Research and development technician jobs in Columbia, SC

Job Details White Oak of Newberry - Newberry, SC Full Time $23.00 - $33.00 Hourly Day Food Service- DietaryDescription White Oak of Newberry is currently seeking a full time RD or DTR for their Newberry location. Full time or part time schedules are negotiable. Competitive salary and excellent benefit options await you! Medical, Dental and Vision Packages Employer paid life insurance plan Long and short term disability options Earn Paid time off from day 1 401K with 50% employer match EDUCATION REQUIREMENTS: Must possess an AS, BS or MS degree in nutrition or dietetics from an accredited college or university; be a member of the Academy of Nutrition and Dietetics; be a Registered Dietitian (RD) or (DTR) in good standing or examination-eligible; be licensed by the state of practice; possess basic keyboarding and computer skills; have legible handwriting; be familiar with regulatory requirements; possess good interpersonal and supervisory skills; be of good physical and mental health Apply today to join our team of dedicated caregivers!!! #SJ

Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn. **Job Overview** We are currently seeking a dynamic, highly motivated, and experienced individual for the position of **Manager, Clinical Systems R&D IT Business Applications** who will serve as the primary liaison between R&D Clinical Operations team and IT, responsible for the delivery and support of technology solutions that align with business needs and operational demands. **_This role requires proficiency in implementing, integration, and managing Medidata & Veeva clinical systems (e.g. CTMS, EDC etc.) in a regulated environment_** **Job Duties and Responsibilities** + Partner with Clinical business stakeholders to co-create technology plans which support their business objectives and operational demands + Continuously assess current systems environment and identify changes (process and/or system) that enhance effectiveness + Assist in the evaluation of new technology systems and/or service providers + Oversee end-to-end management of IT projects-including planning, design, and implementation-ensuring projects are delivered on time, within scope, and with measurable business impact + Work with a team of managed service providers supporting the lines of business technology needs including project delivery, solution design, enhancement requests and support services + Accountable for managing clinical application systems through their full lifecycle, from implementation to ongoing optimization + Lead and initiate troubleshooting quality and/or functionality issues associated with technology systems in scope + Develop and maintain comprehensive project documentation, ensuring centralized storage and accessibility for knowledge management + Manage and prioritize system enhancements and fixes in collaboration with business stakeholders + Provide regular project status reports, manage issues proactively, and adjust schedules as needed while maintaining alignment with the overall program plan + Responsible for timely execution of all GxP system commitments and compliance activities (Backup recovery, Disaster Recovery testing etc.) + Collaborate with cross-functional IT teams to ensure seamless delivery of services, efficient communication, and shared accountability for outcomes + Establish clear performance metrics and service level agreements (SLAs) to monitor IT service delivery, project outcomes, and stakeholder satisfaction + Stay informed of emerging industry trends, best practices, and regulatory changes to proactively recommend technologies and process adaptations that empower the company during phases of rapid expansion + Serve as the IT subject matter expert for application upgrades, integrations, and system enhancements across supported business areas **Key Core Competencies** + Strong understanding of Clinical business processes, requirements and technology systems supporting Clinical Trials (e.g. EDC, CTMS, ETMF, Payments etc.) + 7+ years of progressively increasing experience managing clinical applications in a Pharma/Biotech company + Strong understanding of building and operating a technology support function + Proficient in implementing, integration and managing Medidata & Veeva clinical systems (e.g. CTMS, EDC etc.) in a regulated environment **Education and Experience** + BS/BA degree in a related discipline is required. Training or equivalent experience in IT or business management is beneficial but not required + 7+ years of experience in life sciences with a focus on IT system delivery + 5+ years of experience in implementing, integration and managing Medidata & Veeva clinical systems (e.g. CTMS, EDC etc.) in a regulated environment + Experience in Program & Project Management, including the Software Development Lifecycle and Computer Systems Validation process + Excellent communication skills The base salary range for this role is $127,440 to $159,300. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed. **Confidential Data** : All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential. **Compliance** : Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the "best" industry practices and the highest ethical standards. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. **Mental/Physical Requirements** : Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time. **Sumitomo Pharma America (SMPA)** **is an Equal Employment Opportunity (EEO) employer** Qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn. Sumitomo Pharma America (SMPA) endeavors to make its application process accessible to all. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact SMPA at ********************************************** This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. At Sumitomo Pharma America, our work is guided by the Sumitomo Pharma mission, vision and values, which tie closely to our company's cultural pillars. **Our** **Mission** _To broadly contribute to society through value creation based on innovative research and development activities for the betterment of healthcare and fuller lives of people_ _worldwide_ **Our** **Vision** _For Longer and Healthier Lives, we unlock the future with cutting edge technology and_ _ideas_

