Quality Control Analyst Jobs in Bellefontaine Neighbors, MO

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information St. Louis, MO / Drug Substance Division - The Drug Substance Division is one of the five divisions that make up the Pharma Services Group. We specialize in both small and large molecule development and commercial drug substance services. This allows us to serve the needs of Small/Emerging, Mid-Sized, and Large Pharma sectors globally. Discover Impactful Work: Provide routine analyses in microbiology by following standard practices. Perform microbiological testing of in-process samples, raw materials, buffers, media, etc. per compendial methods. Support internal development and/or manufacturing operations. Make detailed observations and reviews, documents, and communicate test results. Work Schedule: Monday- Friday A day in the Life: Conduct routine bioburden testing of solutions and raw material per compendial methods and established methods. Recognize and report out-of-specification or unexpected results. Clearly and accurately communicate the results of work by generating documentation of the testing/analysis and acquired results. Record and report results of analysis in accordance with prescribed lab procedures and systems. Assist in preparing regulatory documents and other communications with outside agencies, clients, and/or colleagues from other corporate sites. Contribute to writing of SOPs if needed. Perform daily lab cleaning, preventative maintenance of equipment, ordering of supplies, and autoclaving of equipment. Perform all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintain the necessary compliance status required by company and facility standards Keys to Success: Education Bachelor's degree required in a scientific field, preferably a Microbiology or Biology. Experience 2+ years experience working in a cGMP and lab environment or equivalent experience. Knowledge, Skills, Abilities Knowledge of GMP regulations in cGMP manufacturing environment preferred. Excellent problem solving and critical thinking skills Excellent organization and planning skills. Strong attention to detail and ability to adhere to standard procedures. Ability to function in a continually evolving environment. Experience in writing QC investigations Experience in managing projects Ability to work in team environment as well as independently

Analytical Chemist for Pharmaceutical Industry Quality Control experience desired! Target pay: $70k-80k/year Responsibilities: - Perform routine and complex analysis of pharmaceutical products and raw materials using various testing techniques such as GC, HPLC, FTIR, etc. - Ensure analysis adheres to cGMP standards. - Interpret analytical procedures and accurately document work. - Provide expert data interpretation and compare results to specifications. - Summarize laboratory findings and prepare scientific reports. - Maintain lab facilities, equipment, and supplies. - Assist with other assigned tasks and potentially train lab personnel. - Work independently or collaboratively within a scientific team. Requirements: - Expertise in lab equipment and techniques. - Strong problem-solving skills and ability to work independently. - Accurate and compliant work practices. - Effective communication and organizational skills. - Bachelor's degree in a scientific field with extensive chemistry coursework. - Minimum 3-5 years of professional experience in analytical chemistry; preferred MS in Chemistry with 5 years in cGMP-regulated labs. \#p1 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 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. 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.

The Audit and Assurance Department of one of the fastest-growing accounting firms in the country is seeking an Associate who is motivated to learn, excited to collaborate and passionate about delivering outstanding results. This individual will have a direct impact on our firm's mission of serving as a catalyst for those striving to achieve their highest potential. In this role, you will be primarily responsible for planning and conducting audits of client financial statements, assisting with determination of appropriate audit methodology, assisting with performance of risk assessments and developing relationships with client companies. To succeed in this role, you should have a foundational understanding of accounting principles with a desire to build your technical skills and knowledge. This position is open to candidates available to start in September 2026 or January 2027. Additional start dates can be discussed as necessary. What You'll Do: Conduct audits of client company financials to ensure compliance with GAPP and other accounting standards Determine the effectiveness of internal controls and the potential impact of internal control deficiencies Examine records to ensure proper recording and authorization of transactions, compliance with policies, and applicable laws Prepare detailed reports of audit findings and recommendations for client companies Prepare portions of compilation, review, and audit engagements Perform other duties as assigned What We're Looking For: Understanding of audit and attest services Knowledge of FASB standards, GAAP, and GAAS Strong analytical and mathematical abilities Excellent written and verbal communication skills Detail-oriented with strong organizational skills A client service orientation with the ability to interact at all levels of management Ability to work autonomously Proficiency in Microsoft Office, especially Excel and Word Your Qualifications Bachelor's Degree in Accounting required CPA or CPA Candidate

Kindeva Drug Delivery Kindeva Drug Delivery (Legacy Meridian Medical Technologies) is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together, as One Team, we will manufacture many more tomorrows. ROLE SUMMARY The QC Analyst 2 is a second level position with training in statistical sampling, inspection and physical testing of incoming materials for conformance to approved written specifications, Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), and Food and Drug Administration (FDA) regulations. ROLE RESPONSIBILITIES Inspects components, assemblies, drug product containers, packaging and labeling according to approved written material specifications. Performs physical testing of assemblies and finished devices according to approved written material specifications, test records and batch records. Creates in-process and carton labeling according to approved bill of material documents. Follows GMP documentation practices on labeling, logbooks, test records, batch records and other controlled documentation. Understands and utilizes American National Standards Institute (ANSI) sampling plans. BASIC QUALIFICATIONS High School/General Education Development (GED) with three years related experience and/or successful completion of a job-specific training program or equivalent combination of education and experience. Knowledge of cGMP regulations and documentation principles. Experience in use of measurement and testing equipment. #LI-Onsite California residents should review our Notice for California Employees and Applicants before applying. Covid-19: Safety for our employees and our communities is a key priority for Kindeva Drug Delivery. Kindeva encourages everyone who can get vaccinated to get vaccinated. Our Covid-19 task force monitors the external environment and will continue to evaluate our policies and procedures. Equal Opportunity Employer: Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Other details Job Family Apprentice II Job Function Technical Professional Pay Type Hourly

