Chemist jobs in Orem, UT

We are looking to fill a **Scientist 3 - Analytical Chemist** position working as **a full-time employee of Parexel FSP on long-term assignment** onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer any sponsorship.** **Responsibilities** + General understanding of analytical method development and method validation + Hands-on experience with chromatographic analysis using various ultra-high-performance liquid chromatography (UPLC), high-performance liquid chromatography (HPLC), and gas chromatography (GC) techniques + General knowledge of separations science + Experience with Empower chromatographic software and with analysis of drug formulations + Hand-on experience with Fourier transform infrared (FTIR) spectroscopic analysis and ultraviolet-visible (UV-VIS) spectroscopic analysis + Skilled on method and instrument troubleshooting, specifically for HPLC and GC methods and systems **Required Skills** + Strong computer, scientific, and organizational skills + Excellent organization to multi-task and manage multiple ongoing projects in parallel including routine testing (for example, assay and impurity testing) and data processing and interpretation + Excellent communication (oral and written) and attention to detail + Proficient in written and spoken English, is required **Desired Skills and Experience** + Empower software + Analysis of drug products + Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude **Qualifications** + BS degree and 3-5 years of relevant experience, or + MS degree with at least 1-2 years relevant experience **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Performs testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions and maintains appropriate records. List of required skills and day-to-day responsibilities: Performs complex testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions, and maintains appropriate records. May use a variety of analytical instrumentation including HPLC, GC, UV-Vis, and so forth High through put sample preparation Experience with HPLC a plus Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws. Complies with all current Good Manufacturing Practices (cGMP) current Good Laboratory Practices (cGLP) and safety requirements, laboratory, Standard Operating Procedures (SOPs) and Company policies and procedures. Qualifications Bachelors in biological sciences Additional Information All your information will be kept confidential according to EEO guidelines.

• 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 ********************************* ************

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

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

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.

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. About the Role We are establishing a new R&D and pilot production facility in Provo, Utah, focused on advanced ceramic and specialty inks for digital printing applications. We seek an Ink Chemist who is equally comfortable formulating new inks in the lab and working hands-on with inkjet printers. This is a unique opportunity to combine chemistry, materials science, and printing technology in a fast-growing innovation environment. Key Responsibilities Ink Formulation & Development Design and optimize ink formulations (solvent-based, ceramic, and specialty inks). Scale experimental recipes into pilot batches (up to 5 kg) while ensuring reproducibility. Tailor ink properties such as viscosity, surface tension, particle dispersion, and stability to match printhead requirements. Inkjet Printer Operation & Mechanisms Operate, maintain, and troubleshoot inkjet printers and test rigs. Understand printer subsystems (printhead, waveform, drop formation, ink delivery, curing/firing). Run print trials, capture print quality data, and feed results back into ink design. Applied Research & Process Innovation Conduct DOE studies to optimize color calibration, waveform tuning, and print consistency across machines. Explore new pigment systems, dispersants, and solvents to expand ink performance. Collaborate with engineering to adapt inks to different printheads and substrates (e.g., zirconia, metals, ceramics). Incoming Quality Control Perform incoming QC on inks sourced from vendors to ensure they meet required physical property specifications (e.g., viscosity, particle size, stability). Document results and provide feedback to suppliers and internal teams. Vendor Communication Work closely with vendors to discuss formulation changes, improvements, and troubleshooting. Ensure external formulations align with internal performance requirements. Documentation & Communication Keep precise lab notebooks, batch records, and experimental reports. Present results and recommendations to technical leadership and cross-functional teams. Support scale-up into production with well-documented methods. Ensure compliance with lab safety, cleanliness, and chemical handling protocols. Qualifications Education: B.S. or M.S., preferably Ph.D. in Chemistry, Materials Science, Chemical Engineering, Printing Science, or related field. Experience: 2-5 years of experience in inkjet inks, coatings, dispersions, or printing technology. Hands-on experience with inkjet printers and printheads (Seiko, Epson, Xaar, etc.). Track record of bridging chemistry with machine performance. Skills: Strong knowledge of fluid dynamics, surface chemistry, and particle dispersion. Ability to troubleshoot jetting behavior, waveform settings, and print quality defects. Comfortable in both laboratory and pilot production environments. Excellent problem-solving, documentation, and communication skills. Preferred: Experience with ceramic inks or dental materials (zirconia crowns, etc.) Familiarity with color science, VITA shades, and calibration workflows. Knowledge of FDA or ISO regulatory environments for medical/dental materials. What We Offer The chance to work at the intersection of chemistry and printing technology. Competitive compensation and benefits. A role with high visibility and impact in shaping a state-of-the-art ink lab. Growth opportunities in a dynamic, entrepreneurial team. Req ID: J-804 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!

