Quality control analyst jobs in South Carolina - 99 jobs

Clendenin Lumber Co., located in Donald's SC is looking to add a Quality Control Inspector to our team. This is a great opportunity for an individual to join our Kiln Dried Lumber operation as a Quality Control Inspector. This position is responsible for inspecting Hardwood Lumber in accordance with NHLA grading standards as well as proprietary customer requirements. Will be responsible for releasing a product that satisfies industry and customer expectations. All training will be completed in house. Quality Control/Lumber Painter Pay & Benefits: First Shift Full Time Hours Overtime Hours and Pay Full Plan of Benefits Quality Control/Lumber Painter Responsibilities: Learn all general and species-specific aspect of inspecting Hardwood Lumber Working along with a team of 3-4 Lumber Inspectors Conduct live production audits and make records of quality findings Stop production activities when product does not meet industry or customer specifications Adhere to all plant safety and environmental guidelines, policies, and procedures. Assist in downstream packaging requirements Assist in production setup procedures Assist with Yard projects as necessary Strong communication skills and familiarity with working in a team-based environment Other duties as assigned Quality Control/Lumber Painter Qualifications: Previous experience in production quality inspection required Must be self motivated and organized Exceptional negotiation and problem solving skills Ability to work with all levels of management Basic computer skills a must Federal and NY State Labor Laws *************************************************************

Job Requirements TBC

GE Vernova is accelerating the path to more reliable, affordable, and sustainable energy, while helping our customers power economies and deliver the electricity that is vital to health, safety, security, and improved quality of life. Are you excited at the opportunity to electrify and decarbonize the world? Job Description What you'll do: * Perform product audits of gas turbine components, parts, assemblies, and fabrications. * Calibrate non-standard product tools, fixtures, and gauges using standard and special gauging techniques. * Apply geometric, trigonometric, and algebraic relationship in the set up and measurements of complex parts, fixtures, and gauging. * Set up and x-ray production parts, pipe, and welder samples. * Establish radiographic techniques and processes, read and interpret x-ray film or real-time images. * Must maintain accurate records including retrievability. * Perform other related duties. * Perform all duties as part of a team. * The employee is expected to be at their designated workstation ready to work at their assigned starting time. What you'll bring: * Ability to work 2nd shift (3PM - 11PM) * Minimum High School diploma / GED equivalent * Must successfully complete the Quality Assurance Operator Test * Must successfully pass required testing for NDT certification * Prior experience in Quality Operations * Must meet medical/physical Quality Assurance Operator requirements, with or without reasonable accommodation Pay Rate: The pay for this position is $34.70 - $35.96. This position is also eligible for shift premium when you work on an off shift i.e. 2nd or 3rd shift. Plus $1.00 USD an hour on top of base pay. This posting is expected to close on February 23, 2025. Benefits Available to You GE Vernova employees rise to the challenge of building a world that works. In order to meet this mission, we provide varied, competitive benefits to help support our workforce: Our Culture | GE Vernova (gecareers.com) * Our compensation & benefits are designed to reward high performers and help you manage your personal and family needs. We offer a robust benefits package depending on your employment status and your national requirements. * A healthy, balanced lifestyle can mean different things to different people. We've created programs that support the way you live and work today. * GE Vernova invests to provide opportunities to grow your career by providing a path for continued on-the-job learning and development. Inclusion At GE Vernova, we believe in the value of your unique identity, background and experiences. We are committed to fostering an inclusive culture, where everyone feels empowered to do their best work because they feel accepted, respected and that they belong. Click here to learn more: ************************************************** About GE Vernova Gas Power GE Vernova's Gas Power business engineers advanced, efficient natural gas-powered technologies and services, along with decarbonization solutions that aim to help electrify a lower carbon future. It is a global leader in gas turbines and power plant technologies and services with the industry's largest installed base For candidates applying to a U.S. based position only: * The Company pays a geographic differential of 110%, 120% or 130% of salary in certain areas. This posting is expected to remain open for at least seven days after it was posted on December 15, 2025. Available benefits include medical, dental, vision, and prescription drug coverage; access to Health Coach from GE Vernova, a 24/7 nurse-based resource; and access to the Employee Assistance Program, providing 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Vernova Retirement Savings Plan, a tax-advantaged 401(k) savings opportunity with company matching contributions and company retirement contributions, as well as access to Fidelity resources and financial planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability benefits, life insurance and 12 paid holidays. New hires also two weeks of annual vacation (which may be pro-rated based on start date). GE Vernova Inc. or its affiliates (collectively or individually, "GE Vernova") sponsor certain employee benefit plans or programs GE Vernova reserves the right to terminate, amend, suspend, replace, or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a GE Vernova welfare benefit plan or program. This document does not create a contract of employment with any individual.

