Wet chemistry analyst jobs near me

Our client, a global leader in the pharmaceutical manufacturing industry, is seeking a QC Analyst to join their team! - Pay: $25-30/hr ($25/hr for entry level/recent graduate) - Shift: 1st shift M-F GENERAL DESCRIPTION: The QC Analyst I performs testing of samples submitted to the laboratory in a cGMP compliant manner, as well as according to approved written procedures. The QC Analyst I may be required to write or revise SOPs, analytical procedures, or other analytical documentation at the discretion of quality control supervisory staff. KEY DUTIES: Perform testing in accordance with written procedures (i.e. USP/EP/JP grade) Documentation of laboratory activities including worksheet/notebook entries according to procedures that define laboratory documentation practices. Processing of electronic data using procedures that ensure data integrity and security. Ship samples to contract testing facilities. Entry of test results from contract laboratories Review and countersign (when necessary) logbooks, notebooks, and worksheets for the purpose of verifying compliance with written procedures, good documentation practices, data integrity and accuracy of calculations. Transcribe results onto analysis reports. Perform daily standardization and performance verifications on laboratory equipment. Comply with site-wide procedures including but not limited to change control, documentation, deviation reporting, cGMP compliance, safety, and electronic data security. Identify deviations to written procedures. Disposal of laboratory waste on an as needed basis. Identify and report unsafe conditions within the laboratory. Identify OOS results, atypical results, and atypical laboratory events requiring a laboratory investigation; perform investigative testing. SKILLS/ABILITIES: Ability to perform routine analysis, such as wet chemistry and operate basic laboratory equipment. Understands paperwork review process. Ability to follow written procedures and exhibit excellent documentation practices. Basic laboratory knowledge and skills analytical techniques in wet chemistry/chromatography Practical experience with various types of laboratory instrumentation Troubleshooting skills with analytical methodology and instrumentation. Technical writing skills Employee must be able to pass a vision exam prior to employment and annually thereafter. PERSONAL ATTRIBUTES: Proactively achieves results for the best of the organization. Willingness to learn new things. Ability to function in a small company atmosphere. Ability to cope with a rapidly changing work environment. Commitment to teamwork. Commitment to continuous improvement in all areas. Ability to focus attention to details and ensure high quality work. Ability to work safely; seek out and encourage safe practices Responsible for managing their time, organizing their workload to be efficient, and have good organizational and communication skills EDUCATION AND EXPERIENCE: Bachelors Degree in Chemistry with 0-2 years of laboratory experience. Other fields of specialty in Sciences are also acceptable provided sufficient chemistry coursework is completed. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Synthetic Chemist - Material Science | Ohio (On-site) We're working with a global leader in advanced materials, seeking a hands-on chemist to drive innovation and performance breakthroughs in the rubbers space. This is a unique opportunity to join a high-impact team focused on pioneering new additives and sustainable solutions for next-generation products. About the Role: You'll lead investigations into complex chemical systems, collaborating with multidisciplinary experts to engineer transformative products. Reporting directly to technical leadership, you'll have the autonomy to shape research direction, influence product development, and see your innovations swiftly implemented in real-world applications. What You'll Do: Conduct detailed studies of reaction mechanisms, kinetics, and material properties in rubber and polymer systems. Utilize advanced analytical techniques and computational methods to characterize and predict performance outcomes. Develop mechanistic models and propose new pathways for superior material properties. Collaborate with scientists, process experts, and industry partners to integrate insights into product design and manufacturing. Scout and evaluate emerging technologies to drive sustainability and performance, including renewable materials and alternatives to conventional additives. What You Bring: Ph.D. in Organic Chemistry, Physical Chemistry, Polymer Science, or related field. Proficiency with analytical instrumentation and data interpretation. Strong problem-solving skills and ability to apply chemical principles to practical innovations. Excellent communication skills for technical documentation and team collaboration. Prior experience in the rubber industry is a plus.

Are you motivated to leverage your unique skills and experience with an industry leader trusted by the nations' strongest lending institutions? ServiceLink, the unrivaled best in the mortgage industry, seeks an action-oriented professional with a high degree of integrity and sound judgment to fill the position of Quality Control Analyst. The ideal candidate must share our unwavering focus on creating value for our customers and serve as a powerful force to promote unparalleled quality standards. If you thrive in a high-performance, Serve First culture, this may be the perfect position for you. It is an exciting time to join ServiceLink, where empowerment drives entrepreneurship. Applicants must be currently authorized to work in the United States on a full-time basis and must not require sponsorship for employment visa status now or in the future. 3+ years' experience in real estate appraisal quality control review at the AMC or mortgage company level. A DAY IN THE LIFE In this role, you will… · Perform quality control analysis of valuation reports in compliance with regulatory, industry and client requirements · Contact valuation providers to discuss revisions or obtain status as needed · Respond to and satisfy issues in a timely and consistent manner with accurate resolution · Meet daily, weekly, and monthly production goals set forth by management · Provide feedback to QC management that will improve processes and team productivity WHO YOU ARE You possess … · A confident understanding of the mortgage services industry with knowledge of appraisal industry guidelines and products · Prior appraisal or valuation review experience · The ability to multitask in a fast-paced environment, especially the ability to meet tight deadlines for our clients. · Exceptional customer service skills and mentality Responsibilities · Meet or exceed individual and departmental goals related to productivity and quality · Ensure valuation reports meet all regulatory and client standards · Maintain compliance with State and Industry regulations including Appraiser Independence Requirements · Identify any discrepancies or errors in valuation reports and provide detailed revision requests to the provider · Ensure appropriate escalation paths are followed · Ensure that all steps of the QC valuation process are completed accurately and within the required SLA (Service Level Agreement) timeframes · Contact valuation providers (appraisers, agents, etc.) as directed to discuss revisions or obtain status of the order · Attend departmental meetings as required · Participate in overtime, training, and onsite collaboration events as requested · Communicate daily with QC Managers on department operation protocols · Maintain a positive, professional business relationship with vendors and internal staff · Perform all other duties as assigned Qualifications · 3+ years' experience in real estate appraisal quality control review at the AMC or mortgage company level. · College degree preferred. · A penchant for excellence. You will use your strong attention to detail to maintain our quality standards. · The ability to multitask in a fast-paced environment, especially the ability to work in multiple systems at once. · The ability to quickly learn new skills, processes, and procedures. · USPAP certification; if not already certified, this role will require successful completion of the 15 or 7 hr. USPAP training course after hire, and successful maintenance of the certification during employment. · Knowledge of valuation processes, procedures, and technology. · Exceptional customer service, communication and writing skills. We can recommend jobs specifically for you! Click here to get started.

