Research and development technician jobs in Salt Lake City, UT - 111 jobs

Job Description About Scientia Vascular: Our mission is to save lives. Scientia Vascular is a leading innovator and manufacturer of endovascular medical devices. We use micromachining and microfabrication processes to manufacture products that provide physicians with enhanced performance for optimal outcomes for their patients. Position Summary Contributes to the development of medical devices. Main responsibilities are conducting product performance testing and building prototypes for evaluation. Primary Responsibilities Conduct product performance bench testing Build or assemble prototype materials, components, subassemblies and assemblies Construct, operate, troubleshoot, adjust, maintain and test equipment, systems or products Perform testing and analyze data and write reports Review or develop processing or manufacturing instructions Maintain detailed documentation through all phases of development, testing and analysis Record data following good documentation practices Ability to solve problems and work with minimal supervision Perform job functions in accordance with applicable GMP and ISO guidelines Comply with applicable FDA and international regulatory laws/standards Other duties as assigned with or without accommodation. Requirements High School diploma Medical device Tech industry experience is a plus Must have at least 1 year of troubleshooting and testing experience as a technician Computer skills including solid proficiency with Microsoft Excel, Word, Outlook Excellent verbal and written communication skills Working knowledge of GMP, experience with ISO regulations is a plus Must have technical writing experience Must have at least 1 year of experience as a technician in a manufacturing environment Key benefits we provide: Generous Paid Time Off (PTO) Medical, Dental, Vision insurance Paid Parental Leave Paid Holidays 401k Plan (with a generous employer match) Life Insurance (company paid) Short-Term & Long-Term Disability Insurance (company paid) Subscription to Calmhealth.com Employee Assistance Program An environment of belonging where everyone can thrive Commitment to Equal Opportunity: The Scientia Vascular culture is centered on the principals of equal opportunity for all employees. Consistent with our culture, all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, family status, marital status, sexual orientation, national origin, genetics, disability, age, or veteran status, or any other non-merit based or legally protected grounds. Visit our website and learn more about us at ************************

The R&D Technician plays a supporting role in the development and improvement of powder and liquid products, from concept to commercialization. Utilizing best practices and procedures, they are involved in; ideation, formulation, sampling, flavor work, documentation, scale up, and commercialization support, interacting across multiple departments including Marketing, Sales, Quality, Procurement, Operations, etc. DUTIES & RESPONSIBILITIES Support the work of other members of the R&D team throughout the development process Provide support in all stages of formulation, development, and commercialization Communicate with vendors to source existing, novel, or trendy raw materials and obtain relevant documentation Batches and prepares samples for internal and external/client use Accurately maintain vendor information, raw material databases, and other records Supports and performs flavor work for both RTM and RTD supplements Gather information as part of the ideation process for a new project or to improve an existing product Maintains lab organization and sampling protocols Performs physical assays on ingredients, mixed powders, and liquids Filling in (wherever necessary) to cover changing department needs Search for and implement continuous improvement in processes and procedures EDUCATION & EXPERIENCE Related science or laboratory work experience preferred. SKILLS & ABILITIES Ability to read and interpret documents such as laboratory procedure manuals, safety rules, operating maintenance instructions. Ability to calculate figures and amounts such as proportions, percentages and volume. Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. Strong communication skills - written and verbal Experience working independently and as part of a team Some experience working in a food establishment or laboratory Familiarity with product development Experience with flavor systems and sensory evaluation techniques Knowledge of ingredient functionality and nutrition Strong interest in food and health trends Full-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

