Quality control analyst jobs in Rogers, AR - 402 jobs

Yoh is hiring a Quality Assurance Associate for our Pharmaceutical Manufacturing client in St. Louis, Missouri. This is a great opportunity to expand your skillsets and join a growing team! Schedule: 8:00 am - 4:30 pm, Monday - Friday Job Responsibilities: Ensure completion of require training, work (including document review, batch release, QA on-the-floor, AQLs), and timely release of materials and batches. Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP). Responsible for the thorough and efficient review and disposition of completed batch record documentation ensuring adherence to Good Documentation Practices, cGMPs and applicable local procedures. Responsible for performing and / or overseeing performance of Quality Assurance On The Floor tasks including but not limited to performing AQL inspections, performing clearances for manufacturing areas and providing Quality input and guidance to manufacturing personnel. Responsible for with dispositioning finished product, raw materials/ components and intermediates through an all-inclusive documentation review and cross reference of electronic quality systems. Responsible with release of incoming raw materials and components per applicable local procedures. This may include support for labeling dispositioned raw materials and components with appropriate status indicator labels. Ensure a safe and quality working environment through training, awareness, and compliance to safety/Quality guidelines and SOP's. Ensure the maintenance of department, premises and equipment. Perform all work in compliance with site safety and radiation protection guidelines. Assist with quality investigations in order to determine root cause and applicable CAPAs. Skills/Education Required: Associate Degree in life science Bachelor Degree in life science or a related field preferred. Work experience is considered in lieu of degree. Three or more years of quality and production experience in a cGMP environment/facility. #IND-SPG Estimated Min Rate: $27.00 Estimated Max Rate: $29.00 What's In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week) Health Savings Account (HSA) (for employees working 20+ hours per week) Life & Disability Insurance (for employees working 20+ hours per week) MetLife Voluntary Benefits Employee Assistance Program (EAP) 401K Retirement Savings Plan Direct Deposit & weekly epayroll Referral Bonus Programs Certification and training opportunities Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, 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, disability, or status as a protected veteran. Visit ************************************************ to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our Candidate Privacy Notice: **********************************

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: At MilliporeSigma, the Quality Control Logistics Technician 3 will perform a variety of functions according to established protocols in support of the Quality Control testing laboratories. Execute all operations safely, consistently meeting quality and safety standards. Manage diverse sample logistics, including SAP transactions, sampling, weighing, deliveries, retains, and external shipments. Accurately weigh chemicals based on assay requirements and quantities. Safely handle all chemical classes in varying amounts. Support laboratory functions such as equipment upkeep, restocking, waste management, and material transport. Independently evaluate material hazards to establish safe handling and PPE needs. Complete required work to achieve team goals and meet deadlines. Communicate operational status and deviations, maintaining accurate records and logbooks. Physical Attributes: Wear PPE as required. Lift/push/pull up to 80 pounds. Extended work in a dry room environment. Who You Are Minimum Qualifications: High School Diploma or GED. Preferred Qualifications: 2+ years of experience working with SAP quality or inventory systems and transactions. Ability to independently review safety data sheets and determine appropriate handling precautions and personal protective equipment. Experience working with Microsoft Office platforms such as Excel and Word. Strong time management, attention to detail, and drive to perform individually and as a member of a team. Approach all tasks with an independent initiative to create value. Excellent verbal and written communication skills. RSREMD Pay Range for this position: $22.00-$35.00 per hour. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Our client is seeking an Lab Technician - Chemistry to join their team! This position is located in St. Louis, Missouri. Develop and apply analytical methods to determine chemical composition of agrochemical formulations and products using HPLC, UPLC, LC-MS, and GC Perform physical-chemical characterization techniques including density, particle size analysis, viscosity, surface tension, contact angle, and thermal analysis (DSC/TGA) Conduct optical and electron microscopy analyses and spectroscopic techniques such as FTIR, NIR, and UV-Vis Prepare and analyze complex liquid and solid sample matrices for qualitative and quantitative testing Optimize and develop new sample preparation and analytical methods to support pipeline and existing products Lead continuous improvement efforts for existing analytical methods and contribute to new method development Respond to collaborator and stakeholder inquiries, including analytical troubleshooting and data interpretation Analyze data, interpret results, and author clear technical reports for stakeholders across R&D, manufacturing, and product supply Maintain, calibrate, and troubleshoot laboratory instrumentation Perform sample cleanup techniques to enrich active ingredients in complex chemical samples Operate effectively in a fast-paced, high-throughput laboratory environment while managing multiple priorities Desired Skills/Experience: Hands-on experience preparing complex agrochemical or chemical sample matrices Proficiency with HPLC, UPLC, LC-MS, GC, and physical-chemical analytical techniques Strong background in sample preparation and analytical method development Experience with laboratory instrument maintenance and troubleshooting Highly detail-oriented with a strong focus on data quality and accuracy Excellent written and verbal communication skills Self-motivated with the ability to work independently and collaboratively Agile and adaptable to changing scientific and analytical priorities Strong organizational and multitasking skills Commitment to teamwork and cross-functional collaboration Willingness to train and work across multiple analytical disciplines Experience with robotic or automated sample preparation is a plus Benefits: Medical, Dental, & Vision Insurance Plans Employee-Owned Profit Sharing (ESOP) 401K offered The approximate pay range for this position is between $22.00 and $26.00. Please note that the pay range provided is a good faith estimate. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and location. We comply with local wage minimums.

