Scientist Jobs in Syracuse, UT

Meta is seeking a Research Scientist to join Fundamental AI Research (FAIR), a research organization focused on making significant progress in AI. Our organization is motivated by producing new science to understand intelligence and technology towards achieving advanced machine intelligence. The ideal candidate will have established expertise in artificial intelligence and machine learning, particularly in areas such as deep learning, computer vision, and reinforcement learning. **Required Skills:** Fundamental AI Research Scientist, Computer Vision - FAIR Responsibilities: 1. Develop algorithms based on state-of-the-art machine learning and neural network methodologies. 2. Conduct research to advance the science and technology of intelligent machines. 3. Conduct research that enables learning the semantics of data (images, video, text, audio, speech and other modalities). 4. Contribute to and apply research that advances Meta Platforms products. 5. Conduct and collaborate on research projects within a globally-based team. **Minimum Qualifications:** Minimum Qualifications: 6. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience. 7. PhD degree in the field of Artificial Intelligence, Computer Vision, Machine Learning, a related field, or equivalent practical experience. Degree must be completed prior to joining Meta. 8. 2+ years of industry, academic, or government lab experience in computer vision and/or machine learning. 9. First-Author Contributions and / or Publications at peer-reviewed conferences (e.g. CVPR. ECCV, ICCV, NeurIPS, and SIGGRAPH). 10. Experience solving complex problems and comparing alternative solutions, tradeoffs, and diverse points of view to determine a path forward. 11. Experience communicating research for public audiences of peers. 12. Must obtain work authorization in the country of employment at the time of hire, and maintain ongoing work authorization during employment. **Preferred Qualifications:** Preferred Qualifications: 13. 4+ years of work experience in an industry, university, or government lab. **Public Compensation:** $147,000/year to $208,000/year + bonus + equity + benefits **Industry:** Internet **Equal Opportunity:** Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment. Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@fb.com.

The Scientist II is responsible for initiating, directing, and executing scientific research and/or development strategies for bioMérieux through a research staff or individual studies. Scientist II investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products, and problems. Must be familiar with a variety of the field's concepts, practices, and procedures including PCR, real-time RT-PCR, and use of fluorescence-based nucleic acid detection techniques. Relies on experience and judgment to plan and accomplish goals. The position requires expertise in laboratory technical and organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, data analysis, and a dedication to the mission and goals of the department and bioMérieux. The Scientist II normally receives no instructions on routine work, and general instructions on new assignments. Position is ONSITE Full Time Primary Duties * Performs all work in compliance with company policy and within the guidelines of bio Merieux's Quality System. * Follows policies and procedures and conducts oneself professionally and in accordance with the bioMérieux Employment Handbook. * Supervises research associates in daily operations. * Works on complex problems which require expert knowledge of scientific principles and concepts and advanced analytical skills. * Plans, executes, and/or oversees the execution of laboratory research in the service of one or more department projects. * Maintains broad knowledge of state-of-the-art principles and theories. * Makes contributions to literature and presents at conferences. * May advise senior management on research and development project(s). * Participates in development of patent applications. * Responsible for development of a research group. * Required to interact with various company departments. * Uses professional concepts to contribute to the development of company concepts and principles and to achieve objectives in creative and effective ways. * Demonstrates potential for technical proficiency, scientific creativity, collaboration with others, and independent thought. * Ensures data integrity and accurate record-keeping by participating in and overseeing research associates and/or associate scientists in collecting, recording (e.g., via electronic laboratory notebooks and study worksheets), analyzing, and verifying data in compliance with bioMérieux SOPs, WIDs, and Study Protocols. Qualifications: * Requires a PhD in a scientific discipline * Minimum of 6 years' experience in research and/or development environment. Knowledge, Skills, and Abilities * Must demonstrate expertise in molecular biology, microbiology, infectious disease, and/or clinical laboratory diagnostics. * Mastery of common laboratory procedures. * Ability to independently manage projects and employees and report areas of risk as they arise. * Competent in experimental design and data analysis, including statistical assessments. * Demonstrated skills in scientific/technical writing and oral presentations. * Proficiency with Microsoft Office (Outlook, Excel, PowerPoint, and Word).

Newborn Screening Mass Spectrometry Scientist(Chemist/Microbiologist II) Do you have any experience with laboratory testing? Do you want to make a difference in public health? If this is you, then the Utah Public Health Laboratory (UPHL) needs you as a Newborn Screening Mass Spectrometry Scientist. In this role you will perform biochemical and molecular newborn screening testing. UPHL is CLIA certified. You must meet the CLIA requirements (found HERE) to work in this position. PLEASE REVIEW BEFORE APPLYING: Continued employment may be contingent upon the successful completion of a fingerprinting background check. Due to the nature and types of testing samples this position requires compliance with the Utah Department of Health & Human Services Employee Immunization policy. Please click HERE for the most current policy information. A teleworking option is not available for this position. To qualify for this position, you MUST meet CLIA requirements. These requirements can be found HERE. Job Responsibilities: Participating in all high complexity testing functions, including clinical testing with clinical auto-analyzers, analysis and usage of mass spectrometers, molecular testing including quantitative PCR based screening assays, PCR based tests, next-generation sequencing based tests, hemoglobin analysis by isoelectric focusing and HPLC methods Managing inventory control Maintaining instruments and equipment Punching blood clots using high-throughput punching equipment Documenting all activities to meet CLIA requirements Preparing specimens for laboratory analysis following appropriate guidelines and procedures Analyzing and testing newborn dried blood spots (NBS) Reviewing results for mass spectrometry, HPLB, hemoglobin variants by IEF, real-time PCR and DELFIA based assays Reviewing and/or inspecting work for quality, accuracy, and completeness Staying current with all laboratory SOPs Other duties as assigned Minimum Qualifications: Meets CLIA testing personnel qualifications (click HERE to review the standard qualifications) Has experience with mass spectrometry, biochemical, and/or molecular testing applications Is motivated and has attention to detail Can support high-throughput testing Can read and understand technical writings and apply acquired knowledge Schedule: This position will be scheduled for 4 10-hour shifts OR 5 8-hours shifts Monday-Friday with occasional weekends (primarily Saturdays). Scheduled hours are typically from 8:00AM to 6:30PM The Agency: To learn more about UPHL, please click HERE. To learn more about UPHL's Newborn Screening program, please click HERE. Supplemental Information Working Conditions: Risks which require the use of special safety precautions and/or equipment, e.g., working around operating machines, working with contagious diseases or hazardous chemicals, etc. Physical Requirements: Work requires physical exertion. May require the ability to stand; walk over rough surfaces; bend, crouch, stoop, stretch, reach, lift moderately heavy items (up to 50 lbs.) in a recurring manner and/or for long periods of time.

