NMR jobs near me - 16 jobs

Our client is a leading supplier of automotive seating and interior components, specializing in the design and manufacture of high-quality interior systems for major vehicle manufacturers. The company plays a pivotal role in the automotive industry by delivering innovative and sustainable solutions that enhance driving comfort and safety. Location: Columbus, Ohio Metro Area Start: ASAP Type: Contract to hire Position Summary: The Administrator provides administrative assistance in support of the NM Parts Control - New Model activity. This individual must possess an overall knowledge of the operation and provide management with periodic and real-time information. Essential Functions: Control suppliers during New Model maturation process, issue Maker Layouts, Go-Releases, and New Model events. Track / monitor tool & part maturation & part delivery. Interact with suppliers and coordinate all department requests to suppliers during new model development. Support supplier NMR processes to ensure MP ramp up meets customer expectations. Collect trial cost piece pricing with suppliers and correspond with suppliers utilizing various communication skills (verbal and written.) Maintain safe and clean work area (5S). Work to improve knowledge base and problem-solving capabilities. Support planned physical ticketed inventories as needed. Record retention, email, and phone calls daily. Commitment to customer satisfaction (internal & external). Meet daily requirements to support. Support PAR program, Kaizen activities, Eagle finds and WINS group. Review and approve supplier performance data on a monthly basis. Evaluate, control and track direct costs associated with the tooling process by negotiating prices and recommending appropriate design changes. Monitor and track other associated expenses such as accuracy of invoices, shipping and labor costs. Direct Reports: No direct reports

Pulmovant is a Roivant-backed clinical-stage biotechnology company developing innovative therapies for patients suffering from pulmonary diseases. Pulmovant's first program, mosliciguat is designed to provide an effective, once-daily, inhaled treatment option for patients with pulmonary hypertension (PH). Mosliciguat is a novel, potential first-in-class, sGC activator with a differentiated mechanism that may have broad applicability across the PH spectrum. Mosliciguat has been extensively characterized across a robust Phase 1 program with 170 participants dosed to date including patients with PH in the Phase 1b ATMOS study which has produced highly compelling and clinically meaningful efficacy data, as well as a favorable safety profile. Enrollment in a phase 2 trial is ongoing. As part of the Roivant family of companies, Pulmovant leverages the power of collaboration and innovation to drive progress. For more information, please visit ************************** About Roivant: Roivant specializes in developing transformative medicines at an accelerated pace through the launch of nimble biopharmaceutical and health technology entities, each meticulously tailored to address a specific medical need. Since its inception in 2014, Roivant has achieved the following critical milestones in support of its vision: built over 20 Vants; 12 consecutive positive Phase 3 trials; 8 FDA approvals; 5 successful IPOs; >$6B in capital raised; >$10B in global pharma partnerships and proceeds; and continued pipeline expansion across various modalities and therapeutic areas through in-licensing and acquisition of novel product candidates and technology platforms. In addition to a robust clinical stage pipeline, Roivant also incubates discovery-stage companies and health technology startups complementary to its biopharmaceutical business. Title: Manager - CMC Analytical Development (Fully Remote) Summary We are seeking a manager of CMC Analytical Development to help drive successful inhaled product development. The individual will work collaboratively with the Head of Analytical and cross-functionally within CMC to plan, track and report the release, stability and high-quality data packages to support regulatory submissions managed by CMC. This includes, but is not limited to, drug substance, drug product, analytical development, technical transfer, regulatory documentation, project strategy and vendor management. This is an exciting and visible role for a well-qualified and motivated individual. The successful candidate will be an analytical QC expert, with attention to detail and significant experience in analytical method transfer, release and stability testing in late clinical and commercial stage withing the biotechnology industry. The ideal candidate will be detail driven and have a proven track record in managing analytical activities contributing to project success of inhaled products in the pharma/biotech industry, preferably with experience in both small molecule and inhaled therapies. Responsibilities: Support all outsourced analytical testing activities, including method development, transfer, materials testing, in-process controls, lot release, and stability programs. Review chromatographic data, related notebooks and sample results generated at external third-party labs for scientific soundness, completeness, accurate representation of the data, and final reported results. Collaborate with formulation, process development, and quality control teams to troubleshoot and resolve analytical challenges. Manage QC scheduling, sample logistics, and coordination of shipments with internal/external stakeholders. Responsible for review of certificate of analysis, stability reports, data analysis for reporting and shelf-life extensions for DS/DP. Maintain the reference standard and impurity markers qualification and inventory. Monitor data trends, troubleshoot QC method performance, and investigate OOT/OOS results. Collaborate closely with cross-functional teams including drug substance, drug product, QA, and regulatory affairs Qualifications: B.S/M.S. degree in chemistry, biochemistry or equivalent with 8+ years of analytical development experience Broad analytics expertise with widely employed techniques supporting inhaled products- HPLC (UV, RID, ELSD, CAD), GC, MS, NMR, XRPD, DSC/TGA, KF, particle size analysis, APSD, DDU, and dissolution Logical and methodical when solving problems, developing solutions, and making sound recommendations with limited input from senior team members Strong understanding of regulatory requirements for pharmaceutical product development, ICH, FDA, and EMA guidance and GMP requirements governing process development, manufacturing, and stability Experience working with CMC Teams and managing relationships with CMC vendors is strongly preferred Strong analytical, problem solving and critical thinking skills with succinct verbal and written communication skills Detail oriented with excellent organizational skills, sufficient to multi-task in an extremely fast-paced, small company environment with changing priorities while maintaining attention to detail Ability to travel ~10-15% as needed Pulmovant provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We will not accept unsolicited resumes nor outreach from agencies. Please do not send agency resumes to our website or Roivant Sciences and affiliated employees. Thanks!

