Chemist jobs in Columbia, SC

Job Details The Ritedose Corporation - Columbia, SC 2C 4 Year Degree $31.83 - $35.01 Hourly ScienceDescription The Analytical Services Chemist III role is for a laboratory professional with responsible for performing analytical testing related to raw materials, compounding support activities, and final product testing in the Analytical Services Laboratory. In addition, the Analytical Services Chemist III role will support analytical method validations and transfers, as well as product development studies. Responsibilities: Performing chemical raw material (sampling, testing and release), in-process (including product formulation activities), and final product including stability and complaint sample testing. Notify Laboratory Management immediately of out of specification results and assist in the investigations of OOS and deviations as assigned by Laboratory Management. Responsible for performing tests associated with method validations and transfers as assigned, including cleaning and equipment validations. Responsible for laboratory notebook data, batch record data, and report review when assigned. Assist in special projects and regulatory audits as requested by the Laboratory Management. Assist in collaboration of laboratory SOPs when requested. Responsible for assisting with the training of junior personnel when requested. Responsible for ensuring that routine maintenance and troubleshooting of instrumentation, is performed as stated in the instrument manual and contacting the manufacturer for assistance when needed. Responsible for the general maintenance of the Chemistry Laboratory including good housekeeping and a safe working environment. Follow Standard Operating Procedures, documentation, safety, health, and cGMP Guidelines. Qualifications BS degree in Chemistry or related field with a minimum 4 years of experience, or a MS degree in Chemistry or related field with a minimum 2 years of experience, in a pharmaceutical laboratory environment required. Expertise with standard laboratory techniques, wet chemistry tests, titration, spectroscopy, HPLC, GC, and modern Data Acquisition Systems required. Competency with specialized laboratory equipment such as ICP-MS, Malvern PSD, aPSD, Particulate Matter testing, Breathing Simulation Testing, etc. is desirable Strong documentation skills and proficiency with current word processing, spreadsheets, and database software required Must be detail focused, have a strong work ethic, and the ability to participate in and contribute to a team-oriented work environment by developing positive working relationships within the laboratory and between other departments

Job Responsibilities Careers at SCDES: Where Passion Meets Preservation Do you love South Carolina and protecting the environment? Come join our team at SCDES, put your passion to work with us! We are dedicated to protecting the state of South Carolina and we would love to have you as a member of our team! Science| Service| Sustainability This position is for a Chemist II in the Organic Chemistry laboratory of the Analytical and Radiological Environmental Services Division. Primarily performs extractions and analyses of drinking water samples in accordance with EPA methods. * Analysis of various contaminants in the environmental compliance monitoring samples. * Utilize Gas Chromatography/Electron Capture Detector (GC/ECD) instrumentation. * Duties will include, but are not limited to: * Extraction and analysis of drinking water samples for Chlorinated Acid Herbicides by Gas Chromatograph/ECD technique. * Extraction and analysis for Haloacetic Acids (HAAs) and Trihalomethanes (THM) in drinking water samples by GC/ECD technique. * Back-up chemist for extraction and analyses of pesticide and herbicides in water samples by Gas Chromatography/ECD techniques. * The interpretation of generated data while adhering to approved standard operating procedures (SOPs). * Operation and maintenance of analytical instrumentation. * Performing quality control functions associated with sample analysis. * Assist other staff members with glassware preparation, general laboratory cleaning, sample analysis, instrument troubleshooting, and other related duties as dictated by workload assigned by the supervisor. * Communicate effectively with peers, other scientists, and service engineers. * Prepares and participates in emergency response as required. * Perform duties and special projects as assigned by supervisor. * Complete administrative tasks(PCAS, SCEIS related functions, etc.) and documentation as required and requested. Minimum and Additional Requirements * A master's degree in chemistry; * OR a bachelor's degree in chemistry and one year of chemistry experience; * OR a bachelor's degree in the natural or physical sciences* with 16 semester hours in chemistry and two years laboratory experience * A doctorate in chemistry may be substituted for the required work experience Institutions of higher learning must be recognized by the Council for Higher Education Accreditation. * These fields include but are not limited to branches relating to Physics, Chemistry, Biology, etc. ADDITIONAL REQUIREMENTS: * Experience in a laboratory setting related to the area of employment, including experience in operating, maintaining, and interpreting results from advanced analytical instrumentation such as gas or liquid chromatographs, and associated data systems. * Experience with general instrumentation software and Microsoft Office. * Ability to: * Perform scientific mathematical calculations, highly complex tasks, and maintain accurate records. * Communicate effectively with peers, other scientists, and service engineers. * Prioritize tasks and manage time effectively. * Move and change 150-pound gas cylinders using a hand truck. * Adhere to all safety requirements including the wearing of required safety equipment such as eye protection, laboratory coats, and nitrile gloves to assure the safe handling of a myriad of commonly used laboratory chemicals on a daily basis. * Stand for long periods of time and lift at least 50 lbs. to countertop level. * The workplace exposure to chemicals of record will be kept below the published OSHA thresholds through the use of administrative and engineering controls, specialized PPE and through appropriate adjustments in job assignments. * This position requires the strict adherence to approved methods and standard operating procedures for the proper collection of quality and technically defensible data. * This is a laboratory position and as such involves safely working with various types of glassware, the performance of repetitive tasks, and meticulous attention to detail. * Please note that the State of South Carolina will not be responsible for any expenses incurred to attend this interview. * An unofficial copy of all transcripts from institutions of higher learning must be attached to the application. Preferred Qualifications * A Degree in Chemistry. * Two years of Environmental Laboratory employment experience. * Experience with general instrumentation software such Empower, Mass Hunter or Chem Station and Microsoft Office suite. * Knowledge, understanding and experience in the Organic Chemistry Laboratory setting, including but not limited to GC, GC/MS, and HPLC and data interpretation. Additional Comments SCDES is committed to providing equal employment opportunities to all applicants and does not discriminate on the basis of race, color, religion, sex (including pregnancy, childbirth, or related medical conditions, including, but not limited, to lactation), national origin, age (40 or older), disability or genetic information. The Department will not sponsor H1B visas for this position. The South Carolina Department of Environmental Services offers an exceptional benefits package for full time (FTE) employees:? * Health, dental, vision, long-term disability, and life insurance for employees, spouse, and children. Click here for additional information. * 15 days annual (vacation) leave per year * 15 days sick leave per year * 13 paid holidays * Paid parental leave * S.C. Deferred Compensation Program available (S.C. Deferred Compensation) * Retirement benefit choices* * State Retirement Plan (SCRS) * State Optional Retirement Program(State ORP) * Enrollment in one of the listed plans is required for all FTE employees; please refer to the contribution section of hyperlinked retirement sites for the current contribution rate of gross pay.

