Chemist Jobs in Cayce, SC

EMS-Chemie engages in the manufacture and distribution of polymers and other chemicals. Our Polyamides (Business Unit EMS-GRIVORY) are used in applications in the market segments of automotive, industrial and consumer goods, electronics, healthcare, optics and packaging...products you are using in everyday life. We are expanding our quality assurance team in Sumter SC and are looking for a recent graduate with a degree in chemistry and a desire to develop their skill set, learn more about plastics manufacturing and advance in their professional career. We offer a competitive starting salary, relocation assistance, an outstanding benefits package as well as a team motivated to helping you grow. Position Summary: The primary responsibility of the Quality Assurance (QA) Chemist is to ensure products meet or exceed customer requirements. General duties include the monitoring of quality assurance systems including instrumentation calibration, maintenance, cross-checks, methods, procedures, raw materials, and training. Comply with IATF 16949 and ISO 17025 quality system requirements. Supports Production, QA/MT, and Customer Service departments by providing accurate testing results in a timely manner. Appropriately manages all aspects of the Quality Assurance lab including sample flow, material release, off spec handling, supply stock and equipment maintenance. Identify improvement opportunities. Following and ensuring strict safety procedures. Maintain clean and organized work area. What you will be doing: Testing and approval of manufactured products and factored products in line with the quality assurance objectives for the company. Sampling, testing, and release of incoming raw materials. Uphold and follow Quality Policies in order to ensure compliance with IATF 16949 certification and ISO 17025 accreditation. Maintain laboratory equipment to include assurance that instruments are calibrated according to external and internal requirements. Maintain sample stockrooms, laboratory supplies, tools, and other resources to assist in completing tasks. Assist in preparing reports and test certificates. Provide technical problem solving support; support QA compliance and facilitate the release of First-Quality products. Communicate with various departments and salespersons as needed on projects. Revising and/or establishing laboratory instructions. Following and ensuring strict safety procedures. Maintain clean and organized work area. Supports QA/MT, AD/TS, and Sales departments with testing, projects, and other requests. Keeping up-to-date with technical developments, especially those which can save time and improve reliability. Provide proposals and/or credit requests to promote continuous improvements Additional responsibilities as assigned. Educational & Professional Background Bachelors degree required in Chemistry, or related field.

First Quality was founded in 1989 and, in nearly three decades, has grown to be a global privately held company with over 4,000 employees. Its corporate offices are located in Great Neck, New York, with manufacturing facilities and offices in Pennsylvania, South Carolina, Georgia, and Canada. First Quality is a diversified family of companies manufacturing consumer products ranging from Absorbent Hygiene (adult incontinence, feminine care, and baby care), Tissue (bath and towel), and Industrial (print and packaging materials), serving institutional and retail markets throughout the world. First Quality focuses on private label and branded product lines. Our core business philosophy is built on a proud culture driven by safety and quality, respect, humility, integrity, customer focus, and teamwork. With leading edge manufacturing technologies and processes and visionary leadership, First Quality is positioned to continue significant growth in the coming years. We are seeking an experienced Product Development Raw Material Scientist for our First Quality Baby Products facility located in Macon, GA. This position will be responsible for the development and innovation of current and new products that meet and exceed customer/consumer needs while still meeting required cost targets. This position reports directly to the Product Development Leader and plays a crucial role in driving innovation and ensuring the successful launch of high-quality products. Primary responsibilities include: Leads the development of new products from concept through commercialization. Benchmarks competitive products, creates initial specification, produces concept samples, scales up process, confirms process capabilities, and finalizes specifications as needed to ensure successful commercial production. Works in close collaboration with Sales/Marketing, Engineering, and Operations in order to identify opportunities for new products and improvements to current products. Researches and maintains up-to-date information on competitive products and relevant research and patent literature. Works closely with suppliers' technical staff on development efforts. Works with Process Engineers and Quality Assurance to optimize the technical and economic performance of existing products. Maintains extensive contacts with material suppliers to allow development of new materials and optimizes the performance of current raw materials. Responsible for coordinating, analyzing, & documenting Product Development trials while interacting with Process