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Applicants must be currently enrolled in a university-degreed program and have a strong interest in biotechnology, biology, microbiology, and/or diagnostics. Specific duties may include molecular biology work in the laboratory, general laboratory support activities, study planning, data analysis, pr

Company / University Description University of Utah and University of Washington are recruiting a postdoctoral fellow to help develop next-generation biological systems for low-concentration methane capture and conversion. This position brings together expertise in bioreactor engineering, methanotroph biology, computational biophysics, and technology commercialization to address one of the most urgent climate challenges: reducing methane emissions while creating valuable products. The position is jointly mentored by Mary Lidstrom (methanotroph physiology and metabolic engineering), Jessica Swanson (molecular biophysics and efficiency modeling), and Swomitra Mohanty (bioreactor engineering). Role Description The postdoc will play a central role in designing and optimizing continuous methane-fed bioreactors for low-concentration methane conversion. Responsibilities include: • Designing and operating continuous bioreactor systems, • Optimizing gas-liquid mass transfer and reactor performance, • Growing and characterizing Methylotuvimicrobium buryatense 5GB1, • Identifying biological and engineering bottlenecks limiting efficiency, • Generating data to inform scale-up and commercialization strategies Qualifications Required • PhD in Chemical Engineering, Bioengineering, Microbiology, Biomolecular Sciences, or related field, • Hands-on experience with bioreactors, microbial systems, fermentation, or transport phenomena, • Strong experimental skills, • Gas fermentation or gas-liquid reactor experience, • Methanotroph/C1 metabolism experience, • Scale-up experience, • Interest in startups, commercialization, or climate tech More Details: To Apply • Send an email briefly describing why you are interested in this position and why you think you would be a good fit. See above link for further instructions.

Please submit a cover letter with your application for this position Geography:Multiple positions available across the U.S. Territory size and geography may vary and will be assigned based on evolving business needs and the location of the selected candidate Description: Myriad Genetics is seeking an experienced Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within Myriad Genetics. This field-based, scientifically focused role supports liquid and tumor profiling across solid tumors, including MRD testing, NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, and urologists across academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, product, R&D, clinical operations, marketing, commercial teams, and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: * Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGSbased testing. * Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. * Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. * Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. * Contributing to the Somatic Medical Affairs team through collaboration, bestpractice sharing, and training. * Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas. Serves as a Medical/Scientific resource to Clinicians by: * Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility. * Delivering clinical and scientific education (virtual and inperson) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies. * Providing guidance on interpreting MRD or complex NGS reports and integrating results into treatment decisions. * Increasing awareness of Myriad's somatic test portfolio, enhancing appropriate utilization, and supporting evidence-based precision oncology. * Clinical support during KOL meetings with and without commercial partners. Supports Myriad Oncology initiatives and demonstrates business acumen through: * Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory. * Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation. * Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate. * Partnering with cross-functional teams (Medical, Product, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training. * Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates. * Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed. * Educating sales team on current clinical practice, guideline advancements, and aiding in sales training to elevate their skillset. Qualifications: * Advanced scientific or clinical degreerequired: PhD, MS/Genetic Counseling, NP/PA, MD, PharmD or related field. * Minimum of 7 years of clinical, industry, and/or research is required; with at least 5 years being MSL (or similar) experience, preferably within a diagnostic laboratory setting. * Deep understanding ofbiomarkers, targeted therapy pathways, resistance mechanisms, oncology guidelines/management, and molecular profiling and/or MRD testing is required. * Ability to interpret and clearly communicate complex molecular data. * Demonstratedexperience ofengaging clinicians, KOLs, and academic groups. * Excellent presentation, communication, and scientific storytelling skills. * Willing and able to travel. Typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. * Effectively manage travel andmaintainexpenses withinbudget. Significant Work Activities: * Continuous sitting for prolonged periods (> 2 consecutive hours in an 8-hour day) * Keyboard use (greater or equal to 50% of the workday) * Driving a personal vehicle / rental car and flying across the U.S. * Travel: typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. Job Type: Experienced Schedule: Full-time Salary varies on experience and may adjust in predefined locations #LI-remote #LI-MH1

Overview The Lab Automation Engineer II solves key workflow problems in large complex health systems. Supports a full technology stack of automated lab and software sequencing. Responsibility • Design, implement, and test process automation using liquid handlers and other automated equipment., • Utilize programming languages to integrate new or modifications to processes to the robotics software stack., • Work cross-functionally with the science, lab, manufacturing, and maintenance teams., • Design, deploy, and test liquid handler scripts and changes to custom automated work cells., • Make impactful contributions to troubleshooting efforts, analyzing data and helping drive key process-related decisions., • Develop automation related documentation for effective operation and maintenance of automated equipment., • Travel to Myriad locations as needed during certain project phases. Qualifications • Bachelor's degree in molecular biology, bioengineering, chemistry, or related field required., • 2+ years of industry experience., • Experience in programming in at least two of the major liquid handling systems (Tecan, Beckman, Hamilton)., • Experience with molecular biology lab processes., • Software programming experience with Python, C#, or other languages is a plus. Applicant must be a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder) Physical Requirements Lifting Requirements - light work or exerting up to 20 pounds of force frequently. Physical Requirements - stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing or pulling, and reaching. Use of equipment and tools necessary to perform essential job functions. EEO We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. In hiring and all other employment decisions, we prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as any mental health or physical disability needs. #LI-KO1 #LabAutomation #AutomationEngineering #LifeSciencesCareers #EngineeringJobs #Bioengineering #MolecularBiology #LaboratoryAutomation #LiquidHandling #Robotics #ProcessAutomation #HealthTech #BiotechJobs #PythonProgramming #RoboticsEngineering #STEMCareers

Please submit a cover letter with your application for this position Geography:Multiple positions available across the U.S. Territory size and geography may vary and will be assigned based on evolving business needs and the location of the selected candidate Description: Myriad Genetics is seeking an experienced Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within Myriad Genetics. This field-based, scientifically focused role supports liquid and tumor profiling across solid tumors, including MRD testing, NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, and urologists across academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, product, R&D, clinical operations, marketing, commercial teams, and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: * Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGSbased testing. * Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. * Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. * Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. * Contributing to the Somatic Medical Affairs team through collaboration, bestpractice sharing, and training. * Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas. Serves as a Medical/Scientific resource to Clinicians by: * Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility. * Delivering clinical and scientific education (virtual and inperson) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies. * Providing guidance on interpreting MRD or complex NGS reports and integrating results into treatment decisions. * Increasing awareness of Myriad's somatic test portfolio, enhancing appropriate utilization, and supporting evidence-based precision oncology. * Clinical support during KOL meetings with and without commercial partners. Supports Myriad Oncology initiatives and demonstrates business acumen through: * Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory. * Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation. * Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate. * Partnering with cross-functional teams (Medical, Product, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training. * Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates. * Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed. * Educating sales team on current clinical practice, guideline advancements, and aiding in sales training to elevate their skillset. Qualifications: * Advanced scientific or clinical degreerequired: PhD, MS/Genetic Counseling, NP/PA, MD, PharmD or related field. * Minimum of 7 years of clinical, industry, and/or research is required; with at least 5 years being MSL (or similar) experience, preferably within a diagnostic laboratory setting. * Deep understanding ofbiomarkers, targeted therapy pathways, resistance mechanisms, oncology guidelines/management, and molecular profiling and/or MRD testing is required. * Ability to interpret and clearly communicate complex molecular data. * Demonstratedexperience ofengaging clinicians, KOLs, and academic groups. * Excellent presentation, communication, and scientific storytelling skills. * Willing and able to travel. Typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. * Effectively manage travel andmaintainexpenses withinbudget. Significant Work Activities: * Continuous sitting for prolonged periods (> 2 consecutive hours in an 8-hour day) * Keyboard use (greater or equal to 50% of the workday) * Driving a personal vehicle / rental car and flying across the U.S. * Travel: typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. Job Type: Experienced Schedule: Full-time Salary varies on experience and may adjust in predefined locations #LI-remote #LI-MH1

Geography:FL Description: Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: * Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGSbased testing. * Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. * Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. * Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. * Contributing to the Somatic Medical Affairs team through collaboration, bestpractice sharing, and training. * Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas. Serves as a Medical/Scientific resource to Clinicians by: * Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility. * Delivering clinical and scientific education (virtual and inperson) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies. * Providing guidance on interpreting complex NGS reports and integrating results into treatment decisions. * Increasing awareness of Myriad's somatic test portfolio, enhancing appropriate utilization, and supporting evidencebased precision oncology. Supports Myriad Oncology initiatives and demonstrates business acumen through: * Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory. * Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation. * Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate. * Partnering with crossfunctional teams (Medical, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training. * Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates. * Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed. * Educating sales team on current clinical practice, guideline advancements, and aiding in sales training to elevate their skillset. Qualifications: * Advanced scientific or clinical degree required: PharmD, PhD, MS/Genetic Counseling, NP/PA, MD, or related field. * Strong background in oncology, molecular diagnostics, and precision medicine; prior somatic/NGS experience strongly preferred. * 3+ years of clinical, industry, research, or MSL experience preferred. * Understanding of biomarkers, targeted therapy pathways, molecular profiling, resistance mechanisms, and oncology guidelines. * Ability to interpret and clearly communicate complex molecular data. * Demonstrated experience of engaging clinicians, KOLs, and academic groups. * Excellent presentation, communication, and scientific storytelling skills. * Willing and able to travel. Typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. * Effectively manage travel and maintain expenses within appropriate budget. * Significant Work Activities: * Continuous sitting for prolonged periods (> 2 consecutive hours in an 8-hour day) * Keyboard use (greater or equal to 50% of the workday) * Driving a personal vehicle / rental car and flying across the U.S. * Travel: typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. Job Type: Experienced Lifting Requirements -light work or exerting up to 20 pounds of force frequently. Physical Requirements -stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing, or pulling, and reaching. Use of equipment and tools necessary to perform essential job functions.

