Quality control analyst jobs in Millcreek, UT - 69 jobs

Quality Control Technician Kilgore Companies, a Quikrete Materials Company, is looking for a Quality Control Technician at our QC lab in Bluffdale, Utah. This position will be responsible for testing asphalt and aggregate materials for gradation and quality properties in accordance with test methods and specifications. Ready for a fast-paced job where you can provide the literal groundwork that connects communities together? Join Quikrete Materials - a construction materials company leading the industry - where we build the foundation for a better tomorrow. Quikrete Materials consists of more than a dozen local companies that supply aggregates, cement, ready-mix concrete, asphalt paving, and construction services in the United States and western Canada. At Quikrete Materials, we support our teammates who lay the groundwork for our communities and live by our core values: Safety, Integrity, Sustainability, and Inclusivity. We're passionate about our teammates, our work, and our communities. Each of Quikrete's companies celebrates their individual legacies, but together - we are Quikrete Materials. Roles & Responsibilities * Sample and test aggregate materials * Monitor materials daily to ensure our products meet the specified requirements * Follow quality control plans and guidelines * Obtain required quality control certifications in a timely manner * Record and repot tests in quality control database * Safely perform all assigned work * Safely drive a company vehicle Skills & Experience * Be willing to work a flexible schedule, including weekends, nights and anywhere within our work area * Previous testing/quality experience highly desired * High School diploma or GED equivalent is required * Able to read, comprehend, and communicate in English * Excellent math skills are required * Strong computer skills are required Benefits * Recession Resistant Industry * Consistent work, with a work/life balance * Overtime Opportunities * Paid Holidays * Paid Time Off * 401K w/ Company Match Available * Medical / Dental / Vision plan offered * Life Insurance - Company Paid * Short-term / Long-term Disability Insurance - Company Paid Additional Benefits * We care for you and your family: We offer comprehensive medical, dental, and vision insurance plans to support the health of you and your family. * We prepare for the unexpected: We offer life insurance, long-term disability, and short-term disability coverage at no cost to you. * We invest in your career growth with Quikrete Materials and beyond: Get access to our Discover Learning catalog with thousands of available courses to support your professional and personal development. You can learn on-demand, at your own pace, and from any device. * We embrace your well-being: We know that your well-being is more than just physical. We're here to provide teammates with the resources and tools they need to stay healthy and feel supported, including an Employee Assistance Program (EAP) with free counseling, financial resources, and more. * We support your personal goals: We provide a financial foundation as you plan for the future. Our programs, like our 401(k) plan where we match up to 4% of your annual income, are designed to help you prepare and reach your goals for you and your family. * We give you time to recharge: We offer our teammates Paid Time Off (PTO) so they can recharge and relax with family and friends. Get Hired What to Expect During our Hiring Process * Background Check * Motor Vehicle Record Check * 5-Panel Drug Screen * Fit for Duty Baseline Physical (if applicable) * Paid Orientation * A great team to support you throughout your career with Summit Materials companies! Build a Lasting Career with us. Begin Here. Go Anywhere. Apply now! Quikrete Materials consists of more than a dozen local companies that supply aggregates, cement, ready-mix concrete, asphalt paving, and construction services in the United States and western Canada. At Quikrete Materials, we support our teammates who lay the groundwork for our communities and live by our core values: Safety, Integrity, Sustainability, and Inclusivity. We're passionate about our teammates, our work, and our communities. Each of Quikrete's companies celebrates their individual legacies, but together - we are Quikrete Materials. At Quikrete Materials, we provide the foundation to connect our communities today and build a better tomorrow. We value all our communities - including our diverse internal community of teammates that make us stronger. No matter your race, ethnicity, gender, age, or anything that makes you who you are...you belong. Req #: 2378

