Quality Control Analyst jobs in Saint Peters, MO

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 in California, Colorado, District of Columbia, Illinois, Maryland, Minnesota, New Jersey, New York or Washington 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 $94.23 Colorado $30.67 to $81.39 District of Columbia $32.69 to $86.68 Illinois $28.41 to $81.39 Minnesota $30.67 to $81.39 Maryland $30.67 to $81.39 New York/New Jersey $28.41 to $94.23 Washington $32.69 to $86.68 #LI-NA-FY25 Locations

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, Proteins & Nucleotides 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. This position is based in St. Louis at 3500 Dekalb Street. 2nd Shift- 6:30am-7pm (rotational) Safely perform operations to meet quality expectations Perform multi-disciplined, established processes, assays and/or unit operations, primarily those higher level of skill and knowledge Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal) Communicate the status of operations and bring deviations to the attention of supervisor Ensure all applicable logbooks have been filled out completely by current procedures Identify problems and limitations of analysis Perform routine troubleshooting 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 Life Science (Chemistry, Biochemistry, Biology, etc.) or Engineering (Chemical Engineering etc.) 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 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!

The Opportunity: Education: Bachelor's degree in chemistry, Biology, Biochemistry or other science related field. Experience: 3+ years of laboratory experience. Experience in GC, HPLC, required. Conducts routine and non-routine chemical analysis of raw materials, in-process formulations, and final products to specifications. Utilize and operate laboratory equipment and instruments according to laboratory work instructions or procedures such as GC, HPLC, spectrophotometry, and titration. Interpret test results and report findings in a clear, concise, and accurate manner. Performs calculations on data generated for reports and results. Perform technical review of laboratory data. Calibrate and maintain laboratory instruments and equipment. Enter final results and raw data for samples and products in LIMS. Supports investigations to help identify root causes and corrective actions under the guidance of Quality Control Management. Execute method validation and/or method transfers. Handle and dispose of hazardous material using all appropriate safety PPE and equipment. Supports and provides training for new analysts. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at ****************************** and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. For more information about equal employment opportunity protections, please view the Know Your Rights poster. 3rd Party Non-Solicitation Policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.

Why Stifel Stifel strives for a culture that puts its clients and associates first: a culture where everyone belongs, everyone is welcome, and everyone contributes to the success of our clients, their careers, and the firm as a whole. Let's talk about how you can find your place here at Stifel, where success meets success. What You'll Be Doing If you are someone that has a skill set similar to an Internal/External Auditor, likes to be exposed to many areas of a company and people and likes to learn something new on a regular basis, then this job is for you. This is an ever-changing and evolving role. The Operations Control Analyst, under general supervision, will plan and perform operational and regulatory control reviews of various operations departments to evaluate the adequacy and effectiveness of the operations risk management process, system of internal control structure, and the quality of performance in carrying out assigned responsibilities. What We're Looking For Responsible for 17a-5 documentation that includes the identification of risks and controls, evaluating and testing controls, and the attestation process for compliance with 17a-5. Executes operational risk-based reviews that could have financial, compliance, and regulatory components. Reviews and tests manual and automated processes. Collects and analyzes data to identify improvements and efficiencies. Prepares detailed reports of findings and recommendations and communicates results to operations senior management. Examine and evaluate financial and information systems, document findings, and recommend controls to ensure system reliability and data integrity. Examines the systems and processes established by operations to ensure compliance with policies, procedures, laws, and regulations that could significantly impact operations. Examines financial and operating information's accuracy, reliability, timeliness, and integrity and the means used to identify, measure, classify, and report such information. Performs other reasonably related business duties as assigned. What You'll Bring Demonstrated understanding of risk and internal control concepts. Experience in evaluating the design and operating effectiveness of internal controls. Enhanced knowledge of industry rules and regulations. Sound writing and verbal communication skills. Knowledge of finance and accounting principles and practices, the financial markets, banking, and the analysis of reporting of financial data. Ability to use logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or problem approaches. Ability to maintain confidentiality and consider the relative costs and benefits of potential actions to choose quickly and multi-task. Ability to organize, prioritize, and manage multiple tasks, meeting all specific deadlines. Build and maintain collaborative relationships with both internal and external clients. Education & Experience Minimum Required: Bachelor's degree in accounting, finance, business administration, or related field. Minimum Required: 2-4 years of internal audit, accounting and/or regulatory experience. Licenses & Credentials Minimum Required: Commitment to extending technical skills via professional certification and/or licensing (e.g., CPA, CIA, CFE, or CISA; Series 7, 24, 27, or 99). Systems & Technology Proficient in Microsoft Office Suite with knowledge of PowerPoint and Visio. Proficient in BETA system and knowledge of Smartsheet. About Stifel Stifel is more than 130 years old and still thinking like a start-up. We are a global wealth management and investment banking firm serious about innovation and fresh ideas. Built on a simple premise of safeguarding our clients' money as if it were our own, coined by our namesake, Herman Stifel, our success is intimately tied to our commitment to helping families, companies, and municipalities find their own success. While our headquarters is in St. Louis, we have offices in New York, San Francisco, Baltimore, London, Frankfurt, Toronto, and more than 400 other locations. Stifel is home to approximately 9,000 individuals who are currently building their careers as financial advisors, research analysts, project managers, marketing specialists, developers, bankers, operations associates, among hundreds more. Let's talk about how you can find your place here at Stifel, where success meets success. At Stifel we offer an entrepreneurial environment, comprehensive benefits package to include health, dental and vision care, 401k, wellness initiatives, life insurance, and paid time off. Stifel is an Equal Opportunity Employer.

