Chemist Jobs in Kansas

GENERAL STATEMENT OF RESPONSIBILITY: Analyze urine, oral fluid and sweat patch aliquots for the presence of drugs. ESSENTIAL FUNCTIONS: * Operate, monitor, maintain, calibrate, troubleshoot, and record needed documentation on instrumentation; Tecan, Beckman, microplate reader, microplate washer, refractometer, and pH meter. * Proper material labeling, pipetting of controls and samples, transfer and entering of sequences onto designated instruments for analysis, loading of samples on to instruments. * Receive and prepare urine, oral fluids and sweat patch aliquots for testing. * Identify aliquots by batch for computer download. * Operate automated analyzer during testing. * Prepare quality control, maintenance, reagent and other equipment records to document proper execution of procedures in each of these areas. * Review and document proper execution of testing procedures. * Release properly reviewed results to the LIMS. * Maintain and protect the confidentiality of all CRL, CRL subsidiaries, legal entities and client information. * Be able to comply with all applicable federal, state, and local safety and health regulations that would apply to this job. * Keep work area neat and clean. Other duties as assigned JOB QUALIFICATIONS: EDUCATION: A doctoral, master's, bachelor's, or associate degree in medical technology, clinical laboratory, chemical, or biological science. EXPERIENCE: High Complexity Testing: Bachelor's Degree or higher: training/experience as specified in 42CFR493.1489 Acting Technical Supervisor: Education: Bachelor's degree in a chemical or biological or clinical laboratory science, or medical technology from an accredited institution or equivalent. Experience: 4 years of pertinent laboratory experience SKILLS & ABILITIES: * Able to perform analytical technological functions, i.e., communication, analytical thought, mechanical ability * Ability to be at work and on time * Ability and judgment to interact and communicate appropriately with other employees, clients and management PHYSICAL REQUIREMENTS: The physical demands described here are representative of those that must be met to successfully perform the essential functions of this job. Reasonable accommodations may be available to enable qualified individuals with disabilities to perform the essential functions. The following physical attributes are required for this position: * Regularly required to walk between departments * Sitting for extended periods of time * Repetitive use of hands, fingers, wrists, and elbows for operating a computer and telephone * Reaching with hands and arms, and reaching above the shoulder * Bending or stooping * Squatting or crouching * Ability to regularly lift and move up to 25 pounds EQUIPMENT: Must operate and maintain automated testing instrumentation OTHER: Must be able to work overtime as necessary to complete workload. Rotation may include Saturday shift. Specimens consist of body fluids and must be regarded as potentially infectious; exposure to caustics, flammables, solvents, carcinogens, and reactive compounds. The employer shall, in its discretion, modify or adjust this position to meet the company's changing needs. This job description is not a contract and may be adjusted as deemed appropriate in the employer's sole discretion. * denotes essential job function An Equal Opportunity Employer Pay Range: $23.00 - $41.00 Benefits for Full Time Employees: * Medical, Dental, Vision * Life/AD&D * Supplemental Life/AD&D * Section 125 FSA Plan * 401(k) * Short and Long-Term Disability * Paid Time Off * Holidays * Tuition Reimbursement

