Quality control technician jobs in OFallon, MO

Job Overview:Quality Control Technician II - St. Louis, MO The QC Technician II plays a critical role in ensuring that all products manufactured at the facility meet established quality and safety standards. This position performs advanced laboratory testing, sensory evaluations, and quality inspections to support production, compliance, and continuous improvement efforts. The QC Technician II also maintains accurate records, supports audit readiness, and provides technical expertise in both analytical and microbiological testing. Shift & Schedule: This is a full time position working 2nd shift Monday - Friday 12:00pm - 8:30pm. Flexibility to work occasional overtime, including nights, weekends, and/or holidays, is also required. Position ResponsibilitiesPrepare reagents and solutions, perform instrument calibrations and standardizations, and conduct analytical testing (pH, acidity, density, Brix, particle size, absorbance/transmittance, assays). Calculate batch adjustments as needed. File and maintain retained samples for shelf-life studies and investigative testing. Conduct sensory evaluations of raw materials, in-process samples, and finished products to assess appearance, aroma, flavor, and mouthfeel. Compare results against specifications and sensory standards to ensure consistency, detect off-notes, and support product release decisions. Document findings and escalate deviations as appropriate. Maintain the SAP database by entering analytical and qualitative results, and blocking stock when issues are identified. Notify relevant business functions of problems, evaluate non-conformance data, and make recommendations for corrective actions. Verify that all products meet quality specifications through inspections of sanitation, recipe compliance, labeling, fill weights, packaging configuration, and food safety. Document findings, issue reports on deviations, and calculate statistical results for KPI reporting. Maintain accurate and timely documentation of laboratory testing and product evaluations. Upload relevant documentation to shared systems / databases, ensure compliance with retention policies, and provide documentation to support investigations, audits, and customer inquiries. Perform internal audits of compounding, packaging, and finished goods storage areas. Document observations, identify gaps, and recommend improvements to strengthen compliance and efficiency. Perform basic microbiological testing and environmental monitoring as required (e. g. , plating, air/water sampling, yeast and mold counts, and sanitation verification). Document results and escalate out-of-spec findings. Maintain inventory of laboratory supplies-including chemicals, instrumentation materials, microbiological supplies, and sample containers-to ensure adequate availability and prevent testing delays. Other duties as assigned by the manager, supervisor, and lead. Total Rewards: Pay starting at $31. 30 per hour + $1. 50 shift Differential. The employee will move to a higher rate of $32. 99 per hour in the quarter after their 6-month anniversary. Where Applicable: Benefits eligible day one!! Benefits, subject to eligibility, and collective bargaining agreements (where applicable): Medical, Dental, Vision, Disability, Paid Time Off (including vacation and sick time), 401k with company match, Tuition Reimbursement, and Mileage Reimbursement Requirements:Associate degree in a math- or science-related field preferred. Equivalent experience (3+ years in an analytical laboratory or experience as a Quality Technician I) may be substituted. Experience with laboratory instrumentation and SAP data systems preferred. Proficiency in basic computer applications, mathematics, and verbal communication, with the ability to accurately input and manage information. Must be able to learn specific system transactions related to production processes. Strong communication skills with the ability to work effectively in a team environment. Demonstrated ability to apply mathematical concepts and reasoning skills to problem solving and data interpretation. Ability to stand or walk for extended periods in a manufacturing environment. Ability to frequently lift and/or move up to 50 pounds. Ability to perform visual inspections of products and materials. Ability to perform sensory testing, which requires the ability smell and taste product for quality purposes. Company Overview: Keurig Dr Pepper (NASDAQ: KDP) is a leading beverage company in North America, with a portfolio of more than 125 owned, licensed and partner brands and powerful distribution capabilities to provide a beverage for every need, anytime, anywhere. We operate with a differentiated business model and world-class brand portfolio, powered by a talented and engaged team that is anchored in our values. We work with big, exciting beverage brands and the #1 single-serve coffee brewing system in North America at KDP, and we have fun doing it! Together, we have built a leading beverage company in North America offering hot and cold beverages together at scale. Whatever your area of expertise, at KDP you can be a part of a team that's proud of its brands, partnerships, innovation, and growth. Will you join us? We strive to be an employer of choice, providing a culture and opportunities that empower our team of ~29,000 employees to grow and develop. We offer robust benefits to support your health and wellness as well as your personal and financial well-being. We also provide employee programs designed to enhance your professional growth and development, while ensuring you feel valued, inspired and appreciated at work. Keurig Dr Pepper is an equal opportunity employer and recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law. A. I. Disclosure: KDP uses artificial intelligence to assist with initial resume screening and candidate matching. This technology helps us efficiently identify candidates whose qualifications align with our open roles. If you prefer not to have your application processed using artificial intelligence, you may opt out by emailing your resume and qualifications directly to kdpjobs@kdrp. com.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: At MilliporeSigma, the Quality Control Logistics Technician 3 will perform a variety of functions according to established protocols in support of the Quality Control testing laboratories. * Execute all operations safely, consistently meeting quality and safety standards. * Manage diverse sample logistics, including SAP transactions, sampling, weighing, deliveries, retains, and external shipments. * Accurately weigh chemicals based on assay requirements and quantities. * Safely handle all chemical classes in varying amounts. * Support laboratory functions such as equipment upkeep, restocking, waste management, and material transport. * Independently evaluate material hazards to establish safe handling and PPE needs. * Complete required work to achieve team goals and meet deadlines. * Communicate operational status and deviations, maintaining accurate records and logbooks. Physical Attributes: * Wear PPE as required. * Lift/push/pull up to 80 pounds. * Extended work in a dry room environment. Who You Are Minimum Qualifications: * High School Diploma or GED. Preferred Qualifications: * 2+ years of experience working with SAP quality or inventory systems and transactions. * Ability to independently review safety data sheets and determine appropriate handling precautions and personal protective equipment. * Experience working with Microsoft Office platforms such as Excel and Word. * Strong time management, attention to detail, and drive to perform individually and as a member of a team. * Approach all tasks with an independent initiative to create value. * Excellent verbal and written communication skills. RSREMD * Pay Range for this position: $22.00-$35.00 per hour. * The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This role supports manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final QC product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances. They work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes. Hours: Monday - Friday 6am - 2:30pm + rotating Saturdays every 4 weeks Pay: $20.43 - $26.44hr + bonus + FULL benefits after 30 days Location: 7501 & 7405 Page Ave St. Louis, MO Hire Type: Full time/direct hire What You'll Do: Assists in production line Quality investigations and associated problem-solving activities. May coordinate and conduct in-process and final QC product acceptance testing, depending on facility. Investigates production line stoppages to identify corrective actions. Identifies and documents product and process non-conformances. Participates on a Material Review Board to review and process non conformance reports. Reviews DHR's and supports batch record release. Enters and retrieves Quality data from local and global systems. Performs site calibration activities and recordkeeping. Executes environmental monitoring processes and recordkeeping. Verifies calculations, dose ranges, dosimeter placements and special instructions prior to processing and part of final product release. Skills, Abilities, and Experience: Required: Associates Degree in Engineering or Scientific fields + 1yr of experience in manufacturing or repair environment or other technical production tasks. HS Diploma or GED equivilant + 3yrs of expereince in a manufacturing or repair environment. Experince with mathematical skills inlcuding ratios, proportions and basic algebra. PC experience and working familiarity of common desktop applications including Excel and Word. Ability to work in a fast-paced environment with strict deadlines. Ability to generate detailed, high-quality documentation. Ability to work with others in analyzing and solving technical problems. Preferred: Bachelors degree in a scientific, engineering, or manufacturing related field with internship experience. Previous expereince working in a regulated environment (FDA/ISO/EU MDR). Knowledge and experience working in Aseptic gowning. Experience with GDP (Good Documentation Practices) guidelines. Knowledge of 5S manufacturing practices and/or experience working with them in a professional setting. Other: Specific Skills & Competencies: Collaborate with others. Work in a professional manner to support team actions. Effectively manage work tasks. Attention to detail. Drive for continuous improvement. Working Condidtions: Manufacturing/Operations Center Physical Requirements: Lifting, Pushing, & Pulling 25 - 50lbs Bending, Walking, Standing, Sitting, Typing, Hand Manipulation, Visual Acuity, Feet Manipulation What STERIS Offers: We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future. Here is just a brief overview of what we offer: Market Competitive Pay Extensive Paid Time Off and (9) added holidays Excellent Healthcare, Dental and Vision Benefits Long/Short Term disability coverage 401(k) with company match Maternity & Paternal Leave Additional add-on benefits/discounts for programs such as Pet Insurance Tuition Reimbursement and continued educations programs Excellent opportunities for advancement and stable long-term career Pay range for this opportunity is $20.43 - $26.44. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits Open until position is filled. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