Make a meaningful difference: At Thatcher Chemical facilities across the nation, our manufacturing teams create the essential chemistries, processes, and solutions that support clean water, safe environments, reliable infrastructure, and critical industries. From production and quality to logistics and distribution, your precision, dedication, and commitment to continuous improvement help transform raw materials and innovative science into real-world solutions. Your purpose-driven work plays a vital role in protecting public health, supporting communities, and shaping a safer, more sustainable future. Thatcher Company is looking for a Senior R&D Chemist for Concrete Additives to lead the development of construction products at Thatcher Company headquarters, located in Salt Lake City, UT. Compensation $100,000-$150000 Major Accountabilities: •Lead the company's development of new products/technologies for the Construction Market. •Develop manufacturing processes for new products and optimize existing manufacturing processes for the construction division of Thatcher Company. •Support Thatcher's operational excellence group in the scale-up and launch of new products and processes. •Develop finished product specifications and validate analytical test methods which are needed to characterize new construction products. •Improve the existing construction 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 construction industry and develop technical, customer-driven solutions. •Develop a thorough understanding of the construction market through market research and analysis of competitive offerings. •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 construction or a related industry. •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: 100% company-funded Profit-Sharing Plan (up to 25% of salary annually) 401(k) with traditional and Roth contribution options Comprehensive benefits: medical, dental, vision, life insurance, short- and long-term disability, HSA/FSA, 3+ weeks of PTO, and paid holidays Education reimbursement and ongoing professional development The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website. Thatcher is an Equal Opportunity/Affirmative Action employer, including protected Veterans and individuals with disabilities.

Specialist, R&D - Baker (Bread & Laminated Dough) Discover the Craft. Shape the Future. At Bridor North America , we blend the art of European baking with North American innovation , crafting exceptional breads and pastries for the most discerning customers across the U.S. and Canada. As we continue to grow our footprint with our new facility in Salt Lake City, Utah , we're looking for a passionate and skilled R&D Specialist - Baker (Bread & Laminated Dough) who thrives at the intersection of artisan craftsmanship and industrial precision . This is a hands-on role for someone who lives and breathes bakery innovation - from hand-laminating croissants in the lab to scaling new products on state-of-the-art industrial lines. What You'll Do Create & Innovate: Develop new bakery concepts (croissants, breads, and laminated doughs) from artisanal beginnings to full industrial scale. Bridge Art & Industry: Apply traditional baking know-how while adapting recipes and techniques for modern, automated production lines. Collaborate Across Teams: Partner closely with colleagues in Finance, Purchasing, Quality, and Operations to bring projects to life - balancing cost, taste, and texture expectations. Stay Ahead of Trends: Explore new baking styles, ingredients, and processes to keep Bridor at the forefront of bakery innovation. Document & Share: Lead tasting sessions, evaluate results, and communicate your findings clearly with photos and reports. Support Launches: Assist during scale-up and industrial trials, ensuring every new product meets our high standards for quality and consistency. What You Bring Education & Experience Diploma from a recognized baking or pastry school. Minimum 5 years of experience in baking, product development, or food manufacturing. Expertise in artisanal techniques for breads and laminated doughs (croissants, puff pastry, etc.). Experience with industrial bakery lines is an asset. Skills & Qualities Passionate about bakery craftsmanship and innovation. Methodical, curious, and creative problem-solver. Strong interpersonal and teamwork skills with the ability to work cross-functionally. Background in food ingredients or related fields (yeast, flour, chocolate, fillings) preferred. Familiarity with sensory evaluation and product tasting processes. Regulatory & Technical Knowledge Understanding of Canadian and U.S. food regulations (CFIA, Health Canada, FDA, USDA). Knowledge of HACCP, GMP, and BRC standards. Working Conditions Based in Salt Lake City, Utah . Primarily day shift; flexibility may be required. Travel within the U.S. and occasional trips to Canada. Why Join Bridor At Bridor, every baker is a creator, every innovation has a story, and every product reflects our passion for excellence. You'll be joining a collaborative team where ideas rise - just like our dough - in an environment that celebrates craftsmanship, creativity, and growth. Be part of a company that's expanding across North America and shaping the next chapter of premium bakery.

