Research and development technician jobs in Ogden, UT

Job DescriptionSalary: MUSH is a place where driven individuals unlock their highest potential. We believe that change starts within, and as a team, we accomplish extraordinary feats. If you want to build a reputation of doing hard things well, and aspire to make the world a little healthier, MUSH may be a great place for you. Our first product line of ready-to-eat overnight oats pioneers a new category for the breakfast occasion, offering a healthy, satiating, and convenient alternative to traditional morning meals. By making healthy food more accessible, we believe that humankind can feel, think, and do better. Role Description MUSH is seeking a dynamic and open minded teammate to support our Research and Development (R&D) Team at our manufacturing facility in Salt Lake City. The successful candidate has exceptional organization and prioritization skills. General Responsibilities: Support batching for innovation and customer requests Order and maintain inventory for innovation and new ingredients Manage inventory logistics: ingredient labels, shipping boxes, ice packs, shipping labels Operate analytical instruments for QA and secondary supplier approval (pH, viscosity, water activity) Conduct internal sensory testing for secondary supplier approvals Manage formulations and ingredients in Genesis software to ensure accuracy, cost tracking, and efficiency Other duties as assigned Experience Requirements: High School Diploma or GED preferred Strong proficiency in all MS Office/Google applications Problem solving, excellent verbal and oral communication skills Ability to manage multiple priorities and consistently meet time sensitive tasks in a fast paced environment Cultural Expectations: Set an example. Hold yourself accountable to standards of excellence Teammate: know when to follow, know when to lead; always serving others Beginners Mind: provide possibilities, options, and solutions Communicator: use tact and precision to communicate ideas, issues, and feedback Self-Starter: there is no turn-key manual for success, you are helping to build one Results Driven: you demand results, but focus on the robust processes that yield them Attention to Detail: unwavering discipline with little things that make big differences Relationship Builder: customer first mentality with all internal & external counterparts Problem Solver: expect the unexpected; be agile & effective in combating issues Thrive on Adversity: our goals are lofty and our values are grounded in humility. We bite off more than we can chew and roll our sleeves up when the situation calls for it. Fun: check the fun box every day. Love what you do & do it well.

• Perform cleaning of lab glassware in accordance with Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). • Perform lab housekeeping practices. • Must work in compliance with all Company policies and procedures, including safety rules and regulations. Knowledge of the following is helpful: • Current Good Manufacturing Practices (cGMP) and other relevant regulatory requirements. • Basic chemistry laboratory practices and techniques. • Current Company policies, practices and procedures, including safety rules and regulations. Qualifications Minimum Qualifications: High School Diploma or equivalent. Related experience in pharmaceutical manufacturing laboratory is helpful. Additional Information To know more about this position, please contact: Shweta T ********************************* ************

Schedule: Monday - Friday (40 hrs/wk) 8:00 AM - 5:00 PM Department: R&I Innovation - 249 Primary Purpose: Provides services of both a technical and non-technical nature in the laboratory service areas. Works under the direction of an R&D Manager/Supervisor .Duties could include data handling and input, sample handling, preparation of specimens for processing in the laboratory, reagent preparation, handling and storage of glassware and reagents, supply maintenance, and assisting in the performance and documentation of quality control and equipment. This Technician position will also be performing high quality routine venipuncture for R&I. About ARUP: ARUP Laboratories is a national clinical and anatomic pathology reference laboratory and an enterprise of the University of Utah and its Department of Pathology. Based in Salt Lake City, Utah. ARUP proudly hires top talent to create a work environment of diversity, professional growth and continuous development. Our workforce is committed to the important service we provide to over one million patients each month. We always strive for excellence and have a strong desire to have involvement with the advances in medicine and the role laboratory services plays within each patient's life. We never forget that there is a patient behind every specimen we receive. We are looking for individuals who want to contribute to ARUP's culture of accountability, integrity, service, and excellence. Consider joining our dynamic team. Essential Functions: Performs routine venipuncture collections according to department standards. Collects high quality specimens in a timely manner, using established phlebotomy techniques. Performs and documents quality control and equipment maintenance. Understands appropriate specimen collection, handling, and transport. Accurately retrieves and de-identifies specimens according to established departmental procedures. Notifies the appropriate supervisor or designated individual of specimens that meet the rejection criteria for inappropriate samples. Resolves the problem at the direction of the appropriate supervisor or designated individual. Prepares, organizes, and reviews specimens for run set-up according to departmental procedures. Ensures accurate sample order. Maintains cleanliness of work area. Cleans bench tops and equipment after each spill, and daily at the end of the work shift as required. Under supervision, begins training on complex processes and procedures within the group. Assists others in areas of defined competency when assigned workload is complete. Complies with safety and biohazard regulations as outlined in the Laboratory Safety Manual. Observes principles of data security and confidentiality. Maintains ethical standards in the performance of all assignments and in interactions with co-workers and other health care professionals. Other duties as assigned. Physical and Other Requirements: Stooping: Bending body downward and forward by bending spine at the waist. Reaching: Extending hand(s) and arm(s) in any direction. Mobility: The person in this position needs to occasionally move between work sites and inside the office to access file cabinets, office machinery, etc. PPE: Biohazard laboratory environment that requires use of personal protective equipment in accordance with CDC and OSHA regulations and company policies. ARUP Policies and Procedures: To conduct self in compliance with all ARUP Policies and Procedures. Sedentary Work: Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects. Fine Motor Control: Picking, pinching, typing or otherwise working, primarily with fingers rather than with the whole hand as in handling. Vision: Having close, far, and peripheral visual acuity to perform a variety of tasks such as make general observations of depth and distance.

Thatcher Company is looking for a Senior R&D Scientist-Water Processing at Thatcher Company headquarters, located in Salt Lake City, UT. This position will report to the Vice President. Major Accountabilities: Compensation $100,000-$150000 * 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 that 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 that 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 as 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. Additional benefits including health, dental, life insurance, vacation, sick leave, paid holidays and 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.

