Quality control analyst jobs in Springfield, MO - 317 jobs

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.

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. This is a Salary Non -Exempt Role (eligible for payment of overtime in accordance with Fair Labor Standards Act) Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives. We proudly offer * Generous benefit options * Paid training, vacation and holidays * Career advancement opportunities * Education reimbursement * 401k program * And more! Essential job duties * Perform complex testing and data evaluation such as TGA * Perform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues * Participate in or assist with test method validations * Evaluate data for trends * Support supervisors in OOS Investigations and complete CAPA requirements * Interact with outside departments including attending meetings, providing updates, etc. * Coordinate testing performed at outside testing labs, raw materials, etc. * Maintain a detailed and accurate recording of activities and results on paperwork * Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools * Train upon and understand methods, equipment and standard operating procedures * Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures * Support equipment upkeep * Prepare and order supplies, as necessary * Enter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management * Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry * Interact with other departments within the company for testing needs and scheduling * May lead departmental projects with the opportunity to participate in or lead cross-functional teams, including continuous improvement projects and new customer teams * May lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results Good Manufacturing Practices & Good Documentation Practices (GMP & GDP) * Perform all GMP related documentation in compliance with ALCOA and good documentation practices as defined by site SOP's. * Strict compliance with all cGMP documents SOP's, Batch records, protocols, change controls, controlled forms, etc. * Ensure all cGMP applicable training is kept current Do not perform any cGMP task for which have not received appropriate training * Escalate any cGMP concerns to Supervisors and to Quality Department as needed * Perform job functions in compliance with applicable US FDA regulations and current Good Manufacturing Practices. Education, experience, certification and licensures Required Bachelor's degree in Chemistry or related field QC Analyst I: 0-2 Year's Experience QC Analyst II: 3-5 Year's Experience QC Analyst III: 5-7 Year's Experience Preferred Experience working in cGMP or GLP pharmaceutical industry environment Knowledge, skills and abilities * Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public * Ability to meet deadlines and work under pressure with limited supervision * Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently * Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations * Ability to write reports, business correspondence, and procedure manuals * Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations * Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis * Ability to define problems, collect data, establish facts, and draw valid conclusions * Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables * Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems * Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus Physical requirements 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 talk or hear. The employee is frequently required to stand; walk; or sit; use hands to finger, handle, or feel and reach with hands and arms. The employee is occasionally required to climb or balance; stoop, kneel, crouch, or crawl and taste or smell. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Work environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is frequently exposed to fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; risk of electrical shock; explosives; risk of radiation and vibration. The noise level in the work environment is usually moderate. The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel as classified. Management reserves the right to revise or amend duties at any time. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia 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, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

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. This is a Salary Non -Exempt Role (eligible for payment of overtime in accordance with Fair Labor Standards Act) Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives. We proudly offer Generous benefit options Paid training, vacation and holidays Career advancement opportunities Education reimbursement 401k program And more! Essential job duties Perform complex testing and data evaluation such as TGA Perform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues Participate in or assist with test method validations Evaluate data for trends Support supervisors in OOS Investigations and complete CAPA requirements Interact with outside departments including attending meetings, providing updates, etc. Coordinate testing performed at outside testing labs, raw materials, etc. Maintain a detailed and accurate recording of activities and results on paperwork Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools Train upon and understand methods, equipment and standard operating procedures Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures Support equipment upkeep Prepare and order supplies, as necessary Enter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry Interact with other departments within the company for testing needs and scheduling May lead departmental projects with the opportunity to participate in or lead cross-functional teams, including continuous improvement projects and new customer teams May lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results Good Manufacturing Practices & Good Documentation Practices (GMP & GDP) Perform all GMP related documentation in compliance with ALCOA and good documentation practices as defined by site SOP's. Strict compliance with all cGMP documents SOP's, Batch records, protocols, change controls, controlled forms, etc. Ensure all cGMP applicable training is kept current Do not perform any cGMP task for which have not received appropriate training Escalate any cGMP concerns to Supervisors and to Quality Department as needed Perform job functions in compliance with applicable US FDA regulations and current Good Manufacturing Practices. Education, experience, certification and licensures Required Bachelor's degree in Chemistry or related field QC Analyst I: 0-2 Year's Experience QC Analyst II: 3-5 Year's Experience QC Analyst III: 5-7 Year's Experience Preferred Experience working in cGMP or GLP pharmaceutical industry environment Knowledge, skills and abilities Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public Ability to meet deadlines and work under pressure with limited supervision Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations Ability to write reports, business correspondence, and procedure manuals Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis Ability to define problems, collect data, establish facts, and draw valid conclusions Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus Physical requirements 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 talk or hear. The employee is frequently required to stand; walk; or sit; use hands to finger, handle, or feel and reach with hands and arms. The employee is occasionally required to climb or balance; stoop, kneel, crouch, or crawl and taste or smell. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Work environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is frequently exposed to fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; risk of electrical shock; explosives; risk of radiation and vibration. The noise level in the work environment is usually moderate. The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel as classified. Management reserves the right to revise or amend duties at any time. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia 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, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

