Quality control analyst jobs in Columbia, MO

· Coordinate the day to day activities in the Sample Management laboratory · Provide sample tracking and management, tests tracking and timelines and documentation management support to testing laboratories · Maintain a sample inventory program · Report sample metrics on a regular basis · Creation and revision of protocols and SOPs · Maintenance of temperature controlled units · Capable of conducting in depth, complex investigations including and ability to articulate the investigation clearly in writing for submission to the QA group · Use of laboratory and operational software such as LIMS and BMS · Review sample Management documentation in a timely manner Skills: · Some Team Lead and/or Supervisory experience. · Attention to detail, good organizational and interpersonal skills, and problem solving skill. · Ability to prioritize and work under pressure. · Ability to work effectively and to respond quickly in a fast paced environment. · Knowledge of SAP, MS Work and Excel. Qualifications Education: · Bachelor's degree in Life Sciences Additional Information All your information will be kept confidential according to EEO guidelines.

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: Join our St. Louis Cherokee facility at MilliporeSigma, a leading contract development and manufacturing organization (CDMO) and a recognized Center of Excellence for antibody-drug conjugate (ADC) manufacturing. We are seeking passionate and enthusiastic professionals to contribute to our innovative bioconjugate production, leveraging over 35 years of expertise in the field. As a vital part of our dedicated team, you will play a key role in delivering high-quality ADCs that improve the quality of life for patients suffering from cancer and other debilitating diseases. With our state-of-the-art technologies and commitment to excellence, you will ensure the highest standards of quality and compliance in our ADC manufacturing processes. As an Associate Production Scientist - Rotating Shift you will manufacture products according to established protocols under ICH Q7 pharmaceutical regulations, provide technical support to others and perform operations in support of the group and department. Relocation Options Available Job duties include: * Evaluate products per established protocols, providing technical support and performing operations to meet departmental goals. * Safely conduct routine processes and unit operations, including cleaning equipment and work areas, while ensuring quality expectations. * Maintain required training and qualifications, train team members, and act as a technical consultant. * Support facility functions by maintaining equipment, preparing reagents, restocking supplies, and managing waste disposal. * Maintain accurate records and logbooks according to quality guidelines, communicating operational status and concerns to supervision. * Collaborate with other departments, participate in quality audits and customer interactions, and perform procedures independently or in a team. * Improve processes using scientific knowledge and principles, ensuring compliance with change control. * Address unsafe conditions promptly and troubleshoot challenges related to biological processes and GMP compliance. Physical Attributes: * Ability to lift to 50lbs. * Ability to wear personal protective equipment, such as respirator or chemical protective clothing, for extended periods. * Expected on-floor time: (70%) Who you are: Minimum Qualifications: * Bachelor's Degree in a scientific discipline (e.g., Chemistry, Biochemistry, Biology, etc.) * 2+ years industry Production/Laboratory experience * 1 + yeass experience with Antibody Drug Conjugates (ADCs), including knowledge of their formulation and manufacturing processes. Preferred Qualifications: * Experience with Automated Tangential Flow and Automated Chromatography systems. * Familiar with laboratory instruments and production equipment * Familiarity with process techniques, unit operations, and safe chemical handling methods. * Experience with Microsoft Office (Word, Outlook, Excel, etc.). * Mechanical and troubleshooting skills. * Knowledge of cGMP and ICH Regulatory and Quality standards. * Knowledge of Operational Excellence. * Clean room experience * Ability to interact professionally in customer-facing meetings, including challenging discussions on process planning and process execution RSREMD Pay Range for this position: $25.00 - $45.00 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 Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Laboratory Analyst II - Creve Coeur, Missouri Laboratory Analyst II: As a Laboratory Analyst II, you are an integral part of the high-throughput Global Quality Seed Testing Laboratory, supporting Bayer's Product Supply Organization and collaborating with key customers and colleagues across various functions. Your role involves the timely and accurate preparation, evaluation, and recording of seed analyses, ensuring compliance with Bayer's Environmental, Safety, and Health (ESH) policies, Laboratory Quality Management System (QMS), and regulatory requirements. You will participate in the Management of Change process, contribute to continuous improvement initiatives, and engage in Bayer's Environmental, Safety, and Health safety program and cross-site projects. YOUR TASKS AND RESPONSIBILITIES: Prepare, evaluate, and record seed analyses accurately and timely; Complete testing processes under the guidance of peers within squads, E2E, and Unit Leads. This role involves ensuring process controls and effective data management throughout all testing phases. Additionally, the Lab Analyst is expected to facilitate timely problem-solving and error correction as issues arise, thereby contributing to a smooth and efficient workflow within the laboratory; Troubleshoot testing processes and ensure appropriate error resolution; Aid in training new Lab Analysts; Learn and apply scientific methods and non-routine techniques for analysis as directed by protocols and work instructions, including preparation of reagents, media, controls, and sample preparation; Participate in the Management of Change process and updates of testing protocols and work instructions; Work independently within a team environment to ensure compliance with Bayer ESH policies, Laboratory QMS, and regulatory requirements; Provide oversight and task-related feedback to contingent labor; Maintain inventory levels of reagents and consumables; Participate in special projects and teams; Engage in continuous improvement programs to enhance processes and perform root cause analyses and troubleshooting; Actively engage in one PSS programs and initiatives; Participate in Bayer's ESH safety program and cross-site projects and initiatives. WHO YOU ARE: Bayer seeks an incumbent who possesses the following: Required Qualifications: High School Diploma or GED; Flexibility to change shift hours, with weekend and overtime work as required. Preferred Qualifications: Minimum of five years of lab experience with a high school diploma or GED: Bachelor's degree with 0 years of lab experience, or an Associate of Arts (AA) or Associate of Science (AS) degree with two years of lab experience; Strong knowledge of basic laboratory techniques; Fluent in English with the ability to read, write, and speak effectively; Proficiency in Microsoft Office Suite; Ability to work as a team member and effectively communicate within a multicultural environment; Detail-oriented with the ability to multitask in a high throughput environment. Posting will be available until October 22, 2025. Employees can expect to be paid an annual salary range of $47,235.20 - $70,852.80. Additional compensation may include a bonus or commission (if relevant). Other benefits include health care, vision, dental, retirement, PTO, sick leave, etc. If selected for this role, the offer may vary based on market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location: United States : Missouri : Creve Coeur Division: Crop Science Reference Code: 854774 Contact Us Email: hrop_*************