Your work will change lives. Including your own. We are leveraging new technology to create virtuous cycles of learning around datasets to build a next-generation biopharmaceutical company. It's complex biology, decoded. Recursion is a digital biology company industrializing drug discovery. We are working to solve some of the hardest, most meaningful problems facing human health today. Come join us in our mission to decode biology to radically improve lives, while doing the most impactful work of your life. Recursion's Returnship Program Our Returnship program is sponsored by the Women at Recursion Employee Resource Group. The program is aimed at helping those who have taken a hiatus (2+ years) from the STEM industry have the opportunity to return to the workforce in a learning environment with support from teams and mentors. This allows our company to tap into an underutilized pool of talent in Utah, and leverage the experience and skills of previous work and life experiences, while also providing opportunity to learn and develop experience in new cutting-edge tools and technology. This sixteen-week program will enable you to have ownership of projects that can deeply impact the company's mission to radically decode biology and serve patients, while having the guidance, support and mentorship has you re-enter the workforce. Each Returner will be assigned a mentor who will meet with them weekly, as well as weekly seminars on workplace culture, communication and technology. Our returner program lasts 4 months, running from February 2026 through the end of May 2026, with potential for transition into full-time employment depending on performance and availability. This position is mainly based in our Salt Lake City, UT headquarters, with some hybrid working flexibility available. Tissue Culture Core Returnship As the engine for Recursion's biological discovery, the Tissue Culture Core provides and maintains the high-quality cellular models that power our platform. Our diverse and collaborative team combines deep scientific expertise with industrial automation and cutting-edge technology to manage the complete cell culture lifecycle-from sourcing and expansion to rigorous quality control. Our mission is to fuel the search for novel biology and help fulfill Recursion's ultimate goal: getting better drugs to patients, faster.As a key member of the Tissue Culture Core, you will: Drive Large-Scale Cell Production: Manage the end-to-end lifecycle of diverse cellular models, from thaw to cryopreservation. You will execute large-scale expansions using advanced technologies like bioreactors and multi-layer vessels to ensure a consistent, high-quality supply for the Recursion platform. Uphold Quality and Process Excellence: Focus on the quality and robustness of all cellular products. You will help characterize our models, optimize culture protocols, and meticulously document process data to track key metrics and drive continuous improvement in our methodologies. Enable a Data-Driven Platform: Be responsible for the critical delivery of both high-quality cellular materials and the precise, well-documented data that accompanies them. Your work will directly fuel the high-throughput operations of the Recursion OS and contribute to our core mission. The Experience You'll Need Must have 3 years working experience in a research laboratory, preferably with mammalian cell culture -and- Bachelor's Degree or higher in Biology, Biochemistry, Bioengineering, or related major. Must have taken a 2+ year break from employment. A strong sense of curiosity and desire to learn with excellent written and verbal communication skills. Attentiveness to detail and the ability to accurately and honestly record experimental details, cell expansion details, and results. Enjoy working both collaboratively and independently with a team in a laboratory setting. Thrive in fast-paced environments where you'll leverage creativity and independent thinking. The Recursion Community While we offer cutting-edge tools, the secret sauce is our people. Our organization structure and culture isn't driven by politics or ego, it is designed first and foremost to help you do your best work. We live and work by values that we see as the strategic differentiators that give us a competitive advantage, allowing for better and faster work that isn't predicated on burnout and encourages us to make leaps where others take steps. This is a place where people in every role and every level make the bold bets that create large leaps forward on a regular basis! The Perks You'll Enjoy as a Returner Recursionaut Paid sick pay and additional flexibility as needed. Complimentary chef-prepared lunches and well-stocked snack bars (Salt Lake City). One-of-a-kind 100,000 square foot headquarters complete with a 70-foot climbing wall, showers, lockers and bike parking (Salt Lake City). Weekly Returners Skill Development Classes. 1:1 Weekly Mentorship with a member of your team and a member of the Returnship ERG. 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.

RELOCATION ASSISTANCE: Relocation assistance may be available CLEARANCE TYPE: SecretTRAVEL: Yes, 10% of the TimeDescriptionAt Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the world today, and for generations to come. Our pioneering and inventive spirit has enabled us to be at the forefront of many technological advancements in our nation's history - from the first flight across the Atlantic Ocean, to stealth bombers, to landing on the moon. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work - and we have an insatiable drive to do what others think is impossible. Our employees are not only part of history, they're making history. Northrop Grumman, Space Systems, is seeking a Research Engineering Manager 2 to lead our Analytical Chemistry team. This position serves as the department focal point for chemical and analytical laboratory testing supporting all Northrop Grumman programs. The position will be supporting the Propulsion Systems Division at our facility located in Promontory, UT. Role Description and Responsibilities: The Research and Development Analytical Chemistry manager directs a high performing team of approximately 13 individuals who develop and implement chemical, physical and analytical methodologies supporting material characterization and process/production problem-solving for all programs, including internal R&D and environmental testing. The manager is also responsible to: mentor and bring out the best in each team member, help them meet and overcome challenges and progress in their careers, help them feel personal satisfaction in their accomplishments, and convey and implement department and corporate expectations. Job Duties: Direct analytical methodology and maintenance tasks for team Coordinate Team tasks, budgets, and schedules with program managers, IR&D leadership, project engineers, and others in PS Oversee Team member workloads and task progression and completion Mentor Team members in personal growth and career development Lead and document periodic formal and informal performance reviews and determine merits and promotions Review and update standard work requirements and guidelines Determine staffing requirements Support initiatives of engineering leadership Basic Qualifications: B.S. degree in an engineering or science discipline and 8 years experience, M.S. degree in an engineering or science discipline with 6 years experience, or a PhD. Degree in an engineering or science discipline and 4 years experience. Experience with analytical laboratory instrumentation and techniques Working knowledge and/or experience across multiple materials and process disciplines Minimum 4 years experience leading teams and projects Excellent communication, interpersonal skills, and the ability to interface with all levels of employees and management Prior experience guiding and mentoring lower-level colleagues Ability to obtain and maintain a security clearance Must be a U.S. Citizen. Preferred Qualifications: Prior experience working with energetics, pyrotechnics, or solid propellant rocket motor materials. Current active Security Clearance Proven leadership qualities and strong interpersonal skills Prior experience in science/engineering functional management is a plus Position Benefits: As a full-time employee of Northrop Grumman Space Systems, you are eligible for our robust benefits package including: Medical, Dental & Vision coverage 401k Educational Assistance Life Insurance Employee Assistance Programs & Work/Life Solutions Paid Time Off Health & Wellness Resources Employee Discounts Primary Level Salary Range: $139,100.00 - $208,700.00The above salary range represents a general guideline; however, Northrop Grumman considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions.Depending on the position, employees may be eligible for overtime, shift differential, and a discretionary bonus in addition to base pay. Annual bonuses are designed to reward individual contributions as well as allow employees to share in company results. Employees in Vice President or Director positions may be eligible for Long Term Incentives. In addition, Northrop Grumman provides a variety of benefits including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business.The application period for the job is estimated to be 20 days from the job posting date. However, this timeline may be shortened or extended depending on business needs and the availability of qualified candidates.Northrop Grumman is an Equal Opportunity Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO and pay transparency statement, please visit *********************************** U.S. Citizenship is required for all positions with a government clearance and certain other restricted positions.