Who are we? Kodiak is one of the fastest growing food companies that is disrupting the industry with its better-for-you breakfast and snacking options. Our journey with food began by restoring the tradition of whole grain flapjacks and adding some protein to fuel folks' adventures. In the process, we discovered that foods made closer to nature are not only fueling but taste better. So, we set out to inspire wilder, wide-open lives by feeding epic days through real breakfasts. That's one of the reasons we're in the scenic Rocky Mountains of Park City, Utah: to live our purpose and be close to nature. Our mission is to become the most loved, next generation food brand, and we're well on our way. We craft the best-selling whole grain flapjack mix in the nation along with toaster waffles, baking mixes, oatmeal, syrup, and snacking options at all major retailers. We're expanding rapidly as our business continues to grow year-after-year and need to build our team with people that share our passion for the outdoors, bring industry experience, thrive in an entrepreneurial culture, and want to make an impact in the food space. We believe that eating real, good-for-you food, being active outdoors, and preserving nature will restore balance generations before us worked so hard to forge. We embrace the spirit of the Kodiak - a pristine wilderness with a rich ecosystem - and we rely on that spirit of the Kodiak to inspire the work we do, the food we eat, and the way we play. Job Type: Full-Time, Salaried (Exempt) - $80,000 - $90,000 Job Location: Kodiak HQ: Park City, Utah - On-Site / Hybrid Individual base salary for this role ultimately will depend on numerous factors, including but not limited to experience, job-related skills, relevant education or training, certifications, etc. As such, pay for the successful candidate could fall anywhere within the stated range. Beyond base salary, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. This role also is eligible to participate in Kodiak's annual discretionary bonus program, which is dependent on various factors, including individual and company performance. This role will report to the Associate Director, Research & Development and will be responsible for designing research projects, exploring ingredient trends, creating new formulations, product testing, preparing accurate samples, document creation and management. The R & D Food Scientist will work directly with co-manufacturers to align on the ingredients and the formulation for product development and oversee the scale up of innovation and renovation projects. What will this position do? Develop formulas to meet both innovation and renovation briefs. Prepare daily formula test batches for pilot testing. Create prototypes for consumer testing and internal meetings. Work on productivity projects by testing new ingredients and optimizing the formulation. Submit samples for shelf life, allergen, and any additional testing. Research potential new ingredients, ingredient trends, and suppliers. Partner with existing suppliers for rapid prototyping opportunities. Assist with formula documentation creation and management. Partner with co-manufacturing team to align formulas and ingredients for scale up. Develop formulas for back-of-box copy. Maintain and develop positive, professional relationships across all functional areas of the organization - both internal and external - that foster an inclusive and team-oriented culture. What are we looking for? Bachelor's degree in food science or related field, or equivalent experience. At least 5 years of relevant experience in product development or a related industry. Familiarity with food chemistry, safety standards, and regulatory requirements. Detail-oriented, organized, and proactive in approaching tasks. Enthusiastic about learning and open to new challenges. Strong verbal/written communication skills Able to manage multiple projects simultaneously. Demonstrates the ability to work autonomously while also fostering collaborative teamwork. Strong organizational skills, flexible, and able to work with ambiguity Located in or willing to relocate to the Park City area. Open to occasional travel, estimated at approximately 10%. What else do I need to know? This role is based in our headquarters near the ski slopes and mountain trails of Park City, Utah, where we have a hybrid work schedule. We offer competitive compensation and benefits that include: Medical/dental/vision plans 401k match FSA & HSA accounts Life & ADD Insurance Short Term & Long-Term Disability Insurance Cell Phone & Internet Stipend Relocation assistance Annual performance bonus Employee Equity Plan A company fleet of snowboards and other equipment Wellness lifestyle allowance (B.E.A.R Bucks) Mental Health Therapy Benefit & the Calm app All-you-can-eat flapjacks Responsible Time Off Early-out Fridays Parental leave Casual dress code A variety of other Kodiak-unique perks Recognized by Inc and Utah as one of America's best places to work, we are known for our awesome work environment - a fun and authentic place where wins are celebrated, collaboration is king, work is balanced with life, and every individual makes a deep impact. We proactively search for ways to develop each individual along their career path here at Kodiak and beyond. We're inspired and committed to creating natural, authentic food with superior taste to fuel a healthy, active lifestyle. We feel encouraged by some of the trends in food today and believe that with a concerted effort we can make an enormous impact in building momentum for natural, better-for-you foods. We invite you to apply to join our team and leave your legacy on the future of food. At Kodiak, we foster a truly inclusive community that encourages, supports, and celebrates what makes each of us unique. We bring our full authentic selves to work and leverage our diverse backgrounds and perspectives to create a culture of belonging that feeds epic days & wilder lives.

JOB PURPOSE: Alphia, one of the nation's leading custom pet food manufacturing companies, is looking for a skilled R&D Scientist. The R&D Scientist is responsible for managing research and development projects involving new product and process development, production trials, least-cost formulation, product/process improvement, technical sales support, etc. Product area responsibilities will include dry extruded and baked pet foods and snacks/treats. DESCRIPTION OF ESSENTIAL DUTIES: Demonstrate strong project management skills on research and development projects as assigned. Actively participate as a key contributor to new products development. Formulate dry extruded and baked pet foods and snacks/treats according to defined parameters. Oversee/conduct plant trials on assigned projects at various production facilities. Trouble-shoot and resolve production and product quality issues experienced at the plant level. Work effectively on multidisciplinary teams within the company and with external customers and suppliers to accomplish project objectives. Provide technical sales support. Comprehend and apply food science and pet nutrition principles effectively in project work. Prepare and issue specifications for new ingredients and finished products. QUALIFICATION REQUIREMENTS: (To perform this job successfully, and individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required). BS in Food Science, Animal Science, Nutrition, or equivalent required. 5 years of experience in pet food, food science, or related field preferred. Experience in successfully bringing new, innovative products to market. Demonstrated knowledge of ingredient functionality and food manufacturing processes. Strong communication and project management skills. Creativity and problem-solving ability. Collect and interpret data and make recommendations. Experience with working effectively in a plant environment preferred. Knowledge of Good Manufacturing Practices, Microsoft Office, Microsoft Excel.

