhD Degree minimum * Minimum 6+ years of experience (advanced degree inclusive) with photonic integrated circuits (PIC) design using photonic simulation tools (Lumerical, RSoft, or similar guided mode and FDTD solvers) and layout tools (Klayout, GDSFactory, or similar) * Minimum 4+ years' experience (advanced degree inclusive) using and maintaining optical/photonic systems * Due to Contractual requirements, must be a U.S. Person. defined as, U.S. citizen permanent resident or green card holder, workers granted asylum or refugee status * Due to national security requirements imposed by the U.S. Government, candidates for this position must not be a People's Republic of China national or Russian national unless the candidate is also a U.S. citizen. WE VALUE: * PhD Degree minimum (in Optics, Physics, Applied Physics, Electrical Engineering, or a related field) * Experience with design-for-manufacturing * Experience with photonics fabrication processes and metrology * Experience with materials used in visible photonics circuits and optics * Experience in product development regarding photonic design, fabrication and/or packaging of PIC systems * Experience working with cross-disciplinary teams (architecture, physics, fabrication, mechanical engineering, photonics) to develop solutions * Experience leading and mentoring small teams * Broad understanding of optical principles and practices and experience applying this knowledge to projects * Programming experience in Matlab, Python, C * Experience with testing and data analysis (taking, plotting, analyzing, fitting and interpreting relevant data from optical testing experiments) $140,000 - $175,000 a year Compensation & Benefits: Non-Incentive Eligible The pay range for this role is $140,000 - $175,000 annually. Actual compensation within this range may vary based on the candidate's skills, educational background, professional experience, and unique qualifications for the role. Quantinuum is the world leader in quantum computing. The company's quantum systems deliver the highest performance across all industry benchmarks. Quantinuum's over 650 employees, including 400+ scientists and engineers, across the US, UK, Germany, and Japan, are driving the quantum computing revolution. By uniting best-in-class software with high-fidelity hardware, our integrated full-stack approach is accelerating the path to practical quantum computing and scaling its impact across multiple industries. As we celebrate the International Year of Quantum, there has never been a more exciting time to be part of this rapidly evolving field. By joining Quantinuum, you'll be at the forefront of this transformative revolution, shaping the future of quantum computing, pushing the limits of technology, and making the impossible possible. What is in it for you? A competitive salary and innovative, game-changing work Flexible work schedule Employer subsidized health, dental, and vision insurance 401(k) match for student loan repayment benefit Equity, 401k retirement savings plan + 12 Paid holidays and generous vacation + sick time Paid parental leave Employee discounts Quantinuum is an equal opportunity employer. You will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, or veteran status. Know Your Rights: Workplace discrimination is illegal We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description 1.1. Works under the direction of the Quality Assurance Organization and is responsible for providing support and leadership to the QA Team and the Sterilization Dose Audit Program to achieve quality, efficiency, and cost targets, while ensuring compliance to all applicable standards. 2. EDUCATION/CERTIFICATION REQUIREMENTS: 2.1. High school diploma or equivalent required. 2.2. University/Bachelor's Degree or equivalent required, Microbiology preferred. 2.3. Six-sigma certification preferred. 3. KEY SKILLS/KNOWLEDGE REQUIRED: 3.1. SKILL SETS 3.1.1. General knowledge of medical devices preferred. 3.1.2. Knowledge of Good Manufacturing Practices (GMPs) and ISO policy and procedures is preferred. 3.2. COMPUTER SKILLS 3.3. EXPERIENCE 3.3.1. One or more years in microbiological laboratory environment or equivalent training. 3.3.2. One or more years in project management preferred. 4. KEY JOB RESPONSIBILITIES: 4.1. Provide leadership and execution for Sample Item Portions (SIP s) preparation, testing, documentation, reporting, and conclusions. 4.2. Provide leadership and execution for Environmental Monitoring Program (EM) for the Albuquerque Facility. 4.3. Provide leadership of activities and serve as a resource for quality issues and initiatives. 4.4. Provide coaching and mentoring of QA Technicians under the direction of the Quality Assurance Organization. 4.5. Coordinate with Manufacturing Operations to schedule and retrieve audit product samples on a timely manner. 4.6. Perform physical manipulation of product into SIP s under aseptic conditions. 4.7. Aseptically package and ship SIP s to testing laboratories. 4.8. Maintain Laboratory equipment and supplies for SIP s and EM. 4.9. Maintain accurate records verifying that required samples have been collected, processed and dispersed to appropriate testing laboratories. 4.10. Reviewing the incoming data for completeness and adherence to specifications. 4.11. Maintain communication links between different testing laboratories to ensure timely testing and accuracy of samples. 4.12. Create and Maintain laboratory procedures and governing documents. 4.13. Environmental 4.13.1. Participate in implementation of the EMS management system including continual improvement, pollution prevention, objectives and targets, and regulatory compliance. 4.13.2. Implement and follow all applicable EMS procedures. 4.13.3. Adhere to the site's EHS Code of Conduct. 4.14. Other responsibilities may be assigned and not all responsibilities listed may be assigned. 5. POST HIRE TRAINING PLAN REQUIREMENTS: 5.1. Maintain adherence to position training curriculum. 5.2. Training Plan Requirements as identified in Corporate Training Procedure, CP0128. 5.3. Applicable training plan for the area of support. 6. PHYSICAL DEMANDS: 6.1. Requires long walking, standing, bending, stooping and reaching. 6.2. May require lifting of boxes or material not to exceed 50 lbs. 6.3. May require use of a pallet jack. 6.4. Maintain vision certification through the visual acuity testing/process. 6.5. Office deskwork, requiring sitting, walking, using the phone and computer 6.6. Operation of hydraulic and manual cutting equipment daily. 7. WORK ENVIRONMENT: 7.1. Work in office and/or manufacturing environment and/or laboratory environment. 7.2. Flexibility to adjust and rotate the working hours to support Laboratory needs. 7.3. Gowning required as per established procedures. Qualifications EDUCATION/CERTIFICATION REQUIREMENTS: 2.1. High school diploma or equivalent required. 2.2. University/Bachelor's Degree or equivalent required, Microbiology preferred. 2.3. Six-sigma certification preferred. Additional Information For more information, Please contact Sneha Shrivastava **************

Clinical Research Investigator DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an Investigator for our sites in Albuquerque, NM. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes. Responsibilities Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies. Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site. Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants. Interprets protocols and IB and participates in initiatives to strategize for patient recruitment. Carries out clinical evaluation and assessment of participants to ensure eligible participants are enrolled onto studies. Ensures and protects the welfare and safety of participants through ethical conduct. Fulfills and comply with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations. Exercises meticulous attention to detail in documentation and patient care. Requirements Medical License (MD, DO) At least 2 years of experience as a Clinical Research Investigator. Spanish Bilingual a plus.