**Why Oatey?** Since 1916, Oatey has provided reliable, high-quality products for the residential and commercial plumbing industries, with a commitment to delivering quality, building trust and improving lives. Today, Oatey operates a comprehensive manufacturing and distribution network comprised of industry leading family of companies: Oatey, Cherne, Keeney, Quick Drain, Hercules, Dearborn, GF Thompson, William H. Harvey, Masters, Contact, Belanger, Lansas, and Durgo. At Oatey, we're doing big things - and by joining us, you'll have the chance to do big things too. You can build a strong career in an innovative, inclusive, high-performance environment, with the confidence that your company cares - about you, our customers and our world. **Ready to make an impact in a place where you matter?** **Position Summary** This position is responsible for working on New Product Development and Ongoing Business Initiatives from both a formulation and testing and validation perspective. **Position Responsibilities** + Support initiatives to improve performance of new product concepts and existing products, improve cost position, efficiency and reliability of products while ensuring that testing and proof of concept activities are completed on time. + Lead and support technical efforts to support the achievement of the company's business strategies, product roadmaps, and objectives. + Formulation, testing, and validation will require creativity, an understanding of the end user experience, and knowledge of requirements from regulatory agencies such as ISO, IAPMO, ASTM, ICC, NFPA and others as necessary. + Conduct research to identify potential technologies or solutions, jobsite activity and end user immersion, making samples of formulas, developing new formulas, developing and conducting tests to ensure the feasibility of product performance expectations which includes set-up monitoring, observing, analysis, and reporting. + Generate, develop, and communicate data to support the development of new products in addition to producing presentations and presenting to larger audiences. + Test and analyze competitive samples, assist manufacturing and quality teams on both new and existing products, collaborate with compliance and sourcing in addition to chemical engineers and project managers. + Additional responsibilities may be added based on corporate initiatives and needs. + Identifying training needs by evaluating strengths and weaknesses in our manufacturing, technical, and product teams + Develop training materials in collaboration with SME's and schedule and coordinate training for various teams in need + Develop and implement a research plan to obtain unbiased feedback on training, and opportunities for continued training and expertise. + Receive, research, and respond to technical questions from the field. **Knowledge and Experience** + Experience required 5+ years working in a high-volume chemical lab. + Ability to make scale up mixes, develop and follow test protocol, and accurately document findings. + Knowledge and experience using a design process and quality procedures. + Experience or knowledge of analytical test and tools. + Experience working on multiple projects focused on the chemical range of our current technology. + Proven ability to complete tasks on time with limited supervision. + Excellent interpersonal skills in order to communicate to diverse audiences and work in cross functional teams. + Highly organized with written and verbal communication skills. + Ability and desire to learn and demonstrate understanding of complex technical topics. + PC Computer proficiency. + Ability to be accountable for work and transparent with findings and communication. + Ability and desire to live into the corporate mission and values. **Education and Certification** + Bachelor's Degree in chemistry or related field required, or equivalent experience in lieu of degree. + Masters Degree preferred. Compensation Range for the Position 73,236.00 - 95,206.50 - 117,177.00 USD Annual Target Cash Profit Sharing for the Position 8% of Base Salary Offer amount determined by experience and review of internal talent \#LI-ERICA At Oatey we are committed to help our Associates grow their career. Apply today and grow with Oatey! **Oatey Total Rewards** + Generous paid time off programs and paid company holidays to support flexibility and work-life balance + Annual Discretionary Cash Profit Sharing + 401(k) with competitive company match + Market leading health insurance including medical, dental, vision, and life insurance offerings for associates and qualified dependents + Significant company contribution to Health Savings Account with a High Deductible Health Plan (HDHP) + Short-Term and Long-Term Disability income protection coverage at no cost to associates + Paid Maternity and Paid Parental Leave + Tuition reimbursement + A robust suite of complementary benefits to support associate well being **Equal Opportunity Employer** The Oatey family of companies are an equal opportunity employer committed to Diversity, Equity, and Inclusion. We recruit, employ, promote, and offer competitive pay for all jobs without regard to race, color, creed, religion, sex, age, national origin, disability, sexual orientation, or any other characteristic protected by law.

