Chemist jobs in North Carolina

Job DescriptionBenefits: • Company car, • Flexible schedule, • Health insurance, • Opportunity for advancement, • Paid time off, • Profit sharing, • Training & development, • Bonus based on performance, • Competitive salary Environmental Manager Raleigh - Durham NC WTS, a leading By-Product and Waste Management firm, is seeking an experienced Environmental Manager in the Raleigh Durham NC region. The Environmental Manger is responsible for supervision and on-site coordination of services related to the proper disposition and shipment of hazardous wastes, non-hazardous wastes, packaged laboratory chemicals, materials for recycling. Primary tasks include overall site RCRA compliance, waste characterization, profiling, materials collection, and preparation of shipments, while ensuring regulatory compliance. Full Time Position Basic Required Qualifications Astute Chemistry Knowledge * • Degreed Chemist Preferred, • 3-5 Years Experience in Field Chemistry, • Focused ability to recognize and characterize risks associated with a wide variety of chemicals commonly used in various industrial settings., • Chemical Lab Packing Experience Preferred., • Working Knowledge of Hazardous Waste RCRA Regulations, • Experience in Waste Characterization, • Experience in Waste Profiling, • Experience in HW Manifest Preparation, • Working Knowledge of USDOT (PHSMA) Hazardous Materials Regulations, • Experience in HM Characterization, • Practical Knowledge of Pertinent HM Labeling, Marking, Placarding, Segregation, Packaging Regulations, • Experience in HM Shipping Paper Regulations, • Safety Oriented, • Ability to work independently as well as in a team setting, • Ability to travel as needed, • No restrictions on physical activities supplies, on-site container movement, load supervision, • OSHA Haz Wopper Trained, RCRA training, USDOT HM training preferred, • Located in Raleigh Durham region. Re-location possible. This is a remote position.

Clean Harbors in Charlotte, NC is seeking an Environmental Field Chemist (CleanPack Chemist) to handle, segregate, pack, and inspect chemical waste in accordance with Federal/State/Local regulations and our company policies and procedures. This position will work both indoors and outdoors at plants, labs, customer sites and are responsible for assisting with lab packs within customer facilities, household hazardous waste (HHW) collections and lab moves. This is a customer facing position, working at customer sites daily. The Environmental Field Chemist are (NOT) laboratory-based Chemist. The CleanPack Chemist role requires 80% travel across the United States. Clean Harbors is the leading provider of environmental, energy and industrial services throughout the United States, Canada, Mexico and Puerto Rico. Everywhere industry meets environment, Clean Harbors is on-site, providing premier environmental, energy and industrial services. We are solving tough problems through innovation and proven methodology – come be part of the solution with us. Why work for Clean Harbors? • Health and Safety is our #1 priority and we live it 3-6-5!, • Focus on maintaining sustainability and cleaning the Earth, • Pay Range $27.00 - $30.00 per hour, BOE, • Comprehensive health benefits coverage after 30 days of full-time employment including 401K with Company match, • Own part of the company with our Employee Stock Purchase Plan, • Opportunities for growth and development for all the stages of your career, • Ensure that Health and Safety is the number one priority by complying with all safe work practices, policies, and processes and always acting in a safe manner, • Prepare computer generated packing lists, labels, manifest, and land disposal restriction notifications, • Perform inspections of staging, accumulating and storage areas to ensure proper housekeeping procedures and compliance, • Inspect storage area and drums for leaks or spills, • Inspect drums for compliance with labeling regulations, • Collects, segregates, and properly packages waste chemicals for disposal to maximize efficiency and maintain compliance, • Executes Jobs at Clean Harbors customer locations including fortune 500 companies, • Responsible for final preparation and approval of all projects before shipment in accordance with OSHA, EPA, DOT and company policies, • Conducts projects/jobs according to site specific Federal, State, and local regulations and health and safety plans, • Understand customer specific disposal restrictions/special packaging requirements, • Sample and profile of new waste streams or any waste needing analytical testing, • Ensures drum count is correct and that drum conditions are shippable in accordance our company’s policies and procedure, • Follow all local, state (provincial) and federal compliance regulations and rules, • Safely operate vehicles in accordance with U.S. DOT, local, state (provincial) and federal requirements, • Safely observe all corporate operating guidelines and procedures, • Observe all company environmental health and safety operating guidelines, • Valid Driver’s license, • Strong customer service skills, • CDL Class A with hazmat and tanker endorsement, • Ability to operate manual transmission vehicles required, • Willing and able to travel up to 80%, both regionally and across the United States, • Perform physical functions per job requirements, • Successfully complete a background check, drug test, and physical, by position, • Per OSHA's Respiratory Protection Standard, 29 CFR 1910.34, employees in positions requiring respirators are required to meet facial hair standards. Preferred Qualifications:, • College degree in Chemistry or Natural Science, • Waste Disposal – Comprehensive disposal of hazardous and non-hazardous waste at Company-owned facilities, • Recycling Services – Extensive recycling, reuse and reclamation options for materials such as solvents, chemicals, oil and electrical equipment, • Chemical Packing – Safe, efficient handling and disposal of the widest range of chemicals, including reactives and compressed gases, • Household Hazardous Waste (HHW) Services – HHW collection programs of all types and sizes, facilitated by Clean Harbors expert personnel Clean Harbors is an equal opportunity employer. Clean Harbors is committed to providing access, equal opportunity and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation, contact ___ or 1-844-922-5547. Clean Harbors is a Military & Veteran friendly company. Clean Harbors is committed to complying with applicable pay transparency laws and ensuring fair and equitable compensation. The posted salary range reflects the minimum and maximum target for this role. Final compensation may vary based on factors such as location, experience, skills, and business needs. In addition to the base salary, some roles may be eligible for bonus or incentive compensation and a comprehensive benefits package. #CH