This is a full time, non-exempt position. This individual is responsible for completion of activities related to the Quality system. This position regularly interacts and/or collaborates with other departments within BioFire in the execution of their duties. Position follows standard work practices and procedures, and must operate in accordance with FDA, OSHA, ISO, and applicable government regulations and standards. This individual will collect, organize, monitor, and distribute information related to Quality and process improvement functions, possibly including but not limited to compliance to and documentation of Quality Management standards. Typically generates reports using computer skills and distributes those reports to various users in the organization. This individual will follow established procedures to complete tasks within the Quality system. Other responsibilities include assisting with other activities related to the Quality system. This position requires intermediate computer skills, and good attention to detail. After training has been completed, this individual is expected to work independently or cooperatively in the completion of tasks assigned by their direct supervisor. Principal Job Duties and Responsibilities: Perform all work in compliance with company policy and within the guidelines of BioFire's Quality System. Maintains records that comply with regulatory requirements, Good Manufacturing Practices and Standard Operating Procedures. Provides support to all aspects of the Quality System; provides assistance in other Quality Department duties and projects as assigned. Must be able work in a clean-room environment. Performs Functional QC and analysis for all manufactured products, prepares and/or reviews process reports and data. Provides support to all aspects of the Quality System; provides assistance in other Quality department duties and projects as assigned. Training and Education: High School Diploma or equivalent Good computer skills, including proficiency in MS Word, Excel, and PowerPoint. Requires basic laboratory skills, and experience working in a biotech/scientific laboratory setting (i.e. use of pipettes, measurements) Experience: 1-2 years of experience in applicable industry ( g ., ISO 9001, ISO 13485 or GMP) At least one year of laboratory work experience is preferred AS degree in a Biology or Chemical Science may substitute for demonstrated basic laboratory skills (i.e. use of pipettes, measurements) and good computer skills, including proficiency in MS Word and Excel) Benefits: Medical Dental Vision 401k - company match of 5% regardless of participation and up to a total of 9.5% company match if contributing 4 Weeks of PTO 9 Paid Holidays Paid Winter Break from the work week between December 24 thru December 31 Participation in Company's Wellness Program (discounted medical premiums) Multiple Company Sponsored Events Each Year (catered breakfast/lunch, holiday parties, snacks) Stimulating work environment Convenient location near I-15 and Trax Station Free Parking Our EEO Policy BioFire Defense is an equal opportunity employer (M/F/D/V). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law. BioFire Defense complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

The 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

Job Title: Quality Auditor Associate Duration: 5-6 Months (02/09/2026 to 07/31/2026) 3rd shift (10 p.M. 6: 30 a.M. M-F, Onsite) Description: The job requirements include the following essential areas of responsibility: Perform sampling and delivery of intermediate and finished products. Assist with retain sample management. Conduct monthly GMP and batch-specific room audits. Perform in process record review of commercial manufacturing batch records. Review completed swab data and perform subsequent room/equipment release. Ensures compliance with all Company policies and procedures, including safety rules and regulations. Performs related duties as assigned. Materials and samples: Handling of pharmaceutical drug products, including topical patches, ointments, gels, and creams, as well as an oral liquid dosage form (oral suspension) as well as some combination products such nasal sprays, pump products, and vaginal applicators. Our drug products include non-controlled substances as well as some DEA controlled substances (schedule III and IV), as well as hormones. Education/Certification/Experience: Requires a minimum of one year experience in a regulated environment such as pharmaceutical, medical device, nutraceutical, or food processing industries. Requires basic understanding of Good Manufacturing Practice (cGMP) and the application to a production environment. Associate s degree or higher (or equivalent) achieved or in process preferred. Skills/Knowledge/Abilities: Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), EDMS and ERP systems. Self-directed with ability to organize and prioritize work Ability to communicate effectively with excellent written and oral communication skills Ability to interact positively and collaborate with co-workers and management

We are seeking a motivated and detail-oriented Quality Control / Quality Assurance (QC/QA) Specialist with 1-3 years of construction experience to support the successful execution of quality management practices on active construction projects. The QC/QA Specialist will assist in implementing and maintaining the project quality plan, performing inspections, and coordinating quality-related documentation with in owner provided software's to ensure compliance with contract documents, codes, and industry standards. Key Responsibilities: Assist in the development and implementation of project-specific Quality Control Plans Conduct daily field inspections and audits to verify conformance with contract drawings, specifications, and industry best practices Coordinate with subcontractors and trade partners to ensure quality requirements are understood and followed Maintain and organize all QC documentation, including inspection reports, non-conformance reports, testing logs, and material certifications Track and report quality metrics and deficiencies; work with the project team to ensure timely resolution Review submittals, shop drawings, and material certifications for compliance Attend QA/QC and coordination meetings; support third-party testing and inspection agencies Support punch list generation and project turnover documentation Promote a culture of continuous improvement and quality awareness on the job site Coordinate Trade Partner compliance with applicable specification and submit documentation to client interface Inspect and receive shipments of equipment and document with in the client software Qualifications: 1-3 years of QC/QA experience in commercial, industrial, or infrastructure construction Basic understanding of construction documents and specifications Working knowledge of quality management systems, inspection techniques, and common construction codes (e.g., IBC, AWS, ASTM) Strong communication and organizational skills