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. * 2nd Shift- 6:30pm-7am (rotational) * 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 related life science discipline. Preferred Qualifications: * Knowledge in chemistry or biochemistry, math, and general science. * 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 ********************************************************

- Read blueprints and instructions to comprehend the quality expectations for the product and supplies - Approve or reject raw materials with respect to quality standards and record supplier performance - Select output samples and check them using appropriate methods (measuring dimensions, testing functionality, comparing to specifications etc.) - Use automated systems to perform complex testing procedures - Maintain records of testing, information, and various metrics such as number of defective products per day etc. - Inspect procedures of the entire production cycle to ensure they are efficient and comply with safety standards - Monitor the use of equipment to ensure it is safe and well-maintained and discard any that do notmeet requirements - Prepare and submit reports to the quality manager - Read blueprints and instructions to comprehend the quality expectations for the product and supplies - Approve or reject raw materials with respect to quality standards and record supplier performance - Select output samples and check them using appropriate methods (measuring dimensions, testing functionality, comparing to specifications etc.) - Use automated systems to perform complex testing procedures - Maintain records of testing, information, and various metrics such as number of defective products per day etc. - Inspect procedures of the entire production cycle to ensure they are efficient and comply with safety standards - Monitor the use of equipment to ensure it is safe and well-maintained and discard any that do not meet requirements - Prepare and submit reports to the quality manager

About the Role:

9 Suggestions are available **Quality Tech / Quality Control Analyst I - 2nd Shift** Location 9301 Olive Boulevard, St. Louis, Missouri, 63132, United States Category Integrated Supply Chain & Procurement Job Id req473344 JOB DESCRIPTION **Join a team recognized for leadership, innovation and diversity** **Quality Tech - Quality Control Analyst I - 2nd Shift 2p-11p** As a Quality Control Analyst I here at Honeywell, you will play a crucial role in maintaining our organization's commitment to exceptional quality standards. Your responsibilities will involve conducting inspections and tests, analyzing data, and collaborating with cross-functional teams to drive continuous improvement. You'll work out of our St. Louis location onsite. **Position Overview:** Assure acceptance of quality materials, production and shipment of quality parts and conveyor equipment. This will be performed in accordance with customer requirements and Company objectives while ensuring employee safety and job satisfaction. **Key Responsibilities:** Testing and Evaluation: * In process inspection - Check parts and assemblies during the fabrication or build process. Coordinates with shop supervisors to teach and ensure first piece and in process inspections are completed. * Shipping inspection - Check assemblies to design requirements prior to shipping and coordinate resolution with appropriate personnel. * Non-Conformance/RCCA - Follows up and coordinates with originator and/or recipient for clarity and updates. Will ensure timely corrections or improvements in a timely manner. Monitor and evaluate the results of the change to ensure only positive impact of the change. Quality Assurance Process: * Participate in the implementation of quality assurance processes and methodologies. * Support the development and refinement of quality standards and procedures. * Collaborate with development/engineering teams to ensure quality is integrated throughout the product lifecycle. Documentation and Compliance: * Maintain accurate records of testing protocols, results, and discrepancies. * Ensure compliance with industry standards and organizational policies regarding quality assurance. * Calibration & Testing in accordance with ISO requirements. Continuous Improvement: * Work with cross-functional teams to promote ongoing quality improvement initiatives. * Stay current with industry trends, tools, and technologies in quality assurance to enhance efficiency and effectiveness **Additional Information:** The Quality Tech may also be expected to participate in ongoing training and professional development opportunities to better understand quality standards and practices. Organizational Fit: This is a 2nd shift position. The Quality Tech role will be responsible for the evaluation of new QA/QC systems and maintenance of existing QA/QC systems often situated within a dedicated quality assurance team, providing support across various projects and contributing to the overall quality culture within an organization. **BENEFITS OF WORKING FOR HONEYWELL** In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays. The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. **MUST HAVES:** * 5+ years combined experience in Quality Assurance and Manufacturing. * Practical use/application of blueprint reading, root cause analysis and problem solving. **WE VALUE:** * Associate degree, Quality Assurance, Mechanical or Manufacturing Engineering or related field. * Requires exceptional communication skills at all levels. May substitute experience for education as appropriate. * Knowledge of quality standards such as ISO, Six Sigma * Ability to work collaboratively in a team environment. * PC skills with strong knowledge of Office Software such as MS Word, Excel, Access and Power Point **Additional Information** * **JOB ID:** req473344 * **Category:** Integrated Supply Chain * **Location:** 9301 Olive Boulevard,St. Louis,Missouri,63132,United States * Exempt Global (ALL) Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status. ** Recommended jobs based on your profile** No recommendations found Location 2221 Industrial Road, Nebraska City, Nebraska, 68410, United States Integrated Supply Chain & Procurement req471579 Join a team recognized for leadership, innovation and diversity. As an Experienced Manufacturing Engineering Technician here at Honeywell, you will play a crucial role in supporting our manufacturi... Location 315 E Stephenson St, Plant 1, Freeport, Illinois, 61032-4353, United States Integrated Supply Chain & Procurement HRD249906 Improve business and family comfort, protection and productivity. Be part of a team that applies its expertise and knowledge to develop, implement and maintain method and processes in the manufactu... Location 2520 S Walnut Rd, Plant 4, Freeport, Illinois, 61032, United States Integrated Supply Chain & Procurement req468029 Location 2221 Industrial Road, Nebraska City, Nebraska, 68410, United States Integrated Supply Chain & Procurement HRD249201 Location 315 E Stephenson St, Plant 1, Freeport, Illinois, 61032-4353, United States Integrated Supply Chain & Procurement HRD246740 Improve business and family comfort, protection and productivity. As a Manufacturing Engineering Industrial Automation here at Honeywell, you will play a crucial role in ensuring the quality, effic... Location 315 E Stephenson St, Plant 1, Freeport, Illinois, 61032-4353, United States Integrated Supply Chain & Procurement HRD249388 Location United States Integrated Supply Chain & Procurement req460168 Location United States Integrated Supply Chain & Procurement req460247 **Your Privacy**

