Chemist Jobs in Overland, MO

is based in St. Louis, MO. Relocation assistance available. Want to join a world leader? Then Sensient may be for you! At Sensient Technologies, we are experts in science, art, and innovation of color and flavor. We are market savvy and visionary. We are problem solvers and we will be better with you. As the Process Chemist Manager, you will lead a team of four (4) in the optimization and standardization of new and existing manufacturing processes to achieve maximum quality and yield at the lowest manufacturing costs through in-depth process studies and implementation of best practices. You will support key product profitability goals through successful introduction of new R&D scale process to the plant floor. What You'll Do: Manager the continuous optimization of our processes in order to achieve the lowest manufacturing cost while maintaining high quality. Continuously monitor yield and raw material usage of target, take action on issues that arise. Report on performance yield vs std yield. Collaborate with cross functional teams. Assist operations and quality in trouble shooting process problems. Identify and help implement permanent solutions to chronic exceptions. Serve as manufacturing Representative on new product / process introductions into the manufacturing plant. Function as liaison between production and R&D. Drive accountability with our process chemists / operational excellence team. Lead or serve as a key member on assigned quality Improvement Teams. Maintain a trained staff and embrace our coaching and continual improvement approach. Assist in development and maintenance of standard Operation Procedures, Job Models and Exception Condition reports. What You'll Bring: M.S. or PhD Degree in Chemistry with a minimum of 10 years of industry experience. Experience with synthetic reactions, rheology and organic chemistry. Previous operations management experience is a plus. Proven troubleshooting record with emphasis in root cause analysis and cost/benefit evaluation. Willingness to provide hands on support to troubleshoot and commission processes. Food / Pharmaceutical or other FDA regulated industry experience is a plus. What You'll Get: Opportunity to collaborate with your colleagues, onsite 5-days per week. An excellent salary, benefit offering, and development opportunities. A thorough and effective training experience during onboarding and beyond. SPONSORSHIP: Due to our inability to offer visa sponsorship, we can only consider candidates who are authorized to work in the United States without the need for employment visa sponsorship. About Sensient: Sensient Technologies Corporation is a leading global manufacturer and marketer of colors, flavors, and extracts. Sensient employs advanced technologies at facilities around the world to develop specialty food and beverage systems, cosmetic and pharmaceutical systems, specialty colors, and other specialty and fine chemicals. The Company's customers include major international manufacturers representing most of the world's best-known brands. About Sensient Colors: Sensient Colors is a leading developer, producer, and supplier of natural and synthetic color systems for customers around the globe. The Company's high-performance products play a vital role in the manufacture of foods and beverages, cosmetic and pharmaceutical Equal Opportunity Employer #LI-BW1

Want to join a world leader? Then Sensient may be for you! At Sensient Technologies, we are experts in science, art, and innovation of color and flavor. We are market savvy and visionary. We are problem solvers and we will be better with you. As Sr Process Chemist, you will lead the effort in the optimization and standardization of new and existing manufacturing processes to achieve maximum quality and yield at the lowest manufacturing costs through in-depth process studies and implementation of best practices. Support key product profitability goals through successful introduction of new R&D scale process to the plant floor. What You'll Do: Analyze samples from various sources to provide information on compounds or quantities of compounds present. Use analytical techniques and instrumentation, such as ICP, gas and high-performance liquid chromatography (HPLC), ion chromatography, electro chromatography and spectroscopy (infrared and ultraviolet, amongst others). Interpret data (chromatograms and MS data) and meet strict guidelines on documentation when recording data. Report scientific results. Develop techniques/methods for the analysis of raw materials and finished goods for colors and cosmetics. Work collaboratively in cross-functional teams liaise with customers, staff and suppliers. Be aware of, and keep up to date with, health and safety issues. Validate methods and equipment. What You'll Bring: M.S. or PhD Degree in Chemistry with a minimum of 10 years of industry experience. Previous operations management experience is a plus. Experience in organic chemistry, chemical reactions and synthesis, in particular in pigments & dyes Proven troubleshooting record with emphasis in root cause analysis and cost/benefit evaluation. Must be willing to provide hands on support to troubleshoot and commission processes. Food / Pharmaceutical or other FDA regulated industry experience is a plus. What You'll Get: Opportunity to collaborate with your colleagues, onsite 5-days per week. An excellent salary, benefit offering, and development opportunities. A thorough and effective training experience during onboarding and beyond. About Sensient Colors Sensient Color Group is a leading developer, producer and supplier of natural and synthetic color systems for customers around the globe. The Company's high-performance products play a central role in the manufacture of foods and beverages, cosmetic and pharmaceutical colors and coatings, colors for agricultural uses, household cleaners and paper products. The Color Group is located in St. Louis, Missouri. About Sensient Technologies Corporation Sensient Technologies Corporation is a leading global manufacturer and marketer of colors, flavors, and fragrances. Sensient employs advanced technologies at facilities around the world to develop specialty food and beverage systems, cosmetic and pharmaceutical systems, and other specialty and fine chemicals. The Company's customers include major international manufacturers representing most of the world's best-known brands. Sensient is headquartered in Milwaukee, Wisconsin. As a dynamic and diversified global leader, we offer an excellent salary and comprehensive benefits package. For more information, visit our website at ************************ Equal Opportunity Employer #LI-AM1