Come join our amazing team and work remote near Anaheim CA, Westfield IN or Plano TX! The Quality Control Servicing Analyst will be responsible for independently conducting audits of the servicing business units and its affiliates, are in compliance with internal policies and procedures, federal, state, local, and governmental regulatory requirements, and investor/agency/product specific guidelines. Also, ensure that all fraud red flags are identified and fully investigated, and findings are reported, and corrective action is taken. Perform all duties in accordance with the company's policies and procedures and all applicable US state and federal laws and regulations. The target pay for this position is $27.00 - $29.00 an hour. What you'll do: • Conduct scheduled monthly, quarterly, and semi-annual audits on all loan servicing operations business processes and procedures from collections to REO; including but not limited to loan level detail review, control testing, draft and complete audit exception/citation detail and all rebuttal response and support, documentation retrieval, and back-up audit file creation. • Perform OFAC reviews to ensure compliance with federal regulations and company policies. • Validate exception/citation testing and maintain exception issue log tracking and trends. • Conduct audits accurately, ensure proper controls are in place to reduce losses and in accordance with established audit timelines and standards. • Meet with department managers to discuss findings and ensure that where deficiencies are noted that corrective action plans are implemented to remediate those deficiencies in a timely manner. • Identify exception and performance trends and assist in the exception/dispute review and audit rebuttal process. • Complete default servicing fraud investigations and suspicious activity reviews as well as provide investigation support. File Suspicious Activity Reports as required. • Create and maintain documentation of processes, reports, applications, and procedures as per department policy. • Track all completed audits and monitor scores in the quality control system of record. • Review areas of non-compliance and making recommendations on changes to company policies and procedures to ensure compliance for both new requirements as well as external audit findings. • Escalate matters of continued non-compliance and/or recommendations for improvement to quality control leadership team. • Perform compliance testing of new processes implemented and conduct routine compliance monitoring. • Participate in monthly compliance meetings and assist with special audits, as necessary. • Perform other duties and projects as assigned. What you'll need: • High school diploma or equivalent work experience. • Five (5) or more years' experience in mortgage loan servicing. • Two (2) years of Loan Servicing auditing or compliance experience preferred. • Experience with compliance requirements (i.e., FHA, USDA, VA, FHLMC, FNMA) a plus. Our Company: Carrington Mortgage Holdings is a holding company whose primary businesses include asset management, mortgages, real estate transactions and real estate logistics. Collectively, the businesses are vertically and horizontally integrated and provide a broad range of real estate services encompassing nearly all aspects of single-family residential real estate transactions in the United States. Guided by a leadership team with a wealth of industry experience and guided by a consistent philosophy, Carrington maintains the necessary infrastructure to ensure stability and maximize value during any market cycle. We hope you'll consider joining our growing team of uniquely talented professionals as we transform residential real estate. To read more visit: ********************* What We Offer: Comprehensive healthcare plans for you and your family. Plus, a discretionary 401(k) match of 50% of the first 4% of pay contributed. Access to several fitness, restaurant, retail (and more!) discounts through our employee portal. Customized training programs to help you advance your career. Employee referral bonuses so you'll get paid to help Carrington and Vylla grow. Educational Reimbursement. Carrington Charitable Foundation contributes to the community through causes that reflect the interests of Carrington Associates. For more information about Carrington Charitable Foundation, and the organizations and programs, it supports through specific fundraising efforts, please visit: carringtoncf.org. California Privacy Notice: ******************************* # LI-GV1

Description & Requirements Maximus is currently hiring for Quality Control Analysts to join our Veterans Evaluation Services (VES) team. This is a remote opportunity. The Quality Control Analyst is responsible for reviewing Medical Disability Examination ("MDE") reports and Disability Benefits Questionnaires ("DBQs") generated by medical providers for veterans evaluated on behalf of the Department of Veterans Affairs (the "VA"). A Quality Control Analyst works closely with medical providers to ensure MDE reports and DBQs are consistent with the quality and timeliness requirements of the VA. Due to contract requirements, only US Citizens or a Green Card holder can be considered for this opportunity. This class is scheduled to begin on Tuesday, January 20, 2026, no alternate start dates are available. Essential Duties and Responsibilities: * Review MDE (Medical Disability Examination) requests for consistency with the DBQ. * Review MDE reports and DBQs (Disability Benefits Questionnaires) for completeness and typographical and grammatical correctness. * Communicate with medical providers and facilitate any necessary corrections to MDE reports and DBQs prior to submission to the VA. * Verify that any special requests or necessary second reviews have been completed, consistent with the VA's preferences. * Ensure that all diagnostics requested by the medical provider have been completed, reviewed by the medical provider, and are submitted with the final report. * Perform daily queue maintenance to ensure that every case assigned has updated notes and any needed action has been taken. * Communicate with the Medical Advisory Board on cases that need additional review, may be outside the scope of the assigned medical provider's training or expertise, or has presented a problem/issue with the assigned medical provider. * Consistently achieve weekly/monthly qualitative and quantitative goals set by management and VA. * Must be willing and able to work the training schedule of 8:00 AM - 5:00 PM CT, Monday-Friday for 3-4 months with no absences required (this includes pre-planned vacations/trips/appointments etc.) * This class is scheduled to begin on Tuesday, January 20, 2026, no alternate start dates are available. * Must be willing and able to work overtime as needed * Please note upon hire, Veteran Evaluation Services (VES), a Maximus Co. will provide all necessary computer equipment that is to be utilized to fulfil the duties of your role. New hires will not be exempt from using company provided equipment. * Must currently and permanently reside in the Continental US * In accordance with SCA contract requirements, remote work must be conducted from the location specified at the time of hire. Travel is not permitted, and you are required to remain at your designated home location for all work activities. Home Office Requirements Using Maximus-Provided Equipment: * Internet speed of 20mbps or higher required (you can test this by going to (****************** * Connectivity to the internet via either Wi-Fi or Category 5 or 6 ethernet patch cable to the home router * Private work area and adequate power source Minimum Requirements * Associate degree required; Bachelor's degree preferred. * Two (2) years of Quality experience may substitute for educational requirement. * Experience in Healthcare, Quality preferred. * Intermediate knowledge of medical terminology. * Excellent written and oral communication skills. * Excellent analytical skills and attention to detail. * Excellent multi-tasking skills. * Excellent organizational and prioritization skills. * Proficient in the use of Microsoft Office Products. EEO Statement Maximus is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information and other legally protected characteristics. Pay Transparency For positions on this contract, Maximus will pay the prevailing wage rate for the location in which the employee is working, as determined by the Department of Labor. That wage rate will vary depending on locality. An applicant's salary history will not be used in determining compensation. Accommodations Maximus provides reasonable accommodations to individuals requiring assistance during any phase of the employment process due to a disability, medical condition, or physical or mental impairment. If you require assistance at any stage of the employment process-including accessing job postings, completing assessments, or participating in interviews,-please contact People Operations at applicantaccommodations@maximus.com.