The Quality Control Inspector position ensures that the products manufactured by Paul Mueller Company meet the required specifications as directed by company policy, the customer, jurisdictional authority or a combination. This position compares our products to the appropriate specification(s) and/or standard(s) and operates within the limits of company policy and authority delegated by the Quality Assurance Manager. Essential Job Functions * Develop and complete travelers, draft data reports, weld records, and other related project documentation. * Complete and document product inspections and walk-down forms. * Communicate schedule requirements to the Al to ensure data reports are complete on time. * Confirm with manufacturing supervisor that required special testing or documentation is being completed. * Work with the customer's inspection team during FAT as needed. * Verify that the required standards of quality are maintained for the product involved. * Ensure lessons learned applied to future efforts. * Perform other related duties as required and assigned. * Regular, in-person attendance due to necessary teamwork and personal interactive nature of this position. * Overtime may be necessary and required and is dependent on workload. * The ability to work in a constant state of alertness and safe manner. Knowledge, Skills, Abilities (Competencies) * Experience with ASME Code, Section VIII, Division I or equivalent. * Mechanical aptitude with the ability to read and understand manufacturing drawings. * Experience and knowledge of various NDE methods and techniques. * Must be able to work on multiple tasks with little supervision in an organized manner and fast paced environment. * Show initiative to perform duties beyond assignment-specific duties. * Excellent communication skills both orally and written. * Ability to work independently or in a team. * Ability to establish and maintain working relationships with individuals at all levels. * Ability to efficiently utilize Microsoft Office and email. Education and Experience * High school graduate or equivalent required. * Minimum of one (1) year weld inspection experience is preferred. * Knowledge of various fabrication methods and installation procedures; a broad understanding of materials, how to navigate the applicable material specification for characteristics and their tolerances and limitations; and a general understanding of manufacturing equipment and systems Base Compensation Range: $20.13 - $30.20 per hour Variable Compensation Range: Incentive bonus eligibility up to 10% of gross annual salary base on company performance (as of 2024). Health and Ancillary Benefit Overview: * Medical, Dental & Vision Insurance with low employee premiums * Free off-site medical clinic * Company paid Life Insurance & Short-Term Disability * 401k - Employer match of up to 4.0% for coworker contributions of 8.0% or more * Company covers tuition costs up to $5,250.00 annually, contingent on course completion and grades * Paid Time Off and Sick, Family & Parental Paid Time Off * Ten (10) Paid Holidays * Four-day work weeks, varied shifts, and flexible remote work options depending on position * Career progression program for advancement * Free in-house welding, grinding & machine operation school * In-house training program Professional office environment with some time spent in a manufacturing shop. Use of standard office equipment (computers, phones, copiers, and filing cabinets, etc.). Frequent presence on the manufacturing floor as well as field operations. Exposure to conditions, such as: dust, fumes, noise and high-degree varying seasonal temperatures.