Job Description Come join Pajarito Powder and help us change the world. Pajarito Powder is a world leader in the development and commercialization of advanced electrocatalysts for fuel cells and electrolyzers. We manufacture advanced catalysts for hydrogen fuel cells and electrolyzers across PEM, AEM and Alkaline chemistries. Pajarito Powder is poised for rapid growth and needs an R&D Scientist. This is an ideal position for someone seeking a fast-paced challenge. Our manufacturing and R&D team is world class, and the business group is exceptionally experienced. We provide a competitive salary, health, dental, vision and life insurance, paid time off, a collaborative environment, and full vesting of options after four years. Principle Tasks • Prepare compounds, solutions and reagents to synthesize and develop advanced materials per supervisors' guidance and scientific principles. • Determine and evaluate the relationships of chemical and physical properties, composition, structures and reactions of advanced materials using characterization and catalyst performance techniques • Develop, improve and customize equipment, products, formulas, analytical methods and processes per supervisors' guidance and scientific principles • Consult with engineers and scientists on analysis, interpretation and development of tests • Induce chemical reactions with light, energy, heat and chemicals • Document findings and procedures in notebooks, technical papers, and reports, preparing or following specifications and characterization and evaluation standards • Clean and maintain laboratory instruments and equipment, making sure that all the technology is working correctly: if it isn't, troubleshoot the issue or problem. • Conduct quality control tests to ensure no compounds or equipment are contaminated or are working consistently • Order laboratory supplies, equipment, and chemicals as needed to maintain inventory and develop catalysts and processes. • Follow safety protocols, perform safety evaluations on developmental procedures, contribute to safety efforts with peers. • Be familiar with scientific literature to expand technical and scientific knowledge to further R&D operations. Knowledge, Skills, and Abilities • Proficiency and skill with Microsoft Office Suite and company computer systems • Able to work with accuracy and detail oriented • Able to communicate clearly and effectively, both verbally and in writing • Able to interact positively and work effectively with others • Able to independently gather data, compile information, and prepare reports • Able to take initiative in performing job and seek increased responsibilities • Able to multi-task and problem solve with strong analytical skills • Able to organize time, energy, and resources effectively to achieve goals (i.e., organizational skills) • Ability to seek different and novel ways to create efficiencies when working on problems, challenges and issues • Able to perform tasks and duties without constant supervision • Prioritizes and ensures safety of oneself and others Edu/ Training/ exp required • Bachelor's or master's degree in chemistry, chemical engineering, or similar degree from an accredited university/school. • Must possess technical skills and abilities that are generally expected from degreed engineers or chemists • 1 to 3 years of research experience in a chemistry lab • Basic understanding of catalysts and electrochemistry • Basic understanding of Chemical Safety • Use of Microsoft Word, Excel, PowerPoint and Outlook to plan, analyze, and report on projects, experimental data, and logs. • Experience recording and reporting on progress of work and communicating with team and supervisors effectively. Additional Information/Requirements Must be willing to relocate to and work onsite in Albuquerque, NM. For full consideration, applicants must submit a comprehensive resume that addresses the key requirements of the position. Pajarito Powder is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Work Authorization Pajarito Powder will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas such as E, F-1(including those with OPT or CPT), H-1, H-2, L-1, B, J or TN, or who need sponsorship for work authorization now or in the future, are not eligible for hire.

About Sandia Sandia National Laboratories is the nation's premier science and engineering lab for national security and technology innovation, with teams of specialists focused on cutting-edge work in a broad array of areas. Some of the main reasons we love our jobs: * Challenging work with amazing impact that contributes to security, peace, and freedom worldwide * Extraordinary co-workers * Some of the best tools, equipment, and research facilities in the world * Career advancement and enrichment opportunities * Flexible work arrangements for many positions include 9/80 (work 80 hours every two weeks, with every other Friday off) and 4/10 (work 4 ten-hour days each week) compressed workweeks, part-time work, and telecommuting (a mix of onsite work and working from home) * Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and amenities aimed at creating a solid work/life balance* World-changing technologies. Life-changing careers. Learn more about Sandia at: ********************* * These benefits vary by job classification. What Your Job Will Be Like We are seeking a postdoctoral researcher (job title: Postdoctoral Appointee) to join our team and assist with experimental geomechanics, material science, and geothermal energy research. On any given day, you may be called on to: * Support state-of-the-art rock mechanics testing. * Develop and implement laboratory experiments. * Interpret coupled process behavior in materials. * Process and analyze experimental data for subsurface applications. This position is located in Albuquerque, NM, and the annual salary for this position is $98,500. Due to the nature of the work, the selected applicant must be able to work onsite. Qualifications We Require * PhD in geology/geophysics, geomechanics, geotechnical engineering, or other relevant, related discipline * Hands-on experience in laboratory experimentation * Experience with geophysical analysis * Proven record of technical accomplishment and strong written and verbal communication skills, as evidenced by publications in peer-reviewed journals and/or presentations at scientific conferences * Ability to obtain and maintain a DOE L-level security clearance Qualifications We Desire * Familiarity with data acquisition and processing techniques * Experience with experimental rock mechanics research and subsurface energy applications * Proven ability to independently identify and develop innovative solutions to a diverse range of challenges * Excellent oral and written communication skills, including proficiency in technical writing * Strong interpersonal and teamwork skills, with the ability to thrive in a high-functioning environment About Our Team The Geothermal Research Department is an organization that delivers unique solutions for customers who require components and systems capable of operating in harsh and often high-temperature environments. The historical mission of the department was to address technology needs related to the development of geothermal energy (a baseload renewable energy resource); in particular accessing, monitoring and engineering of geothermal resources in subsurface geologic environments. This mission continues, but the capabilities of the organization have also been leveraged to address other issues of national importance. Current activities are broad in scope and require the efforts of multidisciplinary technical teams with expertise in mechanical engineering, drilling technologies, electronics, geosciences, materials, sensors, and explosives/propellants. Our customer base spans a wide variety of governmental and private sponsors, and we work closely with the geothermal power industry, oil & gas developers, service companies, other national laboratories and academia. In addition, the department maintains and continually updates a wide variety of unique testing capabilities for evaluation of technologies in simulated downhole environments. Posting Duration This posting will be open for application submissions for a minimum of seven (7) calendar days, including the 'posting date'. Sandia reserves the right to extend the posting date at any time. Security Clearance Sandia is required by DOE to conduct a pre-employment drug test and background review that includes checks of personal references, credit, law enforcement records, and employment/education verifications. Applicants for employment need to be able to obtain and maintain a DOE L-level security clearance, which requires U.S. citizenship. If you hold more than one citizenship (i.e., of the U.S. and another country), your ability to obtain a security clearance may be impacted. Applicants offered employment with Sandia are subject to a federal background investigation to meet the requirements for access to classified information or matter if the duties of the position require a DOE security clearance. Substance abuse or illegal drug use, falsification of information, criminal activity, serious misconduct or other indicators of untrustworthiness can cause a clearance to be denied or terminated by the DOE, resulting in the inability to perform the duties assigned and subsequent termination of employment. EEO All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status and any other protected class under state or federal law. NNSA Requirements for MedPEDs If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, drug-releasing pump, hearing aids, or diagnostic equipment and other equipment for measuring, monitoring, and recording body functions such as heartbeat and brain waves, if employed by Sandia National Laboratories you may be required to comply with NNSA security requirements for MedPEDs. If you have a MedPED and you are selected for an on-site interview at Sandia National Laboratories, there may be additional steps necessary to ensure compliance with NNSA security requirements prior to the interview date. Position Information This postdoctoral position is a temporary position for up to one year, which may be renewed at Sandia's discretion up to five additional years. The PhD must have been conferred within five years prior to employment. Individuals in postdoctoral positions may bid on regular Sandia positions as internal candidates, and in some cases may be converted to regular career positions during their term if warranted by ongoing operational needs, continuing availability of funds, and satisfactory job performance. Apply for Job * Careers * Sign In * New User

Schedule: Monday - Friday 8AM - 5PM and other shifts as needed. Performs billing research functions to ensure the requisition is ready to bill. Determines appropriate billing codes needed, billing information for data entry of requisitions, and other billing tasks. High degree of initiative and self-motivation needed to be able to troubleshoot billing problems without assistance on a frequent basis. Monitors, summarizes, and reports deficiencies in requisition information received from TRL offsite locations and ordering physicians/clients. ESSENTIAL FUNCTIONS: 1. Performs billing research functions and problem solving activities utilizing internal computer systems and Internet sites as appropriate by locating missing requisitions, status inquiries for patient/client accounts, calling on problems, verifies insurance and diagnosis information, and resolving discrepancies. 2. Determines validity and necessity of obtaining an Advance Beneficiary Notice (ABN) and Uninsured Patient Letter. 3. Enters billing information into billing system and other Business Office applications for scrubber edits (i.e. Rhodes Fusion Scrubber, Antrim, Fast Orders etc.) as appropriate. 4. Meets all Quality Assurance (QA) and production goals. 5. Tracks, logs and provides feedback to appropriate area on missing or inaccurate information by client and/or offsite location. Documents and communicates to Supervisor/Lead to initiate problem solving. 6. Prepare billing reports and perform data analysis of various types, as requested. 7. Communicates effectively and professionally to customers (internal and external). Maintains confidentiality of patient and client information. 8. Perform general clerical functions. Make photocopies; maintain appropriate records, files, and destruction of documents. 9. Responsible for following TriCore safety, personnel, and billing department policies. 10. Participate in training as directed by Supervisor/Manager. The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified. MINIMUM EDUCATION: High school diploma or equivalent. MINIMUM EXPERIENCE: Requires one of the following: One (1) year experience as a Medical Data Entry Specialist in the TriCore Business Office. Minimum of one (1) year laboratory or medical billing experience. Minimum of two (2) years experience within a healthcare medical office in a registration or clerical position. OTHER REQUIREMENTS: Intermediate knowledge and understanding of medical terminology, third party billing requirements, ICD-10 and CPT coding experience. Intermediate PC/data entry skills to include Internet Explorer and Microsoft Office applications. Must type 30 WPM or 9000 keystrokes per hour (typing test required) TriCore is New Mexico s largest laboratory, employing more than 1,400 individuals who serve in a broad range of positions. We are dedicated to improving the quality of care for our communities, and also our employees. We foster a culture of integrity, are dedicated to excellence, and are looking for passionate individuals with a desire to have an impact in patient care, the core of our strategy. We offer excellent benefits including, medical, dental, vision and life insurances, 401(k) retirement plan with employer matching, PTO, and paid holidays, as well as opportunities for continuous learning, education assistance, wellness programs, career advancement, and the ability to share in our genuine commitment to the health of our communities. We offer a variety of shifts at multiple locations.