Thatcher Company, Inc. is a privately owned company based in Salt Lake City, Utah. It is a diversified chemical manufacturer, compounder, re-packager and distributor. Thatcher Company, Inc and its affiliated companies have over 500 employees in 15 locations in the USA. The company was founded in 1967 and is financially strong with excellent growth prospects. The company has never had a losing year, has no outside debt and has financed all its growth internally. Thatcher's diversification, coupled with ever broadening product offerings, allows us to provide job security to our employees and respond to the changing needs of our customers and the marketplace. Our core values include insuring safety in all our activities, proper environment stewardship, a focus on providing our customers superior products and service, insuring employee success, win-win relationships and continuous improvement. The founder of our company set up a defined contribution Profit Sharing Plan to reward the efforts and loyalty of all our employees. It is fully funded by the company and no employee contribution or match is an element of the plan. The plan allows for a yearly contribution of up to 25% of an employee's salary. The results of company operations are reviewed every year to determine the contribution amount for each employee. 2019 marked the 46th consecutive year of maximum funding. Senior Research Scientist, Water Treatment Division Thatcher Company is looking for a Senior Research Scientist to lead water treatment product development at Thatcher Company headquarters, located in Salt Lake City, UT. This position will report to the Vice President of Technical Services and Business Development. Major Accountabilities: * Lead the company's development of new products/technologies for the Water Treatment Market. * Develop manufacturing processes for new products and optimize existing manufacturing processes for the water treatment division of Thatcher Company. * Support Thatcher's operational excellence group in the scale-up and launch of new products and processes. * Develop finished product specifications and validate analytical test methods which are needed to characterize new water treatment products. * Improve the existing water treatment product line and search for opportunities to optimize related manufacturing processes. * Collaborate with Thatcher's marketing and sales departments to understand the needs of the water treatment industry and develop technical, customer-driven solutions. * Develop a thorough understanding of the water treatment market through market research and analysis of competitive offerings. * Understand and maintain a current knowledge of regulatory programs which apply to water treatment operations. * Manage multiple projects simultaneously and communicate project status through written technical reports and live presentations. * Evaluate and approve new raw materials or raw material substitutions as requested by Thatcher's procurement team. * Provide storage and shelf-life recommendations supported by low temperature testing, corrosion studies, and ambient and accelerated aging studies. * Assist the marketing department with the development of technical marketing literature. * Provide both internal and external technical support and guidance. Qualifications Required Qualifications: * PhD in Chemistry (or related field) with a minimum of 2 years of industrial research experience; or MS in Chemistry (or related field) with a minimum of 5 years of industrial research experience; or BS in Chemistry (or related field) with a minimum of 9 years of industrial research experience * Experience with product development and product characterization, preferably in water treatment or related industry. Background in water chemistry will be highly applicable. * Experience with standard wet chemistry techniques, autotitrators and other complex analytical instrumentation such as ICP-OES, ICP-MS, IC, FTIR, GC, and HPLC. * Strong computer literacy and proficient with Microsoft office. Well qualified candidates will have experience working with enterprise resource planning software and laboratory instrumentation software such Masshunter, Empower, OpenLab, IC Magic, ICP Expert, and/or Tiamo. * Proven ability to lead cross-functional teams. * Strong quantitative, problem solving, and decision-making skills. * Strong written and verbal communication skills. Must have a high-level ability to communicate findings concisely and effectively. Why Thatcher is right for you Competitive salary The founder of our company set up a defined contribution Profit Sharing Retirement Plan to reward the efforts and loyalty of all our employees. It is fully funded by the company and no employee contribution or match is an element of the plan. The plan allows for a yearly contribution of up to 25% of an employee's salary. The results of company operations are reviewed every year to determine the contribution amount for each employee. 2019 marked the 46th consecutive year of maximum funding. Additional benefits including health, dental, life insurance, vacation, sick leave, paid holidays and 50% additional education reimbursement. Health Savings Account (HSA) Excellent career opportunities with a growing company A great work environment where your contribution can be recognized, and you can reach your full potential.

About Us: Aliri is committed to solving industry challenges by bringing innovative bioanalysis and spatial solutions to biotech and pharma, as the complexity of the drug development landscape continues to rise. Primary Purpose: Develops and/or validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. Job Duties and Responsibilities: Organizes, conducts and evaluates analytical results and testing in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. Maintains study documentation and laboratory records. Independently sets-up, maintains, operates and performs routine and non-routine maintenance on general equipment as directed. Provides daily updates for individual analytical runs and project status to PAI and or Management. Ensures all data meets acceptance criteria and troubleshoots failures. Ensures all data is analyzed, processed, and compiled in a timely manner Performs peer review of data. Identifies and proactively addresses deviations from normal results and informs Principal Analytical Investigator and/or management of any problems and/or deviations that may affect the integrity of the data; participates in corrective action of problems. Promotes a cohesive team environment. Assists in setting up and performing method development and validation of various analytes in a variety of matrices with supervision. Makes suggestions for modifications in test methods or procedures. Provides input and participates in project meetings, plans, monitors and guides project work. Ability to assist lead chemist on projects, with supervision. Maintains a clean and safe laboratory work environment. Trains and assists less experienced staff. Interacts with internal and external clients Participates in client visits as needed Participates in process improvement initiatives. Effectively plans and utilizes personnel and resources for timely completion of assigned projects. Assists in writing reports, methods, protocols and SOPs. Assists in evaluation of data for incorporation into written reports. Performs other related duties as assigned. Experience: Bachelor's Degree in Chemistry or related Scientific field with 6-8+ years experience is required -OR- Master's Degree or equivalent in Chemistry or related Scientific field with 5+ years' experience is required -OR- Ph.D. or equivalent in Chemistry or related Scientific field with 2+ years experience is required. Knowledge, Skills, and Abilities: Understands the method development and method validation process. Performs complex analytical methods on biological matrices, often involving problem solving situations. Experience with bottom-up protein analysis by LCMS. Applies and interprets scientific theories, concepts, techniques, and regulatory requirements in bioanalytical and mass spectrometry studies and accepts leadership role in developing scientific approaches. Works well in a teamwork setting, for technical direction on complex bioanalytical and mass spectrometry projects. Tracks hours on a consistent project to project basis. Preferred Qualifications: Former Bioanalytical CRO experience; Customer service experience; LIMs experience: Strong written and verbal communication skills. Working Conditions: May work with potentially hazardous substances. Mandatory immunizations and screening as required. Overtime and weekend work as required. Work requires some standing and sitting for long periods of time, including working within a laboratory hood and at standing bench top. Work requires use of PPE (personal protective equipment). Benefits offered to full-time Aliri Bioanalysis employees: Medical and Dental Insurance through United Health Care $6,350 Qualified High Deductible Health Plan with an employer HSA contribution $3,300 Qualified High Deductible Health Plan with an employer HSA contribution $1,500 PPO Copay Plan, with choice of FSA Dental PPO Plan Vision insurance through VSP Additional life insurance options Employer Paid Basic Life & Accidental Death & Dismemberment (AD&D) Accident and Critical Illness and hospital indemnity plan Health savings and Flexible spending accounts Bonus Plans and rewards and recognition programs 401K with matching Fitness and Warehouse Club reimbursements JOB CODE: 1000110