JOB SCOPE: The Quality Control Technician is to be proficient in ensuring quality products and processes are being implemented at Diamond Pet Foods. The Quality Control Technician's overall responsibility, and objective, is to ensure that all aspects of the SQF, Quality, and Food Safety programs are followed by all employees, vendors, and visitors. WORK ENVIRONMENT: Work is performed primarily indoors in an office setting, but employees may be outdoors and near operating equipment, loud noises, and loose particles. Work performed requires employees to operate in all different temperatures/weather, heights, and dusty areas. Long periods of sitting and standing may be required. Employees are required to wear a bump cap, hearing protection, safety shoes/boots, and safety glasses at all times in production areas. DUTIES AND RESPONSIBILITIES: Routinely check paperwork for accuracy and completeness, as well as labels, bags, and seals. Assure checks are clear, documented, legible, and traceable. Notify plant personnel and supervisors on any reports that may negatively impact the quality of the product. Dispose/reject affected product and perform follow-up testing until issue is resolved. Conduct various tests on incoming ingredients for sieve, NIR, moisture, and mycotoxin. Collect routine ingredients and finished samples, as required. Promptly respond to calls for assistance or quality concerns with clear communication. Be a resource and assist in the training and education of new employees. Understand and comply with all Standard Operating Procedures (SOPs), GMP's, and HACCP. Working overtime is MANDATORY and requires full participation. Keep lab, scale, and work areas clean. Maintain assigned portion of master sanitation schedule. Report all safety violations and hazards to the supervisor immediately and participate in all safety programs and procedures. Must always wear PPE when required. Other duties and responsibilities as required or assigned by the supervisor to be accepted with a positive and professional attitude. QUALIFICATIONS: Must hold a valid driver's license. Successful completion of pre-employment screening (drug screen, background check, and physical.) Must be able to lift at least 50 pounds, climb, squat, bend, pull, push, kneel, crouch, etc. Ability to be trained and certified to operate forklifts.

Job Description JOB TITLE: Quality Assurance Associate Founded in 1940 by Sam Young and now led by Jordan Young, Fairfield Processing takes great pride in its rich history as a third generation, family-owned and operated American business providing innovative products and brands to its consumers. Fairfield has built strong consumer loyalty over the decades by delivering consistent, quality products at good value - all with an unconditional guarantee. Working for Fairfield is like being part of a family. Because we believe in you and what you will contribute to our vision, we want the best for you. We understand that what a company has to offer in respect to their Benefit Package can play a major role in the employment decision-making process. That is why we have made it a priority to seek out the best possible benefits for our employees. Benefits Offered: Medical Vision Dental Prescription Plan 401 (k) 9 paid holidays and much more Come join our team! As a Quality Assurance Associate, you will play a crucial role in ensuring that our products meet the highest standards of quality and reliability. You will work closely with the Quality Assurance Supervisor to conduct thorough inspections, tests, and evaluations of our products at every stage; from receiving to delivery. Your attention to detail and commitment to precision will contribute to building and maintaining Fairfield's reputation for excellence in the manufacturing industry. Schedule: 1st Shift: Monday - Friday 6AM-2:30PM, Full-Time, 40 hours per week (overtime may be required when needed.) Schedules are subject to change based on the needs of the operation. 2nd Shift: Monday - Friday 3PM-11:30PM, Full-Time, 40 hours per week (overtime may be required when needed.) Schedules are subject to change based on the needs of the operation. Pay Range: DOE Essential Duties (Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) Complete assigned inspection tasks, ensuring these tasks are reported using the mandated inspection templates, and, when necessary, reorganize tasks to meet deadline changes and updates as communicated by the Plant management team and Quality Assurance Supervisor. Stay constantly up to date on the Quality Manual and Procedures, use of templates, etc. Participate as requested in samples production with the sales and manufacturing teams, as well as managing samples inventory and catalog, including samples disposal calendar. Submit inspection reports to Quality Assurance Supervisor for escalation and suggest corrective actions to the Department management. Participate in the analysis of inspection reports using the Quality SharePoint archive, or other such digital system described in the Quality Manual and Procedures Help maintain vendor scorecards and report to management. Comply with all OSHA safety requirements. Ensure company policies & procedures are followed. Meet all assigned goals and assist others in accomplishing their goals. Education and Qualifications: High school diploma or vocational/technical certification. Must have skills for mathematics and detail. Knowledge of standard quality management tools and systems (MIL-STD, ISO9001) a plus. Strong verbal and written communication skills. Demonstrate strong ability to operate handheld computers and tablets. Knowledge of Enterprise Resource Planning systems and Oracle NetSuite are preferred. Fairfield Guiding Principles Make Products We Want to Use | Operate with Integrity | Strike a Lifestyle Balance | Promote the Giving Spirit Fairfield Processing Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, national origin, gender, sexual orientation, gender identify, age, disability, protected veteran status or any other status protected by law. EEO is the Law.