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

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 ongoing and emerging innovation projects Contribute to cost-saving initiatives Develop methodologies for new analytical tools (e.g., moisture meter, oat-grading sieves) Support product improvement initiatives Build supplier relationships to evaluate new ingredients and technologies Troubleshoot production and QA-related issues Conduct sensory evaluations to support innovation, quality, and supplier approvals Manage formulations and ingredients in Genesis software to ensure accuracy, cost tracking, and efficiency Other duties as assigned Experience Requirements: B.S. Degree (Food Science or Engineering 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 Previous experience in basic and applied research and development preferably in food or beverage companies preferred. Strong background in food science, ingredient interaction, and process development. 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.

Performs cyclotron operation, manufacturing, and quality control for routine and research radiopharmaceuticals for positron emission tomography ( PET ). Incumbent must comply with radiation safety procedures, cGMP, and FDA requirements. Operates, and assists in maintenance and validation of manufacturing and analytical equipment. Follows all standard operating procedures and performs additional duties as directed by management. Must be motivated, team oriented and committed to expanding their knowledge and experience in a clinically oriented academic program. Incumbent will experience moderate exposure to hazardous materials or physical risk, which requires adhering to radiation safety practices. Full time position involving a variable schedule around production demands. The typical work week will be Monday through Friday 11:30 pm - 7:30 am. These time frames may need to be adjusted as production demands change. In very rare instances a weekend shift may be required. Huntsman Cancer Institute is committed to cancer prevention, care, and survivorship for all communities within the area we serve - which includes Idaho, Montana, Nevada, Utah, and Wyoming - with impact worldwide. Partnerships with individuals, communities, and many other entities are crucial to our work. Huntsman Cancer Institute values cancer-related health equity, and inclusion as integral to our guiding principle to serve our patients and their communities, and our commitment to foster a culture of belonging for all within our organization. In your cover letter or during your interview process, we invite you to share how your personal and professional experiences have prepared you to serve as a member of our team as we work to reduce the cancer burden experienced by all people and communities. This may include description of your prior experiences related to research, prevention, clinical care, community engagement/outreach, training, administration, or other areas relevant to Huntsman Cancer Institute's mission and this position. Learn more here Responsibilities As a Radiochemist your duties will be highly varied from time to time and may include but not be limited to: Under the direction of the management, assists with all activities involved in developing and preparing radiopharmaceuticals for clinical and research use. Operates, assists in maintenance and troubleshoots the cyclotron and associated equipment in compliance with protocols and good ALARA radiation safety practices. Operates automated radiochemistry synthesis equipment in compliance with protocols and current Good Manufacturing Practices (cGMP) and FDA regulations. Performs quality control of radiopharmaceuticals according to standard operating procedures. Troubleshoots cyclotron laboratory equipment using mechanical, electrical and basic science skills. Develops and performs new processes or protocols for validation, manufacturing and quality control. Assists management in developing, improving and maintaining protocols, applications, and licenses as required for routine radiopharmaceutical production. Assists in packaging and shipping of radioactive material in compliance with all state and federal regulations. Assists with the return and cleaning of shipping containers as assigned. Assists in preparing regulatory documents for submission to the FDA . Complete and maintain periodic training for GMP , equipment, radiation safety, SOPs, HIPAA , and others as required. Minimum Qualifications · Bachelor of Science Radiochemistry, Chemistry, or Biochemistry. Other science related degrees will also be considered with equivalent experience. · 2+ years of work in a research, analytical or pharmaceutical laboratory. Other types of experience similar to these areas will also be considered. · 2+ years of experience in working with analytical equipment such as HPLC , GC, and IC. · Detail oriented, self-directed, able to work autonomously and able to multitask effectively. · Ability to read, listen and understand technical direction, policies and procedures. · Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description and general responsibilities. · Physical demands: Clear speech, good hearing and at least 20/20 corrected vision (which can include the use of glasses, contact lenses, etc.). Ability to lift up to 110 lbs. · Must satisfactorily pass a background test and not be debarred from any activities related to manufacturing radiopharmaceuticals.