Medical Research Associate- Onsite; Full Time- ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy eNugh to participate in the clinical trial according the protocol of a study. What you will be doing * Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process. * You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures. * Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized. * Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort. Your profile * A strong command of both English and the host country's language is essential, enabling effective communication and collaboration. * A High School Diploma or G.E.D. qualification * If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you. * 1+ years of work experience in a medical or clinical field is preferred * If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage * Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Summary The R&D Application Technician supports the development, testing, and improvement of dietary supplement solid dose products such as tablets, capsules, and powders. This role involves assisting senior R&D staff with product formulation, lab testing, and process optimization under the guidance of more experienced team members. The technician is also responsible for maintaining a clean, safe laboratory environment and following established protocols. --- Key Responsibilities · Assist in Product Development o Support R&D staff in preparing formulations for new and improved dietary supplement products (tablet cores, capsules, powders, and other solid dose forms). o Measure, weigh, and mix ingredients according to established protocols. · Laboratory Testing & Documentation o Operate and maintain lab equipment such as tablet presses, moisture analyzers, disintegration and friability testers, and encapsulation machines under supervision. o Collect and record testing data accurately in a laboratory notebook and digital systems. o Prepare regular progress updates for the R&D team and management as directed. · Process & Procedure Support o Follow standard operating procedures (SOPs) to ensure consistency and compliance in product testing and pilot-scale production. o Assist in troubleshooting minor issues with equipment or formulations, escalating more complex problems to senior staff. o Contribute to documentation such as unit dose specifications, change orders, and basic product labeling details under guidance. · Collaboration & Communication o Communicate effectively with cross-functional teams (Production, Quality, and R&D) about project tasks and progress. o Participate in team meetings to discuss ongoing projects and potential improvements. · Safety & Compliance o Adhere to safety guidelines and wear personal protective equipment (PPE) as required. o Maintain a clean, safe, and organized laboratory environment, including proper handling and disposal of samples and materials. --- Qualifications & Requirements · Education & Experience o High school diploma or equivalent required; post-secondary coursework in science, engineering, or a related field preferred. o 1-3 years of experience in a laboratory, manufacturing, or technical environment, preferably in food, pharmaceutical, or dietary supplement industries. · Technical Skills o Basic understanding of laboratory practices and the scientific method. o Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook). o Familiarity with operating common lab equipment is a plus. · Physical Requirements o Able to lift and move up to 50 lbs. occasionally. o Capable of standing for extended periods and working in both lab and production environments. · Communication o Must be able to understand, speak, read, and write in English to perform essential job functions and comply with documentation requirements. · Other o Willingness to occasionally travel or work flexible hours as needed.

Bookmark this Posting Print Preview | Apply for this Job Posting Details The University of Utah, an AA/EO employer, encourages applications from all qualified individuals, and provides reasonable accommodation to the known disabilities of applicants and employees. The University of Utah values candidates who have experience working in settings with students, staff, faculty and patients from all backgrounds and possess a strong commitment to improving access to higher education, employment opportunities, and quality healthcare for historically underrepresented groups. Position Information Position/Rank Microbiome/Mucosal Immunology Gastroenterology Scientist/Clinician-Scientist Department 00229 - Gastroenterology City Salt Lake City, UT Track Track Dependent on Qualifications New Position to Begin upon hire Details The Division of Gastroenterology within the University of Utah's Department of Internal Medicine announces a new tenure-track physician-scientist faculty position in the field of the Microbiota and Mucosal Immunology. Particular areas of interest include microbiota-immune interactions, mucosal immune pathways that promote health, dietary interactions with the microbiota, or microbial metagenomics, metabolism or ecology within disease states such as Inflammatory Bowel Disease (IBD), primary sclerosing cholangitis, or irritable bowel syndrome. The primary criteria for selection will be excellence and creativity in research and scholarship which includes a successful track-record of publications and funding consistent with rank along with a national presence within their respective field of Gastroenterology & Hepatology. Successful candidates will be expected to establish a rigorous, independent translational research program while integrating seamlessly into our successful clinical program. Candidates will be expected to direct a translational or clinical research program that complements both GI and Internal Medicine goals. Candidates must have an MD or DO degree. Faculty rank will be commensurate with experience and appointments will include competitive salaries and start-up packages. Successful applicants would join faculty within GI and would be integrated within a focused consortium of enthusiastic and well-funded faculty in Mucosal Microbiota and Immunology who are recipients of prestigious new and established investigator awards. The applicant would be part of an emerging, university supported center with a focus on microbiota and mucosal immunology that includes faculty across 13 different departments to nurture inter-disciplinary science in the microbiota field and would be intimately involved with the emerging MAGIC (Microbiota And Gastrointestinal Immunity Consortium) center for microbiota and mucosal oriented research. The MAGIC center has served as the impetus for the novel MAGIC Biobank for prospective collection of human tissues/samples of GI patients for researchers throughout the University. This collective provides infrastructure to conduct gnotobiotic experiments, microbiota analysis, metabolomics, and acquisition of human samples to cultivate basic science and translational discoveries in this space. Minimum Qualifications: PhD, MD, or DO degree, clinicians must be board certified in Gastroenterology and eligible for a Utah Medical License Preferred Qualifications: History of NIH funding in an area appropriate for participation in MAGIC. Contact for Inquiries: If interested in discussing this exciting opportunity, contact Dr. Nicole Frank, ************************* To apply, please submit a curriculum vitae, a brief cover letter, and a 2 page description of anticipated research directions at: ******************************************** Applications reviewed upon receipt. Three references will be obtained at later request. Faculty rank will be commensurate with experience and appointments will include competitive salaries and start-up packages. The University of Utah is located in Salt Lake City, a vibrant and progressive metropolis that sits in the foothills of the Wasatch Mountain Range. This offers a truly unique mix of city life, outdoor activities and a world-class biomedical research program that houses Howard Hughes Investigators, National Academy of Science members and a Nobel Laureate. The University of Utah is adjacent to ARUP national reference laboratory, a worldwide leader in innovative laboratory research and development. Further, the Huntsman Cancer Institute is an NCI designated cancer center at the University of Utah, and provides cutting edge cancer research technologies to support clinically relevant research programs. The University of Utah Health (U of U Health) is a patient focused center distinguished by collaboration, excellence, leadership, and Respect. U of U Health values candidates who are committed to fostering and furthering the culture of compassion, collaboration, innovation, accountability, acceptance, integrity, quality, and trust that is integral to our mission. EEO/Non-Discrimination Information All qualified individuals are strongly encouraged to apply. Veterans' preference is extended to qualified applicants, upon request and consistent with University policy and Utah state law. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities. The University of Utah is an Affirmative Action/Equal Opportunity employer and does not discriminate based upon race, ethnicity, color, religion, national origin, age, disability, sex, sexual orientation, gender, gender identity, gender expression, pregnancy, pregnancy-related conditions, genetic information, or protected veteran's status. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34 CFR part 106. The requirement not to discriminate in education programs or activities extends to admission and employment. Inquiries about the application of Title IX and its regulations may be referred to the Title IX Coordinator, to the Department of Education, Office for Civil Rights, or both. To request a reasonable accommodation for a disability or if you or someone you know has experienced discrimination or sexual misconduct including sexual harassment, you may contact the Director/Title IX Coordinator in the Office of Equal Opportunity and Affirmative Action (OEO/AA). More information, including the Director/Title IX Coordinator's office address, electronic mail address, and telephone number can be located at: *************************************** Online reports may be submitted at oeo.utah.edu Notice The University is a participating employer with Utah Retirement Systems ("URS"). Eligible new hires with prior URS service, may elect to enroll in URS if they make the election before they become eligible for retirement (usually the first day of work). Contact Human Resources at ************** for information. Individuals who previously retired and are receiving monthly retirement benefits from URS are subject to URS' post-retirement rules and restrictions. Please contact Utah Retirement Systems at ************** or ************** or University Human Resource Management at ************** if you have questions regarding the post-retirement rules. This position may require the successful completion of a criminal background check and/or drug screen and immunizations. ************************************ This report includes statistics about criminal offenses, hate crimes, arrests and referrals for disciplinary action, and Violence Against Women Act offenses. They also provide information about safety and security-related services offered by the University of Utah. A paper copy can be obtained by request at the Department of Public Safety located at 1658 East 500 South. Special Instructions for Candidates Please upload a CV in mm/yyyy format for start and end dates Open Date 01/16/2025 Close Date Open Until Filled Yes Requisition Number PRN03755F Type Faculty Posting Specific Questions Required fields are indicated with an asterisk (*). * One measure of faculty diversity at the School of Medicine is the proportion of faculty members who come from a rural background. Did you graduate high school from a town with less than 10,000 persons? * Yes * No Applicant Documents Required Documents * Cover Letter * Curriculum Vitae * Research Statement Optional Documents