Eurofins Scientific is a global leader in providing a unique range of analytical testing services to multiple industries. With over 200,000 analytical methods, Eurofins Scientific helps make life and our environment safer, healthier, and more sustainable. Our network of over 62,000 employees across a network of more than 900 laboratories in 62 countries, strengthens Eurofins Scientific as a leader in scientific testing services. EAG Laboratories, a Eurofins company has over 40 years' experience in materials and engineering testing services. EAG is a global leader in scientific services with a portfolio of analytical methods. We offer a consultative multi-disciplinary approach to solving your materials and engineering related product problems. As thought leaders in investigative science, we set the global standard for materials and engineering testing services. EAG is actively seeking an Analyst (Analytical Chemist) to assist in the formulation of industrial and consumer products. Our laboratory in Maryland Heights, Missouri provides organic chemistry testing specializing in investigative analytical chemistry. Examples of this includes evaluating the label claims of consumer products, reverse engineering pharmaceuticals/nutritional supplements, contaminant identification, determining sources of off odors/flavors/colors, extractables and leachables of consumer electronics, testing medical devices and much, much more. A day in the life: You will be a part of the medical device testing team, which follows ISO 10993-18 to screen medical devices for extractables and leachables in the assembly of a toxicological risk assessment for regulatory approval of the device. A typical week includes preparing GCMS standards and samples, operating and maintaining a variety of GCMS instruments, analyzing data (largely untargeted extractables identification and quantitation), and presenting the data within report templates. Example of a case study: A medical device is extracted in 3 solvents. These extracts are handed off to the GCMS chemist who then runs standards and the extracts on instrument. The GCMS chemist processes all the standard and extract data both qualitatively and quantitatively, identifying the extractables. Example of equipment you will use: Agilent direct injection and headspace GCMS (single quad, high-efficiency source, and time-of-flight) In this position, you will be responsible for: * Applying standard and non-standard techniques, procedures, and criteria to carry out a sequence of related tasks to determine the composition, properties and/or structure of materials. * Performing sample preparation. * Recording test data providing some basic analysis and interpretations. * Maintaining specified records of scientific data. * Preparing reports on analytical results for customers. * Protecting confidential information and proprietary processes. * Handling customer materials and company equipment in a responsible and efficient manner. Qualifications * BS degree in Chemistry and 2+ years of GCMS experience. Desirable MS or PhD in Chemistry with GCMS focus. * Proficient in Microsoft Office and Excel in particular. * Excellent professional, verbal, and written communication skills. * Prefer materials characterization experience and experience in untargeted identification work. We encourage you to apply even if your experience is not a 100% match with the position. We are looking for someone with relevant skills and experience, not a checklist that exactly matches the job description. We want to help you grow and in return, you help us grow into a stronger, more inclusive organization. Physical Requirements: * Must be able to remain in a stationary position 80% of the time. * Ability to continuously operate a personal computer or lab equipment for extended periods of time (4 or more hours). * Ability to operate a keyboard and other lab equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead * Ability to communicate clearly and understandably ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting. * Ability to handle small and fragile devices with tweezers and /or fingers. * Require close distance visual acuity with or without correction (Glasses, Contacts, etc.) * Must be willing and able to wear PPE such as hard-hat, steel-toed shoes, safety glasses, laboratory coat and/or any other devices or equipment that is required. * Learn new tasks, remember processes, maintain focus, complete tasks independently, make timely decisions in the context of a workflow, ability to communicate with visitors, ability to complete tasks in situations that have a speed or productivity quota. * Ability to move equipment or items up to 50 lbs. The essential physical and mental requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. We will consider reasonable accommodations for qualified individuals with disabilities. If you have a disability or special need, we would like to know how we can better accommodate you. Additional Information What It's Like to Work Here: * Teamwork: experience what being a part of the Eurofins-EAG family feels like. Be inspired by your leaders, be encouraged by your teammates and be supported in all parts of your journey while you work with us. * Learning & Development: Develop within the company; be mentored and grown as a leader. * Diversity & Authenticity: we work hard to embrace diversity and inclusion and encourage everyone to bring their authentic selves to work every day. Eurofins EAG Laboratories is an equal opportunity employer and prohibits discrimination, harassment, and retaliation in all of our employment practices. Eurofins EAG Laboratories recruits, hires, trains, promotes and administers all employment-related matters based on an individual's qualifications, abilities, and efforts. Applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship status, sexual orientation, gender identity and/or expression, pregnancy, genetic information, disability, military and/or protected veteran status, and/or any other category protected by applicable federal, state, or local law. Eurofins USA Material Sciences is a Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer If you enjoy being immersed in science or engineering, tackling problems head-on, finding solutions through teamwork, and taking pride in accomplishments, join us today! Check out our other opportunities: ************************** Eurofins USA Material Sciences is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is a global leader in providing a unique range of analytical testing services to multiple industries. With over 200,000 analytical methods, Eurofins Scientific helps make life and our environment safer, healthier, and more sustainable. Our network of over 62,000 employees across a network of more than 900 laboratories in 62 countries, strengthens Eurofins Scientific as a leader in scientific testing services. EAG Laboratories, a Eurofins company has over 40 years' experience in materials and engineering testing services. EAG is a global leader in scientific services with a portfolio of analytical methods. We offer a consultative multi-disciplinary approach to solving your materials and engineering related product problems. As thought leaders in investigative science, we set the global standard for materials and engineering testing services. EAG is actively seeking an Analyst (Analytical Chemist) to assist in the formulation of industrial and consumer products. Our laboratory in Maryland Heights, Missouri provides organic chemistry testing specializing in investigative analytical chemistry. Examples of this includes evaluating the label claims of consumer products, reverse engineering pharmaceuticals/nutritional supplements, contaminant identification, determining sources of off odors/flavors/colors, extractables and leachables of consumer electronics, testing medical devices and much, much more. A day in the life: You will be a part of the medical device testing team, which follows ISO 10993-18 to screen medical devices for extractables and leachables in the assembly of a toxicological risk assessment for regulatory approval of the device. A typical week includes preparing GCMS standards and samples, operating and maintaining a variety of GCMS instruments, analyzing data (largely untargeted extractables identification and quantitation) , and presenting the data within report templates. Example of a case study: A medical device is extracted in 3 solvents. These extracts are handed off to the GCMS chemist who then runs standards and the extracts on instrument. The GCMS chemist processes all the standard and extract data both qualitatively and quantitatively, identifying the extractables. Example of equipment you will use: Agilent direct injection and headspace GCMS (single quad, high-efficiency source, and time-of-flight) In this position, you will be responsible for: Applying standard and non-standard techniques, procedures, and criteria to carry out a sequence of related tasks to determine the composition, properties and/or structure of materials. Performing sample preparation. Recording test data providing some basic analysis and interpretations. Maintaining specified records of scientific data. Preparing reports on analytical results for customers. Protecting confidential information and proprietary processes. Handling customer materials and company equipment in a responsible and efficient manner. Qualifications BS degree in Chemistry and 2+ years of GCMS experience . Desirable MS or PhD in Chemistry with GCMS focus. Proficient in Microsoft Office and Excel in particular. Excellent professional, verbal, and written communication skills. Prefer materials characterization experience and experience in untargeted identification work. We encourage you to apply even if your experience is not a 100% match with the position. We are looking for someone with relevant skills and experience, not a checklist that exactly matches the job description. We want to help you grow and in return, you help us grow into a stronger, more inclusive organization. Physical Requirements: Must be able to remain in a stationary position 80% of the time. Ability to continuously operate a personal computer or lab equipment for extended periods of time (4 or more hours). Ability to operate a keyboard and other lab equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead Ability to communicate clearly and understandably ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting. Ability to handle small and fragile devices with tweezers and /or fingers. Require close distance visual acuity with or without correction (Glasses, Contacts, etc.) Must be willing and able to wear PPE such as hard-hat, steel-toed shoes, safety glasses, laboratory coat and/or any other devices or equipment that is required. Learn new tasks, remember processes, maintain focus, complete tasks independently, make timely decisions in the context of a workflow, ability to communicate with visitors, ability to complete tasks in situations that have a speed or productivity quota. Ability to move equipment or items up to 50 lbs. The essential physical and mental requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. We will consider reasonable accommodations for qualified individuals with disabilities. If you have a disability or special need, we would like to know how we can better accommodate you. Additional Information What It's Like to Work Here: Teamwork: experience what being a part of the Eurofins-EAG family feels like. Be inspired by your leaders, be encouraged by your teammates and be supported in all parts of your journey while you work with us. Learning & Development: Develop within the company; be mentored and grown as a leader. Diversity & Authenticity: we work hard to embrace diversity and inclusion and encourage everyone to bring their authentic selves to work every day. Eurofins EAG Laboratories is an equal opportunity employer and prohibits discrimination, harassment, and retaliation in all of our employment practices. Eurofins EAG Laboratories recruits, hires, trains, promotes and administers all employment-related matters based on an individual's qualifications, abilities, and efforts. Applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship status, sexual orientation, gender identity and/or expression, pregnancy, genetic information, disability, military and/or protected veteran status, and/or any other category protected by applicable federal, state, or local law. Eurofins USA Material Sciences is a Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer If you enjoy being immersed in science or engineering, tackling problems head-on, finding solutions through teamwork, and taking pride in accomplishments, join us today! Check out our other opportunities: ************************** Eurofins USA Material Sciences is a Disabled and Veteran Equal Employment Opportunity employer.

