Quality control analyst jobs in Topeka, KS - 320 jobs

This position is responsible for supporting R&D activities of one or more product lines. The technician will conduct experiments, compile data results, and reactions in support of R&D Sustaining and New Product Developments. They will follow testing plans as laid out by R&D Chemists and Managers and record and report results in a detailed and thorough manner. This position may participate in special studies and be required to conduct testing and work outside of established standard operating procedures. Essential Duties: Conduct routine analytical tests to determine chemical, and physical properties of raw materials, process, and product samples. Manufactures samples and prototype formulations. Tests proposed formulations for performance, lifetime, and manufacturability and suggest modifications as warranted. Conducts competitive product testing, as required. Accurately and thoroughly recording and entering data into electronic systems and R&D lab notebooks. Reports progress on pending projects at regular timeframes. Act with strong listening and analytical skills to develop/maintain relationships and deliver results. Helps maintain laboratory equipment and assists with calibrations. Follows AS9100 Quality Management System as applies to R&D and as defined in the Quality System. Actively participates in company Safety Programs, as required, and practices safe work methods on a daily basis. Actively supports and participates in the site Laboratory Safety and Chemical Hygiene Program. Attends company sponsored training and outside seminars as required. Acts in accordance with company policies, procedures, and corporate ethics. Perform other duties as assigned. Education & Experience: B.S. degree in Chemistry, Chemical Engineering, Material Science, or related field from an accredited college or university. Proficient within Windows based environment. Experienced in Microsoft Office Suite software (Excel, Word, Power Point, Outlook). Experience working with ERP systems, particularly Microsoft Navision, a plus. Proficiency in using standard laboratory equipment. Experience following SOPs and GLPs. Experience working under ISO 9001/AS 9100 Quality Management environments a plus. Exposure to GHS and other regulatory requirements applicable to the supported product line(s) a plus. ITW is an equal opportunity employer. We value our colleagues' unique perspectives, experiences and ideas and create workplaces where everyone can develop their careers and perform to their full potential. As an equal employment opportunity employer, ITW is committed to equal employment opportunity and fair treatment for employees, beginning with the hiring process and continuing through all aspects of the employment relationship. All qualified applicants will receive consideration for employment without regard to race, color, sex, gender identity, sexual orientation, religion, national origin, age, disability, protected Veteran status or any other characteristic protected by applicable federal, state, or local laws.

FUTAMURA USA Futamura is committed to its employees and their families by offering one of the most competitive benefits packages in the market. We can likely beat your current company on insurance premium costs, levels of coverage, out of pocket expenses and savings toward retirement. Medical Insurance 401K + Company Match Dental Insurance Flexible Spending Account Vision Insurance Prescription Benefits Generous Paid Time Off Company-Paid Disability Insurance Company-Paid Life Insurance The Process Chemist performs routine and non-routine analyses of raw materials, in-process samples, and finished products. This role requires strong proficiency in analytical chemistry and the use of a wide range of analytical instruments and test methods to ensure product quality and support manufacturing operations. This position works in our Quality Control Department. Standard schedule is M-F 7:30 to 4 PM with flexibility based on business need. Primary Responsibilities Provide laboratory support for plant trials by performing timely testing, delivering clear feedback, and maintaining a detailed database of trial conditions and outcomes. Update and revise standard operating procedures as needed; support special projects involving analytical method development, instrument troubleshooting, and process validation. Apply effective troubleshooting techniques to identify root causes and develop strategies to resolve issues using all available resources. Collaborate with other departments to jointly troubleshoot process issues related to chemical analysis (e.g., composition, concentration, material properties). Manage time effectively to complete tasks with minimal supervision. Coordinate and plan high-priority work, including organizing meetings, setting timelines, and ensuring project milestones are met. Establish reasonable deadlines for high-priority tasks, communicate timelines to the department head, and provide regular progress updates. Work with technical teams to support research, product development, and process improvements. Perform analytical testing using instruments such as: High-Performance Liquid Chromatography (HPLC) Gas Chromatography (GC) Fourier-Transform Infrared Spectroscopy (FTIR) Automated Titrator Universal Testing Machine (UTM) for tensile, compression, and material strength testing Calculate product characteristics including purity, particle size, and hardness. Record sampling and testing data to maintain accurate and complete quality records. Train lab technicians on laboratory procedures, equipment use, and quality standards. Develop test methods required for quality laboratory analyses. Prepare test solutions, reagents, and compounds for use by plant personnel. Assist the QC Supervisor with analytical problem-solving and instrument-related projects. Perform instrument calibrations. Communicate and coordinate effectively with personnel across departments. Create and maintain Quality Control trend analysis reports for assigned criteria. Enter test results into the manufacturing system and/or communicate findings to the appropriate departments. Perform other duties as assigned. Qualifications Bachelor's degree in Chemistry or a related field. Strong competency in analytical chemistry, including hands-on experience with laboratory instrumentation and analytical techniques. 2-4 years of experience in a Process Chemist or related laboratory role, or an equivalent combination of education and experience. Ability to work independently while adhering to company procedures and guidelines. Demonstrated teamwork and collaboration skills. Strong attention to detail and accuracy. We make NatureFlex and Cellophane packaging films. These are biodegradable and compostable products to help reduce plastic pollution around the world! Since they are made from renewable wood pulp as a raw material, we essentially make transparent paper. Check out the process here. Compostable packaging is a rapidly expanding market. As a result, Futamura is in the process of a major expansion to keep up with the growing demand for our products. We are looking for good people with a drive for advancement to come join our team. The Futamura Group was established in Japan in 1950 and is now a global operation specializing in high added value packaging products. Our products are shipped around the world and are utilized by major brands and specialized markets. EEO/D/M/V/