Job Details KS - Great Bend, KS Full Time Bachelors Degree ScienceJob Posting Date(s) 03/31/2025Description Summary: As a Product Development Chemist, you will be responsible for conducting experiments, analyzing data, and developing innovative solutions across Fuller's product portfolio. You will collaborate with other departments to drive product development and improvement initiatives, ensuring the quality and efficacy of our products. Your role will involve a combination of laboratory work, data analysis, and project management to support the company's objectives. Essential Duties: Conduct experiments to explore new chemical processes, formulations, and materials Design and execute experiments according to established protocols and safety guidelines Analyze experimental data using statistical methods and data visualization tools Interpret results, draw conclusions, and make recommendations for further research or product development Collaborate with other departments to develop new products or improve existing ones Provide technical expertise in chemistry to support product design, formulation, and testing Ensure the quality and safety of products through rigorous testing and analysis Develop and implement quality control procedures to meet regulatory standards and customer requirements Maintain accurate records of experiments, observations, and results, prepare technical reports, presentations and documentation to communicate findings Qualifications Qualifications: Bachelor's degree in Chemistry, Chemical Engineering, or a related field Experience in chemical research and development, preferably in an industrial setting preferred but not essential Proficiency in data analysis software and laboratory information Strong knowledge of chemical principles, laboratory techniques, and instrumentation Excellent communication skills, both verbal and written Detail-oriented with strong organizational and problem-solving skills Ability to work independently and collaboratively in a team environment Commitment to safety, quality, and compliance with regulatory requirements Ability to communicate complex technical concepts effectively to diverse audiences Language Skills: Must be able to read, write and speak English, bilingual a plus. Work Environment: Work is performed under generally good conditions with some machine noise, fumes, oil, and dirt present. Adequate lighting, ventilation is present. Extreme outdoor temperatures will influence the temperature in the production area. Exposure to usual minor shop injuries such as cuts bruises, burns and sprains are inherent in the job. Some exposure to more serious hazards; however, probability of serious injury will be minimized by adherence to established safety regulations. Training will be provided to personnel who may occasionally wear Personal Protective Equipment (PPE). Physical Demands: Essential functions can require: Standing or sitting for extended periods of time. Use hands to touch, handle, or feel objects, tools, or controls. Reach with hands and arms. Talking or hearing. Occasional walking. Stoop; kneel; crouch. Lifting/handling: exert up to 50 pounds occasionally; up to 20 pounds of force frequently; and/or up to 10 pounds of force constantly to move objects. Vision: color; close; peripheral vision; depth perception; and ability to adjust focus. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This job description in no way states or implies that these are the only duties to be performed by this employee. He or she will be required to follow any other instructions and to perform any other duties requested by his or her supervisor.

At Argenta, we're more than a company - we're a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it. Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market. We're in a unique position. We are the world's only combined contract research and contract development and manufacturing organisation (CRO/CDMO) dedicated to animal health. Our uniqueness means: * We are ambitious, growing and building a 'one team' culture, guided by our values. * We are team players; * We are doers; * We are customer-centric; * We are innovators. We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best "paw" forward we will make the lives of the animals we care for, better. With bases in New Zealand, the US, the UK and Europe, our 650+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Let's Make It Happen, Together. TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply. Argenta is looking for an experienced Analytical Chemist to join our Argenta Research team located in Shawnee, Kansas. The Analytical Chemist position is an opportunity for motivated, driven individuals to showcase their ability to multi task and work as a team. The ideal candidate will have a background in formulation including small molecules, monoclonal antibodies, sterile fill and biological as well as analytical chemistry. The Analytical Chemist will provide value through the following responsibilities: * To assist the team with product development/formulation projects all the way to product registration or other suitable client-driven product-cycle end points. * To lead projects on behalf of clients and/or Argenta Research (internal company projects) * Generate, document, and review technical data for internal reports, client reports and CMC regulatory support documents. * Create and maintain activity plans for assigned projects * Communicate and negotiate project activities and timelines * Negotiate with other departments for access to various resources including equipment and assistance Analytical Chemist requirements: * Bachelor's degree or higher in a relevant scientific discipline (Pharmacy / Pharmaceutical Sciences, Chemistry, Biological Sciences) * Preferential past experience in animal health industry * Analytical skills and attention to detail; high degree of accuracy with complex documentation * Experience in a GDP/GLP compliant environment * Problem solver * Strong organizational skills * Communicate multifaceted information simply and clearly * Work well with others * Strong aptitude for technical learning, learn new skills and knowledge * Seeks to understand issues, trends, and opportunities within Argenta and the industry and incorporates this knowledge into daily work * Commitment to continuous improvement This position is subject to a DEA background check post offer and at regular intervals. This position is also required to complete a post offer drug test. Both the background and drug test must comply with company standards or offers of employment will be rescinded. You will also be someone who is aligned with our company values of "We are Doers, We are Team Players, We are Innovators, We are Customer-Centric". We pride ourselves on the uniqueness of our development and manufacturing abilities and the skills and qualities of our team. Want to know more about Argenta? Visit our website ********************* Equal Opportunity Employer