Imagine how your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes. Aortic stenosis and aortic regurgitation impact millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. **How you'll make an impact:** + Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements + Develop and deliver technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities. Act as a mentor to new or junior level employees + Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Boards, Contract, and Training, developing process improvements + Contribute to the development of clinical protocols, informed consent forms, and case report forms. Also contribute to team projects + Validate investigational device accountability by tracking the history of investigational devices from Edwards to the field sites and through final disposition + Verify trial/study data, including maintaining appropriate regulatory documents both internal and external, auditing to be sure the site has the appropriate regulatory documentation to conduct the trial/study, and source documentation is properly recorded + Edit/amend informed consent documents **What you'll need (Required):** + Bachelor's Degree and a minimum of 5 years of work experience in clinical research monitoring, with a strong focus on quality assurance, quality control, and regulatory compliance or equivalent based on Edwards criteria + Experience working in a regulated industry + Experience with electronic data capture + Ability to travel up to 75% for clinical site visits **What else we look for (Preferred):** + Knowledge of cardiovascular physiology and structural heart anatomy + Previous medical device Clinical Research experience in cardiology + Clinical research certification (ACRP or SOCRA, Clinical Coordinator/CRA certification) + Prior clinical research experience with Class III Medical Devices including PMA, IDE and 510(k) + Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families. For Colorado (CO), the base pay range for this position is $106,000 to $149,000 (highly experienced). The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website. Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities. **COVID Vaccination Requirement** Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

The Research Associate will perform a variety of complex studies to include developing aerosol exposure systems, characterizing complex aerosols, documenting laboratory work, maintaining laboratory equipment and supplies. Independently writes proposals, final reports, and cost estimates. Documents laboratory work to acceptable standards and maintains laboratory/medical equipment and supplies in accordance with Standard Operating Procedures (SOPs), protocols and current federal regulations (FDA GLP). The successful candidate will collaborate with scientific staff and will author sections of publications based on research performed as well as perform all other related duties and tasks as required or assigned. May supervise technical staff and provides training. Qualifications Requires a masters degree in a related scientific discipline, engineering or physics and a minimum of 2 years demonstrated research experience; or an equivalent combination of education, training and/or experience from which comparable knowledge, skills and abilities have been attained. Directly-related experience in an aerosol research lab is required for this Research Associate position, as is demonstrated success independently completing aerosol research projects. Experience should include conducting related research, writing reports and protocols, using a scientific approach to analyze, interpret and report data within project deadlines. Must have a demonstrated understanding of science research principles, practices and procedures and the ability to follow and enforce safety procedures. Experience in a broad background of scientific fields including aerosol sciences, mechanical engineering, and analytical chemistry is highly desired. Additional competencies within electrical engineering, toxicology and pharmacology are preferred. Requires strong written and verbal communication skills, the ability to work independently and as a part of a team. Preferred computer proficiency with Microsoft Excel, Word, Internet Explorer, Outlook and the ability to learn department-specific computer systems as needed. A background check is required. Ability to gain and maintain access to Kirtland Air Force base (KAFB) is required. Preferred/Additional Qualifications Experience working with aerosols. Ability to assemble, disassemble and test systems. Must be able to work on weekends, if needed. Job requires attention to detail. Physical Requirements Work is performed in a wet laboratory environment. Will operate standard laboratory equipment and will frequently stand, walk, sit, perform lab- and desk-based computer tasks, perform laboratory techniques requiring grasping/pipetting/hand dexterity, perform repetitive motions and occasionally lift objects that weigh up to 50 pounds. Will wear personal protective equipment which may include a respirator. May work in close proximity to an environment containing research animals and may be required to work with or be in areas where hazardous materials and/or infectious agents are present which may require vaccinations. The above is intended to describe the general requirements for the position and should not be interpreted as an exhaustive statement of physical requirements. The Institute will provide reasonable accommodation to any employee with a disability who requires an accommodation to perform the essential functions of the position. Salary Salary is commensurate with experience. Lovelace Biomedical is an Equal Opportunity Employer

The FOR-NM Project (Forest Research for New Mexico Water and Carbon Management) seeks applications for a Research Scientist 3 position with a focus on data management. We are looking for a motivated and organized person with a background (MS degree preferred) in ecology, data analytics, remote sensing, GIS, and/or hydrology to join our team. This multi-institutional research program spans five institutions across the state of New Mexico including collaboration with Sandia National Laboratory. The project aims to improve management of New Mexico's forested watersheds by addressing key gaps in understanding of water and carbon dynamics in relation to forest management. Duties include collating and managing data with version-controlled programmatic workflows in R and/or Python, including large volumes of high-frequency sensor data and model outputs; working with investigators to design and deliver data products to open access repositories; and training participants to track and quality control data. Interest in participating in field work as approximately 15% of duties is strongly desired. Expertise in working with environmental sensor data and geospatial data (including remote sensing products) is required. This position will be based at the University of New Mexico in Albuquerque, NM. Partial but not fully remote work options can be considered for exceptional candidates. The position will start as soon as possible and will be hired on a 1-year contract, with the expectation of renewal for additional years pending satisfactory performance. The position's online application is open and applications will be reviewed on a rolling basis. See the Position Description for additional information. Conditions of Employment * Successful candidate must submit to a post-offer, pre-employment physical examination and medical history check. Additional health screenings may be required, dependent on the nature of the research conducted, as determined by Employee Occupational Health Services. Minimum Qualifications Bachelor's degree; at least 3 years of experience directly related to the duties and responsibilities specified. Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis. Preferred Qualifications Preferred Qualifications: * Masters in ecology, data analytics, remote sensing, GIS, hydrology, or closely related field * Previous experience working with large datasets * Experience working collaboratively with a team of scientists across multiple institutions * Experience with numerical modeling, remote sensing, and/or environmental sensors * Excellent English verbal communication skills * Experience with programming in R and/or Python, and collaborative version-controlled workflows including Git and/or Jupyter Notebooks * Experience with developing data processing pipelines using R and/or Python Additional Requirements Campus Main - Albuquerque, NM Department AS Biology General Administrative (048F) Employment Type Staff Staff Type Term - Full-Time Term End Date 1 year from start date Status Exempt Pay Monthly: $4,36.27 - $5,950.53 Benefits Eligible This is a benefits eligible position. ERB Statement As a condition of employment, eligible employees working greater than .25 FTE as determined by the New Mexico Education Retirement Act must make mandatory retirement contributions. For more information, review the Benefits Eligibility at a Glance grid. Background Check Required Yes For Best Consideration Date 11/5/2025 Eligible for Remote Work Yes Eligible for Remote Work Statement This position is eligible for a remote work agreement (RWA), to include Hybrid, Application Instructions Only applications submitted through the official UNMJobs site will be accepted. If you are viewing this job advertisement on a 3rd party site, please visit UNMJobs to submit an application. Please submit a resume and cover letter with UNMJobs application. Positions posted with a Staff Type of Regular or Term are eligible for the Veteran Preference Program. See the Veteran Preference Program webpage for additional details. The University of New Mexico is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity Employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, veteran status, disability, or any other protected class. The University of New Mexico requires all regular staff positions successfully pass a pre-employment background check. This may include, but is not limited to, a criminal history background check, New Mexico Department of Health fingerprint screening, New Mexico Children, Youth, and Families Department fingerprint screening, verification of education credentials, and/or verification of prior employment. For more information about background checks, visit ********************************************************** Refer to ********************************************************* for a definition of Regular Staff.