Ready to be pushed beyond what you think you're capable of? At Coinbase, our mission is to increase economic freedom in the world. It's a massive, ambitious opportunity that demands the best of us, every day, as we build the emerging onchain platform - and with it, the future global financial system. To achieve our mission, we're seeking a very specific candidate. We want someone who is passionate about our mission and who believes in the power of crypto and blockchain technology to update the financial system. We want someone who is eager to leave their mark on the world, who relishes the pressure and privilege of working with high caliber colleagues, and who actively seeks feedback to keep leveling up. We want someone who will run towards, not away from, solving the company's hardest problems. Our ******************************** is intense and isn't for everyone. But if you want to build the future alongside others who excel in their disciplines and expect the same from you, there's no better place to be. While many roles at Coinbase are remote-first, we are not remote-only. In-person participation is required throughout the year. Team and company-wide offsites are held multiple times annually to foster collaboration, connection, and alignment. Attendance is expected and fully supported. The Complaints Quality Control (CQC) team plays a critical role in ensuring our global complaints operations are efficient, compliant, and consistently deliver high-quality outcomes. As an Analyst III on the team, you'll conduct quality control (QC) reviews across Consumer Complaints, Regulatory Complaints, and Litigation Support investigations, while helping refine complaint processes and providing actionable feedback to agents. This role requires strong independence, the ability to manage multiple priorities, and a commitment to continuous improvement through open, collaborative feedback. *What you'll be doing (ie. job duties):* * Perform QC reviews of complaint cases based on the quality rubric, ensuring compliance with established guidelines. * Provide constructive feedback to agents based on QC findings to support performance improvement. Feedback will be documented in written reports, and agents may need to set up meetings to discuss and clarify scores if needed. * Assist in refining and updating the complaints review process, contributing feedback and suggestions for ongoing improvements. * Conduct root cause analysis (RCA) to identify trends and areas for process enhancements. * Collaborate with cross-functional teams to improve the efficiency and effectiveness of complaints handling. * Independently balance and prioritize multiple tasks to ensure timely and accurate completion of QC reviews. * Be receptive to feedback from all levels and foster a collaborative environment that encourages open communication and continuous improvement. * Ensure compliance with global regulatory guidelines, including MiCA and CF8, across all complaint handling. * Contribute to reporting and visualizations that highlight complaint trends and areas for process optimization. * Support the troubleshooting and resolution of escalated and complex complaint cases, ensuring alignment with company standards. *What we look for in you (ie. job requirements):* * Minimum of 3 years of relevant experience in financial services, crypto, investigations, legal, or the tech industry, with a focus on complaints handling, compliance, or regulatory matters. * Ability to work independently, manage multiple priorities, and balance tasks with minimal guidance. * Strong analytical skills with the ability to perform root cause analysis and provide actionable insights. * Comfortable providing feedback to agents and open to receiving feedback from peers and leadership. * Exceptional communication skills to collaborate with cross-functional teams and present findings effectively. * Adaptability to thrive in a fast-paced, high-growth environment and adjust priorities as needed. * Proven attention to detail, with a focus on accuracy and quality in QC reviews and reporting. *Nice to haves:* * Experience in project management, analytics, or vendor management. * Advanced degree in business, finance, or customer experience (CX). * Proficiency with tools such as Google apps, JIRA, and Salesforce Service Cloud. * Experience collaborating with external outsource business partners. Position ID: P74727 \#LI-Remote *Pay Transparency Notice*: Depending on your work location, the target annual *base *salary for this position can range as detailed below. Full time offers from Coinbase also include bonus eligibility + equity eligibility + benefits (including medical, dental, vision and 401(k)). Base salary range shown. Total compensation also includes equity and bonus eligibility and benefits: $38.01-$40.01 USD Please be advised that each candidate may submit a maximum of four applications within any 30-day period. We encourage you to carefully evaluate how your skills and interests align with Coinbase's roles before applying. Commitment to Equal Opportunity Coinbase is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation or any other basis protected by applicable law. Coinbase will also consider for employment qualified applicants with criminal histories in a manner consistent with applicable federal, state and local law. For US applicants, you may view the *********************************************** in certain locations, as required by law. Coinbase is also committed to providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please contact us at accommodations*********************************** *Global Data Privacy Notice for Job Candidates and Applicants* Depending on your location, the General Data Protection Regulation (GDPR) and California Consumer Privacy Act (CCPA) may regulate the way we manage the data of job applicants. Our full notice outlining how data will be processed as part of the application procedure for applicable locations is available ********************************************************** By submitting your application, you are agreeing to our use and processing of your data as required. *AI Disclosure* For select roles, Coinbase is piloting an AI tool based on machine learning technologies to conduct initial screening interviews to qualified applicants. The tool simulates realistic interview scenarios and engages in dynamic conversation. A human recruiter will review your interview responses, provided in the form of a voice recording and/or transcript, to assess them against the qualifications and characteristics outlined in the job description. For select roles, Coinbase is also piloting an AI interview intelligence platform to transcribe and summarize interview notes, allowing our interviewers to fully focus on you as the candidate. *The above pilots are for testing purposes and Coinbase will not use AI to make decisions impacting employment*. To request a reasonable accommodation due to disability, please contact accommodations[at]coinbase.com

You could be the one who changes everything for our 28 million members. Centene is transforming the health of our communities, one person at a time. As a diversified, national organization, you'll have access to competitive benefits including a fresh perspective on workplace flexibility. **Kansas City Metro area, KS or MO.** **Up to 25% travel** **HEDIS knowledge and Data interpretation** **Provider performance** **Position Purpose:** Establishes and fosters a healthy working relationship between community physician and small provider practices and WellCare. Educates providers and supports provider practice sites in regards to the National Committee for Quality Assurance (NCQA) HEDIS measures. Provides education for HEDIS measures, appropriate medical record documentation and appropriate coding. Assists in resolving deficiencies impacting plan compliance to meet State and Federal standards for HEDIS. + Under general guidance form Senior Quality Practice Advisors and management, educates community physician and small provider practices in appropriate HEDIS measures, medical record documentation guidelines and HEDIS ICD-9/10 CPT coding in accordance with NCQA requirements. + Collects, summarizes and trends provider performance data to identify and strategize opportunities for provider improvement. + Collaborates with Provider Relations to improve provider performance in areas of Quality, Risk Adjustment and Operations (claims and encounters). + Assists in delivering provider specific metrics and coaches providers on gap closing opportunities. + Assists in identifying specific practice needs where WellCare can provide support. + Partners with physicians/physician staff to find ways to encourage member clinical participation in wellness and education. + Provides resources and educational opportunities to provider and staff. + Captures concerns and issues in action plans as agreed upon with provider. + Documents action plans and details of visits and outcomes. + Reports critical incidents and information regarding quality of care issues. + Communicates with external data sources as needed to gather data necessary to measure identified outcomes. + Provides communication such as newsletter articles, member education, outreach interventions and provider education. + Supports quality improvement HEDIS and program studies as needed, requesting records from providers, maintaining databases, and researching to identify members' provider encounter history. + Ensures that documentation produced and/or processed complies with state regulations and/or accrediting body requirements. + Ensures assigned contract/regulatory report content is accurate and that submission adheres to deadline. + Enter documentation of findings in identified databases and ensure accuracy in medical records for data collection, DE and reporting. + Performs other duties as assigned. + Performs other duties as assigned + Complies with all policies and standards **Kansas City Metro area, KS or MO.** **Up to 25% travel** **HEDIS knowledge and Data interpretation** **Provider performance** **Education/Experience:** **Required A Bachelor's Degree in Healthcare, Public Health, Nursing, Psychology, Health Administration, Social Work or related field or equivalent work experience within a managed care environment related to HEDIS record review, quality improvement, medical coding or transferable skill sets that demonstrates the ability to perform the role. Preferred:** A Master's Degree in Healthcare, Public Health, Nursing, Psychology, Health Administration, Social Work or related field. Candidate Experience: Required: 1+ year of experience in related HEDIS medical record review or quality improvement with experience in data and chart reviews to provide consultation and education to providers and provider staff OR 2 years medical coding or other transferable experience and skill set combination that demonstrates the ability to learn and perform the level of the position. **A license in one of the following is preferred:** Certified Coding Specialist (CCS), Licensed Practical Nurse (LPN), Licensed Master Social Work (LMSW), Licensed Vocational Nurse (LVN), Licensed Mental Health Counselor (LMHC), Licensed Marital and Family Therapist (LMFT), Licensed Certified Social Worker (LCSW), Licensed Registered Nurse (RN), Acute Care Nurse Practitioner (APRN) (ACNP-BC), Other Foreign trained physician/MD, Health Care Quality and Management (HCQM), Certified Healthcare Professional (CHP), Certified Professional in Healthcare Quality (CPHQ). Pay Range: $26.50 - $47.59 per hour Centene offers a comprehensive benefits package including: competitive pay, health insurance, 401K and stock purchase plans, tuition reimbursement, paid time off plus holidays, and a flexible approach to work with remote, hybrid, field or office work schedules. Actual pay will be adjusted based on an individual's skills, experience, education, and other job-related factors permitted by law, including full-time or part-time status. Total compensation may also include additional forms of incentives. Benefits may be subject to program eligibility. Centene is an equal opportunity employer that is committed to diversity, and values the ways in which we are different. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristic protected by applicable law. Qualified applicants with arrest or conviction records will be considered in accordance with the LA County Ordinance and the California Fair Chance Act