Want to work for a company that supports and invests in its employees? Cosmos Corporation has a healthy workplace culture guided by a clear vision, mission, promise, and values! Our culture is intentionally fostered daily by how employees live out our values. The result is a place where employees genuinely enjoy coming to work every day! Cosmos Corporation is a recognized leader in natural health, wellness, and care products. Cosmos creates and distributes people and pet-approved liquid products with the most responsible, effective, high-quality ingredients people trust. Our brands bring innovative products with unique benefits that help people and pets look and feel their very best. We do all of this at our headquarters located in O'Fallon, Missouri. We are looking for a new ideal team player as a process chemist to join the Formulation Team! The Process Chemist is responsible for developing, optimizing, and implementing robust manufacturing processes and formulas to support product development and production. The role involves creating and maintaining master mixing records, conducting pilot and bench batches, troubleshooting with Quality Control, and collaborating with Engineering, Maintenance, and other teams to ensure process efficiency and compliance. This position provides technical support across departments, ensures adherence to GMP and safety practices, and contributes to continuous process improvements to enhance product quality and manufacturing performance. You Key Responsibilities Will Be: Develop, optimize, and scale up robust manufacturing processes for all formulations. Create and maintain master mixing records and documentation for new and existing products. Conduct bench and pilot batches to support formulation and initiation to the mixing team. Collaborate with Quality, Engineering, and Operations to troubleshoot issues and improve efficiencies. Provide technical support across teams and drive continuous improvements in process, quality, and safety. Requirements 5 years of related experience Superior math mathematical skills Excel at problem solving. Excels at computer skills. Experience with formulation in finished goods Bachelor's degree in chemistry, chemical engineering, or related science Your Competencies & Skills You Hold Are as Follows: Collaboration & Communication Team player Analytical & Critical Thinking Skills Technical Proficiency Data Driven Mindset Process & Scale-Up Expertise. Attention to Detail Innovation & Continuous Improvement Ingredient & Formulation Knowledge Adaptability & Learning Agility Safety & Compliance Mindset A Day In the Life At Cosmos: No two days look the same. You might start in the lab running a bench batch to evaluate a new formula, then move to the plant floor to oversee a pilot batch and ensure scale-up parameters align with production equipment. Midday could be spent troubleshooting a manufacturing issue with Quality Control or working with Engineering on process improvements. You will update and refine master mixing records, review data for accuracy, and provide technical guidance to cross-functional teams. Along the way, you will balance hands-on experimentation with problem-solving-leveraging data, technology, and collaboration to keep product quality, efficiency, and innovation at the forefront. Every Wednesday, you will head to the lunchroom at 11:40 a.m. for the weekly Cosmos Minute, where the entire company meets at 11:45 a.m. to learn about other team members and special company announcements at Cosmos. What's In It For You? At Cosmos Corporation we truly care about investing in our employees, these are the benefits and perks at Cosmos! Medical Health Insurance Dental Insurance Vision Insurance Life Insurance Short- & Long-Term Disability Insurance Flexible Spending Accounts Critical Illness Accident Coverage 401(k) Contribution Robust Employee Assistance Program Vacation Time Off 8 Paid Holidays (and sometimes more!) Paid Sick Leave 5 Paid Mission Days Parental Leave Maternal Leave Growth & Development Opportunities Lunch & Learns Employee Referral Bonus Program Cosmos Cash Recognition Program Better Book Club Excellent Culture So much more!! Equal Opportunity Employer Cosmos Corporation is an equal-opportunity employer. We prohibit discrimination and harassment of any kind. Cosmos Corporation makes hiring decisions based solely on qualifications, merit, and business needs at the time. Salary Description $75,000 - $85,000 Per Year

Who are we? Jet Midwest is a full-service commercial aviation company, specializing in the sale and lease of commercial aircraft, engines, and parts as well as aircraft maintenance, repair, and overhaul services to the aviation industry. Position Description: Title: Quality Control Technician Status: Full Time Department: Operatives Summary: The role of Quality Control Technician is directly responsible for Receiving inspections, reviewing and disposing of Return Material Authorizations, Warranty Claims and communications with FAA Certified Repair Stations as well as Jet Midwest Sales and Quality personnel. In addition, the role is responsible for receiving, inspection and reviewing all RMA/Warranty returns, tracking RMA through full disposition, and reviewing and approving re-stocking fees per Warranty Claims. An important responsibility for this role is to act as a liaison with FAA Certified Repair Shops for review and rebuild of RMA material, with Sales Reps for disposition and review of all RMA's, with Purchasing/Repair Reps for disposition of RMA's and to review RMA/Inventory for compliance to FAA/ASA-100 Lead Auditor for ASA-100 & ISO 9001 Quality Systems. Essential Duties & Responsibilities included, but not limited to: Perform preliminary, hidden-damage, in-process, and final inspection on civil aviation articles in accordance with the current maintenance data Ensure that tools and equipment used to make airworthiness determinations are labeled in accordance with the manual Perform incoming review to identify, control, segregate, and maintain all materials according to the manufacturer's requirements or standard industry practices Perform evaluations of various aircraft components I.A.W. current tech data. Perform the initial self-evaluation of work and ensure internal forms and Capability evaluations are completed accurately. Ensure proper documentation has been completed and signoffs performed as required Perform or witness test procedures as required by applicable work instructions, company policies, FAR's, or CMM's Monitor and verify quality in accordance with manuals, instructions, engineering drawings, and any other applicable documentation and work instructions in accordance with regulatory requirements Support training and development activities as needed Maintain maintenance documentation libraries Assist with the acquisition and interpretation of maintenance manuals and work instructions Some after-hours support on evenings and weekends will be required Education & Experience: You have High School Diploma and 3 years minimum of experience in a similar role within the aviation industry You have a minimum of 5 years of experience as a working A&P working on heavy commercial aircraft (Boeing 757, 767, 777, Airbus A330, A320) and associated components You can demonstrate working knowledge of aircraft modifications and documentation requirements You are thoroughly familiar with the inspection methods, techniques, practices, aids, equipment, and tools used to determine the airworthiness of the article on which maintenance, preventive maintenance, or alterations are being performed You have a high-energy personality and desire to learn and grow quickly Can demonstrate a strong track record of excellent decision-making and collaborative work You possess excellent, polished communication skills You can demonstrate proficiency in using the various types of inspection equipment and visual inspection aids appropriate for the article/s being inspected You can read, write, and speak the English language fluently Physical Demands & Work Environment: While performing the responsibilities of the Quality Technician, you will be seated at a desk, using a phone and computer, for much of your workday. When fulfilling inspection duties, physical requirements may include walking long distances, crouching, crawling, standing on ladders or scaffolds, using hoists and lifts, using precision instruments, and other necessary hand tools requiring manual dexterity and visual acuity. These job duties may be performed indoors in a climate-controlled environment, or outdoors in a variety of weather conditions (when safe). This job description is intended to convey information essential to understanding the scope of the Quality Control Technician position and is not intended to be an exhaustive list of knowledge, skills, ability, efforts, duties, responsibilities or working conditions associated with the position. Reasonable accommodations may be made to enable individual with disabilities to perform the essential functions of the job. EOE M/F/D/V Benefits: Eligibility for our comprehensive benefits program starting the 1st of the month after 30 days of full-time employment 401K with company match Robust Paid Time Off 10 paid Holidays Growth opportunities