We're growing and looking for a detail-driven, process-minded Business Analyst to join our Business Operations team. This role is critical to enhancing the quality and consistency of our work through rigorous review programs and operational controls. You'll be a key player in driving continuous improvement, ensuring compliance, and elevating our service delivery. The Gig: * Lead and manage quality assurance initiatives across Business Operations. * Design, test, and refine frameworks for quality review and control programs. * Conduct complex recurring quality audits and controls. * Gather and analyze functional and data requirements to support quality initiatives. * Facilitate discovery sessions and document findings with internal stakeholders. * Collaborate across departments to ensure alignment and timely execution. * Identify gaps and escalate deficiencies in quality programs and propose updates and strategies for mitigation. * Drive process standardization and improvement efforts through creative problem solving and efficiency tool implementation (ie. VBA, SQL, etc) * Own the end-to-end lifecycle of assigned work, from intake to resolution. * Support data analysis and research efforts across departments related to quality and control initiatives. * Maintain confidentiality and uphold company standards. * Other duties as assigned. What you need to make the cut: * Bachelor's degree in Business Systems, Finance, Accounting, or related field (preferred). * 2+ years of operations experience in benefits administration operations, HRIS, payroll, or insurance required. * Proven expertise in internal audit methodologies and operational control design. * Lean Six Sigma or similar methodology experience a plus. * Strong background in process review and risk identification. * Advanced proficiency in Microsoft Excel (pivot tables, lookups, nested functions, advanced functions). * Exceptional time management and organizational skills with the ability to manage conflicting priorities. * Strong critical thinking and problem-solving abilities. * Excellent communication and stakeholder engagement skills. * Project management experience is a plus. The pay range for this position is 45K to 71K per year (pay to be determined by the applicant's education, experience, knowledge, skills, abilities, balanced against internal equity and competitive market based geographic ranges). This role is eligible to participate in the annual bonus incentive plan.

We are seeking a dedicated Analytical Chemist who will be responsible for migrations, extractables and leachables, impurity isolation, identification, and structural characterization studies. The role requires proficiency in LC-MS/MS and GC-MS, as well as strong sample preparation skills. You will work in a GMP analytical laboratory involved with FDA testing and handle pharmaceuticals and food packaging. Reviewing data for technical content and regulatory compliance will be part of your core responsibilities. Responsibilities * Conduct migrations, extractables, and leachables studies. * Isolate, identify, and characterize impurities. * Operate and maintain LC-MS/MS and GC-MS instruments. * Prepare samples for analysis. * Work with pharmaceuticals and food packaging materials. * Review data for technical content and ensure regulatory compliance. Essential Skills * Proficiency in LC-MS/MS and GC-MS. * Strong knowledge in analytical chemistry. * Experience in a GMP laboratory. * Knowledge of FDA compliance. * Sample preparation expertise. Additional Skills & Qualifications * Ph.D. in Chemistry or a related field. * 2-4 years of experience in an analytical laboratory. * Experience with HPLC, GC, HPLC MS/MS, semi-prep chromatography, and lyophilization. * Experience in the isolation and identification of impurities. * Knowledge of migrations, extractables, and leachables. Work Environment The role is based in a lab environment where you will work with extractables and leachables, migrations, and utilize LC-MS/MS technology. You will be part of a high-level pharmaceutical company, providing an excellent opportunity to gain valuable experience in the pharma industry. Job Type & Location This is a Permanent position based out of Painesville, Ohio.k Job Type & Location This is a Permanent position based out of Painesville, OH. Pay and Benefits The pay range for this position is $65000.00 - $85000.00/yr. 401K, medical, dental, vision, PTO, Vacation time Workplace Type This is a fully onsite position in Painesville,OH. Application Deadline This position is anticipated to close on Dec 9, 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.

"Applicants must be legally authorized to work in the United States without the need for sponsorship now or in the future." Voyant Beauty believes our people are more than just employees; they're the driving force behind everything we achieve. Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual's contribution is valued and celebrated. We invest in their growth, providing opportunities for development and advancement within our dynamic team. Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products. We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs. This can include skincare, haircare, bath and body products, fragrances, and more. Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life. Safety is a core value at Voyant Beauty. We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel. If you're seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you. Come join us and be a part of our journey. A Brief OverviewEnsures accuracy and reliability in laboratory testing and analysis. The QC Analytical Chemist is responsible for conducting quantitative and qualitative analysis of raw materials and products, developing analytical methods, and ensuring compliance with industry standards.What you will do Conduct quantitative and qualitative analysis of raw materials and products. Collaborate with production teams to troubleshoot production issues. Ensure compliance with industry standards and regulations. Prepare technical documents and reports. Develop and validate analytical methods. Calibrate and maintain analytical instrumentation. Manage standard chemical inventory and safety protocols. Some duties may vary slightly by location. Education Qualifications Bachelor's Degree in Chemistry or related scientific discipline (Preferred) Experience Qualifications 1-3 years Analytical chemistry in a manufacturing environment (Preferred) 1-3 years Method development and validation (Preferred) Skills and Abilities Analytical Chemistry (High proficiency) Quality Control (Medium proficiency) Laboratory Safety (Medium proficiency) Technical Documentation (Medium proficiency) Regulatory Compliance (Medium proficiency) Data Analysis (Low proficiency) Instrumentation Calibration (Low proficiency) Method Validation (Low proficiency) Chemical Handling (Low proficiency) Collaboration (Low proficiency) To Staffing and Recruiting Agencies:Our company does not accept unsolicited curriculum vitae's or applications from agencies. We are not responsible for any fees related to unsolicited curriculum vitae's or applications and explicitly reserve its right to contact candidates presented in such unsolicited curriculum vitae's or application. Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, color, national origin, sexual orientation, age, disability or veteran status. Voyant Beauty will consider requests for accommodations due to a disability impacting a qualified employee's ability to perform the essential functions of their position consistent with applicable laws. In addition to federal law requirements, Voyant Beauty complies with applicable provincial and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

