Quality control analyst jobs in Kansas - 87 jobs

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: Perform Quality Control activities in support of finished products, which includes testing of raw materials and serum. Perform testing according to approved procedures or compendia (such as USP, EP, ACS) following site quality and safety standards. Testing includes, but is not limited to, environmental monitoring, bioburden analysis, endotoxin testing, microbial limits testing, microbial identification, and growth promotion of microbiological media and reagents. Evaluate results against approved specifications, perform peer review of analytical data, and release data from QC in a timely manner to meet scheduled release dates. Typically performs routine assignments with little direction using existing procedures and practices that require some knowledge of concepts and specialized technical expertise within an analytical/scientific method or operational process. Accountable for the quality of own work. Receives clear instruction, guidance and direction from more senior level roles or even solves problems of low complexity independently by selecting solutions based on fact-based information. Work some weekends or holidays (as required by testing/business needs). Provide complete and accurate records consistent with quality guidelines and GDP requirements. Communicate the status of operations and bring deviations to the attention of the supervisor. Attention to detail. Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal) and ensure equipment and work areas are maintained and clean. Take the necessary action to resolve any unsafe conditions. Who You Are Minimum Qualifications: * Bachelor's Degree in Biology, Chemistry, or other Life Sciences discipline Preferred Qualifications: * 1+ year of laboratory experience in a quality control lab * Good attention to detail * Knowledge of site Quality standards * Familiar with laboratory instruments and production equipment Pay Range for this position: $24-$44 per hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

We are always looking forward to receiving resumes from candidates with skills and technical experience in the aerospace sector. We are very happy to receive speculative resumes if you are looking for a career change within the aerospace industry. Our flexible recruitment services will provide you with the following employment options: * Contract * Contract to Direct * Direct Our experienced consultants are experts in their field and are well placed to advise you on all aspects of aerospace recruitment opportunities, and employment trends.

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.

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.

Basic Function HF Sinclair in El Dorado, Kansas is seeking a Lab Analyst who, under minimal supervision, is responsible for finished product quality control and specification compliance testing including calibration and standardization of test equipment. Job Duties ESSENTIAL JOB DUTIES/RESPONSIBILITIES: (functions considered essential as defined by ADA) Conducts product quality control and specification compliance testing Enters lab results in proper databases and communicates results to assigned area€™s management and other personnel Ensures work area is kept clean and organized Conducts calibration and standardization of testing instruments Executes required assigned area€™s Health Safety & Environmental programs and initiatives. Conducts proficiency sample testing Expected to learn ASTM methods Expected to learn Laboratory Information Management System Special assignments or tasks assigned to the employee by their supervisor, as determined from time to time in their sole and complete discretion. Education Level A minimum of a High School Diploma or equivalent is required. A minimum of 20 hours of progressive level college chemistry is required. Required Skills Intermediate level algebra and proficiency with spreadsheet and word-processing software applications, basic computer skills including Microsoft office. Good mechanical ability and understanding of operational principles of assigned area laboratory testing instruments. Ability to effectively communicate with others, both written and verbal communication. Ability to complete all required classroom and CBT training. Ability to perform basic mathematical calculations, basic reading and writing skills. Work Conditions Petroleum refinery, warehouse/plant environment, out-of-doors, and driver based environment including but not limited to chemicals, pressure vessels, tanks, and rotating equipment. Subject to all temperatures, weather, and varying road conditions. May be required to work flexible hours, including nights, weekends, and a rotating schedule required. Benefits HF Sinclair offers a comprehensive benefits package designed to support the well-being of our employees and their families. Our benefits include, but are not limited to, the following: Medical Insurance Vision Insurance Dental Insurance Paid Time-Off 401(k) Retirement Plan with match Educational Reimbursement Parental Bonding Time Employee Discounts We are committed to fostering a supportive and inclusive work environment, ensuring our employees have the resources needed to thrive professionally and personally. Benefit eligibility is governed by official plan documents, for more details visit Total Rewards.Physical Requirements Job conditions require standing, walking, sitting, twisting, stooping, crouching, kneeling, taking or hearing, making visual inspections, making precise hand and finger movements, reaching or grasping, lifting and/or carrying up to 50lbs, pushing and/or pulling up to 25lbs, ability to operate and drive all assigned company vehicles at company standard insurance rates is essential, valid state driver license. Job conditions may require wearing personal protective equipment (beards not permitted). Our One HF Sinclair Culture: At HF Sinclair, we are united through our One HF Sinclair Culture, which is underpinned by our five core values of Safety, Integrity, Teamwork, Ownership and Inclusion. Developed to empower our people, our five core cultural values are at the heart of everything we do and extend to how we engage our stakeholders. These values influence our decisions, shape our behaviors and keep us connected across the entire organization. We maintain a true Safety culture for our employees, communities, environments and customers. Our goal is to make sure everyone returns home safely each day. We have a long-standing commitment to Integrity and ethical behavior and do what is right for our employees, investors, communities and the environment. We encourage employees to Step Up and Stand Out by championing a culture of Teamwork and Ownership. We foster a culture of Inclusion by encouraging diversity of experiences, viewpoints and backgrounds. What makes each of us different, together makes us stronger.About HF Sinclair Corporation HF Sinclair Corporation, headquartered in Dallas, Texas, is an independent energy company that produces and markets high-value light products such as gasoline, diesel fuel, jet fuel, renewable diesel and other specialty products. HF Sinclair owns and operates refineries located in Kansas, Oklahoma, New Mexico, Wyoming, Washington and Utah and markets its refined products principally in the Southwest U.S., the Rocky Mountains extending into the Pacific Northwest and in other neighboring Plains states. HF Sinclair supplies high-quality fuels to more than 1,500 branded stations and licenses the use of the Sinclair brand at more than 300 additional locations throughout the country. In addition, subsidiaries of HF Sinclair produce and market base oils and other specialized lubricants in the U.S., Canada and the Netherlands, and export products to more than 80 countries. Through its subsidiaries, HF Sinclair produces renewable diesel at two of its facilities in Wyoming and also at its facility in Artesia, New Mexico. HF Sinclair provides petroleum product and crude oil transportation, terminalling, storage and throughput services to its refineries and the petroleum industry.Equal Opportunity Employer HF Sinclair Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status or any other prohibited ground of discrimination.