Benefits: 401(k) Bonus based on performance Flexible schedule Training & development Doping Control Officer I or II (DCO I or DCO II) USADA is seeking a dedicated and driven person to help our organization fulfill its mission to "Stand with athletes to champion their right to clean sport, inspire true and healthy sport, and promote the integrity of sport.” This is an incredibly exciting time to join Team USADA, as we continue to grow our Anti-Doping program and work to support major international competitions such as the Olympic and Paralympic Games in 2026 (Milan), and 2028 (Los Angeles). New team members will have the chance to help ensure USADA is well-positioned in the near and long term for these opportunities as we look to the future with our efforts to protect clean athletes. With the 2028 Games on domestic soil, there will also be opportunities and growth potential over the years for USADA team members to underpin the organizing committee's commitment to a clean Games. REPORTS TO: DC Ops Manager & Asst Manager FLSA: Non-Exempt SUPERVISES: N/A Last revised: July 2025 LOCATION: St. Louis, MO (Must reside w/in 50 miles) Anticipated # of Tests/Year: 20-25 JOB SUMMARY: Responsible for sample collection from athletes. Tasks performed by the Doping Control Officer (DCO) include preparation for, execution of and post-collection administration as it relates to Doping Control both at events and in the out-of-competition setting. DCOs are the field facing representatives of USADA. The primary objective of the DCO is to conduct Doping Control throughout the United States, under direction of the Doping Control Operations team, for Olympic, Paralympic, and Client Services testing teams, in support of USADA's mission and vision. The DCO works with the HQ team to uphold USADA's goals of creating and maintaining a fair and healthy environment for all athletes. The role will include both local and national travel to conduct Doping Control assignments. The following job expectations, responsibilities, and qualifications apply to both the DCO I and DCO II positions, however, in order to qualify for a DCO II level, one must have a valid phlebotomy credential in good standing, as further outlined below. A DCO II is able to serve as a doping control officer that can draw blood. RESPONSIBILITIES: Conduct sample collection sessions in support of the testing programs for the Olympic/Paralympic, and Client Services testing teams, as well as on behalf of other agencies, when requested by USADA. Accept, plan and manage doping control assignments, in accordance with the minimum requirements of the WADA/International Standards, and any minimum criteria established by USADA. Execute logistics aspects as they relate to the doping control process to facilitate successful completion of missions. Conduct doping control, including processing of Samples, in accordance with USADA's protocols and procedures, and in accordance with the WADA Code/International Standards. Recruit and onboard independent contractors to serve in the capacity of a Chaperone*. *( Chaperones may be required in the event the athlete is a minor and/or if the gender of the DCO is not the same as the gender of the athlete being tested ) Witness sample collection or overseeing the witnessing of the sample collection process. Travel (car, plane, train etc.) to various locations to perform sample collections (by the most economical route). Ensure accurate documentation/completion of the doping control process. Ship and submit processed Samples to the specified WADA certified laboratory. Assist in the onboarding and training of new doping control officers. Accountable to the most current version(s) of the DCO Manual, sample collection. documentation and other training resources. Participate in DCO evaluation and support program, continuing education and re-accreditation. Ensure adequate control of document, record and sample collection equipment. Schedule and manage all travel, as well as associated expense reports. Provide witness testimony in Legal cases, such as whereabout failures, other Anti-Doping Rule Violations. Enforce infection control processes at all times that you are working with equipment or athletes. GENERAL: Maintain confidentiality at all times. Have no affiliation with sample collection organizations outside of USADA. Keep USADA aware of issues in the field and/or any conflicts of interest. Recommend necessary updates and revisions to USADA protocol and procedures as related to Doping Control. Projects and other duties, as assigned. REQUIRED QUALIFICATIONS: Skills: Excellent oral and written communication skills. Excellent organizational skills and attention to detail. Demonstrated high proficiency in utilizing technology such as tablets, multiple software platforms, and various applications. Demonstrated ability to: Make decisions in accordance with USADA's protocol and procedures. Multitask and work accurately under pressure. Interact with internal and external customers professionally and in line with USADA's values. Travel, possibly at short notice, to conduct test assignments. Work flexible hours, as needed. Access the internet for daily communication. Values integrity, respect, and justice among internal and external constituents. Perform effectively and collaboratively in a team environment. Meet deadlines and operate with limited supervision. Stand, bend and lift 50 pounds, on a regular basis. Certification: Successful completion of all USADA certification/recertification requirements. Pass bi-annual written and practical exams. Attend DCO training sessions, meetings, conferences. Valid Driver's License in good standing with state requirements where you reside. Must be fully vaccinated against COVID-19. DCO II Additional Requirements: *National Phlebotomy certification from one of the following accredited agencies: ACA- American Certification Agency (certified on/after July 2003) AMT -American Medical Technologists (certified on/after April, 2003) ASCP - American Society of Clinical Pathology (certified on/after June, 2003) NHA- National Healthcareer Association (certified on/after February 2005) NCCT/MMCI- National Center for Competency Testing (certified on/after February 2003) *Applicants who are certified before the above dates must re-take the certifying examination. **A more advanced, applicable credential such as RN, NP or PA will satisfy this requirement. ***CPT I & II in California are acceptable credentials as they require successful completion of a national exam by one of the certifying bodies outlined above. In addition to a current national certification, individuals will be required to ensure compliance with state specific phlebotomy training requirements for the state in which they reside. At least 3 years phlebotomy experience, preferred. Additional Certification(s): Obtain SafeSport Certification (post-offer) DESIRED QUALIFICATIONS: Work experience in Allied Health Professions w/certification and/or License (Athletic Trainer, Physical Therapist, Registered Nurse, Paramedics, etc.) COMPENSATION & TIME COMMITMENT: Compensation is on a per-test basis(piece rate) for out-of-competition (OOC) missions, with compensation typically ranging from $130 to $180 per test dependent on the test parameters. OOC test sessions can vary in length, but generally take 1 to 2 hours for successful completion. In Competition (event) testing is paid at a daily flat rate, typically at $250 per day. Onboarding is anticipated to begin in December/January with a more significant time commitment up front for training. Expect a time commitment of 24-30 hours of time during the first 60 days of onboarding. After that it should only be 2-3 hours of training and updates per quarter, plus the necessary time to complete test assignments. Compensation: $100.00 - $250.00 per day The U.S. Anti-Doping Agency (USADA) is recognized as the national anti-doping organization for Olympic, Paralympic, Pan American and Parapan American sport in the United States. The recognition tasks USADA with drug-testing and results management responsibilities for these athletes, however USADA is equally dedicated to preserving the integrity of sport through research initiatives and educational programs that inspire a commitment to true sport in the next generation of athletes. Internationally, USADA is at the forefront of the anti-doping movement, considered the gold standard in many areas of anti-doping program management. In addition, our employees are held to the same high standards exhibited by athletes who fully embrace true sport: Integrity, Respect, Teamwork, Responsibility, and Courage. Employees at USADA hold positions in areas including: sport testing, elite-athlete education, drug reference resources, science & research, legal affairs, outreach education (TrueSport), communications, business affairs & finance, and information technology. USADA additionally employs approximately 50 doping control officers stationed throughout the country responsible for collecting athletes' samples. USADA's office is located near the Rocky Mountain foothills of northwest Colorado Springs, Colorado, a city that is home to the United States Olympic & Paralympic Committee and numerous Olympic and Paralympic sport national governing bodies.