At Argenta, we're more than a company - we're a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it. Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market. We're in a unique position. We are the world's only combined contract research and contract development and manufacturing organisation (CRO/CDMO) dedicated to animal health. Our uniqueness means: We are ambitious, growing and building a ‘one team' culture, guided by our values. We are team players; We are doers; We are customer-centric; We are innovators . We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best “paw” forward we will make the lives of the animals we care for, better. With bases in New Zealand, the US, the UK and Europe, our 650+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Let's Make It Happen, Together. TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply. Argenta is looking for an experienced Analytical Chemist to join our Argenta Research team located in Shawnee, Kansas. The Analytical Chemist position is an opportunity for motivated, driven individuals to showcase their ability to multi task and work as a team. The ideal candidate will have a background in formulation including small molecules, monoclonal antibodies, sterile fill and biological as well as analytical chemistry. The Analytical Chemist will provide value through the following responsibilities: To assist the team with product development/formulation projects all the way to product registration or other suitable client-driven product-cycle end points. To lead projects on behalf of clients and/or Argenta Research (internal company projects) Generate, document, and review technical data for internal reports, client reports and CMC regulatory support documents. Create and maintain activity plans for assigned projects Communicate and negotiate project activities and timelines Negotiate with other departments for access to various resources including equipment and assistance Analytical Chemist requirements: Bachelor's degree or higher in a relevant scientific discipline (Pharmacy / Pharmaceutical Sciences, Chemistry, Biological Sciences) Preferential past experience in animal health industry Analytical skills and attention to detail; high degree of accuracy with complex documentation Experience in a GDP/GLP compliant environment Problem solver Strong organizational skills Communicate multifaceted information simply and clearly Work well with others Strong aptitude for technical learning, learn new skills and knowledge Seeks to understand issues, trends, and opportunities within Argenta and the industry and incorporates this knowledge into daily work Commitment to continuous improvement This position is subject to a DEA background check post offer and at regular intervals. This position is also required to complete a post offer drug test. Both the background and drug test must comply with company standards or offers of employment will be rescinded. You will also be someone who is aligned with our company values of "We are Doers, We are Team Players, We are Innovators, We are Customer-Centric". We pride ourselves on the uniqueness of our development and manufacturing abilities and the skills and qualities of our team. Want to know more about Argenta? Visit our website ********************* Equal Opportunity Employer

This position is responsible for support of CMC activities as well as working with Scientists and management for specific compound development at CritiTech in support of CritiTech product development and associated affiliates/partners for the global development and regulatory approval of New Chemical Entities (NCE's), Active Pharmaceutical Ingredients (APIs) and support of research and development of any/all product activities. RESPONSIBILITIES Participates in lab development in support of Chemistry, Manufacturing and Controls (CMC) section of NDA or SNDA by direction and interaction with Quality Operations/Regulatory Affairs and CritiTech. Provides analytical support for proof of concept studies, feasibility studies, routine manufacturing, and troubleshooting using CritiTech's Supercritical Precipitation equipment. Provides analytical support for proof of concept studies, feasibility studies, routine manufacturing, and troubleshooting using CritiTech's spray drying equipment. Perform production activities in support of clinical trials, including filling, environmental monitoring, visual inspection, and packaging of vials for further processing. Suggest changes and improvements to CritiTech's analytical services and product characterization, facilities, utilities, and other systems. Performs preventative maintenance and calibration checks on analytical equipment. Participates in the qualification of new equipment and facilities. Generates support data for CritiTech to be used in 3rd party development activities. Generates data in support of CMC documents, including out-of-specification (OOS) or deviation investigations, and helps execute action plans to meet sound scientific practices. Provides technical support for QO on complaint samples and manufacturing/packaging problems. Performs and assists in CritiTech compatibility and feasibility assessments for compounds being considered for development. Participate in the onsite review of data, facilities and laboratory operations of contract manufacturing and analytical laboratory. Suggests changes or edits to appropriate SOP's for CritiTech. Performs release and stability analytical testing with QO in the coordination and management of retest/expiration dating. Executes testing and lab work in support of technology transfer and stability protocols, stability packaging and manufacturing jobs for CritiTech activities. Other duties as assigned. EDUCATION, EXPERIENCE AND SKILLS Required BS in chemistry, biology, engineering or related pharmaceutical field with 3+ years industry background in pharmaceutical product development - or - MS in chemistry, biology, engineering or related pharmaceutical field with 2+ years industry background in pharmaceutical product development. 2+ years preparing and supporting CMC documentation for IND's and NDA's. Experience in working with people in a multi-disciplinary team environment. Preferred Advanced degree in chemistry or pharmacy or equivalent experience. Experience in pharmaceutics, analytical and organic chemistry. Experience in technology transfers to contract facilities. Experience with interactions with regulatory agencies. Experience in preparing and supporting Chemistry, Manufacturing and Control (CMC) documentation regulatory filings. KNOWLEDGE AND SKILLS Knowledgeable (including hands-on experience) in the use of analytical methods for active pharmaceutical ingredients and drug product (i.e. HPLC, GC, IR, etc.) and formulation development/manufacturing and the relation of these to overall pharmaceutical development. Knowledge and understanding of current Good Manufacturing Practices (cGMP) as well as other pertinent national regulations. Current knowledge of CMC regulatory and ICH guidelines. Knowledgeable in the overall drug development process. Knowledgeable in the application of compendia requirements and procedures to testing and developing pharmaceutical products. Leadership Skills - knowledge and interpersonal skills to help others towards the accomplishment of CritiTech's goals and objectives. Analytical and Problem-Solving Skills - ability to identify problems or opportunities using appropriate information; determines the causes and possible solutions to the problem. Teamwork - the ability to work well and manage personnel in a highly cross-functional team environment. Communication Skills - ability to express one's self clearly and concisely to CritiTech personnel over the phone or with others within the team; documents issues and/or concerns concisely and comprehensively; adjusts language and/or terminology appropriate for the audience. Interpersonal Flexibility - ability to adapt to other personalities in a respectful manner that is conducive to goal achievement. Knowledge Sharing - ability to capture knowledge within the organization; improves solutions, processes, an deliverables through the use of information; improves information capital by contributing experience, theories, deliverables, and models for others to use. Resource Management - ability to work with internal and external resources and to coordinate individual goals and objectives to align with business imperatives.