We are looking to fill a **Scientist 3 - Analytical Chemist** position working as **a full-time employee of Parexel FSP on long-term assignment** onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer any sponsorship.** **Responsibilities** + General understanding of analytical method development and method validation + Hands-on experience with chromatographic analysis using various ultra-high-performance liquid chromatography (UPLC), high-performance liquid chromatography (HPLC), and gas chromatography (GC) techniques + General knowledge of separations science + Experience with Empower chromatographic software and with analysis of drug formulations + Hand-on experience with Fourier transform infrared (FTIR) spectroscopic analysis and ultraviolet-visible (UV-VIS) spectroscopic analysis + Skilled on method and instrument troubleshooting, specifically for HPLC and GC methods and systems **Required Skills** + Strong computer, scientific, and organizational skills + Excellent organization to multi-task and manage multiple ongoing projects in parallel including routine testing (for example, assay and impurity testing) and data processing and interpretation + Excellent communication (oral and written) and attention to detail + Proficient in written and spoken English, is required **Desired Skills and Experience** + Empower software + Analysis of drug products + Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude **Qualifications** + BS degree and 3-5 years of relevant experience, or + MS degree with at least 1-2 years relevant experience **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Job DescriptionDescription: Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check, drug screen (subject to applicable law). The hours for this position are Monday - Thursday 3:30pm - 11:30 and Friday 1:30pm - 9:30pm. Summary of the Position: The QLCI reports to Quality Laboratory Management. The QLCI will provide overall support to the laboratory with testing while working in a safe work environment. This is a position that requires the ability to manage time efficiently in order to complete assigned testing. The QLCI shall be willing and able to learn laboratory processes supporting testing as well as instrumentation theory and troubleshooting. Roles and Responsibilities: Testing: The QLCI performs Release, Stability and Special Request testing of finished products and raw material samples following Standard Operating Procedures (SOPs) and in-house test methods, and/or compendial methods. The QLCI is expected to be capable of independently executing in-house methods and procedures and perform them as written with little to no assistance. Teamwork: The QLCI must be flexible to changes with the testing schedule and adapt to laboratory improvements implemented from management and/or teammates. Assists with training of new laboratory personnel and document training in accordance with established laboratory SOPs and the Nutramax training program. Safety Requirements: Must have a Safety-First mindset and being aware of surroundings while working in the laboratory. Maintains a safe work environment and will ensure that all equipment used in the testing procedures are calibrated and properly maintained. General Responsibilities: Train on the operation of the following instrumentation but not limited to: Laboratory Balances, High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Automated Titrators, FTIR, UV/Vis Spectrophotometer, Polarimeter, Dissolution and Disintegration Instrumentation. The operation of additional instrumentation and the need to train on new laboratory test methods when required. Execute projects assigned by management within expected/established deadlines while managing time with testing responsibilities. Stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Laboratory complies in the areas of analytical applications, release specifications, and documentation practices. Ensure competency of ISO 17025 test methods are current. Assist in resolving laboratory Out-Of-Specification (OOS) results in accordance with laboratory investigation procedures if assigned. Perform other assigned duties as may be required in meeting company objectives. Communicate effectively with other departments within the organization and function within a team environment. Regular attendance is required. Minimum Requirements : The QLCI will have 0 - 2 years of laboratory experience working in a cGMP environment preferred. Experience preferred with operation of laboratory instrumentation including Gas Chromatography (GC) and/or Liquid Chromatography (LC). Effective interpersonal, self-motivation skills, and the ability to interact with all levels of personnel are required. Education and Experience: A bachelor's degree in Chemistry. If degree has concentration; Biochemistry, Inorganic, Physical or Polymer Chemistry preferred. Supervisory Responsibilities: None Requirements:

The Quality Control Chemist reports directly to Quality Laboratory Management and plays a key role in supporting laboratory operations through accurate and timely testing. This position requires strong time management skills to meet testing deadlines and a willingness to learn laboratory processes, instrumentation theory, and troubleshooting techniques. Schedule: This position will be on a 2nd shift: Monday - Thursday 3:30pm - 11:30pm and Friday 1:30pm - 9:30pm. Key Responsibilities Testing: + Perform Release, Stability, and Special Request testing on finished products and raw materials in compliance with Standard Operating Procedures (SOPs), in-house methods, and compendial standards. + Execute in-house methods independently and accurately with minimal supervision. Team Collaboration: + Adapt to changes in testing schedules and support continuous improvement initiatives within the lab. + Assist in training new laboratory personnel and document training per established SOPs and Nutramax guidelines. Safety: + Maintain a safety-first approach and remain vigilant of surroundings while performing laboratory tasks. + Ensure all equipment used in testing is properly calibrated and maintained. General Duties: + Train on and operate various laboratory instruments, including but not limited to: Laboratory Balances, HPLC, GC, Automated Titrators, FTIR, UV/Vis Spectrophotometer, Polarimeter, Dissolution and Disintegration instruments. + Complete assigned projects within established timelines while balancing testing responsibilities. + Stay informed on updates from USP, FDA, and other regulatory bodies to ensure compliance with analytical standards and documentation practices. + Assist in investigating Out-of-Specification (OOS) results as needed. + Perform additional duties as required to support company objectives. + Communicate effectively across departments and work collaboratively within a team environment. + Maintain regular and reliable attendance. Skills Chemistry, Quality control, Laboratory, Gmp, Wet chemistry Top Skills Details Chemistry Additional Skills & Qualifications + Experience: 2-5 years in a laboratory setting, a cGMP environment. Familiarity with GC and/or LC instrumentation is preferred. + Skills: Strong interpersonal skills, self-motivation, and ability to work with individuals at all organizational levels. + Education: Bachelor's degree in Chemistry; concentrations in Biochemistry, Inorganic, Physical, or Polymer Chemistry are preferred. Experience Level Intermediate Level Job Type & Location This is a Permanent position based out of Lancaster, SC. Pay and Benefits The pay range for this position is $70000.00 - $80000.00/yr. Comprehensive Health Coverage: Competitive medical, dental, and vision plans for employees and their families.Educational Assistance: Opportunities for training and professional development to support career growth.Supportive Work Culture: A family-oriented environment that values faith, servant leadership, and collaboration.Community Engagement: Volunteer opportunities and mission trips organized by the company to give back locally and internationally.Employee Recognition & Perks: Birthday cards with gift cards, family days at the zoo, Thanksgiving dinners, and other thoughtful gestures.Work-Life Balance: A culture that prioritizes employee well-being and fosters a positive, supportive atmosphere. Workplace Type This is a fully onsite position in Lancaster,SC. Application Deadline This position is anticipated to close on Dec 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins 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. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Eurofins BPT-Columbia is looking for an Associate Scientist to join our Stability and Batch Release team located in Columbia, Missouri. The Associate Scientist position is an entry-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments. The ideal candidate would possess: * Experience with GLP and/or GMP and hands-on experience with HPLC and/or GC desirable. * Experience with LIMS system desirable. * Familiarity and/or experience in a laboratory setting is required. * Good organizational skills; ability to follow direction and good communication skills are required. Qualifications Minimum Qualifications: * Bachelor's degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas is required. * Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information Position is full-time, Monday-Friday, 8am - 4:30 pm., with overtime as needed. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply. We offer excellent full-time benefits including: * comprehensive medical coverage, * life and disability insurance, * 401(k) with company match, * paid holidays and vacation, * dental and vision options. To learn more about Eurofins, please explore our website ****************** . Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Combined Insurance, a Chubb Company, is seeking a Senior Product Development Analyst to join our fast-paced, high energy, growing company. We are proud of our tradition of success in the insurance industry of over 100 years. Come join our team of hard-working, talented professionals! Job Summary The Senior Product Development Analyst supports the expansion and ongoing maintenance of Chubb/Combined North America's insurance product portfolio. This candidate will be collaborating with the Product Innovation Team in all aspects of competitive analysis, product development, contracts, product marketing, distribution support and training and collaborate throughout the enterprise to support cross-functional product implementation. Responsibilities Product Management - Collaborate with Legal/Compliance, Actuarial, Underwriting and new Business Operations, IT and Claims to maintain products. Work with Compliance to monitor and report on our product filings and update tracking reports. Develop and manage product documentation. Product Development - Actively participate in the design and development of innovative, competitive, and compelling products to consistently maintain market leadership and capitalize on new growth opportunities. Draft and revise contract language and support internal and external product approval. Manage relationships and support collaboration with external partners and third-party administrators. Competitive Analysis - Benchmark competitor offerings and industry practices, analyze competitor state product filings, review proposals, marketing materials, social media and attend industry conferences to remain an industry leading carrier. Marketing and Sales Support - Subject matter expert for distribution team and internal and external partners. Review and edit product marketing materials and collateral, maintain product support tools, as well as develop, update, and deliver product training and documentation for multiple sale channels and systems. COMPETENCIES AND SKILLS Draft, interpret, and analyze voluntary life and health insurance contracts. Strong attention to detail, with superior organizational and communication skills Ability to multi-task and successfully manage multiple priority projects. Ability to successfully collaborate as a member of cross functional teams, as well as perform as an individual contributor. Demonstrated ability to meet aggressive deadlines. Quick learner and analytical thinker Education and Experience 5+ years in Group, Worksite and/or Individual Supplemental Health product development and product related functions Experience with Microsoft Office, including Excel, Word and Power Point College degree preferred

Apply Now Why You'll Love This Job We are seeking a motivated individual to join our Quality Assurance team based out of our Gaston, SC facility. The ideal candidate for the Chemist position will be results driven, have self-directing initiative, hands on analytical experience, and excellent problem-solving skills that are complemented by exceptional interpersonal and communication skills Responsibilities The Chemist will be reportable to the Quality Assurance Manager and have responsibilities for the following tasks: * Promote and model behavior-based safety and compliance with all laboratory/hazardous chemical safety procedures * Interface with, train, and lead laboratory analysts * Maintain instrumentation and methods including both qualitative and quantitative techniques as required to support the CA - Columbia site in analytical quality testing * Lead projects for the purchase and installation of new laboratory instruments * Develop and maintain analytical methods * Troubleshoot laboratory technical issues * Serve as a chemical knowledge resource * Ensure proper handling of laboratory waste, including hazardous waste collection and proper movement * Support and implement analytical projects aligned with business objectives * Maintain laboratory statistical process control * Prepare solutions and samples and perform analytical analyses * Collaborate with Quality Assurance, Manufacturing, Maintenance, R&D, and Technical Marketing teams as required. Skills & Qualifications Required: * BS Degree in Chemistry or similar Preferred: * Specialized education or experience in Analytical or Polymer Chemistry * 3+ years' experience with analytical instrumentation * Manufacturing quality control lab experience * Mechanical competence and hands-on instrument troubleshooting * Experience and technical knowledge regarding analytical instruments and techniques including but not limited to: * Dilute Solution Viscometry (IV) * X-Ray Fluorescence Spectrometry (XRF) * Differential Scanning Calorimetry (DSC) * Infrared Spectroscopy (IR) * Karl Fischer * Titrations * Gas Chromatography (GC) * Liquid Chromatography (LC) * Ultraviolet-Visible Spectrophotometer (UV Vis) * Colorimetry * Environmental / Water Lab * Rheology * Applied Statistical Techniques * Computer skills including MS Excel and basic programming * Knowledge of Safety / ISO / Quality / Regulatory Standards * Knowledge of Food Safety Standards * Knowledge of Good Lab Practices, Good Manufacturing Practices, and Good Documentation practices Root cause failure analysis * Excellent written and verbal communication skills * Data-based decision-making skills * Ability to work with small groups to lead improvement projects * Supervisory experience Alpek Polyester USA, LLC is a global leader in the production of PTA (Terephthalic Acid), PET (Polyethylene Terephthalate) Resins, PET Recycling (rPET), and Specialty Polymers. This integrated business services customers all over the world using its global network of manufacturing entities within the Alpek Polyester umbrella. We are committed to improving people's lives through our products, innovations, and a commitment to sustainability and protecting the environment. Alpek Polyester USA, LLC is headquartered in Charlotte, NC with manufacturing facilities in the Carolinas, Mississippi, Indiana, and Pennsylvania. Alpek Polyester USA, LLC is a division of Alpek, the petrochemicals and synthetic fibers business group of Alfa, S.A.B. de C.V., one of Mexico's largest corporations. Alpek Polyester USA, LLC is subject to US Department of Commerce export regulations and thus must hire individuals who meet national security requirements. Interested applicants (or temporary employees) must meet eligibility requirements. Alpek Polyester USA, LLC is an Equal Opportunity Employer. Apply Now Job Number: 160105 Back to All Jobs