Since 1961, Precoat Metals (**************** has been setting the standards in the coil coatings industry worldwide. We are committed to this level of quality in both our product line and customer service, and focus our resources on investigating and implementing new coil coating technologies, developing unique coatings, ink and film systems, and designing multifaceted prints while reducing the cycle time to market. We are able to achieve this "culture of excellence" thru the hard work and talent of the people on our team. Job Description The Product Quality Lab role is a vital part to ensure we are producing a quality product by implementing proper standards and physical test requirements to production. And the experience you have may make you a perfect fit to join our team at our St. Louis, MO plant . Additionally, you will be responsible for insuring coatings are applied within spec and to help insure optimum paint usage through daily audits. Want to take your career to the next level? Working at Precoat Metals can take you down a career path of multiple opportunities. Start your success down a great career path today with Precoat Metals! Some of Your Responsibilities include: Conduct physical quality testing. Maintain paint standard files. Maintain physical test files. Responsible for various in-house quality control audit checks and testing methods. Audit daily paint usage. Audit daily paint DF control. Audit color and gloss trending. Audit requested paint vendor changes on specific coatings. Monitor coating film thickness and conversion coating weights during all production. Assist as backup to the manufacturing line. Qualifications As the selected candidate you will need to have great accuracy with details, regulatory, legal or requirement, timely and concise record keeping, in addition to the following: Strong written and verbal skills with the ability to speak with hourly production workers, management and vendors. Multi-taker within the ability to prioritize and meet critical deadlines. Must be computer literate, familiar with the Windows Operating system. Must be able to work various shifts in a plant environment. Additional Information We are an equal opportunity employer. Precoat Metals is a Drug Free Workplace. $29.85/HR We are an Equal Opportunity Employer. Precoat Metals is a Drug Free Workplace

Job Description Quality Control Inspection Technician Kemco Aerospace Manufacturing, a diversified solutions provider for the defense industry. We manufacture components and parts for fixed wing fighter aircraft, rotary aircraft, and casings for munitions. We employ stringent controls and lean manufacturing practices to deliver certified, precision components that exceed exacting quality, cost, and delivery standards. It is our commitment to total customer satisfaction and integrated customer-to-supplier technology that has earned us preferred supplier status. This is an opportunity to join an organization that enables the manufacture of equipment used to support and equip our service men and women. At Kemco we offer a competitive compensation and benefits package that includes the ability to elect medical, dental, vision and company paid life insurance coverage. The package also includes 8 paid holidays, 3 floating holidays, vacation, and 401k plan with match. Please note that the following duties and requirements described herein are intended to represent general contents of this job: Qualified individuals will possess the following at a minimum: • 3+ years of experience as a CMM operator on a Zeiss or similar machine. • Experience as an operator for a Roamer Arm is a plus. • Excellent skill in blueprint reading and interpretation. • Working knowledge of geometric dimensioning and tolerancing (GD&T) a must. • Knowledge of shop math and some geometry & trigonometry • Ability to analyze data and respond accordingly. • Strong working knowledge of MS Excel and WORD; PC literate • Self-motivated and detail oriented in a fast-paced environment • Good communication skills (verbal and written) • Proficient in use of all standard measuring instruments • Knowledge of S.P.C. and capability studies • Knowledge of C.A.D. software and drawings • ISO-9001/AS9100 knowledge and experience Qualified applicant must meet minimum requirements and complete application, pass drug & background check for consideration. EEOC Employer