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.

The Quality Control Inspector position ensures that the products manufactured by Paul Mueller Company meet the required specifications as directed by company policy, the customer, jurisdictional authority or a combination. This position compares our products to the appropriate specification(s) and/or standard(s) and operates within the limits of company policy and authority delegated by the Quality Assurance Manager. Essential Job Functions * Develop and complete travelers, draft data reports, weld records, and other related project documentation. * Complete and document product inspections and walk-down forms. * Communicate schedule requirements to the Al to ensure data reports are complete on time. * Confirm with manufacturing supervisor that required special testing or documentation is being completed. * Work with the customer's inspection team during FAT as needed. * Verify that the required standards of quality are maintained for the product involved. * Ensure lessons learned applied to future efforts. * Perform other related duties as required and assigned. * Regular, in-person attendance due to necessary teamwork and personal interactive nature of this position. * Overtime may be necessary and required and is dependent on workload. * The ability to work in a constant state of alertness and safe manner. Knowledge, Skills, Abilities (Competencies) * Experience with ASME Code, Section VIII, Division I or equivalent. * Mechanical aptitude with the ability to read and understand manufacturing drawings. * Experience and knowledge of various NDE methods and techniques. * Must be able to work on multiple tasks with little supervision in an organized manner and fast paced environment. * Show initiative to perform duties beyond assignment-specific duties. * Excellent communication skills both orally and written. * Ability to work independently or in a team. * Ability to establish and maintain working relationships with individuals at all levels. * Ability to efficiently utilize Microsoft Office and email. Education and Experience * High school graduate or equivalent required. * Minimum of one (1) year weld inspection experience is preferred. * Knowledge of various fabrication methods and installation procedures; a broad understanding of materials, how to navigate the applicable material specification for characteristics and their tolerances and limitations; and a general understanding of manufacturing equipment and systems Base Compensation Range: $20.13 - $30.20 per hour Variable Compensation Range: Incentive bonus eligibility up to 10% of gross annual salary base on company performance (as of 2024). Health and Ancillary Benefit Overview: * Medical, Dental & Vision Insurance with low employee premiums * Free off-site medical clinic * Company paid Life Insurance & Short-Term Disability * 401k - Employer match of up to 4.0% for coworker contributions of 8.0% or more * Company covers tuition costs up to $5,250.00 annually, contingent on course completion and grades * Paid Time Off and Sick, Family & Parental Paid Time Off * Ten (10) Paid Holidays * Four-day work weeks, varied shifts, and flexible remote work options depending on position * Career progression program for advancement * Free in-house welding, grinding & machine operation school * In-house training program Professional office environment with some time spent in a manufacturing shop. Use of standard office equipment (computers, phones, copiers, and filing cabinets, etc.). Frequent presence on the manufacturing floor as well as field operations. Exposure to conditions, such as: dust, fumes, noise and high-degree varying seasonal temperatures.

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

At Associated Electric Cooperative, we're committed to providing reliable energy to the communities we serve with passion and precision. We're a tight-knit team dedicated to keeping the lights on and the energy flowing smoothly across our expansive network! From technical to operational to professional disciplines, our team brings a wide variety of skills, talents, and expertise to the table. We believe in both dedicating ourselves to excellence and investing in your growth. We are currently seeking applicants for a Chemical Lab Technician 2nd Period in the Chemical Lab of our Power Production division located at our Thomas Hill Energy Center. What You'll Do: Collects, prepares, and analyzes coal samples, water samples, chemical samples, and samples of other materials used in the operation of the power plant. Operates equipment in the laboratory including, but not limited to, sample preparation equipment, laboratory balances, coal analysis equipment, water analysis equipment, and spectrophotometer. Performs routine preventative maintenance and calibration on water and gas monitoring equipment. Adjusts and operates chemical feeding and demineralizing equipment. What You Need: High school diploma or GED required. Must have successfully completed (C average or higher) eight semester hours of college level chemistry and four semester hours of college algebra or higher math. Previous laboratory experience will be considered and is preferred. What Associated provides: We are committed to rewarding talent with top pay. Your efforts will be recognized with a total compensation package that reflects your experience and contributions. Plan for your future with confidence! We offer a robust 401(k) program with a generous employer match to help you build the financial future you deserve. We know how important work-life integration is. Recharge with PTO and enjoy paid holidays, ensuring you have time to unwind and pursue your passions outside of work. Your health matters to us! Stay covered beginning on your first day of employment with our premier healthcare plan that includes medical, dental, and vision coverage for you and your family. At Associated Electric Cooperative, all of our 700+ employees across MO/AR/OK territory play a crucial role in powering our mission! Whether you're an experienced professional or just starting your career, you'll find endless opportunities for career development here. Join us in an environment where your contribution is valued, and your career can thrive as we work together to keep the lights on! Ready to Energize your career? Visit our website at ******************** to learn more about Associated and apply for a position. Equal Opportunity Statement: AECI is fully committed to the concept and practice of equal opportunity in all aspects of employment. Please reference the contact information below if you require assistance in filling out an application. Individuals with disabilities should request reasonable accommodations in accordance with the Americans with Disabilities Act prior to an appointment. An equal opportunity employer and provider/disability/veteran.