Engineering, Operations and Quality Assurance. Organizes trials from the planning stages, monitoring runs and post-trial requirements. Ability to leverage Design of Experiments; Test products to assess product performance and attributes, New raw materials to evaluate their properties and determine their impact on finished goods, and Competitive products (benchmarking). Maintains a historical database, and provide summaries as needed. Responsible for interpreting data for such purposes as quality control, process control, cost savings, and/or product development. Assists in Consumer Usage Testing through product preparation and record keeping as well as data compilation and basic analysis. Maintains excellent data collection and research records. Devises/revises procedures, work instructions, and specifications (raw material, in-process, and finished goods). Ensures that all pertinent FQ GMP and Design Control requirements are met and maintain the necessary records. Prepares product samples for Sales, independent lab assessments, and product safety evaluations. Establishes effective working relationships with other departments (Engineering, Quality, Production Planning, & Production) to achieve product improvement, new product development, cost saving, and/or quality initiatives. Provides recommendations for improvements to our products, testing methods, processes, and potential cost savings. Assists the Product Development Leader with other responsibilities, as requested. The ideal candidate should possess the following: Four-year technical degree (e.g. Materials Science, Chemical Engineering, Mechanical Engineering) or equivalent; additional business studies preferred. Two + years Product Development experience in the Consumer Products or Medical /Healthcare industries, or equivalent combination of education and experience. Ability to define problems, collect data, establish facts, and draw valid conclusions. Excellent project management skills, with the ability to prioritize tasks, meet deadlines, and manage multiple projects simultaneously. Strong analytical skills and attention to detail; strong written and oral communication skills. Self-motivated and proactive attitude, with a passion for innovation and continuous improvement. Proficiency with computer applications, including Microsoft Office. Knowledge of statistical applications preferred. Knowledge of GMP, FDA, ISO 13485, and other applicable quality standards and regulations is preferred. Excellent compensation and benefits, which are effective the first day of employment! First Quality is committed to protecting information under the care of First Quality Enterprises commensurate with leading industry standards and applicable regulations. As such, First Quality provides at least annual training regarding data privacy and security to employees who, as a result of their role specifications, may come in to contact with sensitive data. First Quality is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identification, or protected Veteran status.

The Upstream Engineer/Scientist 2 will provide tech transfer support and technical oversight for a large-scale cell culture in monoclonal antibody manufacturing. Follow Your Genki to North America's largest, state-of-the-art Life Science Manufacturing Facility & CDMO The work we do at FUJIFILM Diosynth Biotechnologies has never been more important-and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people's lives. Join FUJIFILM Diosynth Biotechnologies and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what we call Genki. Join us We are growing our locations and are investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of our Bio CDMO (Contract and Development Manufacturing Organization) business. This will be the largest end-to-end cell culture CDMO provider in North America. The new site will offer end-to-end solutions to our customers looking to manufacture biopharmaceuticals in the US. In addition to drug substance manufacture, it will also provide automated fill-finish and assembly, packaging, and labeling services. The new state-of-the-art facility is located in Holly Springs, North Carolina, United States. Job Description What You'll Do Conducts lab and pilot plant experiments Generates and coordinates execution sampling protocols Serves as subject matter expert (SME) to lead and conduct troubleshooting, process impact assessments, and executes root cause analysis (RCA) and corrective and preventive action (CAPA) in response to deviations Executes and analyzes lab and pilot plant work aimed at solving complex manufacturing problems Leads and supports technology transfer (TT) across multiple unit operation Coordinates, plans, and executes manufacturing process validation runs Supports design and leads generation of sampling plans for process validation reports (PVRs) and investigations Writes and reviews master batch records (MBRs) and standard operating procedures (SOPs), as needed Generates and executes process training and consults on topics related to manufacturing and process Leads technical risk assessments for new manufacturing processes Contributes to the management of manufacturing data (i.e., databasing) and the statistical analysis aimed at both process monitoring and continued process verification Writes documentation for internal and external use, such as manufacturing campaigns summary reports, process performance