Chemist jobs in Chesterfield, MO - 99 jobs

** Veolia in North America is the top-ranked environmental company in the United States for three consecutive years, and the country's largest private water operator and technology provider as well as hazardous waste and pollution treatment leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial and hazardous waste collection and disposal, energy consulting and resource recovery. Veolia helps commercial, industrial, healthcare, higher education and municipality customers throughout North America. Headquartered in Boston, Veolia has more than 10,000 employees working at more than 350 locations across North America. **Job Description** **Position Purpose:** Responsible for leading laboratory technicians in performing routine tasks and simple analysis of hazardous waste samples in accordance with company and regulatory requirements. May perform specialized analysis under the direction of the Lab Manager or Technical Manager to support applied quality assurance and control procedures. Maintain the laboratory as directed for compliance with company hygiene plans. May prepare manifest for waste being shipped off site or review of waste in route to facility for disposal. Ability to review and accept paperwork from sample analysis and other paperwork approvals. **Primary Duties /Responsibilities:** + Under the Lab Supervisor, coordinate analysis of incoming hazardous waste materials, ensuring compliance with regulatory requirements, permits, and safety protocols. + Assist and oversee the logging of all incoming lab samples through manual and electronic systems while verifying proper labels and documentation. + Assists facility personnel with paperwork approval to ascertain accuracy and enhance efficiency and effectiveness in the disposal of hazardous waste materials. + Conduct sample analysis on incoming waste per methods and procedures established by training and knowledge of waste analysis plans. Conducts and oversees QA/QC sample analysis, method development, calibrations, and lab studies. + Ensure proper written and electronic documentation of all test results including QA/QC and audits sample documents prior to approval. Gather appropriate paperwork for management approvals and notifies staff of any incomplete sections needing attention. + Assists in the compiling and reporting of analysis data and reports including QA/QC data for review by staff. + Ability to review and make decisions for inbound container rejection/acceptance to keep the facility in compliance with all permits and regulations. + Authorization shall be obtained under direction of Laboratory Supervisor for waste streams, process samples, sales samples, and production waste streams. This authorization is a mandatory requirement and must be documented per company standards. + Full Signature authority for site generated waste. + Ability to identify and recognize discrepancies on incoming waste and assist the Discrepancy Chemist with the resolution as well as reviewing and suggesting comments to clarify and prevent discrepancies when appropriate. + Assist in the manifesting and documentation of lab waste leaving the facility. Ensuring waste leaves in a timely manner following all site and regulatory requirements. + Prepare and assist in the preparation of reagents, solutions, standards and other laboratory solutions as directed by supervisor per guidance and training. + Maintenance and troubleshooting of analytical equipment, as well as working with outside technical support, coordinating onsite service of analytical equipment and documents in accordance with quality assurance and control compliance. + Perform periodic audits of analytical logs to ensure federal regulation compliance for completeness and error corrections. + Ability to complete analyst training and direct trainers on proper training of analysts, and document said training within Veolia's QA/QC program. + Periodic review of analytical procedures and analysts to ensure compliance. Document supplemental training of analysts as needed. + Comply with federal, state, and local regulatory agencies in the disposal of hazardous waste materials. + Perform other laboratory analysis as requested. + Other duties as assigned by Technical Department **Qualifications** **Education / Experience / Background:** + Bachelor's degree in Chemistry or a related science discipline preferred + 1 to 3 years prior laboratory work experience in environmental or hazardous waste industry preferred + Typically 1-3 years experience in Lab Tech III role **Knowledge / Skills / Abilities:** + Computer proficiency + Strong team player + Organization skills + Excellent interpersonal and communication skills + Time management: the ability to organize and manage multiple deadlines + Strong customer orientation + Analytical Thinker **Required Certification / Licenses / Training:** + 24-Hour HAZWOPER Training **Additional Information** **Annual Pay Range:** Minimum of $64000 to a maximum of $78500 **Benefits:** Veolia's comprehensive benefits package includes paid time off policies, as well as health, dental, vision, life insurance, savings accounts, tuition reimbursement, paid volunteering and more. In addition, employees are also entitled to participate in an employer sponsored 401(k) plan, to save for retirement. Pay and benefits for employees represented by a union are outlined in their collective bargaining agreement. We are an Equal Opportunity Employer! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law.

