Chemist jobs in Kansas - 46 jobs

We are looking to fill a **Scientist 3 - Analytical Chemist** position working as **a full-time employee of Parexel FSP on long-term assignment** onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer any sponsorship.** **Responsibilities** + General understanding of analytical method development and method validation + Hands-on experience with chromatographic analysis using various ultra-high-performance liquid chromatography (UPLC), high-performance liquid chromatography (HPLC), and gas chromatography (GC) techniques + General knowledge of separations science + Experience with Empower chromatographic software and with analysis of drug formulations + Hand-on experience with Fourier transform infrared (FTIR) spectroscopic analysis and ultraviolet-visible (UV-VIS) spectroscopic analysis + Skilled on method and instrument troubleshooting, specifically for HPLC and GC methods and systems **Required Skills** + Strong computer, scientific, and organizational skills + Excellent organization to multi-task and manage multiple ongoing projects in parallel including routine testing (for example, assay and impurity testing) and data processing and interpretation + Excellent communication (oral and written) and attention to detail + Proficient in written and spoken English, is required **Desired Skills and Experience** + Empower software + Analysis of drug products + Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude **Qualifications** + BS degree and 3-5 years of relevant experience, or + MS degree with at least 1-2 years relevant experience **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Education and Experience: Bachelor's degree in chemistry or chemical engineering preferred. Minimum of eight (8) years of plant laboratory, maintenance, or operations experience is required. Skills, Knowledge and Abilities: Must have the ability to perform the physical activities of the job (Includes but not limited to climbing, color vision, depth perception, hearing, seeing, sitting, standing, talking, walking, outside work, etc.). Must be able to read blueprint and electronic schematics. Capable of handling multiple priorities, visualize, analyze and make decisions with limited data, process information in an orderly, accurate and timely manner, and operate within short time frames. Able to apply tact, diplomacy, reason and logic, recognize consequences or erroneous actions, respond quickly, concentrate on tasks and other required functions. Possess a thorough knowledge of water treatment chemistry, power plant operations and maintenance, and a working knowledge of metallurgy and materials. General knowledge of mechanical and electrical technology, construction, equipment operation, and engineering concepts is required. Expected to model Evergy's Talent Framework Behaviors, the foundation for HOW we do our jobs at Evergy. At a minimum, incumbents should be able to demonstrate their ability to progressively develop and exhibit these skills at a proficient level: Evergy's People First Values\: Safety, Integrity, Ownership, Adaptability o Operational Excellence/Execution\: Exerts personal effort and enables the team to achieve performance goals and exhibits a continuous improvement mindset o Decision Making\: Makes informed, objective, timely and ethical decisions o Talent Management\: Takes initiate to develop self and team, acts with a mindset of diversity, equity and inclusion and creates an environment to attract top talent o Strategic Mindset\: Demonstrates sound strategic thinking, knows the business, exercises judgment, influences and persuades. Licenses, Certifications, Bonding and/or Testing: Must possess a valid driver's license. Working Conditions\: Work is both indoor and outdoor, in all types of weather and conditions. Must have a satisfactory work record including good attendance. Must live within 50 minutes' drive time of Jeffrey Energy Center. Evergy has a clear mission - To empower a better