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description 1.1. Works under the direction of the Quality Assurance Organization and is responsible for providing support and leadership to the QA Team and the Sterilization Dose Audit Program to achieve quality, efficiency, and cost targets, while ensuring compliance to all applicable standards. 2. EDUCATION/CERTIFICATION REQUIREMENTS: 2.1. High school diploma or equivalent required. 2.2. University/Bachelor's Degree or equivalent required, Microbiology preferred. 2.3. Six-sigma certification preferred. 3. KEY SKILLS/KNOWLEDGE REQUIRED: 3.1. SKILL SETS 3.1.1. General knowledge of medical devices preferred. 3.1.2. Knowledge of Good Manufacturing Practices (GMPs) and ISO policy and procedures is preferred. 3.2. COMPUTER SKILLS 3.3. EXPERIENCE 3.3.1. One or more years in microbiological laboratory environment or equivalent training. 3.3.2. One or more years in project management preferred. 4. KEY JOB RESPONSIBILITIES: 4.1. Provide leadership and execution for Sample Item Portions (SIP s) preparation, testing, documentation, reporting, and conclusions. 4.2. Provide leadership and execution for Environmental Monitoring Program (EM) for the Albuquerque Facility. 4.3. Provide leadership of activities and serve as a resource for quality issues and initiatives. 4.4. Provide coaching and mentoring of QA Technicians under the direction of the Quality Assurance Organization. 4.5. Coordinate with Manufacturing Operations to schedule and retrieve audit product samples on a timely manner. 4.6. Perform physical manipulation of product into SIP s under aseptic conditions. 4.7. Aseptically package and ship SIP s to testing laboratories. 4.8. Maintain Laboratory equipment and supplies for SIP s and EM. 4.9. Maintain accurate records verifying that required samples have been collected, processed and dispersed to appropriate testing laboratories. 4.10. Reviewing the incoming data for completeness and adherence to specifications. 4.11. Maintain communication links between different testing laboratories to ensure timely testing and accuracy of samples. 4.12. Create and Maintain laboratory procedures and governing documents. 4.13. Environmental 4.13.1. Participate in implementation of the EMS management system including continual improvement, pollution prevention, objectives and targets, and regulatory compliance. 4.13.2. Implement and follow all applicable EMS procedures. 4.13.3. Adhere to the site's EHS Code of Conduct. 4.14. Other responsibilities may be assigned and not all responsibilities listed may be assigned. 5. POST HIRE TRAINING PLAN REQUIREMENTS: 5.1. Maintain adherence to position training curriculum. 5.2. Training Plan Requirements as identified in Corporate Training Procedure, CP0128. 5.3. Applicable training plan for the area of support. 6. PHYSICAL DEMANDS: 6.1. Requires long walking, standing, bending, stooping and reaching. 6.2. May require lifting of boxes or material not to exceed 50 lbs. 6.3. May require use of a pallet jack. 6.4. Maintain vision certification through the visual acuity testing/process. 6.5. Office deskwork, requiring sitting, walking, using the phone and computer 6.6. Operation of hydraulic and manual cutting equipment daily. 7. WORK ENVIRONMENT: 7.1. Work in office and/or manufacturing environment and/or laboratory environment. 7.2. Flexibility to adjust and rotate the working hours to support Laboratory needs. 7.3. Gowning required as per established procedures. Qualifications EDUCATION/CERTIFICATION REQUIREMENTS: 2.1. High school diploma or equivalent required. 2.2. University/Bachelor's Degree or equivalent required, Microbiology preferred. 2.3. Six-sigma certification preferred. Additional Information For more information, Please contact Sneha Shrivastava **************

About Sandia: Sandia National Laboratories is the nation's premier science and engineering lab for national security and technology innovation, with teams of specialists focused on cutting-edge work in a broad array of areas. Some of the main reasons we love our jobs: + Challenging work with amazing impact that contributes to security, peace, and freedom worldwide + Extraordinary co-workers + Some of the best tools, equipment, and research facilities in the world + Career advancement and enrichment opportunities + Flexible work arrangements for many positions include 9/80 (work 80 hours every two weeks, with every other Friday off) and 4/10 (work 4 ten-hour days each week) compressed workweeks, part-time work, and telecommuting (a mix of onsite work and working from home) + Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and amenities aimed at creating a solid work/life balance* World-changing technologies. Life-changing careers. Learn more about Sandia at: ********************* *These benefits vary by job classification. What Your Job Will Be Like: We are seeking a postdoctoral researcher (job title: Postdoctoral Appointee) to join our team and assist with experimental geomechanics, material science, and geothermal energy research. On any given day, you may be called on to: + Support state-of-the-art rock mechanics testing. + Develop and implement laboratory experiments. + Interpret coupled process behavior in materials. + Process and analyze experimental data for subsurface applications. This position is located in Albuquerque, NM, and the annual salary for this position is $98,500. Due to the nature of the work, the selected applicant must be able to work onsite. Qualifications We Require: + PhD in geology/geophysics, geomechanics, geotechnical engineering, or other relevant, related discipline + Hands-on experience in laboratory experimentation + Experience with geophysical analysis + Proven record of technical accomplishment and strong written and verbal communication skills, as evidenced by publications in peer-reviewed journals and/or presentations at scientific conferences + Ability to obtain and maintain a DOE L-level security clearance Qualifications We Desire: + Familiarity with data acquisition and processing techniques + Experience with experimental rock mechanics research and subsurface energy applications + Proven ability to independently identify and develop innovative solutions to a diverse range of challenges + Excellent oral and written communication skills, including proficiency in technical writing + Strong interpersonal and teamwork skills, with the ability to thrive in a high-functioning environment About Our Team: The Geothermal Research Department is an organization that delivers unique solutions for customers who require components and systems capable of operating in harsh and often high-temperature environments. The historical mission of the department was to address technology needs related to the development of geothermal energy (a baseload renewable energy resource); in particular accessing, monitoring and engineering of geothermal resources in subsurface geologic environments. This mission continues, but the capabilities of the organization have also been leveraged to address other issues of national importance. Current activities are broad in scope and require the efforts of multidisciplinary technical teams with expertise in mechanical engineering, drilling technologies, electronics, geosciences, materials, sensors, and explosives/propellants. Our customer base spans a wide variety of governmental and private sponsors, and we work closely with the geothermal power industry, oil & gas developers, service companies, other national laboratories and academia. In addition, the department maintains and continually updates a wide variety of unique testing capabilities for evaluation of technologies in simulated downhole environments. Posting Duration: This posting will be open for application submissions for a minimum of seven (7) calendar days, including the 'posting date'. Sandia reserves the right to extend the posting date at any time. Security Clearance: Sandia is required by DOE to conduct a pre-employment drug test and background review that includes checks of personal references, credit, law enforcement records, and employment/education verifications. Applicants for employment need to be able to obtain and maintain a DOE L-level security clearance, which requires U.S. citizenship. If you hold more than one citizenship (i.e., of the U.S. and another country), your ability to obtain a security clearance may be impacted. Applicants offered employment with Sandia are subject to a federal background investigation to meet the requirements for access to classified information or matter if the duties of the position require a DOE security clearance. Substance abuse or illegal drug use, falsification of information, criminal activity, serious misconduct or other indicators of untrustworthiness can cause a clearance to be denied or terminated by the DOE, resulting in the inability to perform the duties assigned and subsequent termination of employment. EEO: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status and any other protected class under state or federal law. NNSA Requirements for MedPEDs: If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, drug-releasing pump, hearing aids, or diagnostic equipment and other equipment for measuring, monitoring, and recording body functions such as heartbeat and brain waves, if employed by Sandia National Laboratories you may be required to comply with NNSA security requirements for MedPEDs. If you have a MedPED and you are selected for an on-site interview at Sandia National Laboratories, there may be additional steps necessary to ensure compliance with NNSA security requirements prior to the interview date. Position Information: This postdoctoral position is a temporary position for up to one year, which may be renewed at Sandia's discretion up to five additional years. The PhD must have been conferred within five years prior to employment. Individuals in postdoctoral positions may bid on regular Sandia positions as internal candidates, and in some cases may be converted to regular career positions during their term if warranted by ongoing operational needs, continuing availability of funds, and satisfactory job performance. Job ID: 696580 Job Family: 92 Regular/Temporary Position: T Full/Part-Time Status: F