The Department of Chemistry and Biochemistry at John Carroll University seeks to fill a tenure track Assistant Professor position. Full consideration will be given to applications that are complete by November 14, 2025, although applications will be accepted until the position is filled. The anticipated hire start date will be January 2026 or August 2026 depending on the candidate's availability. The primary teaching duties of the successful candidate will be the organic chemistry sequence and potentially inorganic chemistry, general chemistry lecture courses, general-organic-biochemistry lecture and lab, or other courses in their area of specialty. The University is dedicated to teaching excellence that contributes to a rich intellectual environment. Summer teaching may also be available and includes additional compensation. Participation in undergraduate research is expected. Service to the university is required and reflects the institution's mission-driven priorities, community engagement expectations, and shared governance culture. Service to the department and the university is required. Professional and community service are strongly encouraged. These three components (teaching, research and service) are guided by the department's tenure policy. ABOUT THE DEPARTMENT OF CHEMISTRY AND BIOCHEMISTRY The Department of Chemistry and Biochemistry is approved by the American Chemical Society (ACS) and offers a program that leads to a B.S. in Chemistry, with optional concentrations in Biochemistry and Chemical Physics. The department currently includes four full-time tenured faculty, a research scholar in residence, a general chemistry lab coordinator, a half-time administrative assistant, a half-time laboratory technician, and a central stores manager who also serves as the chemical hygiene officer. A fifth tenured professor in chemistry currently serves as Associate Dean in the College of Arts and Sciences. The department graduates 10-20 majors each year, with approximately two-thirds engaging in research projects both on and off campus. The department is equipped with modern instrumentation including a 60 MHz NMR, ESR, GC, GC-MS, HPLC, IR, DSC, Fluorimeter, UV-Vis, Electrochemical, AA, ICP-OES, Microwave Synthesis and Polarimeter. For additional information on the University and the Department, please visit: jcu.edu/academics/chemistry Duties and Responsibilities The primary teaching duties of the successful candidate will be organic chemistry lecture and laboratory courses, and the ability to contribute to the teaching of inorganic chemistry, general chemistry lecture courses, general-organic-biochemistry lecture and lab, or other courses in their area of specialty would also be helpful. Required Qualifications * A Ph.D. in chemistry is required at the time of appointment and some teaching experience is desirable. * The successful candidate will have a strong commitment to undergraduate education in a liberal arts environment and be familiar with pedagogical practices informed by chemistry education research, including active learning approaches. Preferred Qualifications * The ability to teach advanced undergraduate courses in their area of specialization * A fundamental knowledge of and experience with course level assessment of learning outcomes will be an advantage. Normal Work Location, Hours and Conditions University core business hours are generally 8:30 am - 5 pm. However, this position may require work to be performed outside of normal business hours based on department operations. About John Carroll University John Carroll University is a private, coeducational, Jesuit Catholic university, founded in 1886, dedicated to developing people with the knowledge and character to lead and to serve. The University is located in University Heights, Ohio, an attractive residential suburb 10 miles east of downtown Cleveland. Academically, the University consists of the College of Arts and Sciences, the College of Health and the Boler College of Business, which include graduate programs. The University offers more than 70 Academic Programs in the arts, social sciences, natural sciences, and business at the undergraduate level, and in select areas at the master's level. The University enrolls approximately 2,300 undergraduate students and 500 graduate students and has a student-to-faculty ratio of 13:1. John Carroll University is one of 27 Jesuit universities in the United States and has been listed in U.S. News & World Report magazine's top 10 rankings of Midwest regional universities for more than 30 consecutive years.

Title: QC Associate Scientist II Duration: Direct Hire Salary: $75,000-$80,000 MUST BE A US CITIZEN (C2C and Visas not accepted) TOP 5 MUST HAVE SKILLS HPLC & GC hands-on experience in a GMP-regulated environment General analytical techniques (FTIR, KF, UV-Vis, titrations, particle size, etc.) Strong documentation and GDP adherence (ALCOA++ understanding) Experience supporting release testing for raw materials/intermediates/APIs Ability to troubleshoot OOS and support investigations Required Years: 4-5 years of experience in a GMP laboratory Education: Bachelor's degree in Chemistry, Biochemistry, or related scientific field Technology / Instrumentation: HPLC GC FTIR Karl Fischer UV-Vis XRD, NMR, DSC, TGA (nice-to-have) ICP-MS / ICP-AES (preferred but not required) Skills: Chromatography expertise Analytical method execution Data integrity (ALCOA++) Good Documentation Practices (GDP) Strong organizational & communication skills

Lab Analytical Lead- Flavor Creation Glanbia Join this dynamic team focused on delivering better nutrition for every step of life's journey The Opportunity We are seeking an experienced, highly skilled Flavor Analytical Lead to join our Research & Development team. This role is critical in supporting flavor creation, product development, and innovation initiatives through advanced analytical testing. The ideal candidate will bring deep expertise in chromatographic and spectrometric techniques, strong problem‑solving abilities, excellent leadership capability, and the ability to collaborate across functions in a dynamic environment. Essential Functions Analytical Testing & Method Development * Perform qualitative and quantitative analysis of flavors, extracts, and complex mixtures using GC, GC‑MS, GC‑FID, HPLC, SPME, and related analytical techniques. * Conduct extraction, purification, and identification of flavor compounds in raw materials and finished products. * Develop, optimize, and validate analytical methods to support new product development and quality objectives. * Prepare, calibrate, and maintain instrumentation, ensuring high accuracy and reliability in analytical workflows. * Interpret complex analytical datasets and provide clear, actionable