**About ETS:** ETS is a global education and talent solutions organization enabling lifelong learners worldwide to be future-ready. For more than 75 years, we've been advancing the science of measurement to build benchmarks for fair and valid skill assessment across cultures and borders. Our worldwide impact extends through our renowned assessments including TOEFL , TOEIC , GRE and Praxis tests, serving millions of learners in more than 200 countries and territories. Through strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, while Edusoft, Kira Talent, Pipplet, Vericant, and Wheebox enhance our educational technology and assessment platforms across critical markets worldwide. Through ETS Research Institute and ETS Solutions, we're partnering with educational institutions, governments, and organizations globally to promote skill proficiency, empower upward mobility, and unlock opportunities for everyone, everywhere. With offices and partners across Asia, Europe, the Middle East, Africa, and the Americas, we deliver nearly 50 million tests annually. Join us in our journey of measuring progress to power human progress worldwide. **About the role** ETS is seeking a dynamic and strategic Manager of Research Proposal Development to lead the end-to-end proposal process for federal and non-federal funding opportunities. This role is central to advancing ETS's mission by securing resources that fuel innovation across the ETS Research Institute and enterprise-wide initiatives. You'll manage a high-volume pipeline of proposals, guide researchers through complex funding landscapes, and ensure every submission meets the highest standards of quality, compliance, and impact. **What you'll do** Strategic leadership + Serve as a trusted advisor to researchers, guiding engagement with program officers and navigating regulatory requirements-especially with NSF, IES, and other key agencies and foundations. + Interpret funding structures and review cultures to align proposals with agency priorities and long-term trends. + Foster collaboration across ETS and with external partners to support proposal and budget development. + Contribute to the evolution of Strategic Research Alliances' strategy and stay informed on emerging trends and best practices. Proposal development & pipeline management + Identify and share relevant funding opportunities, encouraging timely and strategic proposal submissions. + Provide insights into funding cycles and program structures to align ETS initiatives with external opportunities. + Maintain proposal calendars and assign writers based on expertise and capacity. + Manage a pipeline of 40-60 proposals annually using Salesforce and grants management tools. + Support proposal drafting, including boilerplate content, staffing charts, budget justifications, and organizational materials. + Repurpose technical documentation for future opportunities when appropriate. Quality control & compliance + Review and edit proposals for clarity, consistency, and alignment with funder requirements. + Ensure compliance with federal, state, and institutional guidelines, including FAR and agency-specific standards. + Proactively identify and resolve compliance issues, keeping leadership informed of risks and solutions. Monitoring & reporting + Track proposal outcomes and lead post-submission reviews to drive continuous improvement. + Provide regular status updates and maintain RFP distribution lists. Budget & grant management Draft proposal budgets and narratives aligned with ETS best practices. + Implement process improvements, including external proposal platforms. + Advise leadership on budgetary risks and collaborate with finance teams to monitor project expenses. **What success looks like** + Seamless management of a multimillion-dollar portfolio of research grants. + Formation of high-performing proposal teams. + Proposals meet ETS's editorial and technical standards and are recognized as "best in class." + Grants are implemented effectively and aligned with funder priorities. + ETS intellectual property is protected and aligned with mission-driven goals. + Funders are informed and satisfied with grant progress and outcomes. **Why this role matters** This is a high-impact, high-visibility position. You'll work with confidential materials, lead strategic initiatives, and represent ETS to government agencies and private foundations. Your leadership ensures ETS secures the funding needed to advance research that powers human progress. **Reporting structure** This role reports to the Associate Vice President of Strategic Research Alliances and works closely with the Strategic Research Alliances team, ETS General Counsel, and Finance. \#LI-NK1 + Position requires a Bachelor's degree and 5+ years of directly relevant experience. + Much of the work of the Manager, Research Proposal Development is self-directed. The position reports to the Associate Vice President for Strategic Research Alliances, and by extension to the Senior Vice President, Global Research. + Requires strong writing, interpersonal, and organizational skills, as well as the ability to work effectively as part of a team. + Requires the ability to exercise a significant amount of judgement, technical expertise, professionalism, and experience. + Must be knowledgeable of the policies and procedures of federal funding agencies, private foundations and corporations and other funding bodies. + Must have some knowledge of the electronic proposal submission and project management systems. + Must be able to communicate effectively with ETS researchers and the representatives of federal funding agencies, private foundations and corporations and other funding bodies. + Requires not only operational knowledge but also a scholarly understanding of the evolving funding landscape-including agency missions, program call structures, and peer-review practices-to anticipate shifts in priorities and guide ETS researchers accordingly. + Stakeholders include senior management, departmental professional and support staff and other ETS researchers, external clients, external boards, councils and committees, government organizations and other external agencies. **ETS is mission driven and action oriented** + We are passionate about hiring innovative thinkers who believe in the promise of education and lifelong learning. + We are energized by cultivating growth, innovation, and continuous transformation for the next generation of rising professionals as leaders. Â In support of this ETS offers multiple Business Resource Groups (BRG) for you to learn and advance your career growth! + As a not-for-profit organization we will encourage you to lean in to your passion for volunteering. Â At ETS you may qualify for up to an additional 8 hours of PTO for volunteer work on causes that are important to you! **ETS is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. We believe in creating a work environment where all individuals are treated with respect and dignity.**