MGP Ingredients is a leading supplier of premium distilled spirits and food ingredient solutions. Its Distilling Solutions segment provides bourbons, whiskeys, ryes, gins, and vodkas to craft and multinational brands. MGP's own Branded Spirts business is growing following the 2021 acquisition of Luxco, a top spirits producer, bottler, supplier, and importer as well as the 2023 acquisition of Penelope Bourbon, known for its wide range of uniquely blended expressions. Ingredient Solutions delivers nutritional, functional wheat- and pea-based ingredients aligned with consumer trends. The company operates in locations across the Midwestern U.S., and overseas in Northern Ireland and Mexico. THE OPPORTUNITY We are looking for a Quality Control Technician to join our Luxco team in St. Louis, MO. Under the guidance of the Quality Control Manager, the Quality Control Technicians work closely with the Rectifying and Bottling departments. Working with Rectifying to ensure batching is conducted in a quality manner while ensuring government regulations and internal specifications are met. Working with Bottling department to ensure approved batches are bottled in a quality manner while ensuring government regulations and internal specifications are still being met during the bottling process. Quality Control Technicians aid in ensuring that the quality of the product is carried through to the end consumer. WHAT YOU WILL BE DOING: Responsible for all laboratory analyses of all samples submitted to QC Laboratory to ensure internal specifications and external government regulations are met. Perform beverage laboratory testing, including distillation, titration, specific gravity and proof checks, pH testing, and organoleptic analysis. Inspect and audit production lines to ensure work ticket specifications are met and quality conformance is followed. Operate and calibrate lab instrumentation. Responsible for testing Reverse Osmosis system daily to ensure internal specifications. Perform accurate and timely data entry and record-keeping in Quality Control systems. Communicate effectively with other Luxco departments. All other duties assigned by the Quality Control Manager. WHO WE ARE LOOKING FOR: Minimum of a two-year science degree or Wet Chemistry lab experience. A degree in Chemistry, Biology, or Environmental Sciences. Must possess a strong working knowledge of Microsoft Windows and Office including Excel and Word. Candidate must be self-motivated, dependable, detail-oriented, and able to work independently with little supervision. Laboratory and/or quality control experience is preferred, especially in the food and beverage industry. PHYSICAL REQUIREMENTS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions. While performing the duties of this position, the employee is regularly required to talk or hear. The employee frequently is required to use hands or fingers, handle or feel objects, tools, or controls. The employee is occasionally required to stand; walk; sit; and reach with hands and arms. Specific vision abilities required by this position include close vision, distance vision, and the ability to adjust focus. The noise level in the work environment is usually low to moderate. Includes frequently used office equipment, computer software programs, manuals, books, or other written resources, hand tools, power tools, two-way radios, and other tools/equipment/resources; Includes use of sanitation equipment and lab/field equipment. Various lab equipment, two-way radios will be required to use. If you require a reasonable accommodation in the employee selection process, please direct your inquiries to Caitlin Zbikowski, Talent Manager @ ********************. If the above speaks to you, we're excited to learn more about you! At MGP, we know that our people are our greatest strength. With different perspectives and unique ways of thinking, our employees are as varied as our products. We believe that inclusivity strengthens the organization and champions a company culture that is evolving to reflect all of us. Culture results from our behaviors, our personal commitment, our curiosity, how we collaborate, and the ways we courageously share our perspectives and expect others to do the same. Each of us can make a difference by fostering thinking and actions that empower us to connect, belong and grow together. Compensation is competitive and is commensurate with experience. MGP offers exceptional medical, dental, vision, short and long-term disability, life insurance, 401(k) Match and PTO. All successful candidates for this position will be required to submit to a criminal background check and drug test.

NEWLY WEDS FOODS - GERALD, MO "COME GROW WITH US!" Quality Control Technician - 3rd Shift (11pm-7am) Evaluates finished products for quality and acceptability. Performs all necessary analysis as required and according to product specifications. Communicates product quality issues to Production Supervisors, Production Managers, QC Manager, Shipping personnel and Customer Service. Logs all analysis test results and batch information in the I-Series (AS400) and maintains analysis records and documents necessary for documentation compliance. Monitors line equipment for functionality, safety and cleanliness. Checks metal detectors (CCP), magnets, scales and performs critical control point and GMP audits. Assist in all foreign material and product non-conformance investigations. Performs batch set-up checks, assists in correcting the set ups, and logs descrepancies. Places product on hold as necessary and release when appropriate. Rejects product as necessary and completes rejection forms including root cause and corrective action anlysis. Checks allergen clean out effectiveness as needed. Perform Pre-Op audit when necessary (example: equipment down for maintenance). Performs production scale checks and lab equipment calibration based on calibration schedule. Collect micro samples as needed and places micro hold products on hold. Performs special tasks assigned by the Quality Control Manager. Maintains retain sample area and control sample file. Follows ALL Newly Weds Foods GMP's and Safety/Sanitation Procedures. Hours may vary including possible shift change. This is dependent on plant and production needs. Must be able to work overtime when needed on any shift. Minimum Qualifications: H.S. OR equivalent with 1-2 years related work experience. Highly motivated individual that is committed to the responsibilities of the job. Great work ethic. Great communication skills. Ability to use Quality Control analysis equipment preferred. Mathematical Skills Computer skills and Data Processing skills REQUIRED Ability to climb ladders and work on platforms Able to lift 50 lbs.

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications Ability to work in a highly regulated environment and comply with GMP expectations. • Attention to detail, strong organizational skills in order to start and complete a task.• Ability to handle cold samples for long periods of time and cold environments for short periods of time. Associate Degrees are also acceptable The QC Sample Handling Technician will assist a multi-discipline support staff with primary responsibility for receiving, aliquoting, distributing, and handling materials, as well as with documentation of GMP samples in support of multi-product and multi-site testing laboratories. Additional Information $14/hr 12+ months