future. Evergy chooses to live this mission by valuing People First. We know that to lead the responsible energy transition and provide affordable, reliable, and sustainable service to our customers and communities, we need a team with a variety of backgrounds, perspectives and skills. We are committed to building a team where everyone - regardless of race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status - has a voice and can bring their best every day. Evergy is proud to be an equal opportunity workplace and is an affirmative action employer. JOB TITLE\: Supv Plant Chemist REQUISITION: FOS00HK DEPARTMENT\: Generation - Jeffrey Energy Center LOCATION: St Marys, KS PAY RANGE: $94,600 - $126,100 (Min-Mid) Scheduled Work Hours: Monday - Friday, 6\:00am - 3\:00 pm coverage; some shift work, evenings, nights, and weekends as required. Summary of Primary Duties and Responsibilities\: This position reports directly to the Director of Operations at Jeffrey Energy Center and is the chemistry subject matter expert responsible for managing the reliability, safety, and operation of all water chemistry related activities. These activities include developing sound chemistry standards and procedures. Monitoring all water chemistry processes and developing corrective action plans, minimizing chemistry-induced component failures in all steam and water pressure piping and ultra-pure water production systems. Supervising collective bargaining unit employees. Overseeing both capital and O&M spending for the Chemistry Department. Identifying areas of need for capital improvements. Establishing QA/QC procedures, trending, reporting, and statistical evaluation for data validity. Promoting safety and training functions for the purpose of achieving Company and plant goals and objectives. Develops and provides chemistry training for all personnel as needed. Openly communicates information to the appropriate departments at all levels. Major responsibilities include, but are not limited to: • Monitors all water chemistry processes and develops corrective action plans for all water, steam and other auxiliary water systems that supports power production activities through the development and application of plant specific water and steam quality limits • Optimizes chemistry programs and services by providing technically proficient recommendations for corrective action based upon industry best practices and plant operating experience and provides chemical treatment guidance and training to Operations staff to ensure proper chemical control during off-shift and weekends. • Supervises laboratory and chemical analysis technicians. Develops individual team members for optimum performance. Provides daily observation, instruction, correction and re-enforcement of team members' knowledge and skills and maintain appropriate documentation. Periodically supervises personnel from other departments. • Controls O&M spending by managing overtime, shift schedules, equipment inspections and repairs, and unit performance. • Ensures standards for safety, quality and productivity are met by following established policies and procedures. • Maintains lab records for process and audit purposes • Implements industry regulations, laws, and standards for the purpose of integrating current requirements, technology, and plant equipment changes into programs. • Collaborates with other departments to develop and manage a weekly schedule for equipment maintenance and makes daily work assignments that support the weekly schedule. • Shares information openly to foster an atmosphere of trust and cooperation within support and operations groups. Creates a strategic framework for the effective operation of groups; and provides work direction and resources to effectively operate the plant. • Participates in ensuring the plant meets all environmental regulations by maintaining EPA, KDHE, and OSHA compliance of all applicable areas. • Coordinates activities with chemical vendors and contractors.

