Trabajos Science en North Carolina

Job DescriptionQC / Formulation ChemistSpecialty Chemicals & Coatings Contract Opportunity | Monday-Friday | Modern R&D Laboratory We're seeking a QC / Formulation Chemist to support a growing R&D and quality team focused on specialty coatings and advanced material technologies. This role provides valuable exposure to formulation development, analytical testing, quality investigations, and manufacturing support while working in a state-of-the-art laboratory environment. This is an excellent opportunity for candidates looking to build experience in coatings, specialty chemicals, product development, quality control, and research & development. Why Consider This Opportunity? Gain experience in both Quality and R&D environments Work in a modern, recently developed laboratory facility Hands-on exposure to formulation and scale-up activities Collaborate with experienced scientists and technical teams Build skills with advanced analytical and testing equipment Stable Monday-Friday schedule Excellent opportunity to strengthen your technical experience and expand your career options What You'll Do As a QC / Formulation Chemist, you'll support product development and quality initiatives through laboratory testing, technical investigations, and formulation support activities. Responsibilities include: • Conducting quality control and performance testing on specialty coatings and related materials, • Performing wet chemistry analyses, titrations, and physical property testing, • Executing ASTM and other industry-standard test methods, • Supporting formulation development and optimization projects, • Conducting corrosion, weathering, humidity, and salt spray testing, • Investigating customer complaints through testing and root cause analysis, • Assisting with product scale-up and manufacturing support activities, • Maintaining accurate laboratory records and technical documentation, • Interpreting test results and communicating findings to technical teams, • Collaborating with R&D, manufacturing, and technical service groupsQualificationsRequired, • Bachelor's Degree in Chemistry, • Laboratory testing experience through industry experience, internships, co-ops, or academic research, • Knowledge of analytical chemistry techniques, • Experience with wet chemistry and titration methods, • Strong organizational and documentation skills, • Ability to manage multiple projects in a fast-paced technical environmentPreferred, • Experience with coatings, paints, adhesives, sealants, polymers, or specialty chemicals, • Formulation experience, • Quality Control or Quality Assurance laboratory experience, • Familiarity with ASTM testing methods, • Experience with corrosion, humidity, weathering, or durability testing, • Manufacturing or scale-up support experienceIdeal Candidate This opportunity is well-suited for someone who wants to: Gain exposure to both QC and R&D functions Build formulation and product development experience Work with specialty chemical and coating technologies Develop strong analytical and troubleshooting skills Expand their technical expertise in a professional laboratory environment Work Environment • Monday-Friday schedule (typically 8:00 AM-5:00 PM), • Professional R&D and testing laboratory, • Collaborative technical environment, • Advanced coating and materials testing equipment, • Strong focus on safety, quality, and innovation If you're looking for an opportunity to apply your chemistry experience in a hands-on laboratory setting while gaining exposure to formulation, testing, and product development, we'd love to hear from you. Job Type & Location This is a Contract position based out of Greensboro, NC. Pay and Benefits The pay range for this position is $27.00 - $29.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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) Job Type & Location This is a Contract position based out of Greensboro, NC. Application Deadline This position is anticipated to close on Oct 19, 2026. Workplace Type This is a fully onsite position in Greensboro,NC. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law. If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records. Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.

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 responsibilities include, but are not limited to, the following: • Perform routine sample preparation using wet chemistry techniques, and smoking machines for tobacco products, • Perform analytical testing of tobacco using pH, spectrophotometer, KF and other ancillary laboratory equipment, • Perform all lab work with high degree of accuracy and precision, • Document results accurately in notebooks and computer systems, • Read, understand, and interpret analytical procedures, update procedures as needed, • Perform instrument calibration, recognizes errors, identifies root causes, applies process improvements, • Review and verify data, • Communicate effectively with client staff membersQualifications, • Bachelors 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) The ideal candidate would possess: • 0-2 years working with wet chemistry techniques and ancillary laboratory equipment, • Experience in a cGMP and ISO 17025 environment, • Strong computer, scientific, and organizational skills, • Working knowledge of KF and pH Omnis software helpful, • 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 Monday-Friday, 8-5. Overtime as needed, • May be requested to work on weekends, overtime, and holidays based on business needs, • 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, • 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 Essential Duties and Responsibilities: • 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 routine sample preparation and analyses in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, 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 basic 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 junior level 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, • 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), • 2 – 4 years of related experience Additional Information • Position is Monday-Friday 8am-5pm. Overtime as needed., • May be requested to work on weekends, overtime, and holidays based on business needs, • 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, • 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 Essential Duties and Responsibilities: • 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 routine sample preparation and analyses in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, 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 basic 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 junior level 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, • 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), • 2 – 4 years of related experience Additional Information • Position is Sunday-Thursday 8:00am-5:00pm Overtime as needed, • May be requested to work on weekends, overtime, and holidays based on business needs, • 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, • 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 Description Job Title: Quality Control Laboratory Technician Shift: 2-2-3 schedule (5PM to 5AM) and will train on 8 hour day shift for 3-4 weeks prior to moving to 12-hour shift. Job Description This role is a hands-on, chemistry-focused Quality Control Laboratory Technician position within a large chemical processing facility. You will perform routine and specialized chemical analyses to support production quality, using a variety of laboratory instruments and following established procedures and documentation standards. The position offers the opportunity to grow within the Quality Department and potentially transition into research and development roles over time. Responsibilities • Perform daily quality control testing and chemical analyses on production samples using standard laboratory equipment and specialized instrumentation., • Operate and maintain advanced analytical instruments such as thermogravimetric analysis and differential scanning calorimetry platforms, capillary rheometers, melt indexers, gas chromatographs (GC), and high performance liquid chromatographs (HPLC)., • Conduct wet chemistry procedures, pH measurements, viscosity checks, and other routine assays to ensure products meet established specifications., • Accurately record test results on batch sheets and enter data into the Laboratory Information Management System (LIMS) when required., • Follow Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Standard Operating Procedures (SOPs) for all testing and documentation activities., • Work in accordance with quality standards in an ISO-certified facility, ensuring compliance with internal and external quality requirements., • Troubleshoot basic instrument and testing issues, and escalate complex problems to technical staff as needed., • Communicate test findings clearly and promptly to production and quality teams to support timely decision-making., • Collaborate with technical staff on the night shift, asking questions and seeking guidance to resolve technical or procedural issues., • Maintain a safe and organized laboratory workspace while working with chemical products and processing materials. Essential Skills • Bachelors degree in Chemistry; other scientific degrees may be considered when combined with prior chemical manufacturing experience., • 13 years of experience working in a laboratory setting, preferably within industry., • 13 years of hands-on experience with Gas Chromatography (GC) and High Performance Liquid Chromatography (HPLC)., • Demonstrated proficiency with standard chemical laboratory equipment and instrumentation., • Experience performing chemical analysis and wet chemistry techniques in a quality control environment., • Ability to follow and apply GMP/GLP documentation practices in daily work., • Knowledge of Standard Operating Procedures (SOPs) and the ability to adhere to them consistently., • Familiarity with working in an ISO-certified facility., • Strong troubleshooting abilities related to laboratory tests and instrumentation., • Attention to detail and accuracy in recording and reporting test results. Additional Skills & Qualifications • Experience using a Laboratory Information Management System (LIMS) is a plus., • Experience in chromatography, including GC and HPLC, and related analytical methods., • Experience with thermogravimetric analysis and differential scanning calorimetry is beneficial., • Exposure to capillary rheometry, melt indexers, and viscosity measurements is advantageous., • Previous industry laboratory experience is preferred over purely academic or non-laboratory backgrounds., • Ability to work effectively on a night shift schedule and adapt to a rotating 2-2-3 shift pattern., • Strong communication skills for interacting with technical staff and production personnel., • Interest in long-term career growth within quality control and potential progression into research and development roles. Work Environment This position is based in a large specialty chemicals manufacturing facility on a substantial industrial site. You will work primarily in a laboratory setting that is closely integrated with production areas and deals directly with chemical products. The environment is more industrial than pharmaceutical, and the lab and production spaces are not highly cleanroom-style; candidates should be comfortable working in a setting where surfaces and equipment may be exposed to process materials. The facility operates under ISO certification and emphasizes structured procedures, documentation, and quality-focused culture, offering stability and opportunities for advancement for high-performing laboratory technicians. Job Type & Location This is a Contract to Hire position based out of High Point, NC. Pay and Benefits The pay range for this position is $23.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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) Job Type & Location This is a Contract to Hire position based out of High Point, NC. Application Deadline This position is anticipated to close on Oct 22, 2026. Workplace Type This is a fully onsite position in High Point,NC. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law. If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records. Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.