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

Job Title: Analytical Chemist I Duration: 12 months contract, extendable up to 18 months Note: Client has the right-to-hire you as a permanent employee at any time during or after the end of contract. You may participate in the company group medical insurance plan which includes dental and vision. Job Description: The R&D Pharm Sci. team member will be involved in multiple, on-going projects. Activities include performing analysis in a GXP environment and may include material qualification (excipients or active pharmaceutical ingredients), release testing, and analysis required to support manufacturing functions (engineering, exhibit batches, etc), as well as on-going stability studies. The individual should have good communication and organizational skills and be able to coordinate work with cross-functional team members, peers, and external CROs (Contract Research Organization). Position Responsibilities Perform testing using analytical equipment (i.e. UPLC, HPLC, GC, Karl Fischer, pH, UV-Vis, IR, microscopy, optical rotation) as well as using traditional wet chemistry methods (i.e. titration, TLC, sulfated ash, etc.) Enter experimental information into hard-bound and electronic lab notebooks (i.e. Biovia eLN) and process analytical data accordingly (i.e. Empower 3, Excel, etc). Perform additional data entry, processing, and review within LIMS system (i.e. Thermo LIMS). Coordinate with team members to ensure seamless analytical coverage during manufacturing campaigns and on-going stability studies. Also support new project activities, as needed. Perform analytical method feasibility, development and validation, as necessary. Coordinate with team members to verify each other's data by reviewing eLN and LIMS entries in a timely manner. Take personal responsibility to meet analytical testing and data verification deadlines, as well as safety and training requirements. Author protocols, reports, or other technical documents, and presents project data to group, as needed. Organizational Relationships Primary interaction will be with Pharmaceutical McPherson PEH PharmSci R&D group. Will also work with other product development groups including GTS and Pharmaceutical Center One. Pharmaceutical McPherson Chemistry Quality group. Pharmaceutical McPherson Manufacturing. Possible interaction with CROs Education And Experience Indicate the formal education, certification or license(s) required and/or preferred. Include the minimum number of years of relevant experience required for the position (where legally permissible). BS and 3-7 years experience in a regulated industry (i.e. food, pharmaceutical, biotech, petroleum, etc). MS and 2-5 years experience in regulated industry PhD and 1-5 experience in regulated industry Technical Skills Requirements Indicate the technical skills required and/or preferred, as applicable. Hands-on experience with complex analytical equipment including IR, UV-Vis, imaging systems, chromatography systems (UPLC, HPLC, GC) and chromatography methods (RP, IC, SEC, etc). Experience using simple analytical tools including KF titration, microscope, polarimeter, pH, analytical balances, density meter, osmometer, and etc. is required. Experience with simple and/or complex analytical method verification, development, transfer, or validation strongly preferred. Experience working in a regulated (i.e. FDA, TTB, etc) or GMP environment is strongly preferred. Understanding of various scientific software or software used in pharmaceutical or production environment (i.e. eLN, LIMS, Empower 3, Trackwise, MiniTab, Fusion, etc) would be preferred. Strong analytical reasoning skills. Excellent written and verbal communication skills. Physical Position Requirements Note the physical conditions in which work will be performed, if applicable to the position. Examples: Lifting, sitting, standing, walking, ability to travel, drive, unusual attendance requirements, weekend work or travel requirements, etc. Please include any hazardous materials or non-standard working environment the contractor will have exposure to which may require additional medical testing and/or apparatus fitting for OSHA compliance. May work with hazardous chemicals including acids, bases, oxidizing agents, carcinogens, mutagens, teratogens, etc. Additional medical testing will be required. PPE training, solvent respirator and powder respirator training and fitting will be required. Occasional weekend and evening work is required. May sit or stand at bench for extended periods. Additional Information Anuj Mehta ************