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

An exciting opportunity is available for Analyst, Chemical Marketing Located in Riyadh, KSA. Job Purpose: The job purpose of a Chemical Marketing Analyst is to maximize the value of Tasnee's chemical products by developing and executing comprehensive sales and marketing strategies that drive growth and profitability. This involves monitoring market trends, assessing competitive conditions, and formulating optimal pricing strategies while ensuring alignment with overall business objectives. The role serves as a key liaison between sales teams and other functions such as operations, supply chain, finance, legal, and inventory management to enhance business performance. Additionally, the analyst provides regular market and customer insights to stakeholders, supports sales activities, and implements initiatives aimed at improving efficiency and achieving strategic targets. Role responsibilities: Participate in implementing business and marketing strategies to achieve set goals and objectives. Contribute to sales and marketing activities, growth strategies, and policies for efficient operations. Develop annual sales and marketing agreements covering production, inventory, material allocation, and pricing frameworks. Gather and analyze pricing intelligence to make informed decisions considering regional variations. Manage material allocation and authorize reallocation between regions to maximize netback and meet market targets. Conduct economic impact analysis of pricing options and assess regional sales performance. Collaborate with Finance for performance measurement, reporting, and budget reviews; support procurement in managing overseas hub pricing. Coordinate with production to identify cost improvement projects and evaluate regional representatives for sales performance. Prepare monthly pre-release pricing reports and ensure management is informed of pricing models. Perform market scanning, trend analysis, and forecasting to support sales decisions and strategic initiatives. Create and maintain regular reports, manage market research subscriptions, and maintain a central database of competitive intelligence. Represent Tasnee at regional and international exhibitions and collaborate with global consultants on strategic market projects. Minimum qualification and experience: Bachelor's degree in Marketing, Statistics or Engineering with 3-5 years' experience in Market Intelligence roles with specific experience in the chemicals industry. Exposure to marketing, customer segmentation, report making, competitive intelligence, analysis and forecasting methodologies is preferred. Job Specific Skills: Analytical & Critical Thinking: Ability to interpret data and assess business impact; strong Excel modeling skills. Communication & Presentation: Excellent written and verbal skills; proficient in PowerPoint for reporting. Data & Market Insight: Skilled in sourcing reliable information and understanding macroeconomic trends. Strategic Judgment: Capable of evaluating complex issues and making informed decisions. Collaboration & Leadership: Effective team player with experience leading projects and engaging stakeholders. Problem-Solving: Proven ability to turn creative ideas into practical solutions. Job Post Start Date: 9-November-2025 Job Post Start Date: 9-Februray-2026 Tasnee employs over 4,000 people in Saudi Arabia and we value everyone's contribution in making our business successful. We aim to provide a wide range of career paths and offer everyone the opportunity to broaden their experience, advance and build a professionally rewarding career as we work together to deliver a strong and sustainable business.