Job DescriptionDescription: We are seeking a highly skilled and motivated Senior Formulating Chemist to join our Research & Innovation team in the development of innovative cosmetic products. The ideal candidate will have extensive experience in Skincare and Hair Care formulation, a strong understanding of FDA regulations, and a proven ability to lead projects from concept through commercialization. This role requires technical expertise, cross-functional collaboration, and leadership in driving formulation excellence. Key Responsibilities: 1. Research & Innovation Leadership Lead multiple complex R&I projects with minimal supervision, from ideation through to scale-up and launch. Translate concept briefs into technically sound formulas, applying innovative ingredient solutions and troubleshooting formulation challenges. Identify and implement innovative formulation strategies aligned with consumer trends and brand objectives. Own all technical aspects of formulation development, including prototype creation, stability testing, and batch adjustments to meet key performance and regulatory criteria. 2. Formulation Development Design, develop, and optimize skincare and hair care formulations that meet performance, safety, regulatory, and stability requirements. Solve complex formulation challenges including emulsion stability, texture optimization, and preservative systems. Adapt formulas for different global market needs ( US, CAN, EU, Can, China, etc) 3. Regulatory Compliance & Safety Ensure all formulations comply with applicable FDA regulations for cosmetics and OTC products (if applicable), as well as global regulatory requirements. Maintain a strong understanding of internal development standards, including safety, microbiology, regulatory, and formulation charters. Prepare and maintain documentation for regulatory submissions, ingredient disclosures, and testing requirements. 4. Technical Leadership & Collaboration Provide scientific advisory support across projects, acting as a subject matter expert in formulation science. Coordinate with internal cross-functional teams (Regulatory, Microbiology, Claims, Packaging, and Manufacturing) and external partners to ensure seamless product development. Support scale-up and manufacturing processes in collaboration with Operations and QA/QC teams. 5. Mentorship & Team Development Mentor and train junior chemists and technicians, promoting best practices and fostering a culture of innovation and technical excellence. Team Leadership: May supervise and guide other team members, ensuring alignment with project goals and timelines. 6. Cross-Functional Collaboration Work closely with other departments such as Quality Assurance (QA), Quality Control (QC), Production, Regulatory, Packaging, and Marketing to ensure successful product development, scale-up, and launch. Support seamless communication and coordination across teams to resolve technical challenges and maintain alignment throughout the development process. 7. Technical Tools & Documentation Demonstrate proficiency in R&I lab systems, formulation software, and data analysis tools. Ensure accurate and timely documentation of lab work, formulation revisions, and stability results. Requirements: Qualifications: Bachelor’s degree in Chemistry, Chemical Engineering, Cosmetic Science, or a related field. 5–8+ years of formulation experience in skincare or cosmetic product development. Strong knowledge of FDA regulations and global compliance requirements (CAN, EU, China). Experience working in a regulated environment with an understanding of product safety, efficacy, and microbiological standards. Proficient in managing complex technical projects and leading cross-functional collaboration. Excellent verbal, written, and presentation skills. Strong problem-solving abilities and a proactive mindset. Preferred Experience: Experience of working with OTC products (acne, SPF, anti-dandruff). Familiarity with GMP, ISO 22716, and claims substantiation practices. Prior experience with clean beauty, natural ingredients, or sustainable formulation practices is a plus.

Job DescriptionStructural Integrity Associates, Inc. (SIA) is seeking a Senior Chemistry Consultant for our Nuclear business unit. The ideal candidate will be responsible for primarily BWR chemistry consulting work supporting the energy industry. The role will be to support the Chemistry Services team in BWR chemistry related services and support such as open and closed cooling water, primary chemistry systems, troubleshooting efforts, assessments, chemistry related equipment, and engineering support. The work environment is a dynamic team including potentially utilizing other technical expertise within SIA (e.g., Vessel and Internals, Materials, Vibration, etc.) based on project requirements. The role will support and perform analysis on projects that range from chemical optimization, transient modeling, EPRI research efforts, utility troubleshooting, etc. This is a full-time position that can be fully remote or based in one of Structural Integrity’s offices. Primary Responsibilities: • Participation in utility assessments (e.g., chemistry related system optimization, chemical optimization, troubleshooting, etc.), • Participation in utility equipment upgrades (e.g., PLC panel upgrades, chemical injection skids, etc.), • Participation in business development activities, including learning the business model that makes SIA successful, • Participation in EPRI and SIA related research initiatives, • Writing and reviewing reports generated from assessments and research Required Skills/Qualifications:, • 5-10 years of experience in the Nuclear Industry supporting Chemistry and/or Engineering efforts (specifically BWRs), • BS degree in Nuclear, Chemical Engineering, or other related science, • Project Management experience with multiple work groups, • Ability to travel to support clients and business development efforts (~20%), • Strength in writing technical reports and communication skills, • Previous qualified as a chemistry technician, staff chemist, staff engineer, or Senior Reactor Operator license, • Experience with SampleIQ and Nuclear Chemistry Applications (BWRVIA, etc.), • Significant Project Management experience Export Control Notice: Certain positions at SIA may require access to information and technology which is subject to Export Administration Regulations 15 CFR 730-774, including those of the US Department of Energy (DOE) in 10 CFR 810 and Nuclear Regulatory Commission (NRC) 10 CFR Part 110. Hiring decisions for such positions must comply with these regulations and may result in SIA limiting its consideration of foreign nationals who are citizens of countries that are not on the DOE’s Generally Authorized Destinations List: . About Us: SIA is an engineering consulting firm serving various industries including Nuclear Power, Energy Services, Pipeline Integrity, and Critical Infrastructure. Join a team of internationally recognized experts in a culture based on knowledge, excellence, and respect for one another. Our employees are members of a distinct community of internationally respected professionals committed to quality, engineering innovation and a shared goal of building a safer world. Why Work at SIA? SIA offers a competitive salary and performance-based bonus program. Our retirement benefits include a Traditional 401k, Roth 401k, and an employer match. To help employees maintain a work-life balance, SIA also offers various paid time off including vacation, floating holidays, sick time, and parental leave. Our employees also enjoy a comprehensive benefits program that includes the following: • Medical, dental, and vision insurance, • Life Insurance and AD&D, • Short-term and long-term disability, • Health Savings Account with employer contribution, • Flexible Spending Account for health care and dependent care SIA does not welcome third-party recruiters, employment agencies, headhunters, etc. Please do not reach out to SIA employees requesting a call, sit down, meeting, or email response. Powered by JazzHR GepXmpP6dc

