Quality control analyst jobs in Kansas City, MO - 71 jobs

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 Ensure Part 135 and Part 121 air carrier GMM guidance is followed for maintenance, documentation, return to service and all records are complete 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, CFR'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 Team leadership Project management Professional communication Education & Experience: You possess a current FAA Airframe & Powerplant License are eligible for Inspection Authorization You have High School Diploma and 3 years of experience in a similar role within the aviation industry You have a minimum of 3 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

Company Information 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. We create value for our key stakeholders through three premier brands, Thermo Scientific, Fisher Scientific and Unity™ Lab Services, which offer a unique combination of innovative technologies, convenient purchasing options and a single solution for laboratory operations management. Our products and services help our customers solve complex analytical challenges, improve patient diagnostics and increase laboratory productivity. Visit ********************* Job Description Job Title: Quality Control Scientist I Reports To: Quality Control Supervisor Group/Division: MBD Career Band: Band IV Job Track: Quality Assurance Position Location: Lenexa Kansas Number of Direct Reports none Day/Shift (if applicable): M-F FLSA Status (Exempt/Non-Exempt): Exempt Position Summary: Responsible for all quality control aspects of finished product testing. Ensure that performance of finished product is in compliance with testing standards per IFU and SOP's in addition to customer requirements and regulating agencies' guidelines. Documentation control duties per Quality assurance compliance requirements. Key Responsibilities: Review and maintain product compliance specifications, documentation control. Perform and interpret microbiology testing including growth promotion, biochemical, AST. Gain proficiency on all performance benches. Documentation of testing results and determining disposition. Maintain consistency in training in Master Control. Establish and maintain SOP criteria for inspection/testing. Responsible for maintaining department equipment and requesting consumables as needed. Exercise and monitor GMP compliance in work environment. Work closely with Quality Assurance department as a quality team. Execute Stability Study testing in accordance with QA requirements. Work in conjunction with Customer Service Representatives to achieve on time product releases for standing orders and special products. Work with 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. Assists in maintaining standards in accordance with GMP's/SOP's and ISO regulations. Participate in achieving department goals. Support all company policies. Performs other duties as assigned. Minimum Requirements/Qualifications: 1. Possess at least a 4-year degree in the biological sciences. Must have course work in microbiology with a laboratory or a 4-year degree with 5+ years of microbiology lab experience. 2. A minimum combined 1-2 years of experience of in related QC/QA, microbiology laboratory work in a laboratory setting, or an equivalent combination of education and experience. 3. Familiarity with FDA regulations for medical devices. 4. Possess the ability to manage many tasks and in an organized fashion. 5. Able to communicate effectively with a variety of departments in regard to quality testing parameters. 6. Possess intermediate computer skills, preferably with experience in Microsoft word to include Word, Excel and PowerPoint programs. Experience working in SAP is a plus. 7. Listen to, and follow, written and verbal instructions. 8. Able to adapt and to learn new procedures and to maintain a scientific and objective approach. 9. Must be available to work weekend shifts when needed. 10. Self-motivated, highly responsible and possess a good teamwork spirit. 11. Excellent verbal and written skills in English. Non-Negotiable Hiring Criteria: (Bullet 3-5 key quantifiable skills or position requirements that the candidate must have to be considered for this position.) Candidate must be a good time manager. Candidate must be willing to put in overtime when needed to complete tasks. Candidate must be a good team player/participant on teams. Candidate must have a high sense of responsibility. Candidate must possess critical thinking skills.

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.