The primary responsibility of this position is to analyze drug substances, drug products, and/or stability samples using approved laboratory monographs/specifications, Standard Operating Procedures, and USP/NF methodologies to ensure drug products manufactured at and distributed by PAI meet all quality and compliance requirements. The essential duties and responsibilities listed below are representative of those required on the job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential duties and responsibilities. ESSENTIAL DUTIES AND RESPONSIBILITIES: 1. HPLC/GC Chemists: Shall have an emphasis in HPLC and/or GC methodology and analyses including all applicable preparations (extractions, dissolution, ISE separation, etc.), and training or experience in chromatographic software and instrument troubleshooting. 2. Wet Chemists: Shall have an emphasis in wet chemistry methodology and analyses such as various titrations, dissolution, USP/NF limit tests, Identifications, TLC, etc. 3. Responsible for performing analysis of raw materials, bulk, finished product, and stability samples in a timely and compliant manner, as instructed by QC Supervisor, per applicable SOP's, PAI monographs/specifications, and USP methodology to ensure finished goods are acceptable for distribution. 4. Responsible for documentation of all analyses per applicable SOP's and performance of routine laboratory functions to support manufacturing/production and assure that production schedule is met. 5. Responsible for timely testing and release of manufactured bulk drug products for packaging. 6. Responsible for maintaining clean and organized laboratories. Wash labware and pipettes by loading/unloading dishwasher/pipette washer. 7. Notify Laboratory Coordinator when reagents, standards, and other materials need to be ordered to ensure all resources available for testing. 8. Assist in training and evaluating laboratory personnel to run laboratory equipment for established methods. 9. Assist in review of laboratory documentation. 10. Accountable for the accuracy and timeliness of work, attention to detail, and adherence to test method monograph/specifications. Must follow all applicable Standard Operating Procedures, including all safety procedures and policies. 11. Perform other duties as assigned. 12. For Chemist II, in addition to the tasks listed above, the analyst is able to independently perform multiple different types of testing without significant guidance from management. Analyst will execute OOS investigation plans and routinely serve as second analyst in laboratory investigations. Perform technology transfers and provide coaching and mentorship to junior chemists. 13. For Chemist III, in addition to the tasks listed above, the analyst will routinely troubleshoot critical analytical and technical issues, serve as investigator for laboratory CAPAs, and revise raw material and finished product monographs to ensure compliance with compendial methods. EDUCATION AND/OR EXPERIENCE: This position requires a Bachelors' degree in chemistry, biochemistry, biology or other science field, and/or equivalent combination of education and experience. Working knowledge of Microsoft Office Suite is required. Experience with OpenLab and LIMS software is preferred. Experience in chromatographic software (e.g. Empower) is preferred. B.S. in a science field along with 0-2 years applicable laboratory experience is required. KNOWLEDGE, SKILS & ABILITIES: This position requires the individual be organized, detail-oriented, and self-motivated and to apply advanced mathematical concepts and operations. The ability to apply principles of logical and scientific thinking to a wide range of intellectual and practical problems. Decision making, communication, planning and critical thinking skills are a must. Analytical ability / problem solving, along with accuracy is required. Applicable experience in an analytical laboratory preferred, experience in GMP is ideal. Standard laboratory equipment, including viscometer, centrifuge, analytical balance, conductivity meter, dissolution, apparatus, Karl Fisher, density meter, pH meter, HPLC, GC/FID, GC/Headspace, IR, UV-Vis, AA, polarimeter, particle sizer and analyzer and refractometry. PHYSICAL REQUIREMENTS/WORKING CONDITIONS: The physical requirements and working conditions listed for this job are representative of those required on the job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential duties and responsibilities. Computer keyboarding, computer monitor and mouse use including reaching forward, grasping, finger and wrist manipulations, and neck bending and turning: near vision is necessary for computer monitor use. Frequently required to stand, sit, walk, talk and hear, occasionally required to reach with hands and arms, climb or balance, stoop, kneel, crouch or crawl. Frequently lift up to 30lbs. and occasionally up to 50 lbs. is required. This position is regularly exposed to toxic chemicals. To perform this job successfully, an individual must be able to perform the essential job functions satisfactorily. PAI is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, PAI will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer. PAI uses E-Verify. PAI Pharma is a nicotine-free campus , meaning the use of nicotine products-including cigarettes, vaping, chewing tobacco, and any other nicotine-containing substances-is strictly prohibited on company property. All employees should be able to complete their full shift without the need to use nicotine . By joining PAI Pharma, you agree to adhere to our nicotine-free workplace policy, which supports a healthier environment for all employees. EEO Employer / Veteran / Disabled

The primary responsibility of this position is to analyze drug substances, drug products, and/or stability samples using approved laboratory monographs/specifications, Standard Operating Procedures, and USP/NF methodologies to ensure drug products manufactured at and distributed by Pharmaceutical Associates, Inc. meet all quality and compliance requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES * Follows all policies, procedures, SOPs, cGMPS, Work Instructions, and supervisor instructions. * HPLC/GC Chemists: Shall have an emphasis in HPLC and/or GC methodology and analyses including all applicable preparations (extractions, dissolution, ISE separation, etc.), and training or experience in chromatographic software and instrument troubleshooting. * Wet Chemists: Shall have an emphasis in wet chemistry methodology and analyses such as various titrations, dissolution, USP/NF limit tests, Identifications, TLC, etc. * Responsible for performing analysis of raw materials, bulk, finished product, and stability samples in a timely and compliant manner, as instructed by QC Supervisor, per applicable SOPs, PAI monographs/specifications, and USP methodology to ensure finished goods are acceptable for distribution. * Responsible for documentation of all analyses per applicable SOPs. * Responsible for performance of routine laboratory functions to support manufacturing/production and assure that production schedule is met. * Responsible for the timely testing and release of manufactured bulk drug products for packaging. * Responsible for maintaining clean and organized laboratories. Wash labware and pipettes by loading/unloading dishwasher/pipette washer. * Notify Laboratory Coordinator when reagents, standards, and other materials need to be ordered to ensure all resources available for testing. * Assist in training and evaluating laboratory personnel to run laboratory equipment for established methods. * Assist in documentation review of laboratory notebooks. * Accountable for the accuracy and timeliness of work, attention to detail, and adherence to test method monograph/specifications. For following applicable Standard Operating Procedures, including all safety procedures and policies. For working safely in an effective work team. * Perform any other related duties as required or assigned. EDUCATION / EXPERIENCE * BS in Science + 0 years' experience ADDITIONAL INFORMATION To perform this job successfully, an individual must be able to perform the essential job functions satisfactorily. PAI is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, PAI will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer. PAI uses E-Verify. EEO Employer / Veteran / Disabled First Shift 7:00am - 5:30pm - Monday - Thurs