Job Details Ogden, UT Full Time AnyProduct Development Specialist Product Development Specialist In this role, the Product Development Specialist will utilize their personal experience in product formulation, food safety, and good manufacturing and sanitation practices to provide tactical support to all departments, ensuring NutraSelf products are formulated with the utmost quality. Key Responsibilities: Weigh-up of dietary supplement formulation for beadlets, powders (flavoring), and encapsulation. · Perform benchtop experiments and create new product samples. Maintain an organized and clean lab space. Assist customers and provide them with necessary services pertaining to product development. Work within set procedures to ensure production of quality products, as well as search for cost reductions where possible. Meet all safety expectations including wearing the required personnel protective equipment, cGMP gowning garb and follow all safe practices. Cross training will occur throughout the facility in all aspects of high-speed manufacturing. Work with production and give technical support to assist with manufacturing our products following all production standard procedures (kitting, mixing/blending, beadlet manufacturing, encapsulating, packaging, boxing, and labeling of the product). Prepare and maintain materials and equipment at the start, during, and end of production. Key Competencies: Accountability skills-proactively handle department activities and take ownership for outcomes and needed follow up. Operate with sense of urgency, ensuring departmental tasks completed efficiently and effectively. Team oriented and ability to work effectively with diverse population. Operate with integrity in all situations. Values open communication. Open minded, willing to consider other perspectives that may be different. Excellent communication skills, written & oral. Microsoft computer skills include Excel, Word, PowerPoint, and Outlook Knowledge of basic algebra and the metric system. Must possess a high-level of initiative and dependability. Required Qualifications: Strong knowledge of Label Review/creation, Formulation (capsule, beadlet, & flavoring powders). Must possess good interpersonal and strong communication skills (both written and verbal). Effective organizational, prioritization, and time management. Excellent attention to detail. Always possess a safe attitude. Reliable, motivated, organized and able to work in a dynamic fast-paced team-driven environment. Commitment to Safety, Quality and Productivity. Self-motivated with the ability to take initiative and use sound judgment in day-to-day decision making Punctual and reliable in work attendance Ability to work in a Loud environment with exposure to powder and heavy equipment in a manufacturing atmosphere 18 years of age or older is required. Ability to read and write legibly in English Open to learn various work processes. Ability to work flexible hours and be willing to adapt to changes in orders and tasks. Weekend work may be necessary on occasion. Able to handle the typical stress of meeting deadlines and achieving improved results. Ability to read, interpret and effectively communicate necessary policies and procedures to others. Education and experience: Education: Bachelor's degree in relevant field of study Experience: 0-5 years in a Product Development position, preferably for a Dietary Supplement manufacturing company. Working Conditions: Ability to maintain seated or standing positions for long durations. Prolonged computer use, including screen time and keyboard input, is required. Must be able to lift up to 15 pounds. Required to wear appropriate personal protective equipment (PPE), such as scrubs, hair nets, lab coats, and face masks. Must be able to tolerate various odors and scents in the work environment. Physical activity may include repetitive hand and wrist movements, as well as occasional bending, squatting, and twisting. Flexibility to adjust work hours based on operational demands is necessary. Additional Details: Full Time with Competitive Pay Health Benefits Package Progressive company environment. Position located in Ogden, UT Notice to Recruiters - We do not work with outside recruiting agencies. Please do not solicit. This description is not intended to be an exhaustive list of responsibilities and qualifications. The position, duties, and qualifications are subject to change at any time.

Medical Research Associate - Full Time - Monday - Friday - Salt Lake City, Utah (UT) 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. ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. The Role: * In short, 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 enough to participate in the clinical trial according the protocol of a study. * Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability * Ensures all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. * Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. * Monitors subject safety. • Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. * Performs general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc. Communication/Training/Meetings: * Assist with study setup activities and perform check-in and check-out activities. To be successful in the role, you will have: * Read, write, and speak English; fluent in host country language required. * High School Diploma or G.E.D. required. * Undergraduate degree in a clinical, health- related area and/or minimum 1 year of equivalent work experience with similar position * 1+ years work experience in a medical or clinical field preferred * Basic Life Support (BLS)/Phlebotomist Certification preferred * Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred. Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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 through the form below. 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

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.