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Research & Development In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality. The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation. About the role As an R & D Technician at Reckitt, you will thrive in our fast-paced environment alongside a team of expert scientists dedicated to ensuring product safety and efficacy. Your meticulous attention to detail will be crucial in supporting technical dossier management and analytical lab compliance. This role is not currently sponsoring visas or considering international movement at this time. Your responsibilities * Assist the R&D Analytical Lab and R&D Pilot Plant with placing purchase orders and reconciling accounts and invoices using Excel, SharePoint, and SAP. * Track stability protocols and pull samples at required time points. Route samples for required testing. * Create orders for testing at 3rd party labs where required and ship samples. * Administrate shipment of packages through UPS for the R&D group. * Regularly update the chemical inventory and lab equipment status for the R&D Analytical Lab in lab database. * Organize and maintain stores of lab consumables. * Enter analytical results from 3rd party laboratories in lab database. * Carry out administrative tasks in lab database for routine maintenance. * Organize and maintain archived analytical documentation. * Participate in lab cleanup/5S processes and activities. * Provide general clerical support by assisting with copies, scanning, and updating lists. * Assist in the preparation and maintenance of documents, spreadsheets and presentations using MS Word, Excel and Power Point. * Review analytical lab administrative process and make efficient improvements. * Diagnose and handle business issues as they arise in a logical, self-directed manner and with manager's input as needed. The experience we're looking for * High School Diploma required, Associate degree in a scientific field is a plus. * Laboratory experience preferred; familiarity with laboratory terminology. * Excellent organizational skills. Ability to apply logical thinking to solve a variety of problems. * Interpersonal skills with the ability to work in a team-oriented environment. * Proficient in English. Good verbal and written communication skills. * Ability to display a degree of flexibility regarding changing project priorities. * Knowledge with MS Office Software applications. The skills for success R&D, Product Lifecycle Management, Commercial Awareness, Business Partnership, Collaboration, Partnership building, Collaborator, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Analytical, Formulation, Science, Chemistry. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. US salary ranges USD $62,000.00 - $92,000.00 Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Salt Lake City Job Segment: Counseling, Nutrition, Healthcare

Job Description HemaSource is looking for a detail-focused and analytical Quality Control Analyst to support the intake, evaluation, investigation, and reporting of medical device product complaints. This role directly contributes to patient safety and ensures our products meet global regulatory standards. You will be part of a highly collaborative Quality team that values accuracy, critical thinking, and a commitment to continuous improvement. If you enjoy problem-solving, working with technical data, and partnering across Quality, Engineering, and Regulatory teams, this is an excellent opportunity to grow your career in a fast-paced and mission-driven environment. You will play a vital role in supporting compliance with FDA regulations, international standards, and internal quality system requirements while helping drive improvements in product performance and customer satisfaction. Key Responsibilities Receive, review, and process medical device product complaints, ensuring accurate documentation and timely assessment. Conduct thorough complaint investigations using root-cause analysis and cross-functional input. Ensure compliance with FDA, ISO 13485, EU MDR, and internal quality system requirements. Prepare and submit required regulatory reports (MDRs, vigilance reports) within strict timelines. Analyze complaint data to identify trends and contribute to CAPA and continuous improvement efforts. Communicate clearly with internal teams and external customers regarding complaint status and findings. Maintain accurate, audit-ready records, complaint metrics, and documentation. Manage LMS activities including training assignments, system maintenance, and compliance reporting. Qualifications Bachelor's degree in Life Sciences, Engineering, or related field. 2+ years of medical device complaint handling, post-market surveillance, or quality experience. Familiarity with FDA regulations, ISO 13485, EU MDR, and quality system requirements. Strong analytical, critical-thinking, and problem-solving skills. Excellent written and verbal communication skills. Proficient with Microsoft Office; experience with QMS/ERP/complaint systems preferred. Why Join Us Opportunity to grow in Quality, Regulatory, or Technical Operations. Meaningful work that directly impacts patient safety and product quality. Supportive team environment with clear development pathways. Stable, growing company invested in compliance excellence. Physical Requirements Prolonged computer work. Ability to lift up to 10 lbs. occasionally. Who We Are: HemaSource is an innovative logistics solution partner that combines best-in-class analytics and high-quality medical product supply to specialty ambulatory clinics. Our mission is to drive customer operational efficiencies and related cost savings in high volume ambulatory care clinics. HemaSource's patented data analytics software tool and our superior customer service have enabled us to become the preferred disposables provider to the plasma collection market. Job Posted by ApplicantPro