In 1979, Bettis Asphalt & Construction, Inc. began with a paving and maintenance operation and a dedication to service. Today the organization operates several lines of business that can cover all areas of need in a construction project. The Bettis Group of Companies today include Bettis Asphalt & Construction, Inc., Bettis Asphalt Western Division, Mid-States Materials, LLC, Capital Trucking, LLC, Bettis Contractors, Inc., Capital Crane, LLC, Capital Ready-Mix, LLC, Heartland Rail Services, Koss Construction Company, Midwest Pavement Grinding, LLC, and PCI Mechanical Services. From rock to road, construction to cranes, our ability to handle a complete job ensures both the best price and the best quality. We self-perform the majority of tasks, maintaining strict quality control. Our client list grows steadily because we understand the importance of developing long-term relationships built on trust, performance, and reliability. See The Bettis Companies in action here. Concrete Quality Control Technician Job Overview: Implement company quality control plans for all aspects of our Ready-Mix Concrete operation while maintaining a professional working relationship with the owner's representatives in order to keep the project on schedule and produce a quality product. Ideal Candidate * 2+ years of experience with testing ready mix concrete. * Clean appearance. * Drug free. * A.C.I. Field Technician Grade 1. * Knowledge of concrete mix designs. * Valid driver's license with clean driving record. * Computer literate. * Good background in math. * Good communication skills. * Team player. Essential Duties and Responsibilities * Ensuring quality throughout the entire process of producing ready mix concrete to include raw materials, mix designs and finished products. * Interacting regularly with customers, sales representatives, operation and production employees, vendors and engineers. * Overseeing quality control of concrete on job sites. * Maintain records and write reports regarding job site issues, driver performance and product problems. * Assists in ensuring that job mix formulas are incorporated into mixing plant operations consistent with central laboratory design. * Compiles and reports final summaries of testing results from completed projects. * Will perform other duties as assigned by the Quality Control Manager. Other Duties * Additional duties as assigned by Supervisor Job Requirements and Education * Over 18 years of age * Eligible to work in the United States * Must be able to work flexible hours. 40+ hours per week. Extended hours and travel will be required from time to time. * Valid driver's license and reliable transportation * Complete and pass pre-employment testing, including a drug screen and physical * High school education or GED equivalent * Experience within the Aggregates and/or Construction industry * Ability to establish and maintain effective working relationships with contractors, their employees and state employees. * Ability and knowledge to work with dispatch, sales and customers to create and change mix designs; staying within cost parameters. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job the employee is regularly required to: * Sit * Talk * Hear * Stand * Walk * Bend * Lift and/or move over 50 lbs. Work Environment * Works outdoor exposed to all weather conditions * Exposure to airborne particles * Works near moving mechanical parts Benefits: * 401(k) * 4% match * Profit sharing eligible after 1st year * Health insurance (2 options) * HDHP with Health Savings Account ($500 employer funded) * PPO * Dental insurance * Vision insurance * Paid Holidays * Paid time off Thank you for your interest in applying with one of the Bettis Companies. The Bettis Group of Companies includes: Bettis Asphalt & Construction, Mid-States Materials, Capital Trucking, Bettis Contractors, Bettis Fabrication, Capital Crane, Capital Ready-Mix, Heartland Rail Service, Koss Construction, Midwest Pavement Grinding, PCI and PTMW. If the position you applied for is filled or we feel your experience fits another job, your information may be sent to one of the other Bettis Companies if an opening is available. Capital Ready Mix is an Equal Opportunity Employer and Drug Free Workplace. Women, Minorities, and Veterans are encouraged to apply. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

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: In this role you will support the manufacturing of synthetic oligos nucleotides in an ISO 13485 quality regulated lab. * Set-up and prepare products according to current manufacturing procedures. * Clean-up equipment and working areas after production operations. * Coordinate appropriate disposal of waste and complete compliance documentation. * Communicate and document status of processes, products, and equipment. Communicate the status of production operations and bring deviations to the attention of supervisor. * Provide a complete and accurate batch record at the conclusion of production operations consistent with quality guidelines including Non-Conformance Reports (NCR) if applicable. * Enter hours worked and raw materials used into SAP. * Ensure all applicable logbooks have been filled out completely as required by current procedures. Write and modify production procedures consistent with quality guidelines. Physical Attributes: * Wear appropriate Personal Protective Equipment. Who You Are Minimum Qualifications: * Bachelor's Degree in Biology, Biochemistry or other Life Science discipline. * 1+ years laboratory and/or production experience. Preferred Qualifications: * Experience with laboratory instruments, oligo synthesis, and production equipment. * Experience with process techniques and unit operations. * Experience with problem solving and analytical techniques. RSREMD * Pay Range for this position: $25.00-$46.00. * 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!