We are seeking a skilled Analytical Chemist to support late-stage development and lifecycle management within our Global Technical Operations team. In this dynamic role, you will leverage your expertise in analytical method development, validation, and transfer to both internal and external GMP laboratories. You will play a critical role in the isolation and characterization of trace-level impurities in drug substances and drug products, ensuring the highest standards of data quality and regulatory compliance. This position offers the opportunity to collaborate in a cross-functional environment, working closely with teams in Process Chemistry, Formulation, Quality, Operations, and Regulatory to drive the successful execution of key deliverables. Essential Functions Lead project planning by defining functions, setting timelines, coordinating resources, and ensuring on-time execution. Develop innovative solutions for complex challenges using critical thinking, creativity, and collaboration while considering downstream impacts. Maintain accurate and detailed records in laboratory notebooks and uphold the highest safety standards. Prepare regulatory documentation to support filings and compliance requirements. Provide strategic input to resolve analytical chemistry challenges within Global Technical Operations. Collaborate cross-functionally in a matrix environment to drive project success. Contribute to scientific advancements through new technologies, publications, patents, or trade secrets. Minimum Requirements BA or BS in Analytical Chemistry or related science typically with a minimum of 5 years of pharmaceutical/biotech or related work experience in industry. MS in Analytical Chemistry or related science typically with a minimum of 2 years of pharmaceutical/biotech or related work experience in industry. PhD in Analytical Chemistry or related science Extensive hands-on experience with HPLC/UPLC, LC-MS, GC, GC-MS, TGA, DSC, UV, and IR spectroscopy for drug characterization and quantitation. Expertise in method development, validation, and transfer for small molecules, peptides, and biologics. Strong analytical chemistry problem-solving skills, including trace-level impurity characterization in drug substances and products. Experience with extractable and leachable analysis, biocompatibility testing, and chemical characterization. Knowledge of regulatory standards, including ISO 10993, ISO 18562, EU MDR (GSPR), ICH guidelines, and pharmacopeial requirements. Familiarity with QbD method development tools and regulatory compliance. Self-starter with a strong work ethic, communication, and project management skills. Ability to work independently and collaboratively in a cross-functional team environment. Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Project, Visio) and Adobe. Strong organizational, planning, and interpersonal skills. Preferred Skills Strong familiarity with pharmaceutical GMP and regulatory guidelines Practical experience in bioanalytical chemistry Experience with administration and/or support of Waters Empower Experience with Agilent and Waters analytical instruments and associated software Organizational Relationship/Scope: Position directly reports to the Sr. Manager, Analytical Chemistry. Working Conditions: This position requires frequent work in a research laboratory, both standing at a bench and seated. It also requires reaching into flammable cabinets. This position involves frequent work in an office environment, using a computer to analyze data and write reports and documenting experiments in notebooks. Occasional travel may be required for engagement with external laboratories and collaborators. #LI-LM1

Job Title Analytical Chemist Requisition JR000014859 Analytical Chemist (Open) Additional Locations St. Louis, MO Job Description We are seeking a skilled Analytical Chemist to support late-stage development and lifecycle management within our Global Technical Operations team. In this dynamic role, you will leverage your expertise in analytical method development, validation, and transfer to both internal and external GMP laboratories. You will play a critical role in the isolation and characterization of trace-level impurities in drug substances and drug products, ensuring the highest standards of data quality and regulatory compliance. This position offers the opportunity to collaborate in a cross-functional environment, working closely with teams in Process Chemistry, Formulation, Quality, Operations, and Regulatory to drive the successful execution of key deliverables. Essential Functions * Lead project planning by defining functions, setting timelines, coordinating resources, and ensuring on-time execution. * Develop innovative solutions for complex challenges using critical thinking, creativity, and collaboration while considering downstream impacts. * Maintain accurate and detailed records in laboratory notebooks and uphold the highest safety standards. * Prepare regulatory documentation to support filings and compliance requirements. * Provide strategic input to resolve analytical chemistry challenges within Global Technical Operations. * Collaborate cross-functionally in a matrix environment to drive project success. * Contribute to scientific advancements through new technologies, publications, patents, or trade secrets. Minimum Requirements * BA or BS in Analytical Chemistry or related science typically with a minimum of 5 years of pharmaceutical/biotech or related work experience in industry. * MS in Analytical Chemistry or related science typically with a minimum of 2 years of pharmaceutical/biotech or related work experience in industry. * PhD in Analytical Chemistry or related science * Extensive hands-on experience with HPLC/UPLC, LC-MS, GC, GC-MS, TGA, DSC, UV, and IR spectroscopy for drug characterization and quantitation. * Expertise in method development, validation, and transfer for small molecules, peptides, and biologics. * Strong analytical chemistry problem-solving skills, including trace-level impurity characterization in drug substances and products. * Experience with extractable and leachable analysis, biocompatibility testing, and chemical characterization. * Knowledge of regulatory standards, including ISO 10993, ISO 18562, EU MDR (GSPR), ICH guidelines, and pharmacopeial requirements. * Familiarity with QbD method development tools and regulatory compliance. * Self-starter with a strong work ethic, communication, and project management skills. * Ability to work independently and collaboratively in a cross-functional team environment. * Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Project, Visio) and Adobe. * Strong organizational, planning, and interpersonal skills. Preferred Skills * Strong familiarity with pharmaceutical GMP and regulatory guidelines * Practical experience in bioanalytical chemistry * Experience with administration and/or support of Waters Empower * Experience with Agilent and Waters analytical instruments and associated software Organizational Relationship/Scope: Position directly reports to the Sr. Manager, Analytical Chemistry. Working Conditions: This position requires frequent work in a research laboratory, both standing at a bench and seated. It also requires reaching into flammable cabinets. This position involves frequent work in an office environment, using a computer to analyze data and write reports and documenting experiments in notebooks. Occasional travel may be required for engagement with external laboratories and collaborators. #LI-LM1

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: As the Associate Production Scientist with MilliporeSigma, your role is to support our large-scale Enzymes and Proteins product lines. You will work with other production scientists and operators, and SMEs to ensure successful manufacturing of an established line of products and troubleshoot and investigate process issues that arise. You will write and modify procedures consistent with quality guidelines and identify potential process improvements while interacting cross-functionally with Quality Control, Quality Assurance, Packaging, Materials Management, Engineering and Maintenance. * Day Shift- Monday-Friday 8am-4pm * Safely perform operations to meet quality expectations * Perform multi-disciplined, established processes, assays and/or unit operations, primarily those requiring a higher level of skill and knowledge * Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). * Clean-up equipment and working areas during and after operations * Communicate the status of operations and bring deviations to the attention of supervisor * Ensure all applicable logbooks have been filled out completely as required by current procedures * Participate as needed in quality audits * Accurately perform in-process testing and assays * Identify problems and limitations of analysis * Perform routine troubleshooting * In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles * Participate in process improvements under the guidance of a Supervisor or Scientist * Take the necessary action to resolve any unsafe conditions * Perform and interpret analytical evaluations of products and intermediates Physical Attributes: * Wearing of personal protective equipment such as respirator or chemical protective clothing for extended periods * Lifting and pushing up to 50 pounds Who You Are Minimum Qualifications: * Bachelor's Degree in Chemistry, Biochemistry, Biology, Chemical Engineering, or other life science discipline Preferred Qualifications: * Knowledge in chemistry or biochemistry, math, and general science * Preferably protein extraction and purification * Familiar with laboratory instruments and production equipment * Analytical techniques and equipment * Safe chemical handling methods experience * Good communication skills, verbal and written * Mechanical skills * Troubleshooting skills * Interpersonal skills * Organizational skills RSREMD What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it 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 our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.pe over the past 20 years. Job Description In this role, you will join a team of scientists and engineers focused on developing and optimizing processes for production of polysaccharide conjugate vaccines. Your work will be involved in cutting edge technology development projects to discover the next generation of processes to deliver breakthrough therapeutics. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. Apply technical skills to complete assigned laboratory work within own work group/project team. Support laboratory activities by monitoring lab equipment and maintaining a clean and safe working environment. Effectively document all lab activities in notebooks/elsewhere as required and appropriate, in a timely fashion. Help in authoring technical reports as needed Evaluate data and provide clear reports that can be shared and transferred to and from cross-functional teams with clear communication in both written and oral forms. Provide support and troubleshoot during manufacturing campaign as needed with laboratory experiments. Work collaboratively with colleagues both within the group and cross-functionally; contribute to maintaining and improving upon our safe, effective and efficient lab operations. This role as a contract duration of 18 months. Contract can be extended upon performance. Qualifications Minimum bachelor's degree (BA/BS) in the area of Chemical/Biomedical Engineering, Biology, Biochemistry, Biotechnology, Microbiology, or related fields with 0 to 3 years of experience in a biochemical or chemical laboratory environment. Experience or familiarity with conjugation to large molecules such as polysaccharides or antibody is desirable Running reactions in small and large scale reactors. Purification of large molecules (antibodies, polysaccharides, mRNA) using ultrafiltration-diafiltration and/or column chromatography of biologic products. Familiarity with cGLP/cGMP requirements. Team oriented, with excellent oral and written communication skills Well organized and great attention to detail. Proficiency with personal computers, including word processing, spreadsheets, Spotfire PowerPoint and relevant scientific software. Additional Information What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays This role as a contract duration of 18 months. Contract can be extended upon performance. PHYSICAL/MENTAL REQUIREMENTS: work will be performed in a typical development laboratory environment. WORK LOCATION ASSIGNMENT: Chesterfield, MO Eurofins Lancaster Laboratories Professional Scientific Services (PSS) is a global, award-winning insourcing solution that places our people at our clients' site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries. We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client's quality systems and equipment. Eurofins USA PSS Insourcing Solutions is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