Who We Are Looking For We are looking for a highly skilled scientist-demonstrating a self-reliant approach and proficient in research-to join our team as a research and development scientist focused in mass spectrometry. As part of USANA's in-house team, you will develop and implement robust, reproducible mass spectrometry-based analytical methods for characterizing food, nutrition supplements, and biological samples from clinical research. In this position, you will design and optimize HPLC, ICP-MS, single-and triple-quad mass spectrometry assays as needed to analyze food and supplement products as well as clinical samples. It is expected that you will meet regularly with other team members to coordinate work schedules and relay findings and results, contribute effectively to other groups within R&D-which will include technical report writing and presentation of complex ideas and findings-and assist in the preparation of scientific manuscripts, SOPs, technical reports and other writing endeavors. To be successful in this role, you must be extremely organized, be comfortable working independently, have the capacity to generate, compile, and evaluate materials to support product development and clinical research, and be confident in your research knowledge and expertise. What You Will Also Do as a Research and Development Scientist in Mass Spectrometry * Analyze samples and data and interpret results to ensure robust assay performance * Document experiment results according to company procedures. * Troubleshoot and solve complex technical problems related to assay development * Create and develop standard operating procedures * Report progress to supervisor/management on a regular basis Background and Skills You Need * MS in biology, chemistry, or related field; or bachelor's degree with years of relevant industry experience * Proven experience in mass spectrometer assay development * Strong problem-solving skills with a creative approach to developing innovative solutions * Strong analytical data interpretation and decision-making skills * Ability to work independently and manage multiple projects simultaneously Who We Are Since 1992, USANA has put science first with our focus on in-house research and manufacturing based in Salt Lake City, Utah to drive the creation of supplements that give your body the exact nutrition it needs to thrive. It's why millions across the globe choose USANA as the nutritional provider for themselves and their loved ones. Today we are a billion-dollar company, thanks in part to more than 1,700 employees based around the world. Our Culture Excellence, Health, Integrity, and Community are core to our business. It is our commitment to always strive to be open-minded listeners, hold ourselves and others accountable, be respectful, and celebrate the strength that comes from collaboration. Through initiatives like our Inclusion and Belonging Council, we create a company culture where all members of the USANA family feel cared for, included, and valued. USANA has repeatedly been named one of Utah's Best Companies to Work For by Utah Business magazine, one of America's Best Companies to Work For by Outside Magazine, one of the Best Places to Work for in the Direct Selling Industry by Direct Selling News, and named a top employer by Best of State. What You Will Love About USANA Our science backed mission to improve lives starts with you. With holistic wellness benefits, flexible work, and a culture built on care and connection, we help you thrive, so you can help others around the world do the same. * Health, Dental, Vision, Life and Disability Insurance * On-site medical and mental health clinic for you and your dependents * Flexible paid time off, including sick time, vacation, holidays, family hours, and floating holidays * Paid parental leave for both primary and secondary caregivers * 401k match and profit-sharing bonus * Chiropractor visits, massages, fitness classes, and full-service gym * Free and discounted USANA products * Tuition reimbursement, mentorship opportunities, and learning and development licenses Learn more about working with us by visiting careers.usanainc.com Security notice: USANA Health Sciences will never ask for sensitive personal information during the initial application process or via unsecure channels like email. If you receive such a request, please do not respond and report it to us directly.

Welcome To The Traegerhood: Our business is BBQ, and business tastes good. Traeger invented the wood pellet grill over 30 years ago, and we've been revolutionizing outdoor cooking ever since. We're a team of disruptors, innovators, problem solvers, and food fanatics who are dedicated to bringing people together to create a more flavorful world. From our headquarters in Salt Lake City and beyond, we work tirelessly to provide a world-class experience to our customers, retailers, and especially our employees. If you're a team player who's dedicated to delivering top-quality results every day, then we want you to come cook with us! Traeger is seeking a highly technical, creative Mechanical Engineer to join our APRD team in Salt Lake City, UT. This role is designed for an engineer who is not only capable of solving complex problems but who thrives on becoming a subject matter expert in emerging technologies, transforming ideas into reality through design, prototyping, and innovation. You will be responsible for creating and building new solutions during the advanced development phase and ensuring their successful handoff to execution teams. This includes conceiving and fabricating prototypes that bring concepts to life, clearly demonstrating design intent and engineering vision. From there, you will develop detailed technical documentation that enables seamless transition into production. This role requires more than execution-it demands an innovator, builder, and creator. You will lead technical problem solving, push boundaries with new technologies, and bring a maker's mindset to everything you do. How You Will Help Us Win: Translate consumer insights and research into tangible product innovations that fuel Traeger's pipeline and deliver best-in-class consumer experiences. Serve as a subject matter expert for new technologies, materials, and methods, establishing technical leadership within the organization. Drive the creation of prototypes-ranging from rough mock-ups to precision builds-that communicate vision, function, and manufacturability. Lead advanced development projects through R&D, validation, and transition into execution teams. Apply rigorous engineering analysis (mechanical statics/dynamics, mechanisms, FEA, CFD, cost, and material selection) to inform design decisions. Champion agile, iterative development methods to ensure speed without sacrificing quality. Partner with internal teams, external suppliers, and global resources to develop prototypes and ensure manufacturability. Influence cross-functional teams by integrating process improvements, best practices, and technical excellence into the development cycle. Manage a diverse portfolio of projects, ensuring they meet cost, quality, and timeline goals. What You'll Need to Succeed: Bachelor's degree in Mechanical Engineering. 5-10 years of experience in product development, preferably with consumer products. Proven ability to create, design, and build-from concept sketches to working prototypes. Strong background in Design for Manufacture and Assembly (DFM/DFA) and cost-conscious product development. Advanced skills in CAD (SolidWorks preferred), including solid, surface, and sheet metal modeling. Hands-on experience with prototype fabrication using both hand tools and machine tools. Strong analytical skills with experience in mechanical analysis, FEA, and CFD. Track record of technical innovation, with patents or novel product contributions preferred. Comfortable leading as a technical SME while collaborating cross-functionally across disciplines (SW, FW, EE, ID, Quality, Operations). Experience working with international suppliers and the ability to travel as needed. Highly motivated, detail-oriented, and driven by curiosity, creativity, and craftsmanship. Why You Will Love To Work Here: Be part of the most disruptive force in outdoor cooking Join a true team working towards a common goal Culture of risk-taking, innovation & quality So. Much. Food. Have an outdoor lover's paradise in your backyard Full medical/dental/vision packages to fit your needs 401K to help you plan for the future Tuition reimbursement Individual professional development programs & initiatives to help you grow professionally Great discounts on all things Traeger Did we mention all the food?