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Laboratory Analyst II Laboratory Analyst II: As a Laboratory Analyst II, you are an integral part of the high-throughput Global Quality Seed Testing Laboratory, supporting Bayer's Product Supply Organization and collaborating with key customers and colleagues across various functions. Your role involves the timely and accurate preparation, evaluation, and recording of seed analyses, ensuring compliance with Bayer's Environmental, Safety, and Health (ESH) policies, Laboratory Quality Management System (QMS), and regulatory requirements. You will participate in the Management of Change process, contribute to continuous improvement initiatives, and engage in Bayer's Environmental, Safety, and Health safety program and cross-site projects. YOUR TASKS AND RESPONSIBILITIES: * Prepare, evaluate, and record seed analyses accurately and timely; * Complete testing processes under the guidance of Lab Operations Managers and/or Lab Coordinators, ensuring process control, data management, and timely problem-solving and error correction; * Troubleshoot testing processes and ensure appropriate error resolution; * Aid in training new Lab Analysts; * Learn and apply scientific methods and non-routine techniques for analysis as directed by protocols and work instructions, including preparation of reagents, media, controls, and sample preparation; * Participate in the Management of Change process and updates of testing protocols and work instructions; * Work independently within a team environment to ensure compliance with Bayer ESH policies, Laboratory QMS, and regulatory requirements; * Provide oversight and task-related feedback to contingent labor; * Maintain inventory levels of reagents and consumables; * Participate in special projects and teams; * Engage in continuous improvement programs to enhance processes and perform root cause analyses and troubleshooting; * Actively engage in one PSS programs and initiatives; * Participate in Bayer's ESH safety program and cross-site projects and initiatives. WHO YOU ARE: Bayer seeks an incumbent who possesses the following: Required Qualifications: * High School Diploma or GED; * Flexibility to change shift hours, with weekend and overtime work as required. Preferred Qualifications: * Minimum of five years of lab experience with a high school diploma or GED: * Bachelor's degree with 0 years of lab experience, or an Associate of Arts (AA) or Associate of Science (AS) degree with two years of lab experience; * Strong knowledge of basic laboratory techniques; * Fluent in English with the ability to read, write, and speak effectively; * Proficiency in Microsoft Office Suite; * Ability to work as a team member and effectively communicate within a multicultural environment; * Detail-oriented with the ability to multitask in a high throughput environment. Posting will be available through July 16, 2025. Employees can expect to be paid an annual salary range of $48,240.00 - $72,360.00. Additional compensation may include a bonus or commission (if relevant). Other benefits include health care, vision, dental, retirement, PTO, sick leave, etc. If selected for this role, the offer may vary based on market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location: United States : Missouri : Creve Coeur Division: Crop Science Reference Code: 849302 Contact Us Email: hrop_************* Job Segment: Laboratory, Compliance, Law, Supply, Quality Manager, Science, Legal, Operations, Quality

The QC Equipment Coordinator is responsible for the coordination, maintenance, and management of equipment and instrumentation programs within the department. This position also involves the qualification and validation of new equipment. Responsibilities * Build and maintain equipment and programs using the Calibration Management system. * Ensure equipment calibrations, re-qualification, and preventative maintenance schedules align with GMP procedures. * Coordinate visits and maintain service contracts with outside vendors. * Troubleshoot equipment and perform repairs in-house when possible. * Coordinate and qualify new QC equipment. * Author and archive technical documents such as validation protocols and reports. * Train analysts on equipment usage. * Review reports, identify deviations, and author CAPA's when necessary. Essential Skills * Bachelor's degree in Biology, Chemistry, or a related Science field. * Minimum of 5 years experience in a Quality Control Lab within a pharmaceutical or other FDA-regulated industry. * Experience with Calibration Management Systems. * Experience in validating instrumentation or other LC experience, particularly with HPLC. * Demonstrated analytical and instrumentation skills for troubleshooting and system improvement. * Strong technical writing skills for authoring validation reports. Additional Skills & Qualifications * Experience in microbiology, conductivity, and TOC testing. Work Environment The work environment is a large QC Lab with over 30 people working across two shifts. The laboratory is undergoing changes to become more compliant, with high accountability for accuracy and integrity. There is a culture of respect, which is continuously improving. The work pace is high and the workload is substantial. The standard work hours are Monday to Friday, 7:00 AM to 3:30 PM, with flexibility for the candidate within reasonable day hours. There may be a requirement to work 4 hours a month over a weekend to complete rotations. Pay and Benefits The pay range for this position is $70000.00 - $85000.00/yr. PTO, Medical, Dental Vision, 401K Match, Pet Insurance, paid holidays, etc. Workplace Type This is a fully onsite position in St. Louis,MO. Application Deadline This position is anticipated to close on Jul 22, 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. 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.