TempToFT Please submit resume to **************************************** to apply. Pay Rate/Range: $18-$22/hr Description:The Research and Development (R&D) Technician Apprentice is a member of the engineering team, working under the close guidance of R&D Technicians, R&D Engineers, and the Director of Engineering. The main responsibility is to work with the engineering team to develop new part designs and processes through an understanding of materials and advanced mechanical fundamentals, and to work on multiple projects and platforms under the direction of the Engineering Director. The R&D Technician Apprentice must have the ability to adapt to new process concepts, acquire an advanced level of mechanical ability, and display strong problem solving skills. Job Requirements: Must have good organization skills, problem solving skills and familiarity with computers and MS office. Candidates must have a high school diploma, a valid driver's license, and a minimum of 2 years of experience in a related field. Job Type: Contract-to-Hire Shift/Schedule: Monday-Friday, 7am-3:30pm. Schedule may vary based on the project. The Arnold Group is an Equal Opportunity Employer (EOE) About Us: The Arnold Group (TAG) is a staffing and recruiting firm dedicated to assisting job seekers with employment opportunities. We have been helping people find employment since 1979 and we can help you too. With TAG, you'll have the opportunity to unlock your potential, both professionally and personally. Click here to learn more! The Arnold Group

Science you can trust from concept to consumer. Since 1967, Deibel Laboratories has operated several private food testing facilities providing services in both Microbiology and Chemistry testing. We play an integral role in food and product safety for industry-leading producers, as well as family-run operations much like our own. Our location in Manhattan, KS is currently looking to hire a full-time, entry-level Chemistry Technician. (40 hours/week plus benefits included) We offer a competitive salary based on knowledge and experience. This position includes full health benefits for self and family (employer pays for 90% of employee premiums and 50% of dependents on our base plan). Deibel also offers a self-funded dental plan, vision plan, and 401K option. Check out our website to learn more about what we do at ******************* Compensation : Starting hourly rates $19 - $21 D.O.E. plus a competitive benefits package. Monday - Friday w/ Rotating Saturdays 8am - 4:30pm Required Skills/Abilities: Entry Level Position: We Are Happy to Train Must have an interest in learning basic knowledge of chemical analysis and to accurately perform testing procedures and obtain accurate results. A basic knowledge of personal computers is useful to accurately enter testing data and results. Planning skills are useful to maintain supplies of analysis materials and ensure analysis is completed within a specified time. Basic math skills are essential to complete analysis. Physical dexterity is required for manipulating samples. We'd Love to Hear from People With: Previous experience in manufacturing, production, warehouse, food industry, food service, baking, baristas, or retail. Strong problem-solving skills, ability to multitask, and work in a fast-paced environment. Skills to communicate effectively and develop good working relationships with all employees. A professional workplace appearance, ethical conduct, honesty, and integrity in all communications. A thirst to seek out and participate in appropriate training and professional development. Fluency in written and spoken English is required. Physical Requirements: Safety equipment of gloves, laboratory coat, and eyeglasses may need to be worn depending on the testing process. Extended time spent in a standing position. Ability to lift up to 50lbs occasionally and 10 - 15lbs repeatedly.All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Deibel is committed to fostering a diverse and welcoming workplace with people of all types of backgrounds and experiences.SERVICE - QUALITY - TRANSPARENCY - PARTNERSHIP - EDUCATION - PROFESSIONALISM

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 areaâÂÂs management and other personnel * Ensures work area is kept clean and organized * Conducts calibration and standardization of testing instruments * Executes required assigned areaâÂÂs 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. Experience 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. Supervisory/Managerial Responsibility 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

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. Experience 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. Supervisory/Managerial Responsibility 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.