reports. Leadership & Project Management * Supervise and mentor a small team of analytical scientists, fostering technical development and operational excellence. * Manage customer-driven analytical projects and innovation initiatives, delivering results efficiently and with scientific depth. * Ensure laboratory operations meet internal SOPs, regulatory standards, and safety requirements. Documentation & Cross-Functional Collaboration * Maintain precise documentation for methods, validation protocols, instrument logs, and analytical findings. * Partner closely with flavorists, R&D scientists, quality, and production teams to ensure alignment of analytical insights with development goals. * Support evaluation and implementation of new technologies, equipment, and techniques. The Skills you will bring to the team * Bachelor's degree in Chemistry, Food Science, or a related scientific field. * 10+ years of hands-on experience with GC, GC‑MS, GC‑FID, and related analytical instrumentation. * Strong understanding of analytical chemistry, including extraction techniques, chromatography, and mass spectrometry. * Experience in analytical method development and sample preparation techniques. * Exceptional attention to detail, critical thinking, and problem‑solving abilities. * Strong organization skills with the ability to manage multiple simultaneous priorities. * Excellent communication skills (written and verbal). * Ability to work independently and collaboratively in a fast-paced R&D environment. Preferred * Experience analysing flavor compounds, natural extracts, and food chemistry, including sensory/organoleptic attributes. * Proficiency with SPME headspace, liquid extraction, LC/LC‑MS, and additional spectroscopic methods (NMR, FTIR). * Instrument troubleshooting and routine maintenance experience. * Familiarity with regulated laboratory environments (GMP, GLP). * Experience using ChemStation and/or Empower data systems. * Ability to interpret complex analytical profiles and provide data‑driven recommendations. Physical Requirements * Ability to work safely in a laboratory environment, handling chemical reagents and instrumentation. * Ability to lift up to 25 lbs as needed. * Ability to stand or work at laboratory equipment for extended periods. Where and how you will work The opportunity will be based in Sharonville, OH. What we would like to offer you! The opportunity to develop your career on a global stage, continuous learning through an on-demand learning platform, and a competitive compensation package including staff discounts, generous family leave policy, health & dental plan, competitive salary, 401K. About Glanbia Glanbia is a better nutrition company with three divisions: Performance Nutrition, Health & Nutrition and Dairy Nutrition. Collectively and with our partners we offer an incredible breadth of expertise in nutrition. We employ a team of 5800 people, work with global food and beverage companies, and sell our award-winning and market-leading brands and ingredients in more than 100 countries worldwide At Glanbia, we celebrate diversity, because we know that our individual strengths make us stronger together. We welcome and encourage interest from a variety of candidates, we will give your application consideration, without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. At Glanbia, our culture celebrates individuality, knowing that together we are more. Nearest Major Market: Cincinnati

Apply now Job Title: Post Doc Fellow, Pathology & Lab Medicine Work Arrangement: Current UC employees must apply internally via SuccessFactors Founded in 1819, the University of Cincinnati ranks among the nation's best urban public research universities. Home to 53,235 students, more than 11,000 faculty and staff and 350,000+ living alumni, UC combines a Top 35 public research university with a physical setting The New York Times calls "the most ambitious campus design program in the country." With the launch of Next Lives Here, the Cincinnati Innovation District, a $100 million JobsOhio investment, three straight years of record enrollment, worldwide leadership in cooperative education, a dynamic academic health center and entry into the Big 12 Conference, UC's momentum has never been stronger. UC's annual budget stands at $1.85 billion, and its endowment totals nearly $1.8 billion. Job Overview As one of the oldest medical schools in the country, the UC College of Medicine has a reputation for training best-in-class health care professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients. The Department of Pathology and Laboratory Medicine at the University of Cincinnati includes accomplished physicians, research scientists, clinical laboratory scientists, and administrative, technical, and clerical staff who support our work. The Department of Pathology & Laboratory Medicine is seeking a candidate for a Post Doctoral Fellow position within a well-funded laboratory at the Center for Lipid and Atherosclerosis Studies (CLAS) at the University of Cincinnati, College of Medicine. Essential Functions * Work on projects involving the structure, composition, and function of high-density lipoproteins (HDL) as well as defining how proteins work together on the surface of triglyceride-rich lipoproteins to work against hypertriglyceridemia in cardiovascular disease and diabetes. * Conduct research experiments in lipoprotein metabolism within the pre-determined research scope and methodology. * Gather and analyze data and develop new ideas that promote current research. * Prepare data summaries, reports, manuscripts and presentations of research results. * Participate/assist in manuscript writing for publication in scientific journals and/or presentation; may assist in grant writing. * Keep informed of developments in field to maintain and enhance professional expertise. * May teach techniques to others, train, and mentor junior research staff. * Engage in appropriate training and professional development opportunities. * Play an active role in seeking career and research advice, both from the faculty supervisor and from other faculty members as well. * Perform related duties based on departmental need. This job description can be changed at any time. Required Education Doctoral Degree in the appropriate field or discipline, or the recognized terminal degree. Required Experience * In-depth knowledge of protein structural biology including experimental methods for determining protein structure such as X-ray crystallography, NMR, chemical cross-linking, cryo-EM, etc. * An understanding of protein modeling and simulation. Additional Qualifications Considered May require experience with specialized software programs such as PyMol, Chimera and others. Physical Requirements/Work Environment * Office environment/no