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Laboratory Analyst II Laboratory Analyst II: As a Laboratory Analyst II, you are an integral part of the high-throughput Global Quality Seed Testing Laboratory, supporting Bayer's Product Supply Organization and collaborating with key customers and colleagues across various functions. Your role involves the timely and accurate preparation, evaluation, and recording of seed analyses, ensuring compliance with Bayer's Environmental, Safety, and Health (ESH) policies, Laboratory Quality Management System (QMS), and regulatory requirements. You will participate in the Management of Change process, contribute to continuous improvement initiatives, and engage in Bayer's Environmental, Safety, and Health safety program and cross-site projects. YOUR TASKS AND RESPONSIBILITIES: * Prepare, evaluate, and record seed analyses accurately and timely; * Complete testing processes under the guidance of Lab Operations Managers and/or Lab Coordinators, ensuring process control, data management, and timely problem-solving and error correction; * Troubleshoot testing processes and ensure appropriate error resolution; * Aid in training new Lab Analysts; * Learn and apply scientific methods and non-routine techniques for analysis as directed by protocols and work instructions, including preparation of reagents, media, controls, and sample preparation; * Participate in the Management of Change process and updates of testing protocols and work instructions; * Work independently within a team environment to ensure compliance with Bayer ESH policies, Laboratory QMS, and regulatory requirements; * Provide oversight and task-related feedback to contingent labor; * Maintain inventory levels of reagents and consumables; * Participate in special projects and teams; * Engage in continuous improvement programs to enhance processes and perform root cause analyses and troubleshooting; * Actively engage in one PSS programs and initiatives; * Participate in Bayer's ESH safety program and cross-site projects and initiatives. WHO YOU ARE: Bayer seeks an incumbent who possesses the following: Required Qualifications: * High School Diploma or GED; * Flexibility to change shift hours, with weekend and overtime work as required. Preferred Qualifications: * Minimum of five years of lab experience with a high school diploma or GED: * Bachelor's degree with 0 years of lab experience, or an Associate of Arts (AA) or Associate of Science (AS) degree with two years of lab experience; * Strong knowledge of basic laboratory techniques; * Fluent in English with the ability to read, write, and speak effectively; * Proficiency in Microsoft Office Suite; * Ability to work as a team member and effectively communicate within a multicultural environment; * Detail-oriented with the ability to multitask in a high throughput environment. Posting will be available through July 16, 2025. Employees can expect to be paid an annual salary range of $48,240.00 - $72,360.00. Additional compensation may include a bonus or commission (if relevant). Other benefits include health care, vision, dental, retirement, PTO, sick leave, etc. If selected for this role, the offer may vary based on market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location:United States : Missouri : Creve Coeur Division:Crop Science Reference Code:849302 Contact Us Email:hrop_*************

Job Title Quality Control Technician II - Micro Requisition JR000015031 Quality Control Technician II - Micro (Open) Additional Locations Provides technical support at an entry level. Will evaluate material and product quality by performing various procedures in the microbiology laboratory. This individual performs analysis on Raw Materials, Finished Products, Stability, water, and environmental monitoring samples using established analytical methods. Job Description ESSENTIAL FUNCTIONS: Follow good documentation practices for the accurate and timely documentation of all activities Receive media, reagents and solutions into the laboratory Run autoclave cycles routinely Archive data and files per site procedures Perform routine housekeeping and cleaning Create samples in LIMS and send test results from LIMS to customers Perform water testing for all Mallinckrodt Sites Perform product bioburden testing on incoming raw materials, swabs and finished products Ability to perform gram stain and interpret data Perform environmental monitoring in production Perform microbial limits testing as per USP & Perform endotoxin testing by kinetic methods Perform water sampling in various production areas Follow site HSE Policies and perform GMP walkthroughs Assist with establishing & maintaining safe work standards in the lab Peer review and approve some levels of work Receive and send packages from various MNK sites Order supplies needed for daily activities DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS: LIMS entry of data Use of analytical balance, pH Meter, TOC Analyzer, Kinetic Turbidimetric Analyzer, Autoclave Maintain instrument readiness MINIMUM REQUIREMENTS: Education: Bachelor's Degree in science related field (Chemistry, Microbiology, Biology) or equivalent combination of education, experience, and competencies. Experience: Experience in a cGMP environment is preferred. Working knowledge of instrumentation preferred. Preferred Skills/Qualifications: Use of analytical balance, pH Meter, TOC Analyzer Performs purified & DI water testing as required by USP Performs plant environmental monitoring Basic computer skills and familiarity with Microsoft Office Suite Substantial acquaintance with and understanding of application of basic principles, theories and concepts in Microbiology Basic knowledge and understanding of aseptic technique Use and/or Basic knowledge of industry practices and standards Skills/Competencies: Informing, Customer Focus, Listening, Perseverance, Organizing, function/technical skills, Peer Relationships, Comfort around Higher Management ORGANIZATIONAL RELATIONSHIP/SCOPE: Reports to the Supervisor Quality Microbiology. Contacts involve matters of moderate importance to the organization and include R&D, Marketing, Production Superintendents, Production Engineers, Production Lead Operators, Logistics, Safety and DEA. Infrequent customer contacts on routine matters. WORKING CONDITIONS: 80% Laboratory exposure to plant products, solvents and reagents, some of which are hazardous or potent compounds 20% Office environment Required to work 8 hour shifts, the potential for night, weekend, and holiday work depending on the lab DISCLAIMER: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of employees assigned to this position.