Your work will change lives. Including your own. The Impact You'll Make Recursion is at the forefront of reimagining drug discovery through the integration of automated cell biology, high-dimensional and diverse data sets, and sophisticated analytics and machine learning. We are seeking an in vitro toxicologist who can drive a collaborative effort aimed at identifying and validating novel in vitro safety assessments across our diverse portfolio of drug projects. Currently, our high-throughput platform teams utilize technologies such as brightfield cell imaging and phenomics, high-throughput transcriptomics and fast-proteomics coupled with our advanced machine learning analytics to mine the data for novel relationships and to help decode biology. We see broad opportunities to expand the platform for decoding toxicity/safety and we are seeking for someone with the passion to drive this effort. The goal is to build novel, advanced in vitro toxicology screening to the Recursion platform that to predict toxicities such as cytotoxicity, hepatotoxicity, or cardiotoxicity. Career development opportunities will include the opportunity to work with the early project teams to provide scientific expertise and leadership for the safety assessment of Recursion programs from early discovery through to candidate selection and beyond. You will contribute to the assessment and selection of novel drug targets and the optimisation of novel candidate molecules using innovative molecular and cellular technologies to enhance the safety profile of our drug candidates. In this role, you will Implement innovative experimental or computational strategies using multi-dimensional data to assess and/or provide mechanistic understanding of safety issues. Adapt and apply toxicology screening strategies to predict, assess and mitigate on-target, off-target and other drug-related safety risks in support of the drug discovery portfolio. Provide subject matter expertise on cross-functional project teams within the discovery organization with an opportunity to oversee the preclinical safety strategy in development as projects progress. Act as a key resource for early safety assessment during the discovery phase, providing scientific knowledge and expertise to cross-functional project teams on the appropriate interpretation of in vitro data. Collaborate with external collaborators to ensure best practice for in vitro safety assessment. Partner with the project teams to develop optimal strategies to address specific safety issues within project teams. Provide verbal and written summaries for internal discussions. Present summary data to project teams, senior leadership and external partners as needed. The Team You'll Join Reporting to the Vice President of Toxicology you'll be joining a dynamic toxicology team that works across the portfolio to guide projects through the various stages of discovery and development. This high performing team will work together to continually improve our workflows to drive towards greater efficiency and automation. The Experience You'll Need Pharm D or Ph.D in toxicology, Pathology, Physiology, Biochemistry or expertise in related biological scientific disciplines with preferably 1 or 2 years of postdoctoral experience. Background in cell biology and imaging techniques, or molecular biology running transcriptomic or proteomic experiments with experience in designing and developing high throughput screening assays. Proven ability to troubleshoot technical issues with biological experiments. Skilled in interpreting observed phenotypic signatures to potential mechanisms of toxicity. Highly motivated scientist with the ability to work independently as well as collaborate with stakeholders to drive the development of novel toxicology assays. Stay informed on the latest trends and advancements in advanced in vitro platforms and physiological models, and their potential applications in improving the predictive power of toxicology studies. Keen interest in artificial intelligence and its application to drug discovery. Experience with the use of AI-tools to predict toxicology endpoints. Working Location & Compensation: This position is based at our office located in Salt Lake City. Please note that we are a hybrid environment and ask that employees spend 50% of their time in the office. Relocation support can be provided for this role. At Recursion, we believe that every employee should be compensated fairly. Based on the skill and level of experience required for this role, the estimated current annual base range for this role is $103,000-$175,000. You will also be eligible for an annual bonus and equity compensation, as well as a comprehensive benefits package. #LI-CP1 The Values We Hope You Share: We act boldly with integrity. We are unconstrained in our thinking, take calculated risks, and push boundaries, but never at the expense of ethics, science, or trust. We care deeply and engage directly. Caring means holding a deep sense of responsibility and respect - showing up, speaking honestly, and taking action. We learn actively and adapt rapidly. Progress comes from doing. We experiment, test, and refine, embracing iteration over perfection. We move with urgency because patients are waiting. Speed isn't about rushing but about moving the needle every day. We take ownership and accountability. Through ownership and accountability, we enable trust and autonomy-leaders take accountability for decisive action, and teams own outcomes together. We are One Recursion. True cross-functional collaboration is about trust, clarity, humility, and impact. Through sharing, we can be greater than the sum of our individual capabilities. Our values underpin the employee experience at Recursion. They are the character and personality of the company demonstrated through how we communicate, support one another, spend our time, make decisions, and celebrate collectively. More About Recursion Recursion (NASDAQ: RXRX) is a clinical stage TechBio company leading the space by decoding biology to radically improve lives. Enabling its mission is the Recursion OS, a platform built across diverse technologies that continuously generate one of the world's largest proprietary biological and chemical datasets. Recursion leverages sophisticated machine-learning algorithms to distill from its dataset a collection of trillions of searchable relationships across biology and chemistry unconstrained by human bias. By commanding massive experimental scale - up to millions of wet lab experiments weekly - and massive computational scale - owning and operating one of the most powerful supercomputers in the world, Recursion is uniting technology, biology and chemistry to advance the future of medicine. Recursion is headquartered in Salt Lake City, where it is a founding member of BioHive, the Utah life sciences industry collective. Recursion also has offices in Toronto, Montréal, New York, London, Oxford area, and the San Francisco Bay area. Learn more at ****************** or connect on X (formerly Twitter) and LinkedIn. Recursion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected under applicable federal, state, local, or provincial human rights legislation. Accommodations are available on request for candidates taking part in all aspects of the selection process. Recruitment & Staffing Agencies: Recursion Pharmaceuticals and its affiliate companies do not accept resumes from any source other than candidates. The submission of resumes by recruitment or staffing agencies to Recursion or its employees is strictly prohibited unless contacted directly by Recursion's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Recursion, and Recursion will not owe any referral or other fees. Our team will communicate directly with candidates who are not represented by an agent or intermediary unless otherwise agreed to prior to interviewing for the job.