Veolia in North America is the top-ranked environmental company in the United States for three consecutive years, and the country's largest private water operator and technology provider as well as hazardous waste and pollution treatment leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial and hazardous waste collection and disposal, energy consulting and resource recovery. Veolia helps commercial, industrial, healthcare, higher education and municipality customers throughout North America. Headquartered in Boston, Veolia has more than 10,000 employees working at more than 350 locations across North America. Job Description Position Purpose: Responsible for leading laboratory technicians in performing routine tasks and simple analysis of hazardous waste samples in accordance with company and regulatory requirements. May perform specialized analysis under the direction of the Lab Manager or Technical Manager to support applied quality assurance and control procedures. Maintain the laboratory as directed for compliance with company hygiene plans. May prepare manifest for waste being shipped off site or review of waste in route to facility for disposal. Ability to review and accept paperwork from sample analysis and other paperwork approvals. Primary Duties /Responsibilities: * Under the Lab Supervisor, coordinate analysis of incoming hazardous waste materials, ensuring compliance with regulatory requirements, permits, and safety protocols. * Assist and oversee the logging of all incoming lab samples through manual and electronic systems while verifying proper labels and documentation. * Assists facility personnel with paperwork approval to ascertain accuracy and enhance efficiency and effectiveness in the disposal of hazardous waste materials. * Conduct sample analysis on incoming waste per methods and procedures established by training and knowledge of waste analysis plans. Conducts and oversees QA/QC sample analysis, method development, calibrations, and lab studies. * Ensure proper written and electronic documentation of all test results including QA/QC and audits sample documents prior to approval. Gather appropriate paperwork for management approvals and notifies staff of any incomplete sections needing attention. * Assists in the compiling and reporting of analysis data and reports including QA/QC data for review by staff. * Ability to review and make decisions for inbound container rejection/acceptance to keep the facility in compliance with all permits and regulations. * Authorization shall be obtained under direction of Laboratory Supervisor for waste streams, process samples, sales samples, and production waste streams. This authorization is a mandatory requirement and must be documented per company standards. * Full Signature authority for site generated waste. * Ability to identify and recognize discrepancies on incoming waste and assist the Discrepancy Chemist with the resolution as well as reviewing and suggesting comments to clarify and prevent discrepancies when appropriate. * Assist in the manifesting and documentation of lab waste leaving the facility. Ensuring waste leaves in a timely manner following all site and regulatory requirements. * Prepare and assist in the preparation of reagents, solutions, standards and other laboratory solutions as directed by supervisor per guidance and training. * Maintenance and troubleshooting of analytical equipment, as well as working with outside technical support, coordinating onsite service of analytical equipment and documents in accordance with quality assurance and control compliance. * Perform periodic audits of analytical logs to ensure federal regulation compliance for completeness and error corrections. * Ability to complete analyst training and direct trainers on proper training of analysts, and document said training within Veolia's QA/QC program. * Periodic review of analytical procedures and analysts to ensure compliance. Document supplemental training of analysts as needed. * Comply with federal, state, and local regulatory agencies in the disposal of hazardous waste materials. * Perform other laboratory analysis as requested. * Other duties as assigned by Technical Department Qualifications Education / Experience / Background: * Bachelor's degree in Chemistry or a related science discipline preferred * 1 to 3 years prior laboratory work experience in environmental or hazardous waste industry preferred * Typically 1-3 years experience in Lab Tech III role Knowledge / Skills / Abilities: * Computer proficiency * Strong team player * Organization skills * Excellent interpersonal and communication skills * Time management: the ability to organize and manage multiple deadlines * Strong customer orientation * Analytical Thinker Required Certification / Licenses / Training: * 24-Hour HAZWOPER Training Additional Information Annual Pay Range: Minimum of $64000 to a maximum of $78500 Benefits: Veolia's comprehensive benefits package includes paid time off policies, as well as health, dental, vision, life insurance, savings accounts, tuition reimbursement, paid volunteering and more. In addition, employees are also entitled to participate in an employer sponsored 401(k) plan, to save for retirement. Pay and benefits for employees represented by a union are outlined in their collective bargaining agreement. We are an Equal Opportunity Employer! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law.

**Analytical Chemist - Mid Level** **Analytical Science Hub | Small Molecules Division** Adecco Healthcare & Life Sciences is partnered with a leading agricultural science organization to hire a **Mid-Level Analytical Chemist** to support its **Small Molecules Analytical Science Hub** . This role focuses on performing qualitative and quantitative chemical and physical analyses of agrochemical formulations in support of an active R&D pipeline and existing product portfolio. This position is ideal for a hands-on analytical chemist who thrives in a **high-throughput, fast-paced laboratory environment** and is motivated by solving complex analytical challenges with limited supervision. **Pay: $35- 42.5/hr based on education and experience level** **Position Summary** The Analytical Chemist will perform routine and non-routine analyses of active ingredients in liquid and solid formulations using advanced chromatographic and physical-chemical techniques. The successful candidate will be detail-oriented, adaptable, and capable of independently executing analytical workflows while collaborating with diverse R&D, manufacturing, and product supply stakeholders. **Key Responsibilities** + Perform **qualitative and quantitative analyses** of agrochemical formulations and products using **HPLC, UPLC, LC-MS, and GC** . + Conduct **physical-chemical characterization** including density, particle size analysis, viscosity, surface tension, contact angle, thermal analysis (DSC/TGA), optical/electron microscopy, and **FTIR, NIR, and UV-Vis spectroscopy** . + Prepare complex liquid and solid sample matrices for analytical testing. + Optimize existing analytical methods and **develop new methods** to support R&D pipeline needs and commercial products. + Support analytical troubleshooting, data interpretation, and reporting requests from cross-functional collaborators. + Maintain and troubleshoot laboratory instrumentation to ensure optimal performance and data integrity. + Interpret, document, and present analytical results through written reports and verbal communication to stakeholders across early R&D, manufacturing, and product supply. + Work under general supervision while managing multiple analytical priorities and deadlines. **Required Qualifications** + **Bachelor's degree** in Analytical Chemistry or a closely related scientific discipline. + **1-3 years of hands-on experience** in an analytical chemistry laboratory. + Demonstrated proficiency in **sample preparation and analysis** using HPLC/UPLC/LC-MS/GC. + Experience with **physical-chemical characterization techniques** . + Hands-on experience with **instrument maintenance and troubleshooting** . + Strong attention to detail and commitment to data quality. + Ability to work effectively in a **high-throughput, dynamic laboratory environment** . + Strong written and verbal communication skills. + Self-motivated, adaptable, and collaborative team player. **Preferred Qualifications** + Experience with **sample cleanup and enrichment techniques** . + Exposure to **robotic or automated sample preparation systems** . + Experience supporting both **R&D and manufacturing-facing analytical work** . + Willingness to cross-train and work across multiple analytical disciplines. Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria. **Pay Details:** $30.00 to $42.50 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to ********************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: + The California Fair Chance Act + Los Angeles City Fair Chance Ordinance + Los Angeles County Fair Chance Ordinance for Employers + San Francisco Fair Chance Ordinance **Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