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 (CDMO), the Quality Scientist position will perform quality control activities in support of GMP products within the stability and release ADC (Antibody drug conjugates) team. The position will report to Supervisor of ADC testing team. Shift: Monday through Friday from 2pm-10:30pm. Perform (timely) analytical testing and other activities to support cGMP release, in process and stability testing of drug substances and drug products. Provide complete and accurate records consistent with quality guidelines and good documentation practice (GDP) requirements. Perform data review for GMP testing. Ensure quality through adherence to GMP requirements. Complete the volume of work required to achieve group/departmental goals and meet deadlines and communicate the status of operations and bring deviations to the attention of the supervisor. Participate as needed in quality audits, provide complete and accurate records consistent with quality guidelines and GDP requirements. Provide complete and accurate records consistent with quality guidelines and GDP requirements. Interface with customers and cross-functional departments as needed. Train personnel and act as a technical consultant as needed and lead process improvement initiatives. Perform complex assays and processes requiring a higher level of skill and knowledge as well as identify problems and limitations of the analysis. Perform advanced troubleshooting utilizing technical knowledge and theory. Design basic experiments, evaluate data, and draw conclusions. Provide logical explanations and potential solutions. Conduct training on complex analytical procedures. Train and coach, the associates, and senior associates within the team Contribute to support functions of the lab (eg. Maintain equipment's, prepare reagents, restock lab supplies, and waste disposal). Physical Attributes: Perform tasks while wearing personal protective equipment such as chemical protective clothing, goggles, respirator, gloves, etc. Lift, push, and or pull up to 40 pounds. Who You Are: Minimum Qualifications: Bachelor's degree in chemistry, Biochemistry, Biology, or other life science discipline 10+ years' experience in analytical chemistry. OR Master's degree or higher in life science discipline. 5+ years' experience in analytical chemistry. Preferred Qualifications: 5+ years of cGMP experience in pharmaceutical, biopharmaceutical or similar industry Experience with ICE, Solo VPE, UV-Vis, KF, GC, LCMS, IC, CGE, and HPLC is highly desirable along with Chromeleon software. Strong technical writing and scientific reasoning Experience with Trackwise, Chromeleon, LIMS and SAP. ELISA, Data Integrity, and ALCOA. Strong command of Microsoft excel word, smart sheets and power point. Antibody Drug Conjugate (ADC) testing experience. Experience in lean lab practices and continuous improvement initiatives. Strong technical writing, root cause analysis and scientific reasoning. Able to excel in a team setting in a dynamic environment where shifting priorities are not uncommon. 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 ********************************************************

Workplace Type: Onsite At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. **Position Summary** The QC Laboratory Lead / QC Scientist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This position is responsible for generating leading quality control initiatives with minimal supervision including second sourcing, developing test methods and troubleshooting lab and product issues in accordance with the requirements for ISO, FDA QSR, and STERIS policies. This would include but is not limited to: developing test methodologies and validation methods, and audits. **Duties** * Assist with developing test methodologies and procedures * Assists / trains Lab Techs and Specialist * Works with QS on internal and external audits and audit training * Assists with developing and validating methods * Support and / or develop chemical testing procedures * Support and /or develop technical requirements for raw material specifications based on input from potential vendors, product development staff, and process engineering * Coordinate Failure Investigations by designing and performing lab scale simulation of products made in the plant * Troubleshoots & calibrates Lab equipment * Maintain and order lab supplies * Lead: Assists with directing work of lab employees * Lead: In supervisor's absence will manage day to day operations including, scheduling, submit requisition to obtain lab supplies, and reviewing documentation **Education Degree** * Bachelor's Degree in Science **Requirements** * Minimum 6 years relevant lab testing in a regulated industry (i.e. FDA/ISO13485) required. * Knowledge of standard quality tools such as FMEA (Failure Modes Effect Analysis), Root Cause Analysis, and Statistics #LI-BN1 STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 17,000 associates and Customers in more than 100 countries. If you need assistance completing the application process, please call 1 . This contact information is for accommodation inquiries only and cannot be used to check application status. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity. The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location's HR Office during normal business hours. Location: St. Louis, MO, US, 63133