As the Senior Research Chemist, you will be a key member of the R&D department where innovation and creativity are congruent with sound scientific practices to contribute to the profitability of ICL Phosphate Specialties. This position will support phosphate-based battery material research and development, product stewardship, support sales and marketing teams, providing fast and accurate customer support, compliance with quality, environmental, and adherence to all safety protocols at the site Location: This position will is based at our St. Louis Research and Development Facility located in Webster Groves. I'm interested! What will I get to do in this position? * Provide Research and Development work on phosphate based-battery cathode active materials (CAM) * Provide processes and materials for scale up of battery materials * Develop and establish project objectives, timelines, and key milestones * Familiarize and learn project management tools (Charters, Stage Gate, Gantt Charts) * Complete Applications R&D, Marketing or Operational Excellence Projects * Generate clear and concise reports following the conclusion of a project. Reports may be generated for internal use and for customers * Provide technical support for customer visits, site tours, and audits * Respond to customer requests and questions in a timely manner * Maintain departmental communication by providing progress updates on technical department projects. Progress updates may be reviewed as needed or at scheduled technical meetings * Development and evaluation of battery materials and materials processing * Battery performance testing and electrochemical characterization * Synthesis of battery materials; including supporting scale to production volumes * Research, develop and understand material properties versus battery performance properties and low-cost, environmentally efficient manufacturing What skills and experience do I need to be successful in this role? * M.S. in Chemistry, preferably with focus in Materials Science, Electrochemistry, or High Temperature Processes * 1-3+ years of R&D experience with industrial products * Preference for experience working with Li-ion batteries and related materials * Experience with battery testing and analytical techniques (SEM-EDS, FT-IR, UV-V spectroscopy, Battery cycling, Surface area and X-ray crystallography) * Experience with high temperature synthesis, such as for metal oxides and carbonization/graphitization * Ability to juggle multiple competing priorities * Ability to interpret literature data and reproduce results * Ability to identify and conduct appropriate application testing of formulated products including interpretation and organization of results * Excellent oral and written communication skills * Strong interpersonal and communication skills including effectively interacting with all levels of the organization as well as customers and distributors * Excellent team player * Self-starter: self-driven and creative * Maintains professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks * Ability to travel to customers and ICL plants as required What will set you apart: * Synthesis of lithium iron phosphate cathode active materials * Demonstrated success in developing and commercializing new products Compensation at ICL: If you are hired at ICL, your final base salary compensation will be determined based on factors such as geographic location, skills, education, and/or experience. We also offer a generous benefits package (more information on benefits listed below). Salary Range: $80,000 - $111,000 Annual Bonus Target: 5%, subject to plan provisions. We've Got You Covered ICL is committed to offering you a comprehensive set of benefits to empower you and your family physically, mentally, emotionally, and financially. The benefits we offer to our diverse and inclusive workforce include: * Competitive base pay and performance bonus * Medical, dental, vision, and life benefits that start quickly - the first of the month after hire * Tax-advantaged health savings and spending accounts (when applicable) * Wellness Incentive Program to lower your health insurance cost * Generous Leave and FMLA policies * Prescription program that provides most generic maintenance medications at no cost (including Insulin products & EpiPens) * 401k eligibility from day one of employment with a generous company matching contribution. 100% vested after one year of service * Employee Assistance Program * Student Loan Assistance * Free membership to a program that offers various discounts for travel, entertainment, groceries, and much more About ICL's Lithium Iron Phosphate (LFP) Business: ICL Group, a leading global specialty minerals company, is excited to announce its expansion into the North American battery materials market with the creation of a state-of-the-art battery factory in North St. Louis City. As part of a half-billion-dollar investment, ICL is building a large-scale commercial production plant that will manufacture lithium iron phosphate (LFP) cathode active material (CAM) for the energy storage and electric vehicle markets. If you're ready to drive the future of sustainable energy and work with the latest in cutting-edge technology, this is your opportunity to join an innovative team shaping tomorrow's world. Who is ICL? ICL Group is a leading global specialty minerals company, which creates impactful solutions for humanity's sustainability challenges in the food, agriculture and industrial markets. ICL leverages its unique bromine, potash and phosphate resources, its global professional workforce, and its sustainability focused R&D and technological innovation capabilities, to drive the company's growth across its end markets. Our agricultural products feed the world's growing population, our food additives enable greater access to higher quality food, our potash and phosphate products are essential components for the pharma industry and our bromine-based materials and phosphates contribute to a more energy efficient and environmentally friendly planet. ICL benefits from its advantageous size, geographical spread, and operational flexibility. With a culture based upon leadership, innovation, and sustainability, ICL is well positioned to be an Employer of Choice within the communities in which we operate. ICL shares are dual listed on the New York Stock Exchange and the Tel Aviv Stock Exchange (NYSE and TASE: ICL). The company employs more than 12,500 people worldwide, and its 2023 revenues totaled approximately $7.5 billion. To learn more about ICL, visit the company's global website ****************** EEO-USA Equal Opportunity/Affirmative Action Employer Minorities/Women/Veterans/Disabilities