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 ************

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

At PBI-Gordon Companies, and our subsidiaries PBI-Gordon Corporation, Pegasus Laboratories, and PetAg, Inc, our priority is people, pets, and the places they go. As employee owners, we support each other in building our careers as well as our companies. Our foundation is rooted in integrity, innovation, partnership, and pride. Come grow with us! Join Our Team as a Chemical Batching Technician at PBI Gordon Corporation! Are you ready to roll up your sleeves and be part of a team that formulates products that make a difference? PBI Gordon Corporation is looking for a Formulations I Operator to help manufacture liquid chemical products with precision, safety, and pride. 📍 Location: Shawnee, KS 🕕 Hours: 6:00 AM to 2:30 PM, Monday through Friday - enjoy your afternoons and weekends free! What You'll Do: Safely formulate and prepare chemical batches for packaging or bulk shipment. Operate valves, pumps, agitators, and hoists with confidence. Read and follow batch tickets to stage raw materials accurately. Interface with process controls and HMI panels during mixing. Collect samples for lab analysis and ensure quality standards. Load/unload bulk tanker trucks and raw material containers. Maintain a clean, safe, and organized work environment. What You Bring: Ability to lift up to 55 lbs. and work in outdoor conditions. Willingness to wear PPE and complete safety training. Basic understanding of manufacturing operations. Forklift certification (or willingness to obtain). Strong communication skills and a proactive attitude. Preference given to candidates with chemical manufacturing experience and OSHA familiarity. Why You'll Love It Here: Consistent daytime hours - no nights or weekends! Be part of a safety-first culture. Work with a supportive team and grow your skills. Make a real impact in a hands-on role. Ready to mix things up in your career? Apply today and become a key player in our production process! PBI-Gordon Companies and its subsidiaries are proud to offer a comprehensive benefits package to eligible, full-time employees who work 30 hours per week or more. Full-time employees will become eligible to participate in benefits on the first of the month following their start date, unless stated otherwise below. (Note: Interns do not qualify for eligibility.) Medical Insurance We are committed to helping you and your dependents maintain health and wellness by offering voluntary, competitive medical insurance and prescription drug plan options. Dental Insurance Choose from two voluntary dental plans that are designed to help protect you and your dependents' oral health. Vision Insurance Our voluntary vision insurance plan is designed to help protect you and your dependents eye health. Coverage is available for eye exams, frames, lenses, and contact lenses. Employee owners are responsible for 100% of the cost of this plan. Life Insurance with Accidental Death & Dismemberment (AD&D) We offer a company-paid $50,000 life insurance policy with AD&D. You also have the opportunity to purchase additional life and AD&D insurance for yourself, your spouse and/or your dependent children. The cost for this coverage is based on the amount you elect and your age. Short- and Long-term Disability Our company-paid short-term and long-term disability plans to provide income replacement in the event you are not able to work due to illness or injury. Short-term disability will provide 70% income replacement up to $1,350 per week and long-term disability will provide 60% income replacement up to $5,000 per month. Employee Assistance Program (EAP) EAP Services are company paid to benefit all employee-owners and their families. EAP provides up to six free counseling sessions to help you and your family members manage life stressors, solve personal or relationship concerns, and achieve your goals. Flexible Spending Account (FSA) Flexible Spending Plans offer employee-owners the option to set aside pre-tax monies into a medical reimbursement or dependent care account to help pay for out-of-pocket medical, dental or vision expenses or day care costs. The maximum contributions are determined by the IRS and adjusted annually. This is a use-it-or-lose-it account, meaning any funds remaining in the account following the close of the plan year will be forfeited. Pet Insurance We love our pets! Pet insurance options for your furry friends is offered through the ASPCA. Employee-owners can enroll and pay premiums directly to ASPCA. Paid Holidays & Paid Time Off (PTO) Everyone needs time off to rest and recharge! Paid time off includes Regular PTO, Personal PTO, and specified paid company holidays. * The amount of paid time off (PTO) depends upon the employee's position and years of service. Employee Stock Ownership Plan (ESOP) We act like we own the company because we do! An ESOP provides employees with an ownership stake in the company. It's an additional form of compensation directly tied to PBI-Gordon Companies financial success. All regular employees are eligible to participate in the ESOP the first of the month following 30 days of service. PBI-Gordon Companies contributes approximately 18% of total compensation annually with a six-year vesting schedule. Our ESOP is more than a benefit, it is a key part of a culture, and it can provide significant rewards in retirement! 401(k) Retirement Savings Plan Saving for retirement is one of the most important financial decisions you can make. We offer a 401(k)-retirement savings plan to assist employees with this important financial goal. New employee owners are eligible to participate the first of the month following 30 days of employment. We provide a company match of 100% up to 3% deferral with a three-year vesting schedule. Fitness Reimbursement We believe regular exercise helps improve overall health and job performance. PBI-Gordon will reimburse up to a maximum of $300 annually for gym/fitness memberships. William Everett & Mary Ellen Mealman Scholarship Fund Children or grandchildren of employee-owners may apply for a scholarship under the William Everett & Mary Ellen Mealman scholarship fund. Applicants are awarded based on financial need, academic achievement, and involvement in extracurricular/community activities. Tuition Reimbursement After one full year of employment, employee-owners are eligible for tuition reimbursement for bachelor's level coursework related to their current job or any future job offered at PBI-Gordon Companies. Parental Leave Company paid parental leave is offered to employee-owners following the birth of a child or the placement of a child with an employee in connection with adoption, foster care, or surrogacy. This policy will run concurrently with Family and Medical Leave Act (FMLA) leave, as applicable. If you are a California resident, you have rights under the California Consumer Privacy Act (CCPA). Please see our CCPA disclosure for more information. Employment is contingent upon and may not begin until the successful completion of a pre-employment background check and drug screen. PBI-Gordon and its subsidiaries participate in E-Verify to confirm the identity and employment eligibility of all persons hired to work in the United States. For more information about E-Verify, including your rights and responsibilities, please visit the E-Verify Website.