Job Description ERG is a research and consulting firm that provides a wide range of support to federal, state, and commercial clients. ERG offers multidisciplinary teams with nationally recognized skills in engineering, science, economics, public health, informational technology, and communications. We hire people with the best minds and then provide them with a vibrant and flexible environment in which to develop their careers. The qualified individual must be highly motivated with the skills to prioritize, perform, and communicate effectively in a fast-paced environment. We are an environmental laboratory specializing in ambient air sample analysis. We are seeking an organized and motivated individual for this role. Job Description: • This position will involve preparing and extracting samples, cleaning laboratory glassware, tracking samples through the laboratory sample-tracking system, and performing related support tasksQualifications and Skills:, • Bachelor of Science (B.S.) ERG offers competitive salaries and excellent benefits, including health and dental insurance, life insurance, long-term disability, educational benefits, FSAs, a generous 401k plan, profit sharing, an EAP, 11-20 paid vacation days per year, 10 paid holidays per year, 56 hours or more of sick leave (based on the state you work in) per year (pro-rated for part-time) and more. The salary range for all positions depends on the years and type of experience. ERG is an equal opportunity employer and complies with all applicable EEOC regulations. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual preference, national origin, disability, or status as a protected veteran. Please be aware, the only authentic corporate domain for ERG is https://www.erg.com. ERG may, on occasion, screen applicants via telephone or video interviews via Skype, Teams, GoToMeeting, or another type of video platform. However, any candidate extended a job offer might be asked to meet in person with an ERG employee before providing confidential personal information associated with new employment. If you’re a qualified individual with a disability or a disabled veteran, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access ERG’s online application process as a result of your disability. To request accommodation, please contact Human Resources via email at Resumes-Lex@erg.com or call (781) 674-7293. ERG fosters a friendly, flexible work environment. ERGers are dedicated to serving clients who are committed to making the world a better place. We promote and recognize principles of fairness and respect in the work we do, the partnerships we foster, and the culture we value both within and outside of our organization.

Bench Chemist – Level 1 Location: 100% Onsite Job Type: 12-Month Contract Pay Rate: $26.00/hour (W2) Schedule: Monday–Friday | Day Shift | 40 Hours per Week Anticipated Start Date: November 2, 2026 (alternative start date: November 16, 2026) About the Opportunity Alphanumeric Systems is seeking a detail-oriented and motivated Bench Chemist – Level 1 to support laboratory operations within a pharmaceutical manufacturing environment. This is an excellent opportunity for an entry-level laboratory professional or an individual with experience in raw material sampling and testing who is interested in developing their skills in a regulated environment. The ideal candidate will have strong attention to detail, a willingness to learn, and the ability to follow established procedures. Previous pharmaceutical or Good Manufacturing Practice (GMP) experience is preferred but not required, as training will be provided. Please Note: This position focuses primarily on routine raw material sampling, testing, documentation, and laboratory support rather than advanced research or traditional chemistry experimentation. Key Responsibilities • Perform routine sampling and analytical testing of raw materials, packaging materials, finished products, and environmental samples according to established procedures., • Conduct raw material sampling and testing in accordance with approved methods and quality standards., • Utilize laboratory instrumentation and equipment, which may include HPLC, GC, UV spectroscopy, microscopes, automated systems, and other analytical tools., • Accurately document test results, observations, and laboratory activities in compliance with current Good Manufacturing Practices (cGMP)., • Review and interpret analytical data to ensure accuracy, completeness, and reliability., • Identify and promptly communicate testing discrepancies, deviations, or unexpected results to laboratory supervisors., • Support the review of laboratory documentation, including Standard Operating Procedures (SOPs), testing methods, specifications, and technical reports., • Assist with laboratory equipment maintenance, troubleshooting, and routine operational activities., • Participate in analytical method validation, transfer, and improvement activities as needed., • Complete required training and maintain accurate training documentation., • Collaborate with laboratory personnel and cross-functional teams to support daily operations and quality objectives. Required Qualifications • Associate degree in Chemistry, Biology, Laboratory Science, or a related scientific discipline, or 2–5 years of relevant experience working with raw materials., • Ability to follow detailed written procedures and accurately document work., • Strong attention to detail and commitment to quality and safety., • Basic computer skills and the ability to learn laboratory systems and equipment., • Good communication, organizational, and problem-solving skills., • Willingness to learn new procedures and perform routine, process-driven laboratory activities., • Ability to work independently and collaboratively in a structured laboratory environment., • Ability to work onsite five days per week. Preferred Qualifications • Experience with raw material sampling, handling, or analytical testing., • Previous experience in a pharmaceutical, biotechnology, manufacturing, or quality control laboratory., • Familiarity with GMP/cGMP requirements and laboratory documentation practices., • Experience using analytical laboratory instrumentation., • Knowledge of SOPs, laboratory safety procedures, and quality standards. Additional Position Requirements • Must be available to work a standard Monday–Friday day shift, 40 hours per week., • This position is 100% onsite; remote or hybrid arrangements are not available., • Candidates must be willing and able to complete required Powered Air-Purifying Respirator (PAPR) onboarding and training requirements., • Interviews will be conducted in person. Work Authorization Requirements Applicants must be legally authorized to work in the United States without employer sponsorship, now or in the future. We are unable to provide employment visa sponsorship for this position. We are not accepting applications or candidate submissions from third-party staffing agencies, vendors, or consulting firms. Candidates must apply directly and be eligible for W2 employment. Why Join Alphanumeric Systems? At Alphanumeric Systems, we connect talented professionals with opportunities to contribute to meaningful projects across the life sciences and technology industries. This position offers hands-on experience in a regulated pharmaceutical environment, structured training, and the opportunity to develop valuable laboratory and quality control skills. Apply today to take the next step in your laboratory career!

Job DescriptionTITLE: CHEMISTLOCATION: 4701 International Blvd, Wilson, NC 27893 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., • 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.

Dispersions Specialist (Chemist) DyStar is a leading specialty chemical company with a global presence. We have an immediate need for a Dispersions Specialist in one of our manufacturing plants located in Reidsville, NC. This is an individual contributor role. This role will support our Quality Lab Manager and will provide technical and operational support for production of Dispersions at the Reidsville manufacturing plant and our Tollers. The role will include development of new Dispersions from Lab Trials until Production; production batch supervision; support process and batch troubleshooting; and improve processes to reduce cost and improve sustainability. Primary Responsibilities: • Provides technical and operational support for production of Dispersions at Reidsville site., • Develops new product items in tight cooperation with Product Management from lab sizes over scale up from pilot trials until implementation in the technical plant set-up., • Is the liaison between Quality Control and Production operations., • Improves existing production processes to reduce cost, increase reliability, purity, safety, and improves Sustainability., • Works under and in collaboration with the site Quality Manager to provide in-process and final quality testing for products produced both on site and at tollers considering internal quality procedures and standards as well as the requirements of ISO9001:2015., • Troubleshoots existing production processes and implements new product items in production., • Works with site planning, scheduling and production operators to optimize the production flow and achieve the shortest possible batch cycle time., • Support production operator activities to ensure product is available to meet sales or inventory demand., • Monitors dispersions wastewater (cleaning water) to avoid any contamination of Auxiliaries wastewater., • Supervises the handling of powders to avoid cross-contamination from Dispersions production to other production units., • Supports the Production Manager regarding product cost calculation (effective material consumption and conversion costs)., • Checks and implements advanced technologies to improve costs and efficiency in production. Supervisory Responsibilities: None Education and Experience: • BS Chemistry, Chemical / Process Engineering or related field., • 8+ years of relevant Experience in Production and Quality Control of Dispersions by Physical Operations (Dispersing and Wet Milling)., • 5+ Years experience in supervision of production processes to guarantee best possible output, quality, and costs, • Experience in scale-up of production processes from Lab to technical scale., • Computer skills, including Microsoft Office. Experience with ERP systems a plus. Knowledge/Skills/Abilities: • Experience qualifying raw materials and key intermediates to achieve best costs and stable product quality., • Experience improving lower costs processes with efficiency improvement regarding material and utility consumption., • Written and oral communication skills to explain findings and share results cooperation partners, • Understanding of manufacturing costs. This is an on-site role in Reidsville, NC; not open to remote or hybrid work. Visa sponsorship is NOT available for this role. DyStar is an Equal Opportunity Employer