SUMMARY: Performs chemical and physical testing of samples submitted to SORA Laboratories. Maintains the chemistry and physical testing facilities and supplies in good working order. ESSENTIAL DUTIES AND RESPONSIBILITIES include, but are not limited to, the following. Management retains the right to add to or change the duties of the position at any time. The functions below are to be performed in accordance with all applicable FDA, OSHA, EPA, and ISO standards and regulations. Perform the receipt, compositing, and organization of samples submitted to SORA Labs. Perform and report the assigned testing of samples submitted to the laboratory. Render pass/fail dispositions based on results. Perform and report the routine maintenance and calibration of equipment and instrumentation. Record and peer-review analytical and calibration work performed as required for GMP and laboratory accountability. Organize and maintain the necessary chemical and reagent stocks. Maintain the laboratory facilities in a clean and organized manner. Properly handle and dispose of all hazardous waste generated during routine functions. QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Possess expertise and proficiency with analytical laboratory glassware, equipment and instrumentation. Be able to read, analyze, and interpret methods and standard operating procedures. Be able to work independently in an organized and reliable manner Be willing to work extended hours, weekends and holidays when needed. The position requires extensive standing. The employee is regularly required to walk, sit, and reach with hands and arms. The employee must occasionally lift and/or move up to 50 pounds. EDUCATION AND/OR EXPERIENCE: Requires a Bachelor of Science in Chemistry, Biochemistry or related field. This position requires 0 to 3 years experience. WORK ENVIRONMENT: Work is carried out in an analytical laboratory within a factory setting. There is considerable exposure to raw materials and chemical reagents. Personal Protective Equipment such as lab coats, gloves, safety glasses and respirators must be worn as defined by safety policy. Excited about this role but don't think you meet every requirement listed? We encourage you to apply anyway. You may be just the right candidate for this role or another one of our openings. ADM requires the successful completion of a background check. REF:104074BR About ADM At ADM, we unlock the power of nature to provide access to nutrition worldwide. With industry-advancing innovations, a complete portfolio of ingredients and solutions to meet any taste, and a commitment to sustainability, we give customers an edge in solving the nutritional challenges of today and tomorrow. We're a global leader in human and animal nutrition and the world's premier agricultural origination and processing company. Our breadth, depth, insights, facilities and logistical expertise give us unparalleled capabilities to meet needs for food, beverages, health and wellness, and more. From the seed of the idea to the outcome of the solution, we enrich the quality of life the world over. Learn more at ************ #IncludingYou Diversity, equity, inclusion and belonging are cornerstones of ADM's efforts to continue innovating, driving growth, and delivering outstanding performance. We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments - environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career. We respect and value the unique backgrounds and experiences that each person can bring to ADM because we know that diversity of perspectives makes us better, together. We welcome everyone to apply. We are committed to ensuring all qualified applicants receive consideration for employment regardless of race, color, ethnicity, disability, religion, national origin, language, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law Benefits and Perks Enriching the quality of life for the world begins by taking care of our colleagues. In addition to competitive pay, we support your diverse needs with a comprehensive total rewards package to enhance your well-being, including: Physical wellness - medical/Rx, dental, vision and on-site wellness center access or gym reimbursement (as applicable). Financial wellness - flexible spending accounts, health savings account, 401(k) with matching contributions and cash balance plan, discounted employee stock purchasing program, life insurance, disability, workers' compensation, legal assistance, identity theft protection. Mental and social wellness - Employee Assistance Program (EAP), Employee Resource Groups (ERGs) and Colleague Giving Programs (ADM Cares). Additional benefits include: Paid time off including paid holidays. Adoption assistance and paid maternity and parental leave. Tuition assistance. Company-sponsored training and development resources, such as LinkedIn Learning, language training and mentoring programs. *Benefits may vary for bargained locations, confirm benefit eligibility with your recruiter. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. If hired, employees will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. The pay range for this position is expected to be between:

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!