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

Lab Analyst I- 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. At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an Organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. **The Role: Lab Analyst I** **Location: Lenexa, KS** We're looking for a **Lab Analyst** to join a team of **bioanalytical professionals** supporting groundbreaking clinical research. The **Lab Analyst** will support appropriate development, validation and use of analytical methods through sample processing and analyzation, calibration, data reporting, and quality control testing. **Responsibilities:** + Extraction of bioanalysis samples using various sample preparation techniques for liquid chromatography - mass spectrometry (LC-MS). + Inject and analyze extracted samples using LCMS. + Prepares reagents and quality controls. + Maintains laboratory records physically and electronically. + Maintain clean laboratory bench space. + Ensure compliance with regulatory guidelines such as ICH M10. **To be successful in the role, you will have:** + Good knowledge of Bioanalytical Laboratory processes. + Laboratory Education and a Science Degree. + A detail-oriented mindset and track record of few mistakes, even when performing routine or repetitive tasks. + Ability to apply processes and systems to routine sample processing and instrumental analysis. + Consistent quality work in routine analytical skills. + Good Laboratory Skills (required) + Solid understanding of basic processes in analytical sample analysis, preferred + Experience working in a regulated laboratory environment (GxP) handling biological samples highly preferred. Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and 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 through the form below. \#LI-Onsite \#LI-KM1 **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

Quality control specialists are responsible for inspecting and/or testing products before, during, and after the manufacturing process to ensure that products align with company and legal standards. Requirements Highly Organized Self Motivated Interested in Overtime Passionate Computer Savvy Detail Oriented Key components of Quality Control may include: Inspection: Regularly examining products, materials, or services to identify defects, non-compliance, or deviations from quality standards. Testing: Conducting various tests and measurements to assess the performance, functionality, or characteristics of products or services. Statistical Process Control (SPC): Employing statistical techniques to monitor and control the production processes, ensuring that they remain within acceptable quality limits. Documentation and Records: Keeping detailed records of inspections, tests, and corrective actions taken to maintain traceability and accountability. Corrective Action: Implementing appropriate measures to address any identified quality issues and prevent their recurrence. Training and Education: Providing employees with the necessary skills and knowledge to maintain quality standards effectively. Continuous Improvement: Constantly analyzing data and feedback to identify areas for improvement and enhancing the overall quality management system.

We are looking to fill a **Scientist II or III - Metrology Specialist** position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer sponsorship.** **Metrology specialist is responsible for the oversight of regulated and non-regulated laboratory equipment** . This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement **Qualifications -** B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline + **Scientist II** - B.S. with 1-2 years of relevant experience or M.S. with 0-1 years of relevant experience + **Scientist III** - B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience **Responsibilities** + Prepare, review, and approve instrument/equipment documentation such as master equipment lists, qualification documentation, and calibration documentation + Coordinate service activities across a variety of vendors and service engineers while building and maintaining strong working relationships + Gain a working knowledge of laboratory equipment to facilitate with troubleshooting and/or perform maintenance or calibration activities + Participate in computer system validation activities associated with new or upgraded equipment or software packages + Support the purchase, installation, and equipment qualification of new laboratory equipment + Collaborate with metrology staff across multiple testing labs and sites for process improvement, cross-training and cross-site support + Originate and progress Notice of Event (NOE) and Change Management (CM) records + Perform and document investigations and assist in developing/implementing CAPA plans + Represent the laboratory on all aspects of laboratory equipment during audits + Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures **Required Skills and Experience** + Experience working within a regulated (GMP) laboratory + **Experience maintaining or operating laboratory equipment including HPLCs, GCs, UVs, dissolution systems, or other specialized computerized systems** + Familiarity with standalone computer system validation requirements + Highly organized, and capable of multi-tasking to manage a variety of laboratory equipment or system related schedules, documents, and maintenance tasks + Capable of working independently under moderate supervision + Strong verbal and written communication skills + Strong interpersonal skills. Comfortable interacting with a variety of on-site and off-site collaborators **Desired Skills and Experience** + Experience with maintenance of analytical instrumentation such as HPLC, UPLC, GC, UV, IR, Karl Fischer, and dissolution with ability to troubleshoot them. + Experience with computerized standalone systems GMP validation requirements + Familiarity with authoring relevant instrument standard operating procedures (SOPs) **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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.

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 ************

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

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