**Lead Metrologist -St. Louis, MO** **Pharmaceutical/Biotechnology** **Direct Hire** **M-F; 8am-5pm** **Full Benefits** The Lead Metrologist acts as the **Subject Matter Expert (SME)** , providing hands-on calibration and diagnostic repair while ensuring regulatory compliance and leading team development within the Metrology department in the pharmaceutical space. **Subject Matter Expertise & Technical Execution (Hands-On)** + **Calibration and Diagnostics:** Perform calibration, maintenance, testing, troubleshooting, and diagnostic repair on a variety of complex **analytical instrumentations** used in pharmaceutical laboratories, specifically including **HPLC, GC, and Spectrophotometers** . + **Component Management:** Analyze test results, specify, and request the purchase of necessary components for repairs or upgrades. + **Modification:** Adjust and modify instrument performance and circuitry to meet specific operational requirements and specifications. **Leadership and Team Oversight** + **Technical Guidance:** Provide **oversight and guidance** to other team members, acting as the ultimate technical authority for tasks performed to ensure successful outcomes. + **Training & Development:** **Develop and update training programs** for the department and directly train team members on complex metrology systems and current procedures. + **Audit Representation:** Potentially serve as the departmental representative for the Manager/Supervisor during important client **audits and authority inspections** . **Documentation, Compliance, and Quality Systems** + **Procedure Ownership:** Be accountable for the quality and efficiency of the department by **developing and updating Standard Operating Procedures (SOPs)** . + **Regulatory Documentation:** Write, complete, and review critical quality documents, including **Out-Of-Tolerances (OOTs)** and **Deviations** , and maintain all required logs. + **cGMP Compliance:** Ensure all calibration, maintenance, and documentation activities are completed in a timely manner and remain compliant with **cGMP (current Good Manufacturing Practices)** and other relevant company training requirements. **Qualifications** + Associate's degree with 10+ years related experience or equivalent. + Bachelor's degree with 8+ years of experience in a cGMP GMP facility combined with the soft skills necessary to lead projects, manage documentation, and enforce pharmaceutical quality standards. + Technical field of studies is preferred. + Previous work experience in a GMP facility required. As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

This role can sit anywhere in the US as long as it is near an Accenture Corporate Office We are: Looking to be part of a transformational digital engineering and manufacturing practice? How about an opportunity to help world-class clients solve their biggest challenges and create products and services that customers love - quickly, efficiently and sustainably? Industry X combines Accenture's powerful digital capabilities with deep engineering and manufacturing expertise. We use the power of data and digital to help our clients reimagine the products they make, and how they make them. By connecting engineering and manufacturing operations every step of the way - from how products are designed and engineered, sourced and supplied, manufactured, to how they are serviced and renewed, we help them achieve greater productivity, drive growth and meet their sustainability commitments. Find out more about Industry X. You are: A ambitious Manufacturing Systems (MES) Specialist ready to take on new challenges. As industries head towards Manufacturing and Factory Digitalization, MES stand in the center of manufacturing excellence. The Work: * Lead in the design, development, documentation, and implementation of Körber PAS-X Manufacturing Execution Systems (MES) * Design/Author/Develop/Configure Electronic Batch Records (EBR) * Implement MES solutions and integrate with ERP and control equipment * Documentation of MES configuration and validation of EBRs * Work closely with business management and users to strategically define the needs and design solutions that add value * Document and analyze the information needs of the business and ensure appropriate solutions are delivered according to GxP standards * Respond to requests for client proposals * Manage and develop client relationships Job Requirements: * Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements. Qualification Here's What You Need: * A minimum of 2 years of experience with Körber PAS-X MES solutions in a highly automated Life Sciences manufacturing environment * Bachelor's Degree or equivalent (minimum 3 years work experience). If Associate's Degree, must have equivalent minimum 6 years work experience Set Yourself Apart: * Knowledge of FDA and GMP guidelines * Strong written and oral communication skills * Ability to work in a team-oriented, collaborative environment * Ability to facilitate meetings and follow up with resulting action items * Understanding of Life Sciences validation processes * Working knowledge of software Development Life Cycle (SDLC) and support methodologies Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired as set forth below. We accept applications on an on-going basis and there is no fixed deadline to apply. Information on benefits is here. Role Location Hourly Salary Range California $30.67 to $98.94 Cleveland $28.41 to $79.13 Colorado $30.67 to $85.48 District of Columbia $32.69 to $91.01 Illinois $28.41 to $85.48 Maryland $30.67 to $85.48 Massachusetts $30.67 to $91.01 Minnesota $30.67 to $85.48 New York/New Jersey $28.41 to $98.94 Washington $32.69 to $91.01 #LI-NA-FY25 Locations

Job Title: Analytical Chemist - Mid Level Zip Code: 63017 Keyword's: #Chesterfieldjobs; #Chemistjobs. Job Description: * Will perform analyses of active ingredients in liquid and solid formulations using HPLC/UPLC/LCMS/GC and varied physical-chemistry assay techniques. * Prepare complex liquid and solid matrices for qualitative and quantitative analyses. * Optimize and develop new sample preparation and analytical methods * Write reports and interpret/report analytical results to diverse stakeholders representing early R&D to manufacturing and product supply. REQUIREMENTS & PREFERENCES: * BS in Analytical Chemistry or closely related field. * Hands-on experience and demonstrated proficiency in preparing complex agrochemical sample matrices for analysis with HPLC/UPLC/LCMS/GC and physical-chemical techniques described above. * Experience with robotic sample preparation is desirable. * Able to multitask in high-throughput, fast-paced, dynamic analytical laboratory environment. * 1-3 years of relevant experience. Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, colour, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