Job Description Job Title: Quality Control Chemist Job Description We are seeking a dedicated Quality Control Chemist to perform routine analytical testing of raw materials, in-process samples, and finished products, along with wastewater sampling and adjustments. The role requires strict adherence to standard operating procedures and conducting triplicate assessments on testing procedures to ensure accuracy and compliance. Responsibilities • Ensure compliance with safety, health, and environmental protocols by wearing proper personal protective equipment., • Adhere to the company's Code of Conduct while conducting all business activities., • Perform in-process and finished product testing on various products., • Complete laboratory records and other documentation accurately following good documentation practices., • Communicate with the Shift Production Supervisor regarding in-process batch adjustments based on analytical test results., • Maintain cleanliness of the work area and notify colleagues when consumables need to be ordered., • Keep the workplace organized and orderly., • Understanding and adherence to safety, health, and environmental standards in the laboratory and facility., • Ability to communicate effectively and relate to employees at all levels within the company., • Ability to work independently while adjusting to the priorities of production., • Bachelor's degree in a science discipline, with a preference for Chemistry., • Familiarity with basic laboratory equipment such as GC/LC/FTIR and techniques like titration and liquid-liquid partition., • Previous laboratory experience is preferred., • Basic computer skills, including familiarity with spreadsheet programs., • Strong math and analytical problem-solving skills., • At least 5 years of previous work experience., • Self-motivated and well-organized individual. The pay range for this position is $26.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in SALISBURY,NC. Application Deadline This position is anticipated to close on Oct 15, 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 for other accommodation options.

Job Description We are an emerging technology company hiring A+ players only. As a fast-growing venture-backed advanced materials manufacturer of protective coatings, DetraPel is looking to expand its team to support hyper growth during this next chapter. Previously featured on ABC’s Shark Tank, DetraPel manufactures non-toxic, PFAS-free functional barrier coatings for industrial and consumer applications in Textiles, Paper & Food Packaging, and Contract Aerosol Manufacturing. The Applications Chemist role is a full-time, in-person position focused on translating DetraPel formulations into real-world performance on customer-relevant substrates. You’ll design and run lab application trials (spray and coating), evaluate and report performance data, develop clear SOPs, and collaborate closely with formulation chemists, operations, and manufacturing to move concepts from lab to pilot to production. This is a hands-on lab role (think “applications lab technician with chemistry chops”) for someone who loves process, precision, and measurable results. Compensation: $55,000 - $60,000 yearly Responsibilities: Your Day To Day: Applications Testing & Method Development (35%) • Plan, execute, and document application trials across textiles and paper/packaging using lab-scale tools (airless/air-assisted spray, drawdowns/rod/roll, dip)., • Optimize process parameters (mixing, viscosity/solids, film build, cure/oven settings) to hit target specs., • Evaluate coating performance using relevant standards (e.g., water/oil repellency, grease/oil barrier, Cobb/Kit, contact angle, abrasion/wash durability, adhesion)., • Analyze results in Excel (or equivalent), summarize insights, and communicate recommendations to R&D, Operations, and Commercial teams., • Partner with formulation chemists to iterate final application-ready formulations., • Maintain a clean, organized, and safe lab; adhere to SDS/PPE requirements and good documentation practices., • Calibrate and maintain lab equipment (balances, ovens, mixers, viscometers, goniometer/contact angle - where applicable)., • Education: Bachelor’s degree in Chemistry, Polymer Science, Chemical Engineering (or related field)., • Experience: 1+ year hands-on applications or coatings lab experience (textiles and/or paper/packaging preferred)., • Comfortable with airless/air-assisted spray techniques and common lab coating methods (drawdown/rod/roll, dip)., • Familiarity with textile and paper coating applications; aerosol experience is a plus., • Able to analyze and report data clearly; strong skills in Microsoft Excel and Word., • Detail-oriented, organized, and safety-minded; capable of following and writing SOPs., • Bonus points for exposure to any of the following: contact angle measurement, Cobb/Kit testing, rheology/viscosity control, FTIR/UV-Vis basics, TAPPI/AATCC/ASTM methods, or scale-up support., • Thrive in a fast-paced, collaborative environment and communicate well across R&D, Operations, and Manufacturing., • Excellent project management and organizational skills., • Adaptable and proactive. Ready to pivot and handle ad-hoc needs.About Company DetraPel is the leading provider of performance coatings for various industrial and consumer verticals. We specialize in developing plastic-free, PFAS-free (100% fluorine-free) coatings that provide superior performance without sacrificing sustainability. DetraPel's brands create products for diverse markets, including paper, food packaging, textiles, and healthcare. Our technologies enhance the durability, resistance, and performance of various substrates while still maintaining recyclability, composability, and reliability. Benefits: • Unlimited PTO, • Company healthcare benefits + vision + dental, • 401(k) with company match, • Company-sponsored professional development fund, • Company-sponsored athletic country club membership, • A fun and rewarding place to work with a collaborative team environment, • Quarterly team events