Job DescriptionThe ideal candidate will possess a minimum of 5 years of experience in quality control within the chemical or pharmaceutical industries, demonstrating a robust understanding of analytical techniques and regulatory requirements. DUTIES / RESPONSIBILITESØ Conduct routine and non-routine analysis of raw materials, in-process samples, and finished products to ensure compliance with quality standards.Ø Maintain and calibrate laboratory instruments and equipment.Ø Prepare and review technical documents, including standard operating procedures (SOPs) and test methods.Ø Investigate and resolve quality issues, implementing corrective and preventive actions as necessary.Ø Collaborate with cross-functional teams to support product development and process improvement initiatives.Ø Ensure compliance with all relevant regulatory requirements and safety standards. QUALIFICATIONS / REQUIREMENTSv Bachelor's or Master's degree in Chemistry, Biochemistry, or a related field.v A minimum of 5 years of experience in a quality control role within the pharmaceutical industry or similar environment.v Proficiency in analytical techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy.v Strong knowledge of GMP, GLP, and other regulatory guidelines.v Excellent problem-solving skills and attention to detail.v Effective communication and teamwork abilities. E04JI800n8pv406vc4r

QC Compound Lab Associate IJob Description The QC Compound Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. This position generally works alongside chemists and other technicians, organizing the lab workspace, maintaining cleanliness of equipment, creating chemical solutions, and performing chemical experiments. Works with a team that is dedicated to the formulation, processing and evaluation of additives for use in rubber compounds for tire and has full access to state of the art, industry standard capabilities, located in a highly desirable working environment. Will also be responsible for supporting fundamental programs aimed at providing a sustainable competitive advantage in tire performance and/or cost Essential Duties & Functions Apply training to regularly isolate and prepare samples for chemical analysis Apply knowledge of various chemical analysis techniques to effectively use and calibrate instruments Manage time and resources to effectively meet expected completion dates for requests Document observations and conclusions in clear and concise notes and formal reports Participate in project updates each week Lab scale weighing, mixing and compounding of polymers with various additives for rubber formulations Curing and physical testing of compounds Documentation and reporting of experimental data Assistance with the development of new testing procedures and predictive capabilities for the assessment of tire tread performance properties, whose needs are constantly evolving Training of team members in newly developed test procedures Promote a safe work environment through work practices Under minimal supervision, employee will perform, coordinate, analyze and monitor quality control and product assurance tests and test results to ensure products meet or exceed quality and reliability, specifications and standards Employee will also generate certificate of analysis and approves all raw materials Enforce and follow company policies as required Resolves less complex problems immediately, while more complex problems are typically assigned to next level Perform other duties of equal or less complexity as assigned or directed by management Engage and retain high-performance standards and elevate level of responsibility and performance Skills/Qualifications High-level laboratory skills preferred Safe, careful work habits with attention to detail Must be able to prioritize and multi task Must be able to use Word, Excel, and Outlook Good communication, analytical and troubleshooting skills Good verbal and writing skills Strong interpersonal skills and the ability to work within a team environment recommended Education and/or Experience High School diploma or GED. Prefer Associates degree in Chemistry or laboratory science; or an equivalent combination of education and experience Minimum 1 year work experience in chemical analysis or relevant field preferred 2 years of manufacturing experience preferred Knowledge of laboratory analytical testing procedures and specific lab equipment required to perform quality testing Knowledge of common lab procedures Ability to learn quickly and to apply knowledge on practical problem solving Experience with precise measurements preferred Experience with various types of chromatography, spectroscopy and wet chemical analysis techniques preferred Experience in and/or willing to learn and apply a variety of sample isolation and preparation procedures

QC Compound Lab Associate I Job Description The QC Compound Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. This position generally works alongside chemists and other technicians, organizing the lab workspace, maintaining cleanliness of equipment, creating chemical solutions, and performing chemical experiments. Works with a team that is dedicated to the formulation, processing and evaluation of additives for use in rubber compounds for tire and has full access to state of the art, industry standard capabilities, located in a highly desirable working environment. Will also be responsible for supporting fundamental programs aimed at providing a sustainable competitive advantage in tire performance and/or cost Essential Duties & Functions Apply training to regularly isolate and prepare samples for chemical analysis Apply knowledge of various chemical analysis techniques to effectively use and calibrate instruments Manage time and resources to effectively meet expected completion dates for requests Document observations and conclusions in clear and concise notes and formal reports Participate in project updates each week Lab scale weighing, mixing and compounding of polymers with various additives for rubber formulations Curing and physical testing of compounds Documentation and reporting of experimental data Assistance with the development of new testing procedures and predictive capabilities for the assessment of tire tread performance properties, whose needs are constantly evolving Training of team members in newly developed test procedures Promote a safe work environment through work practices Under minimal supervision, employee will perform, coordinate, analyze and monitor quality control and product assurance tests and test results to ensure products meet or exceed quality and reliability, specifications and standards Employee will also generate certificate of analysis and approves all raw materials Enforce and follow company