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 Technician will be responsible for all aspects of the quality programs and functions. These include maintaining all HACCP, food safety records, plant audits, mock recall programs and training the plant on these issues and procedures. Performs testing to validate the microbiological quality of current and new ingredients, suppliers, and packages. Provides test data to assure the production of high quality products. Tests current and new concentrate ingredients in process and finished concentrates, and beverages products in development and finished products. The QC Technician will also work with the R&D Team on new product launches. ESSENTIAL DUTIES AND RESPONSIBILITIES: Knowledge of all cleaning agents and applications, external, internal, cleaners, and sanitizers. Properly document and follow all procedures set forth in the frequency guide and standards. Ability to properly fill out batch reports, calculate variations in batch sizes, proper attributes, standards, and other data required on batch report documented per formula. Ability to properly measure and follow proper mixing procedures. Ability to evaluate and troubleshoot batch and make corrections. Ability to perform all testing, evaluations, and documentation of results while following procedures. Ability to troubleshoot and take corrective action on the line. Ability to properly prepare batch tanks for batching, tank rinsing, tank sanitation, odor, and tasting. Full knowledge and capabilities to perform internal pest control program, location of stations, checking and cleaning of stations, and proper documentation on hand of pest control program. Assist supervisors in resolving Quality Control issues, tracking quality trends, recommending and implementing plans to improve quality and production efficiency. Responsible for compliance with Federal and State legislation by establishing and enforcing quality standards; testing materials and product. Ability to collect, analyze and summarize process quality information and trends. Computer literacy required with proficiency in Microsoft Office products including Excel and Word. Typically faces situations that have a variety of interpretations and require careful evaluation. LANGUAGE SKILLS: Ability to read, analyze, and interpret common information, reports and other documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or company representatives. Ability to effectively present information to management. 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 walk, stand for long periods of time, sit and talk or hear. The employee frequently is required to use hands and fingers, to handle, or feel, sit for long periods of time, stand frequently, bend, squat, reach and turn to access files and office equipment. Must be able to lift up to 50 pounds. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Field positions will be exposed to various unfamiliar conditions where Personal Protective Equipment (PPE) must be worn and which may include, but are not limited to manufacturing and warehouse plants, and other locations as directed by supervisor. The noise level in the work environment is usually moderate, but increases significantly in warehouse and manufacturing plants. MINIMUM QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. High School Diploma or GED preferred or equivalent experience. 2-3 years hands-on work experience in the carbonated soft drink industry preferred. Experience in quality control testing procedures and internal and external sanitation of beverage equipment with a clear understanding of all aspects of blending, product attributes recordkeeping, yields, etc. Strong computer skills, including Microsoft business applications and various reporting software. Exceptional interpersonal and verbal communication skills Understands and can follow all OSHA required training. Must be 18 years or older Favorable background and drug exam. Ability and willingness to work a flexible Full Time schedule that may include weekends and holidays. Must be able to provide own transportation to various locations in organizational service areas, as required by duties. Shasta Beverages, Inc. provides equal employment opportunities to all applicants for employment without regard to race, color, religion, sex, national origin, age, disability, gender, genetics, gender identity, disabled veterans or sexual orientation.