Make a Difference in YOUR Career! Our vision is both simple and ambitious: to put our drinks on every table. We are the leading global independent beverage solutions provider. We serve a broad range of national and international retailers as well as Global, National and Emerging (GNE) brands. Our products are distributed worldwide from our production sites in Europe, North America, and Australia. Although our own branding may not appear on the labels of the beverages we produce, there is a good chance you are reading this while sipping one of our drinks. Our ambition is to continually improve and it's what keeps us at the top of our game. We are solutions-based. We are innovative. We seek out new challenges and conquer them. This is our company ethos, but it's our people's too: Refresco is at the cutting edge of a fast-moving industry because we have passionate people pushing the boundaries of what's best. Stop and think: how would YOU put our drinks on every table? Contractual hourly wage rate is $23.75 hour - Additional $.20 per hour for 2nd and 3rd shift allowance. Position Description: Reporting to the Quality Supervisor, the Quality Technician is responsible for overseeing day-to-day quality operations for the production lines including the implementation and monitoring of food safety and food quality, sanitation and batching systems to facilitate compliance with company objectives and regulatory requirements. Essential Functions: · Adhere to all health and safety policies/procedures, Good Manufacturing Practices (GMPs) and wear the required personal protective equipment (PPE) while in the warehouse or production areas (including but not limited to hairnets/beard nets, safety glasses, hearing protection, hard toe and slip/oil resistant shoes, appropriate safety gloves, and seatbelts while operating forklifts). · Responsible to adhere to food quality and food safety as per the standard(s) provided by corporate, customer, and/or governing bodies (ex. SQF). · Ensure all products conform to the customer specifications as outlined in SAP system. · Perform analysis on raw materials, finished batches, treated water and/or any other programmed outlines by the department. · Conduct chemical and physical analysis on raw and intermediate processing materials including packaging materials and determine status of materials as acceptable or unacceptable. · Evaluate finished products against current standards by performing audits to monitor all aspects of finished product and packaging integrity. · Check process control parameters to assure proper equipment application and operation is being maintained by performing secure seal, closure torque, can seam checks, and/or any other requirements required by the customer or the company. · Stop any production which may be questionable in terms of Food Safety and immediately alert a member of the management team. · Maintain accurate, legible records of all tests and retests performed. Complete all other required reports (work orders, action reports, etc.) in a timely manner. · Perform analytical tests required to qualify ingredient batches for production. · Perform production line checks at specified intervals. · Ensure accurate test results by maintaining proper operation and calibration of laboratory equipment. · Maintain laboratory cleanliness at all times. · Report all out of specification results to designated leadership. · Complete special projects and other reasonable duties as assigned by leadership. Required Skills: · Working knowledge of Excel, Word, and SAP preferred. · Exposure to using measurement tools and equipment (e.g., calipers, micrometers, CMM machines) preferred. · Organized and detail oriented, adaptable to change. · High level of precision and accuracy in inspection and testing processes. · Familiarity with SQF, SAP, Six Sigma, GMP, and other relevant standards and regulations preferred. · Understanding of Food Safety Requirements. · Able to read and understand metric system. · Food or beverage laboratory experience preferred. Competencies: · Technical: Skilled in maintaining accurate and detailed records of inspections and tests · Integrity: Commitment to maintaining high ethical standards in all quality assurance activities. · Adaptability: Flexibility to adapt to changing production environments and requirements. · Communication: Clear and concise communication with production staff and management Education and Experience: · Highschool diploma or equivalent. · 1 - 3 years of experience in Quality within a manufacturing environment preferred. · In plants co-packaging alcoholic beverages, must be at least 21 years old. Working Conditions: · Work Schedule: Weekdays, weekends, afternoon, evening, and overnight may be required. Overtime scheduled as needed. · Work Environment: Operating in a fast-paced production plant with numerous moving parts. Noise levels require hearing protection and temperatures can get very hot and/or relatively cold (laboratory is temperature controlled). The environment is structured and supervised. Travel Requirements: · 0% travel anticipated. Physical Requirements: R = Rarely (0-15%) O = Occasionally (16-45%) F = Frequently (46-100%) Physical Demand R O F Stand or Sit X Stoop, kneel, crouch, or crawl X Lifting up to 50 lbs. (minimum 5 lbs) X Carry weight, lift X Walking X Driving X Climb (stairs/ladders) or balance X · Visual/Sensory: This position requires attention to detail, requiring attention with one or two senses at a time. · Mental Stress: There is pronounced pressure from deadlines, production quotas, accuracy, or similar demands. Other Duties: · This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice. A Career with Refresco Refresco offers a competitive salary and comprehensive benefits, which include: Medical/Dental/Vision insurance  Health Savings Accounts Life and AD&D Insurance Legal Benefits 401(k) savings plan with company match Paid holidays, vacation, and paid time off  Well-being benefits Discount and Total Rewards Programs Any employment agency, person, or entity that submits a résumé to this career site or a hiring manager does so with the understanding that the applicant's résumé will become the property of Refresco Beverages US, Inc. Refresco Beverages US, Inc. will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person, or entity. Employment agencies that have agreements with Refresco Beverages, Inc., and have been engaged in a search shall submit résumé to the designated Refresco recruiter or, upon authorization, submit résumé to this career site to be eligible for placement fees. Refresco is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, ancestry, religion, sex, national orientation, sexual orientation, age, marital status, disability, gender identity, gender expression, Veteran status, or any other classification protected by federal, state, or local law.

We are seeking a detail-oriented and proactive Quality Assurance Technician to join our team in a fast-paced food manufacturing environment. The QA Technician plays a critical role in ensuring that all products meet company and regulatory standards for safety, quality, and consistency. This position involves monitoring production processes, conducting inspections, and maintaining accurate documentation to support food safety and quality systems. Responsibilities * Perform routine quality checks on raw materials, in-process products, and finished goods. * Monitor and enforce Good Manufacturing Practices (GMPs), sanitation procedures, and food safety protocols. * Conduct environmental and product sampling for microbiological and chemical testing. * Verify compliance with HACCP, FDA, USDA, and other regulatory requirements. * Maintain and calibrate QA equipment, such as scales, thermometers, and pH meters. * Document and report non-conformances, assist in root cause analysis, and support corrective actions. * Collaborate with production and sanitation teams to ensure quality standards are upheld. * Assist in internal audits and support external inspections. * Maintain accurate records of inspections, test results, and quality metrics. * Participate in continuous improvement initiatives and training programs. Essential Skills * Knowledge of HACCP, GMPs, and food safety regulations. * Strong attention to detail and organizational skills. * Ability to work independently and as part of a team. * Proficient in Microsoft Office and basic data entry. Additional Skills & Qualifications * Associate or bachelor's degree in food science, biology, or related field preferred. * 1-2 years of experience in food manufacturing or quality assurance preferred. * Knowledge of chemistry and biology. * Experience in quality control. Work Environment The work schedule consists of 12-hour block shifts, working 2 days on and 2 days off from 6:30 pm to 6:45 am. The position requires flexibility to pick up other shifts when others are on PTO. Saturdays are on an on-call status with each team having a designated Saturday each month. The work environment includes spending half of the shift in the lab testing products and the other half retrieving samples and conducting line checks. The role involves working in cold, wet, or noisy environments and standing for extended periods. Job Type & Location This is a Contract to Hire position based out of Saint Louis, MO. Pay and Benefits The pay range for this position is $20.00 - $23.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Saint Louis,MO. Application Deadline This position is anticipated to close on Dec 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

**Why Us?** We want the best and brightest people to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life. ** Summary** Depending on the laboratory area, will perform analysis on Raw Materials, Intermediates, In-Process, Finished Product, or Stability samples using established analytical methods. **Job Description** **ESSENTIAL FUNCTIONS:** + Follow good documentation practices for the accurate and timely documentation of all activities. + Perform wet chemistry and instrumentation testing. + Follow site HSE Policies. + Assist with establishing and maintaining safe work standards in the lab. + Peer review all levels of work. + Conducts lab investigations. **DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS** **:** + LIMS entry of data + Use of analytical balances, HPLC, GC, KF Titrator, UV, pH Meter + Maintain instrument readiness **MINIMUM REQUIREMENTS** **:** _Education:_ High School Diploma required, associate degree in a science related field or equivalent combined education, experience, and competencies preferred. _Experience:_ Experience in a cGMP environment is preferred. Working knowledge of instrumentation preferred. _Preferred Skills/Qualifications:_ + Working knowledge of wet chemistry required + Working knowledge of instrumentation (GC/LC, UV, AA). + Experience in a cGMP environment is preferred. + Basic computer skills and familiarity with Microsoft Office Suite. + Substantial acquaintance with and understanding of application of basic principles, theories and concept. + Use and/or Basic knowledge of industry practices and standards. + Chromatography (GC/LC) and Spectroscopy experience a plus. **COMPETENCIES:** Informing, Customer Focus, Listening, Perseverance, Organizing, function/technical skills, Peer Relationships, Comfort around Higher Management **ORGANIZATIONAL RELATIONSHIP/SCOPE:** Contacts involve matters of moderate importance to the organization and include R&D, Marketing, Production employees including Engineers, Supervisors, and Operators, Logistics, EHS, and DEA. Infrequent customer contacts on routine matters. **WORKING CONDITIONS:** + 80% Laboratory exposure to plant products, solvents and reagents, some of which are hazardous or potent compounds. + 20% Office environment. + Required to work 8-12 hour shifts, the potential for night, weekend, and holiday work depending on the lab **DISCLAIMER:** _The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills require_ **EEO Statement:** We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. 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. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