PenFed is hiring a (Hybrid) Sr Analyst, Real Estate QC Underwriting at our Omaha, Nebraska; San Antonio, Texas; Eugene, Oregon or Tysons, Virginia location. The primary purpose of this job is to perform quality control reviews for first trust conventional, VA, FHA and equity real estate loans. This role will evaluate the integrity and quality of the credit, compliance, and collateral aspects of the mortgage loan origination process through pre-funding and post-funding loan reviews designed to verify the accuracy and integrity of the information and loan documentation used to support the lending decision for conventional, VA, FHA, and Equity Line of Credit loans. It will validate adherence to PenFed's policies and procedures and secondary marketing investor guidelines. This role requires expertise in evaluating property valuations, including all types of appraisals, AVMs and property condition inspections, with knowledge of Interagency guidelines and Appraisal Independence Requirements. **Responsibilities** Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. This is not intended to be an all-inclusive list of job duties, and the position will perform other duties as assigned. + Conduct reviews of first trust conventional, VA, FHA and equity mortgage loans to ensure that loans were properly underwritten, and that sound judgment was used in the underwriting process. Complete a thorough analysis of loan files to determine member credit worthiness and collateral values were adequate. Review legal and compliance documentation as applicable. + Conduct reviews of mortgage loans to evaluate the accuracy and integrity of the information and loan documentation used to support the lending decision. + Conduct reviews of mortgage loans to ensure compliance with PenFed's policy and procedures, investor, agency, and secondary market requirements. + Analyze and determine accurate defect ratings based on investor's loan eligibility requirements. Evaluate the entire credit package and collateral for residential mortgage loans and ultimately ensure an investment quality loan product. + Follow up on previous deficiencies and examine samples of corrected files. + Ability to work collaboratively with Mortgage Operations, providing clarification of review results as needed. + Understand and interpret all credit underwriting documentation required to be reverified in each loan file and conduct further research as necessary. + Perform peer reviews and provide guidance to junior analysts as needed. + Assist with process testing as assigned and participate in special projects. + Maintain a working knowledge of internal policies, procedure, external regulations, secondary market underwriting guidelines, investor, and private mortgage insurance guidelines. + Maintain current knowledge of Fannie Mae, Veterans Administration (VA), Freddie Mac, FHA and external investors. **Qualifications** Equivalent combination of education and experience is considered. + Bachelor's degree in business, accounting, finance, or another related field required. + Minimum of three (3) years progressive experience in real estate lending with underwriting experience required, preferably in a bank or credit union environment. + Advanced knowledge of real estate loans (origination, processing, closing, funding) required. Broad knowledge of consumer real estate lending, including first trust mortgage loans, home equity loans and lines of credit. + Knowledge of lending compliance regulations and system definitions. + Active or recent VA SAR and/or FHA DE underwriting authority preferred. + Proficiency with Encompass is highly desirable. **Supervisory Responsibility** This position will not supervise employees. **Licenses and Certifications** There are no additional certifications required. **Work Environment** While performing the duties of this job, the employee is regularly exposed to an indoor office setting with moderate noise. *Most roles require working in an office setting with moderate noise and the ability to lift 25 pounds.* **Travel** The ability to travel to various worksites and be on-call may be required. \#LI-Hybrid **Benefits** At PenFed, we offer a robust benefits package designed to support you both personally and professionally. You'll have access to comprehensive health, dental, and vision plans; paid time off; and family-friendly benefits like paid parental leave, care support, and fitness center access. Financial wellness is encouraged through features like a 401(k) match, employee loan discounts, and fully paid life and disability coverage. We also support growth via education assistance, community involvement, and volunteer opportunities. **Our Purpose** Helping members achieve their dreams since 1935. Pentagon Federal Credit Union (PenFed) is one of America's largest federal credit unions, serving 2.8 million members worldwide with $29 billion in assets. PenFed offers market-leading certificates, checking and savings, credit cards, personal loans, mortgages, auto loans, and a wide range of other financial services, always with members' interests in mind. PenFed is federally insured by the NCUA and is an Equal Housing Lender. Berkshire Hathaway HomeServices PenFed Realty, LLC is a full-service real estate company ready to assist our clients with buying, selling and renting a home. The company is a wholly owned subsidiary of PenFed Credit Union and is the largest independently-owned brokerage in the Berkshire Hathaway HomeServices network, placing us in the top 1% of all real estate brokerages in the country. With almost 60 offices and nearly 2,000 world-class sales professionals, we offer complete service coverage in Virginia, Maryland, the District of Columbia, Delaware, Pennsylvania, West Virginia, Florida, Tennessee, Kansas and Texas. In addition, we also offer specialized client services which include management of vacation properties and long-term rentals, corporate relocation services and national referral network. **Equal Employment Opportunity** PenFed management will maintain and observe personnel policies which will not discriminate or permit harassment or retaliation against a person because of race, color, creed, age, sex, gender, gender identity, gender expression, religion, national origin, ancestry, marital status, military or veteran status or obligation, the presence of a physical and/or mental disability or medical condition, genetic information, sexual orientation, and all statuses protected by applicable state or local law in all recruiting, hiring, training, compensation, overtime, position classifications, work assignments, facilities, promotions, transfers, employee treatment, and in all other terms and conditions of employment. PenFed will also prohibit retaliation against individuals for raising a complaint of discrimination or harassment or participating in an investigation of same. PenFed will also reasonably accommodate qualified individuals with a disability so that they can apply for a job or perform the essential functions of a job unless doing so causes a direct threat to these individuals or others in the workplace and the threat cannot be eliminated by reasonable accommodation or if the accommodation creates an undue hardship to PenFed. Contact human resources (HR) with any questions or requests for accommodation at ************.

Responsibilities Peraton is seeking a Quality Control Inspector to join our team of diverse, qualified individuals. The Quality Control Inspector works at the United States Postal Service (USPS) Central Repair Facility (CRF) in Topeka, KS. The CRF is a depot repair facility for USPS mail processing, delivery, and bulk mail systems repairable parts. Examples: repairing printed circuit boards, electrical, electronic, mechanical and electro-mechanical assemblies to component level. The CRF provides depot level maintenance for essential automation, mechanization, retail and bulk mail processing systems used in all mail processing and retail installations. Our Quality Control Inspector verifies and documents a product's degree of conformance or non-conformance with applicable specifications or drawings. Performs inspections on mechanical, electrical, and electronic components and assemblies. Specific tasks include: Performs receiving, incoming, in-process, final, and packing inspections using applicable work instruction, checklists, drawings and specifications Verifies functional tests using approved procedures Maintains records of observations and measurements using designated tags, travelers, and forms Inputs information for electronic material review board (MRB) Certifies special tools and tooling used, as inspection and test media Assists in the maintenance of quality control specification and record files Maintains, logs, and assists in the analysis of data regarding failed individual end items Initiates reports and keep records according to job requirements Uses drawings or component layouts to identify part location on end items Performs other related tasks as assigned #CRF2025 Qualifications Basic Qualifications: High school graduate or equivalent. Formal training with two years' related experience or four years' related experience in lieu of formal training Ability to obtain and maintain a Public Trust clearance U.S. Citizenship required (Must have resided in the U.S. for the past five years with no more than six months travel outside the U.S. during this timeframe) Proficiency using windows based applications and software (Microsoft Office) Basic typing skills are necessary Communicate effectively, both orally and in writing Understand soldering principles, general test equipment, and IPC repair criteria Must have a basic understanding of electromechanical assemblies and electronic equipment configurations to verify conformance to drawing or standards Proficiency in inspecting items to technical specifications Proficiency in identifying discrepancies per standards and express findings in writing Communicate effectively, both orally and in writing Ability to stand on feet for long durations Ability to perform a variety of assembly tasks requiring dexterity and fine motor skills Must be able to perform inspections in the various work areas Preferred Qualifications: ASQ CQI or similar certification J-STD-001 certification Physical Requirements: Heavy work exerting up to 100 pounds of force occasionally, and/or up to 50 pounds of force frequently, and/or up to 20 pounds of force constantly to move objects Physical activity may include kneeling, crouching, reaching, standing, walking, pushing, pulling, lifting, grasping, feeling, talking, hearing and repetitive motion The worker is required to have close visual acuity to perform an activity such as viewing a computer terminal Visual inspection involving small defects, small parts, and/or operation of machines (including inspection) Subject to hazards including a variety of physical conditions, such as proximity to moving mechanical parts, moving vehicles, electrical current Peraton Overview Peraton is a next-generation national security company that drives missions of consequence spanning the globe and extending to the farthest reaches of the galaxy. As the world's leading mission capability integrator and transformative enterprise IT provider, we deliver trusted, highly differentiated solutions and technologies to protect our nation and allies. Peraton operates at the critical nexus between traditional and nontraditional threats across all domains: land, sea, space, air, and cyberspace. The company serves as a valued partner to essential government agencies and supports every branch of the U.S. armed forces. Each day, our employees do the can't be done by solving the most daunting challenges facing our customers. Visit peraton.com to learn how we're keeping people around the world safe and secure. Target Salary Range The rate / range per hour below represents the typical salary range for this position. Salary is determined by various factors, including but not limited to, the scope and responsibilities of the position, the individual's experience, education, knowledge, skills, and competencies, as well as geographic location and business and contract considerations. Depending on the position, employees may be eligible for overtime, shift differential, and a discretionary bonus in addition to base pay. SCA / Union / Intern Rate or Range 26.01 EEO EEO: Equal opportunity employer, including disability and protected veterans, or other characteristics protected by law.