Product Development Chemist Arclin has an immediate full-time, on-site opening for a Product Development Chemist in our Moncure, NC location. About Arclin You can find Arclin everywhere. Our technologies make homes and transportation safer, help crops flourish, keep water clean, protect first responders and members of the military, and preserve the purity of essential pharmaceuticals. These vital, everyday products can't fail, and we’re here to give the world an extra layer of performance and peace of mind. With ~4,000 team members across more than 30 global manufacturing facilities, we operate with the scale to make a global impact and the agility to solve complex challenges at the molecular level. Rooted in scientific discovery and innovation, Arclin’s materials redefine performance across industries - from Firepoint®’s patented intumescent technology that helps stall flames and save lives to the iconic Kevlar® and Nomex® brands trusted to protect those who serve, strengthen aerospace and industrial systems, and perform where reliability and safety are top of mind. As we expand our mission‑critical materials portfolio and shape the next era of performance technologies, we’re looking for people who want to grow, lead, and solve the challenges others can’t. Together, we’ll advance the innovations that keep the world moving. Because at Arclin, our people are truly Vital Beyond Measure. Job Overview: Reporting to the Product Development and Applications Manager, this position is responsible for designing and executing tasks associated with the development of innovative chemistry-based products (resins) to support Arclin’s product development strategy. This position operates within the parameters of Arclin’s policies and procedures and will provide product expertise to R&T, Sales, Manufacturing, and Marketing groups. Responsibilities • Plan and execute projects to develop and optimize quality resin products for Arclin customers. This involves formulating and synthesizing formaldehyde-based resins, conducting lab experiments, performing wet chemistry testing and troubleshooting production issues., • Apply innovative thinking to solve complex scientific and chemical challenges., • Provide technical support to the applications, production and sales groups., • Maintain accurate and complete records of work results and activities., • Maintain a clean and safe lab environment in compliance with Arclin health, safety, and environmental policies and procedures. Ensure that all lab equipment is maintained and operating optimally. Required Qualifications • Bachelors of Science in Chemistry or related field, • 2-3 years of experience in industrial chemical laboratory environment; MS degree will substitute for two (2) years of experience., • Ability to work efficiently and communicate clearly in a cross-functional team., • Capability to prepare written reports with emphasis on technical clarity, accuracy and attention to detail., • Proficiency in the use of computer software (MS Office, Statistical analysis, etc.), • Strong problem solving and troubleshooting skills., • Ability to work with hazardous materials while following Arclin health, safety and environmental regulations. Preferred Qualifications • Ability to construct schedule and goals to effectively execute on projects and tasks., • Demonstrated ability to innovate and think creatively in a scientific context., • Knowledge of formaldehyde-based resin chemistries., • Experience in project planning and design of experiments., • Basic understanding of engineering processes used in resin production.

Key Responsibilities • Perform routine and non-routine raw material testing of commercial, validation and stability samples in accordance to written methodology., • Perform qualitative and quantitative analyses using analytical instrumentation such as HPLC; GC, UV/Vis, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments., • Perform testing in accordance with USP monographs, in-house methods, compendial requirements, and approved test procedures., • Utilize electronic laboratory information systems such as LIMS and Empower for acquisition and processing of analytical data, • Analyze data products approved specifications, notifying management of any OOS and aberrant results, • Actively participate in root cause problem solving during laboratory investigations, provide input for effective corrective and preventive actions, • Perform routine maintenance on lab equipment, as needed., • Support troubleshooting, laboratory investigations, and discrepancy investigations under the direction of a supervisor., • Perform peer review of laboratory testing, as required, • Prepare and/or review test procedures, SOPs, protocols, and other analytical documentation as assigned., • Maintain compliance with all applicable regulatory, safety, and company requirements, including: Chemical waste handling and disposal, Internal laboratory procedures etc., • Maintain a clean, organized, and compliant laboratory environment., • Perform other duties and responsibilities as assigned. Required Qualifications • Bachelor’s degree in Chemistry or another relevant scientific discipline., • A BS in Chemistry or a degree with Chemistry coursework is preferred., • 3–5 years of experience in the pharmaceutical industry., • 2–4 years of hands-on analytical testing experience in a pharmaceutical QC laboratory., • Experience with generic pharmaceutical manufacturing/testing is preferred., • Working knowledge of USP, ICH, and FDA requirements., • Strong knowledge of Good Documentation Practices (GDP) and GMP requirements., • Hands-on experience with analytical techniques such as HPLC, GC, UV-Vis, IR, KF titration, particle size analysis, and other routine QC testing., • Strong attention to detail and ability to accurately document and review analytical data., • Ability to work independently, prioritize tasks, meet established timelines, and make sound decisions., • Ability to learn new procedures, methods, and laboratory techniques quickly., • Strong troubleshooting and problem-solving skills.

Job Description PRIMARY FUNCTION: Plan, direct, and coordinate chemical analytical studies to develop new materials or improve on materials used in the course of manufacturing the company's products. Responsible for plant ISO lead assessor duties. Responsible for environmental compliance. SPECIFIC DUTIES: 1. Evaluate new materials or substitute raw materials from alternate vendors. Conduct critical research chemistries to develop and standardize materials. Produce new formulations for customer or in-house requests., 2. Formulate standardized tests to analyze the quality of materials., 3. Give technical support as required to Research & Development, Sales & Marketing, and Manufacturing. Analyze product failures as returned by customers. Assist in producing new products and prototype parts., 4. Perform in-process analysis, adjustments, and final analysis for the Compounding area. Provide technical support as needed for gel and chemical problems in the Castings area., 5. Perform testing or internal specifications, prepare technical data indicating the testing results., 6. Issue certificate of analysis documentation., 7. Update SDS documentation., 8. Initiate changes to improve product stability, workplace safety, and product safety. Initiate changes to enhance quality, efficiency, and ease of manufacture., 9. Prepare reports and recommendations as to suitability of materials researched and developed and the consistency of material quality supplied by vendors., 10. Handle hazardous material in accordance with established regulations., 11. Maintain ISO procedures and work instructions, records, files, and technical references. Assure all lab instruments are in proper repair and calibration. Keep well informed of new developments in the field of chemistry., 12. Support & maintain facility’s compliance with all applicable federal, state and local environmental regulations, including EPA & NCDEQ (North Carolina Department of Environmental Quality) requirements. QUALIFICATIONS: EDUCATION B.S. Degree in Chemistry. EXPERIENCE 1-3 years experience.

Job DescriptionTITLE: CHEMIST ILocation: WILSON, NC (onsite)Start date: April 28, 2025Duration: Twelve (12 months)Standard Hrs. Per Week: 40 hours per week (Monday thru Thursday)Shift: 7AM-5:30PM 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.

🧪 Quality Control Laboratory Chemist | cGMP 📍 Charlotte Metro Area 💰 Salary range $70k - $80k plus discretionary bonus potential up to 12% 🕰️ Hours: Monday – Thursday 3:30pm – 11:30pm & Friday 1:30pm – 9:30pm 🚨 US Citizens or Green Card Holders only | No C2C Immediate opening for a Quality Control Laboratory Chemist to join an industry-leading health and wellness manufacturer dedicated to improving lives through science, innovation, and uncompromising quality. With a strong reputation for excellence, the company develops trusted products backed by research and produced to the highest standards of quality and compliance. Employees enjoy a collaborative, values-driven culture that emphasizes integrity, continuous improvement, professional growth, and making a meaningful impact every day. If you're looking to join a mission-focused organization where quality matters and people are valued, you'll feel right at home here! Job Summary Support testing activities in a cGMP-regulated environment. The ideal candidate will perform various analytical tests, manage laboratory compliance, and troubleshoot instrumentation. Qualifications • Bachelor’s degree in Chemistry is mandatory., • 2–5 years of industry experience in a cGMP laboratory environment., • Experience with HPLC, GC & LC is mandatory, • Hands-on experience with Empower Software., • Proficient in laboratory analytical techniques such as titrations, gravimetric methods and sample preparation., • Strong understanding of GMP documentation practices. Responsibilities • Perform release, stability, and special-request testing of finished products and raw materials., • Independently execute laboratory methods with minimal supervision., • Operate, maintain, and troubleshoot analytical instrumentation including HPLC, GC, and FTIR., • Assist with laboratory investigations, including Out-of-Specification (OOS) results. Benefits: 🏡 45 Days of Fully Furnished Temporary Housing 💵 $5,000 Relocation Stipend ✈️ Paid Area Exploration Visits 💰 Weekly Pay 🎄 Christmas Eve – New Year's Shutdown 📚 Up to $5,000 Annual Tuition Reimbursement 💪 Gym/Fitness Reimbursement 🛡️ Company-Paid Life Insurance 🩺 Company-Paid Short-Term Disability 🤝 Employee Assistance Program (EAP) 💲 Annual HSA Contribution 👦 Daycare & Private School Tuition Assistance