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 a Process Chemist III, 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: Optimize our process in order to achieve the lowest manufacturing cost while maintaining high quality (25% of time). Continuously monitor yield and raw material usage of target, take action on issues that arise (20% of time). Assist operations and quality in trouble shooting process problems (15% of time). Serve as manufacturing representative on new product / process introductions into the manufacturing plant and function as a liaison between production and R&D (15% of time). Evaluate the impact of raw material from new suppliers prior to introduction into existing processes. Monitor performance in yield and quality (10% of time). Lead or serve as a key member on assigned quality improvement teams (5% of time). Train operations and quality team members when required (5% of time). Assist in development and maintenance of operation procedures, job models and exception condition reports. Identify and help implement solution to chronic exceptions. (5% of time). What You'll Bring: M.S. or B.S Degree in Chemistry or Chemical Engineering with 5+ years of industry experience. Proven troubleshooting record with emphasis on 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. 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

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Description No description available. **Audit and Assurance Associate - Fall 2025** Audit and Assurance St. Louis, MO | Chesterfield, MO | Hybrid The **Audit and Assurance Department** of one of the fastest-growing accounting firms in the country is seeking an **Associate** who is motivated to learn, excited to collaborate and passionate about delivering outstanding results. This individual will have a direct impact on our firm's mission of serving as a catalyst for those striving to achieve their highest potential. In this role, you will be primarily responsible for planning and conducting audits of client financial statements, assisting with determination of appropriate audit methodology, assisting with performance of risk assessments and developing relationships with client companies. To succeed in this role, you should have a foundational understanding of accounting principles with a desire to build your technical skills and knowledge. This position is open to candidates available to start in September 2025 or January 2026. Additional start dates can be discussed as necessary. **What You'll Do:** * Conduct audits of client company financials to ensure compliance with GAPP and other accounting standards * Determine the effectiveness of internal controls and the potential impact of internal control deficiencies * Examine records to ensure proper recording and authorization of transactions, compliance with policies, and applicable laws * Prepare detailed reports of audit findings and recommendations for client companies * Prepare portions of compilation, review, and audit engagements * Perform other duties as assigned **What We're Looking For:** * Understanding of audit and attest services * Knowledge of FASB standards, GAAP, and GAAS * Strong analytical and mathematical abilities * Excellent written and verbal communication skills * Detail-oriented with strong organizational skills * A client service orientation with the ability to interact at all levels of management * Ability to work autonomously * Proficiency in Microsoft Office, especially Excel and Word **Your Qualifications** * Bachelor's Degree in Accounting required * CPA or CPA Candidate **Why You'll Love Working Here:** At Anders, taking care of our employees is a top priority. Our welcoming and collaborative culture will make you feel like a part of the team from day one. From professional development opportunities to benefits that directly impact mental, physical and financial wellness, Anders offers unique incentives that enrich your life and facilitate growth, including our Work Flex program which gives you the opportunity to work at our Chesterfield office, our Downtown St. Louis office, adopt a hybrid approach or even switch between these options as you prefer. Learn more about our full benefit offerings and Work Flex program at our Life at Anders page: All applicants for this position must be authorized to work in the United States now and in the future without requiring sponsorship. For over 55 years, Anders has delivered full-service accounting, tax, audit and advisory services to growth-oriented companies, organizations and individuals. Every day, our partners and staff serve as a catalyst for those striving to achieve their highest potential and carry this mentality on to our clients and community. Ranked #74 on Accounting Today's List of To