At do TERRA we encourage all employees to seek out opportunities that will expand their skill set. We strive to help achieve personal career goals by providing opportunities of growth and movement throughout the company. Job Description: Assists the Quality Control lab through sample submission, data tracking, and CoA release. Job Responsibilities: Receive samples in Labware LIMS for testing in the Quality Control Laboratory Track and file testing data in both Labware LIMS and raw data files Coordinate with Out of House laboratories for testing CoA creation in Labware LIMS CoA release to Quality Assurance Tracking of Out of Specification samples Follow recommendations of deviations pertaining to Quality Control laboratory Administer changes in Labware LIMS, including specification entry and updates Receive, review, and enter projects from outside departments Routinely archive data files and laboratory samples Follow SOPs precisely following GMP compliant practices for data handling Create and track purchase requisitions for orders within the lab Preparation and update of SOPs associated with daily responsibilities Comply with all laboratory safety procedures Utilize multiple tracking programs to maintain efficiency of lab testing Be able to work under pressure and prioritize tasks to achieve daily workload Supports all continuous improvement activities May be asked to perform non-routine work on occasion to assist the Quality Control personnel Must be available to attend ad-hoc meetings, calls, or questions during business hours While the company does strive to maintain a safe workplace, this position requires that employees contribute to a safe work environment by following all safety related procedures and detecting and reporting potential hazards Other duties as assigned Job Qualifications: High School Diploma or GED 1-2 + years full time progressively responsible work in Lab preferred LIMS experience preferred Has basic knowledge of cGMP and laboratory practices Excellent organizational and project management skills Ability to identify problems and work toward solutions creatively and without active supervision Knowledge of record keeping requirements and organization Must be proficient in Microsoft office, basic computer programs, and technical writing Must be able to work in close proximity to products with strong aromas Ability to communicate in a timely manner by reading, writing, and speaking in English. Including in person real-time communication Ability to traverse varying distances and travel between different floors of the building Must be able to elevate and/or move up to 40 pounds with assistance Must be able to stand for extended periods of time Ability to manipulate small objects such as bottle lids, small hand tools, etc. Must maintain positive relationships in the workplace by treating others with respect, dignity, and integrity Must work well in a team environment do TERRA International, LLC. is committed to employing a diverse workforce. Qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, protected veteran status, or disability.

Lab Analyst II - Salt Lake City, UT - Onsite ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Lab Analyst II to join our diverse and dynamic team. As a Lab Analyst II at ICON, you will be responsible for performing intermediate-level laboratory tests and analyses to support clinical research projects. You will contribute to the accuracy and reliability of laboratory data, while adhering to strict quality and regulatory standards, and playing a key role in the daily operations of the lab. What You Will Be Doing: Conducting intermediate-level laboratory tests and analyses in compliance with established protocols and procedures. Accurately recording and documenting test results, maintaining data integrity and quality standards throughout all processes. Operating and maintaining laboratory equipment, including performing routine calibrations, troubleshooting, and preventive maintenance. Assisting in the development and validation of new laboratory methods and protocols to enhance operational efficiency and data quality. Collaborating with cross-functional teams to support project timelines and ensure effective communication of test results and findings. Your Profile: Bachelor's degree in biology, chemistry, or a related scientific field; advanced degree preferred. 2-4 years of experience in a laboratory setting, with a focus on intermediate-level testing and analytical techniques. Strong technical skills and proficiency in using laboratory equipment and software for data analysis and reporting. Excellent attention to detail and organizational abilities, with a commitment to maintaining high-quality standards and compliance. Effective communication and teamwork skills, with the ability to collaborate in a fast-paced and dynamic environment. 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