Job DescriptionSalary: $27 DOE Research Associate is part of a team that supports the analytical studies for regulatory submissions of in vitro diagnostic (IVD) products developed by BioFire Defense. The primary responsibility is to execute and report on performance studies that demonstrate products and devices are functioning in accordance with design and regulatory requirements and specifications. 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 effectively and respectfully communicate and coordinate with peers and supervisors. Other key skills required: Knowledge of microbiology and molecular biology principles, tools, and techniques Knowledge of basic laboratory practices including pipetting, handling of biological and chemical materials, sterile techniques, and contamination control Knowledge of basic statistical and concentration calculations Attention to detail, critical thinking, trouble shooting, and problem solving skills Ability to collaborate in a fast-paced environment Proficiency with Microsoft Office Suite May be required to obtain and maintain a DoD Personnel Security Clearance. Education Minimum of a bachelors degree with emphasis in a science, or related field. Experience Research Associate I Six months experience in an academic, industry, or healthcare laboratory Research Associate II Two years experience in an academic, industry, or healthcare laboratory in addition to experience with real-time PCR and/or sequence analysis and familiarity with Biosafety Level 2 practices Benefits: Medical Dental Vision 401k - company match of 5% regardless of participation and up to a total of 9.5% company match if contributing 4 Weeks of PTO 9 Paid Holidays Paid Winter Break from the work week between December 24 thru December 31 Participation in Company's Wellness Program (discounted medical premiums) Multiple Company Sponsored Events Each Year (catered breakfast/lunch, holiday parties, snacks) Stimulating work environment Convenient location near I-15 and Trax Station Free Parking Our EEO Policy BioFire Defense is an equal opportunity employer (M/F/D/V). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law. BioFire Defense complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

The Research Associate II position supports the performance assessment and validation of molecular in vitro diagnostic products within the Clinical Affairs Lab Operations team. This role contributes to regulatory submissions (e.g., FDA and global agencies) by executing molecular and microbiological experiments such as PCR, nucleic acid extraction, and microbial culture. The associate ensures data integrity through accurate collection, analysis, and documentation in compliance with protocols and safety standards. Operating in a collaborative, fast-paced environment, the role requires technical proficiency, critical thinking, and effective communication to support the department's mission and bioMérieux's goals. Responsible for creating, optimizing ,developing, updating and sustaining diagnostic assays and reagents in a regulated environment, while driving innovative solutions. Design and develop new biomolecules or reagents, collect and manage biological samples to support method/product development. Identify emerging technologies and trends related to diagnostics. Provide technical assistance to support existing products, methods or techniques. Performs analytical verifications and documenting validation activities and outcomes for regulatory submissions. Primary Duties 1. Performs molecular and microbiological experiments (e.g., PCR, nucleic acid extraction, microbial culture) to support diagnostic product validation. 2. Ensures data integrity by collecting, recording, analyzing, and verifying experimental data in compliance with protocols and regulatory standards. 3. Executes study protocols and contributes to their development, optimization, and revision. 4. Conducts routine and complex calculations and laboratory techniques, including solution formulation and microbial enumeration. 5. Analyzes data with minimal supervision and determines appropriate next steps. 6. Communicates findings through written reports and oral presentations to peers and supervisors. 7. Contributes to the writing of study reports for internal and regulatory use. 8. Coordinates with team members and cross-functional groups for lab activities, equipment use, and project execution. 9. Maintains laboratory equipment, supplies, and workspaces according to safety and quality standards. 10. Trains other team members on lab practices and departmental procedures, as appropriate. 11. Develops troubleshooting strategies for unexpected experimental results and proposes solutions. 12. Operates in a Biosafety Level 2/2+ environment, handling pathogenic microbes and human specimens using sterile techniques. 13. Assists with inventory management and stocking of project-specific laboratory supplies. 14. Performs all work in compliance with corporate policies and the Quality Management System.15. Perform all work in compliance with company quality procedures and standards.16. Performs other duties as assigned. Scope and Resources Accountability The Research Associate II is an individual contributor with no direct or indirect supervisory responsibilities. The role operates within the Clinical Affairs Lab Operations team and is accountable for executing laboratory experiments, maintaining data integrity, and supporting regulatory submissions. The position requires coordination across functional groups and contributes to protocol development and troubleshooting, impacting the quality and timeliness of diagnostic product validation. Key Performance Indicators (KPIs) Accuracy and completeness of data recorded in lab notebooks and reports Timely execution of study protocols and experiments Compliance with safety, quality, and regulatory standards Successful contribution to regulatory submissions (e.g., FDA) Effective collaboration and communication within and across teams Number of protocols executed or optimized Training effectiveness for new team members Qualifications Education and Training Bachelor's degree in a scientific discipline Minimum of two years of post graduate experience in an academic, industry, or healthcare laboratory setting.Experience should include: Real-time PCR Sequence analysis Microbiology techniques Familiarity with Biosafety Level 2 practices Knowledge, Skills, and Abilities The role is primarily technical and scientific in nature, focused on laboratory work, data analysis, and regulatory support. There are no specific business strategy, financial, or market-facing responsibilities that require business acumen or understanding of broader business operations. Develops strategies to troubleshoot unexpected experimental results and proposes innovative solutions. Contributes to protocol and process development, optimization, and revision. Demonstrates critical thinking and problem-solving skills to improve experimental design and product performance. Evaluates primers and sequences using bioinformatic tools to support assay development. Comfortable working in a dynamic environment where priorities may shift, requiring adaptability and creative thinking.These skills reflect the ability to innovate within scientific and technical domains, particularly in developing and refining diagnostic tools. Maintaining Focus Detail-oriented in executing laboratory procedures and maintaining accurate records. Ability to follow rules and regulations, including protocols, SOPs, and safety guidelines. Proficiency in laboratory practices, such as sterile technique, pipetting, and contamination control. Comfortable working in a dynamic environment with shifting priorities, requiring sustained attention and adaptability. Strong organizational skills to manage multiple tasks and maintain consistency in data collection and analysis. Ability to remain in a stationary position (often standing) for prolonged periods, supporting physical focus during lab work. Getting Organized Strong organizational skills to manage multiple tasks, experiments, and documentation efficiently. Proficiency in inventory management, including stocking and tracking project-specific laboratory supplies. Ability to maintain laboratory equipment, supplies, and workspaces in accordance with operational, safety, and quality standards. Detail-oriented record keeping, including accurate data entry in electronic lab notebooks and study worksheets. Ability to follow structured protocols and standard operating procedures to ensure consistency and compliance. Comfortable working in a dynamic environment, requiring prioritization and time management. Getting Work Done Through Others Trains other team members on laboratory and departmental practices and procedures, commensurate with experience. Coordinates and collaborates within and across teams and functional groups for routine lab activities, equipment use, and project execution. Shares knowledge, skills, and ideas to support team development and collective success.These responsibilities reflect the ability to support and guide others in completing work, even though the role does not include formal supervisory duties. Managing Work Processes Ability to follow structured protocols, SOPs, and work instruction documents to ensure consistency and compliance. Maintains laboratory equipment, supplies, and workspaces according to operational, safety, and quality standards. Ensures data integrity through accurate collection, analysis, and documentation of experimental results. Executes study protocols and contributes to their development, optimization, and revision. Performs routine and complex lab techniques with minimal supervision, demonstrating independence in managing assigned tasks. Comfortable working in a dynamic environment, managing shifting priorities and timelines effectively. Dealing with Complex Situations Demonstrated critical thinking and problem-solving skills to interpret experimental results and troubleshoot issues. Develops strategies to address unexpected experimental outcomes and proposes scientifically sound solutions. Comfortable working with biosafety level 2/2+ pathogens and human specimens, requiring careful risk assessment and adherence to safety protocols. Ability to work independently on routine tasks and with general supervision on new or complex procedures. Proficiency in data analysis and bioinformatics tools to evaluate sequences and interpret molecular biology results. Adaptability in a dynamic environment, managing shifting priorities and complex workflows. Communicates and coordinates effectively and respectfully with peers and supervisors across teams and functional groups. Collaborates within and across departments, demonstrating awareness of team dynamics and shared goals. Acts as a good lab citizen, contributing to a positive and productive work environment. Understands and adheres to company policies, quality systems, and regulatory requirements, reflecting alignment with organizational standards and expectations.These abilities support effective navigation within the organizational structure and contribute to team cohesion and operational success. Communicating Effectively Strong oral and written communication skills for presenting data, writing reports, and collaborating with peers and supervisors. Ability to communicate data and analyses clearly in written reports and oral presentations. Collaborates respectfully and effectively within and across teams and functional groups. Shares knowledge, skills, and ideas to support team learning and cohesion. Comfortable using Microsoft Office tools (Outlook, Excel, PowerPoint, Word) to support communication and documentation. Relating Skills Collaborates effectively within and across teams and functional groups. Communicates respectfully with peers and supervisors to support a positive and productive work environment. Acts as a good lab citizen, demonstrating teamwork, accountability, and shared responsibility. Shares knowledge, skills, and ideas to foster learning and cooperation among team members. Trains other team members on laboratory and departmental practices, contributing to team development. Developing and Inspiring Others Trains other team members on laboratory and departmental practices and procedures, commensurate with experience. Shares knowledge, skills, and ideas to support team learning and development. Acts as a collaborative team member, contributing to a positive and inclusive lab environment that encourages growth and knowledge exchange.While the role does not include formal leadership or supervisory responsibilities, it supports peer development through mentorship and skill-sharing. Managing Diverse Relationships Collaborates effectively across teams and functional groups, demonstrating adaptability in working with individuals from various scientific and operational backgrounds. Communicates respectfully and professionally with peers and supervisors to maintain productive working relationships. Shares knowledge and skills to support team learning and cross-functional coordination. Operates within a regulated environment, requiring interaction with internal stakeholders such as Quality Assurance, Regulatory Affairs, and R&D. Acting with Honor and Being Open Demonstrates integrity and accountability by ensuring data accuracy and compliance with protocols, SOPs, and regulatory standards. Follows company policies and quality management guidelines, reflecting ethical conduct and transparency in work practices. Communicates respectfully and professionally with peers and supervisors, fostering a culture of openness and trust. Comfortable working with human specimens and biosafety level 2 pathogens, requiring adherence to safety and ethical standards. Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMérieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bio Merieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site ******************************* or contact us at [email protected]. BioMérieux 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 BioMérieux's or its affiliates' application process by contacting us via telephone at **************, by email at [email protected], or by dialing 711 for access to Telecommunications Relay Services (TRS).