This position will require a self-directed, team-oriented individual who will take pride and ownership in their work and is willing to accept total responsibility for the maintenance and sanitation of the semolina delivery system. This position has responsibility for the cleanliness and operation of equipment including silos, blowers, sifters, and roller mill. This position will be responsible for AIB and BRC readiness in all assigned areas. This position will require a Team Oriented attitude to ensure that plant safety, quality, food safety, and operational goals are achieved. Employee Type: Full time Location: MO St Louis Job Type: Production Group Job Posting Title: Quality Technician Job Description: Schedule: Monday - Sunday between 7am - 4pm Work Location: 611 E. Marceau St., St. Louis, MO 63111 Benefits: Medical, Dental, Vision, 401(k) with match, STD/LTD/AD&D/Life, HSA, FSA, EAP, Hospital indemnity, Accident Insurance, Identity and Fraud Protection Plan, Legal, and Critical Illness. Salary, based on experience and other qualifications: $22.80 with $1.50 shift differential Responsibilities: Ownership of the semolina delivery system Areas and equipment must be kept in optimal operational condition and tour and audit ready Perform preventative maintenance and general repair work on semolina delivery systems to identify and eliminate system leaks Direct responsibility for compliance with the Master Sanitation Schedule for the semolina delivery areas and submit daily work assignment sheets Assist with Food Safety and 5S audits regularly to ensure compliance and high standards as required by our Good Manufacturing Practices Ensure compliance with all safety programs by maintaining a hazard free work area and adhering to all OSHA requirements Maintain and clean semolina delivery equipment including delivery lines, couplings, socks, sifters, and mixers. Use and understand the mixing of chemicals for cleaning and sanitizing equipment. Periodically work in confined areas such as interior of semolina silos, dryers and product silos, etc. Perform general structural cleaning of walls, floors, vents, lights, pipes, ceilings and windows. Perform all other tasks assigned. Qualifications/Education/Experience/Skills High School Diploma or GED Must demonstrate effective communication skills and be able to understand and interpret equipment training and policy manuals Demonstrate basic math skills Work independently and on a team Possess a good understanding of Good Manufacturing Practices and HACCP The ability to lift 20 lbs. on a frequent basis and be able to lift up to 55 lbs. unassisted on an infrequent basis Work above ground floor elevations and in environments above 90 degrees continuously Operate a variety of sanitation equipment as necessary (i.e., automatic floor scrubbing equipment, high pressure washers, vacuums, hand jacks and man lifts) Work in confined areas on an infrequent basis Use a variety of power and hand tools Understand the mixing of cleaning chemicals Familiarity with formal safety procedures to maintain the work environment's safety Vision for detailed cleaning and be able to hear audible alarms and verbal communication in noisy environments Must be able to stoop, kneel, crawl, and climb on a semi-frequent basis. EEO Statement: Winland Foods seeks to recruit, develop, and retain the most talented people from a diverse candidate pool, and as a global company we believe our success is enhanced by fostering equity and inclusion in the workplace. Therefore, Winland Foods is committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and teammates without regard to race, color, religion, sex, pregnancy, national origin, age, physical or mental disability, marital status, sexual orientation, gender identity, genetic information, military or veteran status, and any other characteristic protected by applicable law.

Job DescriptionSerioplast, a Global Leader in Rigid Plastic Packaging, is Looking for a Quality Technician for the plants in St. Louis, Missouri! Are you a quality control expert looking for an exciting opportunity to thrive in a fast-paced, global environment? Join us and take your career to new heights! What will you do? Follows the application of safety rules according to company policies and regulations. Maintains order, organization and cleanliness in all assigned areas, working in line with correct workplace hygiene practices, with the aim to be an example to others. Performs controls according to the quality control plan for each product and during technical interventions and product industrialization using lab instruments (scale, caliper, thickness gage, top load tester, torque meter, etc.). Sorts defected bottles, contributes to decisions on discarding or keeping batches and provides support in the evaluation of quality problems. Checks incoming material against quality specifications and verifies documentation compliance. Fills in and verifies quality measurement information in the proper sheets and systems, and timely signals any issues. Creates production stock labels. Performs calibrations and cleaning of measuring instruments within the production or Lab. Is able to run a program on the CMM Machine. Understands the importance of 5S principles and follows their application. Guarantees proper information sharing, reports relevant issues to the Quality Manager Communicates and cooperates with Quality team to ensure quality and hygiene of the final product. Promotes effective communication between team and Manager. Interacts with different business functions to drive high performance culture. What are we looking for? Excellent applied knowledge of measuring instruments and techniques Good knowledge of plastic molding technologies (EBM and/or SBM and/or IM) Good knowledge of ISO standards Basic knowledge of Health, Safety and Environment rules and practices Basic knowledge of Statistical Process Control and statistical analysis Associate's degree or equivalent experience Minimum 3 years' experience working in an ISO certified Quality Lab of a manufacturing company, preferably in the FMCG sector What do we offer? Continuous training: Grow professionally by working alongside industry experts. Dynamic and international environment: Join a team engaged in global projects. Career growth opportunities in an industry leading company. Flexible working hours and smart working (defined days per month). Internal mobility: Opportunities for job rotation and career progression Additional Perks & Benefits: 401(k) 401(k) matching Dental insurance Health insurance Health savings account Paid time off Vision insurance Sounds like a fit? We'd love to hear from you! Want to know more about us? Check out Who We Are and discover what makes us unique! Upon sending their application, the candidate grants specific consent to the processing of personal data, in accordance with current legislation on privacy. The privacy policy is available at the following link: ******************************************************************* Serioplast is an equal employment opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, status as a qualified individual with a disability, or any other characteristic protected by law. Powered by JazzHR oOAoTx8xGE