Logo Posting Number STA00945PO25 Job Family Operational Analysis Job Function Project Management USC Market Title Project Coordinator Link to USC Market Title ************************************ Job Level P3 - Professional Business Title (Internal Title) Research Development Specialist Campus Columbia Work County Richland College/Division Office of Research Department OOR Research Infrastructure Support State Pay Band 7 Approved Starting Salary $59,581 Advertised Salary Range $59,581 Location of Vacancy Part/Full Time Full Time Hours per Week 37.5 Work Schedule Standard working schedule: 8:30am - 5:00pm Must be willing to work a flexible schedule to meet the needs of the department. Basis 12 months Job Search Category Other Professional About USC About University of South Carolina From the Upstate to the Lowcountry, the University of South Carolina system is transforming the lives of South Carolinians through the impact of our eight institutions and 20 locations throughout the state. More than 50,000 students are enrolled at one of eight institutions, including the research campus in Columbia and comprehensive four-year universities in Aiken, Upstate and Beaufort. In addition, our Palmetto College campuses in Salkehatchie, Union, Lancaster and Sumter enable students to earn associate or bachelor's degrees through a combination of in-person, online or blended learning. All of our system institutions place strong emphasis on service - helping to build healthier, more educated communities in South Carolina and beyond. Veterans' Preference Statement The University of South Carolina is committed to equal opportunity and proudly values the skills and experience military veterans bring to our workforce. Across South Carolina, we are making veterans a priority for employment and recognize their vital contributions to our state and our communities. Benefits for FTE Positions The University of South Carolina (USC), through the State of SC and Public Employee Benefit Authority (PEBA), offers employees a valuable benefits package, including health and life insurance, generous paid leave and retirement programs. To learn more about USC benefits, access the "Working at USC" section on the Applicant Portal at *********************** Research Grant or Time-limited positions may be eligible for all, some, or no benefits, based on the grant or project funding. Position Description Advertised Job Summary The Carolina Grants & Innovation Hub is seeking to hire a Research Development Specialist to join our team. The Research Development Specialist in the Carolina Grants & Innovation Hub (CGI Hub) supports research funding competitiveness through strategic management of the OVPR internal funding programs, coordination of limited submission opportunities, and sponsored funding prospecting. This position plays a key role in supporting the CGI Hub's mission to elevate research excellence by connecting researchers to resources, fostering collaboration, and advancing proposal readiness. The Specialist will work closely with stakeholders across USC colleges and campuses to streamline and manage internal competitions, identify funding opportunities, and manage limited submission processes. Reporting to the Associate Vice President for Research Development, this position will exercise independent judgment and discretion in managing OVPR internal funding programs, coordinating limited submission competitions, and carrying out sponsored funding prospecting for faculty research. Job Related Minimum Required Education and Experience Requires a bachelor's degree in a job related field and 3 or more years of job related experience, which may be substituted by an equivalent combination of job related certification, training, education, and/or experience. Required Certification, Licensure/Other Credentials Preferred Qualifications Knowledge/Skills/Abilities * Knowledge of federal and foundation funding landscapes * Excellent organizational and project management skills * Strong written and oral communication abilities * Ability to manage multiple concurrent deadlines with attention to detail * Proficiency in Microsoft Office Suite, database systems, and web-based submission tools * Ability to work independently and collaboratively with a broad range of stakeholders, including faculty and staff Job Duties Job Duty Manage Internal Funding