Job DescriptionDescription: The Quality Control Specialist/Foreman at Weddle and Sons will develop and demonstrate skill in overseeing the day-to-day operations of a residential roofing crew and will show an advanced level of initiative in communication with supervisors, subordinates, and clients. A QCS must be committed to the core values of the company and must show the potential to coach others to higher levels of execution. Working Environment and Expectations: Hours: A typical work week is expected to be not less than 40 hours. Given the seasonality of this business, we expect that there will be many weeks in the middle of the year that requires well over 40 hours of work. At the same time, there will be many weeks in the winter that may require somewhat less than 40 hours. At any time, and especially during the winter months, the service technician and QCS may be asked to assist with various company initiatives. Travel: The service technician and QCS roles are likely to involve occasional travel for company training, and projects. At times, business demand or weather events may require that the service technician and/or QCS spend time working in other company locations. Requirements: Basic knowledge of roofing systems (and ability to learn quickly) with overall technical proficiency Physical fitness sufficient to perform tasks that can be demanding at times Problem-solving ability to troubleshoot roofing (and related) issues: ability to identify symptoms and systematically eliminate potential causes until solving the issue Written and verbal professionalism Customer service skills (listening, positive communication, patience) Competence in grammar and spelling preferred Ability to send clear and mistake-free written communications Good phone demeanor and tone Ability to organize many competing and concurrent workstreams, while prioritizing and following through on commitments

About Thermo Fisher Scientific Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of $12 billion, we have approximately 39,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries. For more information, visit ********************* Position Summary As a Quality Control Scientist I, you will be responsible for all quality control aspects of finished product testing. You will ensure that the performance of finished products complies with testing standards per IFU and SOPs, as well as customer requirements and regulating agencies' guidelines. This role also includes documentation control duties per Quality Assurance compliance requirements. Key Responsibilities Review and maintain product compliance specifications and documentation control Perform and interpret microbiology testing, including growth promotion, biochemical, and AST Gain proficiency on all performance benches Document testing results and determine disposition Maintain consistency in training in Master Control Establish and maintain SOP criteria for inspection/testing Maintain department equipment and request consumables as needed Exercise and monitor GMP compliance in work environment Collaborate closely with the Quality Assurance department as a quality team Execute Stability Study testing in accordance with QA requirements Work with Customer Service Representatives to achieve on-time product releases Participate in the continuous improvement program within the department Work closely with a team in a fast-paced laboratory setting Understand and exercise all safety requirements and procedures Assist in maintaining standards in accordance with GMPs, SOPs, and ISO regulations Participate in achieving department goals and support all company policies Perform other duties as assigned REQUIREMENTS Minimum Qualifications Education: 4-year degree in biological sciences with coursework in microbiology (including laboratory) OR 4-year degree with 5+ years of microbiology lab experience Experience: 1-2 years of experience in related QC/QA or microbiology laboratory work OR an equivalent combination of education and experience Technical Skills: Familiarity with FDA regulations for medical devices Intermediate computer skills, including proficiency in Microsoft Office (Word, Excel, PowerPoint) Experience with SAP is a plus Soft Skills: Ability to manage multiple tasks in an organized fashion Effective communication skills across various departments Ability to follow written and verbal instructions Adaptability and willingness to learn new procedures Scientific and objective approach to work Self-motivation and high sense of responsibility Excellent teamwork spirit Strong verbal and written skills in English Non-Negotiable Hiring Criteria Excellent time management skills Willingness to work overtime when needed to complete tasks Strong team player and participant in team activities High sense of responsibility Critical thinking skills Additional Information Location: Lenexa, KS Shift: Friday - Sunday, 7:00 AM - 5:30 PM Relocation assistance is NOT provided Must be legally authorized to work in the United States without sponsorship Must be able to pass a comprehensive background check, including a drug screening Weekend shift availability required

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description Job Title: Chemist Job ID : LLYJP00006309 Duration: 6+ Months (Possible Of Extension) Location: Overland Park, KS Job Details: QC Chemist position, they will be doing HPLC Analyses with possible dissolution testing. They will be working in a lab environment using GMP skills with a GC headspace, potentially could be running it. They will be an influx of testing required for the lab move which is requiring them to do comparative testing between the two spaces. There is a potential for hormone exposure so there is a respirator testing required. Perform accurate and timely testing of routine and some non-routine lab samples in accordance withappropriate GMP and safety guidelines. Completes second person verification of test results. Participates in laboratory root cause investigations and quality system improvement initiates by executingwell defined protocols and procedures. Shares technical information and best practice within the group. Design and evaluation of experiments, methods development and characterization, support of processdevelopment/optimization and the analysis and interpretation of data. Conduct studies to validate methods, develop methods, evaluate new technologies. Sample Analysis. Sample preparation, instrument set-up and operation, data entry, primary data review. Coordination of method transfers and co-validations. Qualifying, calibrating, and maintaining analytical instrumentation. All laboratory work will be conductedand documented in accordance with the appropriate Quality System. Act as a resource for insuring adherence to quality systems Requirements / have to haves not listed elsewhere Bachelor of Science in Chemistry or related field Request preferences / nice to haves • Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. • Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. • Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. • Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. • Ability to troubleshoot problems and identify solutions. • Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination Primary Position Responsibilities (major or daily tasks) • Perform analytical and physical testing on in-process, finished product and stability samples. • Assist laboratory leader in ensuring compliance with all procedures, safety and regulatory commitments in Quality Control. • Perform review and approval of analytical data. • Maintain analytical methods in the laboratory in a state of validation. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination of problems by identifying and addressing root cause. Qualifications Requirements / have to haves not listed elsewhere Bachelor of Science in Chemistry or related field Request preferences / nice to haves • Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. • Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. • Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. • Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. • Ability to troubleshoot problems and identify solutions. • Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination Primary Position Responsibilities (major or daily tasks) • Perform analytical and physical testing on in-process, finished product and stability samples. • Assist laboratory leader in ensuring compliance with all procedures, safety and regulatory commitments in Quality Control. • Perform review and approval of analytical data. • Maintain analytical methods in the laboratory in a state of validation. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination of problems by identifying and addressing root cause. Additional Information All your information will be kept confidential according to EEO guidelines.