The National Security Customer Group of SAIC is seeking an Information Security Analyst for the Test and Integration Laboratory to support an IT Service Management effort for USTRANSCOM located at Scott Air Force Base (AFB) in Illinois approximately 23 miles from St. Louis, MO. The USTC Managed Information Technology Services (MITS) contract is intended to provide strategic, technical, and program management guidance and support services to facilitate the operations and modernization of the combatant command's infrastructure, systems, and applications. This support will be provided to the USTC Command, Control, Communications & Cyber Systems Directorate (TCJ6). The successful candidate will conduct service transition analysis for the Test and Integration Laboratory and be responsible for working on high-visibility or mission critical aspects of a given program and performing all functional duties with some oversight. Additional responsibilities may include: · Develop and document TIL Plans for all approved Service Design Packages. · Coordinate TIL Plans with and present them to the Government. · Review and participate in engineering and/or release review boards. · Verify as satisfactory the results of all TIL Plans. · Leverage the TIL to test and validate hardware and software interoperability. · Complete and provide evaluation reports. · Provide and execute processes to move applications and hardware through a functional test and security evaluation workflow. · Assist security SME's by capturing artifacts and scheduling scans used in security evaluation reports for all software and hardware on the USTC enterprise. · Work with Domain and Network SMEs to complete integration and functionality verification. · Work with Domain, Network, and Boundary SMEs to actualize mitigations suggested in the security evaluation. This position is for Monday through Friday, normal business hours. However, employee may be required to provide after-hours and weekend support during planned or emergency events. **Qualifications** **Required Qualifications** · BA/BS. · Minimum of nine (9) years of experience. · DoD Secret clearance or higher. · Must have at least one of these IAT Level II certifications: Security+, CECCNA-Security, CySA+ **, GICSP, GSEC, CND, SSCP. · Must have at least one Computing Environment (CE) certification or certificate for the technical area of responsibility for Network support/defense (e.g., Splunk, Cisco, McAfee, etc.) OR Operating System (e.g., Microsoft, Linux, Solaris, etc. **Desired Qualifications** · MA/MS. · ITIL V4 Foundations certification. · Project Management Professional (PMP) or Google Project Management certification. · One of the IAM Level II certifications: CAP, CASP+ CE, CISM, CISSP (or Associate), GSLC, CCISO, HCISPP. Target salary range: $80,001 - $120,000. The estimate displayed represents the typical salary range for this position based on experience and other factors. SAIC accepts applications on an ongoing basis and there is no deadline. Covid Policy: SAIC does not require COVID-19 vaccinations or boosters. Customer site vaccination requirements must be followed when work is performed at a customer site. REQNUMBER: 2415113 SAIC is a premier technology integrator, solving our nation's most complex modernization and systems engineering challenges across the defense, space, federal civilian, and intelligence markets. Our robust portfolio of offerings includes high-end solutions in systems engineering and integration; enterprise IT, including cloud services; cyber; software; advanced analytics and simulation; and training. We are a team of 23,000 strong driven by mission, united purpose, and inspired by opportunity. Headquartered in Reston, Virginia, SAIC has annual revenues of approximately $6.5 billion. For more information, visit saic.com. For information on the benefits SAIC offers, see Working at SAIC. EOE AA M/F/Vet/Disability