Work Schedule 12 hr shift/nights Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps hot/cold, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.) Job Description Job Title: Sr Downstream Processing Technician Dayshift: 6am - 6:30pm Nightshift: 6pm - 6:30am Location/Division Specific Information St. Louis, MO/ Drug Substance Division (Biologics) Are you ready to take your career in manufacturing to the next level? Thermo Fisher Scientific Inc. is currently seeking a highly skilled and motivated Downstream Processing Technician III to join our world-class team in St. Louis. As a leading company in the scientific research industry, we are dedicated to enabling our customers to make the world healthier, cleaner, and safer. In this role, you will have the opportunity to work with a team of exceptional professionals and play a vital role in the flawless execution of manufacturing batch records, work instructions, and SOPs. Your keen attention to detail and proactive approach will ensure that all tasks are completed right the first time. Additionally, you will assist in maintaining the suite, supplies, equipment, logbooks, and data to strict cGMP standards, contributing to the success of our manufacturing operations. A day in the Life: Execution of manufacturing batch records, work instructions and/or SOPs, with focus on proactive ‘right the first time' executions. Assist with batch record reconciliation. Assist in all Department functions, such as maintaining suite, supplies, equipment, logbooks and data in accordance with site SOPs and policies. Documentation of all activities to meet cGMP requirements. Complete document reviews and revisions. Daily record review, tasks, and databases. Actively provide feedback. Participate/Lead in shift exchanges, 1-1's, meetings, attend meetings as needed to facilitate area needs based on changes, etc. (lean activities). Support a quality investigation by answering questions, providing feedback and making suggestions for improvement. Practices and promotes safe work habits and adheres to safety procedures and guidelines. Critical evaluation of processes, including foresight and thinking ahead. Ensure tasks are performed with a method of prioritization - interpret production schedules and complete tasks accordingly. Keys to Success: Education/Experience: Required: High school diploma or equivalent with +2 years of experience OR Bachelor's Degree Preferred Experience: Experience in a manufacturing, operations, production, lab setting or related field Experience in a cGMP environment Knowledge, Skills, Abilities Knowledge Knowledge of cGMP practices, aseptic techniques, or chemical concepts- preferred Subject Matter Expert on processing steps- preferred Skills Critical thinking and problem solving Strong math skills Detail oriented Results Driven MS Office Qualified to train other employees- preferred Abilities Able to demonstrate practical knowledge with successful outcomes Able to recognize problems developing, not just occurring Able to read, write, and communicate in English Able to understand and carry out instructions Reliable Effectively multi-task Able to work in an environment of change Able to work independently and as part of a team Physical Requirements / Work Environment Be willing to wear a full gowning suit which includes: bodysuit, gloves, hair & beard nets, face covers, and safety glasses. (These items are prohibited: makeup, jewelry, nail polish, cologne / perfume, scented lotions or hair care products, etc.) Able to adhere to clean room gowning requirements, including wearing Tyvek, Nitrile, and/or Latex gloves Ability to lift minimum of 25 lbs independently Ability to stand for 80% of shift Join Thermo Fisher Scientific and be part of our ambitious team that strives for excellence in everything we do. We are an equal opportunity employer, committed to fostering an inclusive and diverse workforce. We value the unique perspectives and contributions of all individuals and actively encourage candidates from all backgrounds to apply. To apply, please visit our career website at ***************************** Thermo Fisher Scientific Inc. is an EEO/Affirmative Action Employer and provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. If you require any accommodations during the application process due to a disability, please contact us at ***************. We are here to support you and ensure that you have an equal opportunity to succeed. This telephone line is reserved solely for applicants with disabilities requiring accessibility assistance or accommodations. Messages left for other purposes will not receive a response.

Are you ready to embark on a career where innovation meets excellence? At Jost Chemical Company, we're on a mission to push the boundaries of chemical manufacturing, delivering high-quality products that make a positive impact on global industries. If you're passionate about chemistry, dedicated to precision, and eager to contribute to a company that values both innovation and integrity, explore our exciting job opportunities. Join us in shaping the future of chemical manufacturing at Jost Chemical Company, where your career is more than just a job - it's a journey of growth and achievement. Then, this position is right for you! Founded in 1985, Jost Chemical is a global leader in the manufacture of high purity mineral salts for the nutritional, pharmaceutical and specialty markets. Expansion, growth of capabilities, and investment in people, lab and production equipment have been a part of Jost's company culture for 35 years. To learn more about Jost Chemical please visit ******************** Our offer: * Shift Differential * Medical/Dental/Vision Plan Insurance, Short and Long-Term Disability and Life Insurance first of the month following 60 days. * 401k plan which includes safe-harbor contribution and discretionary match. * Paid Time Off (PTO) Employees eligible first day of employment. * 9 Company Paid Holidays (72 hours) each year. * Uniforms Provided * Foot Protection- annual allowance for all laboratory, maintenance and production employees. * 24-hour access to our free, on-site fitness center. * We provide Individual development, on-the-job training, and development programs designed to enhance your professional growth and development while ensuring you feel valued, inspired and appreciated at work. Jost Chemical is an equal opportunity employer and affirmatively seeks diversity in its workforce. We consider applicants, and make all employment decisions, without regard to race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, or any other legally protected status. We are committed to recruiting and retaining the best talent in the chemical manufacturing industry. Background * Works under general direction of the Quality Control Manager in a c-GMP regulated manufacturing environment operating under Q7A standards. * Employees in positions at this level of the series exercise a considerable degree of independence in conducting a wide range of experiments requiring expertise in the application and adaptation of numerous research techniques and produce desired results. Tasks * Perform analytical testing using wet chemistry techniques and instrumentation on c-GMP regulated products following compendial methods (USP/NF, EP, FCC, JP etc). * Perform microbiological testing on c-GMP regulated products using compendial methods. * Perform routine and non-routine testing using basic and advanced laboratory instrumentation and adhere to a strict calibration / preventative maintenance program. * Interpret analytical data and assist chemical operators and chemical engineers with applying this data to the manufacturing process. * Write research methods, results, and conclusions for publication; may present at professional conferences. * Review scientific literature, abstracts, and applicable method papers; identify appropriate application for current or anticipated research projects. * Maintain data integrity in both written and digital form. * Prepare laboratory test solutions and perform standardizations of volumetric solutions. * May be required to inventory and order laboratory supplies, instruments, and reagents. * Maintain a clean and organized work area. * Maintain and enhance site safety. * Instruct other personnel in specific areas of quality control laboratory testing. * Data mining and trending; Process Validation support; Root Cause Analyses; Problem Solving Tools use; Statistical Data trending; Support for Non-conformance Investigations; Production support activities. Specifications * A.S or B.S. Chemistry or related technical field that included instrumentation, or industry experience. * 0-2 years professional level chemist experience. Knowledge of: * Theories, principles, and methods of instrumental and wet chemistry * Method development and method validation * Mathematics and statistics * Basic analytical laboratory equipment * MS Office software package Skill in: * Working effectively and efficiently on multiple projects at once * Working effectively in a team environment * Responding to rapidly changing demands Ability to: * Lead and/or train others in assigned activities * Follow compendia and other test methods * Develop creative solutions to more varied research procedural problems * Design and manage projects * Identify, gather, process, and record data accurately * Maintain quality, safety, and/or infection control standards * Operate and maintain laboratory equipment * Communicate effectively, orally and in writing (including documenting research methods, results, and conclusions) * Exercise independent judgment