Job ID 251111 Posted 13-Jan-2026 Service line PJM Segment Role type Full-time Areas of Interest Project Management **About the role** The Facility Condition Assessments (FCA) Team at CBRE | Turner & Townsend Inc. is currently seeking a detail-oriented individual who will ensure that the deliverables are accurate, consistent, and conform to the standards and guidelines for the facility condition assessments, capital planning, and asset management reports established by the Building Consultancy group. Primary duties include identifying content issues, developing and enforcing quality standards, and collaborating with teams to provide various client deliverables in a timely manner. **What you'll do** Data Assessment: Review facility condition and asset data for content, structure, and quality, and identify anomalies and inconsistencies. Must have fluency of the English language, as it relates to grammar, punctuation, and spelling. Must be able to compare data criteria/fields for content, agreement, and technical accuracy. Standards Adherence: Collaborate with team members to ensure that the comprehensive quality standards and metrics (e.g., accuracy, completeness, timeliness) are met. Must be able to switch between sets of rules pertaining to each client and project. Data Cleansing and Resolution: Identify and rectify errors, inconsistencies, and redundancies within facility condition assessment and asset datasets. Monitoring and Reporting: Evaluate and provide corrective action of data quality, create reports for facility capital planning engagements. Process Improvement: Recommend changes to existing processes, entry, and deliverable workflow. Must be a team player and not afraid to ask questions. Must be comfortable in a fast-paced, high-volume setting and managing projects and deadlines. **What you'll need** We will provide reasonable accommodations that may be made to enable individuals with disabilities. To perform this job optimally, an individual must be able to perform each crucial duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. + Associate's degree (AA/AS), College Diploma, or equivalent preferred. Minimum of three years of related experience in addition to education. Consideration will be given to a person with 5 years of related experience, regardless of whether they hold a degree. Experience in the Architecture, Engineering, and Construction field is preferred. + Experience with Microsoft Office Suite products. **Additional Skills** + Ability to write in a clear and concise, coherent way using appropriate grammar, spelling, punctuation, and style. Adapt writing style for different audiences, purposes, and formats. + Ability to edit technical documents in a detailed and accurate manner to ensure deliverables are professional and presentable. + Ability to comprehend and interpret instructions, short correspondence, and memos and ask clarifying questions to ensure understanding. Must be detail-oriented and observant + Requires basic knowledge of financial terms and principles. Ability to calculate simple figures such as percentages. + Must have a basic understanding of architectural, mechanical, and electrical equipment and features, and some familiarity with industry standards and language. Turner & Townsend carefully considers multiple factors to determine compensation, including a candidate's education, training, and experience. The minimum salary for this position is 60,000 annually and the maximum salary for this position is 70,000 annually. The compensation that is offered to a successful candidate will depend on the candidate's skills, qualifications, and experience. Successful candidates will also be eligible for a discretionary bonus based on Turner & Townsend's applicable benefit program. This role will provide the following benefits: 401(K), Dental insurance, Health insurance, Life insurance, and Vision insurance. **Equal Employment Opportunity:** CBRE has a long-standing commitment to providing equal employment opportunity to all qualified applicants regardless of race, color, religion, national origin, sex, sexual orientation, gender identity, pregnancy, age, citizenship, marital status, disability, veteran status, political belief, or any other basis protected by applicable law. **Candidate Accommodations:** CBRE values the differences of all current and prospective employees and recognizes how every employee contributes to our company's success. CBRE provides reasonable accommodations in job application procedures for individuals with disabilities. If you require assistance due to a disability in the application or recruitment process, please submit a request via email at recruitingaccommodations@cbre.com or via telephone at *************** (U.S.) and *************** (Canada). CBRE, Inc. is an Equal Opportunity and Affirmative Action Employer (Women/Minorities/Persons with Disabilities/US Veterans)

**Be visionary** Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. **Job Description** **Purpose Statement** **:** The Chemist position is a laboratory position for a chemist, lab technician degreed person with 0 to 5 years industrial experience. The position includes performing various laboratory duties, such as experimentation, testing, sales support, engineering support, and manufacturing support. **Results Expected** **:** 1. Designs, develops, and performs chemical techniques for separation procedures. Develops methods for testing sample introductions for Inductively Coupled Optical Emmision Spectrometers. 2. Evaluate and test Isco instruments and critical components. 3. Communicates in a clear and concise manner, through and written reports, the results of assigned tasks. 4. Practices safe and environmentally sound laboratory techniques. 5. Maintains secrecy of confidential and sensitive information by observing all procedures regarding securing and transmitting privileged information. 6. Collaborates and communicates effectively with other departments as a team member of projects. 7. Responsible for general laboratory maintenance including supply ordering and cleanup. 8. Responsible for other duties assigned by the Separations Laboratory Manager that are within the knowledge level of a college degreed chemistry major. **Job Specifications** **:** + Requires associate's degree in laboratory, Electronic, Industrial, Mechanical, Manufacturing or Engineering Technology or equivalent related schooling and experience. + Experience designing manufacturing support equipment and testing equipment required. + Should possess excellent communication skills, be able to work well with people, also able to work on multiple tasks simultaneously, have a proper sense of urgency to resolve problems that can significantly affect the company's financial performance + Experience with and knowledge of computers and programming is preferred. Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions. Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws. You may not realize it, but Teledyne enables many of the products and services you use every day **.** Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