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: In this role you will be involved with problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing. * Serve as a subject matter expert in analytical development, perform troubleshooting / provide efficient and innovative solutions, and support transfer of analytical methods to GMP QC labs. * Utilize customer-facing skills, document experimental results, communicate results to all stakeholders, author method development and qualification documents, contribute to information for customer proposals. * Serve as a project lead and ensure project deliverables are on quality and on time, develop multiple technical approach plans as needed to solve problems and mitigate risk, ensures process and methods are in place for efficient GMP start. * Lead project teams, influence exemplary work in other team members, lead process improvement initiatives, scout for new technologies / emerging trends, proactively consider the impact of quality, regulatory, manufacturing, and safety requirements when planning project activities. Who You Are: Minimum Qualifications: * Bachelor's Degree in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 6+ years of research experience. OR * Master's Degree in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 2+ years of research experience. OR * PhD in in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 1+ years of research experience. Preferred Qualifications: * Experience with protein characterization via ELISA, SPR, Isoelectric Focusing, CE-based methods, UV-Vis, and/or chromatography (HPLC/GC/IC/UPLC/SEC/HILIC). * Experience with advanced laboratory techniques; theory and practice to enable the development of novel approaches to solve complex process and analytical problems on fast-paced projects with changing priorities. * Knowledge of small molecule or bio-therapeutics drug development process. * Experience with antibody-drug conjugation. * Knowledge in Biochemistry or Organic Chemistry. * Experience in automation in an analytical setting and instrument maintenance and troubleshooting. * Knowledge of Microsoft Word, Excel, and PowerPoint. * Experience with advanced data acquisition and/or statistical software systems. * Ability to coordinate information exchange and manage data generated by contract testing labs. RSREMD Pay Range for this position: $68,700/yr - $132,700 yr. 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!

Job Title: QC ChemistJob Description We are seeking a dedicated QC Chemist to join our contract testing team specializing in the analysis of gases and oils. As a QC Chemist, you will play a crucial role in assisting the laboratory team in testing petroleum, gases, and newly expanded products such as alcohol-based soaps and cleaners. This position offers an opportunity to gain hands-on experience with a variety of testing methods and advanced instrumentation. Responsibilities * Receive, examine, and record inbound samples for testing through a login process. * Deliver test samples to the designated sample staging area. * Monitor the availability of supplies needed for testing processes and communicate any needs to the Laboratory Manager. * Perform testing of samples and quality control specimens using specified methodologies after demonstrating proficiency. * Review test results against specifications and known expectations, and report findings to the laboratory team. * Prepare samples, quality control specimens, reagents, and solutions, and calibrate equipment necessary for testing processes. * Verify and communicate results obtained, ensuring accurate documentation in instrument logs, control charts, and laboratory worksheets. * Maintain a neat, orderly, and safe work environment, adhering to company safety and quality management policies. * Assist in training less experienced employees upon demonstrating sufficient proficiency. Essential Skills * Bachelor's degree in biology, chemistry, biochemistry, or a related field, or equivalent industry experience. * Familiarity with laboratory instrumentation such as HPLC, GC, FT-IR, UV/VIS, NMR, titration, and solution preparation. * Basic proficiency in mathematics, including unit conversions and solution calculations. * Ability to work independently and collaboratively within a team. Additional Skills & Qualifications * An associate degree with relevant experience may be considered. * Experience with ion chromatography, atomic absorption (AA), and other analytical techniques is advantageous. Work Environment The work environment consists of a small, family-oriented office in St. Louis, with a supportive team of approximately 10 people. The lab operates with two core team members. The role offers a flexible shift schedule, including some weekend hours, with a total of 40 hours per week. The team enjoys a tight-knit culture with team lunches and a relaxed atmosphere, contributing to a positive work-life balance. Job Type & Location This is a Contract to Hire position based out of SAINT LOUIS, MO. Pay and Benefits The pay range for this position is $23.00 - $23.00/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 SAINT LOUIS,MO. Application Deadline This position is anticipated to close on Jan 5, 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: 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!