Full-time Description The Quality Control Lab Analyst performs a wide variety of laboratory tests on raw materials, in process samples, finished products, chemicals, using different Laboratory equipment such as HPLC, FTIR, UV-Vis, pH, GC, etc. Schedule is Rotating shifts (every 2 weeks), 4-10 hour shifts per week. Day shift is 7am to 530pm; Night Shift is 5pm to 330am Pay Range is $19 to $25/hour Requirements Conducts Lab testing such as HPLC, FTIR, UV-Vis, pH, GC, etc Perform all routine qualitative and quantitative analyses, from simple to very complex Examine critically test results, entry data into the company ERP computer system. Performs calibrations and standardizations of the Quality Control Laboratory equipment and methods Complies with standard laboratory procedures to maintain the efficiency and effectiveness of the laboratory instruments, titrating solutions, reagents, standards Maintains the housekeeping of the Quality Control Laboratory Participates in and successfully completes all required laboratory training classes Understand and comply with all general safety and environmental requirements for the laboratory and additional specific requirements as contained in the standard methods or in special instructions Review literature related to the general techniques used in the Quality Control Laboratory Learn all of the specific laboratory methods and standard operating procedures outlined by the QC Lab Quality Control Manual Salary Description $19 to $25 / hour

Job DescriptionJob TitleQuality Control LocationGreenville, SC Pay$13 / hr Shift7am - 4:30pm Mon - Thurs and 7:00am - 11:00am Fri Job SummaryWe're looking for a reliable and physically capable Production Associate to join our fast-paced manufacturing team. The ideal candidate will be able to work in a standing position, lift moderate weights, and maintain a high level of productivity in a dynamic environment.Responsibilities Perform production tasks in a fast-paced manufacturing environment Lift and move boxes weighing up to 50 pounds occasionally Stand for long periods without sitting Maintain a clean and organized workspace Meet productivity and quality standards Work scheduled shifts without early departure or absences Preferred Skills Ability to read and write in English Basic math skills Ability to lift and move moderate weights Comfortable working in varying indoor temperatures Ability to stand for long periods Reliable attendance and punctuality Ability to work in a fast-paced environment How to Applyhttps://www.workboxstaffing.com/job-results#/Equal Employment Opportunity