Shape Quality at a Global Manufacturer in Tooele, UT Picture your first morning on 1st shift at Minova's new Tooele facility. You check calibration schedules, set up gauges and scales, and dive into routine testing as production ramps up. By midday, you're logging results, analyzing trends, and partnering with operators to ensure every lot meets internal specifications and customer expectations. In the afternoon, you assist with an internal audit, contribute to corrective actions for a customer complaint, and document improvements that lift quality, efficiency, and cost performance. Why this role matters Minova is a global manufacturing company recognized for safety, quality, and continuous improvement. As a direct-hire Quality professional, you'll be central to maintaining our ISO 9001:2015 Quality Management System and elevating day-to-day quality operations. What you'll handle Conduct routine testing and inspections in accordance with applicable standards Support implementation and upkeep of the ISO 9001:2015 QMS Assist with internal audits and ensure conformance to quality/performance standards Complete accurate documentation, test results, and formal reports Analyze quality data to spot trends and improvement opportunities Support investigations of customer complaints and assist with corrective actions Coordinate calibration of gauges, scales, and test equipment at scheduled intervals Partner with production teams so requirements are understood and met Identify ways to improve quality, efficiency, and cost What you bring Experience in a quality, lab, or manufacturing setting (preferred) Knowledge of quality control practices, testing, and documentation Familiarity with ISO 9001 standards (plus) Strong attention to detail and organization Ability to follow procedures, specifications, and safety requirements Comfort with data and written reporting Team orientation and clear communication skills Schedule, pay, and benefits Direct-hire position 1st shift schedule $23-$25 per hour, based on experience Comprehensive benefits: medical, dental, and vision Paid time off (PTO) and paid holidays 401(k) retirement plan with company match New facility with long-term growth opportunities Location Tooele, Utah Preferred proficiency ISO 9001 Certification Experience Minova and Malone are equal opportunity employers.

Submittal Quality Control Inspector | Salt Lake City, UT Nexeo HR is hiring Quality Control Inspectors to join a leading manufacturing and production company in Salt Lake City, UT. This role is ideal for detail-oriented individuals who enjoy working in a fast-paced manufacturing environment with opportunities for long-term career growth. As a Quality Control Inspector, you will play a key role in ensuring quality assurance and compliance by performing visual and mechanical inspections, verifying materials and assemblies, and using precision tools to confirm product accuracy. Candidates with experience in quality control, inspection, or manufacturing are encouraged to apply. Responsibilities • Perform mechanical and visual inspections of raw materials, components, and sub-assemblies according to inspection plans, blueprints, and specifications • Use precision measurement tools such as microscopes, calipers, and micrometers to perform accurate quality checks • Document inspection results in compliance with quality assurance and manufacturing standards • Support document control processes, including scanning, archiving, and preparing records for shipment • Maintain compliance with FDA regulations, ISO standards, and company quality procedures • Assist with special projects, audits, and process improvements as needed Qualifications • Basic computer proficiency for documenting inspections and accessing quality systems • Strong written and verbal communication skills to interpret work instructions and collaborate with team members • Ability to read and interpret engineering drawings and technical specifications • Familiarity with FDA regulatory standards, ISO 13485, or medical device manufacturing preferred • Strong attention to detail and ability to perform repetitive inspection tasks with accuracy • Manual dexterity and ability to operate standard office and inspection equipment • Ability to sit for extended periods while entering/analyzing data • Must occasionally lift up to 25 lbs Pay Rate $19-$21 per hour Job Type Full-Time Shift/Schedule Day Shift: 6:30 AM - 6:30 PM (rotating schedule) Swing Shift: 6:30 PM - 6:30 AM (rotating schedule) Nexeo Benefits • Medical, Dental, Vision, Limited Life, Short-Term Disability. • Refer a Friend Bonus | Other Financial Incentives (Bonuses). • Weekly Pay | Direct Deposit | Rapid Pay Card. • Hassle-Free Job Search: A Nexeo Recruiter is always available to assist you. Questions? Call or Text our office today! With 100+ jobs available, we're sure to find a job for you. 1745 W 7800 S, West Jordan, UT 84088 (P) (801) 305-1300 Nexeo provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, or genetics. In addition to federal law requirements, Nexeo complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Nexeo expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Quality Control Inspector | Manufacturing Quality Assurance | Mechanical Inspection Specialist | Visual Inspection Technician | Precision Measurement Tools Operator | Micrometer and Caliper Inspection | Medical Device Quality Control | FDA Compliance Specialist | ISO 13485 Inspector | Raw Material Inspection | Sub-Assembly Quality Assurance | Blueprint and Specification Reading | Quality Assurance Technician | Document Control and Archiving | Manufacturing Inspection Professional INDWJ