Science you can trust from concept to consumer. Since 1967, Deibel Laboratories has operated several private food testing facilities providing services in both Microbiology and Chemistry testing. We play an integral role in food and product safety for industry-leading producers, as well as family-run operations much like our own. Our location in Manhattan, KS is currently looking to hire a full-time, entry-level Chemistry Technician. (40 hours/week plus benefits included) We offer a competitive salary based on knowledge and experience. This position includes full health benefits for self and family (employer pays for 90% of employee premiums and 50% of dependents on our base plan). Deibel also offers a self-funded dental plan, vision plan, and 401K option. Check out our website to learn more about what we do at ******************* Compensation : Starting hourly rates $19 - $21 D.O.E. plus a competitive benefits package. Monday - Friday w/ Rotating Saturdays 8am - 4:30pm Required Skills/Abilities: Entry Level Position: We Are Happy to Train Must have an interest in learning basic knowledge of chemical analysis and to accurately perform testing procedures and obtain accurate results. A basic knowledge of personal computers is useful to accurately enter testing data and results. Planning skills are useful to maintain supplies of analysis materials and ensure analysis is completed within a specified time. Basic math skills are essential to complete analysis. Physical dexterity is required for manipulating samples. We'd Love to Hear from People With: Previous experience in manufacturing, production, warehouse, food industry, food service, baking, baristas, or retail. Strong problem-solving skills, ability to multitask, and work in a fast-paced environment. Skills to communicate effectively and develop good working relationships with all employees. A professional workplace appearance, ethical conduct, honesty, and integrity in all communications. A thirst to seek out and participate in appropriate training and professional development. Fluency in written and spoken English is required. Physical Requirements: Safety equipment of gloves, laboratory coat, and eyeglasses may need to be worn depending on the testing process. Extended time spent in a standing position. Ability to lift up to 50lbs occasionally and 10 - 15lbs repeatedly.All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Deibel is committed to fostering a diverse and welcoming workplace with people of all types of backgrounds and experiences.SERVICE - QUALITY - TRANSPARENCY - PARTNERSHIP - EDUCATION - PROFESSIONALISM

Lab Analyst I, Lab Analyst II- Flow Cytometry, Immunoassay, and Small Molecule- Onsite, Lenexa, KS- Full Time 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 Lab Analyst Is and IIs to join our diverse and dynamic team. As a Lab Analyst I or Lab Analyst II at ICON, you will be responsible for conducting routine laboratory tests and analyses to support clinical research studies. You will play an essential role in maintaining accurate data, adhering to standard procedures, and contributing to the overall success of the laboratory operations. What You Will Be Doing: * Performing routine laboratory tests and analyses in accordance with established protocols and procedures. * Recording and documenting test results accurately, ensuring data integrity and compliance with quality standards. * Operating and maintaining laboratory equipment, performing regular calibrations, and troubleshooting as needed. * Supporting quality control activities by participating in the review and verification of test results and procedures. * Collaborating with team members to ensure timely and efficient completion of laboratory tasks and projects. Your Profile: * Bachelor's degree in biology, chemistry, or a related scientific field. * 0-2 years of experience in a laboratory environment, preferably in clinical research or a related industry. * Strong attention to detail and organizational skills, with the ability to follow protocols and maintain accurate records. * Basic proficiency in laboratory techniques and equipment operation, with a willingness to learn and develop new skills. * Good communication and teamwork abilities, with a proactive approach to supporting team objectives and deadlines. #LI-Onsite #LI-HP1 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, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. 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 I, Lab Analyst II- Flow Cytometry, Immunoassay, and Small Molecule- Onsite, Lenexa, KS- Full Time 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 Lab Analyst Is and IIs to join our diverse and dynamic team. As a Lab Analyst I or Lab Analyst II at ICON, you will be responsible for conducting routine laboratory tests and analyses to support clinical research studies. You will play an essential role in maintaining accurate data, adhering to standard procedures, and contributing to the overall success of the laboratory operations. **What You Will Be Doing:** + Performing routine laboratory tests and analyses in accordance with established protocols and procedures. + Recording and documenting test results accurately, ensuring data integrity and compliance with quality standards. + Operating and maintaining laboratory equipment, performing regular calibrations, and troubleshooting as needed. + Supporting quality control activities by participating in the review and verification of test results and procedures. + Collaborating with team members to ensure timely and efficient completion of laboratory tasks and projects. **Your Profile:** + Bachelor's degree in biology, chemistry, or a related scientific field. + 0-2 years of experience in a laboratory environment, preferably in clinical research or a related industry. + Strong attention to detail and organizational skills, with the ability to follow protocols and maintain accurate records. + Basic proficiency in laboratory techniques and equipment operation, with a willingness to learn and develop new skills. + Good communication and teamwork abilities, with a proactive approach to supporting team objectives and deadlines. \#LI-Onsite \#LI-HP1 **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, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. 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 - Night 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 Monday through Friday, from 9:00pm - 5:30am. 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.