Description & Requirements Smurfit Westrock (NYSE:SW) is a global leader in sustainable paper and packaging solutions. We are materials scientists, packaging designers, mechanical engineers and manufacturing experts with a shared purpose: Innovate Boldly. Package Sustainably. Guided by our values of integrity, respect, accountability and excellence, we use leading science and technology to move fiber-based packaging forward. Job Summary The Quality Control Tech is responsible for managing controls and testing materials and finished products to ensure they conform to all applicable company and customer's standards. The Quality Control Tech will test parts across various stages of production cycle (before, in-process, and final) to ensure quality levels are met. The Quality Control Tech will be required to record and maintain data related to the overall quality control process such as logs, traceability forms, and registers. In the absence of the Quality Control Supervisor, this position reports to the Quality Control Lead Technician. Starting M-F 8a-4p overtime and weekends as needed Then site will go to 12hr shifts 2,2,3 schedule HIRING NOW Great Benefits FULL TIME VETERANS ENCOURAGED TO APPLY Essential Accountabilities Duties and responsibilities are not limited to and are as follows: * Perform all work in accordance with the highest standards of SKNA-Vitop safety policies, ensure all safety policies and processes are enforced. * Successfully complete all essential training. * Identify, assess, and verify incoming material. * Complete record of control of incoming raw material. * Observe storage management standards and compliance certificates. * Register batches and ensure their traceability. * Identify and evaluate defects found during the verifications of parts. * Perform dimensional/ functional/visual controls. * Management (identification, segregation, treatment) of the non-conforming material/parts. * Operate label printer. * Fill out and maintain traceability log sheet. * Perform part inspections and various other functions to insure part conformity and quality. * Generate documentation on changes that can be used to control traceability and ensure reproducibility. * Follow established procedures in order to maintain a clean and organized environment. * Adhere to lock-out tag-out policy and procedures. * Work with all departments to meet daily tasks. * Perform all duties safely and efficiently. * Other duties as assigned. Education/Qualification/Experience JOB QUALIFICATIONS * High school education or any equivalent combination of training and experience. * Knowledge and application of measuring instruments. * Experience with basic hand tools required (Calipers, Micrometer, Pin gages). * Minimum of 2 years' experience in a quality function. * Ability to work a flexible schedule, which may include nights, overtime and weekend assignments. * Ability to work in a team environment and rotate jobs or shifts as needed. Knowledge * Knowledge of safety practices and expectations. * Knowledge of quality practices and expectations, and respect for product. * Basic knowledge of manufacturing production processes and quality defects applicable to the plastics processing industry. * Knowledge/respect rules of good behavior "sanitation" and clothing (prohibitions and obligations). * Awareness of the dangers of possible contamination. * Basic knowledge of food quality and safety management systems. * Ability to read and interpret documents such as safety rules, operating and maintenance instructions and procedure manuals. * Ability to effectively communicate. * Knowledge of OSHA requirements to include Machine Guarding and Lockout/Tagout Procedures. * Knowledge of Safety ,5S, LEAN /TPS Toyota Production System a plus. * Understanding standard work (SOP's). * Understands and follows Company's quality and corporate/environmental policies. * Understands and follows procedures and work instructions established by SKNA - Vitop, USA. Skills * Skilled in lifting heavy packages and objects. * Skilled in operating pallet jacks. * Skilled in problem solving. * Basic reading and math. * Basic computer skills (i.e., email, data entry, Microsoft Office-Excel, Word, PowerPoint). * Basic administrative skills (i.e., filing, organization). Physical Requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Must be able to lift and stack objects up to 50 pounds occasionally and frequently exert 50 pounds of force to lift, carry, push, and pull or otherwise move objects. * Work involves periods of sitting, standing, and walking, climbing ladders, staircases, stooping, kneeling, crouching, twisting/turning, and reaching, bending at the waist. Indoor/ out-door work environment with exposure to weather extremes. * Must be able to perceive the nature of sound, utilize near and far vision, depth perception, provide oral information, and possess the manual dexterity to handle and work with various materials and objects which are essential aspects of this position. * The noise level in the work environment is dependent on area of the plant. * Personal Protective Equipment (PPE) (eye protection, ear protection, hand protection and safety shoes) is required for specific tasks and/or area of the plant worked in. SAFETY TERM Smurfit Westrock is committed to a safe and healthy workplace for all of our employees. This commitment is expressed in our Health and Safety (H&S) Policy, the SWR EHS Guidelines, and in the daily safe operations at our world-wide facilities. Working safely is standard practice at SWR -- the safety and health of our employees and the communities we serve is a high priority. Employees must Learn, understand and implement the SWR H&S Guidelines applicable to their job. * Give full support to SWR's safety processes. Individuals will strictly follow rules and guidelines and always uses the right procedure for the job * Ensure that safety and health concerns are given primary consideration in all activities * Assist in the development and accomplishment of safety goals and objectives * Know and understand their individual safety responsibilities. Understands own role in the emergency response plan, and participates in emergency drills * Comply with applicable safety codes, laws, regulations, SWR's Guidelines and standards Candidates are required to undergo a drug screening after receiving a conditional job offer, but before starting employment. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law.

Overview Owen Steel Company is currently recruiting a Quality Control Inspector with 3-5 years of experience in a structural steel fabrication environment. Safety is always first, applicants must be able to work safely and professionally. In this role, a successful applicant will have a strong understanding of welding, fabrication, quality control, and NDE weld inspection methods including VT, UT, and MT. Experience in UT and MT is a plus, but not required. Primary Responsibilities Conduct material verification, fit-up inspections, and final inspections. Read and interpret fabrication drawings for fit-up and final fabrication verification and documentation. Interface effectively with customer QC representatives. Complete reports for all testing and inspections performed. Qualifications and Requirements 3-5 years of experience in a structural steel fabrication environment. AWS Certified Welding Inspector Certification Familiarity with FCAW and SAW welding processes. Proficiency in reading fabrication drawings. Understanding of fabrication codes (AWS D1.1 preferred). Ability to communicate and collaborate effectively with team members and customer QC representatives. Ability to work safely and professionally. Schedule and Location The standard schedule is 10-hour days Monday through Thursday and an 8-hour day on Friday. (Additional overtime may be required based off production needs.) Must be in the plant - no remote option. First shift and second shift opportunities are available. Owen Steel is an Equal Opportunity Employer. The Company offers compensation commensurate with experience, and a benefits package (after 90 days) that includes medical, dental, vision, life insurance, short-term disability, long-term disability and a 401(k) Plan.

Job Title: Welding Inspector Hourly Rate: Depending on Experience. About Us: We are a veteran owned contractor, providing project, maintenance, and outage support throughout the United States. Over the past 15 years we have proven to be a trusted partner for our clients while providing services that help power the world. Summary: We are looking for a skilled QA/QC lead. All applicants must be familiar with ASME Boiler and Pressure Vessel Code, welding processes, SMAW, GTAW and FCAW. Must have a valid CWI with a previous welding background. Familiar with NDT methods, visual, magnetic particle, liquid penetrant, radiography experience helpful. Responsibilities: Properly interpret client specifications, applicable codes and industry standards. Monitor all quality related activities on the project. Review quality inspection personnel qualifications and training requirements. Finalize specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials. Adhere to all site and company rules, regulations, PPE requirements, etc. Use a computer to compile and submit daily reports, inspection reports, and inter-office communications. Pay attention to detail and be capable of recommending and approving repairs as well as performing visual inspections of completed work. Maintain a positive relationship between client, facility, customer, Authorized Inspector and Jurisdiction. Other duties as assigned. Qualifications: Experience working in an industrial setting (nuclear experience considered an asset). Proficient with standard computer software (MS Word and Excel) and be able to write detailed inspection reports while maintaining an organized system of files. 2-3 years of experience in Welding Inspection. Documented NDE experience a plus. VT, MT, PT, UTT Self-motivated with good written and verbal communication skills with a positive team-oriented attitude is required. Must have reliable transportation and be able to travel extensively and work variable hours. Able to pass background screens and drug/alcohol testing as required by our customers. TWIC card a plus. High School Diploma or GED