Job Details Laboratory - St Louis, MO 4 Year Degree $22.00 - $22.00 Hourly None DayNight Shift Analytical Chemist Our mission at Averhealth is to reclaim lives, unite families, and strengthen communities by creating and providing the smartest, most innovative solutions for substance use disorder monitoring and recovery. This is an excellent Entry-Level opportunity for recent grads in Chemistry, Biology, or Biochemistry! We are in need of a determined Analytical Chemists to join our St. Louis Laboratory Team. In this role, you will prepare specimens for routine drug testing following the laboratory's Standard Operating Procedures. The Analytical Chemist will also interface with our instruments (LC/MS/MS and GC/MS) and needs the ability to work safely with instruments/equipment, chemicals, and biological samples. PAY: $22/HR + Company-Paid Training Program + Attendance Bonus Eligibility + Uniform Allowance (post-training) + Referral Bonus Eligibility + Competitive Full-Time Benefits HOURS: Full-Time (40+ hours/week) SHIFTS AVAILABLE Monday - Friday (Nightshift) 9:00pm - 5:30 am ESSENTIAL DUTIES AND RESPONSIBILITIES Locate specific patient samples and perform confirmation assays according to the toxicology testing method requested. Communicate and interact with other departments to solve issues impeding confirmation tests on patient samples Interface with analytical instruments including LC-MS, GC-MS, and Tecan Liquid Handler. Review data generated by LC-MS and GC-MS instrumentation before sending it to data certifiers. Assist with training new staff on sample preparation, LC-MS/GC-MS operation, and data review. Lab maintenance: including, but not limited to, cleaning glassware, restocking/refilling pipette tips, glass vials, centrifuge tubes, etc. Reagent preparation Adhere to all security procedures for ensuring the confidentiality of donor information Adhere to all established guidelines outlined in Averhealth Employee Guidebook Other duties as assigned by the supervisor REQUIREMENTS Bachelor's Degree in Science or equivalent relevant field REQUIRED 1-3+ years experience operating and reviewing data for an LC-MS/MS instrument. ABSciex experience preferred. 1-3+ years experience in a biological laboratory environment. Experience with BOTH LC/MS/MS and/or GC/MS is an added advantage. COMPENSATION AND BENEFITS Pay Dependent on past qualifications and experience We offer Full-Time employees (working over 30 hours per week): Medical, Dental, Vision, Short Term Disability, Long Term Disability and Life Insurance with an employer contribution 3 weeks of Paid Time Off in your first year We offer ALL employees: Company-Paid Training Program Attendance Bonuses Annual Uniform Reimbursement (scrubs) 401k with an employer match Annual Raises Referral Bonuses Instant access to earned wages-no need to wait for your paycheck! Averhealth is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Averhealth is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Averhealth are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Averhealth will not tolerate discrimination or harassment based on any of these characteristics. Physical and Sensory Requirements: Mobility, walking, climbing, sitting, standing, reaching, bending, lifting (minimum of 10 lbs), carrying, pushing, pulling, fine eye-hand coordination, ability to read, write, listen and speak clearly, the ability to understand and follow written and oral instructions and directions, ability to drive a vehicle and travel, and ability to remain calm under pressure. Must be able to sit and/or stand for extended periods of time. Must be able to use computer, monitor, cell phone, mouse and keyboard extensively as well as other general office equipment.

Job Details Education Level: 4 Year Degree Salary Range: $22.00 - $22.00 Hourly Travel Percentage: None Job Shift: Day Night Shift Analytical Chemist Our mission at Averhealth is to reclaim lives, unite families, and strengthen communities by creating and providing the smartest, most innovative solutions for substance use disorder monitoring and recovery. This is an excellent Entry-Level opportunity for recent grads in Chemistry, Biology, or Biochemistry! We are in need of a determined Analytical Chemists to join our St. Louis Laboratory Team. In this role, you will prepare specimens for routine drug testing following the laboratory's Standard Operating Procedures. The Analytical Chemist will also interface with our instruments (LC/MS/MS and GC/MS) and needs the ability to work safely with instruments/equipment, chemicals, and biological samples. * PAY: $22/HR + Company-Paid Training Program + Attendance Bonus Eligibility + Uniform Allowance (post-training) + Referral Bonus Eligibility + Competitive Full-Time Benefits * HOURS: Full-Time (40+ hours/week) SHIFTS AVAILABLE Monday - Friday (Nightshift) 9:00pm - 5:30 am ESSENTIAL DUTIES AND RESPONSIBILITIES * Locate specific patient samples and perform confirmation assays according to the toxicology testing method requested. * Communicate and interact with other departments to solve issues impeding confirmation tests on patient samples * Interface with analytical instruments including LC-MS, GC-MS, and Tecan Liquid Handler. * Review data generated by LC-MS and GC-MS instrumentation before sending it to data certifiers. * Assist with training new staff on sample preparation, LC-MS/GC-MS operation, and data review. * Lab maintenance: including, but not limited to, cleaning glassware, restocking/refilling pipette tips, glass vials, centrifuge tubes, etc. * Reagent preparation * Adhere to all security procedures for ensuring the confidentiality of donor information * Adhere to all established guidelines outlined in Averhealth Employee Guidebook * Other duties as assigned by the supervisor REQUIREMENTS * Bachelor's Degree in Science or equivalent relevant field REQUIRED * 1-3+ years experience operating and reviewing data for an LC-MS/MS instrument. ABSciex experience preferred. * 1-3+ years experience in a biological laboratory environment. * Experience with BOTH LC/MS/MS and/or GC/MS is an added advantage. COMPENSATION AND BENEFITS * Pay Dependent on past qualifications and experience * We offer Full-Time employees (working over 30 hours per week): * Medical, Dental, Vision, Short Term Disability, Long Term Disability and Life Insurance with an employer contribution * 3 weeks of Paid Time Off in your first year * We offer ALL employees: * Company-Paid Training Program * Attendance Bonuses * Annual Uniform Reimbursement (scrubs) * 401k with an employer match * Annual Raises * Referral Bonuses * Instant access to earned wages-no need to wait for your paycheck! Averhealth is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Averhealth is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Averhealth are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Averhealth will not tolerate discrimination or harassment based on any of these characteristics. Physical and Sensory Requirements: Mobility, walking, climbing, sitting, standing, reaching, bending, lifting (minimum of 10 lbs), carrying, pushing, pulling, fine eye-hand coordination, ability to read, write, listen and speak clearly, the ability to understand and follow written and oral instructions and directions, ability to drive a vehicle and travel, and ability to remain calm under pressure. Must be able to sit and/or stand for extended periods of time. Must be able to use computer, monitor, cell phone, mouse and keyboard extensively as well as other general office equipment. Our mission at Averhealth is to reclaim lives, unite families, and strengthen communities by creating and providing the smartest, most innovative solutions for substance use disorder monitoring and recovery. This is an excellent Entry-Level opportunity for recent grads in Chemistry, Biology, or Biochemistry! We are in need of a determined Analytical Chemists to join our St. Louis Laboratory Team. In this role, you will prepare specimens for routine drug testing following the laboratory's Standard Operating Procedures. The Analytical Chemist will also interface with our instruments (LC/MS/MS and GC/MS) and needs the ability to work safely with instruments/equipment, chemicals, and biological samples. * PAY: $22/HR + Company-Paid Training Program + Attendance Bonus Eligibility + Uniform Allowance (post-training) + Referral Bonus Eligibility + Competitive Full-Time Benefits * HOURS: Full-Time (40+ hours/week) SHIFTS AVAILABLE Monday - Friday (Nightshift) 9:00pm - 5:30 am ESSENTIAL DUTIES AND RESPONSIBILITIES * Locate specific patient samples and perform confirmation assays according to the toxicology testing method requested. * Communicate and interact with other departments to solve issues impeding confirmation tests on patient samples * Interface with analytical instruments including LC-MS, GC-MS, and Tecan Liquid Handler. * Review data generated by LC-MS and GC-MS instrumentation before sending it to data certifiers. * Assist with training new staff on sample preparation, LC-MS/GC-MS operation, and data review. * Lab maintenance: including, but not limited to, cleaning glassware, restocking/refilling pipette tips, glass vials, centrifuge tubes, etc. * Reagent preparation * Adhere to all security procedures for ensuring the confidentiality of donor information * Adhere to all established guidelines outlined in Averhealth Employee Guidebook * Other duties as assigned by the supervisor REQUIREMENTS * Bachelor's Degree in Science or equivalent relevant field REQUIRED * 1-3+ years experience operating and reviewing data for an LC-MS/MS instrument. ABSciex experience preferred. * 1-3+ years experience in a biological laboratory environment. * Experience with BOTH LC/MS/MS and/or GC/MS is an added advantage. COMPENSATION AND BENEFITS * Pay Dependent on past qualifications and experience * We offer Full-Time employees (working over 30 hours per week): * Medical, Dental, Vision, Short Term Disability, Long Term Disability and Life Insurance with an employer contribution * 3 weeks of Paid Time Off in your first year * We offer ALL employees: * Company-Paid Training Program * Attendance Bonuses * Annual Uniform Reimbursement (scrubs) * 401k with an employer match * Annual Raises * Referral Bonuses * Instant access to earned wages-no need to wait for your paycheck! Averhealth is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Averhealth is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Averhealth are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Averhealth will not tolerate discrimination or harassment based on any of these characteristics. Physical and Sensory Requirements: Mobility, walking, climbing, sitting, standing, reaching, bending, lifting (minimum of 10 lbs), carrying, pushing, pulling, fine eye-hand coordination, ability to read, write, listen and speak clearly, the ability to understand and follow written and oral instructions and directions, ability to drive a vehicle and travel, and ability to remain calm under pressure. Must be able to sit and/or stand for extended periods of time. Must be able to use computer, monitor, cell phone, mouse and keyboard extensively as well as other general office equipment.