The Lab Technologist II is responsible for conducting laboratory processes that support specimen processing and testing. This position works with department management and quality team members to ensure that laboratory activities are defined, documented, and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation, and continuous improvement projects. Shift: Thursday-Sunday 8:00am-6:00pm Each employee's specific job responsibilities are uniquely defined by their individual training plan and assigned duties, but are generally defined as follows: • Complying with the laboratory's technical, administrative, and safety policies and procedures., • Operating high complexity testing., • Participating in the laboratory's quality assurance plan, adhering to quality control and preventive maintenance policies, and appropriately documenting these activities., • Working as part of a team to produce repeatable quality results., • Maintaining a clean and organized laboratory space., • Participating in proficiency testing in the same manner as routine samples., • Participating in continuing education according to accepted laboratory standards., • Actively participating in successful and timely completion of training and competency assessment as outlined in the laboratory and departmental training programs., • Following the laboratory's policies and procedures whenever test systems are not within acceptable limits and documenting the problem and any corrective action., • Troubleshooting and identifying problems that may adversely affect test performance and/or reporting of test results by initiating corrective action and using the defined electronic system to make the required management notification., • Participates within the departmental team to resolve problems or implement projects., • Serves as a trainer on technical processes within the group., • Doctoral, bachelor's, or master's degree in medical technology or a chemical, physical, biological, or clinical laboratory science., • 6 months of clinical lab experience or equivalent required., • California only: CLS trainee license or a CLS or CGMBS license issued by California., • Familiarity with range of molecular biology techniques (qPCR, DNA extraction, DNA sequencing) and proficiency with molecular biology calculations (dilutions, DNA and protein concentration measurements, enzyme activity measurements)., • Ability to adapt to changes in a fast-paced and evolving work environment., • Some schedule flexibility- occasional overtime hours may be required., • Basic proficiency with computers (Excel, other Office tools) and statistics., • Strong verbal and written communication skills., • Extensive documentation skills and attention to detail skills including the ability to develop and follow written procedures, the ability to organize information, ensures that data is recorded correctly and can be easily understood by others. Lifting Requirements - medium work or exerting up to 50 pounds of force occasionally, 20 pounds of force frequently, and 10 pounds of force consistently. Physical Requirements - stationary positioning, moving, operating, ascending/descending, communicating, observing, reaching, and repetitive motion. Use of equipment and tools necessary to perform essential job functions. Hazards and Atmospheric Conditions - exposure to fumes, dust, extreme temperatures, wet and/or humid, noise, vibration, mists or gases, mechanical hazards, chemical hazards, electrical hazards, and radiant energy hazards. OSHA Category I - duties performed routinely requires exposure to blood, body fluid, and tissue. We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. In hiring and all other employment decisions, we prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as any mental health or physical disability needs.

Geography:San Francisco, CA, Los Angeles, CA, San Diego, CA, Portland, OR, Seattle, WA, Boise, ID Description: Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: • Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGSbased testing., • Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards., • Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting., • Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties., • Contributing to the Somatic Medical Affairs team through collaboration, bestpractice sharing, and training., • Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas. Serves as a Medical/Scientific resource to Clinicians by: • Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility., • Delivering clinical and scientific education (virtual and inperson) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies., • Providing guidance on interpreting complex NGS reports and integrating results into treatment decisions., • Increasing awareness of Myriad's somatic test portfolio, enhancing appropriate utilization, and supporting evidencebased precision oncology. Supports Myriad Oncology initiatives and demonstrates business acumen through: • Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory., • Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation., • Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate., • Partnering with crossfunctional teams (Medical, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training., • Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates., • Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed., • Educating sales team on current clinical practice, guideline advancements, and aiding in sales training to elevate their skillset. Qualifications: • Advanced scientific or clinical degree required: PharmD, PhD, MS/Genetic Counseling, NP/PA, MD, or related field., • Strong background in oncology, molecular diagnostics, and precision medicine; prior somatic/NGS experience strongly preferred., • 3+ years of clinical, industry, research, or MSL experience preferred., • Understanding of biomarkers, targeted therapy pathways, molecular profiling, resistance mechanisms, and oncology guidelines., • Ability to interpret and clearly communicate complex molecular data., • Demonstrated experience of engaging clinicians, KOLs, and academic groups., • Excellent presentation, communication, and scientific storytelling skills., • Willing and able to travel. Typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad., • Effectively manage travel and maintain expenses within appropriate budget. Significant Work Activities: • Continuous sitting for prolonged periods (> 2 consecutive hours in an 8-hour day), • Keyboard use (greater or equal to 50% of the workday), • Driving a personal vehicle / rental car and flying across the U.S., • Travel: typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. Job Type: Experienced Lifting Requirements -light work or exerting up to 20 pounds of force frequently. Physical Requirements -stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing, or pulling, and reaching. Use of equipment and tools necessary to perform essential job functions. EEO We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. In hiring and all other employment decisions, we prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as any mental health or physical disability needs. #LI-MH1 #LI-remote

Geography:TN, GA, SC, NC, AL, MS Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: • Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGSbased testing., • Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards., • Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting., • Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties., • Contributing to the Somatic Medical Affairs team through collaboration, bestpractice sharing, and training., • Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas. Serves as a Medical/Scientific resource to Clinicians by: • Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility., • Delivering clinical and scientific education (virtual and inperson) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies., • Providing guidance on interpreting complex NGS reports and integrating results into treatment decisions., • Increasing awareness of Myriad's somatic test portfolio, enhancing appropriate utilization, and supporting evidencebased precision oncology. Supports Myriad Oncology initiatives and demonstrates business acumen through: • Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory., • Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation., • Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate., • Partnering with crossfunctional teams (Medical, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training., • Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates., • Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed., • Educating sales team on current clinical practice, guideline advancements, and aiding in sales training to elevate their skillset. Qualifications: • Advanced scientific or clinical degree required: PharmD, PhD, MS/Genetic Counseling, NP/PA, MD, or related field., • Strong background in oncology, molecular diagnostics, and precision medicine; prior somatic/NGS experience strongly preferred., • 3+ years of clinical, industry, research, or MSL experience preferred., • Understanding of biomarkers, targeted therapy pathways, molecular profiling, resistance mechanisms, and oncology guidelines., • Ability to interpret and clearly communicate complex molecular data., • Demonstrated experience of engaging clinicians, KOLs, and academic groups., • Excellent presentation, communication, and scientific storytelling skills., • Willing and able to travel. Typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad., • Effectively manage travel and maintain expenses within appropriate budget. Significant Work Activities: • Continuous sitting for prolonged periods (> 2 consecutive hours in an 8-hour day), • Keyboard use (greater or equal to 50% of the workday), • Driving a personal vehicle / rental car and flying across the U.S., • Travel: typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. Job Type: Experienced Lifting Requirements -light work or exerting up to 20 pounds of force frequently. Physical Requirements -stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing, or pulling, and reaching. Use of equipment and tools necessary to perform essential job functions. EEO We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. In hiring and all other employment decisions, we prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as any mental health or physical disability needs. #LI-MH1 #LI-remote

Core Responsibilities • Own the product - Lead the development and lifecycle management of MRD products, translating market and clinical needs into clear product requirements and development priorities., • Drive commercialization activities for the product in the US market, including launch planning, positioning, messaging, and development of sales enablement materials. Lead execution of go-to-market plans to support adoption., • Coordinate closely with R&D, clinical, regulatory, medical affairs, and commercial teams to ensure timely product development and successful market introduction., • Track product performance, gather customer and field feedback, and drive continuous optimization to strengthen clinical value and commercial success., • Monitor clinical trends, customer needs, and competitive dynamics to refine product positioning and identify opportunities for product improvements or new features., • Support development and execution of the product roadmap for MRD, translating strategy into clear product requirements, feature prioritization, and deliverables., • Monitor clinical trends, customer needs, and competitive dynamics to refine product positioning and identify opportunities for product improvements or new features., • Participate in sales meetings, seminars, industry conferences, and tradeshows. Qualifications • Bachelor's degree required; MBA, PhD, MD, or other advanced degree in biochemistry, genetics, molecular genetics or molecular biology preferred., • 5+ years of product management or strategic marketing experience in oncology diagnostics, molecular diagnostics, genomics, or precision medicine., • Experience with NGS-based testing, liquid biopsy, comprehensive genomic profiling, or related technologies, experience in MRD strongly preferred, • Experience supporting product launches or commercialization initiatives in the life sciences or diagnostics space., • Proven ability to lead cross-functional projects and coordinate activities across R&D, clinical, regulatory, and commercial teams., • Strong analytical and communication skills, with the ability to translate complex scientific concepts into clear product requirements and customer-facing messaging., • Ability to work in a fast-paced, collaborative environment and drive execution across multiple stakeholders., • Up to 40% travel anticipated. #LI-PP1