. This National Guard position is for a INTERNAL CONTROL ANALYST (TITLE 5), Position Description Number T59034P1 and is part of the IL 126, National Guard. Responsibilities As a INTERNAL CONTROL ANALYST (TITLE 5), GS-0501-11, you will function as the Financial Management (FM) focal point for the Financial Improvement and Audit Readiness (FIAR) initiative, as well as advise the Comptroller and Wing Commander in all matters relating to FM FIAR within the FM community. Examine all areas to determine the effectiveness of procedures and also determines if supervisors are recording quality data upon which accurate management conclusions and decisions are based. Provide technical internal control advice on military pay, civilian pay, travel pay, disbursing and collection, accounting, vendor and contract pay, budget, and systems administration. Review military pay vouchers, travel payments, and entitlement documents to ensure supporting documents are applicable and valid. Examine all functional areas and determines the effectiveness of procedures, the integrity of financial and accounting data, and other decision-support criteria used by management. Examine all pay-related and accounting and financial functions to ensure internal accounting systems and administrative controls are sufficient to reasonably ensure all obligations and payments comply with applicable laws. Ensure funds are safeguarded against waste, loss and misappropriation, and all remittances and payments are properly accounted. Work closely with the financial management staff to extract needed information for targeting and studying suspected potential weaknesses. Ensure quality assurance standards and internal controls are in place within the comptroller office and reports discrepancies to the FM. Identify needed system changes and conducts system change tests to ensure changes produce the desired matches such as, duplicate payments, collections, and reconciliations. Gather data, track discrepancies, prepare trend charts, and facilitate discussions with personnel at financial or QA meetings. Ensure all open discrepancies are consistently and aggressively addressed and resolved through completion. Cross-feed various reports and bulletins, on a routine basis, through various electronic communications such as, emails and websites throughout the Wing financial management community. **This is NOT an all-inclusive list of duties. ** Requirements Conditions of Employment Acceptance of an excepted service position constitutes concurrence with these requirements as a condition of employment. Males born after 31 December 1959 must be registered for Selective Service. Federal employment suitability as determined by a background investigation. May be required to successfully complete a probationary period. IAW The Fair Chance Act, Agency employees may not request criminal history information at the point of initial application, upon receipt of an application, or prior to, during or after a job interview. If an Optional Form (OF) 306, Declaration of Employment is submitted prior to the point of a conditional offer, questions related to background information section may not be asked. This position is covered by the Domestic Violence Misdemeanor Amendment (30 Sep 96) of the Gun Control Act (Lautenberg Amendment) of 1968. An individual convicted of a qualifying crime of domestic violence may not perform the duties of this position. Irregular and/or overtime (compensatory) hours may be required to support operational requirements or contingencies or may be required to work hours outside of the normal duty day. One year of specialized experience equivalent to the lower grade level in the Federal service in order to be considered for this position. Certification Level 2: THIS IS A FINANCIAL MANAGEMENT Level 2 Certified position designated as such in accordance with the National Defense Authorization Act (NDAA) 2012, Public Law 112-81, Subtitle F-Financial Management, section 1051, amending 10 United States Code, section 1599d. Incumbent of this position is required to comply with all Department of Defense and Department of the Army requirements of this certification program. This certification requirement is a condition of employment for this position. Failure to obtain this certification within the required time may subject the incumbent to adverse action. Participation in direct deposit is mandatory. Recruitment and relocation incentives may be available for this position. Qualifications GENERAL EXPERIENCE: MUST possess the experience, education, or training in collecting and analyzing data effectively, efficiently, and accurately; applying procedures and directives by reading and interpreting program material; presenting formal training presentations and briefing; preparing reports and presentation formats. Time-In-Grade Requirement: Applicants who are current Federal employees and have held a GS grade any time in the past 52 weeks must also meet time-in-grade requirements by the closing date of this announcement. For a GS-11 position you must have served 52 weeks at the GS-09 Level. An SF-50 that shows your time-in-grade eligibility must be submitted with your application materials. SPECIALIZED EXPERIENCE: GS-11 Level - MUST possess the experience, education equivalent to one-year at the next lower GS-09 Level, in providing analytical reasoning in the identification, analysis, and evaluation of financial issues and developing alternative solutions; competencies in analysis, research, writing, and judgment; knowledge and skill in the application of related laws, regulations, precedents, methods and techniques of budgeting; following established methods and procedures; use practical knowledge of the operations, procedures, and policies of specific program areas or functional assignment. OR Education Substitute: Ph. D. or equivalent doctoral degree or 3 full years of progressively higher-level graduate education leading to such a degree or LL. M. , if related. NOTE: You must submit a copy of official transcripts. OR Combination of Specialized Experience and Education: You may meet the qualifications requirement for this position by combining your specialized experience and appropriate graduate level education according to the following formula: (a) your total months of full-time specialized experience as a percentage of a 12-month total; PLUS (b) your total number of qualifying graduate semester or quarter hours as a percentage of three years of progressively higher-level graduate education. The total of the two percentages must equal at least 100 percent. Experience refers to paid and unpaid experience, including volunteer work done through National Service programs (e. g. , Peace Corps, AmeriCorps) and other organizations (e. g. , professional; philanthropic; religious; spiritual; community, student, social). Volunteer work helps build critical competencies, knowledge, and skills and can provide valuable training and experience that translates directly to paid employment. You will receive credit for all qualifying experience, including volunteer experience. Verbiage displayed on your resume or application must contain your own words. You may refer to position descriptions, i. e. the general and specialized experience located within the vacancy announcement, to assist with describing work experiences; however, resumes or applications received in verbatim will not be considered. In your resume you will need to address the general and specialized experience listed below. Please use as much detail as needed, giving dates (months and years) of the experience, position title and how the experience was gained. This information is needed to determine if you are qualified for the position. Education If you are using Education to qualify for this position, applicants may also qualify on the basis of education as follows: To qualify based on education for the GS-11 level, you must have successfully completed a Ph. D. or equivalent doctoral degree or 3 full years of progressively higher-level graduate education leading to such a degree or LL. M. , if related. (Note: You must attach a copy of your official transcripts. ) OR Combination of Specialized Experience and Education: You may meet the qualifications requirement for this position by combining your specialized experience and appropriate graduate level education according to the following formula: (a) your total months of full-time specialized experience as a percentage of a 12-month total; PLUS (b) your total number of qualifying graduate semester or quarter hours as a percentage of three years of progressively higher-level graduate education. The total of the two percentages must equal at least 100 percent. You must provide OFFICIAL transcripts or other documentation to support your educational claims. PLEASE NOTE: Education must be accredited by an accrediting institution recognized by the U. S. Department of Education in order for it to be credited towards qualifications (particularly positions with a positive education requirement). Therefore, applicants must report only attendance and/or degrees from schools accredited by accrediting institutions recognized by the U. S. Department of Education. Applicants can verify accreditation at the following website: *********** ed. gov/admins/finaid/accred/index. html. All education claimed by applicants will be verified by the appointing agency accordingly. FOREIGN EDUCATION: If you are using education completed in foreign colleges or universities to meet the qualification requirements, you must show that the education credentials have been evaluated by a private organization that specializes in interpretation of foreign education programs and such education has been deemed equivalent to that gained in an accredited U. S. education program; or full credit has been given for the courses at a U. S. accredited college or university. For further information, visit: ************ ed. gov/about/offices/list/ous/international/usnei/us/edlite-visitus-forrecog. html Additional Information If you are a male applicant who was born after 12/31/1959 and are required to register under the Military Selective Service Act, the Defense Authorization Act of 1986 requires that you be registered or you are not eligible for appointment in this agency (************ sss. gov/RegVer/wf Registration. aspx). If you are needing some extra information regarding Federal Resumes, you should consider these tips from USA Jobs: USAJOBS Help Center | What should I include in my federal resume.