Alutiiq Operations Services, LLC has an exciting opportunity for a Quality Control Technician supporting Tinker Air Force Base located in Oklahoma City, OK. The Quality Control Technician is responsible for keeping current on procedures, policies, in Control Technician, Quality Control, Technician, QC Manager, Quality Assurance, Equipment Maintenance, Manufacturing

ABOUT THE COMPANY Our founders, food industry veterans Mike and Tisha, knew that food wasn't what it used to be. They wanted to make it better-by creating a new kind of farm. A farm that can grow up to 300 times more food than an open-field farm on a smaller footprint, without use of herbicides, pesticides, or other chemicals that you don't want in your food. A farm powered with 100% renewable energy, growing with 95% less water and delivering food within 48 hours, for longer freshness for our customers and less food waste. 80 Acres Farms is a vertical farming leader, operating commercial farms in Ohio, Kentucky, and soon Georgia in addition to research and development farms in Arkansas and The Hague, Netherlands. All farms utilize state-of-the-art technology and analytics developed by the company's subsidiary, Infinite Acres. 80 Acres Farms-branded salads, microgreens, herbs, and tomatoes are available at retailers and food service distributors from Michigan to Florida, including Kroger, Whole Foods, The Fresh Market, Dorothy Lane Markets, Sysco, and US Foods. 80 Acres Farms is supported by world-class investors and partners, including General Atlantic, Siemens, Barclays, Ocado, and Signify Philips. If you're interested in making a difference, join our team and help us change how the world eats. POSITION OVERVIEW We are looking for self-motivated and driven individuals who can support and promote a team atmosphere. This individual will do so by providing basic crop handling responsibilities, including pruning, and maintaining vine crops; harvesting leafy greens, tomatoes, and herbs; and performing quality inspections. This individual will follow good manufacturing practices critical to food safety and to their team. R&D technicians will gain the hands-on experience and the initial skills needed to help promote advancement within the company. Key Responsibilities Seed & harvest leafy greens, tomatoes, and herbs on commercial scale Basic crop maintenance, such as pruning Complete data collection and documentation to ensure traceability and inventory accuracy Operate machinery including scissor lift, automated seeder, & automated harvester Sanitation of farm materials Follow all GMP's to ensure food safety Priva scheduling changes. Maintaining priva pH and EC sensors. Creating lighting Programs for crop specialists Execute planned trials and scheduled data events in a timely manner by collaborating with the lead crop specialist, operations manager, and other technicians. Clearly communicate SOP's that are associated with the crop program that they are assigned to work with. Help in creating SOP's for specific crop programs. Participate in trial results presentations for trials you have been working on 1:1 with the lead crop specialist. Keep up with maintenance of NCD sensors inside of grow zones. Make decisions on trial changes when needed, with consultation from Crop Specialist. Supervise day-to-day operations of research trials which include system maintenance and plant care. Plant care includes: irrigation scheduling, mixing fertilizer, pollination when needed, harvesting, pruning, seeding, transplanting, pest monitoring, etc. Maintaining seed inventory for crop programs associated with. Meet with the Lead Crop Specialist to go over future trial plans. Other duties assigned Specialized Knowledge, Skills or Abilities Adaptability to fast pace environment and quickly evolving processes Detail and quality oriented Qualifications Basic computer proficiency Ability to operate machinery, use a ladder, & lift 50 lbs Agriculture, science, and/or production background a plus Ability to work weekends, as needed BENEFITS WE OFFER YOU Health, dental, and vision insurance starting day one of employment Two weeks paid vacation One week paid health & wellness time 10 paid holidays Parental leave 401k with up to 4% Company match Annual tuition reimbursement Company-paid life insurance Short and long-term disability insurance ABOUT OUR HIRING PRACTICES Statistics show that underrepresented communities don't apply for a job unless they meet 100% of the qualifications. Don't worry if you think you can't check every box on the list; we'll provide all the on-the-job training you need. 80 Acres Farms is an equal opportunity employer. You're defined by more than just your job title, and we want you to feel comfortable bringing your true self to work. We value your talents, your traditions, your take on the world, and everything else that makes you unique. We strive to be to be a place where a diverse mix of talented people want to come, to stay, and to do their best work. 80 Acres Farms participates in E-Verify. As required by law, your employment with the Company is contingent upon you providing legal proof of your identity and authorization to work in the United States. Employment decisions are made without regard to protected characteristics. All candidates will be given the same consideration.