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Research & Development In R&D, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality. The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our R&D Academy, designed to develop our team and allow you to grow in our great organisation. About the role Perform chemical and/or physical testing on all in-process, finished, validation, and R&D products according to applicable procedures while following all relevant laboratory Test Methods, SOPs, etc. Provide support for or perform calibration, laboratory investigations, and projects as required. Participate in advanced training on equipment and/or methods and assist as needed in validation and method development. Schedule: 6pm-6am Night shift. Will include alternating weekends and some holidays. Your responsibilities * Analyzes sampled materials/goods in accordance with standard methods and specifications, properly records results, and renders a decision concerning acceptability and initiates appropriate paperwork to accept or reject material. * Performs job tasks according to BOMs, Specs, test methods, and SOPs. * Maintains accurate and updated summary records for each material analyzed. * Assists Processing/Mixing Teams with batch process adjustments. * Calculates and assists with the rework of unacceptable batches. * Prepares, dates, and standardizes laboratory reagents as assigned. * Reports inconsistencies in specification, BOM or test methods, including where material test results do not meet specification. * Reviews existing methods and specifications and makes recommendations for changes and/or corrections. The experience we're looking for * B.S. degree in a science field preferably Chemistry with 1-3 years experience in an analytical laboratory of an industrial and/or manufacturing plant environment. * Ability to work with Lab instruments such as GC, NIR, UV/VIS, HPLC etc. * Ability to read, interpret and execute written procedures * Ability to work with minimal supervision/alone * Possess excellent time management, strong analytical and problem-solving skills. * Ability to accurately complete paperwork/documentation, including quality documents * Ability to communicate effectively with supervisors and/or coworkers, contributing individually as well as with team members * Proficiency in Windows-based applications (Word, Excel, etc.) as well as Outlook, Internet Explorer. * Must be able to handle chemicals within permissible level. * Must understand Metric system and be able to convert units * Ability to work with Lab instruments such as GC, NIR, UV/VIS, HPLC etc is a plus * Experience with LIMS, SAP, Quality One, or other similar programs is a plus The skills for success Business Strategy, Task Execution Under Pressure, Makes strategic Business Decisions, Business Acumen, Commercial Awareness, Objective Setting, Accountability, Consumer Insight, Creative Direction, R&D, Change Leadership, Product Lifecycle Management, Business Partnership, Collaboration and partnership building, Relationship Management, Adapt to changes in technological development plans, Ability to challenge the status quo and propose improvement, Innovation Processes, Digital transformation for R&D, Quality and Manufacturing. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. US salary ranges USD $57,000.00 - $85,000.00 US pay transparency The base salary range for this role will vary based on experience in job and industry, training and education, skills relevant to the position, and other factors permitted by law. In addition to the base salary, the position is eligible for an annual discretionary bonus, which is subject to change each year. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, life and disability insurance; paid time off for vacation, sick, and Company recognized holidays; a 401(K) plan; generous paid parental leave; adoption and fertility support; tuition reimbursement; product discounts; and much more! If reasonable accommodation is needed to complete your application, please contact *******************************. Reckitt is committed to the full inclusion of all qualified individuals. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: St Louis Job Segment: Counseling, Nutrition, Healthcare