Quality Control Inspector Stadler has been building trains for over 80 years. With our innovative strength, flexibility, and reliability we are a leading manufacturer of rail vehicles today. In addition to our Swiss locations, around 14,500 employees work at 16 production and components sites at over 80 service locations in Europe, North America, and North Africa. Our passion goes beyond building the trains customers want and people choose to ride. As a complete service provider and dedicated partner in signaling and maintenance, we guarantee safety, availability, and operation. Join our team and help us shape the future of mobility! As a Quality Control Inspector, you will be responsible for the inspection of trains to ensure quality and compliance with engineered drawings, specifications, and documentation within the industry's standards. If you want to be part of a team that builds high quality, state of the art passenger trains, this is the career for you! Key Responsibilities Physically inspect components and systems for in-process and/or completed railcars to determine construction complies with approved drawings and Contract specifications Improve train inspection and testing criteria or procedures, document inspection results, methods, and criteria and report all non-compliances with the specification or approved drawings Perform, and report on, Hold Points and Pre-Shipment inspections Monitor performance of quality control systems and identify problems or areas for improvement and recommend solutions Maintain and review all quality control inspection documentation Investigate and assist in the solution of quality problems Identify, report and recommend solutions for any quality control issues Qualifications High school diploma or GED equivalent; and 1-2 years of experience with high standard of quality Technical skills required, including reading blueprints and drawings Must have excellent interpersonal skills, including strong verbal and written communication Proficient in operating computer software, windows and data base software Highly reliable, great learning skills, management skills and ability to lead cross functional teams Goal-oriented and structured approach in a dynamic environment What we offer Stadler US employee benefits package includes: Competitive Pay (plus Profit Sharing potential) Low-cost, comprehensive Medical / Dental / Vision / Rx plans 401(k) with employer match after 90 days Generous Paid Time Off / 9 Paid Holidays / Extended Paid Holiday (Dec. 25 - Jan 1) Paid training / Career development Tuition and training reimbursement Paid maternity and parental leave Company-paid life and disability insurance Referral bonus program Stadler US is an Equal Opportunity Employe

Stadler offers a wide range of international career opportunities. Here you get the chance to expand your potential, take on meaningful responsibilities, and deliver outstanding performance within dedicated teams. We are looking for motivated individuals who want to shape the mobility of tomorrow with us. Are you ready to achieve great things with us? Join our team and help us shape the future of mobility! HOW YOU CAN MAKE AN IMPACT As a Quality Control Inspector, you will be responsible for the inspection of trains to ensure quality and compliance with engineered drawings, specifications, and documentation within the industry's standards. If you want to be part of a team that builds high quality, state of the art passenger trains, this is the career for you! Key Responsibilities * Physically inspect components and systems for in-process and/or completed railcars to determine construction complies with approved drawings and Contract specifications * Improve train inspection and testing criteria or procedures, document inspection results, methods, and criteria and report all non-compliances with the specification or approved drawings * Perform, and report on, Hold Points and Pre-Shipment inspections * Monitor performance of quality control systems and identify problems or areas for improvement and recommend solutions * Maintain and review all quality control inspection documentation * Investigate and assist in the solution of quality problems * Identify, report and recommend solutions for any quality control issues HOW YOU WILL CONTRIBUTE * High school diploma or GED equivalent; and 1-2 years of experience with high standard of quality * Technical skills required, including reading blueprints and drawings * Must have excellent interpersonal skills, including strong verbal and written communication * Proficient in operating computer software, windows and data base software * Highly reliable, great learning skills, management skills and ability to lead cross functional teams * Goal-oriented and structured approach in a dynamic environment * Must reside in the Salt Lake City Metro area or be able to relocate YOUR BENEFITS YOUR CONTACT PERSON Jennifer Hood Talent Acquisition Specialist ***************