Programs: Coordinate the lifecycle of OVPR internal funding competitions (e.g., SPARC, RISE, ASPIRE, ASPIRE AI, etc.), including RFP management and postings, application intake, eligibility screening, reviewer assignment, communication, award notifications, faculty reporting, and data tracking. Essential Function Yes Percentage of Time 40 Job Duty Coordinate Limited Submissions: Manage the institutional limited submissions process, including opportunity tracking, dissemination, internal competitions, coordination of the reviewers, faculty notifications, and coordination with the Associate Vice President for Research Development for nomination and selection. Essential Function Yes Percentage of Time 20 Job Duty Facilitate Prospecting for Sponsored Funding Opportunities: Identify and disseminate funding opportunities aligned with faculty researcher interests and university research priorities; curate targeted funding lists using funding databases and search tools; collaborate with CGI Hub affiliates, University Libraries, and Corporate and Foundation Relations to ensure strategic coordination and broad dissemination of opportunities; and assist in maintaining funding opportunity web content. Essential Function Yes Percentage of Time 20 Job Duty Data Reporting and Process Improvement: Maintain accurate data on applications, awards, and reviewer participation; prepare periodic reports and contribute to process improvement for internal competitions and limited submissions management. Essential Function Yes Percentage of Time 15 Job Duty Support additional CGI Hub activities and initiatives as needed. Essential Function No Percentage of Time 5 Position Attributes Employees in Safety-Sensitive or Security-Sensitive positions will be subject to pre-employment and post-employment drug testing in accordance with University policy HR 1.95 Drug and Alcohol Testing. Safety Sensitive or Security Sensitive No Hazardous weather category Non-Essential Posting Detail Information Number of Vacancies 1 Desired Start Date Job Open Date 12/03/2025 Job Close Date 12/16/2025 Open Until Filled No Special Instructions to Applicant Positions are advertised for a minimum of five (5) business days on our job website. After five (5) business days, positions can be closed at the discretion of the department at any time. This employment site is updated on a regular basis. The length of the recruitment and screening process may vary from position to position, depending upon a variety of factors. Should review of your qualifications result in a decision to pursue your candidacy, you will be contacted by phone or email. We are only accepting applications submitted by December 16, 2025. Quicklink for Posting ************************************** EEO Statement The University of South Carolina does not discriminate in educational or employment opportunities or decisions for qualified persons on the basis of age, ancestry, citizenship status, color, disability, ethnicity, familial status, gender (including transgender), gender identity or expression, genetic information, HIV/AIDs status, military status, national origin, pregnancy (false pregnancy, termination of pregnancy, childbirth, recovery therefrom or related medical conditions, breastfeeding), race, religion (including religious dress and grooming practices), sex, sexual orientation, veteran status, or any other bases under federal, state, local law, or regulations. Supplemental Questions Required fields are indicated with an asterisk (*). * * Do you have at least a bachelor's degree in a job related field and 3 or more years of job related experience, which may be substituted by an equivalent combination of job related certification, training, education, and/or experience? * Yes * No * * Please describe your experience identifying, curating, and disseminating funding opportunities that align with faculty research interests and institutional research priorities. What setting have you carried out these functions, and please explain. (Open Ended Question) * * Please describe any experience you have in managing internal funding programs (e.g., seed, bridge, pilot, or other internal research funding mechanisms) within a university setting. (Open Ended Question) Applicant Documents Required Documents * Cover Letter * Resume * List of References and Contact Information Optional Documents