The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. Essential Duties: • Assists with stocking project-specific laboratory supplies, including inventorying stock., • Act as a good lab citizen and team member. Coordinate and collaborate within and across teams and functional groups for routine lab activities, cleaning, equipment use, specific assigned tasks and projects, and sharing of knowledge, skills, and ideas., • Work in a Biosafety level 2/2+ environment with potentially pathogenic microbes, patient samples, and body fluids using sterile technique for contamination and infection control., • Ensure data integrity and accurate record-keeping by collecting, recording (in an electronic laboratory notebook and/or study worksheets), analyzing and verifying data in compliance with company standard operating procedures, work instruction documents, and study protocols., • Use and maintain laboratory equipment, supplies/inventory, and workspaces according to operational, quality, and safety requirements as outlined in protocols, standard operating procedures, and work instruction documents., • Perform routine calculations and laboratory techniques including solution formulation, microbial culture and enumeration, nucleic acid extraction and quantification, real-time and/or digital PCR, as well as basic statistical analyses., • Execute study protocols and contribute to protocol and process development, optimization, and/or revision., • Conduct routine data analysis under supervision., • Communicate data and analyses in written reports and oral presentations to peers and supervisors, commensurate with job level., • Contribute to the writing of study reports., • Perform all work in compliance with company quality procedures and standards. Education, Training, and Experience: • High School Diploma, GED or equivalent and 4+ years of experience in an academic, industry, or healthcare laboratory required., • Consistently upholds and reflects the core ethical principles and values that bioMerieux promotes, • Functional skills include critical thinking, adaptability, time management, communication, problem-solving and digital literacy, • Technical learning aptitude to quickly understand and acquire new technical knowledge and skills, • Flexibility, being highly adaptable and resilient to thrive in a dynamic work environment, • Learning agility to be able to learn from experiences and apply that knowledge to new situations, • Detail orientation to complete tasks without errors and produce high-quality work., • Thriving in a fast-paced environment by managing tasks, multitasking, and adapting quickly to maintain productivity, • Practicing time management to allocate tasks, balance priorities, and meet deadlines efficiently, • Ability to work cross-functionally allowing for better collaboration and communication when working across teams to achieve shared objectives, • Ability to cooperate with others at all levels including leadership, • Effective verbal communication skills, • Participating in a way that enhances team performance and cohesion, • Fosters a culture of inclusiveness among all team members, • Actively and attentively listen to others, ensuring a clear understanding of their messages, needs, and concerns., • Demonstrates fundamental awareness and can perform routine tasks with guidance, • Working knowledge of current and evolving microbiology and molecular biology principles, tools, and techniques relevant to developing diagnostic tests for infectious diseases, • Basic competence in laboratory practices including pipetting, handling biological and chemical materials, sterile technique and contamination control, and basic concentration and statistical calculations, • Ability to ascend/descend stairs, ladders, ramps, and the like., • Ability to wear PPE correctly most of the day., • Must be able to lift and safely maneuver 40 lbs., • Manual and visual dexterity to handle small tubes and manipulate very small volumes; reasonable accommodations are applicable. BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at (385) 770-1132, by email at ___, or by dialing 711 for access to Telecommunications Relay Services (TRS).

Geography: Midwest Territory (Most likely will include but may be adjusted: OH, IL, IN, MN, WI, MI) Description: Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: * Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGSbased testing. * Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. * Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. * Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. * Contributing to the Somatic Medical Affairs team through collaboration, bestpractice sharing, and training. * Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas. Serves as a Medical/Scientific resource to Clinicians by: * Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility. * Delivering clinical and scientific education (virtual and inperson) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies. * Providing guidance on interpreting complex NGS reports and integrating results into treatment decisions. * Increasing awareness of Myriad's somatic test portfolio, enhancing appropriate utilization, and supporting evidencebased precision oncology. Supports Myriad Oncology initiatives and demonstrates business acumen through: * Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory. * Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation. * Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate. * Partnering with crossfunctional teams (Medical, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training. * Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates. * Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed. *

BioMerieux is a global leader in developing, manufacturing, marketing, and supporting FDA-cleared molecular diagnostics for infectious disease. These internships offer motivated college or high school students (must be at least 18 years of age) an opportunity to contribute to an early-stage research or product development project and to be immersed in a highly productive and collaborative biotechnology environment. Under the close supervision of a mentorship team, interns may participate in any or all of the following activities, depending on the specific project assigned: (1) perform general laboratory duties; (2) perform wet lab molecular biology work; (3) assist in planning and setup activities for research studies; (4) participate in data analysis and presentation; (5) co-develop and test new research productivity tools; and (6) maintain accurate records of work performed, in accordance with BioMerieux Quality Management System. Internships are available in two R&D groups focused on Panel development and assay design and research focused on investigation and sustainability. Please indicate in your cover letter which area of focus interests you. Internships are considered non-exempt positions; full- and part-time positions will be considered. Specific duties may include molecular biology work in the laboratory, general laboratory support activities, study planning, data analysis, presentation of results, and accurate and thorough recordkeeping. Interns will: • Listen actively while receiving instruction, in order to quickly master assigned duties, • Be present and engaged during scheduled work hours, • Ask questions when any aspect of assigned work is unclear, • Be curious and persistent when solving problems, • Behave professionally while representing BioMerieux, • Participate in research team meetings, • Perform assigned duties with a conscientious and detail-oriented approach, • Prepare preliminary analyses of experimental data for review with mentor, • Assist mentor in preparing presentations of data and conclusions, • Applicants must be currently enrolled in a university-degreed program and have a strong interest in biotechnology, biology, microbiology, and/or diagnostics., • Currently enrolled undergraduate students pursuing a biotechnology-related bachelor's degree are preferred., • Comfort with word processing, spreadsheet, and presentation software, • Strong interest in biotechnology, • Willingness to learn from others, • Ability to respond positively to constructive feedback, • Dependability in maintaining a regular work schedule, • Detail-oriented approach to work, • Positive attitude in the workplace, • Proactive communication style BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at (385) 770-1132, by email at ___, or by dialing 711 for access to Telecommunications Relay Services (TRS).

Geography:MA, NY, NJ, PA, NJ, DC, VA Description: Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: * Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGSbased testing. * Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards. * Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting. * Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties. * Contributing to the Somatic Medical Affairs team through collaboration, bestpractice sharing, and training. * Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas. Serves as a Medical/Scientific resource to Clinicians by: * Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility. * Delivering clinical and scientific education (virtual and inperson) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies. * Providing guidance on interpreting complex NGS reports and integrating results into treatment decisions. * Increasing awareness of Myriad's somatic test portfolio, enhancing appropriate utilization, and supporting evidencebased precision oncology. Supports Myriad Oncology initiatives and demonstrates business acumen through: * Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory. * Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation. * Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate. * Partnering with crossfunctional teams (Medical, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training. * Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates. * Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed. * Educating sales team on current clinical practice, guideline advancements, and aiding in sales training to elevate their skillset. Qualifications: * Advanced scientific or clinical degree required: PharmD, PhD, MS/Genetic Counseling, NP/PA, MD, or related field. * Strong background in oncology, molecular diagnostics, and precision medicine; prior somatic/NGS experience strongly preferred. * 3+ years of clinical, industry, research, or MSL experience preferred. * Understanding of biomarkers, targeted therapy pathways, molecular profiling, resistance mechanisms, and oncology guidelines. * Ability to interpret and clearly communicate complex molecular data. * Demonstrated experience of engaging clinicians, KOLs, and academic groups. * Excellent presentation, communication, and scientific storytelling skills. * Willing and able to travel. Typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. * Effectively manage travel and maintain expenses within appropriate budget. * Significant Work Activities: * Continuous sitting for prolonged periods (> 2 consecutive hours in an 8-hour day) * Keyboard use (greater or equal to 50% of the workday) * Driving a personal vehicle / rental car and flying across the U.S. * Travel: typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. Job Type: Experienced Lifting Requirements -light work or exerting up to 20 pounds of force frequently. Physical Requirements -stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing, or pulling, and reaching. Use of equipment and tools necessary to perform essential job functions.

What You'll Do • Own and evolve Myriad's international product portfolio, aligning strategy to regional market dynamics and growth opportunities, • Partner with Regulatory, Commercial, and Biopharma teams to define and execute international expansion strategies (with emphasis on Japan and Europe), • Lead product positioning and messaging-translating complex science into differentiated, market-ready value propositions, • Build and validate business cases for new opportunities, including market analysis, segmentation, VOC insights, and product requirements, • Drive commercialization strategy, including launch planning, messaging, and enablement for downstream marketing and sales teams, • Continuously assess product and portfolio performance-turning field insights and customer feedback into actionable improvements, • Support market access and reimbursement efforts with clear technical and clinical value articulation, • Represent Myriad at industry events, conferences, and customer engagements, • Stay ahead of market trends, competitive dynamics, and regulatory landscapes across international regions, • Bachelor's degree in life sciences (e.g., biochemistry, genetics, molecular biology); advanced degree preferred, • 12+ years of product management and commercialization experience within biotech, diagnostics, or oncology, • Proven experience commercializing IVD or genomic products in international markets, particularly Japan and Europe, • Deep familiarity with genomic technologies (e.g., NGS, liquid biopsy, precision medicine); MRD experience strongly preferred, • Demonstrated success launching clinical diagnostic products and driving global go-to-market strategy, • Strong track record of influencing cross-functional teams and delivering measurable business impact, • Ability to translate complex data into clear strategy and executive-level communication, • Balance of analytical rigor and creative thinking in product and market strategy, • Comfortable operating in a highly collaborative, matrixed environment We offer a comprehensive and flexible benefits package designed to support your health, well-being, and long-term success: • Medical coverage with 100% preventive care, plus HSA/FSA contributions, • 12 weeks paid parental leave and employer-paid disability, • Flexible discretionary time off (DTO), • 401(k) with employer match and employee stock purchase program, • Student debt repayment and milestone bonuses, • Additional support for family, mental health, and wellness programs #LI-PP1 Physical Requirements Ability to move throughout an office [or lab] setting to perform work tasks. Ability to clearly communicate with coworkers or customers. Use of equipment and tools necessary to perform essential job functions.