qualification (PPQ) protocol and reports, impact assessments etc. Leads training of manufacturing staff and process sciences group on new processes, procedures, and use of equipment in the lab Interprets and utilizes new knowledge to promptly drive data-based decisions Collaborates with the manufacturing department to support commercial and clinical manufacturing campaigns, including on-floor support Leads continuous improvement projects within unit operations, in partnership with manufacturing when applicable, to improve manufacturability, reliability, yield and cost Supports supplier technical evaluations, risk assessments, and raw material evaluation and qualification Other duties, as assigned Knowledge and Skills Proficient knowledge in Design of Experience (DOE) Proficient knowledge in Statistical Process Control Effective communication, both written and oral Ability to effective present information to others Proficient project management skills Advanced problem-solving skills Ability to provide feedback to others, including leaders Ability to develop effective working relationships internally and externally Ability to adapt communication style to differing audiences and advise others on difficult matters Basic Requirements Associate degree in Engineering, Life Science or Chemical Engineering with 4 years of related work experience (e.g., manufacturing); or Bachelor's degree in Engineering, Life Science or Chemical Engineering with 2 years of related work experience (e.g., manufacturing); or Master's degree with no prior experience Experience using quality systems (e.g., deviation management, change control, CAPA, document management system) Experience in contract manufacturing or interacting with contract manufacturers Preferred Requirements Experience working in a Good Manufacturing Practices (GMP) environment To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

All the benefits and perks you need for you and your family: Benefits from Day One Paid Days Off from Day One Whole Person Wellbeing Resources Mental Health Resources and Support $15,000 Sign On Bonus Our promise to you: Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind, and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better. Schedule: 4 days a week, 9hr shifts. 8-10 days of call 1 weekend a month (Fri, Sat, Sun) Shift : Days Location: AdventHealth Redmond The role you’ll contribute: GENERAL SUMMARY : The Cardiac Cath/EP Tech provides direct patient care assisting the physician during cardiac and electrophysiological invasive diagnostic and interventional procedures. Ensures the safe operation of all equipment used in the Cardiac Cath and EP labs. Works under the direction of physician. PRINCIPAL DUTIES AND JOB RESPONSIBILITIES : Performs imaging procedures/treatments according to cardiac catheterization lab practice standards in order to aid in the diagnosis and/or treatment of disease. • Assist with procedure scheduling and preprocedure patient education/instructions when necessary • Prepares the patient for the procedure and monitors, positions and assists patient during procedure • Assists the physician throughout the procedure • Assesses the procedure room for equipment functioning and readiness. • Safely operates cath/EP support equipment for all procedures performed in lab. • Cleans and calibrates equipment • Follows proper infection control procedures • Communicates with the physician and other staff members about patient condition as needed. • Using the electronic medical record, performs procedural documentation for all procedures performed in the cardiovascular/EP labs in a timely manner. • Maintains department inventory • Ensures that department is adequately equipped; keeping supplies organized • Orders supplies as per procedure • Assists in departmental performance Improvement activities including collecting and documenting quality improvement initiatives. • Ensures high quality service in compliance with all federal, state and local accrediting bodies rules, regulations, statutes, requirements, and standards including TJC, measured through quality control, performance improvement and customer satisfaction survey results. • All other duties as assigned Qualifications EDUCATION AND EXPERIENCE REQUIRED: Must be a Registered Nurse, Cardiovasular Tech or Radiology Technologist. Must have a current Georgia license/certification in respective field. Computer proficiency required. Excellent organizational and communication skills. EDUCATION AND EXPERIENCE PREFERRED: Previous experience in Cardiac Catheterization and/or EP lab. LICENSURE, CERTIFICATION OR REGISTRATION REQUIRED: Current Georgia License in respective field. BLS This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances. The salary range reflects the anticipated base pay range for this position. Individual compensation is determined based on skills, experience and other relevant factors within this pay range. The minimums and maximums for each position may vary based on geographical location. Category: Cardiology Organization: AdventHealth Redmond Schedule: Full-time Shift: 1 - Day Req ID: 24006410 We are an equal opportunity employer and do not tolerate discrimination based on race, color, creed, religion, national origin, sex, marital status, age or disability/handicap with respect to recruitment, selection, placement, promotion, wages, benefits and other terms and conditions of employment.