Schedule: Days and shifts scheduled as needed. Job Summary: Under general supervision, performs waived, moderate or high complexity laboratory tests for the purpose of diagnosis and treatment of disease. Performs maintenance, basic troubleshooting and repairs of laboratory equipment. Runs and evaluates quality control testing to ensure equipment is functional prior to patient testing. May assist with the implementation and oversight of waived point of care testing. Staff in this job description meet the qualifications for designation as Testing Personnel for moderate and high complexity testing under CLIA regulations. ESSENTIAL FUNCTIONS: 1. Performs/results and documents clinical laboratory testing exercising independent judgment and responsibility. 2. Notes abnormal patient results and informs supervisor, pathologist, or principal investigator as appropriate. 3. Operates laboratory equipment, interfaces and instruments, performs and documents basic maintenance procedures. 4. Performs routine logging for QC/QA purposes. Collects and compiles QA data as directed. Monitors QC for trends and takes and documents corrective action as needed or directed. 5. Performs troubleshooting procedures. Identifies testing problems and recommends appropriate solutions using defined guidelines. 6. Actively participates in regulatory inspections. 7. Takes inventory as needed or appropriate. Orders supplies for the Section/Department as directed. 8. Assists with training of new staff and/or students. 9. Serves as a liaison with internal and external customers/employees/clients. 10. Depending on the site or department, may participate in the POCT oversight program including but not limited to; a) training lab and non-lab personnel in the use of waived testing. b) Troubleshoot the performance of waived testing, including IT connectivity issues. c) Review the quality performance of waived testing. d) Participate in the implementation, including validation, if necessary, of waived testing. 11. Depending on the site or department, may collect specimens such as blood, urine, sputum and other body fluids and prepare for analysis. The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified. Minimum Qualifications: Selected candidates for the TriCore Laboratory Scientist position will be placed into LS I, LS II, LS III, or LS IV based on education and experience as follows: Laboratory Scientist I: Must meet one of the following per CLIA regulations: Bachelor s degree in biological, or chemical science from an accredited institution. Note- Candidate may qualify with a Bachelor s degree in physical sciences through December 31, 2024, or Associate s degree in laboratory science (biology or chemistry) or medical laboratory technology from an accredited institution, or Have education and training equivalent to an associate degree in a laboratory science, or medical laboratory technology from an accredited institution that includes - At least 60 semester hours, or equivalent, from an accredited institution that, at a minimum, include either: (1) 24 semester hours of medical laboratory technology courses; or (2) 24 semester hours of science courses that include - (i) Six semester hours of chemistry. (ii) Six semester hours of biology; and (iii) Twelve semester hours of chemistry, biology, or medical laboratory technology in any combination, or Have previously qualified or could have qualified as a technologist under CLIA regulations on or before February 28, 1992 No experience required. Laboratory Scientist II: Must meet one of the following: Bachelor s degree in clinical laboratory science, medical laboratory science, or medical technology from an accredited Institution. No experience required, or Bachelor s degree in biology, or chemistry science from an accredited institution AND two years direct clinical laboratory experience, Note: bachelor s degree in physical science acceptable if completed prior to December 31, 2024, or Associate s degree in laboratory science (biology or chemistry) or medical laboratory technology from an accredited institution AND two years direct clinical laboratory experience, or Two years direct clinical laboratory experience AND have education and training equivalent to an associate degree in a laboratory science, or medical laboratory technology from an accredited institution that includes - At least 60 semester hours, or equivalent, from an accredited institution that, at a minimum, include either - (1) 24 semester hours of medical laboratory technology courses; or (2) 24 semester hours of science courses that include - (i) Six semester hours of chemistry. (ii) Six semester hours of biology; and (iii) Twelve semester hours of chemistry, biology, or medical laboratory technology in any combination, or Two years direct clinical laboratory experience AND have previously qualified or could have qualified as a technologist under CLIA regulations on or before February 28, 1992, or Successful completion of a U.S. military medical laboratory training course AND bachelor s degree in biology or chemistry AND one year of direct clinical laboratory testing experience. Laboratory Scientist III: Must meet one of the following: Two years of Laboratory Scientist II at TriCore, or Bachelor s degree in biology, or chemistry science from an accredited institution AND four years direct clinical laboratory experience, Note bachelor s degree in physical science is acceptable if completed prior to December 31, 2024 or Bachelor s degree in clinical laboratory science, medical laboratory science, or medical technology from an accredited Institution, AND two years direct clinical laboratory experience, or Successful completion of a U.S. military medical laboratory training course AND bachelor s degree in biology or chemistry AND three years of direct clinical laboratory testing experience, or Associate s degree in laboratory science (biology or chemistry) or medical laboratory technology from an accredited institution AND four years direct clinical laboratory experience, or Four year s direct clinical laboratory experience AND have education and training equivalent to an associate degree in a laboratory science, or medical laboratory technology from an accredited institution that includes - At least 60 semester hours, or equivalent, from an accredited institution that, at a minimum, include either - (1) 24 semester hours of medical laboratory technology courses; or (2) 24 semester hours of science courses that include - (i) Six semester hours of chemistry. (ii) Six semester hours of biology; and (iii) Twelve semester hours of chemistry, biology, or medical laboratory technology in any combination, or Four years direct clinical laboratory experience AND have previously qualified or could have qualified as a technologist under CLIA regulations on or before February 28, 1992 Laboratory Scientist IV: Must meet one of the following: Bachelor s degree in clinical laboratory science, medical laboratory science, or medical technology from an accredited Institution, AND four years direct clinical laboratory experience, or Bachelor s degree in biology, or chemistry science from an accredited institution AND four years direct clinical laboratory experience. PREFERENCES*: ASCP or AMT certification as a BB, C, CG, H, M, MB, MLT, MLS, SBB, SC, SCYM, SH, SM, or SMB, or ADLM Certification in POCT, or ACHI certification as CHA,CHT or CHS, or NRCC Certification as a Toxicological Chemist or Toxicological Technologist *Certification required for LS IV placement IMMUNIZATION REQUIREMENTS: Prove immunity to Hepatitis B or be immunized or sign a waiver refusing hepatitis immunization. Provide documentation of a tuberculosis (TB) test conducted not more than 90 days prior to date of hire or have a TB test conducted. IN DEPARTMENTS/LOCATIONS WITH DIRECT PATIENT CONTACT: Prove immunity or be eligible to receive rubella, rubeola and varicella immunization. TriCore is New Mexico s largest laboratory, employing more than 1,400 individuals who serve in a broad range of positions. We are dedicated to improving the quality of care for our communities, and also our employees. We foster a culture of integrity, are dedicated to excellence, and are looking for passionate individuals with a desire to have an impact in patient care, the core of our strategy. We offer excellent benefits including, medical, dental, vision and life insurances, 401(k) retirement plan with employer matching, PTO, and paid holidays, as well as opportunities for continuous learning, education assistance, wellness programs, career advancement, and the ability to share in our genuine commitment to the health of our communities. We offer a variety of shifts at multiple locations.