About this role: Wells Fargo Advisors (WFA) is seeking a Supervisory Control Associate responsible for direct support of branches and their responsibilities for remote compliance supervision of Private Client Group (PCG) and Wealth Brokerage Services, (WBS) producing Branch Managers, and Financial Advisors. Learn more about the career areas and lines of business at ********************** In this role, you will: * Participate or conduct compliance, supervision, control reviews, administration and technology * Design risk processes and provide project management support * Identify issues and provide resolution within Insurance or Private Client Groups * Perform basic or tactical ongoing regulatory, compliance and operational reviews as well as other duties related to best practices and opportunities for additional synergies to maximize efficiencies * Receive direction from management and exercise independent judgment while developing an understanding of sales activities using various technological tools and reports to ensure that the activity is in compliance with all regulatory and firm policies * Collaborate and consult with financial advisors, branch managers, supervisory principals and Market Administration Management Required Qualifications: * 6+ months of Supervisory Control, Risk Management Consulting, Property or Casualty Insurance, Insurance Brokerage experience, or equivalent demonstrated through one or a combination of the following: work experience, training, military experience, education * US Only: Successfully completed Financial Industry Regulatory Authority (FINRA) Series 7, 9/10, and 63 examinations (or FINRA recognized equivalents) sufficient to qualify for immediate FINRA registration Desired Qualifications: * Strong analytical skills including strategically analyzing data, diagnosing opportunities, and providing interventions * Solid conflict management and decision-making skills * Excellent verbal, written, and interpersonal communication skills * Ability to work independently while balancing the needs of multiple projects * Ability to be flexible and adjust plans quickly to meet changing business needs * Intermediate Microsoft Office (Word, Excel, and Outlook) skills * Ability to exercise independent judgment and creative problem solving techniques * Ability to interact with all levels of branch associates and business units; including managers and advisors * FINRA registration including Series 65 or 66 (or FINRA recognized equivalents) Job Expectations: * US Only: Registration for FINRA Series 65 or 66 must be completed within a 90 or 180-day time period contingent upon number of license(s) needed if not immediately available to transfer upon hire. FINRA recognized equivalents will be accepted. This will be communicated at time of offer acceptance. * US Only: Obtaining and/or maintaining appropriate FINRA license(s) is required for ongoing employment in this position. Compliance with state law registration and licensing requirements is mandatory. In addition to state registration and licensing requirements, specific product licenses or SAFE licensing may apply. Additional requirements include meeting enhanced financial fitness and criminal background standards. Wells Fargo will initiate the FINRA licensing review process at the time of offer acceptance. For specific FINRA qualification exams obtained after 9/30/2018, the Securities Industry Essentials (SIE) exam co-requisite may also be required. * This role requires a FINRA supervisory license and may require working in the assigned office location for at least one year from the hire date. Any supervisory role employee holding a FINRA supervisory license, who has answered affirmatively to certain Form U4 Section 14 regulatory questions/disclosures, will be ineligible to work from a location other than their assigned office location. This position is subject to FINRA Background Screening Requirements, including successful completion and clearing of a background check. Internal transfers are subject to comply with 17 CFR 240.17f-2 of the Securities Exchange Act of 1934 and FINRA Bylaws, Article III, Section 3, which states that Associated Persons should not be subject to statutory disqualification. Successful candidates must also meet ongoing regulatory requirements including additional screening and are required to report certain incidents. This position is not eligible for Visa sponsorship. Job Locations: * 550 S Tryon St. Charlotte, NC * 550 S 4th St. Minneapolis, MN 55415 * 2801 Market St. F & L Bldg. Saint Louis, MO Pay Range Reflected is the base pay range offered for this position. Pay may vary depending on factors including but not limited to achievements, skills, experience, or work location. The range listed is just one component of the compensation package offered to candidates. $55,300.00 - $98,300.00 Benefits Wells Fargo provides eligible employees with a comprehensive set of benefits, many of which are listed below. Visit Benefits - Wells Fargo Jobs for an overview of the following benefit plans and programs offered to employees. * Health benefits * 401(k) Plan * Paid time off * Disability benefits * Life insurance, critical illness insurance, and accident insurance * Parental leave * Critical caregiving leave * Discounts and savings * Commuter benefits * Tuition reimbursement * Scholarships for dependent children * Adoption reimbursement Posting End Date: 14 Jul 2025 * Job posting may come down early due to volume of applicants. We Value Equal Opportunity Wells Fargo is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other legally protected characteristic. Employees support our focus on building strong customer relationships balanced with a strong risk mitigating and compliance-driven culture which firmly establishes those disciplines as critical to the success of our customers and company. They are accountable for execution of all applicable risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which includes effectively following and adhering to applicable Wells Fargo policies and procedures, appropriately fulfilling risk and compliance obligations, timely and effective escalation and remediation of issues, and making sound risk decisions. There is emphasis on proactive monitoring, governance, risk identification and escalation, as well as making sound risk decisions commensurate with the business unit's risk appetite and all risk and compliance program requirements. Applicants with Disabilities To request a medical accommodation during the application or interview process, visit Disability Inclusion at Wells Fargo. Drug and Alcohol Policy Wells Fargo maintains a drug free workplace. Please see our Drug and Alcohol Policy to learn more. Wells Fargo Recruitment and Hiring Requirements: a. Third-Party recordings are prohibited unless authorized by Wells Fargo. b. Wells Fargo requires you to directly represent your own experiences during the recruiting and hiring process.

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 Responsibilities: • Ability to read and interpret documents such as kit protocols, safety rules, standard operating procedures, equipment use and maintenance instructions. • Ability to multitask and pay close attention to details in fast-paced environment • Set up laboratory equipment and instrumentation required for testing samples. • Test and analyze samples by running an ELISA, RIA or Multiplex immunoassay. • Document results of test samples that include calculating the data and submitting final reports in EXCEL. • Utilize technical knowledge and review of quality control data • Understand and follow all procedures and processes required for ISO 9001 compliance. • The employee may be exposed to a low risk of radiation. • The employee may on occasion be in an area where there is a minimal to low risk of bloodborne pathogens. Qualifications • Bachelor's degree in quality or life science disciplines with one - two years of related experience or Associate's Degree in quality or life sciences with two -four years of related experience and/or training; or equivalent combination of education and experience • Ability to calculate and apply mathematical concepts such as means, standard deviations, coefficient of variations, fractions, percentages, and molar ratios to practical situations used throughout manufacturing. Additional Information All your information will be kept confidential according to EEO guidelines.