Job DescriptionJoin our client's team in Kansas City! Are you passionate about ensuring airworthiness and safety in aircraft maintenance? Our client, a leading aircraft component service organization, is seeking a Quality Control Inspector with a keen eye for detail. If you thrive on precision and excellence, this role is perfect for you.Job Summary: As a Quality Control Inspector, you will play a crucial role in ensuring all maintenance work meets airworthiness standards and regulatory requirements. You will conduct various inspections on aircraft components to determine serviceability and airworthiness, ensuring compliance with technical data and documentation standards. Responsibilities: Perform preliminary, routine, and in-process inspections on aircraft and components. Document maintenance activities following relevant regulations and standards. Conduct final buy-back of maintenance and issue airworthiness releases. Monitor compliance with safety regulations and scrap bin policies. Provide oversight, guidance, and assistance on the floor. Conduct facility audits for regulatory compliance. Complete OJT documentation and maintain training records. Qualifications: Minimum three years of heavy aircraft maintenance or aircraft component maintenance experience. FAA Airframe and Powerplant (A&P) License required. Knowledge of technical and regulatory documentation interpretation. Strong communication skills and ability to work effectively in a team. Proficiency in MS Office and basic computer skills. Ability to work various shifts and schedules. Prior NDI and QC experience preferred. Benefits: We offer a competitive hourly rate, full benefits package, and a dynamic work environment that fosters growth and development. If you are ready to take the next step in your aviation career, apply now for the Quality Control Inspector position at Kansas City.

Wouldn't it be great to build your career at a growing company recognized 6 years in a row from 2019 to 2025 as the winner of Best Places to Work in collections and the 2025 winner of Best Places to Work for Women. At Credit Control, we know without a doubt that our driven, dedicated team members are the foundation of our success. Employees are rewarded with excellent benefits, competitive compensation, and opportunities for growth. Position Overview We are looking for detail-oriented individuals to join our Call Quality Monitoring Team. In this role, you will listen to, and score recorded phone calls to ensure they meet regulatory requirements (FDCPA, HIPAA, state laws) and client/company quality standards. You'll play a crucial role in helping our agents maintain compliance and deliver a positive experience, as outlined in the Position Overview. We are seeking detail-oriented individuals to join our Call Quality Monitoring Team. In this role, you will listen to, and score recorded phone calls to ensure compliance with regulatory standards (FDCPA, HIPAA, state laws) and meet client/company quality standards. You will play a vital role in helping our agents maintain compliance and deliver a positive experience for consumers. Job Duties: Listen to and evaluate inbound and outbound collection calls based on a predetermined scorecard Score calls are based on set criteria such as professionalism, accuracy, compliance, and overall effectiveness. Provide clear, documented feedback to leadership for training and improvement based on observations while monitoring calls Ensures day-to-day operations are conducted in compliance with regulatory and legal requirements, including FDCPA, state regulations, HIPAA, and the company's policies and procedures, by performing ongoing testing of the business's operations and procedures. Review other quality-related documentation or reports assigned by management Skills/Qualifications: Strong listening skills and attention to detail Comfortable working with evaluation forms, checklists, and scoring criteria. Basic proficiency with Microsoft Word and Excel. Good written communication skills. Knowledge of FDCPA and HIPAA is a plus (training provided). High school diploma or equivalent required Job Type: Full-time. This is an in-office position. Salary: $16.00 - $18.00 per hour Benefits: Flexible Schedule Medical/Dental/Vision Life Insurance Paid Time Off Paid Vacation Time Paid Holidays Paid Bereavement Paid Training 401k with company match Annual Retention Bonus Professional Development Grant Program Employee Assistance Program Ongoing Contests & Prizes Annual Company Events Company Referral Program ADP Lifemart Employee Discounts Schedule: 8-hour shift Day shift Holidays Monday to Friday No nights Overtime Education: High school or equivalent (Preferred) Experience: Computer skills: 1 year (Preferred) Data entry: 1 year (Preferred) Microsoft Office: 1 year (Preferred) Work Location: In-office position 3300 Riders Trail South Suite 500 Earth City, Missouri 63045

Mabbett & Associates, Inc. (Mabbett ) is seeking an experienced laboratory analyst to join our team. Responsibilities will include processing and assembling data including primary and secondary reviews, and reporting findings to data users. As an ideal candidate, you have proven experience maintaining lab equipment, testing and analyzing samples, and following scientific best practices. Typical duties and responsibilities Maintain a clean laboratory area by following all laboratory contamination procedures Perform formal chain-of-custody sample receipt, verification of sample information and logging of samples into the Laboratory Information Management System (LIMS) Perform sample preparation on soil and preservation and aliquoting of water samples prior to analysis Perform chemical tests on materials and samples as requested or assigned, including alpha spectrometry, gamma spectroscopy and gross alpha/beta counting by gas flow proportional counters Prepare reagents as needed for the chemical separation processes Manage inventory and supplies Calibrate and clean equipment and replace worn or broken parts to ensure equipment functions properly Adhere to safety standards and regulations, including radiation and chemical safety procedures Willing to work on other projects, to include occasional travel to set up and support laboratory operations Requirements Bachelor's degree in chemistry, biology, or relevant field preferred 2-4 years experience in lab environment or related field Solid analytical skills Good attention to detail Strong computer skills Strong communication skills (oral, written, as well as hearing) Good time management skills Ability to operate electrical and non-electrical laboratory equipment Comfortable handling potentially dangerous substances, such as flammable liquids and biohazards May be required to drive a vehicle (car, truck, and/or van) Must possess a valid driver's license, successfully pass a pre-employment background check, and drug screen that would test for cannabis and other regulated substances under Federal Law.