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

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description: 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.

Quality Control Springfield, Missouri, US + Added - 12/11/2025 Apply for Job _Our client, a leading global CDMO, is looking to hire a QC Deviation Specialist III to join their growing team in Greene County, Missouri!_ **Pay rate:** $45 -$47/hr. **Job type** : 4-month contract (possibility of extension) **Position Summary** The QC Deviation Specialist III will be responsible for leading and executing quality investigations, including deviations and OOS events, within Manufacturing and QC departments. This role ensures compliance with internal procedures, regulatory requirements, and industry best practices while driving continuous improvement through effective root cause analysis (RCA) and implementation of corrective and preventive actions (CAPAs). **Key Responsibilities** + Perform and document Deviation Investigations for Manufacturing and Quality Control operations. + Conduct Root Cause Analyses (RCA) and determine appropriate Corrective and Preventive Actions (CAPAs) to address identified issues. + Partner with Manufacturing, QC, and Quality Assurance teams to support investigations and ensure timely and compliant closure. + Provide coaching and training to staff on deviation investigations, RCA methodologies, and investigator qualification. + Perform and draft Out-of-Specification (OOS) investigations in accordance with internal policies and regulatory standards. + Review and analyze data to identify trends, recurring issues, and opportunities for process improvement. + Support continuous improvement initiatives within the Quality Management System (QMS). + Ensure all activities comply with applicable GMP, ISO, and regulatory requirements. **Qualifications** + Minimum 10 years of relevant experience in Quality Systems Management, with direct experience in manufacturing and quality control deviation management. + Strong knowledge of Root Cause Analysis (RCA) and CAPA development and implementation. + Proven experience writing and managing quality investigations in a regulated industry (e.g., pharmaceutical, biotechnology, medical device, or similar). + Bachelor's degree preferred in a scientific, engineering, or related technical discipline. + Excellent analytical, problem-solving, and communication skills. + Ability to work independently and collaboratively in a cross-functional team environment. **Preferred Qualifications** + Familiarity with Good Manufacturing Practices (GMP) and regulatory guidance (e.g., FDA, EMA, ICH). + Experience using electronic quality systems (e.g., TrackWise, Veeva Vault, or similar). + Prior experience mentoring or training personnel on deviation and CAPA processes. We are 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.

Who we are looking for: Jordan Valley Auto Body Repair is looking for a Quality Control employee. You will be responsible for pre and post repair inspections of vehicles. You will make sure vehicles are moved to where they need to be throughout the repair processes and will be needed to bring vehicle up to the customers once all repairs are completed on a vehicle. You will need to be able to work in a team environment but also a self-starter to work alone to get tasks completed in a timely manner with a high attention to detail. What you will do: Perform thorough pre-repair and post-repair inspections on vehicles Move vehicles to appropriate locations throughout the repair process Coordinate vehicle flow to support shop efficiency Present completed vehicles to customers upon repair completion Ensure all repairs meet company quality and safety standards Work collaboratively with team members while also managing tasks independently Final quality control inspections of vehicles before customers pick up Clean shop and areas as needed Perform additional duties as assigned Maintain a high level of attention to detail and organization What you will need: Ability to read, write, speak and understand English. Candidate must be dependable and a team player Valid driver's license Strong attention to detail is required Good time-management and organizational skills Ability to work independently and as part of a team in a fast-paced body shop Excellent verbal and written communication skills, with the ability to communicate clearly and professionally while maintaining a friendly demeanor Prior body shop experience is preferred but not required. Physical/Mental Requirements: Physical ability to sit, stand or crouch for long periods and lift up to 50 lbs. Compensation: Start rate beginning at $16.80 per hour. Please note that final compensation will be determined based upon the applicant's relevant experience, skillset, location, business needs, market demands, and other factors as permitted by law. No immigration or work visa sponsorship will be provided for this position. #LI-CG1 #Ind123KW