Job Description We are an emerging technology company hiring A+ players only. As a fast-growing venture-backed advanced materials manufacturer of protective coatings, DetraPel is looking to expand its team to support hyper growth during this next chapter. Previously featured on ABC’s Shark Tank, DetraPel manufactures non-toxic, PFAS-free functional barrier coatings for industrial and consumer applications in Textiles, Paper & Food Packaging, and Contract Aerosol Manufacturing. The Polymer Synthesis Chemist role is a full-time, in-person position focused on designing, synthesizing, and scaling bio-based and non-bio-based polymers that meet target barrier and durability requirements. You will own polymer platform development, design and execute lab-scale polymerizations, design and execute characterization and testing, translate results into application-ready formulations, and lead cross-functional work with Applications, Formulation, Operations, and Manufacturing to move programs from lab to pilot to production. You will mentor junior team members and drive continuous improvement. Compensation: $125,000 - $140,000 yearly Responsibilities: Your Day To Day: Polymer Design and Synthesis (40%) • Design and execute polymerizations, including controlled, free radical, step growth, and core-shell approaches., • Select monomers, crosslinkers, surfactants, catalysts, and additives to meet cost, safety, and performance targets., • Own reaction planning, setup, feeds, in-process monitoring, and post-processing., • Maintain detailed batch records and author clear SOPs. Characterization and Data Analysis (20%) • Analyze reports of FTIR, GPC, DSC, and NMR as available. Summarize data in concise reports and presentations., • Execute and document TGA, rheology, particle size, and solids testing as applicable., • Link structure and process variables to key properties such as barrier performance, film formation, adhesion, and flexibility. Formulation and Application Transfer (25%) • Work with Applications and Formulation Chemists to convert neat polymers into final formulations for textiles, paper, and packaging., • Define critical parameters such as solids, viscosity, and cure profile to hit end-use specs. Process Optimization and Scale Up (10%) • Develop process optimizations and scale-up procedures for pilot and production., • Run pilot batches with Operations and Manufacturing, define process windows, and author tech transfer documents and control plans. Safety, Quality, and Lab Operations (5%) • Adhere to all laboratory safety protocols and good documentation practices., • Maintain a clean, organized, and compliant lab environment., • Calibrate and care for lab equipment and manage basic lab inventory.Qualifications:, • Education: Master’s degree in Polymer Chemistry, Chemistry, or Materials Science preferred. Bachelor’s degree considered with a strong record of achievement., • Experience: 7+ years of demonstrated hands-on ownership from synthesis through characterization, formulation transfer, pilot execution, and tech transfer., • Understanding of bio-based and non-bio-based polymer synthesis., • Fully versed in controlled, free radical, step growth, and core shell polymerizations., • Able to interpret FTIR, GPC, DSC, and NMR data., • Proficient in Microsoft Excel and Word with strong data organization and reporting skills., • Plus factors include familiarity with coatings testing, such as viscosity, solids, contact angle, COBB, or KIT, where applicable., • Detail-oriented, organized, and safety-minded; capable of following and writing SOPs., • Thrive in a fast-paced, collaborative environment and communicate well across R&D, Operations, and Manufacturing., • Excellent project management and organizational skills., • Adaptable and proactive. Ready to pivot and handle ad-hoc needs.About Company DetraPel is the leading provider of performance coatings for various industrial and consumer verticals. We specialize in developing plastic-free, PFAS-free (100% fluorine-free) coatings that provide superior performance without sacrificing sustainability. DetraPel's brands create products for diverse markets, including paper, food packaging, textiles, and healthcare. Our technologies enhance the durability, resistance, and performance of various substrates while still maintaining recyclability, composability, and reliability. Benefits: • Unlimited PTO, • Company healthcare benefits + vision + dental, • 401(k) with company match, • Company-sponsored professional development fund, • Company-sponsored athletic country club membership, • A fun and rewarding place to work with a collaborative team environment, • Quarterly team events

Job Description Chemist – North Carolina Are you seeking a position as a Chemist with a well-known chemical manufacturer? Essential Duties and Responsibilities: • Prepare and apply formulations to customer substrates using various methods (e.g., spray, gravure, dip/nip)., • Test finished parts for physical properties, color, aesthetics, and flammability., • Modify existing formulations, simulate customer parts, and scale up production as needed., • Collaborate with cross-functional teams globally to support chemistry development., • Present findings to Technical Sales, Customers, internal R&D, and Applications. Education and Experience: • Bachelor's Degree in Chemistry, Chemical Engineering, Plastic Engineering, Mechanical Engineering, or a related field., • Less than 3 years of industrial experience, with a focus on coatings formulation, color matching, processing, quality control, and technical service. Additional Requirements: • Must be eligible to work in the US.

Job DescriptionTITLE: CHEMIST ILOCATION: WILSON, NC (onsite)DURATION: 6 months (possibility to extend to 12 months)Standard Hrs. Per Week: 36 hours per week (Fri-Sat-Sun)Shift: 6AM-6:30PM Job Summary:Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures. Primary Responsibilities: • Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory., • Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures., • Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs., • Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting., • Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency., • Aid other group members as required., • Ensure that equipment and working areas are maintained with good safety and housekeeping practices., • Re-stock chemicals and consumables used in analysis., • Performs other related assignments and duties as required and assigned. Education and Experience Requirements:, • Must have a BA or BS degree in Chemistry or closely related science., • Minimum of 1-year relevant experience preferred. Necessary Knowledge, Skills, and Abilities:, • Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy – UV/Vis, NIR, IR, or AA/AE)., • Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position.Physical and Environmental:, • Perform job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching. While sitting for an extended period of time on a routine basis, incumbent may use the following equipment: Personal computer, telephone/ other voice communication devices, copier, fax, scanners, or other specialized equipment used in an office setting., • Lift and maneuver equipment and materials weighing up to 20 pounds., • Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums., • Use small hand and power tools to perform incidental maintenance., • Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces., • Ability to work a 10 hour per day/4-day work week Monday through Thursday; 40 hours per week with overtime as required.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Senior Chemist responsibilities include, but are not limited to, the following: • Perform routine and special analyses, utilizing GC / GCMS and other related lab equipment, • Provide support to method development and validation of methods utilizing GC / GCMS and other related lab equipment, • Read, understand, and interpret diverse analytical procedures presented in a variety of written styles, • Perform instrument calibration and instrument troubleshooting, • Review and verify data, compile data packages, • Recognize errors, identify root causes, recommend process improvements, • Revise or write SOP’s as needed, • Work independently and efficiently, • Document work clearly and perform tests accurately, • Communicate effectively with client staff membersQualifications The ideal candidate would possess: • Bachelor’s degree in chemistry, biology, or other related degree concentration, or equivalent directly related experience (2 years of directly related industry experience is equivalent to1 full-time year of college in related major), • 4 years of GC/GCMS experience, • Strong Gas chromatography and mass spectroscopy experience., • Experience in a cGMP and/or ISO 17025 environment, • Strong computer, scientific, and organizational skills, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Additional Information • Position is full-time, 8:00 am- 5:00 pm Overtime as needed., • Candidates currently living within a commutable distance of Winston-Salem, NC, are encouraged to apply, • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays, • #LI-EB1, • Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionTITLE: CHEMISTLOCATION: 4701 International Blvd, Wilson, NC 27893Job Summary:Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures. Primary Responsibilities: • Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory., • Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures., • Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs., • Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting., • Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency., • Ensure that equipment and working areas are maintained with good safety and housekeeping practices., • Re-stock chemicals and consumables used in analysis. Education and Experience Requirements:, • The incumbent must have a BA or BS degree in Chemistry or closely related science., • Minimum of 1 year’s relevant experience preferred. Necessary Knowledge, Skills, and Abilities:, • Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy – UV/Vis, NIR, IR, or AA/AE)., • Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position. Physical and Environmental:, • Perform job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching. While sitting for an extended period of time on a routine basis, incumbent may use the following equipment: Personal computer, telephone/ other voice communication devices, copier, fax, scanners, or other specialized equipment used in an office setting., • Lift and maneuver equipment and materials weighing up to 20 pounds., • Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums., • Use small hand and power tools to perform incidental maintenance., • Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces., • Ability to work a 10 hour per day/4-day work week Monday through Thursday;, • 40 hours per week with overtime as required.