🧪 QC Laboratory Chemist I | cGMP | FDA 📍 Charlotte Metro Area 💰 Salary range $70k - $80k plus discretionary bonus potential up to 12% 🕰️ Hours: Monday – Thursday 3:30pm – 11:30pm & Friday 1:30pm – 9:30pm 🚨 US Citizens or Green Card Holders only | No C2C Immediate opening for a QC Laboratory Chemist I to join an industry-leading health and wellness manufacturer dedicated to improving lives through science, innovation, and uncompromising quality. With a strong reputation for excellence, the company develops trusted products backed by research and produced to the highest standards of quality and compliance. Employees enjoy a collaborative, values-driven culture that emphasizes integrity, continuous improvement, professional growth, and making a meaningful impact every day. If you're looking to join a mission-focused organization where quality matters and people are valued, you'll feel right at home here! Job Summary Support testing activities in a cGMP-regulated environment. The ideal candidate will perform various analytical tests, manage laboratory compliance, and troubleshoot instrumentation. Qualifications • Bachelor’s degree in Chemistry is mandatory., • 2–5 years of industry experience in a cGMP laboratory environment., • Experience with HPLC, GC & LC is mandatory, • Hands-on experience with Empower Software., • Proficient in laboratory analytical techniques such as titrations, gravimetric methods and sample preparation., • Strong understanding of GMP documentation practices. Responsibilities • Perform release, stability, and special-request testing of finished products and raw materials., • Independently execute laboratory methods with minimal supervision., • Operate, maintain, and troubleshoot analytical instrumentation including HPLC, GC, and FTIR., • Assist with laboratory investigations, including Out-of-Specification (OOS) results. Benefits: 🏡 45 Days of Fully Furnished Temporary Housing 💵 $5,000 Relocation Stipend ✈️ Paid Area Exploration Visits 💰 Weekly Pay 🎄 Christmas Eve – New Year's Shutdown 📚 Up to $5,000 Annual Tuition Reimbursement 💪 Gym/Fitness Reimbursement 🛡️ Company-Paid Life Insurance 🩺 Company-Paid Short-Term Disability 🤝 Employee Assistance Program (EAP) 💲 Annual HSA Contribution 👦 Daycare & Private School Tuition Assistance

Job Description Overview MCI is one of the fastest-growing tech-enabled business services companies in the US, delivering Customer Experience (CX), Business Process Outsourcing (BPO) and technology solutions across multiple industries and countries worldwide. Our team uses people, technology and innovation to help organizations improve customer experience and business performance. We are looking for Call Center Representatives to support our "Get Out the Vote" initiative. In this role, you will make outbound phone calls on behalf of the Republican Party to encourage voter turnout for the presidential election. Ideal candidates will be comfortable representing the Republican Party, have excellent communication skills, be eager to learn, and be highly reliable. To be considered for this role, you must complete a full application on our company careers page, including all screening questions and a brief pre-employment test. Responsibilities Key Responsibilities: • Handle inbound and outbound contacts in a courteous, timely, and professional manner, • Listen to customers, understand their needs, and resolve customer issues, • Research systems to find missing information as applicable; coordinate with other departments to resolve issues as applicable, • Follow the processes of the Client program and perform all tasks in a courteous and professional manner, • Utilize systems and technology to complete account management tasks, • Accurately document and process customer claims in appropriate systems, • Follow all required scripts, policies, and procedures, • Utilize knowledge base and training to accurately answer customer questions, • Comply with requirements surrounding confidential information and personal information, • Appropriately escalate customer issues with the managerial team, • Escalate customer issues to the appropriate staff and managerial for resolution as needed., • Ensure first call resolution through problems solving and effective call handling, • Attend meetings and training and review all new training material to stay up-to-date on changes to program knowledge, systems, and processes, • Adhere to all attendance and work schedule requirements Qualifications WONDER IF YOU ARE A GOOD FIT FOR THIS POSITION? All positive, and driven applicants are encouraged to apply. The Ideal candidates for this position are highly motivated and dedicated and should possess the below qualities: • Must be 18 years of age or older, • High school diploma or equivalent, • Experience with data-entry utilizing a computer, • The ability to read and speak English fluently, • Have a wired, high-speed internet connection (Download speed of 20Mbps+), • Excellent organizational, written, and oral communication skills, • The ability to type swiftly and accurately (20+ words a minute), • Ability to work regularly scheduled shifts within our hours of operation including the training period., • Basic knowledge of Microsoft Office Suite (Excel, PowerPoint, Word, Outlook), • Familiarity with computer and Windows PC applications and the ability to learn new and complex computer system applications, • Highly reliable with the ability to maintain regular attendance and punctuality, • The ability to evaluate, troubleshoot, and follow-up on customer issues, • An aptitude for conflict resolution, problem solving and negotiation, • Must be customer service oriented (empathetic, responsive, patient, and conscientious), • Ability to multi-task, stay focused, and self-manage, • Strong team orientation and customer focus, • The ability to thrive in a fast-paced environment where change and ambiguity are prevalent, • Excellent interpersonal skills and the ability to build relationships with your team and customers

Description: \n \n Education Requirements: \n B.S. degree in Chemistry, Biology, Engineering or other STEM related field. \n \n Required Skills: \n\n • Knowledge of continuous improvement principles (e.g. 5S, Kaizen, Hoshin, Standard Work).\n, • Knowledge of routine operation of laboratory equipment including but not limited to: Karl Fisher, pH meter, conductivity meter, UV, HPLC, Dissolution apparatus, etc.\n, • Knowledge of regulatory, cGLP principals and cGMP principles.\n, • Experience using Microsoft Office applications (word, excel, outlook).\n\n \n Preferred Skills: \n 1) Experience operating laboratory equipment: HPLC, dissolution apparatus, FTIR, NIR, etc. \n 2) Experience utilizing Empower. \n 3) Experience utilizing Labware/LIMS. \n 4) Experience performing root cause analysis. \n 5) Technical writing, including but not limited to: updating of standard operating procedures and writing quality notifications. \n 6) Knowledge of Tier processes. \n 7) Experience executing continuous improvement principles (e.g. 5S, Kaizen, Hoshin, Standard work). \n \n Responsibilities: \n Primary responsibilities are routine laboratory analytical testing, documentation, and reporting of potent and non-potent pharmaceutical drug product and drug substances; including but not limited to dissolution, assay/degradate, content uniformity, and identity testing in a GMP laboratory. Additional responsibilities include participating in laboratory investigations, root cause analysis, simple troubleshooting instrumentation issues, and participation in the daily tier process. \n