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description The Scientist I - Analytical Chemist will support the Eurofins Discovery business in contract research services. This role requires applied experience and proven knowledge in analytical chemistry methods with related experience in a contract research organization (CRO) or industry laboratory. Scientist I Analytical Chemist Responsibilities & Duties Include but are not Limited to the Following: * Performs work in a laboratory setting, meeting the physical job requirements of a lab role. * Conducts production assays primarily in ADME Toxicology Services, but may support BioMAP, Immunosignaling, Ion Channel, and/or OncoPanel Services based on business needs. * Develops Liquid Chromatography- Mass Spectrometry (LC-MS) methods for ADME/ DMPK applications * Develops analytical methods supporting project teams both internally and externally for new assay development. * Performs Troubleshooting and Maintenance of Mass Spectrometers and HPLC units. Experience with Sciex or Waters Instrumentation is a plus. * Prepares and manages inventory of buffers, reagents, semi-finished and finished goods. * Provides solutions to more complex problems, identifies and initiates process improvements * Maintains high data quality and reproducibility. * Performs data and report QC review within the department, and may support study director. * Takes ownership of client projects with minimal supervision. * Supports validation of new methods, and contributes to expansion of service/product line, equipment, and data management systems. * Understands and complies with requirements for work performed at a GxP site. * Completes required training and supports 100% of Employee Health and Safety requirements. * Demonstrates proficiency with, care and maintenance of lab equipment and department assets. * Conducts responsible use of confidential IT and business systems, as required. * Adheres to department SOPs and documentation requirements, maintains accurate data management and reporting. * Supports unit goals and demonstrates Eurofins' competencies, as defined in the job plan. * Provides training to colleagues and external end users, when required. * Contributes to scientific community, and site research and development objectives. * Works effectively in a team environment, under minimum direction, to achieve business production, project timelines, and quality objectives. * Adjusts work hours and provides cross-functional support to other departments, as required, and maintains accountability in delivering to client needs/timelines. * Routinely communicates project updates to internal and external clients. * Performs other duties, as assigned/ Qualifications Basic Minimum Education Requirements: * B.S. with minimum 5 years relevant laboratory experience * M.S. with minimum 3 years relevant laboratory experience * Ph.D. with minimum 1 year relevant laboratory experience * Or an equivalent of education and laboratory experience Basic Minimum Work Requirements: * Direct experience with Liquid Chromatography- Mass Spectrometry and/or ultraviolet spectrometry (LC-MS or LC-UV) in a contract research organization or industry laboratory for ADME/ DMPK applications * Experience working in a Quality Management System * Scientific expertise with mass spectrometry-based quantification for ADME/ DMPK applications in biological matrices. * Experience with analytical method development and optimization * Familiarity with concepts of validation of bioanalytical methods in accordance with regulatory (FDA, ICH) guidelines * Experience with liquid handling, automation, solid-phase extraction (SPE), HTS applications, and large-scale screening * Experience in small team leadership and project management * Experience in leading and delivering results in R&D or innovation programs * Authorization to work in the United States indefinitely without restriction or sponsorship. The Ideal Candidate Possesses the Following: * Good communication and interpersonal skills * Demonstrated proficiency in contributing independently on a project team with time and quality deliverables * Ability to read, write, and interpret documents, such as standard operating procedures and technical reports * Ability to perform mathematical calculations, statistical analyses, and data interpretation * Ability to multitask with organization and manage time effectively * Ability to solve practical problems and troubleshooting skills * Ability to work in a laboratory setting, according to physical requirements of a laboratory role * Lab equipment and office computer/software proficiency * Above average oral and written communication skills * Demonstrates a positive attitude, capacity for team environment, and exhibits a genuine interest in drug discovery in support of advancing human health * Ability to develop new methods, and lead research and development projects * Ability to review and QC release data/reports * Ability to lead small, informal sub-teams, train, and train new team members * Ability to conduct mid-size projects with minimal supervision * Ability to contribute to strategic vision, establishment of new service lines, equipment, and data management systems * Ability to easily support cross-functional demands Additional Information Position is full-time working Monday - Friday 8:00pm - 5:00 PM. Candidates currently living within a commutable distance of St. Charles, MO are encouraged to apply. * 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 Eurofins USA Discovery Services is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionDescription: Want to work for a company that supports and invests in its employees? Cosmos Corporation has a healthy workplace culture guided by a clear vision, mission, promise, and values! Our culture is intentionally fostered daily by how employees live out our values. The result is a place where employees genuinely enjoy coming to work every day! Cosmos Corporation is a recognized leader in natural health, wellness, and care products. Cosmos creates and distributes people and pet-approved liquid products with the most responsible, effective, high-quality ingredients people trust. Our brands bring innovative products with unique benefits that help people and pets look and feel their very best. We do all of this at our headquarters located in O'Fallon, Missouri. We are looking for a new ideal team player as a process chemist to join the Formulation Team! The Process Chemist is responsible for developing, optimizing, and implementing robust manufacturing processes and formulas to support product development and production. The role involves creating and maintaining master mixing records, conducting pilot and bench batches, troubleshooting with Quality Control, and collaborating with Engineering, Maintenance, and other teams to ensure process efficiency and compliance. This position provides technical support across departments, ensures adherence to GMP and safety practices, and contributes to continuous process improvements to enhance product quality and manufacturing performance. You Key Responsibilities Will Be: Develop, optimize, and scale up robust manufacturing processes for all formulations. Create and maintain master mixing records and documentation for new and existing products. Conduct bench and pilot batches to support formulation and initiation to the mixing team. Collaborate with Quality, Engineering, and Operations to troubleshoot issues and improve efficiencies. Provide technical support across teams and drive continuous improvements in process, quality, and safety. Requirements: 5 years of related experience Superior math mathematical skills Excel at problem solving. Excels at computer skills. Experience with formulation in finished goods Bachelor's degree in chemistry, chemical engineering, or related science Your Competencies & Skills You Hold Are as Follows: Collaboration & Communication Team player Analytical & Critical Thinking Skills Technical Proficiency Data Driven Mindset Process & Scale-Up Expertise. Attention to Detail Innovation & Continuous Improvement Ingredient & Formulation Knowledge Adaptability & Learning Agility Safety & Compliance Mindset A Day In the Life At Cosmos: No two days look the same. You might start in the lab running a bench batch to evaluate a new formula, then move to the plant floor to oversee a pilot batch and ensure scale-up parameters align with production equipment. Midday could be spent troubleshooting a manufacturing issue with Quality Control or working with Engineering on process improvements. You will update and refine master mixing records, review data for accuracy, and provide technical guidance to cross-functional teams. Along the way, you will balance hands-on experimentation with problem-solving-leveraging data, technology, and collaboration to keep product quality, efficiency, and innovation at the forefront. Every Wednesday, you will head to the lunchroom at 11:40 a.m. for the weekly Cosmos Minute, where the entire company meets at 11:45 a.m. to learn about other team members and special company announcements at Cosmos. What's In It For You? At Cosmos Corporation we truly care about investing in our employees, these are the benefits and perks at Cosmos! Medical Health Insurance Dental Insurance Vision Insurance Life Insurance Short- & Long-Term Disability Insurance Flexible Spending Accounts Critical Illness Accident Coverage 401(k) Contribution Robust Employee Assistance Program Vacation Time Off 8 Paid Holidays (and sometimes more!) Paid Sick Leave 5 Paid Mission Days Parental Leave Maternal Leave Growth & Development Opportunities Lunch & Learns Employee Referral Bonus Program Cosmos Cash Recognition Program Better Book Club Excellent Culture So much more!! Equal Opportunity Employer Cosmos Corporation is an equal-opportunity employer. We prohibit discrimination and harassment of any kind. Cosmos Corporation makes hiring decisions based solely on qualifications, merit, and business needs at the time.