specific unusual physical or environmental demands. Compensation and Benefits UC offers a wide array of complementary and affordable benefit options, to meet the financial, educational, health, and wellness needs of you and your family. Eligibility varies by position and FTE. * Competitive salary range dependent on the candidate's experience. * Comprehensive insurance plans including medical, dental, vision, and prescription coverage. * Flexible spending accounts and an award-winning employee wellness program, plus an employee assistance program. * Financial security via our life and long-term disability insurance, accident and illness insurance, and retirement savings plans. * Generous paid time off work options including vacation, sick leave, annual holidays, and winter season days in addition to paid parental leave. * Tuition remission is available for employees and their eligible dependents. * Enjoy discounts for on and off-campus activities and services. As a UC employee, and an employee of an Ohio public institution, if hired you will not contribute to the federal Social Security system, other than contributions to Medicare. Instead, UC employees have the option to contribute to a state retirement plan (OPERS, STRS) or an alternative retirement plan (ARP). To learn more about why UC is a great place to work, please visit our careers page at ******************************** For questions about the UC recruiting process or to request accommodations with the application, please contact Human Resources at ***********. The University of Cincinnati is an Equal Opportunity Employer. REQ: 97785 SF:OMJ SF:RM SF:HEJ, SF:INS SF:HERC SF:DIV SF:LJN SF:IHE Apply now

Job Location: Paninesville, Ohio Job type: Full-time Type of role: On-site Work Schedule: DuPont Schedule (12-hour rotating shift) About Lubrizol The Lubrizol Corporation, a Berkshire Hathaway company, is a specialty chemical company whose science delivers sustainable solutions to advance mobility, improve wellbeing and enhance modern life. Founded in 1928, Lubrizol owns and operates more than 100 manufacturing facilities, sales, and technical offices around the world and has about 8,000 employees. For more information, visit ***************** We value diversity in professional backgrounds and life experiences. By enabling a consistent, unbiased, and transparent recruitment process, Lubrizol seeks to create a positive experience for candidates so we can get to know them at their best. We recognize unique work and life situations and offer flexibility, ensuring our employees feel engaged and fulfilled in every aspect of life. Join Our Thriving Team at Lubrizol as a Quality Control Lab Analyst Unleash Your Potential. At Lubrizol we're transforming the specialty chemicals market and looking for exceptional talent to join us on this journey. If you are ready to join an international company with talent around the world, and want to make a real impact, we want you on our team. What You'll Do: Performs all QC Lab activities, including but not limited to: all Standard Work Process (SWP), Management Systems, and analytical responsibilities. What We're Looking For: * Provide internal and external customers with the highest level of customer service in responsiveness while performing QC activities. * Interface with all corporate, commercial, supply chain, customer experience, and lab / operations personnel. * Communicate between departments when reporting results and execute SWP / SOP in an exemplary manner. * Perform all test methods without supervision within precision and accuracy standards. * Prepare all solutions needed for testing. * Perform testing on raw material, in-process, finished good, and miscellaneous samples. * Document all data in corresponding laboratory notebook, SAP, LIMS as business needs dictate. * Dispose of all chemicals safely * Perform required testing pertaining to customer complaints, discrepancies, & laboratory investigations. * Report results to operations, in a timely manner. * Review and approve laboratory results as needed. * Assist in the performance of qualifications and validations of instruments, test methods, and basic PMs. * Troubleshoot/self-evaluate OOS results. * Assist in writing SWP, SOPs, methods, protocols, and reports. * Perform daily laboratory maintenance. * Oversee the training of new employee's basic laboratory skills and functions. * Perform simple problem solving and participate in improving daily work Skills That Make a Difference: * Associate degree in chemistry or a related technical field or 5 years' experience in an industrial manufacturing laboratory. * Experience with one of the following analytical techniques: * physical property testing * wet chemistry * advance instrumental analytical techniques. * Highly self-motivated individual, focused on providing high quality laboratory data in an efficient manner, while exhibiting excellent workplace skills. * Solid background in Microsoft Office and computer-based instrument control systems for analytical equipment. * Excellent verbal and written communication skills. * Advanced problem-solving skills and the ability to make competent, independent, decisions in a timely manner to ensure excellent progress on assigned tasks. * Ability to effectively manage multiple and or changing priorities with minimal to no supervision. * Must possess the ability to interact effectively and professionally with internal customers, external customers, vendors, and various stakeholders. Considered a Plus: * Bachelor's degree in chemistry with 1-5 years relevant experience. * Industrial chemical manufacturing laboratory experience is preferred with 1-5 years' experience. * Analytical experience with advanced instrumental techniques like GC, LC, ICP, and NMR. * Analytical experience with wet chemistry and physical property testing. * Experience with LIMS and SAP QM modules. * Experience with proper usage and administration of Lab notebooks / elog notebooks. * Experience with root cause problem solving techniques and tools. * Experience with Statistical Quality Control methodologies. * Experience working in ISO9001/14001 environments. * Experience with internal auditing a plus. Perks and Rewards That Inspire: * Competitive salary with performance-based bonus plans * 401K Match plus Age Weighted Defined Contribution * Competitive medical, dental & vision offerings * Health Savings Account * Paid Holidays, Vacation, Parental Leave * Flexible work environment Learn more at benefits.lubrizol.com! Ready for your next career step? Apply today and let's shape the future together! It's an exciting time to be part of Lubrizol. Lubrizol is not staying put. We are continually learning and evolving. Our passion delivers our success - not only for Lubrizol but for those who count on us every day: our employees, customers, and communities. As a diverse, global team, we work together to solve some of the world's most pressing challenges. We impact everyday lives through science only Lubrizol can deliver, and we never stop pushing to do it better. One of the founding principles of The Lubrizol Corporation more than 90 years ago was treating every employee with dignity and respect. That same commitment is only stronger today. More than that, we are committed to providing an environment where every employee can be the best they can be, no matter their race, color, religion, sex, national origin, sexual orientation, gender identity, disability, or protected veteran status, or any other characteristic. #LI-CS1