State Bank, a growing Community Bank, has an opportunity for a self-motivated and detail-oriented individual to join our Quality Control Team. We are seeking a Full Time Mortgage Quality Control Analyst to work in our Defiance corporate office. This position is responsible for establishing advanced quality controls and implementing continuous improvement standards and procedures for State Bank, including ensuring that mortgage HMDA data is correct and compliant. State Bank offers an extensive benefits package including: competitive compensation, paid vacation and PTO, medical/dental/vision insurance, company-paid life and AD&D insurance, a company-matched 401(k) retirement plan, company-provided short and long-term disability, quarterly incentive payouts, a community volunteer program, and growth opportunities. Apply today and see why State Bank is a great place to work! Equal Opportunity Employer

About Abeona Our Values: Patient First | Innovation | Integrity | Determination | Trust Join us in making cure the new standard of care. At Abeona Therapeutics, we exist for our patients and their caregivers; their needs guide our decision-making. We challenge ourselves to think differently, move quickly, and deliver solutions. We hold ourselves to the highest ethical and quality standards. We persevere with resilience and focus to achieve our mission. We build trust through humility, mutual appreciation, openness, and respect. Company Description Abeona Therapeutics Inc. is a commercial-stage biopharmaceutical company focused on developing cell and gene therapies for serious diseases. Notably, Abeona's ZEVASKYN (prademagene zamikeracel) is the first autologous cell-based gene therapy treating wounds in adults and pediatric patients with recessive dystrophic epidermolysis bullosa (RDEB). The company's cGMP manufacturing facility in Cleveland, Ohio, is dedicated to producing ZEVASKYN. Abeona's portfolio includes adeno-associated virus (AAV)-based gene therapies for ophthalmic diseases with unmet medical needs, and their novel AAV capsids aim to improve treatment outcomes for various debilitating conditions. Position Overview The Quality Control Analyst II performs routine laboratory activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Testing includes qPCR, immunoassays and cell culture-based potency assays. Supports the authorship and revision of GMP documentation. Interacts with employees internal and external to Quality Control. This position will work from 4:00 PM to 12:00 AM, Monday to Friday. Training will be on first shift for four to six months (subject to change based on company need). Essential Duties and Responsibilities * Performs other duties as assigned by management. * Works on QC tasks of diverse scope, requiring basic knowledge of laboratory concepts. * Train new employees on Quality Control process flows and testing methods. * Author and revise existing Standard Operating Procedures (SOPs), testing forms and product specifications (SPCs). * Perform advanced cell culture techniques such as seeding culture dishes, transductions, and immunostaining according to approved test methods. * Completes laboratory work with precision and maintains hardcopy paperwork and electronic data in an organized manner, in compliance with company documentation practices (GDP). * Provides input to improving QC systems and procedures to improve GMP compliance. * Proactively communicates laboratory issues to supervisor or manager. * Supports laboratory investigations related to test failures, discrepancies and deviations. * Helps maintain the laboratories in a GMP compliant state, including participating in cleaning, instrument routine and preventative maintenance, logbook use, etc. Qualifications * BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline with 3 to 5 years of relevant experience. * Experience and knowledge in the pharmaceutical and/or biotech industry within a GMP and/or GLP environments preferred. * Experience in cell culture, immunostaining, and drug product potency testing preferred. * Experience with DEV, CAPA and CR management preferred. * Understanding of basic scientific concepts in one or more areas above. * Experience with relevant analytical lab equipment and computers preferred. * Good mathematical and organizational skills * Ability to interact constructively with co-workers to solve problems and complete tasks * Some weekend work or late nights may be required periodically. 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 experience prolonged sitting, some bending, stooping, and stretching. Hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required. A normal range of hearing and vision correctable to 20/20 is required. Occasional lifting up to 20 pounds is required. Benefits Our values apply to how we view caring for each other as well. While the patient comes first, our employees are vital to making that happen, and so we strive to offer a competitive benefits package that includes: * Medical insurance coverage (multiple options to meet our employees' and their families' needs) * Dental and vision coverage * 401k match plan * Lifestyle spending account * Annual Compensation: $68,000 - $82,000 (includes shift differential) Visa Sponsorship Not Currently Available IMPORTANT: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

About this opportunity : The QC Analyst II is responsible for executing quality control analytical tasks, including in process manufacturing testing, for one or more projects to support testing and release of oligonucleotides. Key Responsibilities: Sample, test and release raw materials and finished products per established procedures with minimal errors Provide analytical support to Manufacturing and Process Development Perform routine analyses using techniques such as: Wet Chemistry, Karl Fischer, UV-Vis, FT-IR, Raman, LC, GC, LCMS, and NMR Train and/or assist other QC Analysts on applicable analytical techniques Assist in the development and/or qualification of test instructions and protocols Author technical documentation (e.g. methods, procedures) Represent Quality Control on internal project teams Perform GDP peer review Maintain laboratory compliance Execute tasks to deliver project results on time Contribute to a positive work atmosphere Responsibilities may also include water system and environmental monitoring testing Job Experience and Technical Skills: Degree in Chemistry or related field. BA/BS with 2+ years of related work experience. Understand and edit laboratory SOPs Operate laboratory instruments Knowledge of undergraduate general chemistry and organic chemistry Basic Word, Excel, and PowerPoint abilities Perform algebraic and basic statistical calculations correctly Proficient in written and spoken English. Experience with technical writing. The annualized salary for this position is between $63,200.00 - $77,400.00.