Driven by integrity and united by the people-and-pet bond, we find strong purpose in the work we do and an even greater joy in those we get to work alongside. Together, we harness the expertise of our long-standing tradition of excellence to embrace possibility and continuously push to do what's never been done before in pet care. Discover your purpose and fuel your passions when you bring your love of pets to a team that prides itself on the power of togetherness-We are Proudly Connected. Purely Driven. Position Summary Quality Assurance and Nestlé Purina Analytical Laboratories department is comprised of talented individuals who possess a genuine love for pets and their families. We thrive on being at the forefront of research, contributing to the innovation and advancements in pet nutrition and quality that sets Nestlé Purina apart. Ensuring the delivery of safe ingredients and sustainable practices to our factories and beyond, we are invigorated by the extensive research and development that goes into our products. Bring your impact to the table and together we will continue to work towards being one of the most trusted companies in pet care. As an Analytical Chemist, you will execute and interpret complex procedures and protocols within a project or goal. You'll be a great fit if you are a self-starter who takes initiative and works independently while collaborating within Nestlé Purina Analytics Laboratories (NPAL). You'll be expected to learn method development, make process improvements, and help draft standard operating procedures (SOP's) in addition to mentoring other team members. * Prepare and interpret reports of complex experiments * Follow established methods and procedures to deliver timely results * Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals * Assist in development and validation of analytical methods in support of projects * Aid in experiments and project assignments Requirements * Bachelor's degree in Chemistry or a related field * 3+ years of analytical lab or industry experience, analytical instrumentation experience, and troubleshooting of assay and equipment issues * 2+ years of experience with chromatography and/or mass spectrometry (HPLC, GC, GCMS, LCMS, etc.) Other * 1+ years of experience working in an ISO 17025 accredited laboratory is preferred Environment includes exposure to Top 14 Allergens. The approximate pay range for this position is $59,000.00 to $90,000.00. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and abilities as well as geographic location of the position. Nestlé offers performance-based incentives and a competitive total rewards package, which includes a 401k with Company match, healthcare coverage and a broad range of other benefits. Incentives and/or benefit packages may vary depending on the position. Learn more at About Us | Making an Impact | Nestle Careers (nestlejobs.com). It is our business imperative to remain a very inclusive workplace. To our veterans and separated service members, you're at the forefront of our minds as we recruit top talent to join Nestlé. The skills you've gained while serving our country, such as flexibility, agility, and leadership, are much like the skills that will make you successful in this role. In addition, with our commitment to an inclusive work environment, we recognize the exceptional engagement and innovation displayed by individuals with disabilities. Nestlé seeks such skilled and qualified individuals to share our mission where you'll join a cohort of others who have chosen to call Nestlé home. The Nestlé Companies are equal employment opportunity employers. All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status or any other characteristic protected by applicable law. Prior to the next step in the recruiting process, we welcome you to inform us confidentially if you may require any special accommodations in order to participate fully in our recruitment experience. Contact us at accommodations@nestle.com or please dial 711 and provide this number to the operator: **************. This position is not eligible for Visa Sponsorship. Review our applicant privacy notice before applying at *********************************** Job Requisition: 377560 Driven by integrity and united by the people-and-pet bond, we find strong purpose in the work we do and an even greater joy in those we get to work alongside. Together, we harness the expertise of our long-standing tradition of excellence to embrace possibility and continuously push to do what's never been done before in pet care. Discover your purpose and fuel your passions when you bring your love of pets to a team that prides itself on the power of togetherness-We are Proudly Connected. Purely Driven. Position Summary Quality Assurance and Nestlé Purina Analytical Laboratories department is comprised of talented individuals who possess a genuine love for pets and their families. We thrive on being at the forefront of research, contributing to the innovation and advancements in pet nutrition and quality that sets Nestlé Purina apart. Ensuring the delivery of safe ingredients and sustainable practices to our factories and beyond, we are invigorated by the extensive research and development that goes into our products. Bring your impact to the table and together we will continue to work towards being one of the most trusted companies in pet care. As an Analytical Chemist, you will execute and interpret complex procedures and protocols within a project or goal. You'll be a great fit if you are a self-starter who takes initiative and works independently while collaborating within Nestlé Purina Analytics Laboratories (NPAL). You'll be expected to learn method development, make process improvements, and help draft standard operating procedures (SOP's) in addition to mentoring other team members. * Prepare and interpret reports of complex experiments * Follow established methods and procedures to deliver timely results * Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals * Assist in development and validation of analytical methods in support of projects * Aid in experiments and project assignments Requirements * Bachelor's degree in Chemistry or a related field * 3+ years of analytical lab or industry experience, analytical instrumentation experience, and troubleshooting of assay and equipment issues * 2+ years of experience with chromatography and/or mass spectrometry (HPLC, GC, GCMS, LCMS, etc.) Other * 1+ years of experience working in an ISO 17025 accredited laboratory is preferred Environment includes exposure to Top 14 Allergens. The approximate pay range for this position is $59,000.00 to $90,000.00. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and abilities as well as geographic location of the position. Nestlé offers performance-based incentives and a competitive total rewards package, which includes a 401k with Company match, healthcare coverage and a broad range of other benefits. Incentives and/or benefit packages may vary depending on the position. Learn more at About Us | Making an Impact | Nestle Careers (nestlejobs.com). It is our business imperative to remain a very inclusive workplace. To our veterans and separated service members, you're at the forefront of our minds as we recruit top talent to join Nestlé. The skills you've gained while serving our country, such as flexibility, agility, and leadership, are much like the skills that will make you successful in this role. In addition, with our commitment to an inclusive work environment, we recognize the exceptional engagement and innovation displayed by individuals with disabilities. Nestlé seeks such skilled and qualified individuals to share our mission where you'll join a cohort of others who have chosen to call Nestlé home. The Nestlé Companies are equal employment opportunity employers. All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status or any other characteristic protected by applicable law. Prior to the next step in the recruiting process, we welcome you to inform us confidentially if you may require any special accommodations in order to participate fully in our recruitment experience. Contact us at accommodations@nestle.com or please dial 711 and provide this number to the operator: **************. This position is not eligible for Visa Sponsorship. Review our applicant privacy notice before applying at *********************************** Job Requisition: 377560 St. Louis, MO, US, 63102 St. Louis, MO, US, 63102