Job DescriptionCompany Description • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices., • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners. Job Description Job Description: Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures. Responsibilities: • Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory., • Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures., • Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs., • Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting., • Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency., • Aid other group members as required., • Ensure that equipment and working areas are maintained with good safety and housekeeping practices., • Re-stock chemicals and consumables used in analysis., • The incumbent must have a BA or BS degree in Chemistry or closely related science., • Minimum of 1-year relevant experience preferred., • Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy – UV/Vis, NIR, IR, or AA/AE)., • Performing job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching. While sitting for an extended period on a routine basis, incumbent may use the following equipment: Personal computer, telephone/ other voice communication devices, copier, fax, scanners, or other specialized equipment used in an office setting., • Lift and maneuver equipment and materials weighing up to 20 pounds., • Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums., • Use small hand and power tools to perform incidental maintenance., • Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces.Additional Information All your information will be kept confidential according to EEO guidelines.

Job DescriptionSalary: Chemtek, a family-owned business with a strong track record of innovation and market changing products in the Industrial Maintenance Chemical business islooking for an experienced Manufacturing Chemist with a strong background in formulation and product development to join our team. In this role, you will be responsible for new product formulation, product testing, quality control, and research & development of industrial cleaning products (I&I cleaners and degreasers). You will play a key part in developing innovative cleaning solutions while ensuring existing products maintain the highest standards of quality and performance. The ideal candidate has at least a Masters degree in Chemistry (or a related field) and 510 years of experience in a formulation manufacturing environment, with a proven track record of taking chemical products from concept through production. This is a great opportunity for someone to help drive our next stage of product development and product improvement. Were a close-knit team that values accuracy, teamwork, and follow-through. If youre organized, proactive, and ready to take ownership of our product development, we want to hear from you. Key Responsibilities • Formulation Development: Develop and optimize new product formulations for industrial cleaners and degreasers, ensuring that new formulas meet targeted performance, physical stability, and safety requirements. This includes reformulating or improving existing cleaning products as needed to enhance efficacy and cost-effectiveness., • Product Testing & Evaluation: Conduct laboratory testing and performance evaluations on formulations to verify cleaning efficacy (e.g. soil removal, foaming, residue analysis) and ensure products meet all quality specifications. Analyze test data to refine formulas and achieve desired product characteristics and compliance with industry standards., • Manufacturing Scale-Up Support: Provide technical support during scale-up from lab to manufacturing, working closely with plant production staff to transition formulations to full-scale production. Troubleshoot any production issues related to formulation stability, separation, or other quality deviations, and implement adjustments to ensure consistent batch manufacturing., • Quality Control & Assurance: Oversee and support quality control activities for both raw materials and finished products. Analyze stability data and conduct root-cause investigations for any non-conformances, such as customer complaints or out-of-specification (OOS) results, to maintain high product quality. Ensure that formulations and processes adhere to internal quality standards and Good Laboratory/Manufacturing Practices., • Documentation & Compliance: Maintain detailed documentation for all formulation work, including laboratory notebooks, batch records, specifications, and test results. Prepare and update technical documents such as Safety Data Sheets (SDS), product labels, and formulation protocols to ensure compliance with safety and labeling regulations for cleaning chemical products. Rigorously enforce safety protocols when handling chemicals and conducting experiments., • Innovation & Continuous Improvement: Stay abreast of industry trends, new raw materials, and emerging technologies in the cleaning chemicals sector. Evaluate competitor products to ensure our companys offerings remain competitive, and identify opportunities for new product development or improvement. Propose and implement R&D process improvements to accelerate time-to-market for new formulations and to reduce costs without compromising quality. Qualifications • Education: Masters degree (M.S.) or higher in Chemistry, Chemical Engineering, or a related field is required. (A Ph.D. is a plus, but a strong M.S. with relevant experience is ideal.), • Experience: 510 years of hands-on experience in formulation chemistry or product development in a manufacturing environment is required, preferably in industrial or specialty chemicals. Candidates should have a proven record of developing chemical products (such as cleaners, detergents, coatings, or similar) from concept through scale-up. Experience in the I&I cleaning chemicals sector or a closely related industry is highly valued., • Formulation Expertise: Strong expertise in formulation of chemical products, particularly cleaners and degreasers. Deep knowledge of surfactants, solvents, emulsifiers, pH adjusters, corrosion inhibitors, and other ingredients used in cleaning formulations is essential. The candidate should understand how to evaluate and optimize these components for performance, stability, and safety., • Scale-Up & Process Knowledge: Experience transitioning formulations from the lab bench to full-scale production is required. Familiarity with manufacturing processes, mixing equipment, and process optimization for chemical products is important. The candidate should be comfortable working in a plant/lab environment and troubleshooting production batches as needed., • Quality & Regulatory: Demonstrated knowledge of quality control practices and regulatory compliance in chemical manufacturing. This includes understanding of safety standards, handling of hazardous materials, and preparation of documentation like Safety Data Sheets and product labels in line with regulatory requirements. Experience ensuring products meet environmental and industry regulations (EPA, OSHA, etc.) for cleaning chemicals is a plus., • Analytical & Problem-Solving Skills: Excellent analytical thinking and problem-solving ability, with the skill to design experiments and solve technical problems related to formulations and manufacturing processes. The ideal candidate can methodically investigate issues (e.g. a formula instability or performance shortfall) and implement effective solutions., • Adaptability: A proactive mindset with enthusiasm for innovation in chemical formulation. The candidate should be self-motivated and able to manage multiple projects, adapt to changing priorities, and maintain a high standard of accuracy and safety in a fast-paced development environment. What We Offer • Competitive Salary with Bonus Opportunitites, • Top-tier benefits,including:, • QESHRA Medical Insurance for employees and families, • 401(k) with company contribution, • Paid vacation, PTO and Sick Leave, • All Holidays plus 8 additioanl days off at Christmas, • Relocation Assistance If you're ready to contribute to a growing company where your attention to detail and relationship-building skills will make a real impact,apply today to join the Chemtek team!