Job Title: Chemist Direct Hire role- relocation assistance offered Salary: $70,000-$80,000/year Job Purpose: The purpose of this role is to provide technical support to sales personnel and customers, assist with product applications and complaints, and develop new application formulations to meet customer requirements for automotive soft trim and weather seal applications. The Chemist will work closely with Manufacturing, Research and Development teams, and Technical Sales for Flame Retardant, Coated Fabrics, and Industrial Coatings markets. This position is responsible for ensuring the highest standards of product quality are adhered to. Essential Duties and Responsibilities: Prepare application formulations and apply them to customer-supplied substrates. Apply formulated coatings using lab or pilot-scale methods such as spray, gravure, dip/nip, pad bath, or similar techniques. Perform testing to customer requirements for physical properties, color/aesthetics, and flammability. Develop innovative approaches to modify existing formulations, simulate customer part construction, conduct testing, and scale up production across various manufacturing locations, if necessary. Collaborate with an interdisciplinary team locally, nationally, and globally to promote the development of chemistry and capabilities. Present and share findings with Technical Sales, Customers, and internal teams (R&D, Applications). Successfully complete Technical Service Request projects in a timely manner, adhering to department guidelines and priorities set by the supervisor. Act as a resource for the Technical Service Group, Quality Control, and Production. Organize and maintain all pertinent testing information in laboratory project files for future reference. Ensure the work area and laboratory space remain clean, organized, and orderly. This role involves supporting customer trials at a Center of Excellence for North American automotive customers, requiring professional customer interaction and presentation. Perform other duties as assigned. Qualifications: A Bachelor's degree in Chemistry, Chemical Engineering, Polymer Science, Plastics Engineering, or a related field. 2 years or more of industrial experience, with a focus on the formulation of specialty coatings, color matching, plant processing procedures, quality control testing, and technical service. Specific or relevant experience with coatings, pigments, flame retardants, OEM specifications, color matching, surface tension testing, and hydrophobicity testing is preferred. Experience with lab equipment, such as Crocking, Abrasion Testers, Humidity Chambers, Weatherometers, W-Flex, Drop Shape Analyzers, Martindale, Flock Peel Testers, and Acoustic Chambers, is a plus. Ability to handle multiple ongoing projects simultaneously without close supervision. Strong communication and organizational skills to effectively interact with both internal and external customers. Must be eligible to work in the US. Additional Skills & Experience: Do you have any experience or skills related to the coatings field, such as compounding coatings, applying coatings via gravure or spray methods, or conducting OEM specifications testing Can your degree in organic chemistry, polymer science, or plastics engineering contribute to the team's goals in the coatings industry? Does your specific or relevant experience with coatings, pigments, flame retardants, OEM specifications, color matching, surface tension testing, and hydrophobicity testing enhance your suitability for this role

Up to $10,000 Sign-on Bonus Based on Eligibility Cath Lab Tech Full Time Days Performs direct and indirect functions in the Cardiac Cath Lab. Assists all Physicians/staff with clinical and technical aspects of cardiovascular care performs miscellaneous duties as assigned. Scrubs monitors and circulates in all invasive procedures in the Cath lab and IVR. (Invasive/surgical and interventional procedures) inventory control. Able to function on all cardiac alerts and STEMI cases. Responsibilities Assesses physical, psychosocial, and growth and development needs of the patient, completes pre, intra and post procedure assessment, informs nurse/MD of any changes in patient's condition. Develops a plan of care for procedure being performed, plan of care is individualized to include specific patient problems, needs and scheduled procedure. Provides teaching and guidance to patient and/or family as well as staff members. Able to execute x-ray for desired views- abdominal aorta gram, runoff, division, storing and printing images, sets priorities for care of patients based on patient's needs and resources available, identifies and performs appropriately in emergency patient care solutions. Knowledge of set up and monitoring of IABP, assists with set-up, insertion and care of temporary and permanent pacemakers. THE CATH LAB TECH FULL TIME DAYS CANDIDATE WILL POSSESS THE FOLLOWING EDUCATION, LICENSE/CERTIFICATIONS, AND EXPERIENCE. Education: Required: Associate Degree in Radiology or equivalent, Basic EKG course. Preferred: Bachelor in Radiology or equivalent. Experience: Required: 6 months in Cath Lab/Cardiac Intervention Lab. Preferred: 1 year experience providing cardiac cath, radiology care Required Certifications/Registrations/Licenses: Required: BLS . ACLS within 6 months of hire. Preferred: RCIS certification ********** Employment practices will not be influenced or affected by an applicant's or employee's race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.