The UNM Comprehensive Cancer Center is seeking a full-time Health Sciences Research Scientist 3 who will be responsible for performing translational cancer research in an NIH-funded laboratory, with a focus on ovarian tumor biology, immunology, and immune therapy, and the development of novel therapeutics for clinical applications. The successful applicant will work independently on complex research projects, under the supervision of a senior Principal Investigator, and will be responsible for supervising junior lab members including fellows, students, and research technicians. The University of New Mexico Comprehensive Cancer Center is the Official Cancer Center of New Mexico and the only National Cancer Institute-designated Cancer Center in a 500-mile radius. Its more than 136 board-certified oncology specialty physicians include cancer surgeons in every specialty (abdominal, thoracic, bone and soft tissue, neurosurgery, genitourinary, gynecology, and head and neck cancers), adult and pediatric hematologists/medical oncologists, gynecologic oncologists, and radiation oncologists. They, along with more than 600 other cancer healthcare professionals (nurses, pharmacists, nutritionists, navigators, psychologists and social workers), provide treatment to 65% of New Mexico's cancer patients from all across the state and partner with community health systems statewide to provide cancer care closer to home. They treated almost 15,000 patients in more than 100,000 ambulatory clinic visits in addition to in-patient hospitalizations at UNM Hospital. A total of nearly 1,855 patients participated in cancer clinical trials testing new cancer treatments that include tests of novel cancer prevention strategies and cancer genome sequencing. The more than 123 cancer research scientists affiliated with the UNMCCC were awarded $38.2 million in federal and private grants and contracts for cancer research projects. Since 2015, they have published nearly 1000 manuscripts, and promoting economic development, they filed 136 new patents and launched 10 new biotechnology start-up companies. Finally, the physicians, scientists and staff have provided education and training experiences to more than 500 high school, undergraduate, graduate, and postdoctoral fellowship students in cancer research and cancer health care delivery. Learn more at ********************** See the Position Description for additional information. Conditions of Employment * Successful candidate must submit to a post-offer, pre-employment physical examination and medical history check. Additional health screenings may be required, dependent on the nature of the research conducted, as determined by Employee Occupational Health Services. Minimum Qualifications Bachelor's degree; at least 3 years of experience directly related to the duties and responsibilities specified. Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis. Preferred Qualifications * PhD in biological sciences, immunology, or a related field * At least one year of prior postdoctoral fellowship training * Demonstrated ability to design and conduct experiments independently * Training in statistical methods and data analysis * Experience mentoring students or other learners * Authorship on publications in cancer biology, immunology or a related field * Experience with flow cytometry, cell culture, in vivo cancer models, gene editing, fluorescence microscopy Additional Requirements Finalists should be prepared to provide official educational transcripts if selected for hire. Applicants must provide names of 3 professional references that the hiring official can contact. Campus Health Sciences Center (HSC) - Albuquerque, NM Department Division of Molecular Medicine (099X) Employment Type Staff Staff Type Term - Full-Time Term End Date 1 year from date of hire Status Exempt Pay $4,073.33 - $5,721.73 Benefits Eligible This is a benefits eligible position. The University of New Mexico provides a comprehensive package of benefits including medical, dental, vision, and life insurance. In addition, UNM offers educational benefits through the tuition remission and dependent education programs. See the Benefits home page for a more information. ERB Statement As a condition of employment, eligible employees working greater than .25 FTE as determined by the New Mexico Education Retirement Act must make mandatory retirement contributions. For more information, review the Benefits Eligibility at a Glance grid. Background Check Required Yes For Best Consideration Date 11/25/2024 Eligible for Remote Work No Eligible for Remote Work Statement Application Instructions Only applications submitted through the official UNMJobs site will be accepted. If you are viewing this job advertisement on a 3rd party site, please visit UNMJobs to submit an application. APPLICANT: Please complete the official application; making sure to include all prior work experience and average hours worked per week. Attach your Current Resume; listing three Professional References. Attach your Cover Letter that details how your experience matches the position as described above; including any Preferred Qualifications. Positions posted with a Staff Type of Regular or Term are eligible for the Veteran Preference Program. See the Veteran Preference Program webpage for additional details. The University of New Mexico is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity Employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, veteran status, disability, or any other protected class. The University of New Mexico requires all regular staff positions successfully pass a pre-employment background check. This may include, but is not limited to, a criminal history background check, New Mexico Department of Health fingerprint screening, New Mexico Children, Youth, and Families Department fingerprint screening, verification of education credentials, and/or verification of prior employment. For more information about background checks, visit ********************************************************** Refer to ********************************************************* for a definition of Regular Staff.