Job DescriptionPosition Summary – The QC Chemist II position performs testing using a variety of analytical techniques. The successful candidate ensures that Testing and Documentation is compliant with GMP regulations and internal procedures. The position will be operating within a GMP environment for an Analytical QC team in a CDMO. Essential Functions • Well versed with various laboratory techniques, including, but not limited to HPLC, GC, titrations, and various wet chemistry techniques., • Carry out routine laboratory work as directed by management and/or senior laboratory personnel with minimal supervision, • Performs complex analyses with moderate supervision., • Conduct routine analytical experiments using established analytical methods and procedures., • Data entry into reports, as directed by senior laboratory personnel., • Verify simple transcription processes, such as checking accuracy of calculations and reviewing daily equipment verifications for compliance., • Support testing for investigations for OOS, OOT, and aberrant results and troubleshooting., • Review and maintain laboratory notebooks., • Ensure data collected is processed and submitted for review in a timely manner., • Aid in investigations for OOS, OOT, and aberrant results and troubleshooting by assisting in root cause determination and report writing., • Maintains laboratory inventory of chemicals, standards, and consumables and orders materials as necessary., • Revises existing methods, SOPs, and Work Instructions as needed. Supervisory responsibilities: • Direct Reports: None, • Indirect Reports: None Key Relationships: • Manufacturing Operations, • Analytical R&D, • Quality Assurance Travel requirements: • N/A Education and Experience • B.S with 4-6 years' experience, or M.S with 3-4 years of experience: focus in chemistry, pharmaceutics or related scientific discipline, • 2-5 years´ experience in a GMP laboratory setting in the pharmaceutical industry, • Must have experience with general laboratory instruments, such as FTIR, Particle Size, Titration Equipment, and UV-Vis, • Must have experience in HPLC testing and troubleshooting, • Must have prior experience with raw materials or finished products testing in a GMP pharmaceutical environment., • Must be well versed with Good Documentation Practices and ALCOA++ principles., • Technical report writing proficiency preferred Knowledge, Skills, and Abilities • Proficiency in Empower, MS Excel, and MS Word, • Speaks, writes, listens and presents information in a logical and articulate manner appropriate for the audience, • Thorough when performing work, conscientious about attending to detail, and uses logical thinking that is well-organized and methodical and has a right first-time mentality Physical Demands and Work Environment While performing the duties of this job, there may be certain physical demands required for the position. • Requires constant standing, walking, seeing, gripping, & hearing, • Requires frequent sitting, bending, pushing, & reaching, • Requires occasional carrying under 20 LBS., • Requires frequent lifting & pulling under 20 LBS, occasionally 20 – 60 LBS., • Requires occasional twisting Other Duties You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked. Limitations and Disclaimer The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently. Powered by JazzHR aS9ej4lZQI

Bench Chemist – Level 1 \n \n Location: 100% Onsite \n Job Type: 12-Month Contract \n Pay Rate: $26.00/hour (W2) \n Schedule: Monday–Friday | Day Shift | 40 Hours per Week \n Anticipated Start Date: November 2, 2026 (alternative start date: November 16, 2026) \n \n About the Opportunity \n Alphanumeric Systems is seeking a detail-oriented and motivated Bench Chemist – Level 1 to support laboratory operations within a pharmaceutical manufacturing environment. \n This is an excellent opportunity for an entry-level laboratory professional or an individual with experience in raw material sampling and testing who is interested in developing their skills in a regulated environment. \n \n The ideal candidate will have strong attention to detail, a willingness to learn, and the ability to follow established procedures. Previous pharmaceutical or Good Manufacturing Practice (GMP) experience is preferred but not required, as training will be provided. \n \n Please Note: This position focuses primarily on routine raw material sampling, testing, documentation, and laboratory support rather than advanced research or traditional chemistry experimentation. \n \n Key Responsibilities \n\n • Perform routine sampling and analytical testing of raw materials, packaging materials, finished products, and environmental samples according to established procedures.\n, • Conduct raw material sampling and testing in accordance with approved methods and quality standards.\n, • Utilize laboratory instrumentation and equipment, which may include HPLC, GC, UV spectroscopy, microscopes, automated systems, and other analytical tools.\n, • Accurately document test results, observations, and laboratory activities in compliance with current Good Manufacturing Practices (cGMP).\n, • Review and interpret analytical data to ensure accuracy, completeness, and reliability.\n, • Identify and promptly communicate testing discrepancies, deviations, or unexpected results to laboratory supervisors.\n, • Support the review of laboratory documentation, including Standard Operating Procedures (SOPs), testing methods, specifications, and technical reports.\n, • Assist with laboratory equipment maintenance, troubleshooting, and routine operational activities.\n, • Participate in analytical method validation, transfer, and improvement activities as needed.\n, • Complete required training and maintain accurate training documentation.\n, • Collaborate with laboratory personnel and cross-functional teams to support daily operations and quality objectives.\n\n \n Required Qualifications \n\n • Associate degree in Chemistry, Biology, Laboratory Science, or a related scientific discipline, or 2–5 years of relevant experience working with raw materials.\n, • Ability to follow detailed written procedures and accurately document work.\n, • Strong attention to detail and commitment to quality and safety.\n, • Basic computer skills and the ability to learn laboratory systems and equipment.\n, • Good communication, organizational, and problem-solving skills.\n, • Willingness to learn new procedures and perform routine, process-driven laboratory activities.\n, • Ability to work independently and collaboratively in a structured laboratory environment.\n, • Ability to work onsite five days per week.\n\n \n Preferred Qualifications \n\n • Experience with raw material sampling, handling, or analytical testing.\n, • Previous experience in a pharmaceutical, biotechnology, manufacturing, or quality control laboratory.\n, • Familiarity with GMP/cGMP requirements and laboratory documentation practices.\n, • Experience using analytical laboratory instrumentation.\n, • Knowledge of SOPs, laboratory safety procedures, and quality standards.\n\n \n Additional Position Requirements \n\n • Must be available to work a standard Monday–Friday day shift, 40 hours per week.\n, • This position is 100% onsite; remote or hybrid arrangements are not available.\n, • Candidates must be willing and able to complete required Powered Air-Purifying Respirator (PAPR) onboarding and training requirements.\n, • Interviews will be conducted in person.\n\n \n Work Authorization Requirements \n Applicants must be legally authorized to work in the United States without employer sponsorship, now or in the future. We are unable to provide employment visa sponsorship for this position. \n \n We are not accepting applications or candidate submissions from third-party staffing agencies, vendors, or consulting firms. Candidates must apply directly and be eligible for W2 employment. \n \n Why Join Alphanumeric Systems? \n At Alphanumeric Systems, we connect talented professionals with opportunities to contribute to meaningful projects across the life sciences and technology industries. This position offers hands-on experience in a regulated pharmaceutical environment, structured training, and the opportunity to develop valuable laboratory and quality control skills. \n \n Apply today to take the next step in your laboratory career!

HPLC is more than a line on your résumé. Ready to put it to work every day? \n \n Job Summary \n We're hiring a Quality Laboratory Chemist I to join our quality control team in Lancaster, SC. Your work will help us evaluate finished products and raw materials with the accuracy and consistency quality demands. You'll spend your first 30 to 60 days learning our methods, then take on increasingly independent testing and assigned projects as you build proficiency. \n \n Schedule: Full-time, fully onsite, second shift. Monday through Thursday, 3:30 p.m. to 11:30 p.m.; Friday, 1:30 p.m. to 9:30 p.m. \n \n What You'll Do \n\n • Perform release, stability, and special-request testing of finished-product and raw-material samples using SOPs, in-house procedures, and applicable compendial methods.\n, • Put your HPLC skills to work and train on other instruments as needed, including GC, titrators, FTIR, UV/Vis, and dissolution equipment.\n, • Record results, prepare reports, review colleagues' work, and support out-of-specification investigations when assigned.\n, • Keep testing on track as priorities change while managing assigned projects to their deadlines.\n, • Maintain a safety-first laboratory, use properly calibrated equipment, and help train new team members as you gain proficiency.\n\n \n What You'll Bring \n\n • Bachelor's degree in Chemistry.\n, • At least three years of hands-on quality control laboratory testing experience.\n, • Practical HPLC experience and the ability to follow written methods accurately with increasing independence.\n, • Experience preparing laboratory reports, peer-reviewing results, and managing projects alongside routine testing.\n, • Strong attention to detail, clear communication, and a collaborative approach to solving problems.\n, • The ability to meet the physical demands of laboratory work, including extended standing and walking and lifting up to 50 pounds.\n\n \n Experience in a cGMP environment is preferred. This is an individual contributor role on a collaborative quality laboratory team. If you enjoy turning careful analytical work into results your colleagues can rely on, apply now and bring your expertise to our second-shift team.