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. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients. We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients. This role will play a key role in executing and reports analytical/chemistry test methods for raw materials, drug substance and drug product for large molecule clinical and commercial products. Key Accountabilities/ Core Job Responsibilities: Performs implementation and execution of routine and ad hoc chemical and analytical testing for raw materials and large molecule drug substance and drug product. Supports the qualification and implementation of USP/EP methods and product specific methods as part of new product introduction and technology transfer. Supports stability testing of drug substance and drug product for all timepoints and conditions. Supports quality events such as CAPA, Change Control, Deviations, and LIR/OOS as subject matter expert for QC Chemistry Generates, analyzes, and reports data and takes appropriate action Works within LabWare LIMS for execution of methods, data trending and report issuance. Reviews documentation for product disposition, generates COA/COC and batch summary reports Works with accuracy, urgency and a continuous improvement perspective Provides flexible support for on-call or outside normal business hours if required Qualifications/Skills: BS in Chemistry or equivalent science 4+ years of experience working in GMP regulated chemistry laboratory Large molecule experience preferred Familiarity with GMP regulations Knowledge of current USP/Ph. Eur./FDA/ISO/GMP standards and guidance Ability to work with independently Build productive relationships with internal teams and external sources Well-developed verbal and written communication skills Excellence in execution through accuracy, right first time and a proactive nature Physical requirements- must be able to put on specialized gowning, lift and manipulate items over 25 lbs, climb ladders, stand for multiple hours at a time Strong collaboration and project management skills Familiar with Master Control and LabWare LIMS Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at ****************************************** This compensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future.This compensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future. Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

This position supports research efforts throughout the system and is accountable to support and/or lead research projects and to ensure that appropriate processes are implemented and maintained according to research protocol. This role will advise research staff regarding project identification, data collection and analysis, computer programming and integration into the Electronic Medical Record. This position designs research and assessment techniques to achieve desired outcomes and/or to comply with regulations, grant requirements, compliance, or clinical excellence initiatives. This position translates pragmatic research into clinical applications (bench-to-bedside), which may involve managing large data bases, creating reports, training clinicians / scientists / associates, and designing metrics to measure outcomes resulting from translational research applied in clinical settings. This position creates the procedures for research data collection and/or electronic medical records and is responsible for managing the ongoing research efforts and integrity of existing data systems and insuring integration across the organization. This position may serve on research committees, developing and reviewing and/or writing grants as part of scientific review groups as needed, mentor junior investigators and work alongside clinicians in developing research ideas, serving on the IRB, reviewing and editing abstracts and manuscripts, serving on external scientific committees on behalf of Intermountain Health or other internal research leadership positions. **Essential Functions** + Routinely writes manuscripts and publishes in peer-reviewed journals, ensuring that research findings are shared with the broader scientific community. + Presents research at national conferences, which helps to establish the researcher's reputation and fosters collaboration with other experts in the field. + Contributes to the writing and submission of competitive grants, which are crucial for securing extramural funding. Demonstrates a strong ability to craft compelling proposals that attract financial support from external sources, enabling the continuation and expansion of research initiatives. + Independently designs studies of low to moderate complexity. Applies for and manages competitive extramural funding to support these projects, showcasing the ability to develop innovative research ideas and secure the necessary resources to bring them to fruition. + Serves as a mentor to more junior investigators and research caregivers, providing guidance and support to foster their professional development. Independently supervises and guides the strategy for a research team, ensuring cohesive work towards common objectives and achieving high standards of research excellence. + Independently oversees a research program consisting of multiple research projects occurring simultaneously. Manages the overall strategy and execution of the program, ensuring that all projects align with organizational goals and are completed efficiently and effectively. + Routinely serves as the principal investigator on studies of moderate to high complexity. Consistently secures competitive extramural funding to support these research activities, demonstrating expertise in managing complex projects and obtaining necessary resources. + Provides research service by serving on institutional committees, taking on administrative roles, or developing organizational strategies and policies. Contributes to the broader mission and governance of the institution, ensuring that research efforts are aligned with institutional priorities and standards. This involvement is critical for shaping the future direction of the organization and promoting a culture of research excellence. + Demonstrates knowledge of quality improvement principles, study design, and statistical modeling to evaluate research activities. Identifies opportunities for improving healthcare delivery across clinical areas and research programs, ensuring that research outcomes lead to tangible improvements in patient care. **Skills** + Study Design + Quality Improvement + Data Management + Research Coordination + Program Management + Risk Assessment + Documentation + Manuscript Writing + Grant Writing + Mentorship **Minimum Qualifications** + MD/DO or Ph.D in a clinical or life science field of study. Degree must be obtained through an accredited institution. Education is verified. + Demonstrated professional experience in research. + Has received or is eligible to receive an academic appointment at Intermountain Health + Demonstrated experience coordinating and training in a healthcare / academic / industry research setting. + Demonstrated experience in study designing, developing, and analyzing research outcome data. + Research and collaboration experience to interact effectively in academic, corporate, and clinical cultures on a national/international basis. + Experience using statistical research methods and their use in outcomes data reporting. + Experience writing manuscripts, sops, technical specifications, and managing implementation projects. + Demonstrated understanding of data management functions and processes. + Ability to travel to various locations. **Preferred Qualifications** + Experience as a 'Principal Investigator' in grant-funded projects of relevant field. + Experience in a role requiring the ability to demonstrate proficiency with MS project and database applications. + Experience in obtaining grants. + Experience in publishing in peer reviewed journals. + Experience in study coordination and collaboration. + Familiarity with statistical and informatics/bioinformatics analysis tools. + Experience working within a hospital clinical area or an understanding of workflows and hospital processes. **Physical Requirements:** **Physical Requirements** + Ongoing need for employee to see and read information, labels, documents, monitors, identify equipment and supplies, and be able to assess customer needs. + Frequent interactions with providers, colleagues, customers, patients/clients and visitors that require employee to verbally communicate as well as hear and understand spoken information, needs, and issues quickly and accurately. + Manual dexterity of hands and fingers to manipulate complex and delicate supplies and equipment with precision and accuracy. This includes frequent computer use for typing, accessing needed information, etc. + For roles requiring driving: Expected to drive a vehicle which requires sitting, seeing and reading signs, traffic signals, and other vehicles. **Location:** Transformation Center **Work City:** Murray **Work State:** Utah **Scheduled Weekly Hours:** 40 The hourly range for this position is listed below. Actual hourly rate dependent upon experience. $54.03 - $85.04 We care about your well-being - mind, body, and spirit - which is why we provide our caregivers a generous benefits package that covers a wide range of programs to foster a sustainable culture of wellness that encompasses living healthy, happy, secure, connected, and engaged. Learn more about our comprehensive benefits package here (***************************************************** . Intermountain Health is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. At Intermountain Health, we use the artificial intelligence ("AI") platform, HiredScore to improve your job application experience. HiredScore helps match your skills and experiences to the best jobs for you. While HiredScore assists in reviewing applications, all final decisions are made by Intermountain personnel to ensure fairness. We protect your privacy and follow strict data protection rules. Your information is safe and used only for recruitment. Thank you for considering a career with us and experiencing our AI-enhanced recruitment process. All positions subject to close without notice.