Specialist, R&D - Baker (Bread & Laminated Dough) Discover the Craft. Shape the Future. At Bridor North America , we blend the art of European baking with North American innovation , crafting exceptional breads and pastries for the most discerning customers across the U.S. and Canada. As we continue to grow our footprint with our new facility in Salt Lake City, Utah , we're looking for a passionate and skilled R&D Specialist - Baker (Bread & Laminated Dough) who thrives at the intersection of artisan craftsmanship and industrial precision . This is a hands-on role for someone who lives and breathes bakery innovation - from hand-laminating croissants in the lab to scaling new products on state-of-the-art industrial lines. What You'll Do Create & Innovate: Develop new bakery concepts (croissants, breads, and laminated doughs) from artisanal beginnings to full industrial scale. Bridge Art & Industry: Apply traditional baking know-how while adapting recipes and techniques for modern, automated production lines. Collaborate Across Teams: Partner closely with colleagues in Finance, Purchasing, Quality, and Operations to bring projects to life - balancing cost, taste, and texture expectations. Stay Ahead of Trends: Explore new baking styles, ingredients, and processes to keep Bridor at the forefront of bakery innovation. Document & Share: Lead tasting sessions, evaluate results, and communicate your findings clearly with photos and reports. Support Launches: Assist during scale-up and industrial trials, ensuring every new product meets our high standards for quality and consistency. What You Bring Education & Experience Diploma from a recognized baking or pastry school. Minimum 5 years of experience in baking, product development, or food manufacturing. Expertise in artisanal techniques for breads and laminated doughs (croissants, puff pastry, etc.). Experience with industrial bakery lines is an asset. Skills & Qualities Passionate about bakery craftsmanship and innovation. Methodical, curious, and creative problem-solver. Strong interpersonal and teamwork skills with the ability to work cross-functionally. Background in food ingredients or related fields (yeast, flour, chocolate, fillings) preferred. Familiarity with sensory evaluation and product tasting processes. Regulatory & Technical Knowledge Understanding of Canadian and U.S. food regulations (CFIA, Health Canada, FDA, USDA). Knowledge of HACCP, GMP, and BRC standards. Working Conditions Based in Salt Lake City, Utah . Primarily day shift; flexibility may be required. Travel within the U.S. and occasional trips to Canada. Why Join Bridor At Bridor, every baker is a creator, every innovation has a story, and every product reflects our passion for excellence. You'll be joining a collaborative team where ideas rise - just like our dough - in an environment that celebrates craftsmanship, creativity, and growth. Be part of a company that's expanding across North America and shaping the next chapter of premium bakery.