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.) Job Description How will you make an impact: Join us at Thermo Fisher Scientific as a QC Scientist I to contribute to global health through quality control testing that ensures the safety and efficacy of pharmaceutical products. You will perform chemical, physical, and microbiological analyses in support of manufacturing operations while following Good Manufacturing Practices (GMP). Working with advanced analytical instruments, you'll conduct testing of raw materials, in-process samples, finished products, and stability samples. Our collaborative environment provides opportunities for continuous learning and career growth as you help deliver vital therapies to patients. We have 3 positions available. A Day in the Life: * Perform testing on In-Process, DS release, DP release, DS stability, DP Stability, and various other non-routine samples, ensuring timely delivery for projects * Conduct GMP testing in an analytical laboratory environment using Separation Techniques, BioAssay Analysis and Compendia test methods (i.e.,Reverse Phase, SEC, Titer concentration, iCE, pH, Osmolarity, Residual DNA, Appearance) * Compiles data for documentation of test procedures, prepares reports. Collaborate with team members and other departments such as quality assurance and data reviewers. * Contributes to the development of new concepts, techniques, and standards. * Recognize and report invalid/ lab incident/ out-of-specification/ out-of-trend results to laboratory management; recommend solutions. * Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, and Safety guidelines. * Participate in laboratory activities, performing safety inspections and ordering supplies. Keys to Success: * Bachelor's degree required, no prior experience required * Preferred Fields of Study: Chemistry, Biology, Biochemistry or related scientific field * Proficiency with analytical techniques including HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods * Experience with microbiological testing, environmental monitoring, and aseptic techniques * Knowledge of GMP regulations, documentation practices, and pharmaceutical quality standards * Strong attention to detail with ability to follow standard procedures and maintain data integrity * Excellent problem-solving skills and logical approach to scientific challenges * Proficient computer skills including Microsoft Office and laboratory information systems * Strong written and verbal communication abilities * Ability to work both independently and collaboratively in a dynamic environment * Physical requirements include standing/walking for extended periods, lifting up to 50 lbs, and manual dexterity * Must be able to work in cleanroom environments wearing required PPE * Ability to work various shifts including nights, weekends, and holidays as needed * Experience in pharmaceutical/regulated environment preferred but not required Excellent Benefits * Benefits & Total Rewards | Thermo Fisher Scientific * Medical, Dental, & Vision benefits-effective Day 1 * Paid Time Off & Designated Paid Holidays * Retirement Savings Plan * Tuition Reimbursement OTHER * Relocation assistance is NOT provided * Must be legally authorized to work in the United States now or in the future, without sponsorship. * Must be able to pass a comprehensive background check, which includes a drug screening

Experiencing together a unique human adventure Animal health is key to the health of the planet. Working at Virbac means taking part in a unique human adventure in which the engagement of each individual contributes to its evolution. Encouraging internal mobility between positions and countries, offering individual development plans and building a partnership based on trust between managers and employees are as many perspectives of motivation for our teams. We also offer them a work environment conducive to exploring new territories and balancing their professional and personal lives. Finally, fostering their engagement to animal health also means listening to them and helping them to acquire new skills, preparing them for the challenges of tomorrow and encouraging them to contribute to an ever more responsible approach to our business. R&D Analytical Development Chemist Virbac Animal Health is seeking an Analytical Development Chemist to join our team. The Analytical Development Chemist develop analytical methodology for performance of routine analytical testing on finished products and stability samples. Design and execute studies to demonstrate the validity of test methods. Perform routine and non-routine testing as required to support R&D. Qualified candidates must possess, at a minimum, a BS in Chemistry or equivalent science degree. 3 to 5 years of experience working in an analytical test lab. This exciting position will work in Bridgeton, MO. It comes with an excellent benefits package including generous time off, 401k + match, life, medical, dental, and vision benefits, and more! Virbac provides numerous career opportunities, thanks to the diversity of its jobs and their international dimension.Joining Virbac means joining dynamic teams ambitious for success.Add Your Talent to Ours!

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description The qualified candidate will be responsible for developing and implementing methods of analysis for characterization of proteins, peptides, vaccines, carbohydrates, and oligonucleotides using advanced analytical techniques. Qualifications • B.S. in chemistry, biochemistry, and biology, or equivalent; industrial experience in analytical characterization is desirable. • The qualified colleague must have knowledge in protein biochemistry and/or protein analytics. • Good communication and writing skills are essential due to the highly matrixed, fast-paced, project-team environment. Additional Information Thanks Warm Regards Ricky Bansal 732-429-1925