Bookmark this Posting Print Preview | Apply for this Job Please see Special Instructions for more details. Please include: * Cover Letter that addresses interest in the position and that specifically highlights experience leading multi-site research projects and using mixed method analyses that is no more than two pages * Curriculum Vitae * Writing sample of one scholarly paper or technical report where you are lead author or major contributor demonstrating mixed methods research skills * Names and contact information for three professional references who can speak to your research skills/experience and collaboration experience Announcement Details Open Date 12/10/2025 Requisition Number PRN43692B Job Title Research Associate Working Title Senior Research Associate (Mixed Methods) Career Progression Track A00 Track Level FLSA Code Professional Patient Sensitive Job Code? No Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary Work schedule: M-F, 8PM-5PM. Travel, nights, and weekends may be needed. The SRA will work on-site at the University of Utah with some travel required. VP Area Academic Affairs Department 00162 - Educational Leadership&Policy Location Campus City Salt Lake City, UT Type of Recruitment External Posting Pay Rate Range $100,000 - $120,000 Close Date 02/25/2026 Priority Review Date (Note - Posting may close at any time) 02/01/2026 Job Summary The Prison Education Action Research Lab in the College of Education at the University of Utah seeks a Senior Research Associate with expertise in mixed methods. The Lab does research that advances educational justice for people and communities impacted by incarceration. We envision a world where colleges and universities lead the way in fostering greater access to opportunity for all people, including those directly impacted by the legal system. The Senior Research Associate (SRA) will undertake a wide range of strategic, academic, and capacity-building activities aimed at enabling and enhancing research on prison higher education and reentry. In collaboration with institutional and program leaders, the SRA will oversee strategic research advancement, communicate research opportunities and findings, foster collaboration within the team, and engage a leadership role on research projects. The person who fills this position will be responsible for training other researchers, supervising research staff, and overseeing graduate assistants, and will serve as primary research liaison to the Lab, the University, and other external partners. The SRA will work under the supervision of the Lab Director. We strongly encourage applications from individuals directly impacted by incarceration and punishment systems. Responsibilities * Serve as the lead/co-lead researcher on multi-PI research projects; * Lead all phases of research design, planning, and execution of mixed methods research projects. This includes reviewing literature, developing research plans, developing data collection instruments and tools, piloting and validating data, analyzing quantitative and qualitative data, and drafting and editing research reports and scholarly manuscripts; * Serve as senior liaison with stakeholders including state agencies and higher education institutions; * Oversee IRB protocols, data use agreements, and compliance monitoring across multiple institutions and jurisdictions; * Lead regular cross-site meetings to align stakeholders; * Coordinate secure data transfers and compliance across states and data providers; * Maintain detailed documentation of data processing pipelines, codebooks, and metadata; * Ensure appropriate data cleaning, harmonization, transformation, and documentation across diverse data sources; * Apply intermediate and advanced statistical models and quantitative research designs; * Design and oversee data linkage strategies across disparate administrative datasets; * Design and conduct qualitative data collection (e.g., interviews, site visits, document analysis) and analysis; * Lead mixed-methods integration to synthesize qualitative and quantitative insights * Interact with stakeholders, partner institutions/organizations, political, governmental, funders, and corporate leaders related to research initiatives; * Develop and present research results, in the form of technical reports, peer-reviewed manuscripts, briefs, presentations, webinars, etc., to inform internal and external stakeholders of research projects; * Mentor, train, and supervise a team of researchers; * Other research related activities as assigned by the Lab Director. Subject to allocation of appropriate funding, Dr. Castro (your supervisor) may authorize support for employee travel to academic conferences and approved professional development activities. All requests for these activities must receive prior approval before the event date. Minimum Qualifications Minimum Qualifications * PhD in education, social sciences, or related field or comparable professional experience; * Advanced knowledge of the field of higher education; * 5+ years of experience in mixed methods research, including longitudinal, administrative, and qualitative data analyses; * Demonstrated experience conducting applied social science and/or educational research, including implementing experimental and quasi-experimental research designs, survey techniques, and program evaluation; * Demonstrated experience with data cleaning, data migration, and management of multiple administrative data sets; * Demonstrated commitment to and knowledge about educational equity and justice; * Ability to work well with and across diverse teams of people; * Strong project management experience coordinating communications and associated logistics on a multi-site research project; * Advanced knowledge of Excel, Python, R, NVivo, Dedoose, Atlas.ti, or other data analysis tools to conduct data analysis; * Proven experience leading teams and managing deadlines; * Experience working both independently and as a collaborative team member; and * Excellent written communication, verbal communication, and organizational skills; and attention to detail. Preferences Type Benefited Staff Special Instructions Summary Please include: * Cover Letter that addresses interest in the position and that specifically highlights experience leading multi-site research projects and using mixed method analyses that is no more than two pages * Curriculum Vitae * Writing sample of one scholarly paper or technical report where you are lead author or major contributor demonstrating mixed methods research skills * Names and contact information for three professional references who can speak to your research skills/experience and collaboration experience Additional Information University of Utah Benefits * Health, dental, and wellness coverage * 14.2% employer contribution to personal retirement account (401a) * Free public transportation pass (Utah Transit Authority) * Paid leave time * Reduced tuition benefits for employee and family members * More information: ********************************* 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. The University of Utah values candidates who have experience working in settings with students and patients from all backgrounds and possess a strong commitment to improving access to higher education and quality healthcare for historically underrepresented students and patients. 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 ************************************ 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. Posting Specific Questions Required fields are indicated with an asterisk (*). Applicant Documents Required Documents * Cover Letter * Curriculum Vitae * Writing Sample 1 * List of References Optional Documents