Performs visual and/or mechanical inspections on component parts to ensure the product quality of production runs. Utilizes inspection equipment (scopes, gauges, etc.) to ensure components meet required specifications. Conduct a variety of mechanical tests on assemblies to ensure unit functions according to specifications. This position also enters in-process information into a computer system as well as assisting in housekeeping within the department to maintain a safe work environment. SAFETY AND ENVIRONMENTAL: All employees are expected to act in a safe manner at all times and ensure that those around them do not put themselves or others at risk. Everyone is personally accountable for his/her own safety as well as their co-workers. Safety and health is a shared responsibility of everyone in the organization and a condition of employment. We value and expect engagement out of all employees. Co-workers share the responsibility for doing the right thing for the environment and carrying out the stewardship principles addressed in our Environmental Policy. We will provide the resources necessary to implement this policy, and management will conduct periodic reviews to ensure its ongoing effectiveness. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform in-process inspections of molded/assembled components per ISO procedures. Compare product with part specifications. Verify specified dimensions and perform color match if required. Read work orders, test manuals and performance specifications to determine testing procedure and equipment to be used Audit production for defective components/finished goods when required. Quarantine product when required Disposition rejected or defective product in accordance with Lead instructions. Generate hold tickets when required for product evaluation. Document all inspection information from in-process checks into computer system. Collect shots for in-process inspections. Check MIU for correct lot number, color, cavitation, mold number, etc. Check components/finished good per ISO procedures to ensure quality of production using various inspection equipment. Perform color matches of components if required. Verify dimensions of parts. Verify internal assembly and alignment of parts according to specifications. Test functional performance of components/finished products under specified instructions. Compare results with specifications and record test data. Analyze test results on defective units to determine extent of failure. Confer with production personnel regarding testing and results. Input of data to the Certificate of Analysis, Excel database Read work order and verify correct/incorrect materials in area. Notify materials handlers to have removed as necessary. Calibrate test instruments according to specifications. Assist in training new hires Performs other duties as assigned Other duties may be assigned. Must follow all work rules and policies QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE: One to three months related experience and/or training LANGUAGE SKILLS: Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence and effectively present information in one-on-one and small group situations to other employees of the organization. MATHEMATICAL SKILLS: Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, percentage, and interpret bar graphs. REASONING ABILITY: Ability to apply commonsense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to handle problems involving several concrete variables in standardized situations. 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 the 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 stand, walk, talk and hear. The employee is frequently required to use hands to finger, handle, or feel; reach with hands and arms; climb or balance; and sit, bend, stoop, twist, kneel, squat, or crawl. The employee must regularly lift and/or move up to 25 pounds, frequently lift and/or move up to 58 pounds, and occasionally lift and/or move up to 100 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing 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 regularly works near moving mechanical parts and is regularly exposed to risk of electrical shock. The employee is frequently exposed to vibration. The employee occasionally works in high, precarious places and is occasionally exposed to fumes or airborne particles. The noise level in the work environment is usually loud. WORK SCHEDULE: 11:00 pm-7:00 am LIMITATIONS AND DISCLAIMER The above is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties and skills required for the position. All job requirements are subject to possible modification to reasonably accommodate individuals with disabilities. Some requirements may exclude individuals who pose a direct threat or significant risk to the health and safety of themselves or other employees. This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position. Employees will be required to follow any other job-related instructions and to perform other job-related duties requested by their supervisor in compliance with Federal and State Laws. Requirements are representative of minimum levels of knowledge, skills and/or abilities. To perform this job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently. Continued employment remains on an “at-will” basis. Silgan is an Equal Opportunity Employer. We consider applicants for all positions without regard to race, color, religion, sex, national origin, age, marital status, or the presence of a disability, which would not prevent the performance of essential job duties with, or without reasonable accommodation of any other protective status. Silgan is a drug-free workplace.

Job Title: QC Scientist IJob Description 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. Work Environment The position is located in Lenexa, Kansas, with working hours from Monday to Thursday or Tuesday to Friday, 7:00 AM to 5:30 PM, and another shift from Friday to Monday, 7:00 AM to 5:30 PM. You will work in a fast-paced laboratory setting, closely with a team, ensuring adherence to GMP and ISO standards. 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 for other accommodation options.

Job Description GENERAL STATEMENT OF DUTIES: Under general supervision, examines and inspects manufactured product and compares it to established standards, Concrete testing noting discrepancies and fabrication errors; performs related work as required or assigned. ESSENTIAL DUTIES: review and interpret plans, specifications and methods to ensure compliance to project specifications use specific tools and instruments in support of related duties prepare and maintain daily logs, reports and inspection records in accordance with customer requests, company policies and procedures perform all occupational safety and hazard procedures in conjunction with all essential duties maintain order and housekeeping in assigned area KNOWLEDGE, SKILLS AND ABILITIES: Knowledge of: industry standards and requirements occupational hazards and proper safety precautions the manufacturing process Skills in: reading and interpreting drawings and specifications operating tools and machines used in the inspection process Ability to: obtain industry certifications and participate in continuing education and training establish and maintain effective working relationships with other employees communicate effectively and at an appropriate level for this classification WORK ENVIRONMENT: Employee may be exposed to: moving mechanical/electrical parts and equipment fumes or airborne particles vibration metal preservatives oils and greases loud noises heat/cold/wet conditions working above ground PHYSICAL DEMANDS: While performing the duties of this classification, the employee is regularly required stand; walk; sit; use hand to finger, handle, or feel objects, tools or controls; reach with hands and arms; stoop, kneel, crouch, bend or twist; talk or hear, see and focus. The employee must regularly lift and/or move heavy objects, up to and exceeding 50 pounds. MINIMUM QUALIFICATIONS: Equivalent combination of experience, education and training which provides the desired knowledge, skills and abilities of this classification. Must successfully complete and possess all required company training and certification before operating any machinery, equipment or tools. Must be able to work overtime on short notice, which could exceed 8 hours per shift and/or 40 hours per work week. #hc80137