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.

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.

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.

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 Title R&D Tire CAD Engineer Department: Research & Development Reports To: R&D Development Engineer / R&D Manager FLSA Status: Non-Exempt The R&D Tire CAD Engineer is responsible for creating 3D models and 2D drawings from conceptual designs. They are also responsible for revising/updating existing drawings as required. All work is done in CATIA V5. Essential Duties & Responsibilities: • Work with conceptual designers and tire development engineers to complete needed 3D & 2D files. • Make necessary design changes requested by designers and engineers • Work with tire development engineers and research engineers to create needed models for predictive modeling • Program and automate 3D & 2D workflows to improve efficiency and accuracy • Ensure compliance with design standards Required Qualifications: Education & Experience: • High school diploma or vocational school diploma required • Associate degree in a technical field preferred • Prior experience in a similar role is highly desirable Knowledge, Skills & Abilities: • Expert in CATIA V5 3D & 2D a must • Problem-solving and troubleshooting capabilities • MS Excel • Results-driven and self-motivated • Ability to work both independently and as part of a team Preferred Qualifications: • Expert in CATIA V5 3D & 2D modeling a must Physical Requirements: • Ability to travel domestically on a very limited basis Work Environment: • Primarily office-based • Must be able to remain stationary for prolonged periods while working on a computer EEO Statement: Giti Tire Mfg. is 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: This job description is intended to describe the general nature and level of work performed by employees in this role. It is not intended to be an exhaustive list of all duties, responsibilities, and qualifications.

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

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.

Preferred Qualifications Experience working with school districts, education agencies, or education nonprofits. Familiarity with fundamental statistical concepts. Familiarity with data infrastructure tools and practices (e.g., data dictionaries, metadata documentation). Experience in qualitative data analysis, particularly coding open-ended responses. Interest in education policy and research, especially issues related to teacher recruitment, retention, and working conditions. Experience with qualitative coding software (e.g., NVivo, MaxQDA) Work Schedule Monday - Friday 8:30am - 5:00pm

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.

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.

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.