Job Description Chemist Wilson NC, 27893 United States Duration: 06+ Months Pay rate: $21 -$23/Hr. Shift-Ability to work a 10 hour per day/4-day work week Monday through Thursday; 40 hours per week with overtime as require Job description: Job Summary Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures. Primary Responsibilities * Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory. * Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures. * Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs. * Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting. * Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency. * Aid other group members as required. * Ensure that equipment and working areas are maintained with good safety and housekeeping practices. * Re-stock chemicals and consumables used in analysis. * Performs other related assignments and duties as required and assigned. * Education and Experience Requirements * The incumbent must have a BA or BS degree in Chemistry or closely related science. Minimum of 1-year relevant experience preferred. Necessary Knowledge, Skills, and Abilities * Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy – UV/Vis, NIR, IR, or AA/AE). * Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position. * Physical and Environmental * Perform job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching. While sitting for an extended period of time on a routine basis, incumbent may use the following equipment: Personal computer, telephone/ other voice communication devices, copier, fax, scanners, or other specialized equipment used in an office setting. * Lift and maneuver equipment and materials weighing up to 20 pounds. * Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums. * Use small hand and power tools to perform incidental maintenance. * Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces. * Ability to work a 10 hour per day/4-day work week Monday through Thursday; 40 hours per week with overtime as required. Benefits: Russell Tobin offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors.

Job DescriptionJob Title: Sr. Quality Specialist I – Method Validation and Development Chemist Location: Wilson, NC Shift Schedule: Monday-Thursday (10 hours). Hours flexible, typically 7:00am-5:30pm $95k – 100k w/ 10% bonus potential (Direct Hire) Primary Responsibilities • Serve as an analytical project lead for all assigned products. Project leads ensure all required testing is completed to support the overall project timeline. • Perform all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures. • Accurately document all necessary and relevant information in a clear concise manner as per cGMPs. • Operate and maintain all analytical instrumentation and equipment as per established procedures. • Write, revise, develop and evaluate operational and maintenance procedures. • Communicate openly within the group to provide and gather information, to optimize the use of resources, and to optimize efficiency. • Provide training and assistance to other group members • Actively participate in investigations, problem solving, and troubleshooting. • Ensure that equipment and working areas are maintained with good safety and housekeeping practices. • Re-stock chemicals and consumables used in analysis. • Prepare and present data summaries (written and oral) as necessary. • Exercises good judgment in interpreting, understanding context, and reporting data. • Proactively identifies potential problems and recommend solutions. • Prepares, writes, and distributes reports as appropriate. • Participates in preparation and revision of job-related controlled documents. • Performs analytical testing of samples under limited direction. • Supports the creation, revision and development of test methods, operational and maintenance procedures, and other job-related controlled documents. • Evaluates accuracy, completeness, and adequacy of reports. • Independently prioritizes workload. • Requires minimal guidance and supervision when conducting routine and non-routine activities in primary discipline. • May interact with other departments/teams within the Company and with external regulatory agencies and business partners. • Performs other related assignments and duties as required and assigned. Education and Experience The incumbent must have a BA or BS degree in Chemistry or closely related science with six years minimum laboratory experience in pharmaceutical or related industries; or a graduate degree (MS Preferred) with 4-7 years’ experience. Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position. Necessary Knowledge, Skills, and Abilities Must demonstrate sound comprehension of multiple analytical technologies (HPLC, GC, Dissolution, Automation, or Spectroscopy – UV/Vis, Raman or IR); and must have a comprehensive knowledge of cGMPs and FDA requirements as well as familiarity with USP and EP monographs. Supervisory Responsibilities (if Applicable) All Sr. Quality Specialist I (Method Development Chemist) report to the Manager/Senior Manager. The Sr. Quality Specialist I may supervise junior staff including temporary staff and interns. Additional Information • Effectively identifies, describes and communicates problem and impact in a timely manner. • Routinely participates in problem resolution. • Identifies, tracks and resolves issues to closure. • Proactively identifies potential problems and recommends possible solutions. • Evaluates accuracy, completeness and adequacy of reports. • Authors, revises and annotates job-related controlled documents. Leadership Competencies: May train Quality colleagues in processes and procedures. • May be responsible for technical supervision of Quality colleagues. This may include: Assigning work, Day-to-day supervision, Input to performance evaluation, Participating in hiring process • Organizes and coordinates activities for assigned projects anticipating future needs