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: * Safely perform multi-disciplined assays and unit operations involving stable isotope products, ensuring all tasks are completed according to established protocols and quality standards. * Maintain a safe work environment by taking immediate action to resolve unsafe conditions, ensuring adequate training for all assignments, and strictly adhering to change control procedures. * Provide complete, accurate records and logbook entries consistent with quality guidelines, ensuring all data is ready for potential participation in quality audits. * Contribute to essential lab support functions, including the preparation of reagents, restocking supplies, equipment maintenance, and responsible waste disposal. * Manage a high volume of work to meet departmental goals and deadlines while maintaining a clean, organized workspace during and after operations. * Provide technical assistance to team members and perform routine troubleshooting of procedures or equipment to maintain workflow continuity. * Interface effectively with other departments and keep supervisors informed on the status of operations, specifically highlighting any deviations from standard protocols. * Identify and implement process improvements through scientific knowledge and committee participation to enhance site performance in areas like safety, cost, and output. Who You Are: Minimum Qualifications: * Bachelor's Degree in Chemistry, Biology, or other Life Science discipline and 1+ years of laboratory work experience. OR * High School Diploma or GED and 4+ years of laboratory work experience. Preferred Qualifications: * Strong mechanical skills with chemical glassware (flasks, fittings, connectors, condensers, and traps) and equipment (heating mantles, stirrers, clamps, and jacks) Hoses (compressed air lines, vacuum lines, cylinder lines, and thermocouples). * Strong troubleshooting skills to troubleshoot chemical reactions, analytical testing, and instrument issues and identify solutions based on knowledge of modern chemistry techniques. * Strong laboratory skills including weighing, measuring, pouring, filtering, making solutions, basic laboratory calculations (pH, molar concentration, percent yield, grams to moles, stoichiometric conversions, and buffer solutions), interpreting analytical data and characterizing and identifying molecular compounds and gases using NMR, HPLC, GC, and MS instruments, among others, and handling chemicals safely wearing personal protective equipment. * Experience with analytical chemistry including instruments and methods, organic chemistry including basic reactions (sn1, sn2, E1, E2, oxidations, reductions, carbonyl reactions, carbon-carbon bond forming reactions, and aromatic reactions), inorganic chemistry including cations, anions, ionic bonding, salts, oxides, and organometallics, and gases including elemental gases, gas mixtures, pressure, temperature, volume, isotopic enrichment. Pay Range for this position: $23 - $37/hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Science & Research Concord, Ohio, US + Added - 19/01/2026 Apply for Job **_We're hiring an Associate Scientist with analytical experience to join a global leader in the development and production of active pharmaceutical ingredients (APIs) for CDMO partners and generic drugs. This is a great opportunity to work with an industry leader that focuses on their expertise and competence in all of the companies processes!_** **Salary:** 70K-80K **Schedule:** M-F 8a-5p **Location:** Lake County, OH **_***Benefits include***_** _PTO, health/vision/dental insurance, HSA, 401(k) with match, and holiday pay!_ **Responsibilities:** + Perform routine HPLC and GC analysis to support API method transfers, including data generation, interpretation, and documentation in compliance with GMP standards + May perform other analytical testing (e.g., FTIR, KF, NMR) + Support GMP method transfers, including protocol/report preparation + Conduct release testing for raw materials, intermediates, and APIs + Investigate out-of-specification (OOS) results and document findings + Ensure timely and compliant data generation to meet project timelines + Review analytical data for accuracy and GDP compliance **Qualifications:** + Bachelor's degree in chemistry or related field + Minimum of 3 years' hands-on experience performing HPLC and GC analysis in a GMP regulated pharmaceutical environment + Demonstrated experience in analytical method transfers + Strong working knowledge of GLP/GMP standards, quality control procedures, and laboratory documentation practices **_***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!***_** INDBH \#LI-DNP We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

AV has an opportunity available for a full-time research scientist to work with the Polymer and Responsive Materials Research Team at Wright Patterson Air Force Base (WPAFB), OH. The successful candidate will join a team of diverse and multi-disciplinary scientists with a broad range of skills including synthetic chemistry, nanomaterial development, mechanical engineering, and polymer modeling. The candidate will be responsible for the design and synthesis of 2D conjugated polymers, such as Covalent Organic Frameworks (COFs), for optoelectronic applications. Successful candidates must possess strong synthesis skills, specifically related to the preparation of low-dimensional organic materials and conjugated polymers, as well as expertise in film fabrication. Furthermore, knowledge of and experience with a wide array of electrochemistry and optoelectronic characterization techniques are highly desired. The candidate will be expected to contribute to the thought leadership of the project and will have the opportunity to expand their skillset in a wide array of materials chemistry and engineering while refining their written and oral communication skills. **Key Responsibilities:** + Design, synthesis, and processing of conjugated polymers or COFs for optoelectronic materials + Electrochemical