The APTIM Federal Services, LLC team at the USEPA Analytical Laboratory Support Program (ALS) has an opening for an analytical chemist to help develop drinking water methods. The chosen candidate will join a group of APTIM chemists on-site at the USEPA Andrew Breidenbach Environmental Research Center (AWBERC) in Cincinnati, OH. Under the general supervision of the ALS management and senior staff, the ideal candidate will design and conduct experiments to develop drinking water methods for a variety of trace contaminants. Key Responsibilities/Accountabilities: Work independently and in a small group designing experiments, conducting extractions, performing analysis, and compiling data Operate GCs, GC/MS, LC-MS/MS, and water quality instruments as needed Abide by USEPA and APTIM safety and quality control procedures Support the quality assurance program with data review and evaluations Communicate effectively within and outside the APTIM group Document experiments and write methods consistent with USEPA and APTIM standards Basic Qualifications: Bachelor's degree in chemistry or related field with 8 years of related experience, a Master's degree with 4 years of experience, or a PhD Ability to communicate and write clearly and concisely Ability to work independently and to take direction from more senior team members as needed ABOUT APTIM APTIM is committed to accelerating the transition toward a clean and efficient energy economy, building a sustainable future for our communities and natural world, and creating a more inclusive and equitable environment that celebrates the diversity of our communities. We specialize in environmental, resilience, and sustainability and energy solutions, as well as technical and data solutions, program management, and critical infrastructure. For every challenge our clients face, there is an opportunity for APTIM to innovate a fit-for-purpose solution that will raise your organization or community to a new standard of excellence. What you can expect from APTIM: Work that is worthy of your time and talent Respect and flexibility to live a full life at work and at home Dogged determination to deliver for our clients and communities A voice in making our company better Investment into your personal and professional development As of the date of this posting, a good faith estimate of the current pay range for this position is $75,000 - $80,000. Compensation depends on several factors including: experience, education, key skills, geographic location of the position, client requirements, external market competitiveness, and internal equity among other employees within APTIM. Employee Benefits APTIM Federal Services, LLC is committed to providing an extensive range of benefits that protect and promote the health and financial well-being of our employees and their families through the APTIM Benefits Marketplace ************************************ Medical, vision, and dental insurance: Through the marketplace, our employees can choose benefits from five metallic levels and 10+ carriers to find the right benefits that work for them in their location. Life insurance Short-term and long-term disability insurance Paid holidays, vacation, and sick leave (eligibility based on company policy and applicable law) 401(k) APTIM offers three 401k plans through the Aon Pooled Employer Plan (PEP). The specific plan you are eligible for depends on the business unit you are in. The details of the largest plan are found here: APTIM 2025 401(k) Plan Features (makeityoursource.com) APTIM - Helpful Documents Watch our video: About APTIM - In Pursuit of Better

What Makes a Honda, is Who makes a Honda Honda has a clear vision for the future, and it's a joyful one. We are looking for individuals with the skills, courage, persistence, and dreams that will help us reach our future-focused goals. At our core is innovation. Honda is constantly innovating and developing solutions to drive our business with record success. We strive to be a company that serves as a source of “power” that supports people around the world who are trying to do things based on their own initiative and that helps people expand their own potential. To this end, Honda strives to realize “the joy and freedom of mobility” by developing new technologies and an innovative approach to achieve a “zero environmental footprint.” We are looking for qualified individuals with diverse backgrounds, experiences, continuous improvement values, and a strong work ethic to join our team. If your goals and values align with Honda's, we want you to join our team to Bring the Future! Job Purpose Works with Real Estate Manager to provide QC support for the real estate department. Responsible for the oversight of operational audits, audit research, compliance monitoring and testing along with all Pre/Post Closing audits in accordance with Freddie Mac requirements &/or other secondary market requirements. The individual will be responsible for the timely submission of departmental audit and investor reporting on an on going basis. Key Accountabilities Conducts Pre & Post Closing Audit functions in accordance with Freddie Mac requirements. Performs other a QC/audit functions as assigned and ensures that all audit responses are complete, accurate, and provided timely. Assists in identifying operational risks and escalating issues to management. Works in conjunction with Real Estate Manager in answering all investor, auditor and regulator questions. Qualifications, Experience, and Skills High School Diploma required Four year college degree is desired Three years experience underwriting real estate loans required Prior working experience with Freddie Mac Working knowledge of State and Federal lending regulations Proficient in Microsoft Word and Excel Excellent verbal and written communication skills Workstyle Office environment On Site position Overtime as necessary Quick response time for occasional urgent situations What differentiates Honda and makes us an employer of choice? Total Rewards: Competitive Base Salary (pay will be based on several variables that include, but not limited to geographic location, work experience, etc.) Regional Bonus (when applicable) Industry-leading Benefit Plans (Medical, Dental, Vision, Rx) Paid time off, including vacation, holidays, shutdown Company Paid Short-Term and Long-Term Disability 401K Plan with company match + additional contribution Relocation assistance (if eligible) Career Growth: Advancement Opportunities Career Mobility Education Reimbursement for Continued learning Training and Development Programs Additional Offerings: Lifestyle Account Childcare Reimbursement Account Elder Care Support Tuition Assistance & Student Loan Repayment Wellbeing Program Community Service and Engagement Programs Product Programs Honda is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, sex, sexual orientation, gender identity and expression, age, disability, veteran status, or any other protected factor.