Lab Analyst II- Onsite, Full-Time; Lenexa, KS ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Lab Analyst II to join our diverse and dynamic team. As a Lab Analyst II at ICON, you will be responsible for performing intermediate-level laboratory tests and analyses to support clinical research projects. You will contribute to the accuracy and reliability of laboratory data, while adhering to strict quality and regulatory standards, and playing a key role in the daily operations of the lab. **What You Will Be Doing:** + Conducting intermediate-level laboratory tests and analyses in compliance with established protocols and procedures. + Accurately recording and documenting test results, maintaining data integrity and quality standards throughout all processes. + Operating and maintaining laboratory equipment, including performing routine calibrations, troubleshooting, and preventive maintenance. + Assisting in the development and validation of new laboratory methods and protocols to enhance operational efficiency and data quality. + Collaborating with cross-functional teams to support project timelines and ensure effective communication of test results and findings. **Your Profile:** + Bachelor's degree in biology, chemistry, or a related scientific field; advanced degree preferred. + 2-4 years of experience in a laboratory setting, with a focus on intermediate-level testing and analytical techniques. + Strong technical skills and proficiency in using laboratory equipment and software for data analysis and reporting. + Excellent attention to detail and organizational abilities, with a commitment to maintaining high-quality standards and compliance. + Effective communication and teamwork skills, with the ability to collaborate in a fast-paced and dynamic environment. **What ICON can offer you:** Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: + Various annual leave entitlements + A range of health insurance offerings to suit you and your family's needs. + Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. + Global Employee Assistance Programme, 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

Summary: Responsible for the inspection of incoming materials and outgoing product at various stages in the production process and data collection of results to generate product quality reports. Inspect printed circuit board (PCB's) assemblies and other incoming materials for compliance to company specifications. Perform First Article Inspection for all new parts and new vendors Generate spreadsheets for data collection and reports Inspect PCB's by using magnifiers or microscope to detect circuit shorts, missing solder and solder bridges, scratches, cracks and other defects. Perform basic assembly tasks on production line (identify components, read B.O.M., drawings, special instructions, completing paperwork, etc). Perform other duties as assigned. Summary: Responsible for the inspection of incoming materials and outgoing product at various stages in the production process and data collection of results to generate product quality reports. Inspect printed circuit board (PCB's) assemblies and other incoming materials for compliance to company specifications. Perform First Article Inspection for all new parts and new vendors Generate spreadsheets for data collection and reports Inspect PCB's by using magnifiers or microscope to detect circuit shorts, missing solder and solder bridges, scratches, cracks and other defects. Perform basic assembly tasks on production line (identify components, read B.O.M., drawings, special instructions, completing paperwork, etc). Perform other duties as assigned. Skills: Proficiency in Microsoft Office Products and Access Ability to use precision measuring instruments and devices Ability to keep accurate records and generate reports Ability to follow company procedures and standards Excellent time management skills with the ability to work with little supervision Physical Requirements: This position requires the ability to lift or move a minimum of 50 lbs. Must have the ability to sit or stand for long periods of time. Education/Experience: High School Diploma or G.E.D. 6 months of electronic or hardware quality control experience Trained to IPC-610 specification Skills & Requirements Skills: Proficiency in Microsoft Office Products and Access Ability to use precision measuring instruments and devices Ability to keep accurate records and generate reports Ability to follow company procedures and standards Excellent time management skills with the ability to work with little supervision Physical Requirements: This position requires the ability to lift or move a minimum of 50 lbs. Must have the ability to sit or stand for long periods of time. Education/Experience: High School Diploma or G.E.D. 6 months of electronic or hardware quality control experience Trained to IPC-610 specification