Duration: 6+ month Job Description: Under general supervision, performs cGMP laboratory analyses of Finished products and in process materials. Performs stability testing for Finished products. Performs maintenance and calibration of analytical instruments. Minimum Qualifications: Bachelor's Degree in Science or related science field from an accredited college or university and one (1) year related laboratory experience or an equivalent combination of education and experience. Experience and Skills: •Usage of GC and HPLC chromatographic equipment, as well as UV/VIS, and FTIR operation methods and techniques. •Business, scientific and personal computer hardware and software applications. •Business English usage, spelling, grammar and punctuation. •Wet Chemistry and Chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures. •Knowledge of or ability to learn FDA, cGLP, cGMP, USP, EP and SOP or other applicable regulatory and safety compliance guidelines. •Performing testing accurately and precisely. •Responding to routine inquiries from management, employees and regulatory agencies. •Communicating clearly and concisely, both orally and in writing. •Managing multiple projects, duties and assignments. •Establishing and maintaining cooperative working relationships with others. Essential functions include: *Carries out responsibilities in accordance with the organization's policies, procedures and state, federal and local laws. *Operates general analytical instruments during the testing of finished products using HPLC, UPLC, GC-FID, UV-VIS, FTIR, automatic titrators, Dissolution Apparatus *Performs physical testing such as viscosity testing, Instron testing, and microscopy . *Performs wet chemistry tests on samples such as pH, titration, gravimetry and prepares standard, sample, and buffer solutions as required by test methods and performs all necessary calculations associated. *Labels, transcribes and records documentation such as report sheets and laboratory notebooks as required by SOPs. *Cleans, maintains and calibrates laboratory equipment to ensure compliance with current Good Manufacturing Procedures (cGMP). *Meets project deadlines and performance standards as assigned. *Complies with all Company policies and procedures, including safety rules and regulations *Performs investigations and troubleshooting of analytical test methods and lab instruments. *Performs investigation and writes reports on findings, conclusion and identify corrective actions/preventative actions. *Carries out quantitative and qualitative analyses in support of method comparisons, method transfers, method validations, product in-use study. *Train junior level scientist and technician and participate in identifying process to improve efficiency in laboratory testing. *Assist in organizing, staging and pulling samples for stability studies. *Assist in creating database for stability sample pull, staging sample and test schedules. *Performs related duties as assigned. Qualifications Minimum Qualifications: Bachelor's Degree in Science or related science field from an accredited college or university and one (1) year related laboratory experience or an equivalent combination of education and experience. Experience and Skills: •Usage of GC and HPLC chromatographic equipment, as well as UV/VIS, and FTIR operation methods and techniques. •Business, scientific and personal computer hardware and software applications. •Business English usage, spelling, grammar and punctuation. •Wet Chemistry and Chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures. •Knowledge of or ability to learn FDA, cGLP, cGMP, USP, EP and SOP or other applicable regulatory and safety compliance guidelines. •Performing testing accurately and precisely. •Responding to routine inquiries from management, employees and regulatory agencies. •Communicating clearly and concisely, both orally and in writing. •Managing multiple projects, duties and assignments. •Establishing and maintaining cooperative working relationships with others. Additional Information All your information will be kept confidential according to EEO guidelines.

The Toxicologist will develop the initial draft of toxicology related projects to safeguard global health. This will include obtaining all necessary information from the client and performing the necessary literature research. This information will then be summarized in a technical format for the project and submitted for peer review. The Toxicologist will also assist with peer review as needed. Education and experience: Required: * Bachelors in Toxicology with 5+ more years working experience OR * Master's degree in Toxicology and 3+ years working experience * ISO 10993 - 17 experience * Performed Toxicological Risk assessments to this standard Preferred (Not Required): * ISO 18562; Inhalation Gas Pathway Device experience * Current American Board of Toxicology Certification * Analytical Chemistry education or working experience Essential Duties: * Review and write Toxicological Risk Assessments and other toxicological related documents (i.e. Opinion Memos for patient safety) * In preparation for assessment deliverable, work cross-functionally with other departments to guide where toxicological expertise is necessary * Communicate with the client to obtain additional information for projects or toxicological related testing * Perform literature research on materials and compounds * Build and implement process improvements * Know and follow the Nelson service standard Competencies of this position * Project Management * Excellent technical writing skills and expertise * Attention to detail * Time management * Able to multi-task and be self-motivated * Knowledge Microsoft Office applications (Word, Excel, PowerPoint, Outlook, etc.) Work Arrangement Flexibility: This role does function remotely, considering applicants can commit any potential travel required. This would include Nelson site visits, trade shows and potentially client meetings as well. Travel requirements: Occasional travel during the business day. Some out of the area and overnight travel may be expected. May be required to attend domestic and international trade shows, seminars and conferences. Physical requirements: Must be able to stand/walk for 10% of the day and 90% of the day sitting at a desk or on the computer. Must be able to attend trade shows, seminars, and conferences. Must be able to occasionally lift a maximum of 45lbs. May require modified work hours to cover travel and work in other time zones.

divstrong Description/strongbr/pThe Toxicologist will develop the initial draft of toxicology related projects to safeguard global health. This will include obtaining all necessary information from the client and performing the necessary literature research. This information will then be summarized in a technical format for the project and submitted for peer review. The Toxicologist will also assist with peer review as needed./p pstrong Education and experience:/strong/p pistrong Required:/strong/i/p ul li Bachelors in Toxicology with 5+ more years working experience OR /li li Master's degree in Toxicology and 3+ years working experience/li li ISO 10993 - 17 experience ul li Performed Toxicological Risk assessments to this standard/li /ul/li /ul pistrong Preferred (Not Required):/strong/i/p ul li ISO 18562; Inhalation Gas Pathway Device experience/li li Current American Board of Toxicology Certification /li li Analytical Chemistry education or working experience/li /ul pstrong Essential Duties:/strong/p ul li Review and write Toxicological Risk Assessments and other toxicological related documents (i.e. Opinion Memos for patient safety)/li li In preparation for assessment deliverable, work cross-functionally with other departments to guide where toxicological expertise is necessary/li li Communicate with the client to obtain additional information for projects or toxicological related testing/li li Perform literature research on materials and compounds/li li Build and implement process improvements/li li Know and follow the Nelson service standard/li /ul pstrong Competencies of this position/strong/p ul li Project Management/li li Excellent technical writing skills and expertise/li li Attention to detail/li li Time management /li li Able to multi-task and be self-motivated/li li Knowledge Microsoft Office applications (Word, Excel, PowerPoint, Outlook, etc.)/li /ul pstrong Work Arrangement Flexibility:/strong/p pThis role does function remotely, considering applicants can commit any potential travel required. This would include Nelson site visits, trade shows and potentially client meetings as well./p pstrong Travel requirements:/strong/p pOccasional travel during the business day. Some out of the area and overnight travel may be expected. May be required to attend domestic and international trade shows, seminars and conferences./p pstrong Physical requirements:/strong/p pMust be able to stand/walk for 10% of the day and 90% of the day sitting at a desk or on the computer. Must be able to attend trade shows, seminars, and conferences. Must be able to occasionally lift a maximum of 45lbs. iMay require modified work hours to cover travel and work in other time zones./i/p p /pbr/br//div