The Quality Control Coordinator is responsible for the Document Control and the Monthly Training Program. The Quality Control Coordinator must assist with internal and external audits, maintain policies, procedures, facility forms, logs and records. Benefits: Medical Insurance Prescription Drug Plan Dental/Vision Insurance Employee Incentive Plan Flexible Spending Account Cash Accumulation Plan-401K Life/AD&D Insurance Short- Term/Long-Term Disability Vacation Plan Paid Holidays Employee Assistance Program Adoption Assistance Program Tuition Reimbursement Maternity/Paternity Leave Pet Insurance Essential Functions: Works with Food Safety Manager and QC Manager in internal and external audits to ensure compliance for NWF to ensure successful audit completion. Facilitates annual document review per schedule and record requests per plant calendar. Completes document updates as needed to meet updated requirements or per management request. Works with various departments to maintain SSOPs, plant maps, employee training records, SDS catalog, Maintenance, QC and EHS records. Responsible for obtaining copies of all records pertaining to QC, Food Safety and Maintenance such as annual testing, GFSI certifications, equipment calibrations, safety inspections and licenses. Performs data entry of Environmental Monitoring Program results and generates monthly reports. Verifies sanitation records. Assists with tracking and trending. Responsible for retention of documents. Perform other duties or special projects as needed. Minimum Qualifications: Minimum of three years of working in the food industry with internal/external audit experience. Strong computer skills including Microsoft Office and Lotus Notes. Strong communication, analytical abilities and organizational skills. PCQI trained or will obtain within 12 months of hire date. Ability to work within a food plant environment. Preferred Qualifications: Degree in Food Science, Microbiology, Environmental Health or related Science field. Work Environment: General Office Setting 60% Food Production Area 40% Disclaimer: The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job. New Weds Foods is an Equal Opportunity Employer.

Opal Foods is currently accepting applications for the position of full time Quality Control Technician for our Missouri Processing Plants. This position is responsible for ensuring that all products meet or exceed USDA and customer specifications. Also monitors the food safety and sanitation procedures to ensure compliance with the company quality policy. Position Responsibilities: Perform pre-op sanitation inspection Monitor and record condition of nest run product Monitor and record condition of finished product Verify labeling and packaging of finished product Verify and record operating parameters of processing equipment in accordance with HACCP and GMP programs Monitor and record sanitation conditions of facility during processing Properly maintain all test instruments and supplies Any other tasks/job duties as assigned by the leadership team Requirements: (knowledge, experience, skills, education) Follow all Opal Foods Policies and Procedures including but not limited to Safety, Bio-security, FDA, SQF, HACCP and GMP Excellent attention to detail, ability to complete work tasks efficiently and be able to speak, read and write in English Ability to establish and maintain good working relationships with employees, customers and visitors - this position requires a "team" attitude Ability to multitask, be flexible and be able to adapt to change and variety in the workplace High school diploma or equivalent Food manufacturing and/or quality control experience preferred Requirements: (physical) Requires walking, standing, bending, stooping, turning, reaching, manual dexterity, eye-hand coordination to obtain readings and verify code dates Must be able to stand for extended periods while hand candling eggs Must be dependable and be able to work flexible hours, including weekends and holidays Must have a flexible schedule to help other departments should they need assistance on a particular day. About Opal Foods: Opal Foods formed in 2014 and is a partnership between Rose Acre Farms and Weaver Brothers. Our foundation is our commitment to our team, the quality of our product, our customers' satisfaction, and the welfare of our animals. Opal Foods provides high-quality, nutritious, affordable eggs to its customers through their farms based in Missouri, Colorado, and Iowa with its headquarters in Neosho, MO. For information on Opal Foods, please visit our website at ******************* Benefits: Opal Foods, LLC offers a comprehensive benefits package. This package includes options for medical, dental, vision, flexible spending accounts, life insurance, dependent life insurance, and disability that will all become effective the first of the month after your hire date. Opal Foods, LLC also provides a matching 401K plan. Opal Foods is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.

Reports To: Department Supervisor FLSA Status: Hourly Non-Exempt 3rd Shift Hours: 10:30pm-7:00am Overtime required based on production need. Pay: $18.50/hour GUARANTEED $0.50 RAISE AFTER 90 DAYS. Summary Tests and inspects products at various stages of production process and compiles and evaluates statistical data to determine and maintain food quality and reliability of products by performing the following duties. Essential Duties and Responsibilities include the following. Other duties may be assigned. Collects the production paperwork. Verifies the production room has been sanitized and swabbed. Selects products for tests at specified stages in production process, and tests products for variety of qualities such as dimensions, performance and chemical characteristics. Records test data, applying statistical quality control procedures. Recommends modifications of existing food quality or production standards to achieve optimum food quality within limits of equipment capability. Assures compliance to all applicable regulatory agencies including USDA, FDA, Bureau of Weights and Measures, State and Local regulations. Maintains current HACCP plan of both USDA and FDA products. Competencies To perform the job successfully, an individual should demonstrate the following competencies: Problem Solving - Identifies and resolves problems in a timely manner; Works well in group problem solving situations. Written Communication - Writes clearly and informatively; Able to read and interpret written information. Organizational Support - Follows policies and procedures. Quality - Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality. Quantity - Meets productivity standards; Completes work in timely manner; Strives to increase productivity. Safety and Security - Observes safety and security procedures; Reports potentially unsafe conditions; Uses equipment and materials properly. Adaptability - Adapts to changes in the work environment; Able to deal with frequent change, delays, or unexpected events. Attendance/Punctuality - Ability to maintain regular and punctual attendance. Dependability - Follows instructions, responds to management direction; Commits to long hours of work when necessary to reach goals; Completes tasks on time or notifies appropriate person with an alternate plan. Initiative - Asks for and offers help when needed. Requirements Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and/or Experience One year certificate from college or technical school; or three to six months related experience and/or training; or equivalent combination of education and experience. Language Skills Must be able to speak, read and write in English. Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Mathematical Skills Ability to calculate figures and amounts such as proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry. Reasoning Ability Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Computer Skills To perform this job successfully, an individual should have basic knowledge of computers and the ability to input data into a computer. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to physically perform the following: Lift 50 pounds 25 times during the shift Stand and/or walk for the duration of the shift Use hands to finger, grip, handle, or feel and reach with hands and arms Talk and hear Occasionally required to climb or balance and stoop, kneel, crouch, or crawl Close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly exposed to wet, humid, hot and/or cold conditions; moving mechanical parts; fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to high, precarious places. The noise level in the work environment is usually loud