We are seeking a skilled, reliable Quality Control Laborer to join our growing company. In this position, you will be responsible for attaining production goals, and following all site health and safety regulations. A strong work ethic and attention to detail are essential. General Labor Duties and Responsibilities Follow project instructions from manager or supervisor Follow all health and safety regulations when operating machinery Ensure regulated and proper headgear, earplugs, gloves, safety glasses, and clothing are worn Complete all assigned tasks in a timely and efficient manner Safely operate a variety of tools including hand-held banders, banding tables, tagging guns, and hand tools Clean and clear debris and hazardous materials Ensure equipment and tools are cleaned and stored properly Verify lumber dimensions and counts Ensure compliance with Chemical Safety and SDS sheets General Labor Requirements and Qualifications Must be 18 years of age Ability to physically stand, bend, squat, and lift up to 40 to 60 pounds Ability to work outside in all weather Positive attitude and work ethic Basic Mechanical Functions Able to work independently or as an active member of a team Excellent interpersonal skills and communication with all levels of management Confined Space Entry training is a plus but not required Prior experience in a setting where mobile equipment and pedestrians interact is a plus but not required

Start your new career as a Quality Control Inspector with MAU at AFL in Duncan, SC. As a Quality Control Inspector, you will perform in-process and final inspections of fiber optic cable products to ensure they meet AFL's high-quality standards and customer specifications. This is a temp-to-hire opportunity. What We Offer: * Pay of $21.01 per hour * 8% shift differential for night shifts * Paid breaks * Health Benefits: Medical, Dental, and Vision * 401(k) retirement plan * Life Insurance * Vacation and Holiday pay * Training and advancement opportunities What We're Looking For: * High School Diploma or GED - preferred * 1+ year of experience in machine operation or machine setup * Ability to read and use micrometers and calipers * Mechanically inclined with strong attention to detail * Ability to multitask in a fast-paced environment * Able to lift up to 50 lbs. * Willing to work 12-hour night shifts (7:00 PM - 7:00 AM) on a 2-2-3 rotation * Must be available for training on day shift (7:00 AM - 7:00 PM) * Willingness to work weekends and overtime as needed What You'll Do as a Quality Control Inspector: * Perform in-process and final inspections to verify compliance with quality standards * Conduct dimensional, physical, and visual inspections based on specifications * Use an OTDR to test the transmission capabilities of fiber in cable * Prepare cables for testing and document inspection results * Maintain calibration records and ensure inspection equipment is operational * Log inspection activities in Oracle, QTS, and internal systems * Create and manage test documentation and packages for special customer requirements * Generate Non-Conformance Reports (NCMIRs) as needed * Inspect and test Returned Material Authorizations (RMAs) * Re-inspect reworked products to confirm compliance * Assist with Factory Acceptance Testing (FAT) conducted by third parties * Support safety initiatives and corrective actions * Train new final inspectors Walk-In Interview Hours: * Monday & Thursday: 9:00 AM - 11:30 AM * Tuesday & Thursday: 1:30 PM - 4:00 PM

Greenwood Mills, Inc., a family-owned textile manufacturing business located in Greenwood, SC that makes cloth for our US Military, employee uniforms, and more! We have been in business for more than 135 years! Currently seeks motivated employees to be the final inspection before the cloth is sent to customers! This is a critical piece to our operation and we need you! You will be shown the area with more description during the interview. Job Objective: Visually Inspects cloth for final quality check. Visually inspects cloth on grading machine Separates into A1 & A2 or seconds category and records on supplied tickets. Must be able to push rolls of cloth weighing up to 1200 pounds and sew together with sewing machine on dolly. Brush off grading frame at end of each shift and remove trim waste from sewing machine basket. Record yards on batch up rolls. Check defect and remove defect when needed. Doff roll from batcher and any small cuts of off quality that is doffed from take up of grading frame. Count picks in cloth with pick glass. Must be able to use and read measuring tape. Must be able to read basic written instructions and perform basic math calculations with calculator. Must be able to doff and lift damaged cloth weighing 15 to 20 pounds. Must be able to work with little supervision. Must be able to distinguish colors. Must follow prescribed safety rules for job assignment. Must be able to wear respirator/dust mask, hearing protection, and other required pieces of equipment. Must be able to meet plant work schedules and attendance requirements as stipulated in company policies. Schedule 2nd shift 4pm - 12am Competitive Benefits: Medical, Dental, Vision, Teladoc Basic Term Life/Accidental Death Insurance Short Term Disability, Long Term Disability Voluntary Life Insurance Free Employee Assistance Program Free Onsite Nurse/Clinic Identity Theft Assistance/ Travel Assistance 401K Company Holidays Pay rate: $13.10 Hourly with $1.00 shift premium (3rd shift) Advancement opportunities/ internal growth available! No textile experience is needed, although prior textile or manufacturing experience is a plus. We are looking for new hires who wish to build a career with us. Join our team! Greenwood Mills, Inc. is an equal opportunity employer. It is our policy to ensure that all employment opportunities are available to associates and applicants on the basis of their individual willingness and ability to do the job.