Basic Function HF Sinclair in El Dorado, Kansas is seeking a Lab Analyst who, under minimal supervision, is responsible for finished product quality control and specification compliance testing including calibration and standardization of test equipment. Job Duties ESSENTIAL JOB DUTIES/RESPONSIBILITIES: (functions considered essential as defined by ADA) * Conducts product quality control and specification compliance testing * Enters lab results in proper databases and communicates results to assigned areas management and other personnel * Ensures work area is kept clean and organized * Conducts calibration and standardization of testing instruments * Executes required assigned areas Health Safety & Environmental programs and initiatives. * Conducts proficiency sample testing * Expected to learn ASTM methods * Expected to learn Laboratory Information Management System Special assignments or tasks assigned to the employee by their supervisor, as determined from time to time in their sole and complete discretion. Education Level A minimum of a High School Diploma or equivalent is required. A minimum of 20 hours of progressive level college chemistry is required. Required Skills Intermediate level algebra and proficiency with spreadsheet and word-processing software applications, basic computer skills including Microsoft office. Good mechanical ability and understanding of operational principles of assigned area laboratory testing instruments. Ability to effectively communicate with others, both written and verbal communication. Ability to complete all required classroom and CBT training. Ability to perform basic mathematical calculations, basic reading and writing skills. Work Conditions Petroleum refinery, warehouse/plant environment, out-of-doors, and driver based environment including but not limited to chemicals, pressure vessels, tanks, and rotating equipment. Subject to all temperatures, weather, and varying road conditions. May be required to work flexible hours, including nights, weekends, and a rotating schedule required. Benefits HF Sinclair offers a comprehensive benefits package designed to support the well-being of our employees and their families. Our benefits include, but are not limited to, the following: * Medical Insurance * Vision Insurance * Dental Insurance * Paid Time-Off * 401(k) Retirement Plan with match * Educational Reimbursement * Parental Bonding Time * Employee Discounts We are committed to fostering a supportive and inclusive work environment, ensuring our employees have the resources needed to thrive professionally and personally. Benefit eligibility is governed by official plan documents, for more details visit Total Rewards. Physical Requirements Job conditions require standing, walking, sitting, twisting, stooping, crouching, kneeling, taking or hearing, making visual inspections, making precise hand and finger movements, reaching or grasping, lifting and/or carrying up to 50lbs, pushing and/or pulling up to 25lbs, ability to operate and drive all assigned company vehicles at company standard insurance rates is essential, valid state driver license. Job conditions may require wearing personal protective equipment (beards not permitted). Our One HF Sinclair Culture: At HF Sinclair, we are united through our One HF Sinclair Culture, which is underpinned by our five core values of Safety, Integrity, Teamwork, Ownership and Inclusion. Developed to empower our people, our five core cultural values are at the heart of everything we do and extend to how we engage our stakeholders. These values influence our decisions, shape our behaviors and keep us connected across the entire organization. We maintain a true Safety culture for our employees, communities, environments and customers. Our goal is to make sure everyone returns home safely each day. We have a long-standing commitment to Integrity and ethical behavior and do what is right for our employees, investors, communities and the environment. We encourage employees to Step Up and Stand Out by championing a culture of Teamwork and Ownership. We foster a culture of Inclusion by encouraging diversity of experiences, viewpoints and backgrounds. What makes each of us different, together makes us stronger. About HF Sinclair Corporation HF Sinclair Corporation, headquartered in Dallas, Texas, is an independent energy company that produces and markets high-value light products such as gasoline, diesel fuel, jet fuel, renewable diesel and other specialty products. HF Sinclair owns and operates refineries located in Kansas, Oklahoma, New Mexico, Wyoming, Washington and Utah and markets its refined products principally in the Southwest U.S., the Rocky Mountains extending into the Pacific Northwest and in other neighboring Plains states. HF Sinclair supplies high-quality fuels to more than 1,500 branded stations and licenses the use of the Sinclair brand at more than 300 additional locations throughout the country. In addition, subsidiaries of HF Sinclair produce and market base oils and other specialized lubricants in the U.S., Canada and the Netherlands, and export products to more than 80 countries. Through its subsidiaries, HF Sinclair produces renewable diesel at two of its facilities in Wyoming and also at its facility in Artesia, New Mexico. HF Sinclair provides petroleum product and crude oil transportation, terminalling, storage and throughput services to its refineries and the petroleum industry. Equal Opportunity Employer HF Sinclair Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status or any other prohibited ground of discrimination. Nearest Major Market: Wichita

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

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 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

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

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.

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.

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

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

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.

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst - 10hr Day Shift position at its facility in Winfield, 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 Thursday through Sunday, from 7:00am - 5:30pm. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from

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.

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

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.