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Chemist Group Leader responsibilities include, but are not limited to, the following: • Applies GMP/GLP in all areas of responsibility, as appropriate, • Applies the highest quality standard in all areas of responsibility, • Demonstrates and promotes the company vision, • Demonstrates strong client service skills, teamwork, and collaboration, • Proactively plans and multitasks to maximize productivity, • Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration, • Regular attendance and punctuality, • Ensure that the quality policy program is understood, implemented, and maintained at all levels of the organization; identify, prevent, or correct any departures from the quality system, • Perform work for both routine and non-routine work as specified by separate and applicable technical job description for individual, • Develop and implement operational improvements, • Supervise others in performing client’s service requirements, • Coach, train, and develop others within the group with respect to their personal development and effective implementation of operational improvements, • Coordinate workflow and perform daily monitoring to meet TAT, • Conduct semiannual performance reviews, interview applicants, keep training records up to date for assigned employees, perform succession planning in preparation for growth, • Confront and address problems, concerns, and performance issues, • Coach and develop individual and team to maximize performance, • Foster motivation and morale, • Monitor and approve employees’ time worked through time-entry system, • Support and promote company policies and procedures, • Expand self-awareness and develop leadership skills as defined; attend applicable leadership training based on identified needs, • Perform and/or assign other duties as requested to ensure smooth operation of department, • Perform all functions in support of and in compliance with all state and federal employment regulations, • Conducts all activities in a safe and efficient manner, • Lead team, schedule and train employees, • Ensure adherence to Quality System and efficiency standards in laboratory operations, • Coordinate workflow and ensure enough coverage and performance to meet turnaround times, • Foster motivation and teamwork, • Oversee lab for preparation of samples for tobacco smoke analysis using rotary and linear smoking machines, and FSC lab for regulatory compliance testing, • Work closely with other labs leaders to ensure appropriate scheduling of samples for analysis, • Participate in lab testing activities as needed, • Document test results in notebooks; write SOP’s, protocols and reports, • Review data, data notebooks and reports, • Perform instrument calibration, instrument troubleshooting, recognize errors, identify root causes, apply process improvement; maintain excellent working knowledge of smoking machine operation, • Communicate effectively with client staff members, • Performs other duties as assignedQualifications, • At least 2 years laboratory or quality control experience, • Bachelor’s degree in science or related discipline, or equivalent directly-related experience, • Experience in the tobacco industry, • Experience in GMP/GLP and or ISO compliance laboratory environment, • Strong leadership, initiative, and teambuilding skills, • Strong computer, client service, scientific, and organizational skills, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Additional Information • Position is full-time, Monday-Friday, 8:00 am - 5:00 pm., • Candidates currently living within a commutable distance of Winston-Salem, NC are encouraged to apply, • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays, • #LI-EB1, • Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description • Applies GMP/GLP in all areas of responsibility, as appropriate, • Applies the highest quality standard in all areas of responsibility, • Demonstrates and promotes the company vision, • Demonstrates strong client service skills, teamwork, and collaboration, • Proactively plans and multitasks to maximize productivity, • Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration, • Regular attendance and punctuality, • Applies 17025 compliance standards in all areas of responsibility, as appropriate, • Performs complex analyses and non-routine testing in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g. ICP, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.), • Operates and maintains job related equipment as required, • Performs advanced troubleshooting of laboratory equipment, • Performs supporting verification, calibration, and maintenance tasks (e.g., balance calibration and pipet verifications), • Performs laboratory tasks as assigned following supervisor direction, SOPs, WI and other documentation, • Assists other staff in the edits and updates of SOPs, WI and other documentation, • Follows all Good Documentation Practices appropriately, including digital platforms, • Maintains working areas appropriately (cleaning, disinfecting, etc…), • Possesses strong organizational skills, • Provides clear feedback, • Keeps accurate records, follows instructions, and complies with company policies, • Proactively checks and stays current with all training across multiple learning platforms, • Provides instruction/training to new staff, • Recognizes errors, identifies root causes, and applies process improvements, • Provides analyses support for method validation as needed, • Evaluates, reviews, and approves data by other analysts, • Independently drafts, edits and updates SOPs, WI and other documentation, • Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision, • Makes recommendations for technical improvements, as needed, • Communicates effectively with client staff members, • Conducts all activities in a safe and efficient manner, • Performs other duties as assignedQualifications, • Bachelor's degree in Chemistry, Biology, or other related degree concentration, or equivalent directly related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major), • 4 – 7 years of related experience, • GMP experience a plus; experience in the tobacco industry a plus Additional Information • Position is full-time, Monday-Friday, 8:00 am - 5:00 pm., • Candidates currently living within a commutable distance of Winston-Salem, NC are encouraged to apply, • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays, • #LI-EB1, • Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionSalary: 70000 to 90000 Company Background:Farmina is nature and science in perfect harmony. Our mission is to develop the best all-natural, nutritious, and scientifically validated food that dogs and cats will love. Farmina is an innovative Pet Nutrition Company focusing on servicing dog and cat pet parents to make the best personalized nutritional decisions for their pet's well-being while providing life changing solutions along the way. We at Farmina firmly believe in our company motto: Happy pet. Happy you. Position Purpose The Lead Chemist will oversee analytical testing and laboratory operations to ensure the highest standards of quality, safety, and compliance in pet food manufacturing. This role requires strong expertise in classical wet chemistry, instrumental analysis, and regulatory compliance, with an emphasis on nutritional, contaminant, and safety testing. The Lead Chemist will serve as the technical expert, supporting method development, staff training, and implementation of advanced analytical instrumentation. Requirements • Bachelors degree in Chemistry, Food Science, or related field (Masters preferred)., • Minimum 5 years of laboratory experience in food, feed, or pet food testing with increasing responsibility., • Proficiency in wet chemistry techniques and operation of analytical instruments (NIR, spectrophotometer, ICP, UPLC)., • Strong knowledge of nutritional, contaminant, and microbiological testing methods., • Experience with method development, validation, and regulatory compliance., • Demonstrated leadership skills with ability to supervise and train laboratory staff., • Strong analytical problem-solving, organizational, and communication skills., • Preferred: HACCP certification and PCQI (Preventive Controls Qualified Individual) certification. Work Environment • Laboratory and production plant environment., • Must be able to stand for extended periods and occasionally lift up to 25 lbs., • Exposure to laboratory chemicals, heat, and standard lab hazards. Key Responsibilities • Perform and oversee routine testing for ash, protein, fat, fiber, moisture, and peroxide values using traditional AOAC methods., • Conduct and validate testing using Soxhlet extraction, Kjeldahl analysis, fiber extraction, muffle furnace, titrations, and polarimetry., • Apply aseptic sampling techniques, incubation, autoclaving, and microbiological assays (including mycotoxin analysis and VIDAS)., • Operate and maintain advanced laboratory equipment such as NIR spectrometer, ICP-AES, and UPLC systems., • Lead implementation of ICP-AES for heavy metals and mineral analysis, and UPLC for vitamins and amino acid profiling., • Ensure laboratory practices comply with GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), HACCP, and FSMA guidelines., • Prepare, review, and approve test results, analytical reports, and Certificates of Analysis., • Train and mentor laboratory staff on methods, equipment, and regulatory requirements., • Investigate analytical deviations, identify root causes, and implement corrective/preventive actions., • Support R&D and Quality Assurance teams with method validation, product formulation testing, and troubleshooting., • Maintain laboratory safety programs, calibration schedules, and inventory of reagents/standards. Benefits: • Empower 401k, • Hartford Company Paid AD&D, • Hartford Voluntary AD&D, • Hartford Voluntary Long-term Disability Insurance, • Harford Voluntary Child Life, • Hartford Short-term Disability Insurance, • Colonial Life Critical Illness, • Colonial Life Term Life, • Colonial Life Whole Life, • Health FSA, • Dependent Care FSA, • Colonial Medical Bridge, • Colonial Accident, • Harford Voluntary Life Dependents, • Hartford Voluntary AD&D Dependents, • Hospital Indemnity, • NYC Commuter Benefits, • Employee Pet Food Discounts, • Paid Maternity Time Off, • Paid Paternity Time Off, • Paid Adoption Time Off, • Pet Wellness Insurance Farmina is An Equal Opportunity Employer