Clarkson Construction Company is a leading firm in the heavy civil construction industry, with a proud history of delivering complex infrastructure projects across the Kansas City region. Our portfolio spans grading, paving, and bridge construction, underscoring our commitment to excellence and innovation. Clarkson Construction Company offers a supportive and dynamic work environment where innovation and hard work are recognized and rewarded. We believe in investing in our employees through professional development and advancement opportunities. Join us and be a part of a team that shapes the infrastructure in and around one of America's most vibrant cities. Job Summary: The Senior Quality Technician plays a vital role in ensuring materials and construction processes meet all project and agency specifications for MoDOT and KDOT projects. This position performs and oversees testing and inspection of concrete, aggregates, soils, and cement-treated base in both field and laboratory environments. The Senior Quality Technician verifies compliance with contract documents, leads and mentors other technicians, and supports Quality Control Managers in implementing Clarkson's quality management program. This role requires strong technical knowledge of materials testing procedures, field inspection practices, and agency documentation standards. The ideal candidate will be comfortable working independently on active construction sites, coordinating directly with project engineers, superintendents, and client representatives to address quality concerns in real time. Essential Functions / Responsibilities: Perform and lead field inspections and materials testing for concrete, aggregates, soils, asphalt, and cement-treated base in accordance with MoDOT, KDOT, ASTM, and AASHTO procedures. Inspect rebar placement, formwork, subgrade preparation, and material delivery to verify compliance with approved plans and specifications. Conduct field testing such as moisture/density (nuclear gauge) and plastic concrete properties, ensuring timely and accurate results. Review and interpret test data and inspection results, identify deviations from specifications, and recommend corrective actions as needed. Train and mentor Quality Technicians in approved test procedures, equipment operation, calibration, and proper documentation. Coordinate with Project Managers, Superintendents, and client representatives to ensure timely communication and resolution of quality-related issues. Oversee collection and submission of test results, inspection reports, and documentation through company systems, or equivalent platforms. Assist Quality Control Managers with implementation of project-specific quality plans, materials documentation, and agency submittal requirements. Maintain, calibrate, and verify testing equipment to ensure reliability and accuracy of results. Support continuous improvement initiatives by identifying opportunities to enhance testing efficiency, accuracy, and safety practices. Demonstrate leadership in maintaining safe work practices and compliance with OSHA, Clarkson safety policies, and PPE requirements. Stay current with MoDOT and KDOT material testing procedures and certification requirements, participating in ongoing training and recertification as needed. Perform other related duties as assigned to support overall project quality and success. Knowledge, Skills, and Abilities: Comprehensive understanding of MoDOT and KDOT specifications and testing procedures for concrete, asphalt, soils, aggregates, and cement-treated base materials. Hands-on experience performing field inspections and quality testing, including concrete testing, rebar inspection, subgrade evaluation, density testing, and mix verification. Ability to interpret construction plans, standard drawings, and material specifications to ensure conformance and document field conditions accurately. Proficient in analyzing test results, identifying deviations from specification, and implementing corrective measures with project teams. Strong documentation and reporting skills, including completion and submittal of test forms, inspection reports, and daily summaries in compliance with project and agency standards. Effective communication and coordination skills to interface with contractors, engineers, and project management on quality-related matters. Leadership ability to mentor and train technicians on approved testing methods, safety procedures, and documentation practices. Proficiency in Microsoft Office (Excel, Word, Outlook) and familiarity with digital data management and document control systems. Commitment to safety, accuracy, and continuous improvement, promoting a culture of quality and accountability in all testing and inspection activities. Ability to work independently in the field, manage multiple testing priorities, and adapt to changing site and schedule conditions. Other Responsibilities: Report to work on time and prepared for scheduled assignments. Communicate any absences or delays to the supervisor as early as possible. Travel to local jobsites as required. Successfully pass a pre-employment drug screening and background check. Qualifications Requirements: High School Diploma or GED. Basic computer skills including Excel, Word, and Outlook. KDOT/ MoDOT Certifications ACI Concrete Certification Nuclear Gauge Certification Physical Requirements and Working Environment: Ability to sit, climb, balance, stoop, kneel, crouch or crawl, walk, stand; Able to frequently lift and/or move up to 10 lbs. and lift and/or move up to 50 lbs. This position requires in-person work. Work is often performed next to live traffic, in outdoor weather conditions, with and around large heavy civil construction machinery. Work is also performed in a lab setting. May be exposed to extreme outdoor weather conditions. Must be willing to work non-traditional hours, including night shifts and overtime, as assigned.

Essential Job Functions: * Adhere to all health and safety policies/procedures, Good Manufacturing Practices (GMPs) and wear the required personal protective equipment (PPE) while in the warehouse or production areas (including but not limited to hairnets/beard nets, safety glasses, hearing protection, hard toe and slip/oil resistant shoes, appropriate safety gloves, and seatbelts while operating forklifts). * Responsible to adhere to food quality and food safety as per the standard(s) provided by corporate, customer, and/or governing bodies (ex. SQF). * Ensure all products being run conform to the customer product specifications as outlined in SAP system, and conduct analysis on raw deliveries, finished batches and treated water. * Conduct chemical and physical analysis on raw and intermediate processing materials including packaging materials and determine status of materials as acceptable or unacceptable. * Evaluate finished products against current standards by performing audits to monitor all aspects of finished product and packaging integrity. * Investigate all out of specification conditions and make recommendations for corrective action and document. * Enter data into and confirm batches in SAP. * Check process control parameters to assure proper equipment application and operation is being maintained by performing secure seal, closure torque and seaming checks. * Effectively perform BBSO audits and provides feedback to the employee observed. * Can send professional emails as required to provide effective communication to all levels of the organization. * Understands how to generate a Process Order (COR1) and print batch sheet in emergency situations with Manager approval. * Stop any production which may be questionable in terms of Food Safety and immediately alert a member of the management team. * Maintain accurate, legible records of all tests and retests performed. Complete all other required reports (work orders, action reports, etc.) in a timely manner. * Perform analytical tests required to qualify ingredient batches for production. * Perform production line checks at specified intervals. * Ensure accurate test results by maintaining proper operation and calibration of laboratory equipment. * Maintain laboratory cleanliness at all times. * Report all out of specification results to designated leadership. * Complete special projects and other reasonable duties as assigned by leadership. * Has demonstrated Tier I skills have been sustained at an acceptable level with limited supervision. Required Skills: * Working knowledge of Excel, Word, and SAP preferred. * Exposure to using measurement tools and equipment (e.g., calipers, micrometers, CMM machines) preferred. * Organized and detail oriented, adaptable to change. * Ability to apply statistical methods to analyze data and identify trends. * High level of precision and accuracy in inspection and testing processes. * Familiarity with ISO, Six Sigma, GMP, and other relevant standards and regulations * Understanding of Food Safety Requirements. * Able to read and understand metric system.