About the opportunity SWCA Environmental Consultants is expanding our team and actively looking for dynamic individuals who are following their passion in delivering the highest-quality project work.OurSalt Lake Cityofficeislooking for a self-motivatedProject-LevelEnvironmental Plannerwith attention to detail and strong communication skills. Depending upon experience and qualifications, this individual can get hired as either an assistant project environmental planner, an associate environmental planner, or a project environmental planner. Individuals need to be willing and able to work with peers across various offices and accomplish tasks associated with a variety of projects in any given week. The ability to work directly with clients is imperative.The interest in pursuing new business is also desirable. This is a regular status, full-time position, reporting to one of SWCA's Sr. Project Managers out of ourSalt Lake Cityoffice. Work can be based in the office, or in a hybrid work arrangement or distributed, for those located in the region. This position is available at the below levels and title will be based on years of relevant experience: • Assistant ProjectEnvironmental Planner- Typically with three (3) years of relevant industry experienceand expertise, • Association ProjectEnvironmentalPlanner - Typically with five (5) years of relevant industry experienceand expertise Please also submit a cover letter to be considered for this role. Please highlight in your cover letter if you have relevant government experience, especially Federal agency experience. Application deadline: Our team will begin reviewing applications immediately, and interviews will be scheduled with qualified candidates on a rolling basis. The application process will remain open until we have received a robust pool of qualified candidates. Once we have identified suitable individuals, we may close the application process without prior notice. We appreciate the time and effort invested by all applicants and will carefully consider each submission. SWCA Environmental Consultantsis a growing,1,800 staff+,employee-owned firm, providing a full-spectrum of environmental services.Our Vision (the North Star)isto makeSWCA the best workplace and industry leader in sustainability, bringing sound science and creative solutions to global environmental challenges while maintaining a dedication to employee-ownership.We live our core values: we collaborate as#OneSWCA;weare#AlwaysLearning, we#NeverSettle,and we#GiveBack. What you will accomplish You will be responsible for performing NEPA compliance and non-NEPA environmental planning efforts across a wide range of natural resource, land use, and infrastructure projects. These could include environmental impact analyses, facilitating public and agency outreach, and providing quality assurance and leadership during the development of Environmental Assessments (EAs) and Environmental Impact Statements (EISs).Fajer question - any non-NEPA planning? Associate Project Environmental Planner responsibilities include more complex activities and potentially more project management work. Specific responsibilities include: • Contribute topreparingEAs and EISs addressing the development for a wide variety of projects, revision of federalresource management plans (RMPs) andland use plans, issuance of rights-of-way, approvals, and/or leases, policy amendments, etc. In addition, this position will help lead, write, and managetasks forthe preparation of NEPA documents related to projects managed by federal agencies or for those that occur on federal lands., • Participate in non-NEPA environmental planning, including land use and resource management planning, planning level environmental analyses, feasibility and constraint analyses, regulatory strategy development, permitting support, and pre-decisional planning activities that help clients evaluate constraints, risks, and opportunities early in project development., • Support business line growth objectives and participate or lead parts of the development of EAs and EISs, including NEPA documents, for business lines that may include land use planning, generation, transmission, mining, and others., • Assist teams by providing technicalassistancefor the preparation of key aspects of NEPA documents and the NEPA process, including Pre-NOI activities and project planning; development of the description of the proposed action and purpose and need; NEPA document structuring and content planning; public scoping; public comment review and response; and Records of Decisions and Findings of No Significant Impact., • Provide expertise to SWCA project managers on NEPA and other planning projects. Required Qualifications • A minimum of a bachelor's degree in environmental planning, environmental science, biology, environmental science, natural resource management, planning, geology, or another science-related field., • A minimum of three (3) years of NEPA document preparation A working knowledge of federal and state environmental regulations including NEPA, the Federal Land Policy and Management Act (FLPMA), the Clean Water Act (CWA), the Endangered Species Act (ESA), the National Historic Preservation Act (NHPA), and the ability to support project preparation of plans to satisfy regulatory compliance. Preferred Qualifications • Five(5) or more years of NEPA document preparation and 5 yearsof experience in environmental consulting. A working understanding of agency internal processes and procedures and positive existing relationships with federal land management and regulatory agencies, such as the BLM, BOEM, USFS, NPS, BOR, DOE, Federal Energy Regulatory Commission (FERC), Natural Resource Conservation Service (NRCS), and/or U.S. Fish and Wildlife Service (USFWS) is strongly preferred., • Experience with public lands, natural resource issues, wind and solar projects, transportation projects, transmission lines, and/or oil and gas projects, and/or infrastructure projects in the western US., • Excellent verbal and written communication skills; interpersonal skills and emotional intelligence; attention to detail; and organization, schedule, and budget management skills., • Experience with supporting business development with federal agencies, resource management plans (RMPs), mining, oil and gas, and renewable energy developers or other non-federal applicants that seek permits or leases from federal agencies helpful. SWCA is a 100% employee-owned, and we build our success together. With offices across the United States, SWCA is one of the largest environmental compliance firms and ranks among Engineering News-Record's Top 200 Environmental Firms. We offer a supportive, team-oriented work environment and competitive wages and benefits, including an 100% employee stock ownership plan (retirement).If you are seeking an opportunity to work in a culture of exceptionally skilled and diverse professionals who embrace sound science and creative solutions, then SWCA will be a great fit for you! If you need assistance accessing SWCA's website, completing the online application, or require accommodations at any point during the hiring process due to a disability, please contact us at___or call 1-480-581-5378. We're committed to providing an inclusive and supportive experience for all candidates. This contact information is specifically for accommodation requests; other inquiries will not receive a response. SWCA is committed to salary equity and salary transparency for all its employees. In alignment with this commitment, SWCA posts good faith pay ranges in all its advertised job postings to promote pay equity and transparency. An employee in thisSalt Lake City, UT-basedposition can expect a salary of: Assistant Project Environmental Planner -- $28.09/hour to $36.04/hour; Associate Project Environmental Planner -- $66,144/year to $84,885/year. Actual pay within this range may depend on experience, qualifications, geographic location, client requirements where applicable, and other factors permitted by law. Candidates are also encouraged to consider SWCA's Total Rewards package, which includes a competitive benefits package (___), forward-thinking workplace flexibility, outstanding corporate culture, award-winning career development, and more. EOE - women, minorities, individuals with disabilities and veterans are encouraged to apply.At SWCA Environmental Consultants, we celebrate diversity and are committed to creating an inclusive work environment. We strongly encourage candidates from all backgrounds, including those with diverse experiences and veterans, to apply. We believe that a diverse and inclusive workforce enhances creativity, innovation, and overall organizational success. SWCA continues to invest deeply in career development programs, delivering our award-winning Career Landscape support resources to accelerate the growth of our staff. We recognize the valuable skills and experiences our internal team members bring to SWCA's continued success. Qualified internal candidates are encouraged to apply and will be seriously considered for this position. We believe in promoting from within, where possible, providing our existing employees with compelling opportunities to advance theircareers. #LI-NP1

Geography:TX, LA Description: Myriad Genetics is seeking a Medical Science Liaison (MSL) to support the Somatic / Tumor Genomics portfolio within the Precision Oncology business unit. This field based, scientifically focused role supports liquid and tumor profiling across solid tumors, including NGS based assays, biomarker driven therapy selection, resistance mechanisms, and treatment monitoring. The MSL will engage with medical oncologists, gynecologic oncologists, surgeons, molecular pathologists, urologists, academic centers, and community oncology practices. This individual will serve as a conduit of clinical expertise, scientific exchange, and insights that inform medical strategy. This position reports to the Director of Medical Affairs, Somatic, and partners closely with Medical Affairs colleagues, R&D, clinical operations, marketing, commercial teams (if role design includes sales support), and cross-functional leadership. Responsibilities: Maintain MSL Expertise through: • Demonstrating deep knowledge of Myriad's liquid and tumor profiling portfolio, including biomarkers, targeted therapies, immuno-oncology, therapy selection pathways, tumor biology, and NGSbased testing., • Staying current on emerging clinical data, guidelines (NCCN, ASCO, ESMO), competitive trends, and evolving precision oncology treatment standards., • Attending and representing Myriad at national and regional medical conferences for scientific engagement and insight reporting., • Building and maintaining relationships with regional and national KOLs in oncology, molecular pathology, and related specialties., • Contributing to the Somatic Medical Affairs team through collaboration, bestpractice sharing, and training., • Continually advances and grows with market issues, trends, monitors the competitive landscape, and product knowledge specific to key therapeutic areas. Serves as a Medical/Scientific resource to Clinicians by: • Responding to scientific and medical inquiries on somatic testing, assay selection, biomarker interpretation, therapy alignment, and clinical utility., • Delivering clinical and scientific education (virtual and inperson) to oncologists, surgeons, molecular pathologists, APPs, health systems, tumor boards, and professional societies., • Providing guidance on interpreting complex NGS reports and integrating results into treatment decisions., • Increasing awareness of Myriad's somatic test portfolio, enhancing appropriate utilization, and supporting evidencebased precision oncology. Supports Myriad Oncology initiatives and demonstrates business acumen through: • Identifying opportunities for scientific engagement, educational support, and clinical collaboration within the territory., • Communicating clinical landscape insights to Medical Affairs leadership to inform strategy, product evolution, and evidence generation., • Participating in advisory boards, expert panels, KOL roundtables, publication planning discussions, and PLR (Promotional Literature Review) activities as appropriate., • Partnering with crossfunctional teams (Medical, R&D, Marketing, Market Access, Training) on clinical content development and internal scientific training., • Supporting scientific review, interpretation, and development of clinical messaging for new data, assays, or product updates., • Attending sales meetings and partnering with area sales manager and marketing to facilitate and/or present information, as needed., • Educating sales team on current clinical practice, guideline advancements, and aiding in sales training to elevate their skillset. Qualifications: • Advanced scientific or clinical degree required: PharmD, PhD, MS/Genetic Counseling, NP/PA, MD, or related field., • Strong background in oncology, molecular diagnostics, and precision medicine; prior somatic/NGS experience strongly preferred., • 3+ years of clinical, industry, research, or MSL experience preferred., • Understanding of biomarkers, targeted therapy pathways, molecular profiling, resistance mechanisms, and oncology guidelines., • Ability to interpret and clearly communicate complex molecular data., • Demonstrated experience of engaging clinicians, KOLs, and academic groups., • Excellent presentation, communication, and scientific storytelling skills., • Willing and able to travel. Typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad., • Effectively manage travel and maintain expenses within appropriate budget. Significant Work Activities: • Continuous sitting for prolonged periods (> 2 consecutive hours in an 8-hour day), • Keyboard use (greater or equal to 50% of the workday), • Driving a personal vehicle / rental car and flying across the U.S., • Travel: typical travel is expected to be at 50-60%, however may be up to 80% at times depending on territory/needs. Travel will include occasional weekends for conferences/meetings and must be willing to undergo territory changes as deemed appropriate by Myriad. Job Type: Experienced Lifting Requirements -light work or exerting up to 20 pounds of force frequently. Physical Requirements -stationary positioning, moving, operating, ascending/descending, communicating, observing, pushing, or pulling, and reaching. Use of equipment and tools necessary to perform essential job functions. EEO We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. In hiring and all other employment decisions, we prohibit discrimination and harassment on the basis of any protected characteristic, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as any mental health or physical disability needs. #LI-MH1 #LI-remote