and optoelectronic characterization of COFs or conjugated polymers + Collaboration with other experts to further characterize and expand the applicability of synthetic platforms beyond the chemistry + Communicate methodologies effectively both written and verbal to a community of peers + Manage and mentor the research and professional development of junior team members **Requirements:** + This position is working within a government facility and requires US Citizenship (and may require the ability to obtain a security clearance). + PhD in Chemistry, Polymer Science, Chemical Engineering, Materials Science, or a related field of study required + 0-3 years' experience + Ability to understand and apply principles of organic polymer synthesis to develop next-generation materials systems + Strong quantitative and problem-solving skills + Strong oral and written communication skills + Willingness to collaborate and communicate with other scientists with professionally and personally diverse backgrounds + Familiarity with productivity software suites (Microsoft Office, Google Suite) that are used for email, word processing, spreadsheets, presentations, cloud file sharing, and virtual meetings **Additional Skills Preferred:** + Familiarity with the synthesis and processing of COFs or conjugated polymers + Electrochemical characterization skills (e.g., Cyclic Voltammetry, Spectro-electrochemistry, etc.) + Experience in characterization of crystalline porous materials (e.g., PXRD, Grazing incidence X-ray, gas sorption, etc.) + Knowledge and understanding of electronic-structure theory of organic materials + Design, synthesis, and characterization of organic molecules (e.g., NMR, FT-IR, Mass Spec, UV-Vis, PL, Raman, etc.) **Clearance Level** No Clearance The salary range for this role is: AeroVironment considers several factors when extending an offer, including but not limited to, the location, the role and associated responsibilities, a candidate's work experience, education/training, and key skills. **ITAR Requirement:** _T_ _his position requires access to information that is subject to compliance with the International Traffic Arms Regulations ("ITAR") and/or the Export Administration Regulations ("EAR"). In order to comply with the requirements of the ITAR and/or the EAR, applicants must qualify as a U.S. person under the ITAR and the EAR, or a person to be approved for an export license by the governing agency whose technology comes under its jurisdiction. Please understand that any job offer that requires approval of an export license will be conditional on AeroVironment's determination that it will be able to obtain an export license in a time frame consistent with AeroVironment's business requirements. A "U.S. person" according to the ITAR definition is a U.S. citizen, U.S. lawful permanent resident (green card holder), or protected individual such as a refugee or asylee. See 22 CFR § 120.15. Some positions will require current U.S. Citizenship due to contract requirements._ **Benefits** : AV offers an excellent benefits package including medical, dental vision, 401K with company matching, a 9/80 work schedule and a paid holiday shutdown. For more information about our company benefit offerings please visit: ********************************* . We also encourage you to review our company website at ******************** to learn more about us. Principals only need apply. NO agencies please. **Who We Are** Based in California, AeroVironment (AVAV) is a global leader in unmanned aircraft systems (UAS) and tactical missile systems. Founded in 1971 by celebrated physicist and engineer, Dr. Paul MacCready, we've been at the leading edge of technical innovation for more than 45 years. Be a part of the team that developed the world's most widely used military drones and created the first submarine-launched reconnaissance drone, and has seven innovative vehicles that are part of the Smithsonian Institution's permanent collection in Washington, DC. Join us today in developing the next generation of small UAS and tactical missile systems that will deliver more actionable intelligence to our customers so they can proceed with certainty - and succeed. **What We Do** Building on a history of technological innovation, AeroVironment designs, develops, produces, and supports an advanced portfolio of unmanned aircraft systems (UAS) and tactical missile systems. Agencies of the U.S. Department of Defense and allied military services use the company's hand-launched UAS to provide situational awareness to tactical operating units through real-time, airborne reconnaissance, surveillance, and target acquisition. _We are proud to be an EEO/AA Equal Opportunity Employer, including disability/veterans. AeroVironment, Inc. is an Equal Employment Opportunity (EEO) employer and welcomes all qualified applicants. Qualified applicants will receive fair and impartial consideration without regard to race, sex, color, religion, national origin, age, disability, protected veteran status, genetic data, sexual orientation, gender identity or other legally protected status._ **ITAR** U.S. Citizenship required **About AV:** **AV isn't for everyone. We hire the curious, the relentless, the mission-obsessed. The best of the best.** We don't just build defense technology-we redefine what's possible. As the premier autonomous systems company in the U.S., AV delivers breakthrough capabilities across air, land, sea, space, and cyber. From AI-powered drones and loitering munitions to integrated autonomy and space resilience, our technologies shape the future of warfare and protect those who serve. Founded by legendary innovator Dr. Paul MacCready, AV has spent over 50 years pushing the boundaries of what unmanned systems can do. Our heritage includes seven platforms in the Smithsonian-but we're not building history, we're building what's next. **If you're ready to build technology that matters-with speed, scale, and purpose-there's no better place to do it than AV.** **Careers at AeroVironment (*****************************************