Salary: $19.00 Hourly At Thorne, we work to deliver high-quality, science-backed solutions to empower individuals to take a proactive approach to their well-being. Each day begins with a mission to help others discover and achieve their best health. We count on our team members to challenge and push the boundaries to make that happen. At Thorne, you'll be joining a team of more than 750 passionate individuals committed to our cause of providing superior health solutions at every age and life stage. Position Summary: At Thorne, quality is a standard we stand by, where science meets precision to create high-quality health and wellness products. Our hourly quality control inspector roles offer hands-on experience in a clean, safe, and innovative manufacturing environment with opportunities for growth and development. Whether examining, testing, or operating high-tech machinery ensuring products meet our strict quality standards, every team member plays a critical role in delivering trusted solutions to our customer. To learn more about our quality control inspector role - watch below! * Quality Control Inspector This application is for 2nd Shift positions, 3:00pm-11:30pm. All shifts include Saturdays plus overtime as required to meet production needs. What You Need * Minimum High school diploma or GED is required. Prior manufacturing experience preferred. * Ability to work overtime as required. * Must be able to safely work with ingredients and products that are derived from possibly allergenic sources including, but not limited to, nuts, soy, dairy, fish, and shellfish. Physical Demands * Must be able to work while using a half-mask respirator or a full-air respirator for up to six hours at a time and be able to follow Thorne Research's Respiratory Protection Program guidelines. * Must be able to work in a stationary position as well as move about unassisted. * Must be able to safely and carefully operate and use assigned equipment and machinery * Must be able to stoop, kneel, crouch, or crawl as circumstances arise during the course of a shift. * Must be able to operate, activate, use, prepare, and clean equipment, occasionally grasping with force and using twisting wrist movements. * Must be able to hear and converse with supervisors and other employees. * Must be able to work independently with limited supervision. * Must be able to interact with other departments to ensure compliance with specifications and to facilitate the acceptance of parts. * Must be able to complete all required training levels. * Must be able and willing when needed to assist and train new QC Inspectors. * Must be able to see and read small print and be able to distinguish colors. * Must be able to work in a moderate noise level environment. * Must be able to work a 12-, 10- or 8-hour shift and overtime as assigned. * Must be able to move or lift items weighing up to 50 pounds from floor to table and from table to floor, occasionally, during a 12-, 10- or 8-hour shift unassisted. Must have assistance when lifting items weighing over 50 pounds. * Must have sufficient range of motion with arms and hands to reach overhead and to the side, often repetitively, during a 12-, 10- or 8-hour shift. * Must be able to ascend/descend a ladder while carrying up to 20 pounds of materials. * Must be able to work in a fast-paced environment. What We Offer * Competitive compensation * 100% company-paid medical, dental, and vision insurance coverage for employees * Company-paid short- and long-term disability insurance * Company- paid life insurance * 401k plan with employer matching contributions up to 4% * Gym membership reimbursement * Monthly allowance of Thorne supplements * Paid time off, volunteer time off and holiday leave * Training, professional development, and career growth opportunities Thorne is the leader in science-backed health and wellness solutions committed to helping individuals live healthier longer. As the top recommended clinical brand by healthcare practitioners, Thorne offers a comprehensive range of products including nutritional supplements and health tests designed to meet the unique needs of individuals at every stage of life. Founded in 1984, Thorne products are formulated with the highest-quality ingredients, supported by clinical research, and rigorously tested to ensure purity, potency, and efficacy. Thorne is trusted by 47,000+ health-care professionals, thousands of professional athletes, more than 100 professional sports teams, multiple U.S. National Teams, and more than five million consumers. For more information, visit Thorne.com. THORNE IS AN EQUAL OPPORTUNITY EMPLOYER

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst position at its facility in Gaffney, SC. Ideal candidates will possess the following: * An Associate degree in Biology or related field (required); BS or BA in the biological sciences or related field (preferred) * Proficiency with data entry and computer applications * Ability to multitask and work in a fast-paced environment * Strong written and verbal communication skills * Strong attention to detail * Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. This is a full-time position in which the employee will be eligible for standard benefits after a brief waiting period. The schedule for this position is Monday through Friday, from 10:00pm to 6:30am. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from