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: Join our St. Louis Cherokee facility at MilliporeSigma, a leading contract development and manufacturing organization (CDMO) and a recognized Center of Excellence for antibody-drug conjugate (ADC) manufacturing. We are seeking passionate and enthusiastic professionals to contribute to our innovative bioconjugate production, leveraging over 35 years of expertise in the field. As a vital part of our dedicated team, you will play a key role in delivering high-quality ADCs that improve the quality of life for patients suffering from cancer and other debilitating diseases. With our state-of-the-art technologies and commitment to excellence, you will ensure the highest standards of quality and compliance in our ADC manufacturing processes. As an Associate Production Scientist - Rotating Shift you will manufacture products according to established protocols under ICH Q7 pharmaceutical regulations, provide technical support to others and perform operations in support of the group and department. Relocation Options Available Job duties include: * Evaluate products per established protocols, providing technical support and performing operations to meet departmental goals. * Safely conduct routine processes and unit operations, including cleaning equipment and work areas, while ensuring quality expectations. * Maintain required training and qualifications, train team members, and act as a technical consultant. * Support facility functions by maintaining equipment, preparing reagents, restocking supplies, and managing waste disposal. * Maintain accurate records and logbooks according to quality guidelines, communicating operational status and concerns to supervision. * Collaborate with other departments, participate in quality audits and customer interactions, and perform procedures independently or in a team. * Improve processes using scientific knowledge and principles, ensuring compliance with change control. * Address unsafe conditions promptly and troubleshoot challenges related to biological processes and GMP compliance. Physical Attributes: * Ability to lift to 50lbs. * Ability to wear personal protective equipment, such as respirator or chemical protective clothing, for extended periods. * Expected on-floor time: (70%) Who you are: Minimum Qualifications: * Bachelor's Degree in a scientific discipline (e.g., Chemistry, Biochemistry, Biology, etc.) * 2+ years industry Production/Laboratory experience * 1 + yeass experience with Antibody Drug Conjugates (ADCs), including knowledge of their formulation and manufacturing processes. Preferred Qualifications: * Experience with Automated Tangential Flow and Automated Chromatography systems. * Familiar with laboratory instruments and production equipment * Familiarity with process techniques, unit operations, and safe chemical handling methods. * Experience with Microsoft Office (Word, Outlook, Excel, etc.). * Mechanical and troubleshooting skills. * Knowledge of cGMP and ICH Regulatory and Quality standards. * Knowledge of Operational Excellence. * Clean room experience * Ability to interact professionally in customer-facing meetings, including challenging discussions on process planning and process execution RSREMD Pay Range for this position: $25.00 - $45.00 The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Research & Development - Method Development / Method Validation Chemist Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry and is the most respected name in our industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. The position requires the performance of variety of task including development and validation of analytical method, work with HPLC (High Performance Liquid Chromatography), manage a variety of research projects, and qualitatively/quantitatively testing client samples. This position requires knowledge of commonly used concepts, practices, procedures, and instrumentation used in a chemistry laboratory. Research Scientist II manages projects with some supervision and reports to the lab supervisor. The Research Scientist II must be able to think and work independently, yet share ideas and work toward team goals. The ability to express thoughts in a clear concise manner both orally and written is also expected. Works to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities. Some highlights.. Attractive Relocation Package available! Great Benefits Excellent Work/Life Balance Fantastic work environment 100% Company-paid Medical and Dental Insurance 401K Retirement with Company Match This is a full-time role Work Schedule: Days and hours of work are Monday through Friday, 8:30 a.m. to 5 p.m. Flexible hours such as early, late and weekend shift may be required. Work Restrictions: Because of vital nature of this work, we do not allow medical marijuana cards and we do random drug testing on all of our employees. Essential Functions... Qualitatively and quantitatively test of client samples. Development and validation of analytical methods. Manage research projects and coordinate project related works between different departments of ARL. Write research protocol, project report and working instruction. Communication with client regarding the project/sample test status. Use HPLC, IC and LCMSMS. Position Requirements... A BS in chemistry or related science with 4+ years industrial experience in MDMV Chemistry in the bio-technology and/or Pharmaceutical space. PhD in chemistry with 4+ years industrial experience in MDMV Chemistry in the bio-technology and/or Pharmaceutical space preferred. or related science with 0-2 years industrial experience Communication Proficiency. Work Environment... This job operates in a laboratory environment. Physical Demands... This position often requires standing for prolong periods of time; dexterity in fingers and hands to perform complex and precise manipulations; ability to walk and stood; ability to lift and move up to 50 lbs; see in the normal visual range including the ability to distinguish colors and shades and hear in the normal audio range with or without correction. AAP/EEO Statement ARL Bio Pharma, Inc. provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law. ARL Bio Pharma, Inc. expressly prohibits any form of workplace harassment based on race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law. Improper interference with the ability of ARL Bio Pharma, Inc. employees to perform their job duties may result in discipline up to and including discharge. Further, the company takes affirmative action to ensure that applicants and employees are treated without regard to any of these characteristics.