Why Us? We want the best and brightest people to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life. Summary Depending on the laboratory area, will perform analysis on Raw Materials, Intermediates, In-Process, Finished Product, or Stability samples using established analytical methods. Job Description ESSENTIAL FUNCTIONS: Follow good documentation practices for the accurate and timely documentation of all activities. Perform wet chemistry and instrumentation testing. Follow site HSE Policies. Assist with establishing and maintaining safe work standards in the lab. Peer review all levels of work. Conducts lab investigations. DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS: LIMS entry of data Use of analytical balances, HPLC, GC, KF Titrator, UV, pH Meter Maintain instrument readiness MINIMUM REQUIREMENTS: Education: High School Diploma required, associate degree in a science related field or equivalent combined education, experience, and competencies preferred. Experience: Experience in a cGMP environment is preferred. Working knowledge of instrumentation preferred. Preferred Skills/Qualifications: Working knowledge of wet chemistry required Working knowledge of instrumentation (GC/LC, UV, AA). Experience in a cGMP environment is preferred. Basic computer skills and familiarity with Microsoft Office Suite. Substantial acquaintance with and understanding of application of basic principles, theories and concept. Use and/or Basic knowledge of industry practices and standards. Chromatography (GC/LC) and Spectroscopy experience a plus. COMPETENCIES: Informing, Customer Focus, Listening, Perseverance, Organizing, function/technical skills, Peer Relationships, Comfort around Higher Management ORGANIZATIONAL RELATIONSHIP/SCOPE: Contacts involve matters of moderate importance to the organization and include R&D, Marketing, Production employees including Engineers, Supervisors, and Operators, Logistics, EHS, and DEA. Infrequent customer contacts on routine matters. WORKING CONDITIONS: 80% Laboratory exposure to plant products, solvents and reagents, some of which are hazardous or potent compounds. 20% Office environment. Required to work 8-12 hour shifts, the potential for night, weekend, and holiday work depending on the lab DISCLAIMER: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills require EEO Statement: We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. 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.

Job Description Clarkson Construction Company is a leading firm in the heavy civil construction industry, with a proud history of delivering complex infrastructure projects across the Kansas City region. Our portfolio spans grading, paving, and bridge construction, underscoring our commitment to excellence and innovation. Clarkson Construction Company offers a supportive and dynamic work environment where innovation and hard work are recognized and rewarded. We believe in investing in our employees through professional development and advancement opportunities. Join us and be a part of a team that shapes the infrastructure in and around one of America's most vibrant cities. Job Summary: The Senior Quality Technician plays a vital role in ensuring materials and construction processes meet all project and agency specifications for MoDOT and KDOT projects. This position performs and oversees testing and inspection of concrete, aggregates, soils, and cement-treated base in both field and laboratory environments. The Senior Quality Technician verifies compliance with contract documents, leads and mentors other technicians, and supports Quality Control Managers in implementing Clarkson's quality management program. This role requires strong technical knowledge of materials testing procedures, field inspection practices, and agency documentation standards. The ideal candidate will be comfortable working independently on active construction sites, coordinating directly with project engineers, superintendents, and client representatives to address quality concerns in real time. Essential Functions / Responsibilities: Perform and lead field inspections and materials testing for concrete, aggregates, soils, asphalt, and cement-treated base in accordance with MoDOT, KDOT, ASTM, and AASHTO procedures. Inspect rebar placement, formwork, subgrade preparation, and material delivery to verify compliance with approved plans and specifications. Conduct field testing such as moisture/density (nuclear gauge) and plastic concrete properties, ensuring timely and accurate results. Review and interpret test data and inspection results, identify deviations from specifications, and recommend corrective actions as needed. Train and mentor Quality Technicians in approved test procedures, equipment operation, calibration, and proper documentation. Coordinate with Project Managers, Superintendents, and client representatives to ensure timely communication and resolution of quality-related issues. Oversee collection and submission of test results, inspection reports, and documentation through company systems, or equivalent platforms. Assist Quality Control Managers with implementation of project-specific quality plans, materials documentation, and agency submittal requirements. Maintain, calibrate, and verify testing equipment to ensure reliability and accuracy of results. Support continuous improvement initiatives by identifying opportunities to enhance testing efficiency, accuracy, and safety practices. Demonstrate leadership in maintaining safe work practices and compliance with OSHA, Clarkson safety policies, and PPE requirements. Stay current with MoDOT and KDOT material testing procedures and certification requirements, participating in ongoing training and recertification as needed. Perform other related duties as assigned to support overall project quality and success. Knowledge, Skills, and Abilities: Comprehensive understanding of MoDOT and KDOT specifications and testing procedures for concrete, asphalt, soils, aggregates, and cement-treated base materials. Hands-on experience performing field inspections and quality testing, including concrete testing, rebar inspection, subgrade evaluation, density testing, and mix verification. Ability to interpret construction plans, standard drawings, and material specifications to ensure conformance and document field conditions accurately. Proficient in analyzing test results, identifying deviations from specification, and implementing corrective measures with project teams. Strong documentation and reporting skills, including completion and submittal of test forms, inspection reports, and daily summaries in compliance with project and agency standards. Effective communication and coordination skills to interface with contractors, engineers, and project management on quality-related matters. Leadership ability to mentor and train technicians on approved testing methods, safety procedures, and documentation practices. Proficiency in Microsoft Office (Excel, Word, Outlook) and familiarity with digital data management and document control systems. Commitment to safety, accuracy, and continuous improvement, promoting a culture of quality and accountability in all testing and inspection activities. Ability to work independently in the field, manage multiple testing priorities, and adapt to changing site and schedule conditions. Other Responsibilities: Report to work on time and prepared for scheduled assignments. Communicate any absences or delays to the supervisor as early as possible. Travel to local jobsites as required. Successfully pass a pre-employment drug screening and background check. Qualifications Requirements: High School Diploma or GED. Basic computer skills including Excel, Word, and Outlook. KDOT/ MoDOT Certifications ACI Concrete Certification Nuclear Gauge Certification Physical Requirements and Working Environment: Ability to sit, climb, balance, stoop, kneel, crouch or crawl, walk, stand; Able to frequently lift and/or move up to 10 lbs. and lift and/or move up to 50 lbs. This position requires in-person work. Work is often performed next to live traffic, in outdoor weather conditions, with and around large heavy civil construction machinery. Work is also performed in a lab setting. May be exposed to extreme outdoor weather conditions. Must be willing to work non-traditional hours, including night shifts and overtime, as assigned.