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 serves as Lab Analyst for the Environmental Affairs (EA), Bureau of Regional and Laboratory Services (BRLS)/ Division of Air Quality Analysis/Analytical Laboratory - Columbia. Job Responsibilities * Serves as Lab Analyst for the Environmental Affairs (EA), Bureau of Regional and Laboratory Services (BRLS)/ Division of Air Quality Analysis/Analytical Laboratory - Columbia. * Prepares and analyzes samples for the presence of inorganic compounds using ICP/MS, Ion Chromatography, and other methods as assigned. Serves as backup analyst as needed. * Logs in samples and results for assigned analyses. Calculates, records, and interprets air quality analysis results for Division reports. Prepare collection media for shipment to field staff as requested. * Performs quality assurance activities such data review, data validation, reviewing and writing Standard Operating Procedures (SOPs), and quality control tracking. * Reviews Federal reference and equivalent methods relevant to laboratory procedures. * Researches methodology and revises as necessary to meet the laboratory's analytical needs. * Assists in response to emergencies involving spills, odors complaints, etc. Minimum and Additional Requirements * A bachelor's degree in chemistry and experience in a laboratory setting related to the area of employment, including experience in operating and interpreting test results from complex analytical instrumentation such as gas, ion or liquid chromatographs or atomic absorption spectrophotometers; * OR a bachelor's degree in the natural sciences with academic credits in chemistry and experience in a laboratory setting related to the area of employment, including experience in operating and interpreting test results from complex analytical instrumentation such as gas, ion or liquid chromatographs or atomic absorption spectrophotometers. * A doctorate in chemistry may be substituted for the required work experience. 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 move at least 30 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. Preferred Qualifications * A chemistry degree and two (2) years of employment experience in an environmental laboratory setting. * Knowledge of GC, HPLC, GC/MS, and associated data systems used for the analysis of organic contaminants. * 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 (2) years of laboratory experience. 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.

The Analytical Scientist III plays a key role in developing, validating, and optimizing analytical methods independently. This position leads method development initiatives, ensures timely completion of projects, and provides technical oversight through report reviews and regular updates. The ideal candidate demonstrates urgency, initiative, and consistency in managing tasks and major projects. Support Quality Release testing, special requests, and stability studies for raw materials and finished products using SOPs, in-house methods, compendial standards, or methods under development. Evaluate testing methodologies across various sample matrices and review results from contract labs to confirm compliance with agreed methods and parameters. Instrumentation & Software Troubleshoot analytical instruments including HPLC, GC, ICP-MS/OES, and LC-MS/MS. Apply strong knowledge of experimental design, chemical principles, and instrumentation theory. Proficient in laboratory software such as Empower, Tiamo, MassHunter, and MassLynx for chromatographic and spectroscopic analysis. Mentorship & Collaboration Actively mentor and train junior chemists in laboratory techniques and data interpretation. Provide technical leadership in optimizing analytical methods for both marketed and developmental products. Assist in onboarding and training new personnel following SOPs and established programs. Safety Compliance Maintain a safety-first approach, adhering to all safety protocols and regulatory requirements. Manage hazardous waste in compliance with RCRA and SCDHEC regulations. Ensure proper calibration and maintenance of laboratory instruments. General Duties Plan and coordinate analytical activities to ensure successful project execution. Serve as a liaison for resolving product quality and technical issues. Collaborate with cross-functional teams (Operations, Innovations, Marketing, etc.) to address quality and compliance concerns. Develop and validate robust analytical methods for raw materials, finished products, and stability studies. Execute method transfer protocols and maintain ISO 17025 competency. Stay current with scientific advancements and act as a subject matter expert for the Quality department. Skills fda, Hplc, Analytical chemistry, Chemistry, Analytic, Laboratory, Wet chemistry, Method validation, Pharmaceutical, Uv/vis, Ftir, Chromatography, Icp, Gcms, Gas chromatography Top Skills Details fda,Hplc,Analytical chemistry Additional Skills & Qualifications Ability to develop chromatographic, spectroscopic, titrimetric, and wet chemistry methods. Skilled in troubleshooting laboratory instruments and interpreting complex data. Advanced knowledge of instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS/MS, GC-MS, ICP-MS/OES, and HPTLC. Familiarity with botanical compound characterization and analytical column selection. Strong understanding of sample preparation techniques and statistical analysis (DOE, trend analysis). Thorough knowledge of FDA, ICH guidelines, and GMP/GLP compliance. Education & Experience Bachelor's degree in Chemistry with 7+ years of experience in method development and validation within a GMP environment; or Master's/Ph.D. with 5+ years of relevant experience. Hands-on bench experience is required. Job Type & Location This is a Permanent position based out of Lancaster, SC. Pay and Benefits The pay range for this position is $80000.00 - $110000.00/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 12, 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.