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.

Company Information About Thermo Fisher Scientific Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of $12 billion, we have approximately 39,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries. We create value for our key stakeholders through three premier brands, Thermo Scientific, Fisher Scientific and Unity™ Lab Services, which offer a unique combination of innovative technologies, convenient purchasing options and a single solution for laboratory operations management. Our products and services help our customers solve complex analytical challenges, improve patient diagnostics and increase laboratory productivity. Visit ********************* Job Description Job Title: Quality Control Scientist I Reports To: Quality Control Supervisor Group/Division: MBD Career Band: Band IV Job Track: Quality Assurance Position Location: Lenexa Kansas Number of Direct Reports none Day/Shift (if applicable): M-F FLSA Status (Exempt/Non-Exempt): Exempt Position Summary: Responsible for all quality control aspects of finished product testing. Ensure that performance of finished product is in compliance with testing standards per IFU and SOP's in addition to customer requirements and regulating agencies' guidelines. Documentation control duties per Quality assurance compliance requirements. Key Responsibilities: Review and maintain product compliance specifications, documentation control. Perform and interpret microbiology testing including growth promotion, biochemical, AST. Gain proficiency on all performance benches. Documentation of testing results and determining disposition. Maintain consistency in training in Master Control. Establish and maintain SOP criteria for inspection/testing. Responsible for maintaining department equipment and requesting consumables as needed. Exercise and monitor GMP compliance in work environment. Work closely with Quality Assurance department as a quality team. Execute Stability Study testing in accordance with QA requirements. Work in conjunction with Customer Service Representatives to achieve on time product releases for standing orders and special products. Work with the continuous improvement program within the department. Work closely with a team in a fast-paced laboratory setting. Understand and exercise all safety requirements and procedures. Assists in maintaining standards in accordance with GMP's/SOP's and ISO regulations. Participate in achieving department goals. Support all company policies. Performs other duties as assigned. Minimum Requirements/Qualifications: 1. Possess at least a 4-year degree in the biological sciences. Must have course work in microbiology with a laboratory or a 4-year degree with 5+ years of microbiology lab experience. 2. A minimum combined 1-2 years of experience of in related QC/QA, microbiology laboratory work in a laboratory setting, or an equivalent combination of education and experience. 3. Familiarity with FDA regulations for medical devices. 4. Possess the ability to manage many tasks and in an organized fashion. 5. Able to communicate effectively with a variety of departments in regard to quality testing parameters. 6. Possess intermediate computer skills, preferably with experience in Microsoft word to include Word, Excel and PowerPoint programs. Experience working in SAP is a plus. 7. Listen to, and follow, written and verbal instructions. 8. Able to adapt and to learn new procedures and to maintain a scientific and objective approach. 9. Must be available to work weekend shifts when needed. 10. Self-motivated, highly responsible and possess a good teamwork spirit. 11. Excellent verbal and written skills in English. Non-Negotiable Hiring Criteria: (Bullet 3-5 key quantifiable skills or position requirements that the candidate must have to be considered for this position.) Candidate must be a good time manager. Candidate must be willing to put in overtime when needed to complete tasks. Candidate must be a good team player/participant on teams. Candidate must have a high sense of responsibility. Candidate must possess critical thinking skills.