Job Title: Analytical Chemist I Duration: 12 months contract, extendable up to 18 months Note: Client has the right-to-hire you as a permanent employee at any time during or after the end of contract. You may participate in the company group medical insurance plan which includes dental and vision. Job Description: The R&D Pharm Sci. team member will be involved in multiple, on-going projects. Activities include performing analysis in a GXP environment and may include material qualification (excipients or active pharmaceutical ingredients), release testing, and analysis required to support manufacturing functions (engineering, exhibit batches, etc), as well as on-going stability studies. The individual should have good communication and organizational skills and be able to coordinate work with cross-functional team members, peers, and external CROs (Contract Research Organization). Position Responsibilities Perform testing using analytical equipment (i.e. UPLC, HPLC, GC, Karl Fischer, pH, UV-Vis, IR, microscopy, optical rotation) as well as using traditional wet chemistry methods (i.e. titration, TLC, sulfated ash, etc.) Enter experimental information into hard-bound and electronic lab notebooks (i.e. Biovia eLN) and process analytical data accordingly (i.e. Empower 3, Excel, etc). Perform additional data entry, processing, and review within LIMS system (i.e. Thermo LIMS). Coordinate with team members to ensure seamless analytical coverage during manufacturing campaigns and on-going stability studies. Also support new project activities, as needed. Perform analytical method feasibility, development and validation, as necessary. Coordinate with team members to verify each other's data by reviewing eLN and LIMS entries in a timely manner. Take personal responsibility to meet analytical testing and data verification deadlines, as well as safety and training requirements. Author protocols, reports, or other technical documents, and presents project data to group, as needed. Organizational Relationships Primary interaction will be with Pharmaceutical McPherson PEH PharmSci R&D group. Will also work with other product development groups including GTS and Pharmaceutical Center One. Pharmaceutical McPherson Chemistry Quality group. Pharmaceutical McPherson Manufacturing. Possible interaction with CROs Education And Experience Indicate the formal education, certification or license(s) required and/or preferred. Include the minimum number of years of relevant experience required for the position (where legally permissible). BS and 3-7 years experience in a regulated industry (i.e. food, pharmaceutical, biotech, petroleum, etc). MS and 2-5 years experience in regulated industry PhD and 1-5 experience in regulated industry Technical Skills Requirements Indicate the technical skills required and/or preferred, as applicable. Hands-on experience with complex analytical equipment including IR, UV-Vis, imaging systems, chromatography systems (UPLC, HPLC, GC) and chromatography methods (RP, IC, SEC, etc). Experience using simple analytical tools including KF titration, microscope, polarimeter, pH, analytical balances, density meter, osmometer, and etc. is required. Experience with simple and/or complex analytical method verification, development, transfer, or validation strongly preferred. Experience working in a regulated (i.e. FDA, TTB, etc) or GMP environment is strongly preferred. Understanding of various scientific software or software used in pharmaceutical or production environment (i.e. eLN, LIMS, Empower 3, Trackwise, MiniTab, Fusion, etc) would be preferred. Strong analytical reasoning skills. Excellent written and verbal communication skills. Physical Position Requirements Note the physical conditions in which work will be performed, if applicable to the position. Examples: Lifting, sitting, standing, walking, ability to travel, drive, unusual attendance requirements, weekend work or travel requirements, etc. Please include any hazardous materials or non-standard working environment the contractor will have exposure to which may require additional medical testing and/or apparatus fitting for OSHA compliance. May work with hazardous chemicals including acids, bases, oxidizing agents, carcinogens, mutagens, teratogens, etc. Additional medical testing will be required. PPE training, solvent respirator and powder respirator training and fitting will be required. Occasional weekend and evening work is required. May sit or stand at bench for extended periods. Additional Information Anuj Mehta ************