We Deliver the Goods: * Competitive pay and benefits, including Day 1 Health & Wellness Benefits, Employee Stock Purchase Plan, 401K Employer Matching, Education Assistance, Paid Time Off, and much more * Growth opportunities performing essential work to support America's food distribution system * Safe and inclusive working environment, including culture of rewards, recognition, and respect Position Summary: Responsible for managing accounts in geographical area providing assistance and training to such accounts by maintaining proper functioning of various beverage and chemical equipment. Installs and tests various equipment. Assists customers and sales people to determine best equipment or products for application. Communicates and interacts with customers, vendors and company personnel in a professional and courteous manner while providing accurate and timely information. Functions as a team member within the department and organization, as required, and perform any duty assigned to best serve the company. Position Responsibilities: * Manage accounts in geographical area and provide assistance and training to such accounts. * Maintain proper functioning of various beverage and chemical equipment. * Install and test various equipment. * Assist customers and sales people determine best equipment or products for application. * Provide face-to-face customer service in various situations. * Drive to customer sites to assist in correcting problems. * Prepare schedules for service or installation. * Performs other related duties as assigned. EEO Statement Performance Food Group and/or its subsidiaries (individually or collectively, the "Company") provides equal employment opportunity (EEO) to all applicants and employees, regardless of race, color, national origin, sex, marital status, pregnancy, sexual orientation, gender identity, religion, age, disability, genetic information, veteran status, and any other characteristic protected by applicable local, state and federal laws and regulations. Please click on the following links to review: (1) our EEO Policy; (2) the "EEO is the Law" poster and supplement; and (3) the Pay Transparency Policy Statement. Required Qualifications High School Diploma or Equivalent 6 - 12 months equipment sales and / or maintenance Preferred Qualifications 1 - 2 years equipment sales and / or maintenance within foodservice industry.

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 for other accommodation options.

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 Associate Production Scientist - Night Shift at our 3300 South Second/Cherokee site will be responsible for the large-scale manufacturing of Life Science products. This role involves utilizing standard organic chemistry processes to ensure the efficient and effective production of high-quality products. Job duties include: * Production shifts consist of 12-hour shifts (6 PM - 6:30 AM) with a two-week rotation: Week 1 (Monday, Tuesday, Friday, Saturday) and Week 2 (Sunday, Wednesday, Thursday) * Take the necessary action to maintain a safe working environment. * Carry out production operations and communicate status to Manufacturing Supervision. * Provide technical leadership during the manufacturing process. * Ensure cleaning protocols are followed and recorded. * Prepare production areas, chemicals, and equipment for operations. * Conduct analytical tests and assess results during production. * Advise chemical processors on key in-process decisions based on test results. * Write and revise Master Manufacturing Procedures. * Prepare and review Operating Procedures to ensure compliance. * Participate in quality audits. * Provide complete and accurate records consistent with quality guidelines. * Provide technical support and training to personnel as well as cross-functional teams. Physical Attributes: * Lift, push pull, or move up to 55 pounds while wearing personal protective equipment, including respirators, for an extended time. Also able to move 300+ pounds with mechanical or team member assistance. * Perform tasks while wearing personal protective equipment, such as respirators or chemical protective clothing, for long durations. * Walk, reach above shoulders, stoop, kneel, twist, crouch, and/or stand and perform repetitive movements for extended periods of time. * Ability to talk, hear, taste and smell. Specific vision requirements of this job include close vision, distance vision, color vision, peripheral vision, depth vision, and the ability to adjust focus. Who you are: Minimum Qualifications: * Bachelor's degree in Chemistry, Biochemistry, Chemical Engineering or other scientific discipline OR * Associate Degree in Chemistry, Biochemistry, Chemical Engineering or other scientific discipline with 5 + years large scale chemical manufacturing experience Preferred Qualifications: * 1+ year production experience. * Detail oriented with excellent organizational, written, and verbal communication skills. * Logical approach to problem solving. * Experience with customer interaction. * Knowledge of Process Improvement methodology (e.g., PDSA, Lean Manufacturing, and/or Six Sigma). Pay Range for this position: $24.00 - $41.00. 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!