Benefits: * 401(k) * Bonus based on performance * Flexible schedule * Training & development Doping Control Officer I or II (DCO I or DCO II) USADA is seeking a dedicated and driven person to help our organization fulfill its mission to "Stand with athletes to champion their right to clean sport, inspire true and healthy sport, and promote the integrity of sport." This is an incredibly exciting time to join Team USADA, as we continue to grow our Anti-Doping program and work to support major international competitions such as the Olympic and Paralympic Games in 2026 (Milan), and 2028 (Los Angeles). New team members will have the chance to help ensure USADA is well-positioned in the near and long term for these opportunities as we look to the future with our efforts to protect clean athletes. With the 2028 Games on domestic soil, there will also be opportunities and growth potential over the years for USADA team members to underpin the organizing committee's commitment to a clean Games. REPORTS TO: DC Ops Manager & Asst Manager FLSA: Non-Exempt SUPERVISES: N/A Last revised: July 2025 LOCATION: Fayetteville, AR (Must reside w/in 50 miles) Anticipated # of Tests/Year: 30-40 JOB SUMMARY: Responsible for sample collection from athletes. Tasks performed by the Doping Control Officer (DCO) include preparation for, execution of and post-collection administration as it relates to Doping Control both at events and in the out-of-competition setting. DCOs are the field facing representatives of USADA. The primary objective of the DCO is to conduct Doping Control throughout the United States, under direction of the Doping Control Operations team, for Olympic, Paralympic, and Client Services testing teams, in support of USADA's mission and vision. The DCO works with the HQ team to uphold USADA's goals of creating and maintaining a fair and healthy environment for all athletes. The role will include both local and national travel to conduct Doping Control assignments. The following job expectations, responsibilities, and qualifications apply to both the DCO I and DCO II positions, however, in order to qualify for a DCO II level, one must have a valid phlebotomy credential in good standing, as further outlined below. A DCO II is able to serve as a doping control officer that can draw blood. RESPONSIBILITIES: * Conduct sample collection sessions in support of the testing programs for the Olympic/Paralympic, and Client Services testing teams, as well as on behalf of other agencies, when requested by USADA. * Accept, plan and manage doping control assignments, in accordance with the minimum requirements of the WADA/International Standards, and any minimum criteria established by USADA. * Execute logistics aspects as they relate to the doping control process to facilitate successful completion of missions. * Conduct doping control, including processing of Samples, in accordance with USADA's protocols and procedures, and in accordance with the WADA Code/International Standards. * Recruit and onboard independent contractors to serve in the capacity of a Chaperone*. *(Chaperones may be required in the event the athlete is a minor and/or if the gender of the DCO is not the same as the gender of the athlete being tested) * Witness sample collection or overseeing the witnessing of the sample collection process. * Travel (car, plane, train etc.) to various locations to perform sample collections (by the most economical route). * Ensure accurate documentation/completion of the doping control process. * Ship and submit processed Samples to the specified WADA certified laboratory. * Assist in the onboarding and training of new doping control officers. * Accountable to the most current version(s) of the DCO Manual, sample collection. documentation and other training resources. * Participate in DCO evaluation and support program, continuing education and re-accreditation. * Ensure adequate control of document, record and sample collection equipment. * Schedule and manage all travel, as well as associated expense reports. * Provide witness testimony in Legal cases, such as whereabout failures, other Anti-Doping Rule Violations. * Enforce infection control processes at all times that you are working with equipment or athletes. GENERAL: * Maintain confidentiality at all times. * Have no affiliation with sample collection organizations outside of USADA. * Keep USADA aware of issues in the field and/or any conflicts of interest. * Recommend necessary updates and revisions to USADA protocol and procedures as related to Doping Control. * Projects and other duties, as assigned. REQUIRED QUALIFICATIONS: Skills: * Excellent oral and written communication skills. * Excellent organizational skills and attention to detail. * Demonstrated high proficiency in utilizing technology such as tablets, multiple software platforms, and various applications. Demonstrated ability to: * Make decisions in accordance with USADA's protocol and procedures. * Multitask and work accurately under pressure. * Interact with internal and external customers professionally and in line with USADA's values. * Travel, possibly at short notice, to conduct test assignments. * Work flexible hours, as needed. * Access the internet for daily communication. * Values integrity, respect, and justice among internal and external constituents. * Perform effectively and collaboratively in a team environment. * Meet deadlines and operate with limited supervision. * Stand, bend and lift 50 pounds, on a regular basis. Certification: * Successful completion of all USADA certification/recertification requirements. * Pass bi-annual written and practical exams. * Attend DCO training sessions, meetings, conferences. * Valid Driver's License in good standing with state requirements where you reside. * Must be fully vaccinated against COVID-19. DCO II Additional Requirements: * *National Phlebotomy certification from one of the following accredited agencies: * ACA- American Certification Agency (certified on/after July 2003) * AMT -American Medical Technologists (certified on/after April, 2003) * ASCP - American Society of Clinical Pathology (certified on/after June, 2003) * NHA- National Healthcareer Association (certified on/after February 2005) * NCCT/MMCI- National Center for Competency Testing (certified on/after February 2003) * Applicants who are certified before the above dates must re-take the certifying examination. A more advanced, applicable credential such as RN, NP or PA will satisfy this requirement. * CPT I & II in California are acceptable credentials as they require successful completion of a national exam by one of the certifying bodies outlined above. * In addition to a current national certification, individuals will be required to ensure compliance with state specific phlebotomy training requirements for the state in which they reside. * At least 3 years phlebotomy experience, preferred. Additional Certification(s): * Obtain SafeSport Certification (post-offer) DESIRED QUALIFICATIONS: * Work experience in Allied Health Professions w/certification and/or License (Athletic Trainer, Physical Therapist, Registered Nurse, Paramedics, etc.) COMPENSATION & TIME COMMITMENT: * Compensation is on a per-test basis(piece rate) for out-of-competition (OOC) missions, with compensation typically ranging from $130 to $180 per test dependent on the test parameters. OOC test sessions can vary in length, but generally take 1 to 2 hours for successful completion. * In Competition (event) testing is paid at a daily flat rate, typically at $250 per day. * Onboarding is anticipated to begin in December/January with a more significant time commitment up front for training. Expect a time commitment of 24-30 hours of time during the first 60 days of onboarding. After that it should only be 2-3 hours of training and updates per quarter, plus the necessary time to complete test assignments.