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

Find your future at National Beef! National Beef of Liberal, Kansas is seeking a qualified professional to join our team as a Microbiology Laboratory Technician. With competitive pay and benefits, stable work, and an environment that is caring and supportive, National Beef could become your next career move! Hours for this position are 9:00 pm to 5:30 am Monday through Friday (Saturdays and Sundays as needed) Competitive Wages and Benefits: Family-friendly benefits including Health, Dental and Vision Paid vacation Paid holidays Employee meat purchase program Responsibilities Microbiology Laboratory Technician responsibilities include but are not limited to: Follows instructions on project methodology from laboratory management staff Ensures correctness and accuracy of information presented to Food Safety Center on samples Makes note of any sample and chain of custody differences in appropriate sample discrepancy logbook Efficiently performs tasks with a focus on speed and accuracy, ensuring timely completion while maintaining high quality and productivity standards in all assigned duties Run tests as specified for National Beef and as directed by laboratory management Inputs all data and information from received samples into electronic data base system Prints and fills out required paperwork for samples received during shift Responsible for following all policies, procedures, and protocols as approved by upper management for sample setup Read tests results on all samples being analyzed Checks completed paperwork for accuracy and as a part of the dual check program will check other technicians work before turning it in Assists the inventory clerk, when needed, with the receiving of incoming supplies, recording of data into receiving logbook (s) and stocking Inspects all received supplies making note of the condition, lot numbers, and expiration dates in the appropriate supply usage log Assists with the daily monitoring of temperature accuracy and records all temperatures for incubators, refrigerators, and freezers on log-sheet Enters results and prints completed reports for issuance while maintaining accuracy of all data outlined in the reports Issues completed reports for received samples to appropriate customers Properly implements all procedure modifications as outlined by laboratory management staff Directs all question concerning reports to a member of laboratory management staff Completes media growth and sterility quality assurance controls Responsible for maintaining adequate levels of testing supplies Completes supply re-order log for needed supplies Ensures specified daily housekeeping duties are performed Responsible for completing weekly housekeeping tasks and log sheet Utilizes any available time to cross train in other areas Assists laboratory technicians in other areas in day to day duties when time permits or when needed Responsible for maintaining accurate records for quality system traceability Ensures all decontamination steps for all samples that have been completed Completes all environmental quality assurance checks Carries out necessary testing as outlined by laboratory management for any pending results that have been determined by other team members Performs and completes any other duties assigned by FSCML management staff This is a safety sensitive position. This position is not remote. Qualifications Qualified Candidates for the Microbiology Laboratory Technician should possess the following: Minimum of a High school diploma or equivalence with some college background or an Associate's degree - College degree preferred Good written and oral communication skill in English Self-Starter while being a team player Ability to handle multi-tasking - not afraid to get dirty Excellent organizational skills which allows for multitasking is a must Previous laboratory experience or science related course work preferred (must provide credentials/college completed course work) Excellent customer service skills with all levels- Upper management, Vendors, and production employees Must possess computer skills in Microsoft Programs (Excel, Word, Access, Power-Point, Outlook/email) Schedule flexibility, including additional hours and weekends as needed Must be willing to be cross trained in many facets of laboratory work Must be at least 18 years of age or older. Applicants must be authorized to work for ANY employer in the U.S. We are unable to provide visa sponsorship at this time. Company Overview National Beef is a leader in producing fresh, chilled and further processed beef products for customers in the U.S. and worldwide. We offer a variety of employment opportunities in our production, packaging, and hide tanning facilities that stretch from the western plains to the east coast. We strive to be the preferred employer in every one of those communities, whether it's measured by the number of people employed or the good we do in the area. We invite you to join our family, wherever you call home. National Beef is an equal opportunity employer committed to workplace diversity. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, natural origin, age, gender identity, protected veterans status, or status as a disabled individual. #IND

Find your future at National Beef! National Beef of Liberal, Kansas is seeking a qualified professional to join our team as a Microbiology Laboratory Technician. With competitive pay and benefits, stable work, and an environment that is caring and supportive, National Beef could become your next career move! Hours for this position are 9:00 pm to 5:30 am Monday through Friday (Saturdays and Sundays as needed) Competitive Wages and Benefits: Family-friendly benefits including Health, Dental and Vision Paid vacation Paid holidays Employee meat purchase program Responsibilities Microbiology Laboratory Technician responsibilities include but are not limited to: Follows instructions on project methodology from laboratory management staff Ensures correctness and accuracy of information presented to Food Safety Center on samples Makes note of any sample and chain of custody differences in appropriate sample discrepancy logbook Efficiently performs tasks with a focus on speed and accuracy, ensuring timely completion while maintaining high quality and productivity standards in all assigned duties Run tests as specified for National Beef and as directed by laboratory management Inputs all data and information from received samples into electronic data base system Prints and fills out required paperwork for samples received during shift Responsible for following all policies, procedures, and protocols as approved by upper management for sample setup Read tests results on all samples being analyzed Checks completed paperwork for accuracy and as a part of the dual check program will check other technicians work before turning it in Assists the inventory clerk, when needed, with the receiving of incoming supplies, recording of data into receiving logbook (s) and stocking Inspects all received supplies making note of the condition, lot numbers, and expiration dates in the appropriate supply usage log Assists with the daily monitoring of temperature accuracy and records all temperatures for incubators, refrigerators, and freezers on log-sheet Enters results and prints completed reports for issuance while maintaining accuracy of all data outlined in the reports Issues completed reports for received samples to appropriate customers Properly implements all procedure modifications as outlined by laboratory management staff Directs all question concerning reports to a member of laboratory management staff Completes media growth and sterility quality assurance controls Responsible for maintaining adequate levels of testing supplies Completes supply re-order log for needed supplies Ensures specified daily housekeeping duties are performed Responsible for completing weekly housekeeping tasks and log sheet Utilizes any available time to cross train in other areas Assists laboratory technicians in other areas in day to day duties when time permits or when needed Responsible for maintaining accurate records for quality system traceability Ensures all decontamination steps for all samples that have been completed Completes all environmental quality assurance checks Carries out necessary testing as outlined by laboratory management for any pending results that have been determined by other team members Performs and completes any other duties assigned by FSCML management staff This is a safety sensitive position. This position is not remote. Qualifications Qualified Candidates for the Microbiology Laboratory Technician should possess the following: Minimum of a High school diploma or equivalence with some college background or an Associate's degree - College degree preferred Good written and oral communication skill in English Self-Starter while being a team player Ability to handle multi-tasking - not afraid to get dirty Excellent organizational skills which allows for multitasking is a must Previous laboratory experience or science related course work preferred (must provide credentials/college completed course work) Excellent customer service skills with all levels- Upper management, Vendors, and production employees Must possess computer skills in Microsoft Programs (Excel, Word, Access, Power-Point, Outlook/email) Schedule flexibility, including additional hours and weekends as needed Must be willing to be cross trained in many facets of laboratory work Must be at least 18 years of age or older. Applicants must be authorized to work for ANY employer in the U.S. We are unable to provide visa sponsorship at this time. Company Overview National Beef is a leader in producing fresh, chilled and further processed beef products for customers in the U.S. and worldwide. We offer a variety of employment opportunities in our production, packaging, and hide tanning facilities that stretch from the western plains to the east coast. We strive to be the preferred employer in every one of those communities, whether it's measured by the number of people employed or the good we do in the area. We invite you to join our family, wherever you call home. National Beef is an equal opportunity employer committed to workplace diversity. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, natural origin, age, gender identity, protected veterans status, or status as a disabled individual. #IND