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.

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.) Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Division / Site Information Join Thermo Fisher Scientific's Pharma Services Group, where quality and compliance are at the core of everything we do. This role supports GMP manufacturing and quality control laboratories responsible for testing biopharmaceutical products across early-stage clinical development through commercial release. You will work on-site in a regulated laboratory environment, collaborating with cross-functional teams to ensure the highest standards of product quality, safety, and complian DESCRIPTION: You'll perform sophisticated analyses to ensure product quality and safety in our laboratories. As a QC Scientist II, you'll conduct complex analytical testing to support GMP manufacturing of biopharmaceutical products, from early-stage clinical development through commercial release. You'll work with analytical instruments and technologies while making a meaningful impact on patient health through precise quality control testing. Working with cross-functional teams, you'll execute validated test methods, participate in method development and validation activities, investigate out-of-specification results, and maintain detailed documentation of analyses. You'll contribute to continuous improvement initiatives and help establish robust analytical processes while adhering to cGMP requirements and safety standards. A Day in the Life You will: Perform complex analytical testing in support of GMP manufacturing, including in-process, release, and stability testing Execute validated test methods and support method development, validation, and transfer activities Operate and troubleshoot analytical instrumentation such as HPLC, GC, CE, ELISA, PCR, and other bioanalytical platforms Investigate out-of-specification (OOS), out-of-trend (OOT), and atypical results, including root cause analysis and technical report authorship Maintain accurate, thorough, and compliant documentation in accordance with cGMP and data integrity requirements Utilize Laboratory Information Management Systems (LIMS) and quality management systems to document and review data Support health authority and internal audits, inspections, and regulatory commitments Collaborate with manufacturing, quality assurance, and development teams to resolve issues and improve analytical processes Participate in continuous improvement initiatives to enhance laboratory efficiency, compliance, and robustness Follow all safety, aseptic technique, and environmental monitoring requirements Keys to SuccessEducation Advanced degree (MS or PhD) in Chemistry, Biology, Biochemistry, or a related scientific field with no prior experience, or Bachelor's degree in a scientific discipline with 2+ years of experience in a GMP-regulated laboratory environment performing analytical testing Experience Hands-on experience with analytical techniques such as HPLC, GC, CE, ELISA, PCR, and other bioanalytical methods Experience working in a cGMP-regulated environment Demonstrated experience investigating OOS results and authoring technical documentation Experience with method validation and method transfer activities preferred Familiarity with health authority audits and regulatory inspections Knowledge, Skills, and AbilitiesKnowledge Strong understanding of cGMP regulations, quality control principles, and data integrity requirements Knowledge of aseptic techniques and environmental monitoring procedures Skills Proficiency with Microsoft Office applications Experience with LIMS and electronic quality management systems Strong problem-solving, analytical, and organizational skills Excellent written and verbal communication skills Abilities Ability to work independently and collaboratively in a fast-paced laboratory environment Ability to manage multiple priorities while maintaining attention to detail Willingness to work flexible schedules, including occasional weekend work Physical Requirements / Work Environment Ability to lift up to 30 pounds Ability to stand for extended periods Willingness to wear required PPE, including lab coat, safety glasses, and gloves Work performed in a laboratory environment with exposure to chemicals and biological materials Benefits We offer competitive remuneration, an annual incentive plan, and a comprehensive benefits package starting Day 1, including: Medical, Dental, and Vision coverage Paid Time Off and designated paid holidays Retirement Savings Plan Tuition Reimbursement Career development and growth opportunities Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization and an inclusive culture that values Integrity, Intensity, Involvement, and Innovation. Relocation assistance is NOT provided Must be legally authorized to work in the United States without sponsorship, now or in the future. Must be able to pass a comprehensive background check, which includes a drug screening.

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