Are you ready to embark on a career where innovation meets excellence? At Jost Chemical Company, we're on a mission to push the boundaries of chemical manufacturing, delivering high-quality products that make a positive impact on global industries. If you're passionate about chemistry, dedicated to precision, and eager to contribute to a company that values both innovation and integrity, explore our exciting job opportunities. Join us in shaping the future of chemical manufacturing at Jost Chemical Company, where your career is more than just a job - it's a journey of growth and achievement. Then, this position is right for you! Founded in 1985, Jost Chemical is a global leader in the manufacture of high purity mineral salts for the nutritional, pharmaceutical and specialty markets. Expansion, growth of capabilities, and investment in people, lab and production equipment have been a part of Jost's company culture for 35 years. To learn more about Jost Chemical please visit ******************** Our offer: * Shift Differential * Medical/Dental/Vision Plan Insurance, Short and Long-Term Disability and Life Insurance first of the month following 60 days. * 401k plan which includes safe-harbor contribution and discretionary match. * Paid Time Off (PTO) Employees eligible first day of employment. * 9 Company Paid Holidays (72 hours) each year. * Uniforms Provided * Foot Protection- annual allowance for all laboratory, maintenance and production employees. * 24-hour access to our free, on-site fitness center. * We provide Individual development, on-the-job training, and development programs designed to enhance your professional growth and development while ensuring you feel valued, inspired and appreciated at work. Jost Chemical is an equal opportunity employer and affirmatively seeks diversity in its workforce. We consider applicants, and make all employment decisions, without regard to race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, or any other legally protected status. We are committed to recruiting and retaining the best talent in the chemical manufacturing industry. Background * Works under general direction of the Quality Control Manager in a c-GMP regulated manufacturing environment operating under Q7A standards. * Employees in positions at this level of the series exercise a considerable degree of independence in conducting a wide range of experiments requiring expertise in the application and adaptation of numerous research techniques and produce desired results. Tasks * Perform analytical testing using wet chemistry techniques and instrumentation on c-GMP regulated products following compendial methods (USP/NF, EP, FCC, JP etc). * Perform microbiological testing on c-GMP regulated products using compendial methods. * Perform routine and non-routine testing using basic and advanced laboratory instrumentation and adhere to a strict calibration / preventative maintenance program. * Interpret analytical data and assist chemical operators and chemical engineers with applying this data to the manufacturing process. * Write research methods, results, and conclusions for publication; may present at professional conferences. * Review scientific literature, abstracts, and applicable method papers; identify appropriate application for current or anticipated research projects. * Maintain data integrity in both written and digital form. * Prepare laboratory test solutions and perform standardizations of volumetric solutions. * May be required to inventory and order laboratory supplies, instruments, and reagents. * Maintain a clean and organized work area. * Maintain and enhance site safety. * Instruct other personnel in specific areas of quality control laboratory testing. * Data mining and trending; Process Validation support; Root Cause Analyses; Problem Solving Tools use; Statistical Data trending; Support for Non-conformance Investigations; Production support activities. Specifications * A.S or B.S. Chemistry or related technical field that included instrumentation, or industry experience. * 0-2 years professional level chemist experience. Knowledge of: * Theories, principles, and methods of instrumental and wet chemistry * Method development and method validation * Mathematics and statistics * Basic analytical laboratory equipment * MS Office software package Skill in: * Working effectively and efficiently on multiple projects at once * Working effectively in a team environment * Responding to rapidly changing demands Ability to: * Lead and/or train others in assigned activities * Follow compendia and other test methods * Develop creative solutions to more varied research procedural problems * Design and manage projects * Identify, gather, process, and record data accurately * Maintain quality, safety, and/or infection control standards * Operate and maintain laboratory equipment * Communicate effectively, orally and in writing (including documenting research methods, results, and conclusions) * Exercise independent judgment