We are seeking a Quality Control (QC) Chemist to support analytical testing and ensure product quality in a regulated environment. The QC Chemist will perform routine and non-routine testing of raw materials, in-process samples, and finished products following Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory requirements. Key Responsibilities: Perform analytical testing using techniques such as HPLC, GC, FTIR, titration, and wet chemistry methods. Conduct raw material, in-process, and final product testing to ensure compliance with specifications. Maintain, troubleshoot, and calibrate laboratory instruments. Document all testing and results accurately in lab notebooks, LIMS, and batch records. Support method validation, method development, and transfer activities as needed. Follow SOPs, cGMP, GLP, and regulatory guidelines. Work cross-functionally with QA, R&D, and manufacturing teams to maintain product quality. Qualifications & Skills: Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field. 3+ years of experience in a QC laboratory within pharma, biotech, or medical devices. Hands-on experience with analytical instrumentation (HPLC, GC, UV-Vis, FTIR, etc.). Strong understanding of GMP, GLP, and regulatory compliance. Excellent attention to detail, documentation, and problem-solving skills.

Job Details: Job Title: "Quality Control Associate " Duration: 12 months Contract Internal ID: 25-36468 Pay Rate: $28 to $32/hr on W2 (without benefits) Schedule: Sunday-Wed or Wed-Sat, 10 hours per day/ 40 hour work week Must have skills: Basic science background (science degree or prior laboratory experience) Environmental monitoring experience or Microbiology experience is a plus. Knowledge of Aseptic technique. Proficient in good documentation practices (GMP experience not required but basic laboratory writing skills/GDP/GLP knowledge preferred) Job Responsibilities: Under general supervision, this position will perform routine sampling and testing in a GMP Manufacturing facility in support of the Microbiology and Environmental Monitoring group. This position will be responsible for one or more of the following activities: Assist with environmental monitoring performance qualification. Execute routine sample collection for environmental monitoring in classified areas Assist with clean utilities performance qualifications, including water for injection, clean steam, clean compressed air, oxygen, and carbon dioxide distribution systems Execute sample collection for routine utilities monitoring Assist with general lab startup activities Perform routine tasks such as cleaning and inventory management Support routine activities over the weekends and public holidays as required Skills: Some lab experience is preferred. Experience with environmental monitoring preferred but not required Knowledge of aseptic technique Experience with Good Documentation Practices/Good Laboratory Practices preferred Good writing and verbal communication skills About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions 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 status as a protected veteran. Details: Name: Shalini L Email ID: ******************************

Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules - both New Chemical Entities (NCE's) and New Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. POSITION SUMMARY: This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Perform IOQ/Calibration for instruments in QC lab at Monroe with guidance of CQA. Execute and complete procedures and systems for RM, PM, FD and in process testing in QC lab. Provide information, data for evaluation and execution of stability study as per Quality and regulatory requirement. Timely complete testing and ensure compliance during analytical TT and AMV performed in QC lab. Able to be a qualified trainer for QC related systems and SOP's and responsible that personnel are appropriately trained. As a member of Site Investigation Team (SIT) needs to investigate quality events and perform Root Cause Analysis (RCA). OVERALL JOB RESPONSIBILITIES: Be cost effective and vigilant of laboratory reagents, glassware, etcetera to ensure department is within the Revenue and Capex Budget as per spent analysis project. Execute and maintain quality system controls to ensure no critical