policies as required Resolves less complex problems immediately, while more complex problems are typically assigned to next level Perform other duties of equal or less complexity as assigned or directed by management Engage and retain high-performance standards and elevate level of responsibility and performance Skills/Qualifications High-level laboratory skills preferred Safe, careful work habits with attention to detail Must be able to prioritize and multi task Must be able to use Word, Excel, and Outlook Good communication, analytical and troubleshooting skills Good verbal and writing skills Strong interpersonal skills and the ability to work within a team environment recommended Education and/or Experience High School diploma or GED. Prefer Associates degree in Chemistry or laboratory science; or an equivalent combination of education and experience Minimum 1 year work experience in chemical analysis or relevant field preferred 2 years of manufacturing experience preferred Knowledge of laboratory analytical testing procedures and specific lab equipment required to perform quality testing Knowledge of common lab procedures Ability to learn quickly and to apply knowledge on practical problem solving Experience with precise measurements preferred Experience with various types of chromatography, spectroscopy and wet chemical analysis techniques preferred Experience in and/or willing to learn and apply a variety of sample isolation and preparation procedures

Job Responsibilities Careers at SCDES: Where Passion Meets Preservation Do you love South Carolina and protecting the environment? Come join our team at SCDES, put your passion to work with us! We are dedicated to protecting the state of South Carolina and we would love to have you as a member of our team! Science| Service| Sustainability The purpose of this position is to serve as a chemist in the Inorganic Chemistry Automated Analysis Section preparing and analyzing samples for Nitrate/Nitrite, Nitrite, Total Organic Carbon (TOC), Total Phosphorus, Ortho phosphorus, Carbon Oxygen Demand (COD), Fluoride, and Chloride. Operates and maintains analytical instrumentation to include but not limited to, flow injection analyzers, TOC analyzer, Ion Chromatography, and UV-vis Spectroscopy. Responsibilities: * Checks pH of samples upon receipt and discard expired samples according to the sections waste management plan. * Coordinates with others in the lab to order supplies and submit work orders. * Performs maintenance on all instruments that the analyst is responsible for and assists other analysts as needed with shared duties including but not limited to: morning and afternoon temperature checks, daily balance checks, routine maintenance on Deionized water systems and dishwasher systems, and the preparation of wash and preservative acids. Performs the preparative and interpretative phases of the analysis process to include, but not limited to, preparing calibration standards, spike solutions, reagents, and cleaning the laboratory. Interprets, calculates, and records data. Ensures supportive QC functions are performed. * Review DES SOPs and its reference methods annually, updating SOP as needed. Prepares and participates in emergency response as required. Ensures safe work practices by attending all safety meetings, annual review of the safety manual, and adherence to the safety policies as prescribed by the Hayne Building Safety Manual and the Agency. * Perform other duties as required, which includes attending periodic staff meetings and training. Minimum and Additional Requirements * A bachelor's degree in chemistry * or a bachelor's degree in the natural or physical sciences* with 16 semester hours in chemistry and one year of laboratory experience. * These fields include but are not limited to branches relating to Physics, Chemistry, Biology, etc. ADDITIONAL REQUIREMENTS: * Experience in a laboratory setting related to the area of employment, including experience in operating, maintaining, and interpreting results from advanced analytical instrumentation such as gas or liquid chromatographs, and associated data systems. * Experience with general instrumentation software and Microsoft Office. * Ability to: * Perform scientific mathematical calculations, highly complex tasks, and maintain accurate records. * Communicate effectively with peers, other scientists, and service engineers. * Prioritize tasks and manage time effectively. * Move and change 150-pound gas cylinders using a hand truck. * Adhere to all safety requirements including the wearing of required safety equipment such as eye protection, laboratory coats, and nitrile gloves to assure the safe handling of a myriad of commonly used laboratory chemicals daily. * Stand for long periods of time and lift at least 50 lbs. to countertop level. * The workplace exposure to chemicals of record will be kept below the published OSHA thresholds through the use of administrative and engineering controls, specialized PPE and through appropriate adjustments in job assignments. * This position requires the strict adherence to approved methods and standard operating procedures for the proper collection of quality and technically defensible data. * This is a laboratory position and as such involves safely working with various types of glassware, the physical shaking of samples, the performance of repetitive tasks, and meticulous attention to detail. * Must be able to occasionally work outdoors in various weather conditions. Must be able to drive an agency vehicle and occasionally travel overnight for training and emergency response purposes. * Prior to possible selection for this position, candidates will have to attend an in-person interview. Please note that the State of South Carolina will not be responsible for any expenses incurred to attend this interview. * An unofficial copy of all transcripts from institutions of higher learning must be attached to the application. * An official transcript will be required prior to hiring. Preferred Qualifications Preference will be given to candidates with employment experience in a inorganic chemistry laboratory setting. Please complete the State application to include all current and previous work history and education. A resume will not be accepted or reviewed to determine if an applicant has met the qualifications for the position. * Applicants meeting preferred qualifications will be given priority consideration over persons who do not meet preferred qualifications. Applications must be accurate and complete. Additional Comments SCDES is committed to providing equal employment opportunities to all applicants and does not discriminate on the basis of race, color, religion, sex (including pregnancy, childbirth, or related medical conditions, including, but not limited, to lactation), national origin, age (40 or older), disability or genetic information. The Department will not sponsor H1B visas for this position. The South Carolina Department of Environmental Services offers an exceptional benefits package for full time (FTE) employees:? * Health, dental, vision, long-term disability, and life insurance for employees, spouse, and children. Click here for additional information. * 15 days annual (vacation) leave per year * 15 days sick leave per year * 13 paid holidays * Paid parental leave * S.C. Deferred Compensation Program available (S.C. Deferred Compensation) * Retirement benefit choices* * State Retirement Plan (SCRS) * State Optional Retirement Program(State ORP) * Enrollment in one of the listed plans is required for all FTE employees; please refer to the contribution section of hyperlinked retirement sites for the current contribution rate of gross pay.