GAI Consultants, Inc. is seeking experienced Lead Wetland Delineators to support projects throughout the greater Southwest US region. Ideal candidates will be excited to conduct field work and have a proven track record of independently or as part of a team conducting field investigations related to wetland and watercourse delineation, stream assessments, general biological assessment, and vegetation mapping in a variety of Southwestern US terrestrial habitats, as well as experience with reviewing, managing, and analyzing field data and contributing to environmental reports on time and within budget. The field work will support a variety of project types and stages, including siting/routing/due diligence studies, National Environmental Policy Act (NEPA) compliance, natural resources/waters impact avoidance and permitting, and construction support. These positions are regular, full-time positions with the opportunity for overtime supporting projects throughout the Southwestern US. This role will support both field and desktop-based tasks, depending on business needs. This position is eligible for remote employment, but requires candidates to be located within the Southwestern US region. Position Responsibilities: • Work independently or as part of team to conduct wetland/water jurisdictional delineation surveys, vegetation mapping and general biological resources site assessments., • Participate in pre-field planning and post-field data analysis, processing, and management in support of technical report preparation, under the direction of the project's Environmental Task Manager., • Utilize desktop resources and other digital tools (i.e., topographic maps, aerial photographs, etc.), industry-related GPS-based field data platforms/software (Field Maps, Survey123, etc.) and other tools for the preparation and execution field studies., • Assist with the preparation of technical reports associated with the data collected in the field., • Collect and maintain accurate field reports and data logs using digital forms and collaborative databases., • Collaborate with multidisciplinary teams and provide additional support to the Environmental Team as needed., • Ability to read, analyze, and interpret industry protocols, technical reports and procedures, and governmental regulations regarding regulated wetlands and waterbodies., • Ability to work well as part of a field team (including subconsultants), • Applicants must be able to provide progressive professional experience conducting jurisdictional delineations of state and federal waters/wetlands in the Southwest to be considered for the position., • Minimum 5 years' experience routinely performing wetland/water field studies for private or public sector projects in the environmental consulting industry., • For Lead Wetland Delineators: at least three of the five years' experience must be related to conducting field work as field crew lead for projects in the environmental consulting industry., • Bachelor's degree in Biology, Botany, Wildlife Biology, Ecology, Environmental Science, Natural Resources, or a closely related discipline., • Knowledge regarding current Clean Water Act Section 404 and Section 401 regulatory policy, as well as the currently accepted field assessment protocols and associated field instruments to determine jurisdiction of wetlands and waters., • Familiarity with relevant Federal, State, and local regulations including but not limited to federal and state Endangered Species Acts (ESAs), NEPA, and Clean Water Act (CWA) permits., • Strong knowledge of Southwest US flora and fauna, especially state and federally listed special-status plant and animal species., • Ability and willingness to travel to project site locations within the Southwest US region, including field work assignments requiring overnight stays., • Ability and willingness to hike long distances (up to ~10-12 miles/day) and conduct fieldwork in a variety of terrains (desert, grasslands, wetlands/riparian, etc.) over multiple days for long hours (up to 12 hours/day) in various weather conditions, while carrying equipment and supplies weighing up to 50 pounds., • up to 75% travel, • Comfortable with conducting field work on active construction sites in the presence of construction crews., • This position requires punctuality, professionalism, and preparation to enter the field and successfully perform the required work independently or part of a field team. Candidates must be able to follow instructions from project managers and field leads but also think critically through unplanned situations that arise while onsite all while maintain a positive attitude., • Must have a valid driver's license and be able to operate a 4-wheel drive vehicle in off-road conditions; utility terrain vehicle (UTV) operation experience is a plus., • Proficient with using GPS units and electronic data forms (cell or tablet) in the field to collect, organize, and manage data to support defensible and accurate technical reports., • Experience and interest in conducting focused surveys and habitat suitability assessments for common and special-status plant and wildlife species Southwestern US is highly desirable., • Experience with preparing and reviewing environmental reports using the data collected in the field., • Experience with managing field teams., • This position is responsible for participating in the successful delivery of scope, schedule, budget, and quality of data associated with project field efforts (wildlife, botanical, water, etc.)., • Minimum 5 years' experience routinely performing wetland/water field studies for private or public sector projects in the environmental consulting industry., • Execution of project task deliverables, which could include involvement with subconsultant partners., • Ability to develop and implement day-to-day routines for accomplishing assigned tasks through clear communication and collaboration with the project team., • Strong verbal and written communication skills., • Ability to collaborate and communicate with peers and supervisors., • Ability to read, analyze, and interpret industry protocols, technical reports and procedures, and governmental regulations., • Ability to write detailed and comprehensive field reports and other task-related correspondence. GAI offers skilled professionals like you an exceptional place to work, grow, lead, and achieve. Explore an array of opportunities in locations across the U.S. and join accomplished colleagues in tackling challenging projects for a range of markets. Enjoy work location and scheduling flexibility; your choice of comprehensive, personalized benefits; a range of employee wellness programs and discounts; and more. Feel good about being part of a collaborative team that's committed to supporting the communities we serve. Join GAI and distinguish yourself in a company poised for unlimited growth. Benefits To Working at GAI Include: Competitive Pay & Recognition • Market based, competitive compensation, • Medical, dental, and vision plans, • Company paid short-term and long-term disability, • Company paid life insurance, • Generous paid time off + 7 paid holidays, • An additional floating holiday-use it for what matters to you, • 401(k) with company match, • Tuition reimbursement, • Support and rewards for professional development and certifications EducationBachelors of Environmental and Earth Science (required) Experience5 years: Related Experience (required) Licenses & CertificationsDriver's License (required) Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the ___ notice from the Department of Labor.