Trove Brands is a privately-held house of brands including BlenderBottle , Owala , EcoBrite™, and Whiskware . Our patented and best-selling products are designed to simplify and improve everyday life with leading-edge innovation, incomparable quality, and aspirational style. A career at Trove Brands is not about punching the clock. It's about embracing exciting and fast-paced opportunities that sharpen your skills, drive innovation, and play an integral role in growing our global reach. Your work will not only impact the company, it will impact the lives of millions of people around the world. When you step up to a career at Trove, you step up to cutting-edge excellence. You sign up for bold action and invigorating synergy. You agree to face-and break through-new challenges every single day. Job Description We are seeking a highly motivated and detail-oriented R&D Scientist I to join our dynamic Research & Development team, with a focus on sports nutrition product innovation. This role requires prior experience directly formulating and flavoring products across a variety of delivery matrices, including powders, ready-to-drink (RTD) beverages, baked/freeze-dried goods, and extruded items. The ideal candidate will combine a strong scientific foundation with creativity and practical hands-on execution to deliver innovative, consumer-accepted products from concept to commercialization. This is an exciting opportunity for someone who thrives in a collaborative, fast-paced environment and is passionate about performance nutrition, functional ingredients, and food science. Key Responsibilities: Flavoring products. Hands-on development of innovative sports nutrition products in various delivery formats. Utilize the latest research and trends in nutritional science and biochemistry to guide development decisions and optimize product efficacy. Apply a deep understanding of physical and organic chemistry principles to drive product optimization and flavor development. Participate in and contribute to sensory evaluation studies; collect and interpret data to guide formulation adjustments for consumer acceptability. Conduct stability testing and troubleshoot formulation challenges with minimal supervision. Collaborate cross-functionally with Marketing, Project Management, Supply Chain, Quality Assurance, Regulatory, Legal, and external partners to ensure timely and compliant product launches. Operation of laboratory equipment including mixers, pH meters, Brix refractometers, density testers, and other analytical tools. Develop formulas considering ingredient claims, interactions in formulation, and implications for certificate of analysis standards. Manage multiple product development projects simultaneously, ensuring they are completed on time, within budget, and in alignment with strategic goals. Ensure exemplary record keeping, reporting, and documentation of all project activities in both written and electronic formats. Maintain a clean, organized, and safe laboratory environment in compliance with internal policies and safety standards. Awareness of regulatory requirements to ensure product claims and nutrition facts panels meet applicable standards (FDA, DSHEA, etc.). Coordinate and communicate effectively with contract manufacturing organizations (CMOs); support scale-up trials and commercial production activities. Refine and standardize raw material specifications. Qualifications Must have a strong background in flavoring theory and application. Understanding of ingredient functionality, food chemistry, and sensory science. Proficient in formulating food and beverage products with time and budget constraints. Demonstrated ability to work independently and manage multiple priorities effectively in a dynamic environment. Excellent communication and interpersonal skills; ability to explain technical concepts to cross-functional stakeholders. Detail-oriented with strong analytical, organizational, and project management abilities. Familiarity with Microsoft Office Suite (Excel, Word, PowerPoint); experience with formulation and nutritional software (e.g., ESHA) is a plus. Experience with basic statistical analysis tools and research methodologies. Strong problem-solving mindset with a proactive and flexible approach to R&D challenges. Bachelor of Science (B.S.) in Food Science, Food Chemistry, Nutritional Sciences, or a related scientific discipline. Preferred: Advanced coursework or background in nutritional biochemistry. Minimum of 2+ years of relevant experience in food product development, preferably in sports nutrition, functional foods, or nutraceuticals. Hands-on experience with contract manufacturing or co-manufacturing environments is highly desirable. Flavoring products and experience working through various food matrices for ideal organoleptics, stability, making label claims is key. Understanding of regulatory frameworks related to food labeling and nutrition claims. Willingness to travel up to 25% for production trials, vendor visits, and other project needs. Additional Information Our culture is passionate, entrepreneurial, and energetic. We value innovation through collaboration. And while we work smart and hard, we also connect and celebrate with equal gusto. We host team-building activities, athletic events, and seasonal celebrations to foster community and reward accomplishments. Bottom line? You'll love it here. Among the many benefits our team members enjoy are: Comprehensive medical, dental, and vision care 401k package with employer matching Paid Time Off Maternity/Paternity leave Full indoor basketball/volleyball court Fully equipped fitness center (cardio, weights, functional fitness area, lockers and showers, etc.) Yoga studio Meditation/Nap room And much more! Trove Brands is an equal opportunity employer. This is a fully in-office position in Lehi, Utah. Phone calls regarding this position are not accepted.

We are seeking an R&D Product Development Scientist to join our team at our headquarters in Salt Lake City. This position requires a drive to innovate and develop new materials in the dental industry. Experience in progressing ideas from concept to prototype and/or managing multiple projects from prototype to production is highly recommended. This person will be working mostly onsite in the South Jordan location, in state candidates will be given first priority. This position will report to the R and D Chemical Development Manager and will join a team of 6 other scientists in this particular part of a larger R and D group. JOB FUNCTIONS: Backgrounds in chemistry, material science, chemical engineering, and/or a related field is preferred. Develop, improve, and customize products and formulas Explore, innovate, and create new chemistries, materials, and technologies Design and implement experiments Collaborate with a dynamic team to generate new products Conduct research and remain current on applicable technologies Scale up chemical synthesis and material batches from benchtop to production WHAT YOU'LL NEED TO SUCCEED: B.S. in Chemistry, Chemical Engineering, Material Science, or related scientific field with R&D experience is ideal Ability to communicate effectively, both verbally and written Ability to effectively use computer software including Microsoft Office Suite WHAT WE'RE LOOKING FOR IN YOU: Self-driven and motivated Strong mechanical aptitude Strong organizational skills including the ability to manage multiple priorities Ability to effectively use laboratory and processing equipment Passion for completing challenging projects Strong analytical, deductive, and inductive reasoning abilities Be able to work effectively as a part of a multi-functional team Ultradent is an Equal Opportunity Employer. We are a global culture where differences and perspectives are sought after, welcomed, and embraced. We consider all qualified applicants fairly, based on their experience, skills, and potential to contribute to our team. Our core values - Integrity, care, quality, innovation, and hard work- guide us daily. These values, when balanced, shape our workplace culture and ensure that we remain focused on our vision while maintaining a professional and inclusive environment. VEVRAA Federal Contractor: For more information please contact us at ************************ PWDNET