GE Vernova is accelerating the path to more reliable, affordable, and sustainable energy, while helping our customers power economies and deliver the electricity that is vital to health, safety, security, and improved quality of life. Are you excited at the opportunity to electrify and decarbonize the world? Job Description What you'll do: * Perform product audits of gas turbine components, parts, assemblies, and fabrications. * Calibrate non-standard product tools, fixtures, and gauges using standard and special gauging techniques. * Apply geometric, trigonometric, and algebraic relationship in the set up and measurements of complex parts, fixtures, and gauging. * Set up and x-ray production parts, pipe, and welder samples. * Establish radiographic techniques and processes, read and interpret x-ray film or real-time images. * Must maintain accurate records including retrievability. * Perform other related duties. * Perform all duties as part of a team. * The employee is expected to be at their designated workstation ready to work at their assigned starting time. What you'll bring: * Ability to work 3rd shift (11PM - 7 AM) * Minimum High School diploma / GED equivalent * Must successfully complete the Quality Assurance Operator Test * Must successfully pass required testing for NDT certification * Prior experience in Quality Operations * Must meet medical/physical Quality Assurance Operator requirements, with or without reasonable accommodation Pay Rate: The pay for this position is $34.70 - $35.96. This position is also eligible for shift premium when you work on an off shift i.e. 2nd or 3rd shift. Plus $1.00 USD an hour on top of base pay. This posting is expected to close on February 23, 2025. Benefits Available to You GE Vernova employees rise to the challenge of building a world that works. In order to meet this mission, we provide varied, competitive benefits to help support our workforce: Our Culture | GE Vernova (gecareers.com) * Our compensation & benefits are designed to reward high performers and help you manage your personal and family needs. We offer a robust benefits package depending on your employment status and your national requirements. * A healthy, balanced lifestyle can mean different things to different people. We've created programs that support the way you live and work today. * GE Vernova invests to provide opportunities to grow your career by providing a path for continued on-the-job learning and development. Inclusion At GE Vernova, we believe in the value of your unique identity, background and experiences. We are committed to fostering an inclusive culture, where everyone feels empowered to do their best work because they feel accepted, respected and that they belong. Click here to learn more: ************************************************** About GE Vernova Gas Power GE Vernova's Gas Power business engineers advanced, efficient natural gas-powered technologies and services, along with decarbonization solutions that aim to help electrify a lower carbon future. It is a global leader in gas turbines and power plant technologies and services with the industry's largest installed base For candidates applying to a U.S. based position only: * The Company pays a geographic differential of 110%, 120% or 130% of salary in certain areas. This posting is expected to remain open for at least seven days after it was posted on December 15, 2025. Available benefits include medical, dental, vision, and prescription drug coverage; access to Health Coach from GE Vernova, a 24/7 nurse-based resource; and access to the Employee Assistance Program, providing 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Vernova Retirement Savings Plan, a tax-advantaged 401(k) savings opportunity with company matching contributions and company retirement contributions, as well as access to Fidelity resources and financial planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability benefits, life insurance and 12 paid holidays. New hires also two weeks of annual vacation (which may be pro-rated based on start date). GE Vernova Inc. or its affiliates (collectively or individually, "GE Vernova") sponsor certain employee benefit plans or programs GE Vernova reserves the right to terminate, amend, suspend, replace, or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a GE Vernova welfare benefit plan or program. This document does not create a contract of employment with any individual.

The primary responsibility of this position is to analyze drug substances, drug products, and/or stability samples using approved laboratory monographs/specifications, Standard Operating Procedures, and USP/NF methodologies to ensure drug products manufactured at and distributed by Pharmaceutical Associates, Inc. meet all quality and compliance requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES Follows all policies, procedures, SOPs, cGMPS, Work Instructions, and supervisor instructions. HPLC/GC Chemists: Shall have an emphasis in HPLC and/or GC methodology and analyses including all applicable preparations (extractions, dissolution, ISE separation, etc.), and training or experience in chromatographic software and instrument troubleshooting. Wet Chemists: Shall have an emphasis in wet chemistry methodology and analyses such as various titrations, dissolution, USP/NF limit tests, Identifications, TLC, etc. Responsible for performing analysis of raw materials, bulk, finished product, and stability samples in a timely and compliant manner, as instructed by QC Supervisor, per applicable SOPs, PAI monographs/specifications, and USP methodology to ensure finished goods are acceptable for distribution. Responsible for documentation of all analyses per applicable SOPs. Responsible for performance of routine laboratory functions to support manufacturing/production and assure that production schedule is met. Responsible for the timely testing and release of manufactured bulk drug products for packaging. Responsible for maintaining clean and organized laboratories. Wash labware and pipettes by loading/unloading dishwasher/pipette washer. Notify Laboratory Coordinator when reagents, standards, and other materials need to be ordered to ensure all resources available for testing. Assist in training and evaluating laboratory personnel to run laboratory equipment for established methods. Assist in documentation review of laboratory notebooks. Accountable for the accuracy and timeliness of work, attention to detail, and adherence to test method monograph/specifications. For following applicable Standard Operating Procedures, including all safety procedures and policies. For working safely in an effective work team. Perform any other related duties as required or assigned. EDUCATION / EXPERIENCE BS in Science + 0 years' experience ADDITIONAL INFORMATION To perform this job successfully, an individual must be able to perform the essential job functions satisfactorily. PAI is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, PAI will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer. PAI uses E-Verify. EEO Employer / Veteran / Disabled