Job Details Hazelwood, MO Full Time High School $20.00 - $25.00 Hourly None GraveyardDescription Join the 125-year legacy of Potter Electric Signal Co. Potter has been a part of the St. Louis community since 1898 and we are very proud of our rich history in the fire and life safety industry. Potter's mission is to be the "Symbol of Protection" for fire and life safety solutions worldwide by combining the latest technology in fire protection with the dedicated manpower for which we have been known for over one hundred years. Our vision is to provide industry leading quality solutions, products and services for the protection of life, property and the environment. With unwavering dedication to our customers, Potter looks to continue as the industry standard in both product and service with increased focus on international expansion. Each employee at Potter takes great pride in knowing that every product we assemble, service, and sell is for the purpose of saving lives around the world. We strive to provide employment opportunities to those individuals who are performance driven, team players, take pride in their work, and are enthusiastic and passionate about their job. Potter Global Technologies and our private equity firm, KKR, value our employees and all that they do. KKR offers a unique benefit and opportunity for all employees to participate in an ownership program of Potter Global Technologies. Being a co-owner allows each employee to play a more direct role in the business itself and reap the financial benefits of the Company's success. Summary of the Position The Quality Control Inspector is responsible for maintaining product quality. This role performs t ests and inspects products, processes, and procedures at various stages of production process to compile and evaluate statistical data to determine and maintain quality and reliability of products. Primary Responsibilities Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Support in-process inspection of all products. Accurately record test data, using Epicor, Microsoft Office, and other computer programs. Communicate and coordinate findings with Quality Management and Quality Engineering. Understand customer expectations of and needs from all product. Prepare data for further analysis, as needed. Attend Meetings on the factory floor. Secondary Responsibilities Associate degree in technical field, plus two years of related experience in Quality Control, or combination of relevant education, experience, and training. Proven and successful track record working in a similar role, highly desired. ISO 9001 or other standards experience (ex. IATF 16949, ISO 17025, VDA) highly desired. Experience in Fire, Automotive or Aerospace industry, a plus. Quality certification, such as from ASQ, advantageous. Required Skills/Abilities Ability to multitask with attention to detail in a fast-paced, dynamic environment. Ability to excel in ambiguous circumstances or situations. Ability to effectively communicate with multi-functional partners over a wide range of subject areas. Knowledge of manufacturing environment. People skills, ability to motivate, engage and coach all levels of employees. Qualifications Work Environment/Physical Demands/Travel This job operates in a warehouse/manufacturing setting where hand tools and parts are used to assemble products, such as pliers, screwdrivers, box cutters, power tools, screws, automatic tape dispensers. This position must be able to lift 25 pounds at times. Must be able to access and navigate each department at the organization's facilities. Preferred Qualifications Experience in Quality Control Knowledge and experience in manufacturing Proven and successful track record working in a similar role. PCB troubleshooting experience. ISO 9001 or other standards experience (ex. IATF 16949, ISO 17025, VDA). Experience in Fire, Automotive or Aerospace industry. Associate degree in technical field. This is a full-time position, on-site at the manufacturing facility. The weekly hours worked are 40 hours per week. There may be a need for overtime work. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of an employee for this job. Activities, duties and responsibilities may change at any time with or without notice.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Apply today for a rewarding career with opportunities for growth!! We are looking to fill entry level positions in our environment testing lab. Must live a commutable distance to Earth City, MO. We are looking for to fill full-time year round positions for 1st in our Earth City, MO laboratory. Compensation is $17-20/hour (DOE) The Analyst I prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins Quality Assurance programs and SOP's. Responsibilities include, but are not limited to, the following : Demonstrates and promotes the company vision Regular attendance and punctuality Applies GMP/GLP in all areas of responsibility, as appropriate Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include: Preparation of samples using standard techniques Performing chemical analysis using standard techniques Calculating data Recording and reporting data and any unusual test occurrences to the supervisor Performing routine instrument maintenance Responsible for performing job functions in compliance with Eurofins' EHS and QA standards Responsible for general housekeeping in his/her work area Ability to become trained and competent on complex instrumentation including but not limited to gas chromatography, gas chromatography/mass spectrometry, atomic absorption, ICP, and instrument specific data systems. Works under close supervision using routine and standard methods Aliquots and weighs samples Washes glassware Conducts all activities in a safe and efficient manner Performs other duties as assigned The ideal candidate would possess : Reading, writing and speaking skills Problem solving skills Team participation and meeting management skills Time management and organization skills Ability to use calculator/mathematical formulas and concepts Ability to complete work within time and quality constraints Can work independently following written or verbal instructions Cooperate and coordinate both orally and in writing Able to follow and learn appropriate protocols in one or more of the following disciplines: Organic preparation Metals preparation and analysis Gas Chromatography Gas Chromatography/Mass Spectrometry Radio Chemistry Wet Chemistry High Resolution preparation and analysis Low Resolution preparation and analysis Qualifications Basic Minimum Qualifications (BMQ): A minimum of an Associate of Science degree in Chemistry or equivalent experience Experience in an environmental lab is a plus At least 1-2 year's preparation, analytical experience, or combination, at company or equivalent experience elsewhere preferred Demonstrated effective communication skills and relate well to people in direct communication Consciousness of and a positive attitude toward quality, service and safety procedures Sound reasoning, good judgment and decision making Strong organization and problem solving skills Detail oriented, ability to handle multiple tasks simultaneously and able to coordinate multiple priorities Versatility, flexibility in dealing with people Ability to synthesize and retain information Computer skills, experience with LIMs software a plus Ability to perform basic math skills including multiplication, division and algebra Work independently Work within time constraints Must be able to lift up to 25 lbs frequently, and up to 50 lbs occasionally Willingness to put in overtime hours, as necessary to meet work needs Must be able to pass a pre-employment background check and drug screen Authorization to work in the United States indefinitely without restriction or sponsorship Professional working proficiency in English is a requirement, including the ability to read, write and speak in English. Perform other duties as assigned Disclaimer: This position description is written as a guideline to inform employees of what is generally expected of them at each job level. The description is not intended to be all encompassing or limiting in any manner; rather, it is hoped it will add understanding and better reflect the work performed at all levels of employment. Duties and responsibilities other than those listed may be included as needed within the work group or the company as a whole. Additional Information Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. We do not offer Visa Sponsorship for this role. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description National Carwash Solutions has grown over the past 50 years to become North America's largest equipment, service, and cleaning solutions provider in the car wash industry. Our world-class brands are backed by the largest service network in the country with more than 300 dedicated service professionals and growing! Come join us for an extraordinary career in a high growth, team-oriented company! The Gig: The Chemical Technician plays a critical role in our engagement and customer longevity. It is responsible for ensuring maximum customer satisfaction, troubleshooting and resolving immediate issues, proactively addressing any potential issues and identifying areas of opportunity as it relates to the customer experience. The typical number of sites this role is responsible for is 50-75 sites per month. What You'll Do: Provide professional, expert solutions to all customers, to enable their business to be profitable and leave their customers satisfied with a clean, shiny, dry vehicle every time they use our products Site Preventative Care & troubleshooting: Titration of product as needed Volumemetrics for product as needed Minor chemical equipment/application repairs Customer Satisfaction: Responsible for site chemical conversions & installations, and keeping the customers informed of progress Monitor customer levels and responsible for Chemical Inventory & replenishment orders placed at sites under responsibility Maintain Wash Key Reporting - Service Report Conduct NCS Site Surveys using the template Support & execute on corporate accounts (CTC) per the protocols Provide on-site revenue program training Conduct Technical & Chemistry basic training with appropriate location personnel Maintain accurate and up-to-date computer files (SF, Portal, Google & CTM) of customers and their issues Analyze customer outputs, and make recommendations on technical updates or ways to increase efficiency and wash counts for the designated site. Customer Expansion: Identify areas of opportunity for our account, conduct an initial intake discussion and communicate to sales management This individual is expected to comply with all applicable OSHA, EPA, Local Regulatory Law, and company safety policies. Management retains the discretion to add or change the duties of this position at any time. Qualifications: Associate Degree in Business Administration or related field preferred; or equivalent practical experience. Car Wash experience is preferred but not required Basic mechanical knowledge & aptitude Ability to communicate internally and externally across all levels of the organization Good microsoft office skills and basic knowledge of a computer Demonstrated ability to provide the highest level of customer service and support. Ability to function with minimal supervision and work in a team environment. Must be a self-starter and be extremely motivated. Exemplary organizational skills and attention to detail Ability to support overnight travel up to 40% based on territory & customer needs Grow your career supported by an energized and passionate team, professional development, training, flexibility and opportunities for advancement. We offer competitive wages and benefits including comprehensive health, dental and vision coverage, matching 401(k), paid time off and more. National Carwash Solutions is a proud equal opportunity employer. We are a drug free, EEO employer committed to a diverse workforce. We will consider all qualified candidates regardless of race, color, national origin, sex age, marital status, personal appearance, sexual orientation, gender identity, family responsibilities, disability, education, political affiliation or veteran status.