Medical Research Associate - Full Time - Monday - Friday - Salt Lake City, Utah (UT) 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. ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. The Role: + In short, 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 enough to participate in the clinical trial according the protocol of a study. + Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability + Ensures all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. + Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. + Monitors subject safety. - Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. + Performs general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc. Communication/Training/Meetings: + Assist with study setup activities and perform check-in and check-out activities. To be successful in the role, you will have: + Read, write, and speak English; fluent in host country language required. + High School Diploma or G.E.D. required. + Undergraduate degree in a clinical, health- related area and/or minimum 1 year of equivalent work experience with similar position + 1+ years work experience in a medical or clinical field preferred + Basic Life Support (BLS)/Phlebotomist Certification preferred + Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred. Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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 through the form below. **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

Medical Research Associate - Full Time - Monday - Friday - Salt Lake City, Utah (UT) 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 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. The Role: In short, 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 enough to participate in the clinical trial according the protocol of a study. Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability Ensures all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. Monitors subject safety. • Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. Performs general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc. Communication/Training/Meetings: Assist with study setup activities and perform check-in and check-out activities. To be successful in the role, you will have: Read, write, and speak English; fluent in host country language required. High School Diploma or G.E.D. required. Undergraduate degree in a clinical, health- related area and/or minimum 1 year of equivalent work experience with similar position 1+ years work experience in a medical or clinical field preferred Basic Life Support (BLS)/Phlebotomist Certification preferred Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred. Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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 through the form below. 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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised 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