Laboratory Concord, Ohio, US + Added - 06/05/2025 Apply for Job Our client is a contract research and development manufacturing service provider to chemical-based industries, and they're looking for a **Method Development Associate Scientist** to join their growing team! + Direct Hire + Salary: $70-80K + Shift: 1st shift 8a-5p M-F **Position Summary** We are seeking a detail-oriented and proactive Associate Scientist to join our cGMP Laboratory. This role involves supporting analytical stability studies in compliance with regulatory guidelines. The ideal candidate will have hands-on experience with small molecule drug substances and drug product batch release and stability testing, and experience working in a cGMP environment. + We are seeking an Associate Scientist with at least 2 years of experience in a GMP analytical laboratory environment. + The ideal candidate will have hands-on experience with HPLC, NMR, and Mass Spectrometry, supporting small molecule drug substance and product testing. + Responsibilities include conducting stability studies, batch release testing, and generating analytical data using techniques such as FTIR, GC, KF, XRD, DSC, and TGA. + Strong documentation practices, attention to detail, and ability to work cross-functionally are essential. + Must have experience with HPLC, NMR and Mass Spec and coming from a GMP Lab environment and have 2 years of relevant analytical Lab environment experience. Minimum B.S. in chemistry with 2+ years related pharmaceutical analytical laboratory experience or equivalent combination of education and experience is required _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!_ INDBH \#LI-DNP: We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Job type: Full-time Type of role: On-site Work Schedule: DuPont Schedule (12-hour rotating shift) The Lubrizol Corporation, a Berkshire Hathaway company, is a specialty chemical company whose science delivers sustainable solutions to advance mobility, improve wellbeing and enhance modern life. Founded in 1928, Lubrizol owns and operates more than 100 manufacturing facilities, sales, and technical offices around the world and has about 8,000 employees. For more information, visit **************** . We value diversity in professional backgrounds and life experiences. By enabling a consistent, unbiased, and transparent recruitment process, Lubrizol seeks to create a positive experience for candidates so we can get to know them at their best. We recognize unique work and life situations and offer flexibility, ensuring our employees feel engaged and fulfilled in every aspect of life. Join Our Thriving Team at Lubrizol as a Quality Control Lab Analyst Unleash Your Potential. At Lubrizol we're transforming the specialty chemicals market and looking for exceptional talent to join us on this journey. If you are ready to join an international company with talent around the world, and want to make a real impact, we want you on our team. What You'll Do: Performs all QC Lab activities, including but not limited to: all Standard Work Process (SWP), Management Systems, and analytical responsibilities. What We're Looking For: Provide internal and external customers with the highest level of customer service in responsiveness while performing QC activities. Interface with all corporate, commercial, supply chain, customer experience, and lab / operations personnel. Communicate between departments when reporting results and execute SWP / SOP in an exemplary manner. Perform all test methods without supervision within precision and accuracy standards. Prepare all solutions needed for testing. Perform testing on raw material, in-process, finished good, and miscellaneous samples. Document all data in corresponding laboratory notebook, SAP, LIMS as business needs dictate. Dispose of all chemicals safely Perform required testing pertaining to customer complaints, discrepancies, & laboratory investigations. Report results to operations, in a timely manner. Review and approve laboratory results as needed. Assist in the performance of qualifications and validations of instruments, test methods, and basic PMs. Troubleshoot/self-evaluate OOS results. Assist in writing SWP, SOPs, methods, protocols, and reports. Perform daily laboratory maintenance. Oversee the training of new employee's basic laboratory skills and functions. Perform simple problem solving and participate in improving daily work Skills That Make a Difference: Associate degree in chemistry or a related technical field or 5 years' experience in an industrial manufacturing laboratory. Experience with one of the following analytical techniques: physical property testing wet chemistry advance instrumental analytical techniques. Highly self-motivated individual, focused on providing high quality laboratory data in an efficient manner, while exhibiting excellent workplace skills. Solid background in Microsoft Office and computer-based instrument control systems for analytical equipment. Excellent verbal and written communication skills. Advanced problem-solving skills and the ability to make competent, independent, decisions in a timely manner to ensure excellent progress on assigned tasks. Ability to effectively manage multiple and or changing priorities with minimal to no supervision. Must possess the ability to interact effectively and professionally with internal customers, external customers, vendors, and various stakeholders. Considered a Plus: Bachelor's degree in chemistry with 1-5 years relevant experience. Industrial chemical manufacturing laboratory experience is preferred with 1-5 years' experience. Analytical experience with advanced instrumental techniques like GC, LC, ICP, and NMR. Analytical experience with wet chemistry and physical property testing. Experience with LIMS and SAP QM modules. Experience with proper usage and administration of Lab notebooks / elog notebooks. Experience with root cause problem solving techniques and tools. Experience with Statistical Quality Control methodologies. Experience working in ISO9001/14001 environments. Experience with internal auditing a plus. Perks and Rewards That Inspire: Competitive salary with performance-based bonus plans 401K Match plus Age Weighted Defined Contribution Competitive medical, dental & vision offerings Health Savings Account Paid Holidays, Vacation, Parental Leave Flexible work environment Learn more at benefits.lubrizol.com! Ready for your next career step? Apply today and let's shape the future together! It's an exciting time to be part of Lubrizol. Lubrizol is not staying put. We are continually learning and evolving. Our passion delivers our success - not only for Lubrizol but for those who count on us every day: our employees, customers, and communities. As a diverse, global team, we work together to solve some of the world's most pressing challenges. We impact everyday lives through science only Lubrizol can deliver, and we never stop pushing to do it better. One of the founding principles of The Lubrizol Corporation more than 90 years ago was treating every employee with dignity and respect. That same commitment is only stronger today. More than that, we are committed to providing an environment where every employee can be the best they can be, no matter their race, color, religion, sex, national origin, sexual orientation, gender identity, disability, or protected veteran status, or any other characteristic. #LI-CS1