At Superior, we act like we own the company because we do. We are 100% employee-owned organization that thrives on a culture of cooperation, commitment, and stewardship. We invest in our people and processes so that we can best serve our customers and grow responsibly. We shy away from "this is the way we've always done it," and gravitate towards "this make a lot of sense." We are looking for people that want to feel invested in making a difference that ultimately affects the company's bottom line, and yours as well. Oh, and by the way, we distribute solvents, chemicals, and composites. We also take customer's hazardous waste, and we repurpose it. And we're really good at all of the above because we've been doing it successfully since 1932. Superior is currently seeking an experienced Quality Control Chemist for our Arnold, MO location. This is a Monday through Friday position with working hours 8am-5pm. The position will perform quality control testing on incoming and outgoing products using the following instrumentation: Gas Chromatograph, Karl Fischer, viscometer, etc. Successful candidate will: Possess strong problem-solving skills and initiative Work well under pressure and handle multiple tasks effectively and efficiently Display exceptional organizational skills and ability to prioritize work assignments Demonstrate ability to work in teams with members from various disciplines Display significant attention to detail Requirements: 4-year degree required (chemistry/biology/science) Prior quality control experience (preferred) Familiar with analytical equipment - specifically, GC, KF, viscometer Excellent computer and communication skills Superior offers a competitive compensation package which includes Medical Insurance (an HDHP option - 100% premium paid, and a highly subsidized PPO option with very affordable premiums), Employee Stock Ownership Plan (ESOP), 401K, Flexible Spending, PTO, Paid Holidays, Life, Dental, Vision, STD and LTD. We hire based on character as well as experience! EOE including disability/veteran/drug free

Eurofins Scientific is a global leader in providing a unique range of analytical testing services to multiple industries. With over 200,000 analytical methods, Eurofins Scientific helps make life and our environment safer, healthier, and more sustainable. Our network of over 62,000 employees across a network of more than 950 laboratories in 60 countries, strengthens Eurofins Scientific as a leader in scientific testing services. EAG Laboratories, a Eurofins company has over 40 years' experience in materials and engineering testing services. EAG is a global leader in scientific services with a portfolio of analytical methods. We offer a consultative multi-disciplinary approach to solving your materials and engineering related product problems. As thought leaders in investigative science, we set the global standard for materials and engineering testing services. EAG is actively seeking an Analyst to assist in chemical testing of industrial and consumer products. Our laboratory in Maryland Heights, Missouri provides organic chemistry testing specializing in investigative analytical chemistry. Examples of this includes evaluating the label claims of consumer products, reverse engineering pharmaceuticals/nutritional supplements, contaminant identification, determining sources of off odors/flavors/colors, extractables and leachables of consumer electronics, testing medical devices and much, much more. Example of a case study: Clients approach us to develop and validate methods for analysis of various kinds of products. Every day and every project are different. We participate in each stage of the process and help guide our clients to appropriate testing for their desired purpose. Clients have asked us to develop and validate methods for assay of drug content, drug uniformity, product impurities, observed particulate characterization, residual solvent content, molecular weight confirmation, In-vitro cytotoxicity / irritation / sensitization, etc. Example of equipment you will use: LC GC GPC NMR Dissolution ICP Data processing software Example of materials we use: Polymers, solvents, any kind of sample imaginable! In this position, you will be responsible for: Applying standard and non-standard techniques, procedures, and criteria to carry out a sequence of related tasks to determine the composition, properties and/or structure of materials. Performing sample preparation. Recording test data providing some basic analysis and interpretations. Maintaining specified records of scientific data. Preparing reports on analytical results for customers. Protecting confidential information and proprietary processes. Handling customer materials and company equipment in a responsible and efficient manner. Employees are expected to comply with ISO 27001 standard and company requirements for Information security. Qualifications BS/MS degree in Chemistry and 1-3+ years of Industry experience. LC/GC & laboratory experience/familiarity with several techniques. Proficient in Microsoft Office and Excel in particular. Excellent professional, verbal, and written communication skills. Excellent attention to detail & critical observer of results and processes. An understanding of method development and validation processes in a regulated space. Desire to learn and understand new processes/instruments/techniques. Prefer materials characterization experience and experience in untargeted identification work. Preferred experience working with USP products. We encourage you to apply even if your experience is not a 100% match with the position. We are looking for someone with relevant skills and experience, not a checklist that exactly matches the job description. We want to help you grow and in return, you help us grow into a stronger, more inclusive organization. Physical Requirements: Must be able to remain in a stationary position 80% of the time. Ability to continuously operate a personal computer or lab equipment for extended periods of time (4 or more hours). Ability to operate a keyboard and other lab equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead Ability to communicate clearly and understandably ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting. Ability to handle small and fragile devices with tweezers and /or fingers. Require close distance visual acuity with or without correction (Glasses, Contacts, etc.) Must be willing and able to wear PPE such as hard-hat, steel-toed shoes, safety glasses, laboratory coat and/or any other devices or equipment that is required. Learn new tasks, remember processes, maintain focus, complete tasks independently, make timely decisions in the context of a workflow, ability to communicate with visitors, ability to complete tasks in situations that have a speed or productivity quota. Ability to move equipment or items up to 50 lbs. The essential physical and mental requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. We will consider reasonable accommodations for qualified individuals with disabilities. If you have a disability or special need, we would like to know how we can better accommodate you. Additional Information Schedule: Mon-Fri 8am-5pm What It's Like to Work Here: • Teamwork: be inspired by your leaders, be encouraged by your teammates, and be supported in all parts of your journey while you work with us. • Learning & Development: take on career development programs and goal setting to create big possibilities for your career and life. Develop within the company; be mentored and grow as a leader. • Diversity & Authenticity: we work hard to embrace diversity and inclusion and encourage everyone to bring their authentic selves to work every day. Benefits & Perks to Foster Work/Life Balance: ✓ Medical, Dental and Vision Coverage ✓ 401k Company Matching ✓ Paid Time Off ✓ Wellness Program ✓ Education Assistance ✓ …and more! Eurofins EAG Laboratories is an equal opportunity employer and prohibits discrimination, harassment, and retaliation in all of our employment practices. Eurofins EAG Laboratories recruits, hires, trains, promotes and administers all employment-related matters based on an individual's qualifications, abilities, and efforts. Applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship status, sexual orientation, gender identity and/or expression, pregnancy, genetic information, disability, military and/or protected veteran status, and/or any other category protected by applicable federal, state, or local law. Eurofins USA Material Sciences is a Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer If you enjoy being immersed in science or engineering, tackling problems head-on, finding solutions through teamwork, and taking pride in accomplishments, join us today! Check out our other opportunities: ************************** Eurofins USA Material Sciences is a Disabled and Veteran Equal Employment Opportunity employer.