SummaryEngineer II to support sustainability and development of medical devices for BD's healthcare products.Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. BD (Becton Dickinson and Company), a leading global medical technology company, is seeking a Research and Development Engineer II to work on the sustainability and development of medical devices for BD's healthcare products. They assume the technical role of projects and champion technical and architectural excellence. The candidate should be passionate about solutions to clinician and patient unmet needs, and enjoy the details involved with the long-term outlook of technological solutions to clinical needs. The position is an exciting opportunity to make a meaningful, positive impact on patients throughout world by leveraging cutting edge technologies. This role offers competitive compensation and relocation packages. Duties and Responsibilities: An understanding of medical device regulations, design controls Follows and executes testing according to existing methods Understands and can develop protocols, test methods, statistical analysis, test report generation Participates in the documentation of sustainability and product development risk activities and design controls Applies engineering principles to solve basic engineering problems Authors a requirements document for a subsystem or simple component or a section of a requirements'document for a larger system Participates in Voice of Customer activities Understands the budgeting process and provides inputs to budget owners Requests and receives quotes; orders project supplies Reports to manager on progress on tasks that were assigned to them; Completes management updates as requested by manager Works in a cross-functional team and participates in cross-functional activities Correctly selects and applies analytical methods to interpret small, well characterized data sets; Able to extract key information and its relative importance from data sets; Able to define conclusions from the data set and present the conclusions logically and in an understandable way for technical individuals Actively participates in team meetings, makes recommendations, accepts commitments, and delivers on commitments Participates in problem solving activity in a team setting Participates in project planning, estimating task duration, and resource needs Communicates upcoming milestones frequently to team members Interacts with product managers and more experienced engineers to understand the business aspects of product development Participates and contributes on project teams where technical issues and product development challenges had driven unique solutions Qualifications Bachelor's or Post Graduate degree (preferred) in STEM or related field 0 - 5+ years of professional experience in product engineering Experience gained in a classroom and/or internship or Co-op setting Strong technical degree work demonstrated At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. Required Skills Optional Skills . Primary Work LocationUSA UT - Salt Lake City BASAdditional LocationsWork Shift

We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. BD (Becton Dickinson and Company), a leading global medical technology company, is seeking a Research and Development Engineer II to work on the sustainability and development of medical devices for BD's healthcare products. They assume the technical role of projects and champion technical and architectural excellence. The candidate should be passionate about solutions to clinician and patient unmet needs, and enjoy the details involved with the long-term outlook of technological solutions to clinical needs. The position is an exciting opportunity to make a meaningful, positive impact on patients throughout world by leveraging cutting edge technologies. This role offers competitive compensation and relocation packages. Duties and Responsibilities: * An understanding of medical device regulations, design controls * Follows and executes testing according to existing methods * Understands and can develop protocols, test methods, statistical analysis, test report generation * Participates in the documentation of sustainability and product development risk activities and design controls * Applies engineering principles to solve basic engineering problems * Authors a requirements document for a subsystem or simple component or a section of a requirements'document for a larger system * Participates in Voice of Customer activities * Understands the budgeting process and provides inputs to budget owners * Requests and receives quotes; orders project supplies * Reports to manager on progress on tasks that were assigned to them; Completes management updates as requested by manager * Works in a cross-functional team and participates in cross-functional activities * Correctly selects and applies analytical methods to interpret small, well characterized data sets; Able to extract key information and its relative importance from data sets; Able to define conclusions from the data set and present the conclusions logically and in an understandable way for technical individuals * Actively participates in team meetings, makes recommendations, accepts commitments, and delivers on commitments * Participates in problem solving activity in a team setting * Participates in project planning, estimating task duration, and resource needs * Communicates upcoming milestones frequently to team members * Interacts with product managers and more experienced engineers to understand the business aspects of product development * Participates and contributes on project teams where technical issues and product development challenges had driven unique solutions Qualifications * Bachelor's or Post Graduate degree (preferred) in STEM or related field * 0 - 5+ years of professional experience in product engineering * Experience gained in a classroom and/or internship or Co-op setting * Strong technical degree work demonstrated At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. Required Skills Optional Skills . Primary Work Location USA UT - Salt Lake City BAS Additional Locations Work Shift

Salt Lake City Regular MERIEUX NUTRISCIENCES As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years. If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us! YOUR DAY TO DAY LIFE We are looking for a Chemist 1 in 1945 Fremont Drive, Salt Lake City, UT 84104 USA. Your mission will be to: The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. * Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) * Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. * Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. * Calculate the concentration of components present in samples and post results. * Wash glassware as needed and prepare samples as needed. * Prepare standards or reagents that are needed for the analysis procedure. * Maintain knowledge of Laboratory Information Management System (LIMS) required to complete job responsibilities. * Maintain clean laboratory by washing countertops, sweeping floors, storing analysis materials, etc. * Initiate and investigate customer complaint and non conformances Determine root cause and corrective action * Review batches and respond to out of specification results or questionable data. * Maintain equipment records in appropriate software systems. Meet the housekeeping schedule on time. * This position has the responsibility and authority to identify departures from the quality system or test procedures and document such observations in accordance with the prescribed non conformance system and the supervisor is notified. * Responsibility to support laboratory management in the implementation maintenance and improvement of the management system. * Adhere to all safety policies. * Perform other related tasks as needed YOUR PROFILE A basic knowledge of instrumentation and theory including HPLC, GC, ICP and AA is helpful. Basic knowledge of food science is helpful to analyze the chemical content of samples. Associates degree required, Bachelors preferred. Required skills: One - two years experience. This position requires a general knowledge of chemistry to perform analyses. A general knowledge of the Laboratory Information Management System and Laboratory Instrument Data systems are required to process client data. The incumbent needs a broad knowledge of analytical chemistry to perform analysis procedures. Manual dexterity is needed to pipet samples where required. Analytical skills are necessary for completion of tasks within the department. Work Environment: The incumbent works in a laboratory setting with proper lighting and temperature control. Occasional exposure to laboratory fumes, chemicals, and materials will occur when in the laboratory. Safety equipment of gloves, laboratory coat and eyeglasses may need to be worn depending on the testing process. The incumbent may use the autoclave daily to complete the analysis process. Continuous lifting of analysis materials weighing up to 50 pounds are necessary to transport media materials. The incumbent can expect extended time spent in a standing position. The incumbent should be able to detect slight variation in shades of colors. WHY JOIN US? * Because you would contribute to an inspiring Public Health purpose, supported by long-term and visionary shareholders. * Because you would have an impact on our strategic pillars that build on 50 years of experience and expertise. * Because you would be part of a community of an enthusiastic and skilled group of people who love co-building together and serving a purpose bigger than them. * Because you would be welcome as you are, in a diverse and open-minded environment that is rich in our singularities and differences. * Because you would grow in an international group of more than 8200 fantastic team members, with plenty of opportunities to learn and share. Ready for the journey? To apply please click on 'Apply now' button