The primary responsibility of this position is to analyze drug substances, drug products, and/or stability samples using approved laboratory monographs/specifications, Standard Operating Procedures, and USP/NF methodologies to ensure drug products manufactured at and distributed by PAI meet all quality and compliance requirements. The essential duties and responsibilities listed below are representative of those required on the job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential duties and responsibilities. ESSENTIAL DUTIES AND RESPONSIBILITIES: 1. HPLC/GC Chemists: Shall have an emphasis in HPLC and/or GC methodology and analyses including all applicable preparations (extractions, dissolution, ISE separation, etc.), and training or experience in chromatographic software and instrument troubleshooting. 2. Wet Chemists: Shall have an emphasis in wet chemistry methodology and analyses such as various titrations, dissolution, USP/NF limit tests, Identifications, TLC, etc. 3. Responsible for performing analysis of raw materials, bulk, finished product, and stability samples in a timely and compliant manner, as instructed by QC Supervisor, per applicable SOP's, PAI monographs/specifications, and USP methodology to ensure finished goods are acceptable for distribution. 4. Responsible for documentation of all analyses per applicable SOP's and performance of routine laboratory functions to support manufacturing/production and assure that production schedule is met. 5. Responsible for timely testing and release of manufactured bulk drug products for packaging. 6. Responsible for maintaining clean and organized laboratories. Wash labware and pipettes by loading/unloading dishwasher/pipette washer. 7. Notify Laboratory Coordinator when reagents, standards, and other materials need to be ordered to ensure all resources available for testing. 8. Assist in training and evaluating laboratory personnel to run laboratory equipment for established methods. 9. Assist in review of laboratory documentation. 10. Accountable for the accuracy and timeliness of work, attention to detail, and adherence to test method monograph/specifications. Must follow all applicable Standard Operating Procedures, including all safety procedures and policies. 11. Perform other duties as assigned. 12. For Chemist II, in addition to the tasks listed above, the analyst is able to independently perform multiple different types of testing without significant guidance from management. Analyst will execute OOS investigation plans and routinely serve as second analyst in laboratory investigations. Perform technology transfers and provide coaching and mentorship to junior chemists. 13. For Chemist III, in addition to the tasks listed above, the analyst will routinely troubleshoot critical analytical and technical issues, serve as investigator for laboratory CAPAs, and revise raw material and finished product monographs to ensure compliance with compendial methods. EDUCATION AND/OR EXPERIENCE: This position requires a Bachelors' degree in chemistry, biochemistry, biology or other science field, and/or equivalent combination of education and experience. Working knowledge of Microsoft Office Suite is required. Experience with OpenLab and LIMS software is preferred. Experience in chromatographic software (e.g. Empower) is preferred. B.S. in a science field along with 0-2 years applicable laboratory experience is required. KNOWLEDGE, SKILS & ABILITIES: This position requires the individual be organized, detail-oriented, and self-motivated and to apply advanced mathematical concepts and operations. The ability to apply principles of logical and scientific thinking to a wide range of intellectual and practical problems. Decision making, communication, planning and critical thinking skills are a must. Analytical ability / problem solving, along with accuracy is required. Applicable experience in an analytical laboratory preferred, experience in GMP is ideal. Standard laboratory equipment, including viscometer, centrifuge, analytical balance, conductivity meter, dissolution, apparatus, Karl Fisher, density meter, pH meter, HPLC, GC/FID, GC/Headspace, IR, UV-Vis, AA, polarimeter, particle sizer and analyzer and refractometry. PHYSICAL REQUIREMENTS/WORKING CONDITIONS: The physical requirements and working conditions listed for this job are representative of those required on the job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential duties and responsibilities. Computer keyboarding, computer monitor and mouse use including reaching forward, grasping, finger and wrist manipulations, and neck bending and turning: near vision is necessary for computer monitor use. Frequently required to stand, sit, walk, talk and hear, occasionally required to reach with hands and arms, climb or balance, stoop, kneel, crouch or crawl. Frequently lift up to 30lbs. and occasionally up to 50 lbs. is required. This position is regularly exposed to toxic chemicals. To perform this job successfully, an individual must be able to perform the essential job functions satisfactorily. PAI is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, PAI will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer. PAI uses E-Verify. PAI Pharma is a nicotine-free campus, meaning the use of nicotine products-including cigarettes, vaping, chewing tobacco, and any other nicotine-containing substances-is strictly prohibited on company property. All employees should be able to complete their full shift without the need to use nicotine. By joining PAI Pharma, you agree to adhere to our nicotine-free workplace policy, which supports a healthier environment for all employees. EEO Employer / Veteran / Disabled 4:00PM-2:30AM

Job Description Greenwood Mills, Inc., a family-owned textile manufacturing business located in Greenwood, SC that makes cloth for our US Military, employee uniforms, and more! We have been in business for more than 135 years! Currently seeks motivated employees to be the final inspection before the cloth is sent to customers! This is a critical piece to our operation and we need you! You will be shown the area with more description during the interview. Job Objective: Visually Inspects cloth for final quality check. Visually inspects cloth on grading machine Separates into A1 & A2 or seconds category and records on supplied tickets. Must be able to push rolls of cloth weighing up to 1200 pounds and sew together with sewing machine on dolly. Brush off grading frame at end of each shift and remove trim waste from sewing machine basket. Record yards on batch up rolls. Check defect and remove defect when needed. Doff roll from batcher and any small cuts of off quality that is doffed from take up of grading frame. Count picks in cloth with pick glass. Must be able to use and read measuring tape. Must be able to read basic written instructions and perform basic math calculations with calculator. Must be able to doff and lift damaged cloth weighing 15 to 20 pounds. Must be able to work with little supervision. Must be able to distinguish colors. Must follow prescribed safety rules for job assignment. Must be able to wear respirator/dust mask, hearing protection, and other required pieces of equipment. Must be able to meet plant work schedules and attendance requirements as stipulated in company policies. Schedule 2nd shift 4pm - 12am Competitive Benefits: Medical, Dental, Vision, Teladoc Basic Term Life/Accidental Death Insurance Short Term Disability, Long Term Disability Voluntary Life Insurance Free Employee Assistance Program Free Onsite Nurse/Clinic Identity Theft Assistance/ Travel Assistance 401K Company Holidays Pay rate: $13.10 Hourly with $1.00 shift premium (3rd shift) Advancement opportunities/ internal growth available! No textile experience is needed, although prior textile or manufacturing experience is a plus. We are looking for new hires who wish to build a career with us. Join our team! Greenwood Mills, Inc. is an equal opportunity employer. It is our policy to ensure that all employment opportunities are available to associates and applicants on the basis of their individual willingness and ability to do the job.