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

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst at its facility in Lawrence, KS. Ideal candidates will possess the following: - A BS or BA in the biological sciences or related field (required) - Strong attention to detail - Proficiency with data entry and computer applications - Ability to multitask and work in a fast-paced environment - Strong written and verbal communication skills - Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. This is a full-time position and employees will be eligible for standard benefits after a brief waiting period. The schedule for this position is Sunday through Thursday, from 7:00am - 3:00pm. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from

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 Ensure Part 135 and Part 121 air carrier GMM guidance is followed for maintenance, documentation, return to service and all records are complete 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, CFR'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 Team leadership Project management Professional communication Education & Experience: You possess a current FAA Airframe & Powerplant License are eligible for Inspection Authorization You have High School Diploma and 3 years of experience in a similar role within the aviation industry You have a minimum of 3 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 7:30AM-4:00PM Monday thru Friday.

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: Perform accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. Completes second person verification of test results. Participates in laboratory root cause investigations and quality system improvement initiates by executing well defined protocols and procedures. Shares technical information and best practice within the group. Design and evaluation of experiments, methods development and characterization, support of process development/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 conducted and documented in accordance with the appropriate Quality System. Act as a resource for insuring adherence to quality systems. 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. 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 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. Additional Information All your information will be kept confidential according to EEO guidelines.

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.

Bioanalytical Lab Analyst II - 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 II** to join our diverse and dynamic **quality control (QC)** team within the **LC-MS** department. The **Lab Analyst II (QC)** will review chromatograms in the LC-MS analysis software, interpret and verify results in LIMS. Additionally, the **Lab Analyst II (QC)** will be responsible for independently reviewing results generated during sample analysis and method validation testing, according to our Standard Operating Procedures (SOPs). **What You Will Be Doing:** + Accurately recording and documenting test results, maintaining data integrity and quality standards throughout all processes. + Review results generated using various techniques for bioanalysis and method validation. + Review chromatograms in the LCMS analysis software. Interpret and verify results in the Lab Information Management System (LIMS). + Review documentation in both paper based and electronic laboratory notebooks. + Collaborating with team members to ensure timely and efficient completion of laboratory tasks and projects. **Your Profile:** + Effective communication and teamwork skills when executing logical problem solving and experimental strategy. + Bachelor's degree in biology, chemistry, or a related scientific field; advanced degree preferred. + 2-4 years of experience in a laboratory setting, with a focus on intermediate-level testing and analytical techniques. + Strong technical skills and proficiency in using laboratory equipment and software for data analysis and reporting. + Excellent attention to detail, and willingness to learn analytical chemistry and LC-MS/MS workflows. + Commitment to maintaining high-quality standards and compliance. **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

Bioanalytical Lab Analyst II - 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 II to join our diverse and dynamic quality control (QC) team within the LC-MS department. The Lab Analyst II (QC) will review chromatograms in the LC-MS analysis software, interpret and verify results in LIMS. Additionally, the Lab Analyst II (QC) will be responsible for independently reviewing results generated during sample analysis and method validation testing, according to our Standard Operating Procedures (SOPs). What You Will Be Doing: * Accurately recording and documenting test results, maintaining data integrity and quality standards throughout all processes. * Review results generated using various techniques for bioanalysis and method validation. * Review chromatograms in the LCMS analysis software. Interpret and verify results in the Lab Information Management System (LIMS). * Review documentation in both paper based and electronic laboratory notebooks. * Collaborating with team members to ensure timely and efficient completion of laboratory tasks and projects. Your Profile: * Effective communication and teamwork skills when executing logical problem solving and experimental strategy. * Bachelor's degree in biology, chemistry, or a related scientific field; advanced degree preferred. * 2-4 years of experience in a laboratory setting, with a focus on intermediate-level testing and analytical techniques. * Strong technical skills and proficiency in using laboratory equipment and software for data analysis and reporting. * Excellent attention to detail, and willingness to learn analytical chemistry and LC-MS/MS workflows. * Commitment to maintaining high-quality standards and compliance. 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

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.

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 for other accommodation options.