Formulation R&D Technician- Oral Product Development Humanwell Pharmaceuticals US, St Louis, MO Interested candidate, please submit resumes to email: ******************** Summary Humanwell Pharmaceutical US, Inc., based in St Louis, MO, is committed to advancing pharmaceutical research and development, with a particular emphasis on novel therapeutics that address unmet medical needs. The organization strives to enhance the quality of life for patients and shape a healthier future. Humanwell seeks individuals motivated by a desire to make a meaningful impact and is currently recruiting a dedicated Formulation R&D Technician. The individual will collaborate closely with senior scientists and management to execute hands-on pharmaceutical development activities. Primary Duties and Responsibilities Maintain compliance, cleanliness, and organization within the operational areas of the pilot plant. Set up, operate, maintain, and sanitize a broad array of formulation equipment and testing instruments, including but not limited to scales, high shear and fluid bed granulators, blenders, tablet press, film coater, homogenizer, density tester, and hardness tester. Document laboratory activities in accordance with Good Documentation Practices. Summarize study outcomes and assist in the preparation of technical reports and presentations. Independently plan and accomplish assigned responsibilities within established timelines as directed by supervisory personnel. Conduct physical inventory for both controlled and non-controlled substances. Contribute to the development, revision, and delivery of training on manufacturing Standard Operating Procedures (SOPs). Comply with current Good Manufacturing Practices (cGMP) and all applicable regulatory guidelines. Work extended hours occasionally, as necessitated by project requirements. Be available to travel up to 10% of the time. Perform additional duties and assignments as required. Required Qualifications and Skills: Bachelor's or Master's degree in Pharmaceutical Science, Chemical Engineering, Chemistry, or a closely related discipline. Preferably possesses relevant experience within the pharmaceutical industry. Preferably possesses hands-on experience in pharmaceutical research and development as well as GMP manufacturing environments. Demonstrates willingness and capability to comply with FDA, OSHA, and DEA regulations. Exhibits a proven ability to collaborate effectively as part of a cross-functional team. Displays excellent oral and written communication skills. Job Type: Full-time Job Location: Ballwin, MO

At the dawn of the new millennium, a unique information technology company was born: HCL Technologies. As narrated in the video below, HCL Technologies has demonstrated remarkable growth through the recent economic downturn, emerging as one of only eight 21st century listed technology companies in the world to cross $1bn in Net Profit, $6bn in Revenue and $15bn in Market Capitalization. Job Description • Molecular biologist to aid in characterization of recombinant mammalian cell lines. Requires BS/MS in molecular biology or related field and at least one year of laboratory experience. • Must be familiar with general cell culture techniques (ex. aseptic passaging of cell lines), RNA, cDNA and genomic DNA preparation, DNA/RNA electrophoresis, and Northern and Southern analyses. • Experience with molecular cloning techniques such as plasmid construction, preparation and analysis, DNA sequencing technologies and analysis of DNA sequencing data multiple sequence alignments, identification of mutant sequences, in silico protein translation, etc. would be a definite plus MOST CRITICAL SKILLS: gDNA/RNA preparation; northern/southern blot analysis. Additional Skills:REQUIRED PERSONALITY TRAITS: team oriented, fast learner, good attention. MOST CRITICAL SKILLS: gDNA/RNA preparation; northern/southern blot analysis. Additional Information Best Regards, Anuj Mehta ************

Leidos is in search of an Environmental Chemist/Data Validator. This role will primarily provide support to the United States Army Corps of Engineers (USACE) Formerly Utilized Sites Remedial Action Program (FUSRAP) St. Louis project. At Leidos, we deliver innovative solutions through the efforts of our diverse and talented people who are dedicated to our customer's success. We empower our teams, contribute to our communities, and operate sustainably. Everything we do is built on a commitment to do the right thing for our customers, our people, and our community. Our Mission, Vision, and Values guide the way we do business. This role will start on site 100% of the time, with the opportunity for a hybrid work situation in the future. Office support will be conducted at the St. Louis, MO (Earth City) office. It is expected the candidate will be within commutable distance to this location. The anticipated salary range for this position is between $69,000 and $79,000. Due to contract requirements; U.S. Citizenship or U.S. Permanent Residency is required. The Challenge: * Perform validation of laboratory data packages of radiological data received from analytical laboratories * Evaluate lab reports for completeness, assess quality control results, and assign validation flags to reported concentrations based on the validation criteria * Enter data into project database, and perform quality control checks on data entry * Prepare written narratives to describe validation findings and write quality assurance/quality control reports * Prepare sample information for field work including database setup of sample IDs, labels and chain-of-custody documents, and evaluate compliance with planning documents * Query data in response to project management needs; evaluate accuracy of final data relative to the reported data * Track samples from collection through laboratory receipt, analysis, and reporting, and evaluate documents for accuracy and completeness * Routine communication and coordination with management and staff to ensure overall project objectives are satisfied Basic Qualifications: * B.S. degree in chemistry (preferred) or other closely related science * 2+ years' relevant laboratory experience performing environmental analyses (radiological preferred) * Excellent attention to detail and time management * Must be able to organize and prioritize to accommodate crucial deadlines * Self-starter with excellent verbal, interpersonal and written communication skills * Knowledgeable of computer software programs including spreadsheets, database, and other Microsoft Office products (Excel, Word, Access) Preferred Qualifications: * At least 4 years' relevant experience validating radiological analytical data and performing environmental data or database management. * Experience with radiological laboratory methods, QA/QC elements, and record keeping. * Familiarity with laboratory instrumentation systems. * Proficient with computer software programs including spreadsheets, database, and other Microsoft Office products * Experience with environmental data validation practices/policies/procedures especially the Department of Defense Quality Systems Manual and U.S. Environmental Protection Agency National Functional Guidelines for Data Review. * Experience with environmental databases such as ERPIMS, EQuIS, ADR.net or FUDSChem, or data management software such as MS Access and SQL. If you're looking for comfort, keep scrolling. At Leidos, we outthink, outbuild, and outpace the status quo - because the mission demands it. We're not hiring followers. We're recruiting the ones who disrupt, provoke, and refuse to fail. Step 10 is ancient history. We're already at step 30 - and moving faster than anyone else dares. Original Posting: November 26, 2025 For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. Pay Range: Pay Range $59,150.00 - $106,925.00 The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.

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