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, as a Associate Scientist- Production, at our 3300 South Second Ave/ Cherokee site, you will manufacture products according to established protocols, provide technical support to others and perform operations in support of the group and department. * Rotating schedule Monday- Friday (1st, 2nd and 3rd shift (including evenings and nights). This role will eventually be rolled into a 24/7 schedule * Evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. * Safely perform operations to meet quality expectations. * Maintain required training to perform tasks/assignments. * Perform routine processes and unit operations. * Clean equipment and working areas during and after operations. * Support functions of the facility (e.g., maintain equipment, prepare reagents, and restock supplies, waste disposal). * Communicate the status of operations and convey concerns to the supervisor. * Provide complete and accurate records consistent with quality guidelines. * Ensure all applicable logbooks are completed as required by current procedures. * Interact with other departments as needed and performs procedures independently and part of a team. * Participate as needed in quality audits and customer interactions. * Improve processes through application of scientific knowledge, experience, and principles, in compliance with change control. * Take action to resolve unsafe conditions. * Train team members and act as technical consultant. Physical Attributes: * Ability to lift to 50lbs. * Personal protective equipment such as respirator or chemical protective clothing for extended periods. Who you are: Minimum Qualifications: * Bachelor's Degree in a scientific discipline (e.g., Chemistry, Biochemistry, Biology, etc.) OR * Associate Degree and 2+ years industry Production/Laboratory experience Preferred Qualifications: * Familiar with laboratory instruments and production equipment * Process techniques and 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. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it 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 our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************

Job Details Laboratory - St Louis, MO 4 Year Degree $21.00 - $21.00 Hourly None DayPart-time Analytical Chemist (weekends) Our mission at Averhealth is to reclaim lives, unite families, and strengthen communities by creating and providing the smartest, most innovative solutions for substance use disorder monitoring and recovery. This is an excellent Entry-Level opportunity for recent grads in Chemistry, Biology, or Biochemistry! We are in need of a determined Analytical Chemists to join our St. Louis Laboratory Team. In this role, you will prepare specimens for routine drug testing following the laboratory's Standard Operating Procedures. The Analytical Chemist will also interface with our instruments (LC/MS/MS and GC/MS) and needs the ability to work safely with instruments/equipment, chemicals, and biological samples. PAY: $21/HR + Company-Paid Training Program + Uniform Allowance (post-training) + Referral Bonus Eligibility HOURS: Part-Time (less than 20 hours/week) SHIFTS AVAILABLE Saturday & Sunday (Midshift) 12:00 pm - 8:30pm ESSENTIAL DUTIES AND RESPONSIBILITIES Locate specific patient samples and perform confirmation assays according to the toxicology testing method requested. Communicate and interact with other departments to solve issues impeding confirmation tests on patient samples Interface with analytical instruments including LC-MS, GC-MS, and Tecan Liquid Handler. Review data generated by LC-MS and GC-MS instrumentation before sending it to data certifiers. Assist with training new staff on sample preparation, LC-MS/GC-MS operation, and data review. Lab maintenance: including, but not limited to, cleaning glassware, restocking/refilling pipette tips, glass vials, centrifuge tubes, etc. Reagent preparation Adhere to all security procedures for ensuring the confidentiality of donor information Adhere to all established guidelines outlined in Averhealth Employee Guidebook Other duties as assigned by the supervisor REQUIREMENTS Bachelor's Degree in Science or equivalent relevant field REQUIRED 1-3+ years experience operating and reviewing data for an LC-MS/MS instrument. ABSciex experience preferred. 1-3+ years experience in a biological laboratory environment. Experience with BOTH LC/MS/MS and/or GC/MS is an added advantage. COMPENSATION AND BENEFITS Pay Dependent on past qualifications and experience We offer ALL employees: Company-Paid Training Program Annual Uniform Reimbursement (scrubs) 401k with an employer match Annual Raises Referral Bonuses Instant access to earned wages-no need to wait for your paycheck! Averhealth is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Averhealth is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Averhealth are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Averhealth will not tolerate discrimination or harassment based on any of these characteristics. Physical and Sensory Requirements: Mobility, walking, climbing, sitting, standing, reaching, bending, lifting (minimum of 10 lbs), carrying, pushing, pulling, fine eye-hand coordination, ability to read, write, listen and speak clearly, the ability to understand and follow written and oral instructions and directions, ability to drive a vehicle and travel, and ability to remain calm under pressure. Must be able to sit and/or stand for extended periods of time. Must be able to use computer, monitor, cell phone, mouse and keyboard extensively as well as other general office equipment.

Job Title Analytical Chemist Requisition JR000014859 Analytical Chemist (Open) Additional Locations St. Louis, MO Job Description We are seeking a skilled Analytical Chemist to support late-stage development and lifecycle management within our Global Technical Operations team. In this dynamic role, you will leverage your expertise in analytical method development, validation, and transfer to both internal and external GMP laboratories. You will play a critical role in the isolation and characterization of trace-level impurities in drug substances and drug products, ensuring the highest standards of data quality and regulatory compliance. This position offers the opportunity to collaborate in a cross-functional environment, working closely with teams in Process Chemistry, Formulation, Quality, Operations, and Regulatory to drive the successful execution of key deliverables. Essential Functions * Lead project planning by defining functions, setting timelines, coordinating resources, and ensuring on-time execution. * Develop innovative solutions for complex challenges using critical thinking, creativity, and collaboration while considering downstream impacts. * Maintain accurate and detailed records in laboratory notebooks and uphold the highest safety standards. * Prepare regulatory documentation to support filings and compliance requirements. * Provide strategic input to resolve analytical chemistry challenges within Global Technical Operations. * Collaborate cross-functionally in a matrix environment to drive project success. * Contribute to scientific advancements through new technologies, publications, patents, or trade secrets. Minimum Requirements * BA or BS in Analytical Chemistry or related science typically with a minimum of 5 years of pharmaceutical/biotech or related work experience in industry. * MS in Analytical Chemistry or related science typically with a minimum of 2 years of pharmaceutical/biotech or related work experience in industry. * PhD in Analytical Chemistry or related science * Extensive hands-on experience with HPLC/UPLC, LC-MS, GC, GC-MS, TGA, DSC, UV, and IR spectroscopy for drug characterization and quantitation. * Expertise in method development, validation, and transfer for small molecules, peptides, and biologics. * Strong analytical chemistry problem-solving skills, including trace-level impurity characterization in drug substances and products. * Experience with extractable and leachable analysis, biocompatibility testing, and chemical characterization. * Knowledge of regulatory standards, including ISO 10993, ISO 18562, EU MDR (GSPR), ICH guidelines, and pharmacopeial requirements. * Familiarity with QbD method development tools and regulatory compliance. * Self-starter with a strong work ethic, communication, and project management skills. * Ability to work independently and collaboratively in a cross-functional team environment. * Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Project, Visio) and Adobe. * Strong organizational, planning, and interpersonal skills. Preferred Skills * Strong familiarity with pharmaceutical GMP and regulatory guidelines * Practical experience in bioanalytical chemistry * Experience with administration and/or support of Waters Empower * Experience with Agilent and Waters analytical instruments and associated software Organizational Relationship/Scope: Position directly reports to the Sr. Manager, Analytical Chemistry. Working Conditions: This position requires frequent work in a research laboratory, both standing at a bench and seated. It also requires reaching into flammable cabinets. This position involves frequent work in an office environment, using a computer to analyze data and write reports and documenting experiments in notebooks. Occasional travel may be required for engagement with external laboratories and collaborators. #LI-LM1