Newco Enterprises is a leading manufacturer of commercial coffee machines that has been brewing up innovations for 50 years. Founded in 1974, Newco has grown from humble beginnings into an industry leader known for its commitment to quality and customer satisfaction. Our state-of-the-art, climate-controlled manufacturing facility houses the latest Amada metal fabrication machinery, positioning us for even higher levels of quality and efficiency. Why join Newco: Our facility is climate controlled and clean. Competitive benefits package that includes health, dental, vision, and long/short term disability. Paid time off. 401(k) plan with company match. Advancement opportunities. Stable work environment. We've been around 50 years and are excited for the next 50! Responsibilities: Perform quality inspection of fabricated, assembled products and parts supplied by vendors. Conduct first piece, in-process and final inspections for discrepancies and deviations from standard specifications. Record results of inspections, prepare inspection reports, and work with engineering to resolve quality issues Inspect incoming products using gauges, calipers, protractors and vision Examine material or product for surface defects Compare product with work order, bill of material, or sample model to ensure completion of assembly Requirements 3+ years experience performing component and assemble inspection functions in a manufacturing environment. Proficient in the use of inspection tools. i.e. Calipers, protractors and pin gauges Fully developed math skills Functional knowledge of computers (Excel, Word, electronics file organization) Interpretation of engineering drawings, suppliers drawings and written specifications Good communication skills both written and verbal Color recognition - Able to differentiate between wire colors (red, green, blue, orange, yellow, etc.,) Able to detect mild chemical fragrances involved in chemically cured products Functional knowledge of electronic multi-meters - preferred Functional knowledge of variable power supplies - preferred Experience with interpretation of electrical schematics - preferred

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make In this role, you will develop, validate, and transfer analytical methods. You will support Production with investigations and cleaning validations, and assist Pharm Tech in the evaluation of APIs, excipients, and components. You will also collaborate with QC on analytical method optimization, analyst training, and laboratory investigations. Additionally, you will mentor junior chemists and write and review analytical methods, protocols, investigations, and reports. ROLE RESPONSIBILITIES Identifies and implements improvements in analytical testing methods. Mentor and trains junior chemists in analytical methods and technologies. Performs method development and validation for analytical procedures. Executes method transfer and developmental protocols. Participates in new instrument qualification. Participates, examines and solves technical problems associated with the manufacture and handling of products and components Performs all activities under cGMP following company policies. Updates existing test methods. Also, writes and reviews analytical methods, protocol and reports BASIC QUALIFICATIONS Minimum Bachelor degree in a science field with 5 years' experience in GMP environment. Experience with analytical techniques like HPLC, GC/MS, LC/MS, FTIR preferred, familiarity with organic synthesis desired. Familiarity with EMPOWER software desired. #LI-Onsite #LI-BM1 California residents should review our Notice for California Employees and Applicants before applying. 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. Do you see yourself as part of the Kindeva mission? Click Apply Now Today! Other details Job Family D - Quality - Analytical Quality Development Job Function D - Quality Pay Type Salary

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 * 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 FLSA * Nonexempt

Full-time Description We are looking for a Quality Control Technician to join our team. In this role you will ensure quality control for the specific parts in accordance with established company and customer standards. Provide verbal and/or written test results to management and production staff in a timely manner. At Addman you'll be part of a skilled and growing team pushing the limits of aerospace and additive / subtractive manufacturing. ESSENTIAL JOB FUNCTIONS: Uses a variety of inspection instruments (calipers, micrometers, CMMs, etc.) and calculations to determine conformity to blueprints. Performs visual inspections under magnification to determine conformity to standards. Reviews certifications from suppliers and vendors to determine conformity to blueprints. Maintains records of results using various databases. Coordinates work to ensure that tasks are completed in a timely manner and according in order of priority. Requirements ITAR REQUIREMENTS: This position is subject to the International Traffic in Arms Regulations (ITAR) which requires U.S. citizen status. SKILL REQUIREMENTS: Commitment to a safety culture where safety is the first consideration before starting any task. Proficient with the use of manual inspection equipment. Experience programming using Calypso is preferred, but not required. Selects and uses appropriate inspection equipment and techniques. Interpret drawings and specifications. Experience conducting audits and creating corrective actions. Determines acceptability of quality of work. Meets time and quality standards. Seeks out additional duties when it is needed. Brings up potential problems with suggested solutions. Promotes a positive environment through what is said and by setting an example. QUALIFICATIONS: Graduate of related two-year vocational school program and two years related work experience and/or training; or equivalent combination of education and experience is preferred, but not required. Able to work in a dynamic environment with changing priorities to exceed customer expectations. Works independently, has a strong work ethic, is self-motivated and able to complete tasks with minimal supervision. Ability to work on cross-functional teams to support the core business, ensuring quality products are delivered on time. Computer aptitude (Outlook, PowerPoint, Word, and Excel). Ability to read, write, and communicate in the English language. Must be a team player and willing to learn new skills and concepts. Eligible to work in the United States without company sponsorship.