Job DescriptionCompany Description Veolia has acquired Clean Earth. As Clean Earth completes its integration into Veolia, recruiting and hiring for this role is being managed in partnership with the Clean Earth talent acquisition team. Veolia in North America is the top-ranked environmental company in the United States for three consecutive years, and the country’s largest private water operator and technology provider as well as hazardous waste and pollution treatment leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial and hazardous waste collection and disposal, energy consulting and resource recovery. Veolia helps commercial, industrial, healthcare, higher education and municipality customers throughout North America. Headquartered in Boston, Veolia has more than 10,000 employees working at more than 350 locations across North America. Job Description Performs various assigned tasks and physical labor to ensure proper off-site treatment and disposal of customers’ hazardous waste materials in accordance with environmentally responsible and cost-effective practices and Clean Earth policies, practices, and procedures. Primary Responsibilities (Essential Functions): PRINCIPAL DUTIES AND RESPONSIBILITIES: • Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations. • Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract. • Assists other business groups, i.e., Depack, Retail and HHW, for both internally and onsite as needed. • Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle • Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR’s), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures. • May require obtaining and maintaining a Commercial Driver’s License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers’ job locations. • Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA’s) procedures including development of on-site Health &Safety plans/JSA’s as outlined in the procedures and policies, • Performs other duties as assigned. Qualifications Preferred Qualifications: EDUCATION/CREDENTIALS: Entry Level Associates Degree in genereal science (BS preferred) is required for the Lab Pack Chemist MEASURES OF PERFORMANCE Completion of the following curriculum: • 40-hour OSHA HAZWOPER (29 CFR 1910.120), • Acquisition of Commercial Driver’ s License (B or C) with Hazmat Endorsement, • Clean Earth Lab Pack I Training – (24 hours), • RCRA/DOT refresher course, • Department of Transportation, • Lab Pack definitions and procedures, • Lab pack Field Program, • Introduction to High Hazardous Cylinder Assessment course, • Customer Interactions, • Waste Management Methods, • On-Site Expectations, • Manifest/ LDR Completion, • Health & Safety course(s), • Customer Approach, • 40 hours Depack Experience This position requires a CDL B to be obtained within a 6-month period from your start date. Failure to obtain a CDL B within the 6-month period will mean you are no longer eligible for the Lab Pack Chemist position. This position is also contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements. Additional Information Benefits: Comprehensive benefits package includes paid time off policies, as well as health, dental, vision, life insurance, tuition reimbursement, paid volunteering and more. In addition, commencing no later than January 1, 2027, benefits package will include participation in an employer sponsored 401(k) plan, to save for retirement. Pay and benefits for employees represented by a union are outlined in their collective bargaining agreement. We are an Equal Opportunity Employer! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law

Job Description Position Summary – The Chemist III/Sr. Chemist Raw Materials ensures that testing, data review, and documentation is compliant with GMP regulations, internal procedures, and applicable compendial requirements. The position will be operating within a GMP environment for a Quality Control CDMO. The ideal candidate will additionally possess superior communication skills, presenting to internal and external clients Essential Functions • Schedule the QC laboratory Raw Materials workload appropriately to meet manufacturing release testing schedules, stability pull dates and timelines., • Monitor weekly laboratory and data review activities for accuracy and track hours needed for completion of tasks., • Oversight for review of QC and Raw Material data for compliance with specifications and regulatory requirements, • Interact with third party laboratories for microbial and analytical testing of raw materials, • Generate and/or review shipping paperwork for third part testing and prepare samples for shipment., • Create purchase requisitions for lab supplies and third-party testing, • Perform weekly laboratory audit inspections, • Perform sampling of raw materials as needed, • Review third party laboratory investigations and protocols., • Execute intermediate to advanced chemical and instrumental testing of raw materials using HPLC, GC, FTIR, UV-Vis, Karl Fischer titration, and wet chemistry., • Ensure all testing meets compendial standards (USP/EP/JP) and regulatory expectations. Conduct peer reviews of data, Certificates of Analysis (COAs), and laboratory logbooks., • Author and review GMP documentation including Standard Operating Procedures (SOPs), protocols, deviations, Corrective and Preventive Actions (CAPAs), and change controls., • Provide technical guidance to junior analysts. Lead method verification, validation, and method transfer activities for incoming raw materials., • Oversee the calibration, maintenance, and troubleshooting of laboratory equipment., • Other duties as assigned Supervisory responsibilities • Direct Reports: No, • Indirect Reports: None Key Relationships • Manufacturing Operations, • Quality Assurance, • Analytical R&D, • Program Management Travel requirements: • None Education and Experience • Minimum BA or BS in a scientific discipline required, • Minimum 5-8 years of Analytical chemistry experience with a cGMP/GLP environment, preferably at a CDMO or pharmaceutical company. Knowledge, Skills, and Abilities • Knowledge of cGMPs, • Good communication, organization and computer skills are required., • Knowledge of Empower required; LIMS and Microsoft Office programs knowledge is desired., • Ability and willingness to work additional hours as required by business need, • At least 5 years’ experience in a CRO environment, • Experience with USP, EP and JP monographs., • Experience with laboratory equipment such as HPLC (UV, Ion detectors, RI detectors), GC (Headspace, FID, TCD), FTIR, Auto Titrators, Karl Fischer Titrators (Volumetric and Coulometric), and Particle size., • Excellent interpersonal skills and ability to establish and maintain effective working relationships with both internal and external stakeholders, • Excellent verbal and written communication skills, • Ability to work with minimal supervision, • Experience in Data Review of Analytical data per GDP guidelines., • Proven ability to review and evaluate the compliance and completeness of analytical data., • Able to multi-task productively, applying time management processes and procedures effectively., • Works toward common goals by supporting, encouraging, and sharing information with colleagues., • Strong analytical skills and ability to understand business and financial implications of contracts, • Self-directed Physical Demands and Work Environment While performing the duties of this job, there may be certain physical demands required for the position. • Requires frequent sitting and walking, • Requires carrying under 20 LBS, occasionally 20 – 60 LBS, • Requires pushing, & pulling under 20 LBS, occasionally 20-60 LBS, • Requires occasional bending, twisting, reaching, & gripping, • Requires constant seeing & hearing Other Duties You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked. Limitations and Disclaimer The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently. Powered by JazzHR 9s721DUGQ2

Job Description Position Summary – The Quality Control Raw Materials Chemist I performs testing using a variety of analytical techniques. The successful candidate ensures that Testing and Documentation is compliant with GMP regulations and internal procedures The ideal candidate will additionally possess superior communication skills. The position will be operating within a GMP environment for a Quality Control CDMO. Essential Functions • Perform testing of raw materials, packaging components, and other samples., • Well versed with various laboratory techniques, including, but not limited to HPLC, GC, titrations, and various raw materials testing techniques., • Conduct routine analytical experiments using established analytical methods and procedures., • Data entry into reports, as directed by senior laboratory personnel., • Verify simple transcription processes, such as checking accuracy of calculations and reviewing daily equipment verifications for compliance., • Support testing for investigations for OOS, OOT, and aberrant results and troubleshooting., • Review and maintain laboratory notebooks., • Ensure data collected is processed and submitted for review in a timely manner., • Maintains laboratory inventory of chemicals, standards, and consumables and orders materials as necessary., • Aid in investigations for OOS, OOT, and aberrant results and troubleshooting by assisting in root cause determination., • Generate and/or review shipping paperwork for third party testing and prepare samples for shipment., • Create purchase requisitions for lab supplies and third-party testing, • Perform weekly laboratory audit inspections, • Perform sampling of raw materials as needed, • Other duties as assigned Supervisory responsibilities: • Direct Reports: None, • Indirect Reports: None Key Relationships: • Manufacturing Operations, • Quality Assurance, • Analytical R&D, • Program Management Travel requirements: • None Education and Experience • Minimum BA or BS in a scientific discipline required, • Minimum 2 – 4 years in a Quality Control setting for Raw Materials Knowledge, Skills, and Abilities • Knowledge of cGMPs, • Good communication, organization and computer skills are required., • Knowledge of Empower and Microsoft Office (Excel, Word) is required; LIMS knowledge is desired., • Ability and willingness to work additional hours as required by business needs, • Experience with testing per USP, EP, BP, and JP monographs., • Ability to interpret various compendial guidelines to ensure specifications meet regulatory requirements., • Experience with laboratory equipment such as HPLC (UV, Ion detectors, RI detectors), GC (Headspace, FID, TCD), FTIR, Auto Titrators, Karl Fischer Titrators, Coulometric Karl Fischer Titrators, Melting Point Apparatus, Muffle Furnace, UV-Vis, Refractometers, and Particle size., • Excellent interpersonal skills and ability to establish and maintain effective working relationships with both internal and external stakeholders, • Ability to work with modest supervision, • Able to multi-task productively, applying time management processes and procedures effectively., • Self-directed Physical Demands and Work Environment While performing the duties of this job, there may be certain physical demands required for the position. • Requires constant standing, walking, seeing, gripping, & hearing, • Requires frequent sitting, bending, pushing, & reaching, • Requires constant carrying under 20 LBS, occasionally 20 – 60 LBS., • Requires frequent lifting & pulling under 20 LBS, occasionally 20 – 60 LBS., • Requires occasional twisting Other Duties You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked. Powered by JazzHR V5qtfE57G1