Quality Control Concord, Ohio, US + Added - 20/01/2026 Apply for Job Pay Rate Low: 75000 | Pay Rate High: 90000 **_We're hiring an Associate Scientist with analytical experience to join a global leader in the development and production of active pharmaceutical ingredients (APIs) for CDMO partners and generic drugs. This is a great opportunity to work with an industry leader that focuses on their expertise and competence in all of the companies processes!_** **Schedule:** M-F 8a-5p **Location:** Lake County, OH **_***Benefits include***_** _PTO, health/vision/dental insurance, HSA, 401(k) with match, and holiday pay!_ **Responsibilities:** + Perform routine HPLC and GC analysis to support API method transfers, including data generation, interpretation, and documentation in compliance with GMP standards + May perform other analytical testing (e.g., FTIR, KF, NMR) + Support GMP method transfers, including protocol/report preparation + Conduct release testing for raw materials, intermediates, and APIs + Investigate out-of-specification (OOS) results and document findings + Ensure timely and compliant data generation to meet project timelines + Review analytical data for accuracy and GDP compliance **Qualifications:** + Bachelor's degree in chemistry or related field + Minimum of 3 years' hands-on experience performing HPLC and GC analysis within GMP pharmaceutical manufacturing + Demonstrated experience in analytical method transfers + Strong working knowledge of GLP/GMP standards, quality control procedures, and laboratory documentation practices **_***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!***_** INDBH \#LI-DH3 We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Science & Research Concord, Ohio, US + Added - 15/01/2026 Apply for Job Pay Rate Low: 75000 | Pay Rate High: 90000 _Our client, a leading contract manufacturer and research organization of API's, is looking for a skilled_ **_QC Associate Scientist I & II_** _to join their team in Lake County, OH!_ **Location:** Lake County, OH Positions: QC Associate Scientist (level I & II openings) **Salary:** $75,000 - $80,000 per year (level I), $80,000-$90,000 (level II) **Employment Type:** Full-time **Position Summary** The QC Associate Scientist I/II will support a GMP-regulated API analytical laboratory by performing routine and non-routine analytical testing, method transfers, and investigations. This role requires strong expertise in HPLC and GC analysis, experience working within cGMP environments, and the ability to collaborate cross-functionally to support project timelines and quality objectives. **Responsibilities** + Perform routine HPLC and GC analyses in a GMP API analytical laboratory. + Execute and support GMP analytical method transfers, including preparation of transfer protocols and final reports. + Conduct additional analytical techniques as needed, including but not limited to: FTIR, IC, Karl Fischer (KF), XRD, NMR, DSC, TGA, particle size analysis, Titrations, UV-Vis spectroscopy, and optical rotation. + Coordinate release testing for raw materials, intermediates, and active pharmaceutical ingredients (APIs). + Perform out-of-specification (OOS) investigations and support root cause analysis. + Ensure timely and compliant generation of analytical data to meet project and regulatory timelines. + Review analytical data for technical accuracy and adherence to good documentation practices. + Maintain compliance with cGMP, GLP, and laboratory safety requirements. + Collaborate effectively with Quality Assurance, Production, and Technical teams. + Perform other duties as assigned. **Qualifications** + Bachelor's degree (B.S.) in Chemistry or related scientific discipline required. + Minimum of 5 years of experience in a pharmaceutical analytical laboratory or equivalent combination of Strong hands-on experience with HPLC and GC instrumentation. + Proficient with standard laboratory equipment (balances, pipettes, pH meters, etc.). + Solid understanding of analytical chemistry principles and laboratory safety practices. + education and experience. + Demonstrated experience working in cGMP/GLP environments, including QC or stability testing. + Experience interacting with Quality Assurance and regulatory documentation. _*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! *_ _INDBH_ We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Quality Control Concord, Ohio, US + Added - 13/01/2026 Apply for Job _Our client, a leading contract manufacturer and research organization of API's, is looking for a skilled QC Associate Scientist to join their team in Lake County, OH!_ **Salary:** $75,000 - $80,000 per year **Employment Type:** Full-time **Position Summary** The QC Associate Scientist will support a GMP-regulated API analytical laboratory by performing routine and non-routine analytical testing, method transfers, and investigations. This role requires strong expertise in HPLC and GC analysis, experience working within cGMP environments, and the ability to collaborate cross-functionally to support project timelines and quality objectives. **Responsibilities** + Perform routine HPLC and GC analyses in a GMP API analytical laboratory. + Execute and support GMP analytical method transfers, including preparation of transfer protocols and final reports. + Conduct additional analytical techniques as needed, including but not limited to: FTIR, IC, Karl Fischer (KF), XRD, NMR, DSC, TGA, particle size analysis, Titrations, UV-Vis spectroscopy, and optical rotation. + Coordinate release testing for raw materials, intermediates, and active pharmaceutical ingredients (APIs). + Perform out-of-specification (OOS) investigations and support root cause analysis. + Ensure timely and compliant generation of analytical data to meet project and regulatory timelines. + Review analytical data for technical accuracy and adherence to good documentation practices. + Maintain compliance with cGMP, GLP, and laboratory safety requirements. + Collaborate effectively with Quality Assurance, Production, and Technical teams. + Perform other duties as assigned. **Qualifications** + Bachelor's degree (B.S.) in Chemistry or related scientific discipline required. + Minimum of 5 years of experience in a pharmaceutical analytical laboratory or equivalent combination of Strong hands-on experience with HPLC and GC instrumentation. + Proficient with standard laboratory equipment (balances, pipettes, pH meters, etc.). + Solid understanding of analytical chemistry principles and laboratory safety practices. + education and experience. + Demonstrated experience working in cGMP/GLP environments, including QC or stability testing. + Experience interacting with Quality Assurance and regulatory documentation. _*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! *_ \#INDH \#LI-DNP We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.