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 bachelor's 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.

Interested in working with us, but don't see the right role posted today? Share your resume with us here! We'll keep it on hand in case other opportunities arise in the future. In the meantime, please keep an eye on our job board for new postings.

AND SCOPE: This scientist will be responsible for developing formulas (liquid, powder, capsule), flavor work, and validating methods to support manufacturing and new products; instrumentation or equipment set up, troubleshooting, maintenance, and blend validation, and training other formulators in the lab. ESSENTIAL RESPONSIBILITES: Create new formulas for customers and formulate great tasting products Performs technical support for new product, to ensure product is ready for production run Creates the Batch Records for production runs. Troubleshoots any issues related to the materials of the product run Finds solutions to help machines run better for the product run Approves all changes to Batch Records Gather and compile supplier documentation. Note: This description is not intended to be all inclusive. Employee may be requested to perform other duties as requested. EDUCATION AND EXPERIENCE: Undergraduate degree in Food Science with 3-5 years experience in related field. Related manufacturing experience (5 years) primarily in formulation and flavor work. We work with many pre-workout/energy brands, so experience working with caffeine is a plus. SKILLS AND ABILITIES: Highly motivated, creative and independent performer with the ability to operate in a fast-paced, high pressure environment. Ability to interpret a variety of instructions furnished in written, oral, or schedule form. High ethical standards with the ability to maintain confidentiality of information. Excellent written and verbal communication skills. Strong analytical, critical thinking and communications skills. Ability to work both independently and in a team environment Must be able to follow all safety guidelines. PHYSICAL DEMANDS: The employee may be required to lift and/or move up to 30 lbs. WORK ENVIRONMENT: Laboratory environment which may include long hours standing, sitting, bending, twisting, walking, climbing stairs, strong and/or unusual odors. Powered by JazzHR 3Kqf7TA5Tp

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

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.