Immediate need for a talented Chemist - I (Assistant). This is a 06+ Months Contract opportunity with long-term potential and is located in Wilson, NC (Onsite). Please review the job description below and contact me ASAP if you are interested. \n \n Job ID:26-31756 \n \n Pay Range: $25 - $28.06/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). \n \n Key Responsibilities: \n \n\n • Perform routine laboratory testing and analysis of pharmaceutical products.\n, • Ensure accurate documentation and compliance with GMP/GLP quality standards.\n, • Conduct testing including dissolution, assay/degradate, content uniformity, and identity testing.\n, • Participate in laboratory investigations and root cause analysis.\n, • Troubleshoot simple instrumentation issues and engage in daily tier processes.\n\n \n Key Requirements and Technology Experience: \n \n\n • B.S. degree in Chemistry, Biology, Engineering, or other STEM-related field.\n, • Knowledge of continuous improvement principles (e.g., 5S, Kaizen, Hoshin, Standard Work).\n, • Experience using laboratory equipment including HPLC and dissolution apparatus.\n, • Familiarity with regulatory cGLP and cGMP principles.\n, • Proficiency in Microsoft Office applications (Word, Excel, Outlook).\n, • Experience operating laboratory equipment: FTIR, NIR, etc.\n, • Experience utilizing Empower and Labware/LIMS.\n, • Experience performing root cause analysis and technical writing.\n, • Knowledge of Tier processes and executing continuous improvement principles.\n\n \n Our client is a leading Pharmaceutical Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. \n \n Pyramid Consulting, Inc. 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. \n \n By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.

Company Profile: Evergreen Strategeum is a premier market and business intelligence solution provider, blending generative AI with expert analysis to deliver crucial, relevant insights for enterprises and business leaders. Job Summary: To provide fact-based research and forward-thinking insight into regional and global geopolitical dynamics that have impacts on international trade and business. Key Responsibilities: Conduct investigative research into current issues in diplomacy, international relations, economy and trade, and security dynamics. Track ongoing events including legislation, negotiation, conflict and crisis. Interview subject-matter experts for research purposes. Prepare research report, briefing, and presentation for stakeholders. Qualifications: At least 1 year of professional experience in research, government, or consulting. Educational background in intelligence, political science, international relations, geopolitics, law, or other related fields. Excellent analytical skills and ability to stay informed about current events and latest developments related to the applicant’s specialized areas. Salary & Reward: Negotiable after interview and probation, starting at USD4,200.00 per • month, performance bonus not included.

Job Description Description Product Development Chemist Arclin has an immediate full-time, on site opening for a Product Development Chemist in our Moncure, NC location. About Arclin You can find Arclin everywhere. Our technologies make homes and transportation safer, help crops flourish, keep water clean, protect first responders and members of the military, and preserve the purity of essential pharmaceuticals. These vital, everyday products can't fail, and we’re here to give the world an extra layer of performance and peace of mind. With ~4,000 team members across more than 30 global manufacturing facilities, we operate with the scale to make a global impact and the agility to solve complex challenges at the molecular level. Rooted in scientific discovery and innovation, Arclin’s materials redefine performance across industries - from Firepoint®’s patented intumescent technology that helps stall flames and save lives to the iconic Kevlar® and Nomex® brands trusted to protect those who serve, strengthen aerospace and industrial systems, and perform where reliability and safety are top of mind. As we expand our mission‑critical materials portfolio and shape the next era of performance technologies, we’re looking for people who want to grow, lead, and solve the challenges others can’t. Together, we’ll advance the innovations that keep the world moving. Because at Arclin, our people are truly Vital Beyond Measure. Job Overview: Reporting to the Product Development and Applications Manager, this position is responsible for designing and executing tasks associated with the development of innovative chemistry-based products (resins) to support Arclin’s product development strategy. This position operates within the parameters of Arclin’s policies and procedures and will provide product expertise to R&T, Sales, Manufacturing, and Marketing groups. Responsibilities • Plan and execute projects to develop and optimize quality resin products for Arclin customers. This involves formulating and synthesizing formaldehyde-based resins, conducting lab experiments, performing wet chemistry testing and troubleshooting production issues., • Apply innovative thinking to solve complex scientific and chemical challenges., • Provide technical support to the applications, production and sales groups., • Maintain accurate and complete records of work results and activities., • Maintain a clean and safe lab environment in compliance with Arclin health, safety, and environmental policies and procedures. Ensure that all lab equipment is maintained and operating optimally. Required Qualifications • Bachelors of Science in Chemistry or related field, • 2-3 years of experience in industrial chemical laboratory environment; MS degree will substitute for two (2) years of experience., • Ability to work efficiently and communicate clearly in a cross-functional team., • Capability to prepare written reports with emphasis on technical clarity, accuracy and attention to detail., • Proficiency in the use of computer software (MS Office, Statistical analysis, etc.), • Strong problem solving and troubleshooting skills., • Ability to work with hazardous materials while following Arclin health, safety and environmental regulations. Preferred Qualifications • Ability to construct schedule and goals to effectively execute on projects and tasks., • Demonstrated ability to innovate and think creatively in a scientific context., • Knowledge of formaldehyde-based resin chemistries., • Experience in project planning and design of experiments., • Basic understanding of engineering processes used in resin production.

Job DescriptionBench Chemist - Level 1Location: 100% Onsite Job Type: 12-Month Contract Pay Rate: $26.00/hour (W2) Schedule: Monday-Friday | Day Shift | 40 Hours per Week Anticipated Start Date: November 2, 2026 (alternative start date: November 16, 2026) About the OpportunityAlphanumeric Systems is seeking a detail-oriented and motivated Bench Chemist - Level 1 to support laboratory operations within a pharmaceutical manufacturing environment. This is an excellent opportunity for an entry-level laboratory professional or an individual with experience in raw material sampling and testing who is interested in developing their skills in a regulated environment. The ideal candidate will have strong attention to detail, a willingness to learn, and the ability to follow established procedures. Previous pharmaceutical or Good Manufacturing Practice (GMP) experience is preferred but not required, as training will be provided. Please Note: This position focuses primarily on routine raw material sampling, testing, documentation, and laboratory support rather than advanced research or traditional chemistry experimentation. Key Responsibilities: • Perform routine sampling and analytical testing of raw materials, packaging materials, finished products, and environmental samples according to established procedures., • Conduct raw material sampling and testing in accordance with approved methods and quality standards., • Utilize laboratory instrumentation and equipment, which may include HPLC, GC, UV spectroscopy, microscopes, automated systems, and other analytical tools., • Accurately document test results, observations, and laboratory activities in compliance with current Good Manufacturing Practices (cGMP)., • Review and interpret analytical data to ensure accuracy, completeness, and reliability., • Identify and promptly communicate testing discrepancies, deviations, or unexpected results to laboratory supervisors., • Support the review of laboratory documentation, including Standard Operating Procedures (SOPs), testing methods, specifications, and technical reports., • Assist with laboratory equipment maintenance, troubleshooting, and routine operational activities., • Participate in analytical method validation, transfer, and improvement activities as needed., • Complete required training and maintain accurate training documentation., • Collaborate with laboratory personnel and cross-functional teams to support daily operations and quality objectives. Required Qualifications: • Associate degree in Chemistry, Biology, Laboratory Science, or a related scientific discipline, or 2-5 years of relevant experience working with raw materials., • Ability to follow detailed written procedures and accurately document work., • Strong attention to detail and commitment to quality and safety., • Basic computer skills and the ability to learn laboratory systems and equipment., • Good communication, organizational, and problem-solving skills., • Willingness to learn new procedures and perform routine, process-driven laboratory activities., • Ability to work independently and collaboratively in a structured laboratory environment., • Ability to work onsite five days per week. Preferred Qualifications: • Experience with raw material sampling, handling, or analytical testing., • Previous experience in a pharmaceutical, biotechnology, manufacturing, or quality control laboratory., • Familiarity with GMP/cGMP requirements and laboratory documentation practices., • Experience using analytical laboratory instrumentation., • Knowledge of SOPs, laboratory safety procedures, and quality standards. Additional Position Requirements: • Must be available to work a standard Monday-Friday day shift, 40 hours per week., • This position is 100% onsite; remote or hybrid arrangements are not available., • Candidates must be willing and able to complete required Powered Air-Purifying Respirator (PAPR) onboarding and training requirements., • Interviews will be conducted in person. Work Authorization RequirementsApplicants must be legally authorized to work in the United States without employer sponsorship, now or in the future. We are unable to provide employment visa sponsorship for this position. We are not accepting applications or candidate submissions from third-party staffing agencies, vendors, or consulting firms. Candidates must apply directly and be eligible for W2 employment. Why Join Alphanumeric Systems?At Alphanumeric Systems, we connect talented professionals with opportunities to contribute to meaningful projects across the life sciences and technology industries. This position offers hands-on experience in a regulated pharmaceutical environment, structured training, and the opportunity to develop valuable laboratory and quality control skills. Apply today to take the next step in your laboratory career!