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Title: Quality Engineer/Scientist II Requisition ID: When you're part of the team at ThermoFisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. Location/Division Specific Information St. Louis, MO/Biologics Division How will you make an impact? The Quality Engineer/Scientist II will operate in a high-throughput environment, completing investigations on behalf of the various QC testing groups, but primarily for QC Analytical. This person is responsible for leading multiple investigations simultaneously and ensuring on-time completion through dedication, tenacity and relationship building with our partners in QA and the various testing groups. As a strong individual contributor, the Quality Engineer/Scientist III will maintain a steady record closure rate while working on moderate complexity investigations, with some variance in difficulty based on what becomes available. They will also assist more junior investigators when needed and will participate in QC compliance activities related to audits and continuous improvement. What will you do? • Occasionally conduct RAPID meetings with QA and QC staff • Use TrackWise software to author investigations • Be responsible for compliance-related deliverables including: audit support/observation response, presentations to senior management and site leadership, and generating trend reports to better understand the weaknesses in our organization and make suggestions for improvement • Support compliance culture initiatives and assist manager and supervisor with implementing these changes. • Develop the team through creation/delivery of proactive and reactive trainings. • Assist with the development of tools and resources to improve our investigative process. • Assist Scientist I investigators when needed • Average 1 deviation/OOS/CAPA record closures per week • Complete overdue assessments and file record extensions as required • Author/revise SOPs (limited) • Assist with formulating continuous improvement strategies and timelines • Other job duties as assigned How will you get here? • Minimum of an Associate's degree • Bachelor's degree in science related field is a plus but not required • 3 or more years working in a GMP regulated environment or Quality Role (QA or QC) • 2 or more years as an investigation writer, CAPA developer, or auditor. • TrackWise and TapRooT experience is preferred. Knowledge, Skills, Abilities • Knowledge of GMP regulations • Knowledge of Good Laboratory Practices (GLP) and Good Documentation Practices (GDP) • Able to read, write, and communicate in English. • Able to use standard computer programs such as SmartSheet, PowerBI, MS Excel, Word, and PowerPoint. • Able to inspire innovation and team effectiveness. • Able to work in an evolving environment and adapt to a variety of internal customer's needs • Strong computer, scientific, and organizational skills. • Strong communication skills including active listening, facilitation, and escalation • Enjoys collaborative efforts both internal and external to the department Physical Requirements / Work Environment: Wear gloves and other PPE to enter laboratory spaces Sit for extended periods of time. This role requires a lot of desk time and meeting time. Benefits: We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, resolve difficult scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! **************************** Disclaimer: This job description presents the general content and requirements for the performance of this job. The description is not to be construed as an extensive statement of work, responsibilities, or requirements. Managers and supervisors may assign other duties as needed. Nothing contained herein should be construed to describe an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully abide by all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. Thermo Fisher Scientific is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We strive to build an inclusionary work environment and prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

A career with MilliporeSigma is an ongoing journey of discovery: our 57,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany. At MilliporeSigma, the Quality Control Scientist position is responsible for overseeing and leading out of specification investigations and non-conformance deviation investigations associated with release, stability and in-process samples. The Quality Control Department at this site supports quality functions for Active Pharmaceutical Ingredients (APIs) under Good Manufacturing Practice guidelines (ICHQ7). The position is also responsible for execution and management of quality control CAPA projects and change controls. The QC Scientist must demonstrate strong technical knowledge, be familiar with scientific/regulatory principles, possess initiative, and maintain a strong commitment to scientific excellence. Manage and lead Quality Control OOS and deviation investigations to adequately identify root cause and assign appropriate corrective and preventative actions (CAPAs) to prevent recurrence. Interact with the laboratory, manufacturing, quality assurance, packaging and development personnel to ensure adequate root cause is identified. Work within various internal departments to improve and execute processes used in an ICHQ7 environment. Write, review, and approve operating procedures, specifications, and other QC controlled documents. Occasionally support and perform detailed data review for analytical data packets generated by quality control for compliance with cGMP, internal SOPs and Specifications. Who You Are: Basic Qualifications: Bachelor's degree in Chemistry, Biochemistry, Biology or related life science discipline 5+ years of experience within a cGMP environment 1+ years of experience working with ICH Q7 Strong technical writing, scientific reasoning and attention to detail Preferred Qualifications: API manufacturing and testing knowledge and/or experience 5+ years of work experience in pharmaceutical, biopharmaceutical or similar industry Knowledge of 21CFR210 and ICH Q7. Experience using root cause analysis tools such as Fishbone, 5Whys, and pareto charts Experience in OOS/OOT investigations, CAPA and non-conformance deviations Good computer skills, including proficiency in MS Word, MS Excel, MS PowerPoint, and the ability to learn and operate other specific application software Excellent written and verbal communication and customer interfacing skills Excellent writing skills and experience writing technical documentation and reports RSRMS What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life! Curious? Apply and find more information at ************************* The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