Dandy is transforming the massive and antiquated dental industry-an industry worth over $200B. Backed by some of the world's leading venture capital firms, we're on an ambitious mission to simplify and modernize every function of the dental practice through technology. As we expand our reach globally, Dandy is building the operating system for dental offices around the world-empowering clinicians and their teams with technology, innovation, and world-class support to achieve more for their practices, their people, and their patients. Shade &Aesthetic crown development requires precise traceability, attention to detail, and disciplined execution across a multi-step physical + digital workflow. Today, this workflow spans: Pre-milled crown inventory Geometry-specific design UUID + QR code association Pegging and shade execution Manual firing AOI (automated optical inspection) High-quality documentation for engineering analysis Any breakdown of lost crowns, mixed geometries, incorrect QR associations, missing photos invalidates the experiment (DOE) and slows learning. This role exists to: Own the physical execution layer of aesthetic crown experiments and DOE's for overall machine metrics and yield improvements. Act as the single point of accountability from crown prep → post-firing documentation Ensure engineering can trust the data because the process was executed flawlessly! Offer growth and development to an individual through technical experimentation and process improvement. Core Requirement: Availability & Responsiveness Must be available on-site in Provo (MST) within but not precisely core testing hours: 8:00 AM - 6:00 PM Monday to Friday This role supports live experiments, machine availability, and engineering iteration cycles Delays or gaps in availability directly block testing velocity What This Role Must Do (End-to-End Ownership) Understand the Active DOE Know what experiment is being run Understand: What problem we are trying to solve or prove/disprove What variable is changing What must remain controlled Execute the workflow exactly as defined by the DOE Documentation or Test Method (doc) (This role does not design the experiment but must deeply understand it.) Manage Pre-Milled / SAT Crown Inventory Maintain awareness of: Which crown geometries are currently in stock Which geometries are required for upcoming tests Aesthetic crown testing starts with pre-milled crowns If crowns are not available: Prepare crowns via sandblasting / recycling or Initiate or coordinate new crown milling Geometry Discipline & Organization Crowns are designed on specific geometries Each crown is milled out of a base shade (A1, B1, C1 and D2) and then get's shaded up. We must ensure extreme precision on matching shades. Each crown must: Stay paired with the correct geometry Never be mixed or substituted mid-flow Physical organization is critical to prevent invalid test results UUID, QR Code & Design Association Each crown design has: A UUID A QR code The role ensures: Correct crown geometry is placed into the correct bin Each bin has the correct QR code Pegging scans: Bin QR code Peg QR code This “marries” the design file → peg → physical crown This step guarantees the right shade design is applied to the right geometry Shade Injection & Retrieval Use of Akribis and P&T User interfaces. Apply changes on machine parameters as printhead voltage, temperatures, etc. Ability to perform printer start-up in case it's not being used or in production. Ability and knowledge to check and ensure optimal printer operation before running tests Pre-milled crowns are injected just before shade Crowns are retrieved immediately after shade Crowns are then delivered to the manual firing station Critical rule: No crowns lost. No ambiguity. Full accountability start to finish. Manual Firing & Post-Processing Track crowns through manual firing Ensure fired crowns remain correctly identified and grouped Photography & Engineering Documentation Take high-quality photos of each crown: Multiple angles Consistent lighting Clear detail Photos must be: Associated with the correct UUID Matched to the testing sheet showing intended design outcome These images are used directly for engineering evaluation and decisions R&D Storage & Long-Term Traceability Store completed crowns in the Engineering R&D locker Maintain labeling and organization so crowns can be retrieved later for: Comparisons Audits Follow-up testing Nice to Have Prior experience operating or supporting industrial equipment, printers, or automated machines. Background as a technician or field service technician is a plus, but not required. Basic familiarity with inkjet or printing equipment (loading parts, starting jobs, monitoring runs). Comfort following standard operating procedures (SOPs) and checklists exactly as written. Ability to recognize when a machine or process is not behaving normally and escalate issues appropriately. Willingness to perform simple machine setup, startup, and recovery tasks under guidance. Experience working in lab, pilot line, or manufacturing environments with physical parts and traceability requirements. General mechanical aptitude and comfort working around equipment. Req ID: J-917 For full-time positions, Dandy offers a wide range of best-in-class, comprehensive, and inclusive benefits tailored to each country where we operate. Our local benefits packages typically include healthcare, dental, mental health support, parental planning resources, retirement savings options, and generous paid time off-ensuring our team members are supported no matter where they live and work. Dandy is proud to be an equal-opportunity employer. We are committed to building a diverse and inclusive culture that celebrates authenticity to win as one. We do not discriminate on the basis of race, religion, color, national origin, gender, gender identity, sexual orientation, age, marital status, disability, protected veteran status, citizenship or immigration status, or any other legally protected characteristics. Dandy also fully complies with the Americans with Disabilities Act (ADA). We are dedicated to embracing challenges and creating an accessible, inclusive workplace for all individuals. If you require any accommodations for your interview or have any questions beforehand, rest assured that we will do everything we can to meet your needs. Visit Dandy Careers for more!

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** Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of 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, or any other protected status.