Work Schedule: This position follows a day-shift schedule from Thursday to Monday. Candidates may select either a four-day, 10-hour schedule (4/10s) or a five-day, 8-hour schedule (5/8s), depending on operational needs. The focus is on developing your technical knowledge and skills to solve more complex problems. Become familiar with all basic microbiological testing including but not limited to media making, Total Plate Count, Enterobacteriaceae, Yeast and Mold using Petrifilm and Petriplate methods: also presence/absence of E coli, Salmonella, Staphylococcus, and Pseudomonas testing RESPONSIBILITIES * If appropriate, uses laboratory equipment and instruments with minimal supervision * Perform calibrations, and maintain calibration records * Able to keep detailed and complete records * Able to think analytically * Have a good sense of timeliness and cleanliness * Proficient in Excel, MS Office * Ability to be flexible * Ability to work as a team member * Keep labs clean and organized QUALIFICATIONS * BS in a scientific area, preferably microbiology/biology * Knowledge of microbiology and chemistry * Knowledge of testing of natural products and ingredients * Knowledge of GMP and GLP requirements * Experience in environmental testing and allergen testing * Capable of using laboratory equipment and documentation systems. * Ability to write reports and communicate results * Ability to work as a team member Nature's Sunshine is dedicated to being a Force of Nature that champions social and environmental wellness. We are focused on building a team of professionals with diverse backgrounds and experiences to become the natural supplement company of the future. By celebrating the individuality and unique perspectives of our workforce, we empower our employees to share the healing power of nature with more people around the world. And through our commitment to sustainable processes, renewable energy usage and waste reduction initiatives, we're devoted to preserving nature and its power for future generations. We believe we are stronger together, and our ongoing commitment to diversity, equity, inclusion and belonging ensures that every employee is treated with fairness and respect. Because doing what's right-in the right way-is how we succeed as a company and a society.

We are looking to fill a **Scientist II or III - Metrology Specialist** position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer sponsorship.** **Metrology specialist is responsible for the oversight of regulated and non-regulated laboratory equipment** . This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement **Qualifications -** B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline + **Scientist II** - B.S. with 1-2 years of relevant experience or M.S. with 0-1 years of relevant experience + **Scientist III** - B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience **Responsibilities** + Prepare, review, and approve instrument/equipment documentation such as master equipment lists, qualification documentation, and calibration documentation + Coordinate service activities across a variety of vendors and service engineers while building and maintaining strong working relationships + Gain a working knowledge of laboratory equipment to facilitate with troubleshooting and/or perform maintenance or calibration activities + Participate in computer system validation activities associated with new or upgraded equipment or software packages + Support the purchase, installation, and equipment qualification of new laboratory equipment + Collaborate with metrology staff across multiple testing labs and sites for process improvement, cross-training and cross-site support + Originate and progress Notice of Event (NOE) and Change Management (CM) records + Perform and document investigations and assist in developing/implementing CAPA plans + Represent the laboratory on all aspects of laboratory equipment during audits + Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures **Required Skills and Experience** + Experience working within a regulated (GMP) laboratory + **Experience maintaining or operating laboratory equipment including HPLCs, GCs, UVs, dissolution systems, or other specialized computerized systems** + Familiarity with standalone computer system validation requirements + Highly organized, and capable of multi-tasking to manage a variety of laboratory equipment or system related schedules, documents, and maintenance tasks + Capable of working independently under moderate supervision + Strong verbal and written communication skills + Strong interpersonal skills. Comfortable interacting with a variety of on-site and off-site collaborators **Desired Skills and Experience** + Experience with maintenance of analytical instrumentation such as HPLC, UPLC, GC, UV, IR, Karl Fischer, and dissolution with ability to troubleshoot them. + Experience with computerized standalone systems GMP validation requirements + Familiarity with authoring relevant instrument standard operating procedures (SOPs) **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Performs testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions and maintains appropriate records. List of required skills and day-to-day responsibilities: Performs complex testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions, and maintains appropriate records. May use a variety of analytical instrumentation including HPLC, GC, UV-Vis, and so forth High through put sample preparation Experience with HPLC a plus Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws. Complies with all current Good Manufacturing Practices (cGMP) current Good Laboratory Practices (cGLP) and safety requirements, laboratory, Standard Operating Procedures (SOPs) and Company policies and procedures. Qualifications Bachelors in biological sciences Additional Information All your information will be kept confidential according to EEO guidelines.

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.

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.

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.