About this opportunity : The QC Analyst II is responsible for executing quality control analytical tasks, including in process manufacturing testing, for one or more projects to support testing and release of oligonucleotides. Key Responsibilities: * Sample, test and release raw materials and finished products per established procedures with minimal errors * Provide analytical support to Manufacturing and Process Development * Perform routine analyses using techniques such as: Wet Chemistry, Karl Fischer, UV-Vis, FT-IR, Raman, LC, GC, LCMS, and NMR * Train and/or assist other QC Analysts on applicable analytical techniques * Assist in the development and/or qualification of test instructions and protocols * Author technical documentation (e.g. methods, procedures) * Represent Quality Control on internal project teams * Perform GDP peer review * Maintain laboratory compliance * Execute tasks to deliver project results on time * Contribute to a positive work atmosphere * Responsibilities may also include water system and environmental monitoring testing Job Experience and Technical Skills: * Degree in Chemistry or related field. BA/BS with 2+ years of related work experience. * Understand and edit laboratory SOPs * Operate laboratory instruments * Knowledge of undergraduate general chemistry and organic chemistry * Basic Word, Excel, and PowerPoint abilities * Perform algebraic and basic statistical calculations correctly * Proficient in written and spoken English. Experience with technical writing. The annualized salary for this position is between $63,200.00 - $77,400.00.

Full-time Description Company Background: Headquartered in Akron, OH, Flexsys is a chemical manufacturing company with operations in the US, Europe, Latin America, and Asia. It produces tire additives that enhance the strength and durability of tires for leading manufacturers around the world. We are a global supplier of rubber chemicals and solutions including insoluble sulfur, anti-degradants, and stabilizers. The company's singular focus is on delivering better solutions for manufacturers of tires and other rubber products that enhance product performance, optimize production efficiency, and ensure supply chain success. As the largest manufacturer of tire-industry additives in the world, and a newly independent entity, Flexsys brings a track record of innovation, quality, specialized expertise, a highly collaborative approach, and a commitment to growth - working together with our customers as a valuable partner, helping to meet their critical objectives. General Description: Flexsys has an immediate opening for a Laboratory Analyst in the Akron Rubber Laboratory. The rubber laboratory functions as both a research lab and quality control lab for Flexsys products developed and used in the rubber industry. The Laboratory Analyst is located in Akron but is a part of the global tire additives team providing support to production facilities in the America's, Europe, and Asia/Pacific regions. The laboratory collaborates closely with the tire additives research and development teams to provide research support in new product development and quality assurance of our products. The Laboratory Analyst position promotes continuous on-the-job learning and provides an environment focused on working in a highly integrated team setting. If you are excited to work in a highly innovative environment and want to work for a company with a collaborative spirit, we would love to hear from you. Performing routine sample analysis including, but not limited to: o Accurate and precise weighing of chemicals. o Ability to follow sample preparation in accordance with customer requests. o Operating internal mixers and two-roll mills. o Perform physical, mechanical, and rheological laboratory testing using automated and manual laboratory instrumentation. o Work safely around chemicals and machinery. o Follow Standard Operating Procedures. o Maintain a clean work area. o Assist in preventative maintenance of equipment. o Using a Laboratory Information System to report results. o Supporting all initiatives to improve the laboratory. Requirements o Minimal Education level - High School Graduate or equivalent. o Ability to function in a high-paced, quality-focused laboratory environment. o Ability to work in high-performing teams both safely and responsibly. o High sense of urgency and self-starter mentality. o Strong written and verbal communication skills. o Ability to quickly adapt to a dynamic environment. o Ability to focus on multiple projects at a time. o Ability to lift to 50 pounds. An ideal candidate would possess the following: o Previous laboratory experience and/or industrial experience. o Hands on rubber mixing and milling would be ideal but not required. o Familiar with ASTM testing. o Experience with internal mixers. o Mechanical Aptitude. o Strong knowledge of Microsoft Excel and Word. An Equal Opportunity Employer (EOE): race/color/religion/sex/sexual orientation/gender identity/ national origin/disability

About Our Team At Tolco Corporation, we are the trigger sprayer experts. With a foundation of over 64 years of selling best-in-class cleaning tools, our major product categories focus on dispensing, including trigger sprayers, pumps, bottles and closures. We attribute our success to our dedicated team who strive to provide quality customer service and take pride in providing fast and efficient shipping. We often collaborate across teams to get the job done; however, we don't take ourselves too seriously. It is important for us to have fun too! About You The ideal candidate is a detail-oriented problem-solver with a strong commitment to quality. A proactive mindset, technical aptitude, and strong communication skills are essential to thrive in this role. If you take pride in ensuring products meet high standards and enjoy working in a structured, process-driven environment, we encourage you to apply. Job Summary The Quality Control Analyst ensures that all inbound and returned products meet Tolco's quality standards through systematic inspection, documentation, and testing. This role involves evaluating product performance, chemical resistance, output, and compliance with specifications, while also inspecting goods produced or assembled by Tolco as directed by the manager. This position reports to the Quality Control Manager. Job Responsibilities Perform timely inspections of inbound goods against Tolco's product specifications Select samples from the warehouse/receiving area and transport them (using non-motorized handcart) to the inspection station Conduct functional tests to verify proper operation, chemical resistance, output and performance Use testing equipment to measure product compliance Evaluate customer-returned products as directed by the QC Manager to determine root causes of defects or failures Inspect internally produced or assembled goods before outbound shipment to ensure compliance with quality standards Record test results and document inspection findings Maintain organized and up-to-date quality records in the Quality Control Master Specification Worksheet Requirements Education & Experience: Associates Degree in Quality Assurance Mgmt preferred, and/or minimum of 3+ years experience in quality control, inspection, or manufacturing Certifications: Quality Control/Inspection (i.e. CQT or CQI) preferred but not required Technical Skills: Basic computer skills, including proficiency in Microsoft 365, Google Suite and an ERP Physical Requirements: Ability to lift/move items up to 50 lbs and stand for extended periods of time Soft Skills: Detail-oriented, analytical, and able to follow standardized procedures Benefits and Other Important Information This is a full-time, on-site position 8am-5pm, Monday-Friday. Tolco offers a comprehensive benefits package, including medical, dental, vision, voluntary life insurance, 401k disbursements, paid vacation, and more. More About Tolco Tolco Corporation is a leading manufacturer of cleaning tools used in the Janitorial, Beauty & Barber, Animal Health, and Auto Detailing markets. Our major product categories focus on dispensing, which include trigger sprayers, pumps, bottles, and containers. Additionally, we offer over 1000 products, and carry items in the restroom care, floor & window cleaning, utility, and safety categories. Tolco is a third-generation family business operating out of Toledo, OH since 1961.