Job Description Certerra Southwest, a leading engineering consulting firm in the western United States, has an excellent opportunity for an Entry Level Environmental Scientist in several of our offices. 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, New Mexico, Utah, and Nevada. A willingness and ability to learn new skills in challenging field and office assignments in a collaborative setting wins the day! 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. Candidates must be able to travel, and work nights, weekends, and extended hours, depending on the project requirements. Potential responsibilities Support field projects including groundwater monitoring, soil sampling, vapor sampling, and operations/maintenance of remediation systems. Support planning and design of environmental systems and processes to mitigate/control the discharge of pollutants. Monitor, record, and report environmental field measurements. Conduct field investigations and inspections to review and evaluate compliance with regulatory requirements, permits, and specifications involving water, wastewater, air emissions, hazardous waste, and petroleum storage tank systems. Collect soil samples from borings using a variety of drilling rigs for environmental and geotechnical testing, prepare lithologic, and perform field screening for environmental contaminants. Install groundwater monitoring wells, vadose zone wells, and vapor sampling ports per project specifications. Log and track data, prepare spreadsheets, prepare calculations for use in exposure assessments and fate and transport modelling. Conduct literature research for use in interpreting areas of waste management, disposal, and releases to the environment. Read, review, interpret, and analyze existing and historical data about past investigative activities to develop conceptual site models. Prepare detailed report narratives and supporting documentation describing and summarizing research, field activities, and analytical results. Physical Requirements Work outside in extreme weather conditions (heat and cold) Ability to lift/carry 50 pounds Ability to carry and climb ladders Use and control handheld power tools Be able to wear a respirator, safety harness and other safety equipment, as needed Stand for extended periods of time. Key Credentials OSHA 40-Hour HAZWOPPER Training. Experience with MS Office, CADD, Salesforce, and or Deltek Advantage State or Federal level certifications for asbestos, lead, indoor air quality, industrial hygiene, or environmental management Clean driving record BS in Engineering or Physical Science WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee occasionally works near moving mechanical parts in outside weather conditions and is occasionally exposed to wet and/or humid conditions, and fumes or airborne particles. The noise level in the work environment is usually moderate. 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 based on their ability, competence, and performance of the essential functions of their positions. There will be no discrimination based on 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 people will be hired based on 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.

Summary The R&D Application Technician supports the development, testing, and improvement of dietary supplement solid dose products such as tablets, capsules, and powders. This role involves assisting senior R&D staff with product formulation, lab testing, and process optimization under the guidance of more experienced team members. The technician is also responsible for maintaining a clean, safe laboratory environment and following established protocols. --- Key Responsibilities · Assist in Product Development o Support R&D staff in preparing formulations for new and improved dietary supplement products (tablet cores, capsules, powders, and other solid dose forms). o Measure, weigh, and mix ingredients according to established protocols. · Laboratory Testing & Documentation o Operate and maintain lab equipment such as tablet presses, moisture analyzers, disintegration and friability testers, and encapsulation machines under supervision. o Collect and record testing data accurately in a laboratory notebook and digital systems. o Prepare regular progress updates for the R&D team and management as directed. · Process & Procedure Support o Follow standard operating procedures (SOPs) to ensure consistency and compliance in product testing and pilot-scale production. o Assist in troubleshooting minor issues with equipment or formulations, escalating more complex problems to senior staff. o Contribute to documentation such as unit dose specifications, change orders, and basic product labeling details under guidance. · Collaboration & Communication o Communicate effectively with cross-functional teams (Production, Quality, and R&D) about project tasks and progress. o Participate in team meetings to discuss ongoing projects and potential improvements. · Safety & Compliance o Adhere to safety guidelines and wear personal protective equipment (PPE) as required. o Maintain a clean, safe, and organized laboratory environment, including proper handling and disposal of samples and materials. --- Qualifications & Requirements · Education & Experience o High school diploma or equivalent required; post-secondary coursework in science, engineering, or a related field preferred. o 1-3 years of experience in a laboratory, manufacturing, or technical environment, preferably in food, pharmaceutical, or dietary supplement industries. · Technical Skills o Basic understanding of laboratory practices and the scientific method. o Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook). o Familiarity with operating common lab equipment is a plus. · Physical Requirements o Able to lift and move up to 50 lbs. occasionally. o Capable of standing for extended periods and working in both lab and production environments. · Communication o Must be able to understand, speak, read, and write in English to perform essential job functions and comply with documentation requirements. · Other o Willingness to occasionally travel or work flexible hours as needed. --- Work Environment · Primarily operates in a laboratory and office setting. · Occasionally operates in production or warehouse areas where noise and airborne particles (dust, powders, etc.) may be present. · Must comply with safety regulations, including wearing hearing protection and other PPE when required. --- Note: This job description is not intended to be all-inclusive. Duties and responsibilities may be assigned or modified as business needs evolve. Employment remains on an “at will” basis. Salary is commensurate with experience and market conditions.

The Toxicologist will develop the initial draft of toxicology related projects to safeguard global health. This will include obtaining all necessary information from the client and performing the necessary literature research. This information will then be summarized in a technical format for the project and submitted for peer review. The Toxicologist will also assist with peer review as needed. Education and experience: Required: Bachelors in Toxicology with 5+ more years working experience OR Master's degree in Toxicology and 3+ years working experience ISO 10993 - 17 experience Performed Toxicological Risk assessments to this standard Preferred (Not Required): ISO 18562; Inhalation Gas Pathway Device experience Current American Board of Toxicology Certification Analytical Chemistry education or working experience Essential Duties: Review and write Toxicological Risk Assessments and other toxicological related documents (i.e. Opinion Memos for patient safety) In preparation for assessment deliverable, work cross-functionally with other departments to guide where toxicological expertise is necessary Communicate with the client to obtain additional information for projects or toxicological related testing Perform literature research on materials and compounds Build and implement process improvements Know and follow the Nelson service standard Competencies of this position Project Management Excellent technical writing skills and expertise Attention to detail Time management Able to multi-task and be self-motivated Knowledge Microsoft Office applications (Word, Excel, PowerPoint, Outlook, etc.) Work Arrangement Flexibility: This role does function remotely, considering applicants can commit any potential travel required. This would include Nelson site visits, trade shows and potentially client meetings as well. Travel requirements: Occasional travel during the business day. Some out of the area and overnight travel may be expected. May be required to attend domestic and international trade shows, seminars and conferences. Physical requirements: Must be able to stand/walk for 10% of the day and 90% of the day sitting at a desk or on the computer. Must be able to attend trade shows, seminars, and conferences. Must be able to occasionally lift a maximum of 45lbs. May require modified work hours to cover travel and work in other time zones.