GAI Consultants, Inc. is seeking experienced Wetland Delineators to support projects throughout the greater Southwest US region. Ideal candidates will be excited to conduct field work and have a proven track record of independently or as part of a team conducting field investigations related to wetland and watercourse delineation, stream assessments, general biological assessment, and vegetation mapping in a variety of Southwestern US terrestrial habitats, as well as experience with reviewing, managing, and analyzing field data and contributing to environmental reports on time and within budget. The field work will support a variety of project types and stages, including siting/routing/due diligence studies, National Environmental Policy Act (NEPA) compliance, natural resources/waters impact avoidance and permitting, and construction support. These positions are regular, full-time positions with the opportunity for overtime supporting projects throughout the Southwestern US. This role will support both field and desktop-based tasks, depending on business needs. This position is eligible for remote employment, but requires candidates to be located within the Southwestern US region. Position Responsibilities: • Work independently or as part of team to conduct wetland/water jurisdictional delineation surveys, vegetation mapping and general biological resources site assessments., • Participate in pre-field planning and post-field data analysis, processing, and management in support of technical report preparation, under the direction of the project's Environmental Task Manager., • Utilize desktop resources and other digital tools (i.e., topographic maps, aerial photographs, etc.), industry-related GPS-based field data platforms/software (Field Maps, Survey123, etc.) and other tools for the preparation and execution field studies., • Assist with the preparation of technical reports associated with the data collected in the field., • Collect and maintain accurate field reports and data logs using digital forms and collaborative databases., • Collaborate with multidisciplinary teams and provide additional support to the Environmental Team as needed., • Ability to read, analyze, and interpret industry protocols, technical reports and procedures, and governmental regulations regarding regulated wetlands and waterbodies., • Ability to work well as part of a field team (including subconsultants), • Applicants must be able to provide progressive professional experience conducting jurisdictional delineations of state and federal waters/wetlands in the Southwest to be considered for the position., • Minimum 5 years' experience routinely performing wetland/water field studies for private or public sector projects in the environmental consulting industry., • Bachelor's degree in Biology, Botany, Wildlife Biology, Ecology, Environmental Science, Natural Resources, or a closely related discipline., • Knowledge regarding current Clean Water Act Section 404 and Section 401 regulatory policy, as well as the currently accepted field assessment protocols and associated field instruments to determine jurisdiction of wetlands and waters., • Familiarity with relevant Federal, State, and local regulations including but not limited to federal and state Endangered Species Acts (ESAs), NEPA, and Clean Water Act (CWA) permits., • Strong knowledge of Southwest US flora and fauna, especially state and federally listed special-status plant and animal species., • Ability and willingness to travel to project site locations within the Southwest US region, including field work assignments requiring overnight stays., • Ability and willingness to hike long distances (up to ~10-12 miles/day) and conduct fieldwork in a variety of terrains (desert, grasslands, wetlands/riparian, etc.) over multiple days for long hours (up to 12 hours/day) in various weather conditions, while carrying equipment and supplies weighing up to 50 pounds., • Comfortable with conducting field work on active construction sites in the presence of construction crews., • This position requires punctuality, professionalism, and preparation to enter the field and successfully perform the required work independently or part of a field team. Candidates must be able to follow instructions from project managers and field leads but also think critically through unplanned situations that arise while onsite all while maintain a positive attitude., • Must have a valid driver's license and be able to operate a 4-wheel drive vehicle in off-road conditions; utility terrain vehicle (UTV) operation experience is a plus., • Proficient with using GPS units and electronic data forms (cell or tablet) in the field to collect, organize, and manage data to support defensible and accurate technical reports., • Experience and interest in conducting focused surveys and habitat suitability assessments for common and special-status plant and wildlife species Southwestern US is highly desirable., • Experience with preparing and reviewing environmental reports using the data collected in the field., • Experience with managing field teams., • This position is responsible for participating in the successful delivery of scope, schedule, budget, and quality of data associated with project field efforts (wildlife, botanical, water, etc.)., • Execution of project task deliverables, which could include involvement with subconsultant partners., • Ability to develop and implement day-to-day routines for accomplishing assigned tasks through clear communication and collaboration with the project team., • Strong verbal and written communication skills., • Ability to collaborate and communicate with peers and supervisors., • Ability to read, analyze, and interpret industry protocols, technical reports and procedures, and governmental regulations., • Ability to write detailed and comprehensive field reports and other task-related correspondence. GAI offers skilled professionals like you an exceptional place to work, grow, lead, and achieve. Explore an array of opportunities in locations across the U.S. and join accomplished colleagues in tackling challenging projects for a range of markets. Enjoy work location and scheduling flexibility; your choice of comprehensive, personalized benefits; a range of employee wellness programs and discounts; and more. Feel good about being part of a collaborative team that's committed to supporting the communities we serve. Join GAI and distinguish yourself in a company poised for unlimited growth. Benefits To Working at GAI Include: Competitive Pay & Recognition • Market based, competitive compensation, • Medical, dental, and vision plans, • Company paid short-term and long-term disability, • Company paid life insurance, • Generous paid time off + 7 paid holidays, • An additional floating holiday-use it for what matters to you, • 401(k) with company match, • Tuition reimbursement, • Support and rewards for professional development and certifications EducationBachelors of Environmental and Earth Science (required) Experience5 years: Related Experience (required) Licenses & CertificationsDriver's License (required) Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the ___ notice from the Department of Labor.

About the opportunity SWCA Environmental Consultants is expanding our team and looking for Temporary Staff-Level Biologists with backgrounds in botany, wildlife biology, wetland ecology, avian, and/or environmental science to support our Salt Lake City office. These are temporary, hourly positions that will support a variety of natural resources projects and field efforts at sites throughout Utah and the Intermountain West. Candidates local to Utah (or neighboring states) familiar with flora and fauna of Utah, conducting field surveys, and 4x4 truck, ATV, and trailer towing experience are strongly preferred. Applicants should be able to work outdoors in a team or independently for 40 hours or more per week (travel included) with flexible scheduling based on project and client needs. Applicant must be willing to participate in a drug and alcohol screening as part of the pre-employment process, as some projects require such screenings. This position can hire at three different levels: • Natural Resources Technician - Typically with a few months of relevant experience and expertise, • Assistant Staff Biologist - Typically with up to one (1) year or relevant experience and expertise. Our Vision (the North Star): Help drive SWCA to be the best workplace and industry leader in sustainability, bringing sound science and creative solutions to global environmental challenges while maintaining a dedication to employee-ownership. Core Values: We are #OneSWCA and collaborate across all of our offices, programs, and disciplines. We are #AlwaysLearning, we #NeverSettle and we #GiveBack. We are 100% employee-owned, and we build our success together. It is imperative for the successful candidate to fit SWCA's unique culture. Do you appreciate sustainability and environmental awareness? Is giving back to your community a priority? SWCA is a team of scientists, planners, technical experts, and corporate services professionals that are committed to our culture. Purpose: Our company's purpose is to preserve natural and cultural resources for tomorrow while enabling projects that benefit people today. You are invited to be a part of our success story. What you will accomplish • Follow established scientific protocols to conduct wildlife, vegetation, and wetland field surveys, complete environmental inspections, wildlife and vegetation baseline studies, habitat assessments, noxious weed mapping, stormwater inspections, and reclamation monitoring, • Assist with tasks to collect and/or manage natural resources and wetland data in the field or office. Technicians are expected to work efficiently to complete assigned tasks in a manner that ensures the data are accurate, complete, and verifiable, • Use topographic maps, aerial photographs, GPS units, and other mapping tools to determine exact locations of project areas, habitat types, species of interest, and associated landforms, • Photograph and record appropriate habitat, species, and geographic landforms relative to suitable habitat requirements and ecological classifications, • Operate SWCA vehicles, assure they will perform safely, and notify appropriate person if vehicle needs maintenance, • Ability to perform all work with a focus on safety in a remote field setting for long hours, sometimes in inclement weather, rugged terrain, and at high altitudes is required; the ability to carry equipment and supplies weighing up to 40 pounds and walk up to 12 miles per day is required, • Communicate frequently and openly with team members and supervisors to ensure that task objectives and methods are clearly understood, task progress is shared, and questions or needs are promptly addressed. This includes initiating and/or responding to communication requests before, during, and after task implementation as part of a real-time, collaborative work effort, • Project work may include electrical transmission, renewable generation projects (wind, solar, geothermal), oil and gas development, transmission/pipelines, transportation, mining, and state and federal agency clients, • Adhere to SWCA's safety program while looking out for the safety of others, promptly communicating and mitigating safety hazards, • For Assistant Staff Biologist and Staff Biologist positions, a key element of your job will be to supervise a small crew while conducting environmental fieldwork. This includes:, • Independently assigning and directing the activities of others on behalf of SWCA, often in remote areas without immediate guidance from senior managers, to ensure quality and on-time delivery., • Ensuring that employees understand their responsibilities and delegated tasks and being held accountable if crew members under your supervision are not performing their activities correctly, productively, and safely., • Serving as a conduit of communication between employees and senior managers, including communicating issues to relevant senior managers., • Receiving and resolving complaints from employees in the field., • Minimum of B.A. or B.S. in Biology, Ecology, Environmental Science, Natural Resource Management field preferred, • A minimum of 6 months' experience with field-based natural resources scientific data collection and attention to detail, • Must have experience with accurate natural resources data collection procedures and data QA/QC, • Familiarity with Intermountain West flora and fauna; botany and/or wetland delineation experience a plus, • Familiarity with Microsoft Office 365, ArcGIS, and other software suites, • Must have valid driver's license and be able to meet SWCA's driver requirements, • Ability to work long days outdoors for extended periods of time (up to 14 days) in a safe and productive manner, • Ability to maintain a positive attitude while working closely with a small team in a dynamic work environment, • Ability to travel and work remotely as required, • Ability to work independently and as a member of a team with excellent team collaboration skills, • Excellent communication and organizational skills SWCA Environmental Consultants is a growing employee-owned firm, providing a full spectrum of environmental services. With offices across the United States, SWCA is one of the largest environmental compliance firms and ranks among Engineering News-Record's Top 200 Environmental Firms. If you would like to contact SWCA regarding the accessibility of our website or need assistance completing the online application process due to a disability, please email ___ or call 480-581-5378. This contact information is for disability accommodation requests only. All other inquiries will not receive a response. SWCA is committed to salary equity and salary transparency for all its employees. In alignment with this commitment, SWCA posts good faith pay ranges on all its advertised job postings to promote pay equity and transparency. An employee in this Salt Lake City office -based position can expect a salary of: Natural Resources Technician -- $19.24/hour to $25.48/hour; Assistant Staff Biologist -- $21.32 to $27.56/hour; Staff Biologist -- $23.92/hour to $31.20/hour. Actual pay within this range may depend on experience, qualifications, geographic location, client requirements where applicable, and other factors permitted by law. EOE - women, minorities, individuals with disabilities, and veterans are encouraged to apply. At SWCA Environmental Consultants, we celebrate diversity and are committed to creating an inclusive work environment. We strongly encourage candidates from all backgrounds, including those with diverse experiences and veterans, to apply. We believe that a diverse and inclusive workforce enhances creativity, innovation, and overall organizational success. SWCA continues to invest deeply in career development programs, delivering our award-winning Career Landscape support resources to accelerate the growth of our staff. We recognize the valuable skills and experiences our internal team members bring to SWCA's continued success. Qualified internal candidates are encouraged to apply and will be seriously considered for this position. We believe in promoting from within, where possible, providing our existing employees with compelling opportunities to advance their careers. #LI-JR1 #IND-SWCA