Quality Inspector - CMM / PCMM Our Quality Department is seeking a qualified individual with experience inspecting machined and fabricated metal parts and assemblies using Coordinate Measuring Machines (CMM) and Portable Coordinate Measuring Machines (PCMM). The successful candidate will work with minimal supervision and possess strong mathematical skills, a solid working knowledge of Geometric Dimensioning and Tolerancing (GD&T), and excellent computer, reasoning, and communication skills. WE OFFER GREAT BENEFITS! * Monthly Manufacturing Performance Incentives with the opportunity to earn up to $550 per month. * Weekly payroll * Start accruing vacation from day one! Accrued each pay period, you will receive 96 hours of vacation in your first year. That increases to over three weeks of vacation (136 hours) after three years. * Anniversary paid day off awarded each year. * Nine (9) paid holidays including the day after Thanksgiving, Christmas Eve, and New Year's Eve. * Complete benefits package including Health, Dental, Vision, and Voluntary Life. * Benefits Provided by Seyer Industries: HealthiestYou (Teledoc services), Basic Life Insurance, Accidental Death and Dismemberment, Employer Assistance Program (EAP), Short-term and Long-term disability. * 401(k) with employer match - Seyer Industries will match 100% of the first 3% of pay you contribute to the plan; plus 50% of next 2% contributed. Skills & Qualifications * Previous experience reading and interpreting manufacturing drawings and CAD models * Working knowledge of Geometric Dimensioning and Tolerancing (GD&T) * Ability to set up and use standard precision inspection tools * Ability to operate and care for stationary ZEISS CMMs and PCMMs * Experience using Verisurf software for inspection and measurement (preferred) * Familiarity with Windows-based file structures and Microsoft Office applications * Strong mathematical skills * Good organizational skills ABOUT SEYER INDUSTRIES Founded in 1957, Seyer Industries is a small business located in St. Peters, Missouri, specializing in high-complexity machined parts and assemblies for the aerospace and maritime industries. Seyer is a turnkey supplier with extensive capabilities, including CNC machining, design engineering, mechanical assembly, painting, kitting, welding, and NADCAP-certified penetrant and magnetic particle inspection. Our team is comprised of individuals proudly committed to the objectives of quality and productivity. All job offers are contingent on the successful completion of a pre-employment drug test and background check. EOE disability/veteran - We are an Equal Opportunity Employer and do not discriminate. 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.