WGNSTAR is a dynamic and growing company with a global footprint. Primarily focused on the semiconductor industry, we provide a platform for you to expand your career with knowledge gained on the job, and tailored development. We know we need talented people like you that hold similar values, which is why we do not put limits on learning, development, industry, and personal growth. Start your path to a WGNSTAR career today! Schedule: Sunday, Monday, Tuesday, alternating Wednesday, 6:00 AM - 6:00 PM Pay Rate: $23, hourly Location: Lehi, Utah Position Type: Full-Time Benefits: This position is eligible for WGNSTAR's full benefits package, including Medical, Dental, Vision, and 401(k). Additional benefits are listed at the end of this posting. Principal Duties and Responsibilities: Perform chemical and gas container changeouts. Perform chemical offloads. Respond quickly to potentially critical situations, perform rapid and accurate situational assessments, and troubleshoot system components. Review recommended operating procedures to ensure best practices are in place and documented properly. Review, maintain, comprehend, and follow Work Plans, Sequence of Operations, Standard Operating Procedures, P&IDs, and Process Flow Diagrams. Keep operational areas at a high level of operational readiness, housekeeping, organization, orderliness, and free of hazards. Receive, stock, and deliver chemicals and gases. Collect chemical system samples and deliver them to the lab. Requirements: Ability to be SCBA certified and clean-shaven. Ability to be forklift certified on-site. Experience with MS Office, Word, Excel, and PowerPoint. Proven ability to follow procedures and work with minimal supervision. Flexible with job responsibilities and shift assignments. Proven time management, organization, and prioritization skills. Proven ability to multitask in a high-paced environment. Physical Effort/Activities: May be required to walk up to 5+miles per day, able to be on feet for 8-10 hrs at a time, ability to bend, twist, push/pull, crouch, kneel in confined spaces, work at heights, on a ladder, and lift up to 50 pounds. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions of this job. Additional Benefits: Paid Vacation, Select Holidays, Overtime Opportunities, On-site Facilities & Career Development Opportunities. The people who thrive most at WGNSTAR are those individuals who perform well in a team environment, enjoy interacting and engaging with several different stakeholders, and adapt quickly to changing environments, while leveraging their skills, quality, and knowledge to drive themselves and their teams towards continuous improvement and success. This is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed by job holders within this job. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities or working conditions associated with the position. This position is not eligible for visa sponsorship. All applicants must be legally authorized to work in the United States without the need for current or future sponsorship (e.g., H-1B, O-1, etc). Additionally, WGNSTAR does not participate in the STEM OPT extension program for this role. Equal opportunities and Social Governance WGNSTAR is an Equal Opportunity Employer, drug free workplace, and complies with ADA regulations as applicable. WGNSTAR places an immense emphasis on equal employment, encourages diversity in the workplace, and applies an open-door policy for inclusion of all employees. Our diversity program encourages people from any gender, background, ethnicity, culture, education, and experience to join the company and more importantly build a career through employee development. Through our Global wellness programs, WGNSTAR ensures our employees and families have access to a full range of wellness services through our Employee Assistance Program (EAP). In the communities that surround our business operations, we support individual and group sponsorships for local sports and those that are vulnerable in society.

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!

Required Qualifications Student at Weber State University Successful completion of Principles of Chemistry I Chem 1210 lecture and 1215 lab or higher level chemistry courses and labs. Excellent verbal communication skills. Ability to work well with others and attention to details. Preferred Qualifications Preference given to Chemistry and Biochemistry majors/or other related majors. Preference given to applicants who are Federal Work Study eligible. Work Study is preferred for this position but is open for students as well. If you are unsure if you are eligible for Federal Work Study program, please contact Financial Aid at ************.

Quality Control Technician Kilgore Companies, a Quikrete Materials Company, is looking for a Quality Control Technician at our QC lab in Mona, Utah. This position will be responsible for testing asphalt and aggregate materials for gradation and quality properties in accordance with test methods and specifications. Ready for a fast-paced job where you can provide the literal groundwork that connects communities together? Join Quikrete Materials - a construction materials company leading the industry - where we build the foundation for a better tomorrow. Quikrete Materials consists of more than a dozen local companies that supply aggregates, cement, ready-mix concrete, asphalt paving, and construction services in the United States and western Canada. At Quikrete Materials, we support our teammates who lay the groundwork for our communities and live by our core values: Safety, Integrity, Sustainability, and Inclusivity. We're passionate about our teammates, our work, and our communities. Each of Quikrete's companies celebrates their individual legacies, but together - we are Quikrete Materials. Roles & Responsibilities * Sample and test aggregate materials * Monitor materials daily to ensure our products meet the specified requirements * Follow quality control plans and guidelines * Obtain required quality control certifications in a timely manner * Record and repot tests in quality control database * Safely perform all assigned work * Safely drive a company vehicle Skills & Experience * Be willing to work a flexible schedule, including weekends, nights and anywhere within our work area * Previous testing/quality experience highly desired * High School diploma or GED equivalent is required * Able to read, comprehend, and communicate in English * Excellent math skills are required * Strong computer skills are required Benefits * Recession Resistant Industry * Consistent work, with a work/life balance * Overtime Opportunities * Paid Holidays * Paid Time Off * Employees age 18 and over that have been an employee for at least six months are eligible to enroll in the 401(k) Plan. Once you have met the eligibility requirements, you can join the plan on the first day of each quarter coinciding or next following the date the requirements have been met (January, April, July, and October). Enrollment information will be mailed to your home address on file. * Medical / Dental / Vision plan offered * Life Insurance - Company Paid * Short-term / Long-term Disability Insurance - Company Paid Additional Benefits * We care for you and your family: We offer comprehensive medical, dental, and vision insurance plans to support the health of you and your family. * We prepare for the unexpected: We offer life insurance, long-term disability, and short-term disability coverage at no cost to you. * We invest in your career growth with Quikrete Materials and beyond: Get access to our Discover Learning catalog with thousands of available courses to support your professional and personal development. You can learn on-demand, at your own pace, and from any device. * We embrace your well-being: We know that your well-being is more than just physical. We're here to provide teammates with the resources and tools they need to stay healthy and feel supported, including an Employee Assistance Program (EAP) with free counseling, financial resources, and more. * We support your personal goals: We provide a financial foundation as you plan for the future. Our programs, like our 401(k) plan where we match up to 4% of your annual income, are designed to help you prepare and reach your goals for you and your family. * We give you time to recharge: We offer our teammates Paid Time Off (PTO) so they can recharge and relax with family and friends. Get Hired What to Expect During our Hiring Process * Background Check * Motor Vehicle Record Check * 5-Panel Drug Screen * Fit for Duty Baseline Physical (if applicable) * Paid Orientation * A great team to support you throughout your career with Summit Materials companies! Build a Lasting Career with us. Begin Here. Go Anywhere. Apply now! Quikrete Materials consists of more than a dozen local companies that supply aggregates, cement, ready-mix concrete, asphalt paving, and construction services in the United States and western Canada. At Quikrete Materials, we support our teammates who lay the groundwork for our communities and live by our core values: Safety, Integrity, Sustainability, and Inclusivity. We're passionate about our teammates, our work, and our communities. Each of Quikrete's companies celebrates their individual legacies, but together - we are Quikrete Materials. At Quikrete Materials, we provide the foundation to connect our communities today and build a better tomorrow. We value all our communities - including our diverse internal community of teammates that make us stronger. No matter your race, ethnicity, gender, age, or anything that makes you who you are...you belong. Req #: 2320