Position Overview This position is responsible for the management of reprocessing and infection control activities associated with the endoscopic product portfolio. The Director of Endoscopy Infection Control is the primary company resource and subject matter expert for the Endoscopy Division as it relates to the cleaning, high-level disinfection and/or sterilization of Fujifilm endoscopy products. This role works cross-functionally with customers, third-party companies and internal stakeholders including sales/sales management, field personnel, international liaisons, and marketing/R&D groups in Japan to ensure that the Fujifilm reprocessing recommendations satisfy US market needs and comply with industry infection control guidelines. Company Overview At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier world, and we need passionate, driven people like you to help us get there. Our cutting-edge healthcare solutions span diagnostic imaging, enterprise imaging, endoscopic and surgical imaging, as well as in-vitro diagnostics. But we don't stop at healthcare; our Non-Destructive Testing (NDT) team harnesses advanced radiography solutions to keep transportation infrastructure, aerospace, and oil and gas assets safe and running smoothly. Ready to innovate, collaborate, and make a difference? Join us and bring your big ideas to life while working in a dynamic, flexible environment that fuels your creativity and drive. Our headquarters is in Lexington, Massachusetts, an inspiring healthcare research hub in a historic town. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: Job Description Duties and Responsibilities: * Collaborate with headquarter liaisons and teams to effectively communicate subsidiary needs and US requirements for reprocessing and infection control issues. * Develop or/and support validation program for testing of endoscope designs and reprocessing instructions, working with Fujifilm Tokyo and independent microbiology laboratories as necessary. * Partner with Fujifilm Japan to support FDA requests and requirements including 522 Postmarket Surveillance Studies and Human Factors Testing of Fujifilm products, as necessary. * Serve as technical writer/reviewer to develop and/or revise endoscope operation and reprocessing manuals based upon latest industry guidelines and review/improve product labeling for accuracy, consistency and ease of understanding. Review operation manuals for any comments/instructions related to reprocessing. * Develop policies, policy statements, customer, and sales rep notifications regarding infection control/reprocessing issues. * Serve as a senior corporate source of education & information for infection control/reprocessing issues. * Establish educational tools and review training aids (such as QRGs, slide presentations) on reprocessing and infection control practices. * Assist sales management and Product Management with development and maintenance of luminary customers in key target markets in US. * Represent the company on national committees and at meetings/seminars developing reprocessing guidelines. Keep Fujifilm Tokyo well informed of any new reprocessing/infection control trends and/or guidelines. * Have adaptable learning skills and an established track record of being a subject matter expert on reprocessing and infection control matters. * Work with third-party companies including AER and sterilizer OEMs to validate and expand reprocessing options for Fujifilm endoscopes. * Oversee/manage HCUS Clinical Education Manager responsible for reprocessing training of HCUS personnel and customer in-services. * Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO standard requirements and all other applicable laws, regulations, and standards. Qualifications: * Bachelor's degree in biology or microbiology is required. A Master's degree preferred. * Minimum of 10-12 years' experience in medical device reprocessing, (cleaning, disinfection and sterilization) validation studies and infection control best practices including a strong background of flexible endoscopes. * 3-5 years' experience as an accredited microbiologist is preferred. * Extensive cleaning/reprocessing knowledge of medical devices is required. * Background/experience working with the FDA and knowledge of the biological evaluation of medical devices (Biocompatibility). * Highly focused and results-oriented; able to identify goals and priorities and resolve issues in initial stages. * Demonstrated ability to work independently and in a close team environment, self-starter who can motivate others. * Possess exceptional communication/interpersonal, analytical, and problem-solving skills. * Work remotely * Proficient computer skills using Word, Excel, PowerPoint. * Effective Time Management skills. * High command and literacy in endoscopic application * Strong analytical and critical thinking skills * Ability to read, analyze, and interpret essential job-related documents. * Ability to present and speak effectively and professionally to all internal and external customers. Physical requirements: The position requires the ability to perform the following physical demands and/or have the listed capabilities: * Frequently required to stand; walk; use hands to finger, handle or feel objects, ability to use a keyboard, reach with hands and arms; balance; stoop, kneel, crouch; and talk or hear. * Occasionally lift and/or move up to 30 lbs. * Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception, and the ability to adjust focus. Travel: Applicants to positions where vendor credentialing or other similar requirements exist to enter facilities will be required to comply with the credentialing requirements of the facilities, including complying with vaccine requirements. For all positions, the Company encourages vaccination against COVID-19 and requires that the successful candidate hired be willing to test for the COVID-19 virus periodically and wear a face covering indoors as required, absent being granted an accommodation due to medical or sincerely held religious belief or other legally required exemption. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department ( or (330) 425-1313). Job Locations US-Remote Posted Date 2 days ago (5/13/2026 7:49 PM) Requisition ID 2026-37543 Category Executive Management Company (Portal Searching) FUJIFILM Healthcare Americas Corporation

Core Qualifications - 3+ years of research, academic, or industry experience in Machine Learning, or Data Science, or Software Engineering, or Computer Science, or Statistics, or Biology, or Electrical/Mechanical/Civil Engineering, or Physics, or Chemistry, or Mathematics, or Materials Science, or o

Company / University Description University of Utah and University of Washington are recruiting a postdoctoral fellow to help develop next-generation biological systems for low-concentration methane capture and conversion. This position brings together expertise in bioreactor engineering, methanotroph biology, computational biophysics, and technology commercialization to address one of the most urgent climate challenges: reducing methane emissions while creating valuable products. The position is jointly mentored by Mary Lidstrom (methanotroph physiology and metabolic engineering), Jessica Swanson (molecular biophysics and efficiency modeling), and Swomitra Mohanty (bioreactor engineering). Role Description The postdoc will play a central role in designing and optimizing continuous methane-fed bioreactors for low-concentration methane conversion. Responsibilities include: • Designing and operating continuous bioreactor systems, • Optimizing gas-liquid mass transfer and reactor performance, • Growing and characterizing Methylotuvimicrobium buryatense 5GB1, • Identifying biological and engineering bottlenecks limiting efficiency, • Generating data to inform scale-up and commercialization strategies Qualifications Required • PhD in Chemical Engineering, Bioengineering, Microbiology, Biomolecular Sciences, or related field, • Hands-on experience with bioreactors, microbial systems, fermentation, or transport phenomena, • Strong experimental skills, • Gas fermentation or gas-liquid reactor experience, • Methanotroph/C1 metabolism experience, • Scale-up experience, • Interest in startups, commercialization, or climate tech More Details: To Apply • Send an email briefly describing why you are interested in this position and why you think you would be a good fit. See above link for further instructions.

Job details Entry-Level Microbiology Lab Analyst - Salt Lake City, UT Location: Salt Lake City, UT 84123 Schedule Available: Job Summary Join our premier client in Salt Lake City as an Entry-Level Microbiology Lab Analyst! Perfect for recent graduates or those starting their microbiology careers, this role supports critical lab functions and environmental monitoring tasks. Responsibilities • Assist with prep work for microbiology testing, • Perform water testing and environmental monitoring in a hooded, benchtop laboratory environment, • Conduct incubation, membrane filtration, and test preparation, • Perform colony enumeration, • Utilize a manifold for sample processing, • Execute additional duties as assigned Qualifications • Bachelor's degree in Biology, Microbiology, Chemistry, or related field, • Coursework, experience, or demonstrated interest in microbiology, • 6+ months of production lab experience preferred, • Must not have allergies to latex or antibiotics, • Must not be colorblind, • Able to maintain short nails (no long nails that could puncture gloves Apply now for consideration! 10209679

Neurodegenerative diseases are one of the largest medical challenges of our time.Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine.D

Job Description Job Title: Environmental Equipment Coordinator Job Description The Environmental Coordinator oversees the full lifecycle of equipment orders, from initial customer contact through shipment, receipt, and return. This role combines hands-on shipping and receiving with responsive customer service, ensuring that high-value environmental equipment is accurately processed, tested, and delivered on time. The position offers training on industry trends, the opportunity to work closely with leading environmental organizations, and the chance to grow within a small, collaborative team. Responsibilities • Handle incoming and outgoing orders for environmental equipment., • Receive orders via phone, email, and web, and respond promptly and professionally to customer inquiries and requests., • Review each order for completeness and enter any missing or required information into the company’s system., • Collect equipment from the appropriate storage locations, verify item details, and confirm that the correct products are prepared for each order., • Test equipment to ensure it is functioning properly before shipment and document any relevant test results or observations., • Package equipment securely for shipment, following internal standards to protect high-value items during transit., • Coordinate shipments and track orders through to customer receipt, maintaining clear and accurate documentation of all order movements., • Manage returns once customers have finished using the equipment, including receiving, inspecting, and documenting returned items., • Maintain accurate inventory records by documenting orders in and out, updating stock levels, and supporting inventory control activities., • Provide courteous, solutions-focused customer service by phone and email, addressing questions, issues, and special requests related to equipment and orders., • Perform administrative and clerical tasks related to order processing, purchase orders, and data entry to support smooth daily operations., • Multitask effectively between hands-on shipping and receiving duties and customer service responsibilities in a fast-paced environment., • 1–2 years of experience in customer service or shipping and receiving, preferably within the environmental industry., • Proven ability to handle shipping and receiving tasks, including order processing, packaging, and documentation., • Strong customer service skills with experience communicating by phone and email in a professional manner., • Proficiency with Microsoft Office and comfort working within a Windows PC environment., • Experience with order entry, data entry, and order management processes., • Ability to manage order fulfillment from receipt through shipment and return., • High attention to detail when working with high-value equipment and critical order information., • Ability to multitask effectively between hands-on shipping work and customer service support., • Capability to work in person on site to handle physical packages and equipment., • Knowledge of environmental or engineering equipment., • Bachelor’s degree in environmental science or a related field such as biology or chemistry., • Experience with inventory management and tracking., • Familiarity with Point of Rental or similar order management systems., • Interest in environmental industries and willingness to learn industry trends. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program About Aston Carter: Aston Carter provides world-class corporate talent solutions to thousands of clients across the globe. Specialized in accounting, finance, human resources, talent acquisition, procurement, supply chain and select administrative professions, we extend the capabilities of industry-leading companies. We draw on our deep recruiting expertise and expansive network to meet the evolving needs of our clients and talent community with agility and excellence. With offices across the U.S., Canada, Asia Pacific and Europe, Aston Carter serves many of the Fortune 500. We are proud to be a ClearlyRated Best of Staffing® double diamond winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options.