We are looking to fill a **Scientist II or III - Metrology Specialist** position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer sponsorship.** **Metrology specialist is responsible for the oversight of regulated and non-regulated laboratory equipment** . This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement **Qualifications -** B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline + **Scientist II** - B.S. with 1-2 years of relevant experience or M.S. with 0-1 years of relevant experience + **Scientist III** - B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience **Responsibilities** + Prepare, review, and approve instrument/equipment documentation such as master equipment lists, qualification documentation, and calibration documentation + Coordinate service activities across a variety of vendors and service engineers while building and maintaining strong working relationships + Gain a working knowledge of laboratory equipment to facilitate with troubleshooting and/or perform maintenance or calibration activities + Participate in computer system validation activities associated with new or upgraded equipment or software packages + Support the purchase, installation, and equipment qualification of new laboratory equipment + Collaborate with metrology staff across multiple testing labs and sites for process improvement, cross-training and cross-site support + Originate and progress Notice of Event (NOE) and Change Management (CM) records + Perform and document investigations and assist in developing/implementing CAPA plans + Represent the laboratory on all aspects of laboratory equipment during audits + Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures **Required Skills and Experience** + Experience working within a regulated (GMP) laboratory + **Experience maintaining or operating laboratory equipment including HPLCs, GCs, UVs, dissolution systems, or other specialized computerized systems** + Familiarity with standalone computer system validation requirements + Highly organized, and capable of multi-tasking to manage a variety of laboratory equipment or system related schedules, documents, and maintenance tasks + Capable of working independently under moderate supervision + Strong verbal and written communication skills + Strong interpersonal skills. Comfortable interacting with a variety of on-site and off-site collaborators **Desired Skills and Experience** + Experience with maintenance of analytical instrumentation such as HPLC, UPLC, GC, UV, IR, Karl Fischer, and dissolution with ability to troubleshoot them. + Experience with computerized standalone systems GMP validation requirements + Familiarity with authoring relevant instrument standard operating procedures (SOPs) **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

The Quality Control Chemist reports directly to Quality Laboratory Management and plays a key role in supporting laboratory operations through accurate and timely testing. This position requires strong time management skills to meet testing deadlines and a willingness to learn laboratory processes, instrumentation theory, and troubleshooting techniques. Schedule: This position will be on a 2nd shift: Monday - Thursday 3:30pm - 11:30pm and Friday 1:30pm - 9:30pm. Key Responsibilities Testing: * Perform Release, Stability, and Special Request testing on finished products and raw materials in compliance with Standard Operating Procedures (SOPs), in-house methods, and compendial standards. * Execute in-house methods independently and accurately with minimal supervision. Team Collaboration: * Adapt to changes in testing schedules and support continuous improvement initiatives within the lab. * Assist in training new laboratory personnel and document training per established SOPs and Nutramax guidelines. Safety: * Maintain a safety-first approach and remain vigilant of surroundings while performing laboratory tasks. * Ensure all equipment used in testing is properly calibrated and maintained. General Duties: * Train on and operate various laboratory instruments, including but not limited to: Laboratory Balances, HPLC, GC, Automated Titrators, FTIR, UV/Vis Spectrophotometer, Polarimeter, Dissolution and Disintegration instruments. * Complete assigned projects within established timelines while balancing testing responsibilities. * Stay informed on updates from USP, FDA, and other regulatory bodies to ensure compliance with analytical standards and documentation practices. * Assist in investigating Out-of-Specification (OOS) results as needed. * Perform additional duties as required to support company objectives. * Communicate effectively across departments and work collaboratively within a team environment. * Maintain regular and reliable attendance. Skills Chemistry, Quality control, Laboratory, Gmp, Wet chemistry Top Skills Details Chemistry Additional Skills & Qualifications * Experience: 2-5 years in a laboratory setting, a cGMP environment. Familiarity with GC and/or LC instrumentation is preferred. * Skills: Strong interpersonal skills, self-motivation, and ability to work with individuals at all organizational levels. * Education: Bachelor's degree in Chemistry; concentrations in Biochemistry, Inorganic, Physical, or Polymer Chemistry are preferred. Experience Level Intermediate Level Job Type & Location This is a Permanent position based out of Lancaster, SC. Pay and Benefits The pay range for this position is $70000.00 - $80000.00/yr. Comprehensive Health Coverage: Competitive medical, dental, and vision plans for employees and their families. Educational Assistance: Opportunities for training and professional development to support career growth. Supportive Work Culture: A family-oriented environment that values faith, servant leadership, and collaboration. Community Engagement: Volunteer opportunities and mission trips organized by the company to give back locally and internationally. Employee Recognition & Perks: Birthday cards with gift cards, family days at the zoo, Thanksgiving dinners, and other thoughtful gestures. Work-Life Balance: A culture that prioritizes employee well-being and fosters a positive, supportive atmosphere. Workplace Type This is a fully onsite position in Lancaster,SC. Application Deadline This position is anticipated to close on Dec 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. Eurofins 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 Organizations. The Group also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Job Summary: Eurofins BPT-Columbia is looking for an Associate Scientist to join our Biochemistry Method Development and Validation team located in Columbia, Missouri. The Associate Scientist position is an entry-level professional position involved in day-to-day activities in a laboratory setting under prescribed procedures (protocols, standard operating procedures, methods, etc.) * Follow cGMP processes and procedures and adhere to all regulatory requirements * Run a variety of equipment including HPLC, CE, pH meter, analytical balance, and pipetting, among other techniques * Perform various tasks and analyses of bio/pharmaceutical ingredients and products * Review or prepare standards and samples for analysis * Ensure that clients receive quality data by reviewing laboratory data for accuracy * Other job duties as assigned Qualifications Minimum Qualifications: * Bachelor's degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas. * Authorization to work in the U.S. without restriction or sponsorship The Ideal Candidate Would Possess: * Hands-on experience with laboratory analytical instrumentation (HPLC, CE, pH meter, analytical balance, pipettes). * Interest in learning complex analytical procedures supporting bio-pharma product testing. * Familiarity and/or experience in a laboratory setting. * Good organizational skills; ability to follow direction and good communication skills are required. * Working knowledge of Microsoft Word and Excel. Additional Information Position is full-time, Monday-Friday, 8:00 a.m.-4:30 p.m. with additional hours, as needed. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply. We offer excellent full-time benefits including: * Comprehensive medical coverage, * Life and disability insurance, * 401(k) with company match, * Paid holidays and vacation, * Dental and vision options. Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