The Research Technologist assists in study execution; collects samples from and administers agents to research animals in accordance with IACUC standards with a large focus on necropsy on multiple species. Participation in other pathology and study specific related duties (tissue collection, trimming, specimen processing and management, etc.) will be required. This position will involve preparing various study supplies for the rest of the team, including label making and labeling, helping ensure we do not run out of supply stock, and handling samples post-collection, including shipping samples, transferring samples, and archiving samples. Documents laboratory work to very high, accepted standards and maintains laboratory/medical equipment and supplies in accordance with Standard Operating Procedures (SOPs), protocols and regulations. The successful candidate will assist in administrative functions of study execution such as labeling collection tubes and transporting supplies to appropriate area. Individual will complete moderately complex work assignments as well as documenting laboratory work and maintaining laboratory equipment and supplies, and performing all other related duties and tasks as required or assigned. Qualifications Requires a bachelor's degree in a related scientific discipline or with comparable course work; or an equivalent combination of education, training and/or experience from which comparable knowledge, skills and abilities have been attained. Requires strong written and verbal communication skills, the ability to work independently and as a part of a team. Must have working knowledge of Microsoft Office, as well as the ability to learn department-specific computer systems as needed. Ability to gain and maintain access to Kirtland Air Force base (KAFB) is required. Preferred/Additional Qualifications Physical Requirements Work is performed in a wet laboratory environment. Will operate standard laboratory equipment and will frequently stand, walk, sit, perform lab- and desk-based computer tasks, perform laboratory techniques requiring grasping/pipetting/hand dexterity, perform repetitive motions and occasionally lift objects that weigh up to 50 pounds. Will wear personal protective equipment which may include a respirator. May work in close proximity to an environment containing research animals and may be required to work with or be in areas where hazardous materials and/or infectious agents are present which may require vaccinations. The above is intended to describe the general requirements for the position and should not be interpreted as an exhaustive statement of physical requirements. The Institute will provide reasonable accommodation to any employee with a disability who requires an accommodation to perform the essential functions of the position. Salary Salary is commensurate with experience + $500 sign-on bonus. Lovelace Biomedical is an Equal Opportunity Employer

About Sandia Sandia National Laboratories is the nation's premier science and engineering lab for national security and technology innovation, with teams of specialists focused on cutting-edge work in a broad array of areas. Some of the main reasons we love our jobs: * Challenging work with amazing impact that contributes to security, peace, and freedom worldwide * Extraordinary co-workers * Some of the best tools, equipment, and research facilities in the world * Career advancement and enrichment opportunities * Flexible work arrangements for many positions include 9/80 (work 80 hours every two weeks, with every other Friday off) and 4/10 (work 4 ten-hour days each week) compressed workweeks, part-time work, and telecommuting (a mix of onsite work and working from home) * Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and amenities aimed at creating a solid work/life balance* World-changing technologies. Life-changing careers. Learn more about Sandia at: ********************* * These benefits vary by job classification. What Your Job Will Be Like Are you passionate about working in collaboration with a hardworking team of neuroscientists, computer scientists, mathematicians, and engineers? Our team is seeking a computational neuroscience postdoctoral appointee to conduct research at the interface of neuroscience, artificial intelligence, and implementing neural-inspired algorithms on conventional and specialized hardware. On any given day, you may be called on to: * Draw inspiration from neuroscience to develop novel algorithms to tackle real-world problems. * Develop neurobiological models at differing levels of biological complexity, ranging from neural network theory to neural circuit models constrained by current understanding of biophysical mechanisms underlying sensory processing and learning. * Work with computer scientists, mathematicians, and engineers to abstract neural computations such as dendritic computation, short-term plasticity, and microcircuit computations for incorporation into artificial intelligence algorithms and human-made computing systems. * Develop techniques for mapping novel brain-inspired and AI models onto existing and emerging neuromorphic hardware. This includes analyzing, benchmarking, and modeling neuromorphic architectures. * Publish research results in journals and professional conference venues. * Due to the nature of the work the selected applicant must be able to work onsite in Albuquerque, New Mexico Relocation will be provided for those that qualify. Relocation will be provided for those that qualify. Qualifications We Require * Possess, or are pursuing, a PhD in theoretical neuroscience, computer science, mathematics, physics or a relevant field; PhD must be conferred within five years prior to employment. * Experience with theoretical or practical aspects of either neural algorithms, artificial intelligence models, or neuromorphic hardware. * Experience in a common programming language such as Python or C++. * Able to obtain and maintain a DoE Q clearance. Qualifications We Desire * Interest in developing neural-inspired (e.g., spiking neural network, population codes) and cutting-edge artificial intelligence algorithms (e.g. transformer models, RNNs, diffusion models) or in the deployment and application of such algorithms. * Experience with specialized computational architectures such as GPUs, FPGAs, neuromorphic processors. * Experience with neural network modeling languages (PyTorch, Tensorflow, Keras, etc) or neural modeling languages (Brian, NEST, etc). * Prior peer-reviewed publications in top-tier journals are highly desirable. * Desire to work as part of a collaborative, multi-disciplinary team. About Our Team The department of Cognitive & Emerging Computing (Org. 01421) pursues foundational research and development of:- emerging general-purpose energy-efficient and beyond-Moore computing paradigms;- cognitive, brain-inspired and neuromorphic computing, human-machine interface technologies;- advanced heterogeneous architectures based on integrated commodity components, special purpose accelerators, neural architectures and algorithms. Posting Duration This posting will be open for application submissions for a minimum of seven (7) calendar days, including the 'posting date'. Sandia reserves the right to extend the posting date at any time. Security Clearance Sandia is required by DOE to conduct a pre-employment drug test and background review that includes checks of personal references, credit, law enforcement records, and employment/education verifications. Applicants for employment need to be able to obtain and maintain a DOE Q-level security clearance, which requires U.S. citizenship. If you hold more than one citizenship (i.e., of the U.S. and another country), your ability to obtain a security clearance may be impacted. Applicants offered employment with Sandia are subject to a federal background investigation to meet the requirements for access to classified information or matter if the duties of the position require a DOE security clearance. Substance abuse or illegal drug use, falsification of information, criminal activity, serious misconduct or other indicators of trustworthiness can cause a clearance to be denied or terminated by DOE, resulting in the inability to perform the duties assigned and subsequent termination of employment. EEO All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status and any other protected class under state or federal law. NNSA Requirements for MedPEDs If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, drug-releasing pump, hearing aids, or diagnostic equipment and other equipment for measuring, monitoring, and recording body functions such as heartbeat and brain waves, if employed by Sandia National Laboratories you may be required to comply with NNSA security requirements for MedPEDs. If you have a MedPED and you are selected for an on-site interview at Sandia National Laboratories, there may be additional steps necessary to ensure compliance with NNSA security requirements prior to the interview date. Apply for Job * Careers * Sign In * New User

Schedule: Days and shifts as needed. Job Summary: Under general supervision, performs waived, moderate or high complexity laboratory tests for the purpose of diagnosis and treatment of disease. Performs maintenance, basic troubleshooting and repairs of laboratory equipment. Runs and evaluates quality control testing to ensure equipment is functional prior to patient testing. May assist with the implementation and oversight of waived point of care testing. Staff in this job description meet the qualifications for designation as Testing Personnel for moderate and high complexity testing under CLIA regulations. ESSENTIAL FUNCTIONS: 1. Performs/results and documents clinical laboratory testing exercising independent judgment and responsibility. 2. Notes abnormal patient results and informs supervisor, pathologist, or principal investigator as appropriate. 3. Operates laboratory equipment, interfaces and instruments, performs and documents basic maintenance procedures. 4. Performs routine logging for QC/QA purposes. Collects and compiles QA data as directed. Monitors QC for trends and takes and documents corrective action as needed or directed. 5. Performs troubleshooting procedures. Identifies testing problems and recommends appropriate solutions using defined guidelines. 6. Actively participates in regulatory inspections. 7. Takes inventory as needed or appropriate. Orders supplies for the Section/Department as directed. 8. Assists with training of new staff and/or students. 9. Serves as a liaison with internal and external customers/employees/clients. 10. Depending on the site or department, may participate in the POCT oversight program including but not limited to; a) training lab and non-lab personnel in the use of waived testing. b) Troubleshoot the performance of waived testing, including IT connectivity issues. c) Review the quality performance of waived testing. d) Participate in the implementation, including validation, if necessary, of waived testing. 