Job Description Tear the roof off your expectations, and build your career with us! At Advocate Construction, we’re not just builders, we’re the guardians of dreams and champions of the communities where we live and work. Here, passion meets profession, and potential finds its wings. It’s where growth, life-changing benefits, and award-winning workplace culture shine. It’s not just about the highs of success; it’s about the journey to get there – one paved with empowerment, that celebrates every voice, and reverberates through the impact we make within our walls and throughout our communities where we live and serve. People are the heart and soul of everything we do, and we believe there’s no better investment than in them; both professionally and personally. Join our construction team as a Quality Control Specialist to play an integral role in our customer's experiences! This position interacts with both customers and contractors and involves the following general job duties and responsibilities: The Quality Control Specialist is the frontline presence of the Construction Department in the field. By actively resolving issues, performing detailed inspections, and maintaining high standards, this role plays a critical part in ensuring customer satisfaction and strengthening trust between departments. Conduct thorough quality control walks at job sites after construction is completed. Carefully compare the work ticket against the actual work completed to ensure alignment. Cross-check the contractor completion form against the work ticket, verifying that the entire scope of work has been executed as outlined. Serve as the primary communicator between field conditions and office operations. Leverage excellent customer service skills to address and resolve customer issues with professionalism and empathy. When necessary, develop a comprehensive plan for repairs, generate a detailed work order based on your findings, and perform minor repairs as needed. Apply strong problem-solving skills to independently assess situations and find effective solutions. Provide status updates and communicate potential risks or delays identified in the field. Requirements: Must be able to successfully pass a comprehensive background check, including criminal and MVR checks. Must possess and maintain a valid driver's license. Must be physically capable of climbing a ladder and walking on a roof. Must be able to lift 70 lbs. Must be comfortable and able to thrive while working outdoors in various weather conditions. Must be flexible and willing to work non-traditional hours or overtime when required. Requirements: Must be able to pass a thorough background check Must possess a valid drivers license Must be able to climb a ladder and walk a roof Must be able to lift 70 lbs. Must thrive in the outdoors in various weather conditions Must be able to work non-traditional hours or overtime when required Benefits Package Comprehensive Health Coverage: Medical Insurance Dental Insurance Vision Insurance Life Insurance Short-Term Disability Insurance Long-Term Disability Insurance Flexible Spending Account (FSA) Health Savings Account (HSA) Financial Well-being: 401(k) Retirement Plan with Company Match: The company will match a percentage of your contributions to the 401(k) plan, helping you save for retirement. Employee Assistance Program (EAP) : Confidential support for personal and work-related challenges. Time Off: Paid Time Off (PTO) to use for vacation, illness, and personal time. Paid Holidays: The company observes major holidays with paid time off. Additional Perks: Company Truck Program : Eligible employees are provided with a choice of program that may include a company truck for work or reimbursement for use of their personal vehicle. Cell Phone and Internet Stipend : Monthly reimbursement for cell phone and internet expenses. Professional Development : The company invests in employees' growth through continuing training and annual work retreat trips. Company Culture: Regular social events and outings to foster camaraderie and a positive work environment To adhere to Colorado pay transparency requirements, the pay for this position is 28.00 - 31.00 per hour. Advocate Construction is an equal-opportunity employer committed to diversity and inclusion in the workplace. We 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.

Top Secret Clearance Jobs is dedicated to helping those with the most exclusive security clearance find their next career opportunity and get interviews within 48 hours. Make an impact by joining ServiceSource, a champion for people with disabilities. Explore new opportunities! ServiceSource is an organization of talented people who drive innovation, embrace change, and serve humanity. Job Summary Interpret, build upon, and comply with ServiceSource quality assurance standards. Maintain complaint and nonconformance processing through records and tracking systems, including root-cause analysis and corrective actions. Document quality assurance activities with internal reporting and audits. Develop improved standards for production and design, and create testing protocols for implementation across all service lines. Identify training needs and take action to ensure companywide compliance. Primary Duties Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. These duties and responsibilities will be rated on the Annual Performance Review: Develop Quality Assurance Surveillance Plan for assigned annexes and assist Annex managers in developing meaningful key performance indicators. Conduct and document contract surveillance of contract Required Service (RS) and assist managers to resolve performance issues. Make recommendations for corrective action and actively work with management team to ensure an acceptable level of quality is maintained. Coordinate and manage the document change process and maintain current revisions via a SharePoint web-based document management server. Review and manage quality control; run searches on database to scan for errors, generate reports and apply corrections accordingly. Additional Responsibilities Perform root cause analysis on quality defects. Formulate and maintain quality assurance objectives complementary to corporate policies and goals. Prepare and maintaining documentation and reports on quality issues, statistical reviews and relevant quality documentation Review all data obtained during all quality assurance activities to ensure consistency with company policies and procedures. Recommend improvements to the production process to ensure quality control. Develop new approaches to solve problems identified during quality assurance activities. Maintain a working knowledge of government and industry quality assurance codes and standards. Train and guide staff on new standards, procedures and processes Design and implement quality assurance training programs to key personnel in conjunction with managers. Record and investigate customer complaints regarding quality of services performed. Perform random inspections, validate inspection methods, and interact with customers regarding quality of services provided. Customer complaint and dispute resolution. Perform other related duties as assigned. Qualifications: Education, Experience, and Certification(s) Associate degree (AA) or equivalent from two-year college or technical school preferred. At least 5 years' experience in quality assurance and/or quality control performing the Primary Duties, or related work experience required. Demonstrated experience developing quality assurance/quality control surveillance plans, key performance indicators, and statistical reviews and relevant documentation required. Ability to obtain and maintain a Top Secret/SCI government security clearance with polygraph is required. Knowledge, Skills, And Abilities Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs. Basic ability to operate a computer using Microsoft Office software. Must have knowledge of creating spreadsheets and graphs. Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand; reach with hands and arms; and talk or hear. The employee is occasionally required to walk, sit, and climb ladders. The employee may occasionally lift or move products and supplies, up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, depth perception, and ability to adjust focus. Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. The noise level in the work environment is usually quiet. What We Offer - for Benefit Eligible Employees May Include: Because ServiceSource hires the best people, we work hard to provide benefits that make their lives better, so we offer a comprehensive benefit program which features: Health coverage for you and your family through Medical, Dental, and Vision plans. Financial protection with 100% company paid Disability, Life, Accidental Death & Dismemberment insurance. A 403(b)-Retirement plan in which the company matches dollar for dollar on a generous percentage matching up to 3% of your contribution. Tax advantages through Flexible Spending and Health Savings accounts that allow you to pay for specific healthcare and dependent care expenses with pre-tax dollars. To help you manage your work and life needs, we offer an Employee Assistance Program, Wellness Program, and Tuition Assistance. A generous paid time-off program in which the benefits increase based on your tenure with the company. ServiceSource is committed to hiring and retaining a diverse workforce and building an inclusive workplace. We are an Equal Opportunity and Affirmative Action Employer, making employment decisions without regard to a person's race, color, religion, sex (including pregnancy, sexual orientation, gender identity and transgender status), national origin, age (40 or older), veteran status, disability, or any other protected class. We are an E-Verify Employer and a drug-free workplace. Pre-employment background checks are required for all employment positions. PAY TRANSPARENCY POLICY STATEMENT: The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information