Job Description COMPANY OVERVIEW: Certerra is a growing national provider of testing, inspection, and certification services that support innovation in new product development, quality assurance, for project delivery, and engineered solutions for asset management. We are passionate about contributing to the sustainable development of the communities we serve. We are a national firm with a global reach serving national and international clients from 30+ offices located in 10 states and are ranked on ENR’s Top 500 list alongside the nation’s top firms. With a 60-year history, Certerra has a passion for high-end services, constant innovation, and investment in the development of world-class laboratory facilities, and interactive management technologies. Each member of our staff is committed to service, innovation, and the success of our clients. Certerra is a consulting firm with over 65 years of quality service that offers professional services in the southwestern United States in the fields of geotechnical engineering, environmental engineering, construction materials engineering and testing, nondestructive testing, and welding inspection. Job Description: Certerra Southwest, a leading engineering consulting firm, has an excellent opportunity for an Environmental Scientist working into Project Management in our Salt Lake City, UT office. The successful candidate will conduct a variety of field and office duties to support senior team leaders. Project assignments will take you to locations throughout the southwestern United States, but primarily in Arizona. This position requires a hard-working, safe, efficient and dedicated employee that is excited to receive training on the job and expand their current skill set. General responsibilities: (Include but are not limited to:) • Conduct field sampling and inspections for soil, groundwater, air, and building materials. • Conduct Phase I Environmental Site Assessments (ASTM E1527-21) including historical records review, site reconnaissance, and preparation of technical reports., • Perform Phase II environmental investigations including soil, groundwater, and soil vapor sampling under the direction of project managers., • Perform asbestos building inspections and bulk sampling in accordance with AHERA and state regulatory requirements., • Conduct lead-based paint inspections and risk assessments using XRF analyzers and paint chip sampling techniques., • Perform indoor air quality (IAQ) monitoring including collection of samples for VOCs, mold spores, particulate matter, and other indoor contaminants., • Document field activities through field notes, photographs, and site sketches., • Communicate with clients and contractors during field activities. Required Job Qualifications: • Environmental science, biology, chemistry, industrial hygiene or similar background., • 1-3 years of experience in environmental or industrial hygiene consulting., • Experience with environmental sampling techniques including soil, groundwater, air, and building materials., • Knowledge of federal and state environmental regulations (EPA, OSHA, ADEQ, etc.)., • Strong technical writing and data organization skills., • Certifications such as AHERA Building Inspector, AHERA Contractor/Supervisor, Lead Inspector/Risk Assessor, or 40-hour HAZWOPER are preferred., • A valid driver’s license with a clean driving record • Pass a pre-employment drug screen Physical Demands: • Physical examination required to obtain medical clearance to work, • Ability to stoop, kneel and to routinely lift and carry 50 pounds, • Ability to travel for field work and some overnight stays, • Able to work in variable outside conditions, including extreme heat or cold EOC Statement: We are an Equal Opportunity Employer. This Company is dedicated to both the letter and the spirit of the equal opportunity employment laws. All applicants and all employees will be evaluated on the basis of their ability, competence, and performance of the essential functions of their positions. There will be no discrimination on the basis of race, sex, national origin, religion, age 40 and over, disability, sexual orientation, marital status, or any other classification which may be protected by federal, state, or local laws. In compliance with the Americans with Disabilities Act, we specifically offer equal opportunity for all employees or job applicants who may have a physical or mental disability. Such persons will be hired on the basis of their ability to perform the essential functions of the job in question. Likewise, their work will be evaluated on their performance of these essential functions. We will offer reasonable accommodation to individuals with disabilities, to the extent that Company resources allow without undue hardship. As part of our equal employment policy, there will be no wage differentials based on gender, between men and women employed in the same establishment, on jobs that require equal skill, effort, and responsibility, and which are performed under similar working conditions

Job Description Welcome to DiscGenics, a pioneering, late-clinical stage biopharmaceutical company dedicated to advancing regenerative cell-based therapies for patients suffering from degenerative diseases of the spine. Privately held and passionately driven, our mission is to enhance lives by alleviating pain and restoring function through innovative treatment. At DiscGenics, we are committed to improving the quality of life for individuals debilitated by degenerative diseases of the spine. Our focus lies in developing cutting-edge therapies that offer hope and tangible results, fostering a future where patients can regain mobility and comfort. Our team is characterized by a relentless pursuit of excellence and a nimble approach to addressing challenges. Our core values of Integrity, Innovation, Accuracy, Teamwork, and Stewardship guide everything we do. Join us at DiscGenics and be part of a transformative journey where your contributions have the potential to impact the lives of millions. Together we innovate with purpose and compassion, striving towards a future where pain and limitations of degenerative spine diseases are a thing of the past. Discover more about us at discgenics.com and see how you can contribute to revolutionizing patient care through regenerative therapies. Job Summary: The Quality Control Analyst will have the unique experience of assisting the Quality Control laboratory move from concept to realization as part of a new company build-out. The QC Analyst performs quality control analysis of raw material, and finished product using USP compendial tests or in-house developed analytical test methods and will play a role in transitioning analytical methods from development/qualification into QC-ready validated methods. This role will function as a hybrid QC/Analytical Sciences resource, focusing on method optimization, robustness, and lifecycle management to ensure methods are fit for purpose for routine QC use. The position will work cross-functionally to perform equipment qualifications and test method optimization, bridging, and validation activities that are reliable, repeatable, and adhere to quality procedures. This candidate will also help manage compliance programs for QC. This role interacts with all levels of the organization. Delivers collaborative and positive leadership to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. Duties and Responsibilities • Demonstrates high-level of proficiency with, and ability to troubleshoot, multiple raw material and cell culture test assays and instrumentation including cell-based potency assays, cell culture, ELISA, etc., • Perform qualification/re-qualification requirements for laboratory equipment., • Lead and execute method validation, transfer, and lifecycle management activities in alignment with ICH guidelines (e.g., ICH Q2) and regulatory expectations., • Optimize and refine existing analytical methods to improve robustness, reproducibility, and suitability for routine QC release and stability testing., • Design and execute method bridging/comparability studies when method changes are required, ensuring appropriate statistical evaluation and documentation., • Writes SOPs and work instructions for current and future laboratory operations, including use, maintenance, and qualification of equipment, laboratory investigations, sampling procedures, and test methods., • Receives and maintains traceability of test samples, reagents, and materials per Approved procedures., • Author and approve Out of Specification (OOS) records and Laboratory Investigation Records (LIR) by facilitating implementation of meaningful corrective and preventative actions for laboratory-related issues., • Prepares and analyzes periodic summary reports of quality control test results using Statistical Process Controls. Tracks and trends OOSs. Identifies and elevates adverse trends to CAPA process and management review., • Prepares QC data trending for quality management review meetings., • Provides oversight of contract lab facilities., • Assist in development and maintenance of the product stability program. Qualifies, maintains, and monitors stability chambers., • Qualified trainer for test methods, • Manages QC on the job training. Tracks training metrics., • Provides technical support for LIMS function for QC assays., • Collaborate closely with Analytical Development, Process Development, and Manufacturing to support PPQ readiness and regulatory submissions., • Support PPQ activities by ensuring validated methods are in place and performing as expected during commercial release., • 3-10 or more years of experience in a laboratory setting., • 3-10 or more years of experience in a GMP (Good Manufacturing Practices) type environment., • Experience with analytical/cell-based QC instruments., • Strong understanding of analytical method validation, transfer, and comparability principles, • Experience with statistical analysis applied to method performance (precision, accuracy, linearity, and robustness), • Independence and creative problem-solving abilities., • Ability to handle highly confidential business information., • Exceptional time management and multi-tasking skills., • Team leadership skills and team player., • Adheres to company values of Integrity, Innovation, Accuracy, Teamwork and Stewardship., • Regular and predictable attendance., • Ability to report to work responsive, free from sedatives, and in a non-sedative state., • B.S./B.A. in Engineering, Biology, Chemistry, Industrial Sciences, or related field., • 3-10 years of experience in a GMP (Good Manufacturing Practices) related field., • Experience in Pharmaceutical, Biologics, Medical Device or Cell/Gene Therapy industry., • Preferred: Experience supporting late-stage development and PPQ/Validation readiness Position requires qualified individuals to see, hear and speak (verbally and audibly). Required to ascend and descend stairs; sit, stand, lift, bend, stoop, crawl and kneel. The employee must also use hands to finger, handle or feel. Occasionally reaching with hands and arms, climbing or balancing are required. May be asked to drive or travel by car, air, or other transportation for business purposes. May be required to lift and carry 20 pounds. Must be able to function effectively with noise in a lab environment. Natural and regular stressors occur on the job. Disclaimer: Please note: DiscGenics reserves the right to change, modify, suspend, interpret, or cancel in whole, or in part, any of the duties outlined above, at any time, and without advance notice to the employee.

Benefits This is a full-time or part-time REMOTE position You’ll be able to choose which projects you want to work on You can work on your own schedule Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work Responsibilities Give AI chatbots

Benefits This is a full-time or part-time REMOTE position You’ll be able to choose which projects you want to work on You can work on your own schedule Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work Responsibilities Give AI chatbots

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