11. Depending on the site or department, may collect specimens such as blood, urine, sputum and other body fluids and prepare for analysis. The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified. Minimum Qualifications: Selected candidates for the TriCore Laboratory Scientist position will be placed into LS I, LS II, LS III, or LS IV based on education and experience as follows: Laboratory Scientist I: Must meet one of the following per CLIA regulations: Bachelor s degree in biological, or chemical science from an accredited institution. Note- Candidate may qualify with a Bachelor s degree in physical sciences through December 31, 2024, or Associate s degree in laboratory science (biology or chemistry) or medical laboratory technology from an accredited institution, or Have education and training equivalent to an associate degree in a laboratory science, or medical laboratory technology from an accredited institution that includes - At least 60 semester hours, or equivalent, from an accredited institution that, at a minimum, include either: (1) 24 semester hours of medical laboratory technology courses; or (2) 24 semester hours of science courses that include - (i) Six semester hours of chemistry. (ii) Six semester hours of biology; and (iii) Twelve semester hours of chemistry, biology, or medical laboratory technology in any combination, or Have previously qualified or could have qualified as a technologist under CLIA regulations on or before February 28, 1992 No experience required. Laboratory Scientist II: Must meet one of the following: Bachelor s degree in clinical laboratory science, medical laboratory science, or medical technology from an accredited Institution. No experience required, or Bachelor s degree in biology, or chemistry science from an accredited institution AND two years direct clinical laboratory experience, Note: bachelor s degree in physical science acceptable if completed prior to December 31, 2024, or Associate s degree in laboratory science (biology or chemistry) or medical laboratory technology from an accredited institution AND two years direct clinical laboratory experience, or Two years direct clinical laboratory experience AND have education and training equivalent to an associate degree in a laboratory science, or medical laboratory technology from an accredited institution that includes - At least 60 semester hours, or equivalent, from an accredited institution that, at a minimum, include either - (1) 24 semester hours of medical laboratory technology courses; or (2) 24 semester hours of science courses that include - (i) Six semester hours of chemistry. (ii) Six semester hours of biology; and (iii) Twelve semester hours of chemistry, biology, or medical laboratory technology in any combination, or Two years direct clinical laboratory experience AND have previously qualified or could have qualified as a technologist under CLIA regulations on or before February 28, 1992, or Successful completion of a U.S. military medical laboratory training course AND bachelor s degree in biology or chemistry AND one year of direct clinical laboratory testing experience. Laboratory Scientist III: Must meet one of the following: Two years of Laboratory Scientist II at TriCore, or Bachelor s degree in biology, or chemistry science from an accredited institution AND four years direct clinical laboratory experience, Note bachelor s degree in physical science is acceptable if completed prior to December 31, 2024 or Bachelor s degree in clinical laboratory science, medical laboratory science, or medical technology from an accredited Institution, AND two years direct clinical laboratory experience, or Successful completion of a U.S. military medical laboratory training course AND bachelor s degree in biology or chemistry AND three years of direct clinical laboratory testing experience, or Associate s degree in laboratory science (biology or chemistry) or medical laboratory technology from an accredited institution AND four years direct clinical laboratory experience, or Four year s direct clinical laboratory experience AND have education and training equivalent to an associate degree in a laboratory science, or medical laboratory technology from an accredited institution that includes - At least 60 semester hours, or equivalent, from an accredited institution that, at a minimum, include either - (1) 24 semester hours of medical laboratory technology courses; or (2) 24 semester hours of science courses that include - (i) Six semester hours of chemistry. (ii) Six semester hours of biology; and (iii) Twelve semester hours of chemistry, biology, or medical laboratory technology in any combination, or Four years direct clinical laboratory experience AND have previously qualified or could have qualified as a technologist under CLIA regulations on or before February 28, 1992 Laboratory Scientist IV: Must meet one of the following: Bachelor s degree in clinical laboratory science, medical laboratory science, or medical technology from an accredited Institution, AND four years direct clinical laboratory experience, or Bachelor s degree in biology, or chemistry science from an accredited institution AND four years direct clinical laboratory experience. PREFERENCES*: ASCP or AMT certification as a BB, C, CG, H, M, MB, MLT, MLS, SBB, SC, SCYM, SH, SM, or SMB, or ADLM Certification in POCT, or ACHI certification as CHA,CHT or CHS, or NRCC Certification as a Toxicological Chemist or Toxicological Technologist *Certification required for LS IV placement IMMUNIZATION REQUIREMENTS: Prove immunity to Hepatitis B or be immunized or sign a waiver refusing hepatitis immunization. Provide documentation of a tuberculosis (TB) test conducted not more than 90 days prior to date of hire or have a TB test conducted. IN DEPARTMENTS/LOCATIONS WITH DIRECT PATIENT CONTACT: Prove immunity or be eligible to receive rubella, rubeola and varicella immunization. TriCore is New Mexico s largest laboratory, employing more than 1,400 individuals who serve in a broad range of positions. We are dedicated to improving the quality of care for our communities, and also our employees. We foster a culture of integrity, are dedicated to excellence, and are looking for passionate individuals with a desire to have an impact in patient care, the core of our strategy. We offer excellent benefits including, medical, dental, vision and life insurances, 401(k) retirement plan with employer matching, PTO, and paid holidays, as well as opportunities for continuous learning, education assistance, wellness programs, career advancement, and the ability to share in our genuine commitment to the health of our communities. We offer a variety of shifts at multiple locations.

This position will be located in the UNM Prevention and Population Sciences (PPS) division and will be part of a multi-disciplinary group of researchers who are conducting a range of studies designed to improve health-related social needs and health. This position will work with existing principal investigators in PPS to plan, design, and conduct research and present findings for multiple research studies. The Senior Research Scientist 1 will apply advanced analytic techniques to develop research designs, create data collection and sampling plans, and analyze data. This position will obtain and analyze administrative data as well as primary data. This position will also communicate research findings to the scientific community in peer-reviewed journal articles and also to policymakers via presentations, research briefs, or other means. The Senior Research Scientist 1 is expected to be familiar with advanced statistical techniques in areas such as power calculations, weighting, and sample plans. This position will also contribute to the preparation of grant and contract proposals. Duties and responsibilities for this position may include: * Assist in developing research designs for complex projects. * Undertaking power calculations to determine sample sizes and research designs. * Develop sample plans for data collection. * Assist in original data collection for multimodal research projects. * Obtain, clean and analyze administrative data. * Create data analysis plans and analyze data according to plans. Analyses will include stratified and clustered data, so advance modeling and analysis techniques will be required. * Report results from research by preparing articles for peer-reviewed journals. * Communicate findings from multiple projects to policymakers and other stakeholders, through in-person presentations, research briefs and other means. * Contribute to the preparation of grant and contract proposals. * Performs other job-related duties as assigned. See the Position Description for additional information. Conditions of Employment * Successful candidate must submit to a post-offer, pre-employment physical examination and medical history check. Additional health screenings may be required, dependent on the nature of the research conducted, as determined by Employee Occupational Health Services. Minimum Qualifications Master's degree; at least 5 years of experience directly related to the duties and responsibilities specified. Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis. Preferred Qualifications * Familiarity with health promotion and improving health-related social needs with diverse populations in New Mexico. * Advanced degree in statistics or other field with extensive statistical training. * Experience analyzing primary data as well as administrative data. Additional Requirements Campus Health Sciences Center (HSC) - Albuquerque, NM Department Peds Prvn and Population Sciences (997E) Employment Type Staff Staff Type Term - Part-Time Term End Date 06/30/2026 Status Exempt Pay Monthly: $4,875.87 - $6,976.67 Benefits Eligible This is a benefits eligible position. The University of New Mexico provides a comprehensive package of benefits including medical, dental, vision, and life insurance. In addition, UNM offers educational benefits through the tuition remission and dependent education programs. See the Benefits home page for a more information. ERB Statement As a condition of employment, eligible employees working greater than .25 FTE as determined by the New Mexico Education Retirement Act must make mandatory retirement contributions. For more information, review the Benefits Eligibility at a Glance grid. Background Check Required Yes For Best Consideration Date 1/13/2026 Eligible for Remote Work Yes Eligible for Remote Work Statement This position is eligible for a hybrid schedule. Application Instructions Only applications submitted through the official UNMJobs site will be accepted. If you are viewing this job advertisement on a 3rd party site, please visit UNMJobs to submit an application. A complete application will consist of current resume, cover letter and reference. Please describe in your cover letter how you meet the preferred qualifications for the position. Include three references in your resume. The references must be professional references, preferably supervisors. Finalists should be prepared to provide official educational transcripts if selected for hire. Positions posted with a Staff Type of Regular or Term are eligible for the Veteran Preference Program. See the Veteran Preference Program webpage for additional details. The University of New Mexico is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity Employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, veteran status, disability, or any other protected class. The University of New Mexico requires all regular staff positions successfully pass a pre-employment background check. This may include, but is not limited to, a criminal history background check, New Mexico Department of Health fingerprint screening, New Mexico Children, Youth, and Families Department fingerprint screening, verification of education credentials, and/or verification of prior employment. For more information about background checks, visit ********************************************************** Refer to ********************************************************* for a definition of Regular Staff.