Science you can trust from concept to consumer. Since 1967, Deibel Laboratories has operated several private food testing facilities providing services in both Microbiology and Chemistry testing. We play an integral role in food and product safety for industry-leading producers, as well as family-run operations much like our own. Our location in Manhattan, KS is currently looking to hire a full-time, entry-level Chemistry Technician. (40 hours/week plus benefits included) We offer a competitive salary based on knowledge and experience. This position includes full health benefits for self and family (employer pays for 90% of employee premiums and 50% of dependents on our base plan). Deibel also offers a self-funded dental plan, vision plan, and 401K option. Check out our website to learn more about what we do at ******************* Compensation: Starting hourly rates $19 - $21 D.O.E. plus a competitive benefits package. Monday - Friday w/ Rotating Saturdays 8am - 4:30pm Required Skills/Abilities: Entry Level Position: We Are Happy to Train Must have an interest in learning basic knowledge of chemical analysis and to accurately perform testing procedures and obtain accurate results. A basic knowledge of personal computers is useful to accurately enter testing data and results. Planning skills are useful to maintain supplies of analysis materials and ensure analysis is completed within a specified time. Basic math skills are essential to complete analysis. Physical dexterity is required for manipulating samples. We'd Love to Hear from People With: Previous experience in manufacturing, production, warehouse, food industry, food service, baking, baristas, or retail. Strong problem-solving skills, ability to multitask, and work in a fast-paced environment. Skills to communicate effectively and develop good working relationships with all employees. A professional workplace appearance, ethical conduct, honesty, and integrity in all communications. A thirst to seek out and participate in appropriate training and professional development. Fluency in written and spoken English is required. Physical Requirements: Safety equipment of gloves, laboratory coat, and eyeglasses may need to be worn depending on the testing process. Extended time spent in a standing position. Ability to lift up to 50lbs occasionally and 10 - 15lbs repeatedly. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Deibel is committed to fostering a diverse and welcoming workplace with people of all types of backgrounds and experiences. SERVICE - QUALITY - TRANSPARENCY - PARTNERSHIP - EDUCATION - PROFESSIONALISM

Lab Analyst II - On-Site - US, 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. Title: Lab Analyst II Location: On-Site (Lenexa, KS) Job Type: PRN The Role: The Lab Analyst operates and maintains instrumentation and performs diagnostic clinical laboratory testing. * Routine sample processing with different analytical instruments and methodologies. * Interpret data and quality control data. * Identify and report irregularities identified with any aspects of work. * Recognize, exemplify, and adhere to ICON's values which center around our commitment to People, Clients, and Performance. * Ensures on-time task completion to support the overall goal of on-time study completion. * Perform assays for the routine batch analysis of physical/chemical analysis samples involving simple to complex analytical techniques. Perform laboratory work to GMP or GxP standard. * Work in compliance with study plans and validation plans and all relevant SOPs. * Document all work and results accurately, completely, and compliant with GMP or GxP regulations and SOPs. * Generate high-quality analytical results. Ensure the smooth transfer of data and participate in the evaluation and interpretation of data. * Operate general laboratory equipment and instrumentation systems and utilize automated data collection/reporting systems. * Maintain instruments. * Work in compliance with GMP or GxP. * Generate laboratory reports for work performed. * Perform routine maintenance and calibration of instrumentation. * To undertake other reasonably related duties as may be assigned from time to time. To be successful in the role, you will have: * Bachelor's Degree - Preferably in a science-related field of study * Clinical laboratory experience is required. * Certified clinical laboratory scientist preferred. Preferred Qualifications: * MLS (ASCP) or MT (ASCP) 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, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. 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