Job DescriptionSalary: $20 - $22 DOE This is a full time, non-exempt position. This individual is responsible for completion of activities related to the Quality system. This position regularly interacts and/or collaborates with other departments within BioFire in the execution of their duties. Position follows standard work practices and procedures, and must operate in accordance with FDA, OSHA, ISO, and applicable government regulations and standards. This individual will collect, organize, monitor, and distribute information related to Quality and process improvement functions, possibly including but not limited to compliance to and documentation of Quality Management standards. Typically generates reports using computer skills and distributes those reports to various users in the organization. This individual will follow established procedures to complete tasks within the Quality system. Other responsibilities include assisting with other activities related to the Quality system. This position requires intermediate computer skills, and good attention to detail. After training has been completed, this individual is expected to work independently or cooperatively in the completion of tasks assigned by their direct supervisor. Principal Job Duties and Responsibilities: Perform all work in compliance with company policy and within the guidelines of BioFires Quality System. Maintains records that comply with regulatory requirements, Good Manufacturing Practices and Standard Operating Procedures. Provides support to all aspects of the Quality System; provides assistance in other Quality Department duties and projects as assigned. Must be able work in a clean-room environment. Performs Functional QC and analysis for all manufactured products, prepares and/or reviews process reports and data. Provides support to all aspects of the Quality System; provides assistance in other Quality department duties and projects as assigned. Training and Education: High School Diploma or equivalent Good computer skills, including proficiency in MS Word, Excel, and PowerPoint. Requires basic laboratory skills, and experience working in a biotech/scientific laboratory setting (i.e. use of pipettes, measurements) Experience: 1-2 years of experience in applicable industry ( g ., ISO 9001, ISO 13485 or GMP) At least one year of laboratory work experience is preferred AS degree in a Biology or Chemical Science may substitute for demonstrated basic laboratory skills (i.e. use of pipettes, measurements) and good computer skills, including proficiency in MS Word and Excel) 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.

Lab Analyst 1 - Lenexa, KS - Onsite ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Lab Analyst I to join our diverse and dynamic team. As a Lab Analyst I at ICON, you will be responsible for conducting routine laboratory tests and analyses to support clinical research studies. You will play an essential role in maintaining accurate data, adhering to standard procedures, and contributing to the overall success of the laboratory operations. What You Will Be Doing: Performing routine laboratory tests and analyses in accordance with established protocols and procedures. Recording and documenting test results accurately, ensuring data integrity and compliance with quality standards. Operating and maintaining laboratory equipment, performing regular calibrations, and troubleshooting as needed. Supporting quality control activities by participating in the review and verification of test results and procedures. Collaborating with team members to ensure timely and efficient completion of laboratory tasks and projects. Your Profile: Bachelor's degree in biology, chemistry, or a related scientific field. 0-2 years of experience in a laboratory environment, preferably in clinical research or a related industry. Strong attention to detail and organizational skills, with the ability to follow protocols and maintain accurate records. Basic proficiency in laboratory techniques and equipment operation, with a willingness to learn and develop new skills. Good communication and teamwork abilities, with a proactive approach to supporting team objectives and deadlines. 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