Job Details Education Level: 4 Year Degree Salary Range: $21.00 - $21.00 Hourly Travel Percentage: None Job Shift: Day Part-time Analytical Chemist (weekends) Our mission at Averhealth is to reclaim lives, unite families, and strengthen communities by creating and providing the smartest, most innovative solutions for substance use disorder monitoring and recovery. This is an excellent Entry-Level opportunity for recent grads in Chemistry, Biology, or Biochemistry! We are in need of a determined Analytical Chemists to join our St. Louis Laboratory Team. In this role, you will prepare specimens for routine drug testing following the laboratory's Standard Operating Procedures. The Analytical Chemist will also interface with our instruments (LC/MS/MS and GC/MS) and needs the ability to work safely with instruments/equipment, chemicals, and biological samples. * PAY: $21/HR + Company-Paid Training Program + Uniform Allowance (post-training) + Referral Bonus Eligibility * HOURS: Part-Time (less than 20 hours/week) SHIFTS AVAILABLE Saturday & Sunday (Midshift) 12:00 pm - 8:30pm ESSENTIAL DUTIES AND RESPONSIBILITIES * Locate specific patient samples and perform confirmation assays according to the toxicology testing method requested. * Communicate and interact with other departments to solve issues impeding confirmation tests on patient samples * Interface with analytical instruments including LC-MS, GC-MS, and Tecan Liquid Handler. * Review data generated by LC-MS and GC-MS instrumentation before sending it to data certifiers. * Assist with training new staff on sample preparation, LC-MS/GC-MS operation, and data review. * Lab maintenance: including, but not limited to, cleaning glassware, restocking/refilling pipette tips, glass vials, centrifuge tubes, etc. * Reagent preparation * Adhere to all security procedures for ensuring the confidentiality of donor information * Adhere to all established guidelines outlined in Averhealth Employee Guidebook * Other duties as assigned by the supervisor REQUIREMENTS * Bachelor's Degree in Science or equivalent relevant field REQUIRED * 1-3+ years experience operating and reviewing data for an LC-MS/MS instrument. ABSciex experience preferred. * 1-3+ years experience in a biological laboratory environment. * Experience with BOTH LC/MS/MS and/or GC/MS is an added advantage. COMPENSATION AND BENEFITS * Pay Dependent on past qualifications and experience * We offer ALL employees: * Company-Paid Training Program * Annual Uniform Reimbursement (scrubs) * 401k with an employer match * Annual Raises * Referral Bonuses * Instant access to earned wages-no need to wait for your paycheck! Averhealth is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Averhealth is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Averhealth are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Averhealth will not tolerate discrimination or harassment based on any of these characteristics. Physical and Sensory Requirements: Mobility, walking, climbing, sitting, standing, reaching, bending, lifting (minimum of 10 lbs), carrying, pushing, pulling, fine eye-hand coordination, ability to read, write, listen and speak clearly, the ability to understand and follow written and oral instructions and directions, ability to drive a vehicle and travel, and ability to remain calm under pressure. Must be able to sit and/or stand for extended periods of time. Must be able to use computer, monitor, cell phone, mouse and keyboard extensively as well as other general office equipment. Our mission at Averhealth is to reclaim lives, unite families, and strengthen communities by creating and providing the smartest, most innovative solutions for substance use disorder monitoring and recovery. This is an excellent Entry-Level opportunity for recent grads in Chemistry, Biology, or Biochemistry! We are in need of a determined Analytical Chemists to join our St. Louis Laboratory Team. In this role, you will prepare specimens for routine drug testing following the laboratory's Standard Operating Procedures. The Analytical Chemist will also interface with our instruments (LC/MS/MS and GC/MS) and needs the ability to work safely with instruments/equipment, chemicals, and biological samples. * PAY: $21/HR + Company-Paid Training Program + Uniform Allowance (post-training) + Referral Bonus Eligibility * HOURS: Part-Time (less than 20 hours/week) SHIFTS AVAILABLE Saturday & Sunday (Midshift) 12:00 pm - 8:30pm ESSENTIAL DUTIES AND RESPONSIBILITIES * Locate specific patient samples and perform confirmation assays according to the toxicology testing method requested. * Communicate and interact with other departments to solve issues impeding confirmation tests on patient samples * Interface with analytical instruments including LC-MS, GC-MS, and Tecan Liquid Handler. * Review data generated by LC-MS and GC-MS instrumentation before sending it to data certifiers. * Assist with training new staff on sample preparation, LC-MS/GC-MS operation, and data review. * Lab maintenance: including, but not limited to, cleaning glassware, restocking/refilling pipette tips, glass vials, centrifuge tubes, etc. * Reagent preparation * Adhere to all security procedures for ensuring the confidentiality of donor information * Adhere to all established guidelines outlined in Averhealth Employee Guidebook * Other duties as assigned by the supervisor REQUIREMENTS * Bachelor's Degree in Science or equivalent relevant field REQUIRED * 1-3+ years experience operating and reviewing data for an LC-MS/MS instrument. ABSciex experience preferred. * 1-3+ years experience in a biological laboratory environment. * Experience with BOTH LC/MS/MS and/or GC/MS is an added advantage. COMPENSATION AND BENEFITS * Pay Dependent on past qualifications and experience * We offer ALL employees: * Company-Paid Training Program * Annual Uniform Reimbursement (scrubs) * 401k with an employer match * Annual Raises * Referral Bonuses * Instant access to earned wages-no need to wait for your paycheck! Averhealth is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Averhealth is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Averhealth are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Averhealth will not tolerate discrimination or harassment based on any of these characteristics. Physical and Sensory Requirements: Mobility, walking, climbing, sitting, standing, reaching, bending, lifting (minimum of 10 lbs), carrying, pushing, pulling, fine eye-hand coordination, ability to read, write, listen and speak clearly, the ability to understand and follow written and oral instructions and directions, ability to drive a vehicle and travel, and ability to remain calm under pressure. Must be able to sit and/or stand for extended periods of time. Must be able to use computer, monitor, cell phone, mouse and keyboard extensively as well as other general office equipment.

At Superior, we act like we own the company because we do. We are 100% employee-owned organization that thrives on a culture of cooperation, commitment, and stewardship. We invest in our people and processes so that we can best serve our customers and grow responsibly. We shy away from "this is the way we've always done it," and gravitate towards "this make a lot of sense." We are looking for people that want to feel invested in making a difference that ultimately affects the company's bottom line, and yours as well. Oh, and by the way, we distribute solvents, chemicals, and composites. We also take customer's hazardous waste, and we repurpose it. And we're really good at all of the above because we've been doing it successfully since 1932. Superior is currently seeking an experienced Quality Control Chemist for our Arnold, MO location. This is a Monday through Friday position with working hours 8am-5pm. The position will perform quality control testing on incoming and outgoing products using the following instrumentation: Gas Chromatograph, Karl Fischer, viscometer, etc. Successful candidate will: Possess strong problem-solving skills and initiative Work well under pressure and handle multiple tasks effectively and efficiently Display exceptional organizational skills and ability to prioritize work assignments Demonstrate ability to work in teams with members from various disciplines Display significant attention to detail Requirements: 4-year degree required (chemistry/biology/science) Prior quality control experience (preferred) Familiar with analytical equipment - specifically, GC, KF, viscometer Excellent computer and communication skills Superior offers a competitive compensation package which includes Medical Insurance (an HDHP option - 100% premium paid, and a highly subsidized PPO option with very affordable premiums), Employee Stock Ownership Plan (ESOP), 401K, Flexible Spending, PTO, Paid Holidays, Life, Dental, Vision, STD and LTD. We hire based on character as well as experience! EOE including disability/veteran/drug free

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 - Day 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 AM - 6:30 PM) 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 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). RSREMD What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it 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 our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************