Provide technical oversight and guidance to project teams, including collaboration with geologists, engineers, and field staff.

Exploration Geologist | Remote + Field Work | Full-time, Direct-Hire | Mining. We're partnering with a growing exploration company to find a Mid-to-Senior Exploration Geologist to join their team. This is a fantastic opportunity for a field-focused geologist who wants to play a key role in advancing

Dispersions Specialist (Chemist) DyStar is a leading specialty chemical company with a global presence. We have an immediate need for a Dispersions Specialist in one of our manufacturing plants located in Reidsville, NC. This is an individual contributor role. This role will support our Quality Lab Manager and will provide technical and operational support for production of Dispersions at the Reidsville manufacturing plant and our Tollers. The role will include development of new Dispersions from Lab Trials until Production; production batch supervision; support process and batch troubleshooting; and improve processes to reduce cost and improve sustainability. Primary Responsibilities: • Provides technical and operational support for production of Dispersions at Reidsville site., • Develops new product items in tight cooperation with Product Management from lab sizes over scale up from pilot trials until implementation in the technical plant set-up., • Is the liaison between Quality Control and Production operations., • Improves existing production processes to reduce cost, increase reliability, purity, safety, and improves Sustainability., • Works under and in collaboration with the site Quality Manager to provide in-process and final quality testing for products produced both on site and at tollers considering internal quality procedures and standards as well as the requirements of ISO9001:2015., • Troubleshoots existing production processes and implements new product items in production., • Works with site planning, scheduling and production operators to optimize the production flow and achieve the shortest possible batch cycle time., • Support production operator activities to ensure product is available to meet sales or inventory demand., • Monitors dispersions wastewater (cleaning water) to avoid any contamination of Auxiliaries wastewater., • Supervises the handling of powders to avoid cross-contamination from Dispersions production to other production units., • Supports the Production Manager regarding product cost calculation (effective material consumption and conversion costs)., • Checks and implements advanced technologies to improve costs and efficiency in production. Supervisory Responsibilities: None Education and Experience: • BS Chemistry, Chemical / Process Engineering or related field., • 8+ years of relevant Experience in Production and Quality Control of Dispersions by Physical Operations (Dispersing and Wet Milling)., • 5+ Years experience in supervision of production processes to guarantee best possible output, quality, and costs, • Experience in scale-up of production processes from Lab to technical scale., • Computer skills, including Microsoft Office. Experience with ERP systems a plus. Knowledge/Skills/Abilities: • Experience qualifying raw materials and key intermediates to achieve best costs and stable product quality., • Experience improving lower costs processes with efficiency improvement regarding material and utility consumption., • Written and oral communication skills to explain findings and share results cooperation partners, • Understanding of manufacturing costs. This is an on-site role in Reidsville, NC; not open to remote or hybrid work. Visa sponsorship is NOT available for this role. DyStar is an Equal Opportunity Employer

We're hiring a Quality Laboratory Chemist I to join our quality control team in Lancaster, SC. Bachelor's degree in Chemistry.

This involves formulating and synthesizing formaldehyde-based resins, conducting lab experiments, performing wet chemistry testing and troubleshooting production issues. Bachelors of Science in Chemistry or related field. Knowledge of formaldehyde-based resin chemistries.

Knowledge of formaldehyde-based resin chemistries. This involves formulating and synthesizing formaldehyde-based resins, conducting lab experiments, performing wet chemistry testing and troubleshooting production issues. Bachelors of Science in Chemistry or related field.

We're hiring a Quality Laboratory Chemist I to join our quality control team in Lancaster, SC. Bachelor's degree in Chemistry.

Chemist – Personal Care & Skincare Formulation. For a Chemist who enjoys creative formulation, solving technical challenges and seeing products successfully reach the market, this is a genuinely compelling opportunity.

Product Development Chemist Arclin has an immediate full-time, on-site opening for a Product Development Chemist in our Moncure, NC location. About Arclin You can find Arclin everywhere. Our technologies make homes and transportation safer, help crops flourish, keep water clean, protect first responders and members of the military, and preserve the purity of essential pharmaceuticals. These vital, everyday products can't fail, and we’re here to give the world an extra layer of performance and peace of mind. With ~4,000 team members across more than 30 global manufacturing facilities, we operate with the scale to make a global impact and the agility to solve complex challenges at the molecular level. Rooted in scientific discovery and innovation, Arclin’s materials redefine performance across industries - from Firepoint®’s patented intumescent technology that helps stall flames and save lives to the iconic Kevlar® and Nomex® brands trusted to protect those who serve, strengthen aerospace and industrial systems, and perform where reliability and safety are top of mind. As we expand our mission‑critical materials portfolio and shape the next era of performance technologies, we’re looking for people who want to grow, lead, and solve the challenges others can’t. Together, we’ll advance the innovations that keep the world moving. Because at Arclin, our people are truly Vital Beyond Measure. Job Overview: Reporting to the Product Development and Applications Manager, this position is responsible for designing and executing tasks associated with the development of innovative chemistry-based products (resins) to support Arclin’s product development strategy. This position operates within the parameters of Arclin’s policies and procedures and will provide product expertise to R&T, Sales, Manufacturing, and Marketing groups. Responsibilities • Plan and execute projects to develop and optimize quality resin products for Arclin customers. This involves formulating and synthesizing formaldehyde-based resins, conducting lab experiments, performing wet chemistry testing and troubleshooting production issues., • Apply innovative thinking to solve complex scientific and chemical challenges., • Provide technical support to the applications, production and sales groups., • Maintain accurate and complete records of work results and activities., • Maintain a clean and safe lab environment in compliance with Arclin health, safety, and environmental policies and procedures. Ensure that all lab equipment is maintained and operating optimally. Required Qualifications • Bachelors of Science in Chemistry or related field, • 2-3 years of experience in industrial chemical laboratory environment; MS degree will substitute for two (2) years of experience., • Ability to work efficiently and communicate clearly in a cross-functional team., • Capability to prepare written reports with emphasis on technical clarity, accuracy and attention to detail., • Proficiency in the use of computer software (MS Office, Statistical analysis, etc.), • Strong problem solving and troubleshooting skills., • Ability to work with hazardous materials while following Arclin health, safety and environmental regulations. Preferred Qualifications • Ability to construct schedule and goals to effectively execute on projects and tasks., • Demonstrated ability to innovate and think creatively in a scientific context., • Knowledge of formaldehyde-based resin chemistries., • Experience in project planning and design of experiments., • Basic understanding of engineering processes used in resin production.

QC Laboratory Chemist I | cGMP | FDA.

Quality Control Laboratory Chemist | cGMP. Quality Control Laboratory Chemist.

This involves formulating and synthesizing formaldehyde-based resins, conducting lab experiments, performing wet chemistry testing and troubleshooting production issues. Bachelors of Science in Chemistry or related field. Knowledge of formaldehyde-based resin chemistries.

We're hiring a Quality Laboratory Chemist I to join our quality control team in Lancaster, SC. Bachelor's degree in Chemistry.

Quality Control Laboratory Chemist | cGMP. Quality Control Laboratory Chemist.

QC Laboratory Chemist I | cGMP | FDA.

Masis Professional Group in Charlotte, NC, is seeking a QC Laboratory Chemist I to join an industry-leading health and wellness manufacturer dedicated to quality and innovation. Bachelor’s in Chemistry and 2–5 years' experience required.

Job Title Environmental Engineer, Geologist or ScientistIntern/Co-Op Job Details Primary Location US-NC-Raleigh ID 2026-4983 Category Co-Op/Intern Position Type Limited Term Remote No Additional Location US-NC-Wilmington Overview Do you want to build an impactful career to change the world for the b

Project Manager / Professional Geologist. Our client is a reputable Environmental, Geotechnical, and Civil Engineering firm serving the Mid-Atlantic and Southeast. Due to continued growth, they are seeking a Project Manager / Professional Geologist to support DOT project work in North Carolina.