Job DescriptionShape Quality at a Global Manufacturer in Tooele, UT Picture your first morning on 1st shift at Minova's new Tooele facility. You check calibration schedules, set up gauges and scales, and dive into routine testing as production ramps up. By midday, you're logging results, analyzing trends, and partnering with operators to ensure every lot meets internal specifications and customer expectations. In the afternoon, you assist with an internal audit, contribute to corrective actions for a customer complaint, and document improvements that lift quality, efficiency, and cost performance. Why this role matters Minova is a global manufacturing company recognized for safety, quality, and continuous improvement. As a direct-hire Quality professional, you'll be central to maintaining our ISO 9001:2015 Quality Management System and elevating day-to-day quality operations. What you'll handle Conduct routine testing and inspections in accordance with applicable standards Support implementation and upkeep of the ISO 9001:2015 QMS Assist with internal audits and ensure conformance to quality/performance standards Complete accurate documentation, test results, and formal reports Analyze quality data to spot trends and improvement opportunities Support investigations of customer complaints and assist with corrective actions Coordinate calibration of gauges, scales, and test equipment at scheduled intervals Partner with production teams so requirements are understood and met Identify ways to improve quality, efficiency, and cost What you bring Experience in a quality, lab, or manufacturing setting (preferred) Knowledge of quality control practices, testing, and documentation Familiarity with ISO 9001 standards (plus) Strong attention to detail and organization Ability to follow procedures, specifications, and safety requirements Comfort with data and written reporting Team orientation and clear communication skills Schedule, pay, and benefits Direct-hire position 1st shift schedule $23-$25 per hour, based on experience Comprehensive benefits: medical, dental, and vision Paid time off (PTO) and paid holidays 401(k) retirement plan with company match New facility with long-term growth opportunities Location Tooele, Utah Preferred proficiency ISO 9001 Certification Experience Minova and Malone are equal opportunity employers.

WGNSTAR is a dynamic and growing company with a global footprint. Primarily focused on the semiconductor industry, we provide a platform for you to expand your career with knowledge gained on the job, and tailored development. We know we need talented people like you that hold similar values, which is why we do not put limits on learning, development, industry, and personal growth. Start your path to a WGNSTAR career today! Schedule: Sunday, Monday, Tuesday, alternating Wednesday, 6:00 AM - 6:00 PM Pay Rate: $23, hourly Location: Lehi, Utah Position Type: Full-Time Benefits: This position is eligible for WGNSTAR's full benefits package, including Medical, Dental, Vision, and 401(k). Additional benefits are listed at the end of this posting. Principal Duties and Responsibilities: * Perform chemical and gas container changeouts. * Perform chemical offloads. * Respond quickly to potentially critical situations, perform rapid and accurate situational assessments, and troubleshoot system components. * Review recommended operating procedures to ensure best practices are in place and documented properly. * Review, maintain, comprehend, and follow Work Plans, Sequence of Operations, Standard Operating Procedures, P&IDs, and Process Flow Diagrams. * Keep operational areas at a high level of operational readiness, housekeeping, organization, orderliness, and free of hazards. * Receive, stock, and deliver chemicals and gases. * Collect chemical system samples and deliver them to the lab. Requirements: * Ability to be SCBA certified and clean-shaven. * Ability to be forklift certified on-site. * Experience with MS Office, Word, Excel, and PowerPoint. * Proven ability to follow procedures and work with minimal supervision. * Flexible with job responsibilities and shift assignments. * Proven time management, organization, and prioritization skills. * Proven ability to multitask in a high-paced environment. Physical Effort/Activities: May be required to walk up to 5+miles per day, able to be on feet for 8-10 hrs at a time, ability to bend, twist, push/pull, crouch, kneel in confined spaces, work at heights, on a ladder, and lift up to 50 pounds. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions of this job. Additional Benefits: Paid Vacation, Select Holidays, Overtime Opportunities, On-site Facilities & Career Development Opportunities. The people who thrive most at WGNSTAR are those individuals who perform well in a team environment, enjoy interacting and engaging with several different stakeholders, and adapt quickly to changing environments, while leveraging their skills, quality, and knowledge to drive themselves and their teams towards continuous improvement and success. This is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed by job holders within this job. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities or working conditions associated with the position. Apply for this job