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. If you enjoy a challenging and fast paced environment that provides opportunity to learn and utilize a multitude of QC instrumentation and methodology, the Virbac QC Lab has an immediate opening for a QC Analytical Chemist or Chemist Principal in the Finished Product/Stability group. In this role, you will be responsible for the testing of multiple product lines for Product release, Stability conformance, and In-Process evaluations. You will be working in a GMP regulated environment on a daily basis evaluating products to ensure that they meet quality standards and product specifications. A Bachelor's degree in Chemistry, Biology, Biochemistry or other related science field is required. An Associate's degree in Chemical Technology may be considered as well, dependent on the years of related experience. Experience using the following types of instrumentation is desired: HPLC, GC, UHPLC, UV-vis, pH meter, Rheometer, Densitometer, Friabilator, Hardness Tester, Karl Fisher Autotitrator, Drying and Vacuum ovens, and analytical balances. Success in this role is dependent on an individual's ability to perform work assignments independently, understand cGMP rules and regulations and be able to consistently and accurately execute all testing and document according to them. This individual must be able to follow procedures as written, manage time proficiently, maintain an organized work area and efficient dataflow, consistently maintain a high degree of focus with great attention to detail, and execute all GMP requirements for working in a Pharmaceutical environment. Individuals that are accountable, cooperative, flexible, self-motivated, and possess great organizational skills are desired for this role. This role requires standing, lifting, reaching, and moving on a consistent basis. All chemists in the QC lab utilize various chemicals, reagents, and solvents on a routine basis. Personal protective gear is provided and is required to be worn while in the QC lab (safety glasses, lab coat, and gloves). Excellent time management skills and the ability to transition proficiently to different test assignments are key bench skills required for this position. This challenging position is located in Bridgeton, MO and comes with an excellent benefits package including generous time off, 401k + match, life, medical, dental, 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!

QC Scientist I Job ID: 24-02347 Job title: QC Scientist I- Gel Electrophoresis Duration: 6 Months assignment What will you do? * Conduct routine compendial, purity, and impurity testing of pharmaceutical release, stability, and in-process samples by internally developed, qualified, and validated test methods. * Support qualification and validation of test methods for pharmaceutical concentration, purity, and impurity testing. * Assists in preparing regulatory documents and other communications with outside agencies, clients, and/or colleagues from other corporate sites. * Perform all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintain the necessary compliance status required by company and facility standards. Education * Associates Degree with 2 or more years of relevant work experience or a Bachelor's degree with GPMP laboratory experience, STEM degree preferred, technical skills, a * HS Diploma or GED required Experience * 0 - 1 year of experience in the biopharmaceutical or pharmaceutical industry. Knowledge, Skills and Abilities * Good knowledge and understanding of chemistry and analytical instrumental technologies * Good knowledge of qualitative and quantitative chemical or microbiological analysis. * Good presentation skills to present information to customers, clients, and other employees. * Routine use of MS Excel, MS PowerPoint, MS Access, and MS Word is essential. * Ability to write standard operating procedures, simple protocols, and reports. * Scientific techniques including: Protein Concentration via Shimadzu and SoloVPE, Residual DNA via Real Time PCR (Polymerase Chain Reaction), Capillary Gel Electrophoresis, Imaged Capillary Isoelectric Focusing (iCIEF), Dot Blot, Compendial Testing: pH and osmolality * Job details *

This lab supports those functions in high volume in the spring so the seed treatment can get into the ground in time for spring planting. Main responsibilities of this role will be to perform QC for microbial products which includes viability assays, pH measurement, microbial morphology inspection with microscope, colony PCR, etc. Will be responsible for basic plating, pipetting, and plant based assays. This role requires a lot of repeat testing but consistency and attention to detail are key throughout. They will be testing for multiple commercial product lines, probably equating to 1000s of samples. This will involve basic pipetting, colony counting, aseptic technique and sample prep. Some work will be done by hand, other functions are more automated. ● Deliver time-sensitive QC projects on time with required standards and documentations, according to SOPs ● Use aseptic techniques to sample microbial products with serological pipettes, run plate-based serial dilution, plate diluted microbial products with spread or spot plating techniques. ● Support all general lab operations necessary to keep the lab running safely and efficiently, including waste removal, hazardous waste disposal, safety policies, equipment maintenance, etc. Skills qc testing, plate based assays, Assay, Aseptic technique, Plating, pipetting, multichannel pipetting Top Skills Details qc testing, plate based assays, Assay, Aseptic technique, Plating, pipetting Additional Skills & Qualifications ● Ideal to have BS degree or equivalent lab experience, preferably in Microbiology or a related field required. ● Aseptic technique and plating experience, as well as pipetting required (does not have to be multi-channel pipetting for these roles) ● Plate-based assay experience very helpful ● Ability to follow SOPs. Good organization skills with attention to details. ● Ability to work independently. ● Ability to lift 50 lbs. Experience Level Entry - Intermediate Level Pay and Benefits The pay range for this position is $25.00 - $27.00 * 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 St. Louis,MO. Application Deadline This position will be accepting applications until Jan 18, 2025. 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. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.