About Scientia Vascular: Our mission is to save lives. Scientia Vascular is a leading innovator and manufacturer of endovascular medical devices. We use micromachining and microfabrication processes to manufacture products that provide physicians with enhanced performance for optimal outcomes for their patients. Position Summary Contributes to the development of medical devices. Main responsibilities are conducting product performance testing and building prototypes for evaluation. Primary Responsibilities Conduct product performance bench testing Build or assemble prototype materials, components, subassemblies and assemblies Construct, operate, troubleshoot, adjust, maintain and test equipment, systems or products Perform testing and analyze data and write reports Review or develop processing or manufacturing instructions Maintain detailed documentation through all phases of development, testing and analysis Record data following good documentation practices Ability to solve problems and work with minimal supervision Perform job functions in accordance with applicable GMP and ISO guidelines Comply with applicable FDA and international regulatory laws/standards Other duties as assigned with or without accommodation. Requirements High School diploma Medical device Tech industry experience is a plus Must have at least 1 year of troubleshooting and testing experience as a technician Computer skills including solid proficiency with Microsoft Excel, Word, Outlook Excellent verbal and written communication skills Working knowledge of GMP, experience with ISO regulations is a plus Must have technical writing experience Must have at least 1 year of experience as a technician in a manufacturing environment Key benefits we provide: Generous Paid Time Off (PTO) Medical, Dental, Vision insurance Paid Parental Leave Paid Holidays 401k Plan (with a generous employer match) Life Insurance (company paid) Short-Term & Long-Term Disability Insurance (company paid) Subscription to Calmhealth.com Employee Assistance Program An environment of belonging where everyone can thrive Commitment to Equal Opportunity: The Scientia Vascular culture is centered on the principals of equal opportunity for all employees. Consistent with our culture, all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, family status, marital status, sexual orientation, national origin, genetics, disability, age, or veteran status, or any other non-merit based or legally protected grounds. Visit our website and learn more about us at ************************

Make a meaningful difference: At Thatcher Chemical facilities across the nation, our manufacturing teams create the essential chemistries, processes, and solutions that support clean water, safe environments, reliable infrastructure, and critical industries. From production and quality to logistics and distribution, your precision, dedication, and commitment to continuous improvement help transform raw materials and innovative science into real-world solutions. Your purpose-driven work plays a vital role in protecting public health, supporting communities, and shaping a safer, more sustainable future. Thatcher Company is looking for a Senior R&D Chemist-Waste Water Treatment at Thatcher Company headquarters, located in Salt Lake City, UT. 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. 100% company-funded Profit-Sharing Plan (up to 25% of salary annually) 401(k) with traditional and Roth contribution options Comprehensive benefits: medical, dental, vision, life insurance, short- and long-term disability, HSA/FSA, 3+ weeks of PTO, and paid holidays Education reimbursement and ongoing professional development The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website. Thatcher is an Equal Opportunity/Affirmative Action employer, including protected Veterans and individuals with disabilities.

AND SCOPE: This scientist will be responsible for developing formulas (liquid, powder, capsule), flavor work, and validating methods to support manufacturing and new products; instrumentation or equipment set up, troubleshooting, maintenance, and blend validation, and training other formulators in the lab. ESSENTIAL RESPONSIBILITES: Create new formulas for customers and formulate great tasting products Performs technical support for new product, to ensure product is ready for production run Creates the Batch Records for production runs. Troubleshoots any issues related to the materials of the product run Finds solutions to help machines run better for the product run Approves all changes to Batch Records Gather and compile supplier documentation. Note: This description is not intended to be all inclusive. Employee may be requested to perform other duties as requested. EDUCATION AND EXPERIENCE: Undergraduate degree in Food Science with 3-5 years experience in related field. Related manufacturing experience (5 years) primarily in formulation and flavor work. We work with many pre-workout/energy brands, so experience working with caffeine is a plus. SKILLS AND ABILITIES: Highly motivated, creative and independent performer with the ability to operate in a fast-paced, high pressure environment. Ability to interpret a variety of instructions furnished in written, oral, or schedule form. High ethical standards with the ability to maintain confidentiality of information. Excellent written and verbal communication skills. Strong analytical, critical thinking and communications skills. Ability to work both independently and in a team environment Must be able to follow all safety guidelines. PHYSICAL DEMANDS: The employee may be required to lift and/or move up to 30 lbs. WORK ENVIRONMENT: Laboratory environment which may include long hours standing, sitting, bending, twisting, walking, climbing stairs, strong and/or unusual odors.