We are seeking a dedicated and detail-oriented Quality Control Technologist to join our team in Lenexa, Kansas. This role is crucial in ensuring that all quality control aspects of finished product testing meet compliance standards, customer requirements, and regulatory guidelines. You will play a key role in maintaining documentation control duties as per quality assurance compliance requirements. Responsibilities + Review and maintain product compliance specifications and documentation control. + Perform and interpret microbiology testing, including growth promotion, biochemical, and AST. + Gain proficiency on all performance benches and document testing results to determine product disposition. + Maintain consistency in training in Master Control and establish SOP criteria for inspection/testing. + Maintain department equipment and request consumables as needed. + Exercise and monitor GMP compliance in the work environment. + Collaborate closely with the Quality Assurance department as part of the quality team. + Execute Stability Study testing in accordance with QA requirements. + Coordinate with Customer Service Representatives to ensure timely product releases. + Participate in the continuous improvement program within the department. + Adhere to all safety requirements and procedures and assist in maintaining standards according to GMP and ISO regulations. + Support all company policies and participate in achieving department goals. + Perform other duties as assigned. Essential Skills + Possess at least a 4-year degree in biological sciences with coursework in microbiology and a laboratory component or a 4-year degree with 5+ years of microbiology lab experience. + Minimum 1-2 years of experience in QC/QA or microbiology laboratory work, or an equivalent combination of education and experience. + Familiarity with FDA regulations for medical devices. + Ability to manage tasks in an organized fashion and communicate effectively with various departments. + Intermediate computer skills, preferably with Microsoft Word, Excel, and PowerPoint. + Experience working in SAP is a plus. + Ability to follow written and verbal instructions and adapt to new procedures. + Self-motivated, highly responsible, with excellent teamwork spirit. + Excellent verbal and written communication skills in English. Additional Skills & Qualifications + Availability to work weekend shifts when needed. + Good entry-level job in the field of microbiology. Job Type & Location This is a Contract position based out of Lenexa, KS. Pay and Benefits The pay range for this position is $20.00 - $20.00/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 Lenexa,KS. Application Deadline This position is anticipated to close on Jan 28, 2026. 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Lab Analyst III (Bioanalytical) - Full Time, Benefits - Greater Kansas City, KS (Lenexa) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Looking to grow your career in support of real scientific advancements that bring new medicine to patients? Our bioanalytical teams in the Greater Kansas City area are growing! Join a culture that values you for your attitude, not just your experience. We are currently seeking a Lab Analyst III to join our diverse and dynamic team. This Lab Analyst III will join our bioanalytical LC-MS team and will be responsible for performing advanced laboratory tests and analyses to support complex clinical research studies. You will play a critical role in ensuring the accuracy and reliability of laboratory data, mentoring junior analysts, and contributing to the continuous improvement of laboratory operations and methodologies. What You Will Be Doing: * Conduct advanced laboratory assays and analyses on bioanalytical samples for pharmaceutical companies. Follow established protocols and procedures to ensure data accuracy and integrity. * Perform LC-MS assays for the routine batch analysis of bioanalytical samples involving simple to complex analytical techniques. Perform laboratory work to GLP and GCP standard. * Interpret complex test results for clinical research projects, and provide accurate, complete, compliant reports following GLP or GCP regulations. * Ensure smooth transfer of high-quality analytical results to PIs and participate in evaluation and interpretation of data. * Generate Laboratory Reports for work performed. * Lead quality control activities, including equipment calibration, troubleshooting, and validation of laboratory processes. * Prepare buffers and solutions, dispose of expired reagents, and order and maintain laboratory supplies like reagents and equipment. * Maintain accurate records of maintenance and calibrations in database system. * Collaborate with cross-functional teams to develop and optimize new laboratory methods and workflows to improve efficiency and quality. * Mentor and train junior lab analysts, providing guidance on laboratory best practices and complex analytical techniques. Your Profile: * Bachelor's degree in biology, chemistry, or a related scientific field; advanced degree preferred. * 3-5 years of experience in an academic or industry laboratory setting, with expertise in LC-MS testing procedures and data analysis. * Proficiency in operating and maintaining complex laboratory equipment and software for data management and reporting. * Ability to follow instructions, handle routine tasks with precision, and high focus to detail. * Strong analytical problem-solving and experimental strategy skills, with a commitment to maintaining high-quality standards and compliance. * Excellent communication and leadership abilities, with experience mentoring and guiding junior team members. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

In a world of vibrant color, INX stands out by blending art, science, and sustainability into every drop of ink we make. We're globally recognized for our innovation, and we're A Great Place to Work-Certified™ company! INX International is the third largest producer of inks in North America with full-service subsidiaries in Europe and South America. We offer a complete line of ink and coating solutions technology for commercial, packaging and digital applications. We expertly blend pioneering technology with a deep commitment to the environment. Dedicated to coloring a safe and sustainable future one print at a time, you can see our color chemistry on beverage cans, food and household packaging, clothing, banners, billboards and more. Investing in and protecting our employees is the key to our success. Our average employee has been with us 12 years, and we recognize the significant experience and the continuous dedication of our team members. We're actively seeking new talent with new ideas as we continue to provide sustainable products, service and innovation to the printing and packaging markets. Join us in coloring a safe and sustainable future! Job Description Are you detail-oriented and enjoy putting out a high-quality product? We are seeking a Quality Control Technician for our Ink Lab. Check out this opportunity to be part of our team and contribute to our growth and success. As a Quality Control Tech, you will be responsible for: Performing quality control testing of production batches of inks and coatings Completing associated clerical work (entering results into SAP, printing labels, filing, etc.) Performing 5S cleaning and maintaining the area Establishing and maintaining accurate and complete quality records in SAP Performing color quality tests; making batch additions and adjustments Implementing necessary and timely batch corrections directly to Production Calibrating and verifying test equipment Investigating and analyzing non-conforming batches (internal and external) Supporting Lean Manufacturing Ensuring sample retention management Performing some customer proofing Qualifications To perform your job as expected, you will be required to: Have a high school diploma or GED equivalent Be able to pass a color vision test Demonstrate proficiency with Microsoft Suite programs (MS Office) and other computer skills Be flexible to cover other shifts if needed Have excellent verbal, written, reading comprehension and good math skills Have 6 to 12 months previous Lab/QC related work experience Be able to stand for long periods of time In addition to these qualifications, we will consider it a plus if you have: An understanding of manufacturing operations and basic aspects of printing technologies Experience working in a high volume department Prior experience in Lean Manufacturing facility Trade or Tech school Availability and willingness to work overtime as needed SAP Knowledge Previous experience in the ink industry Additional Information We offer a competitive salary with excellent benefits including medical, dental, vision, life insurance, disability, pet insurance, HSA and FSA, long-term care, 401(k), and more. Through our programs, which now include Paid Volunteer Time Off and Paid Parental Leave, we support the needs of our employees, their dependents, and their communities by providing a benefit package that is easy to understand, easy to access, and affordable for all our employees. Don't just choose a job; choose a career that emphasizes employee growth in a safe, environmentally conscious culture. Embark on your Colorful Career with us! We require post-offer, pre-employment drug screens, physicals, and background checks. Equal Opportunity Employer: disability/veteran.