Job Description We’re looking for a food industry Chemist Lab Lead with pet food/food science lab experience. Experience with lab safety, food safety, chemital testing, Microbiology lab experience required, PCR, rapid testing experience, experience with advanced lab equipment. A solid understanding of regulatory compliance is a must with FDA, USDA, AAFCO, cGMP. This is a full-time Direct Hire position. Responsibilities: • Chemically test foods daily, • Daily lab testing raw materials, • Oversee sampling and testing standards and procedures, • Maintain compliance with all food regulatory standards, • Maintain continuous improvement and scientific testing procedures, • Documentation and report tests, • Food testing experience, • Laboratory safety, • Testing raw foods, • Rapid testing, • Great work life balance, • Excellent benefits, • Paid vacations

This is a hands-on position suited for a chemist who thrives in an applied science environment and is eager to contribute to innovative solutions in a fast-paced industry.

We are looking for an to join our team to train AI models.You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.In this role you will need to hold an expert understanding of chemistry- a completed or in pr

We are looking for an to join our team to train AI models.You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.In this role you will need to hold an expert understanding of chemistry- a completed or in pr

This is a technical and supervisory position.Perform chemical analysis for Textile Center clients accurately, in accordance with industry standards, if applicable, and in a timely manner.Develop new test procedures and protocols, where applicable, with appropriate costing and pricing.Provide written

R&D Analytical Chemist Accentuate Staffing is partnering with a fast-growing pharmaceutical company who is hiring for an R&D PDM Assistant. This is a contract-to-hire opportunity, offering competitive pay and benefits, working onsite in Wilson, NC. The ideal candidate has 1–2 years of analytical laboratory experience, strong knowledge of GMP/GLP, and attention to detail in regulated environments. Responsibilities: • Support analytical method transfer, validation, and USP verification studies in accordance with ICH and USP guidelines., • Conduct USP compendial testing (e.g., assay, dissolution, content uniformity, identification)., • Maintain accurate laboratory documentation and support investigations and root cause analysis., • Assist with equipment qualification, lab start-up activities, SOP development, and compliance with GMP and GLP standards., • Participate in laboratory audits, ensuring readiness and adherence to quality and safety standards., • Bachelor’s degree in Chemistry, Pharmaceutical Science, Biochemistry, or related field., • 1–2 years of analytical laboratory experience in a regulated industry (pharma, healthcare, manufacturing)., • Familiarity with GMP, GLP, GDP, and USP standards., • Strong organizational skills, attention to detail, and proficiency with Microsoft Office., • Experience with chromatography, mass spectrometry, or raw material testing preferred., • Strong interpersonal and communication skills to collaborate across multifunctional tea

* Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures. • Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory., • Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures., • Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs., • Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting., • Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency., • Aid other group members as required., • Ensure that equipment and working areas are maintained with good safety and housekeeping practices., • Re-stock chemicals and consumables used in analysis., • Performs other related assignments and duties as required and assigned. The incumbent must have a BA or BS degree in Chemistry or closely related science. Minimum of 1-year relevant experience preferred. Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy UV/Vis, NIR, IR, or AA/AE). Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position. • Perform job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching. While sitting for an extended period of time on a routine basis, incumbent may use the following equipment: Personal computer, telephone/ other voice communication devices, copier, fax, scanners, or other specialized equipment used in an office setting., • Lift and maneuver equipment and materials weighing up to 20 pounds., • Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums., • Use small hand and power tools to perform incidental maintenance., • Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces., • Ability to work a 10 hour per day/4-day work week Monday through Thursday; 40 hours per week with overtime as required. Work Location: Wilson -Onsite Standard Hrs. Per Week: 36 hours per week (Fri-Sat-Sun) Weekend Shift: 6AM-6:30PM (Sept 2025- End of Assignment) Training Shift: *Please note, the worker will start on 1st shift (7:00am-5:30pm) till Sept 2025 for training period, then they will begin the weekend shift.

We are looking for an to join our team to train AI models.You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.Scroll down to find the complete details of the job offer, including experience required and