A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit ****************** Position Summary: The Analyst, QC Aseptic Control (Night Shift) is responsible for reviewing sampling and laboratory data and autonomously performing tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. The position requires operating equipment in various classified/non-classified areas up to a Grade A aseptic environment and in a laboratory setting, and includes the maintaining of gowning qualification. **This is a Night Shift position - 12-hour rotating schedule from 6pm - 6:30am (2 days on /2 days off /3 days on)** Position Responsibilities: Supports coordination of workflow for Environmental Monitoring team. Verifies QC data, while monitoring for trends and abnormalities. Performs project work and leads laboratory investigations. Trained and able to perform all Environmental Monitoring technician responsibilities (including maintaining aseptic qualification) when needed. Review completed production documentation (for example: logbooks) for quality, completeness, and cGMP (Good Manufacturing Practices) compliance. Troubleshoots methods and processes. Train others on systems, software, equipment, machines, procedures, and/or processes. Answer compliance and process questions from others. Communicate policies and procedures to employees. Fill in for Analyst II/Team Lead when absent. Gather, organize, and communicate operational information to others. Lead and coordinate investigations and studies with little supervision. Lead process improvement activities and teams to meet strategic goals. Other duties that support Environmental Monitoring, Operations, or Laboratory processes may be assigned. Minimum Qualifications: General experience in a pharmaceutical production or quality control environment (GMP/GDP) Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language. Good attention to detail is required. Must be capable of keeping accurate records and performing mathematical calculations Preferred Qualifications: Bachelor's degree, scientific discipline Significant experience in a sterile or cGXP environment Lab experience is a plus Sponsorship or support for work authorization, including visas, is not available for this position. Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $24.00 - $34.50 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.

Laboratory Analyst Imagine your future with us! At ALS, we encourage you to dream big. When you join ALS, you join a purpose and values-driven team that empowers you to innovate, create, and thrive. Our global team turns up each day with passion and commitment to do amazing things, always challenging our thinking to find ways to solve some of the world's most complex problems for a safer, healthier world. Responsibilities About the role ALS Food Safety provides an extensive range of food analytical testing services, including food production environments and raw and cooked meat, dairy, produce, seafood, and animal feeds. We work closely with our clients to ensure their needs are met now and in the future. Due to growth, ALS is currently recruiting for Laboratory Analysts in our Marshfield, WI Food Lab. We will train the right candidates! Entry Level Laboratory Analysts perform basic laboratory tests. Analysts receive, log, and prepare samples and perform analysis according to procedures and test methods. Duties include: Perform calculations as required when conducting analytical preparations. Calibrate equipment as required. Maintains an understanding of and ensures compliance to Quality System including the manual, system procedures (QMSPs). Perform housekeeping duties as required. About you High school diploma or equivalent Good communication and collaboration skills (Teamwork!) Multi-tasked, organized, and detail oriented. Problem solving capabilities. Previous experience working in another laboratory on in the food safety sector. Life Science degree a plus! Working conditions 4/10 work schedule. Position requires significant time working in a laboratory environment between ten to twelve (10-12) hours per business day. Must be able to stand, bend, push, pull, stoop and crouch up to 80% of the time while performing the duties of this position. Must be able to lift (with both hands) and/or move up to 50 pounds and occasionally lift and/or move heavier loads with assistance. Working at ALS Our people are our most valuable asset and drive our success at ALS. We are a diverse community of dedicated professionals united by our passion to make a difference in the world. We reward excellence and uphold our values in our work and how we treat each other. At ALS, you'll be supported to expand your skills and develop new ones so you can reach your full potential. We invest in our people with a range of programs and provide opportunities across the company, giving our people scope to grow diverse careers and develop as leaders. We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and the communities where we work. Our benefits include: Structured wage increases Food Safety Incentive program Comprehensive benefit package including medical, dental, and vision coverage, life and disability insurance, retirement plan with company match, employee assistance and wellness programs, access to company perks) Additional vacation days for years of service Business support for education or training after 9 months with the company Learning & development opportunities (unlimited access to e-learnings and more) About ALS ALS is a global leader in scientific testing, providing comprehensive testing solutions to clients in more than 60 countries across a wide range of industries, including environment, food and beverage, mining, personal care, pharmaceutical, healthcare and equipment reliability. Using state-of-the-art technologies and innovative methodologies, our dedicated international teams deliver the highest-quality testing services and personalized solutions supported by local expertise. We help our clients leverage the power of data-driven insights for a safer and healthier world. Everyone matters ALS is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society ALS is a VEVRAA Federal Contractor. EOE AA Minority, Female, Veteran, Individuals with Disabilities. Click Here to view the EEO is the Law poster Click Here to view the FMLA Law poster Click Here to view the EPPA Law Poster Click Here to view the Pay Transparency Provision Click Here to view company E-Verify Participation Poster