16Consultancy is a dynamic and forward-thinking business consulting company based in Singapore, specializing in gathering and analyzing industry insights. We guide clients towards informed decisions with expertise in sourcing, purchasing trends, and product development across various sectors, primarily focusing on actionable intelligence. Visit us at our website. Job Overview We are seeking skilled Food Industry Consultants specializing in Supply Chain Procurement for a part-time, remote, freelance, or hybrid position with 16Consultancy. This role requires at least 2 year of professional experience. The ideal candidate will have a passion for the food industry, with a particular focus on the freeze-dried fruit sector. Qualifications and Skills Proven experience in supply chain management within the food industry, particularly in the freeze-dried fruit sector. Strong background in global sourcing strategies to efficiently manage and optimize supply chain operations. Comprehensive knowledge and experience in procurement contracts, ensuring favorable terms for the business. Demonstrated ability to identify and select suitable suppliers that match business needs and quality standards. Experience working as a category buyer, focusing on product lines and market trends to enhance procurement strategy. Exceptional analytical skills to assess market trends and identify opportunities for cost-saving in supply chain activities. Strong communication skills to effectively negotiate with suppliers and liaise across different stakeholders internally. Proven capacity to work independently in a flexible, remote, or hybrid setting without compromising productivity. Roles and Responsibilities Analyze and enhance supply chain processes within the food industry, specifically targeting the freeze-dried fruit sector. Identify potential suppliers and establish procurement contracts that align with the strategic goals of the business. Conduct in-depth market research to track purchasing trends and provide insights for product development and sourcing strategies. Ensure compliance with industry standards and regulations related to food supply chain operations and procurement practices. Collaborate with cross-functional teams to support the design and implementation of supply chain improvement initiatives. Maintain and expand professional relationships with suppliers and industry stakeholders to foster long-term partnerships. Deliver actionable recommendations to improve sourcing efficiency while reducing costs and maintaining quality standards. Prepare detailed reports and presentations to convey analysis results and project outcomes to clients and management.

Quality Control Technician The purpose of this position is to oversee quality control of concrete both at job sites and plant locations. The Quality Control Technician will interact regularly with customers and batch personnel. We are looking for a team player who is able to make decisive educated decisions in the moment or know when to contact proper authorities to help make the right choices. Someone who takes pride in their work and takes care of their equipment. Work experience in Quality Control and the Ready Mix Concrete Industry are a plus. You will deal with a variety of individuals on a daily basis both within the company and outside through customers and state and local officials. THE IDEAL CANDIDATE 2+ years of experience with testing ready mix concrete. A.C.I. Field Technician Grade 1 / MoDOT certified. Knowledge of concrete mix designs. Ability to establish and maintain effective working relationships with contractors, their employees and state employees. Ability and knowledge to work with dispatch, sales, and customers to create and change mix designs, staying within cost parameters. RESPONSIBILITIES Overseeing quality control of concrete on job sites and plant sites. Maintain records and draft reports regarding job site issues, driver performance and product problems. Perform air tests, slump tests, unit weights and making of cylinders. Compiles and reports final summaries of testing results from completed projects. Will perform other duties as assigned by the Quality Control Manager. REQUIREMENTS 2+ years of experience with testing ready mix concrete. A.C.I. Field Technician Grade 1 / MoDOT certified. High school graduate or G.E.D. equivalent. Must be able to work flexible hours. 40+ hours per week. Clean appearance. Drug free. Valid driver's license with clean driving record. Computer literate. Good background in math. Excellent communication skills. Team player. Must be able to do moderately strenuous work, ability to lift over 50 pounds and endure extended periods of standing/walking as well as continuous strenuous activities such as frequent reaching, bending, or lifting. This position is an outdoor position exposed to all weather conditions. Working in a manner to ensure your personal safety and that of fellow employees by following Company safety guidelines and following Company policies.