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

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

Job Title: QC Scientist IJob Description We are seeking a dedicated and detail-oriented Quality Control Technologist to join our team in Lenexa, Kansas. This role is crucial in ensuring that all quality control aspects of finished product testing meet compliance standards, customer requirements, and regulatory guidelines. You will play a key role in maintaining documentation control duties as per quality assurance compliance requirements. Responsibilities + Review and maintain product compliance specifications and documentation control. + Perform and interpret microbiology testing, including growth promotion, biochemical, and AST. + Gain proficiency on all performance benches and document testing results to determine product disposition. + Maintain consistency in training in Master Control and establish SOP criteria for inspection/testing. + Maintain department equipment and request consumables as needed. + Exercise and monitor GMP compliance in the work environment. + Collaborate closely with the Quality Assurance department as part of the quality team. + Execute Stability Study testing in accordance with QA requirements. + Coordinate with Customer Service Representatives to ensure timely product releases. + Participate in the continuous improvement program within the department. + Adhere to all safety requirements and procedures and assist in maintaining standards according to GMP and ISO regulations. + Support all company policies and participate in achieving department goals. + Perform other duties as assigned. Essential Skills + Possess at least a 4-year degree in biological sciences with coursework in microbiology and a laboratory component or a 4-year degree with 5+ years of microbiology lab experience. + Minimum 1-2 years of experience in QC/QA or microbiology laboratory work, or an equivalent combination of education and experience. + Familiarity with FDA regulations for medical devices. + Ability to manage tasks in an organized fashion and communicate effectively with various departments. + Intermediate computer skills, preferably with Microsoft Word, Excel, and PowerPoint. + Experience working in SAP is a plus. + Ability to follow written and verbal instructions and adapt to new procedures. + Self-motivated, highly responsible, with excellent teamwork spirit. + Excellent verbal and written communication skills in English. Additional Skills & Qualifications + Availability to work weekend shifts when needed. + Good entry-level job in the field of microbiology. Work Environment The position is located in Lenexa, Kansas, with working hours from Monday to Thursday or Tuesday to Friday, 7:00 AM to 5:30 PM, and another shift from Friday to Monday, 7:00 AM to 5:30 PM. You will work in a fast-paced laboratory setting, closely with a team, ensuring adherence to GMP and ISO standards. Job Type & Location This is a Contract position based out of Lenexa, KS. Pay and Benefits The pay range for this position is $20.00 - $20.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Lenexa,KS. Application Deadline This position is anticipated to close on Jan 28, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Full-time Description Main Responsibilities Being the last line of defense in production for ensuring quality Verifying sizes, counts, and order breakdowns- ensuring 100% accuracy of order Monitoring print quality; quickly and clearly communicating about all aspects of the job to Press Operator: report defects, errors, questions, concerns immediately Performing other screenprinting duties, as needed: taping and cleaning screens, with the overall focus on facilitating print jobs in a timely manner Ensuring that printed jobs are taken to post-production, after shirts are printed Requirements The person in this position must have the following characteristics: Communicative: able to talk to Press Operators and other departments when a miscount or mess-up occurs Quick and Agile: able to address and resolve issues on the floor Team Player: able to ask for help when needed and offer help without being asked Detail-oriented: conduct precise counts, with zero tolerance for error Productive: able to take initiative and manage time efficiently (i.e., not wasting time waiting for shirts to come down the dryer - find other work to do) Salary Description starting $13/hour

The Lab Analyst role reports to the Plant Chemist/Lab Leader as part of the site quality assurance laboratory. The Lab Analyst is responsible for using analytical methods to provide prompt and accurate testing of industrial chemicals for conformance to quality specifications, for operational process control, to fulfill special customer requirements, or in support of troubleshooting or improvement projects. Responsibilities & Accountabilities * Follow all safety rules and actively promote safety through reporting safety observations, performing job safety analyses, completing safety inspections and walkthroughs, participating in safety meetings, etc. * Directly responsible for understanding, promoting and upholding the Eastman Basic Safety Expectations * Perform routine testing to determine and report final product quality status to manufacturing * Perform routine testing to support unit production as specified by the manufacturing units * Accurately input all data into LIMS system and record test results in a legible manner on designated forms * Check operation of testing equipment, troubleshoot equipment to identify and/or correct source of problem, and notify the chemist of any abnormalities or maintenance requirements * Conduct job tasks in a professional manner utilizing good housekeeping practices and laboratory technique Experience & Education * Minimum of 1 years laboratory experience in a technical environment *Bachelor's/Associate's degree in a STEM field, such Chemistry or Chemical Technology preferred, but not required Job Skills * Strong attention to detail and safe work practices * Familiarity in GC, HPLC, and wet chemistry techniques * Ability to work in a team/collaborative environment * Strong communication and multitasking skills * Computer skills: Microsoft Office (Outlook, Word, Excel, PowerPoint), and LIMS preferred * Experience with cGMP and ISO 9001 requirements a plus Schedule * Position requires working a rotating 12- hour shift. Successful applicants must be flexible and willing / able to provide overtime coverage when needed (including evenings and holidays) and work a 12-hour rotating shift schedule (days and nights) if needed to support business requirements. Brown & Root Industrial Services is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, disability, sex, sexual orientation, gender identity or expression, age, national origin, veteran status, genetic information, union status and/or beliefs, or any other characteristic protected by federal, state, or local law. BENEFITS: Brown and Root offers a selection of competitive lifestyle benefits which include a 401K plan with company match, medical, dental, vision, life insurance, AD&D, flexible spending account, disability, paid time off, and flexible work schedule. We support career advancement through professional training and development. The Lab Analyst role reports to the Shift Team Leader/Lab Manager as part of the site quality assurance laboratory. The Lab Analyst is responsible for using analytical methods to provide prompt and accurate testing of industrial chemicals for conformance to quality specifications, for operational process control, to fulfill special customer requirements, or in support of troubleshooting or improvement projects. Responsibilities & Accountabilities * Follow all safety rules and actively promote safety through reporting safety observations, performing job safety analyses, completing safety inspections and walkthroughs, participating in safety meetings, etc. * Directly responsible for understanding, promoting and upholding Basic Safety Expectations both for themselves and the people around them * Perform routine testing to determine and report final product quality status to manufacturing * Perform routine testing to support unit production as specified by the manufacturing units * Accurately input all data into LIMS system and record test results in a legible manner on designated forms * Check operation of testing equipment, troubleshoot equipment to identify and/or correct source of problem, and notify the chemist of any abnormalities or maintenance requirements * Conduct job tasks in a professional manner utilizing good housekeeping practices and laboratory technique.