**Compensation: $115,000 - $125,000 per year + up to 12% discretionary bonus** **About the Role** The Analytical Scientist III is responsible for independently leading the development, validation, and optimization of analytical methods for complex formulations in a GMP-regulated environment. This role requires a deep understanding of laboratory instrumentation, strong troubleshooting ability, and the capacity to guide peers through technical projects. Candidates must be authorized to work in the United States without the need for employer sponsorship. **Key Responsibilities** + Design, develop, and validate robust analytical methods for raw materials and finished products across a range of sample types (including complex nutraceutical matrices). + Support Quality Release, Stability, and Special Request testing using SOPs, in-house methods, compendial standards, and methods in development. + Evaluate testing methodologies and results, including those from external contract labs. + Troubleshoot and maintain advanced analytical instrumentation (HPLC, GC, ICP-MS/OES, LC-MS/MS, etc.). + Serve as a technical mentor and train junior chemists in method development, validation, and troubleshooting. + Write and review technical documents including validation protocols, reports, and method transfer documentation. + Collaborate with cross-functional teams, including product innovation and commercial support groups, to meet project timelines and resolve technical issues. + Participate in laboratory safety programs and maintain a strong safety culture. + Maintain expertise in emerging technologies, industry trends, and regulatory updates. **Education & Experience** **Required:** + Bachelor's degree in Chemistry with **7+ years** of relevant experience in method development and validation in a GMP environment. **OR** + Master's or Ph.D. in Chemistry with **5+ years** of relevant experience in a GMP environment. **Technical Qualifications** + **Hands-on expertise** with laboratory instrumentation including: + HPLC, GC, LC-MS/MS, GC-MS, FTIR, UV-Vis, ICP-MS/OES, HPTLC + Proficient in **Empower chromatography software** . + Strong troubleshooting skills with chromatographic systems (HPLC and GC). + Deep understanding of **botanical compound characterization** , spectroscopic techniques, and mass spectrometry. + Familiarity with **statistical analysis** , including design of experiments and data trend evaluation. + Strong knowledge of FDA and ICH guidelines; familiarity with maintaining laboratory accreditations (e.g., ISO 17025, NSF).As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Job DescriptionDescription: Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check and drug screen (subject to applicable law). Summary of the Position: The Analytical Scientist III will be expected to develop, validate, optimize and lead practical analytical methods with no supervision. Responsible to lead peers for timely completion, review of method development / analytical technical reports and weekly updates. Must be able to complete assigned tasks and major projects consistently with urgency and initiative. Roles and Responsibilities: Testing: Willingness to assists with Quality Release testing as needed, Special Request testing of finished products and raw materials and Stability samples either following Standard Operating Procedures (SOPs) and in-house test methods, compendial methods or methods still in the development phase. · Capable of assessing testing methodologies and their application to different sample matrix including evaluation of testing results from contract laboratories to ensure agreed upon methods and testing parameters were properly followed. Laboratory Instrumentation/Software: Ability to troubleshoot all Analytical instruments such as HPLC, GC, ICP-MS/OES and LC-MS/MS. Good knowledge of experimental design, chemical theory and analytical instrumentation theory for HPLC, GC, ICP-MS/OES and LC-MS/MS. · Proficient in Empower, Tiamo, MassHunter and MassLynx software and other laboratory software used in the Quality Laboratory environment for chromatographic and spectroscopic methods. Mentoring and Teamwork: Takes initiative to consistently act as a mentor to others and helps others without having to be asked. Is flexible to changes in priorities with projects and assignments and can adapt to laboratory improvements implemented from management and/or peers. · Has the aptitude to take the lead and provide technical support with the optimization of analytical methods used for marketed products and products in the development phase. · Can mentor and train junior chemists in the proper execution of laboratory techniques including interpretation of development and validation studies. Assists with training of new laboratory personnel in accordance with established laboratory SOPs and the Nutramax training program. Possesses techniques and tools to successfully train others with empirical data to support training. Safety Requirements: Participates without hesitation in all safety initiatives, consistently exhibits an excellent safety record and ensures proper safety practices are followed in the laboratory. · Responsible for producing and handling hazardous waste from point of generation to satellite storage. Hazardous waste produced is managed in accordance with RCRA and SCDHEC regulations and includes: proper containers, accumulation, labeling, marking and storage. Must have a Safety-First mindset and be aware of surroundings while working in the laboratory. Maintains a safe work environment and ensures all instruments used in testing procedures are calibrated and properly maintained. General Responsibilities: · The Analytical Scientist III is capable of planning, directing, layout design and coordination of analytical activities in order to ensure the success of projects from initiation through completion and full implementation. · Acts as a liaison to resolve product quality, technical or operational issues and support of commercial products. · Capable of working with outside departments such as Operations, Innovations, Marketing, Purchasing and Engineering to investigate external and internal quality and compliance related issues. · Familiarity and supportive of all Analytical projects and Special Request testing. · Works closely with the Innovations team to be aware of timely testing of samples to facilitate decision making. · Effective and practical development and validation of scientifically sound analytical methods to ensure analysis and prompt release of raw materials, finished products and stability studies. · Design and execute method transfer protocols of analytical methods oriented to the timely manner release of Quality Laboratory samples. Ensure competency of ISO 17025 test methods are current as needed. Maintain current knowledge of latest technological and scientific trends and serves as an expert resource for the Quality department. Perform other assigned duties as may be required in meeting company objectives. Communicate effectively with other departments within the organization and function within a team environment. Regular attendance is required. Minimum Requirements: · Understands urgency and initiative to drive projects/assignments to completion. · Capable of developing analytical methods for chromatographic, spectroscopic, titrimetric and wet chemistry analyses. · Is proficient with laboratory instrument troubleshooting. · Intermediate to advanced understanding in most laboratory instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS/MS, GC-MS, ICP-MS/OES and HPTLC. · Has knowledge in the characterization and elucidation of botanical compound structures by study of the compound structure, spectroscopic methods and mass spectrometry. · Knowledge required in the selection of analytical columns for chromatographic analyses, proper techniques or technologies and the selection for proper reagents to design effective analytical methods in timely manner. · Knowledge in effective sample preparation techniques to support high number of samples for testing such as liquid-liquid extraction, derivatization, chemical manipulation and mechanical manipulation. · Knowledge of statistical techniques, such as data trend analysis and design of experiments is highly desirable. Proficient in reviewing and interpretation of laboratory data. · Detailed knowledge in principles of routine laboratory operations. · Thorough working knowledge of industry regulations, FDA and ICH guidelines; experience implementing and maintaining adherence to pharmaceutical and/or nutritional supplement GLP/GMP is strongly desired. · Proven ability to communicate effectively and cooperatively within all levels of an organization. · Strong communicator both verbal and written. · Demonstrated aptitude to function in a dynamic fast-paced environment. Education and Experience · A bachelor's degree in Chemistry with 7 years of experience in method development and validation of analytical methods for nutraceuticals and/or pharmaceutical samples in a GMP environment. If degree has concentration; Biochemistry, Inorganic, Physical or Polymer Chemistry preferred; or, a Master's/Ph.D. degree in Chemistry with a minimum of 5 years of technical experience in a GMP environment. · Must have prior experience of working on the bench as this position is primarily on the bench working in the laboratory. Supervisory Responsibilities: None Requirements:

Job DescriptionWe are seeking a motivated individual to join our Quality Assurance team based out of our Gaston, SC facility. The ideal candidate for the Chemist position will be results driven, have self-directing initiative, hands on analytical experience, and excellent problem-solving skills that are complemented by exceptional interpersonal and communication skills ResponsibilitiesThe Chemist will be reportable to the Quality Assurance Manager and have responsibilities for the following tasks: Promote and model behavior-based safety and compliance with all laboratory/hazardous chemical safety procedures Interface with, train, and lead laboratory analysts Maintain instrumentation and methods including both qualitative and quantitative techniques as required to support the CA - Columbia site in analytical quality testing Lead projects for the purchase and installation of new laboratory instruments Develop and maintain analytical methods Troubleshoot laboratory technical issues Serve as a chemical knowledge resource Ensure proper handling of laboratory waste, including hazardous waste collection and proper movement Support and implement analytical projects aligned with business objectives Maintain laboratory statistical process control Prepare solutions and samples and perform analytical analyses Collaborate with Quality Assurance, Manufacturing, Maintenance, R&D, and Technical Marketing teams as required. Required SkillsRequired: BS Degree in Chemistry or similar Preferred: Specialized education or experience in Analytical or Polymer Chemistry 3+ years' experience with analytical instrumentation Manufacturing quality control lab experience Mechanical competence and hands-on instrument troubleshooting Experience and technical knowledge regarding analytical instruments and techniques including but not limited to: Dilute Solution Viscometry (IV) X-Ray Fluorescence Spectrometry (XRF) Differential Scanning Calorimetry (DSC) Infrared Spectroscopy (IR) Karl Fischer Titrations Gas Chromatography (GC) Liquid Chromatography (LC) Ultraviolet-Visible Spectrophotometer (UV Vis) Colorimetry Environmental / Water Lab Rheology Applied Statistical Techniques Computer skills including MS Excel and basic programming Knowledge of Safety / ISO / Quality / Regulatory Standards Knowledge of Food Safety Standards Knowledge of Good Lab Practices, Good Manufacturing Practices, and Good Documentation practices Root cause failure analysis Excellent written and verbal communication skills Data-based decision-making skills Ability to work with small groups to lead improvement projects Supervisory experience Alpek Polyester USA, LLC is a global leader in the production of PTA (Terephthalic Acid), PET (Polyethylene Terephthalate) Resins, PET Recycling (rPET), and Specialty Polymers. This integrated business services customers all over the world using its global network of manufacturing entities within the Alpek Polyester umbrella. We are committed to improving people's lives through our products, innovations, and a commitment to sustainability and protecting the environment. Alpek Polyester USA, LLC is headquartered in Charlotte, NC with manufacturing facilities in the Carolinas, Mississippi, Indiana, and Pennsylvania. Alpek Polyester USA, LLC is a division of Alpek, the petrochemicals and synthetic fibers business group of Alfa, S.A.B. de C.V., one of Mexico's largest corporations. Alpek Polyester USA, LLC is subject to US Department of Commerce export regulations and thus must hire individuals who meet national security requirements. Interested applicants (or temporary employees) must meet eligibility requirements. Alpek Polyester USA, LLC is an Equal Opportunity Employer.

QC Compound Lab Associate I Job Description The QC Compound Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. This position generally works alongside chemists and other technicians, organizing the lab workspace, maintaining cleanliness of equipment, creating chemical solutions, and performing chemical experiments. Works with a team that is dedicated to the formulation, processing and evaluation of additives for use in rubber compounds for tire and has full access to state of the art, industry standard capabilities, located in a highly desirable working environment. Will also be responsible for supporting fundamental programs aimed at providing a sustainable competitive advantage in tire performance and/or cost Essential Duties & Functions Apply training to regularly isolate and prepare samples for chemical analysis Apply knowledge of various chemical analysis techniques to effectively use and calibrate instruments Manage time and resources to effectively meet expected completion dates for requests Document observations and conclusions in clear and concise notes and formal reports Participate in project updates each week Lab scale weighing, mixing and compounding of polymers with various additives for rubber formulations Curing and physical testing of compounds Documentation and reporting of experimental data Assistance with the development of new testing procedures and predictive capabilities for the assessment of tire tread performance properties, whose needs are constantly evolving Training of team members in newly developed test procedures Promote a safe work environment through work practices Under minimal supervision, employee will perform, coordinate, analyze and monitor quality control and product assurance tests and test results to ensure products meet or exceed quality and reliability, specifications and standards Employee will also generate certificate of analysis and approves all raw materials Enforce and follow company policies as required Resolves less complex problems immediately, while more complex problems are typically assigned to next level Perform other duties of equal or less complexity as assigned or directed by management Engage and retain high-performance standards and elevate level of responsibility and performance Skills/Qualifications High-level laboratory skills preferred Safe, careful work habits with attention to detail Must be able to prioritize and multi task Must be able to use Word, Excel, and Outlook Good communication, analytical and troubleshooting skills Good verbal and writing skills Strong interpersonal skills and the ability to work within a team environment recommended Education and/or Experience High School diploma or GED. Prefer Associates degree in Chemistry or laboratory science; or an equivalent combination of education and experience Minimum 1 year work experience in chemical analysis or relevant field preferred 2 years of manufacturing experience preferred Knowledge of laboratory analytical testing procedures and specific lab equipment required to perform quality testing Knowledge of common lab procedures Ability to learn quickly and to apply knowledge on practical problem solving Experience with precise measurements preferred Experience with various types of chromatography, spectroscopy and wet chemical analysis techniques preferred Experience in and/or willing to learn and apply a variety of sample isolation and preparation procedures