and major market complaints. Take appropriate steps to reduce wastages and losses in the analysis process and build improved efficiency Perform day to day activities for the chemical laboratory which shall include testing of in- process, RM, PM and FP samples, Swab sample and Tech Transfer (as applicable). Ensuring compliance to systems and procedures throughout product lifecycle. Communicate with Supervisor and/or report any preparations or data that may result in an Incidence & OOS. Ensure that the QC Laboratory is in a ready state of compliance for internal and external audits. Execute technology transfer of analytical methods for new products. Execute cleaning validation of new products. Assist in the monitoring of changes in the monographs Pharmacopoeia requirements, Regulatory agencies recommendations and implement the same in QC Lab. Apply CAPA for Lab failures in OOS. Complete and maintain certified investigator training requirements to ensure SIT representation for identified area(s). Performing the investigation of quality events assigned using root cause analysis tools defined by company procedures, maintain timelines for closure of investigations assigned and to identify and initiate CAPA's. Participate in continuous improvement initiatives for investigations and associated investigation certification process. Work with CIT team as needed for Major and Critical Investigations to align with corporate guidelines. Comply with applicable FDA and international regulatory laws/standards and the Code of Conduct. Maintain knowledge of current regulatory requirements and standards as they pertain to the Stability and Quality Control departments. Represent Glenmark as appropriate in FDA, notified body, internal and other regulatory audits. Work in close collaboration and support with other members of the CMC team responsible for drug product development and support to management, as necessary Domestic and international travel up to 5% may be required to accompany technical staff in the factory acceptance and inspection of laboratory equipment. Ensure training of QC Analyst (Entry level Positions) Perform the Tracking System Deployment for Stability Samples/ Process Validation Samples etc. Perform the Training Tracking Tool/Software for QUALITY Assurance and Quality Control. Education : A minimum of a Bachelor's degree in Chemistry / Pharmaceutical Sciences or Equivalent. Experience: • 4+ years in the field of Pharmaceutical (manufacturing facility). • Background in the functional areas of Quality Control in Stability, Finished Goods and some Raw Materials with a some experience in Analytical R&D. Extensive knowledge in general laboratory equipment including but not limited to: GC, HPLC, Polarography, Particulate Matter, UV-Vis and FTIR Knowledge and Skill: Knowledge of cGMP, Validations and Qualifications, regulatory guidelines, US Pharmacopoeias, Internal auditing, Handling of regulatory Inspections, well acquainted with QMS, well versed with Change control/deviations and market compliant management system. Skills in coordination of calibration and preventative maintenance services, including but not limited to: setting up vendor contracts, processing quotes, generating purchasing orders and handling vendor invoices. Technical writing skills to generate SOPs and serve as the Subject Matter Expert. Completed training on Six Sigma, certified Green belt professional. Support the Management to organize and maintain the QC team, good communications skills, front runner, and GMP trainer. Will be an added advantage if the individual has dealt with multiple audits personally.

Perform sampling tasks throughout the plant site, field and off sites to support critical and core analysis for our operations, ensuring these samples are representative of the source. The Lab Sampling Technician will carry out routine and non-routine lab sampling of waters, sweet and sour gases and oils. Accountabilities / Responsibilities: • Support lab operation, safety and environmental systems • Support stake holders on projects, R&D and operations optimization • Troubleshoot plant process/sampling issues • Look for and lead efforts to improve processes and procedures as it relates to position • Carry out routine and non-routine lab sampling • Communicate with Operations on plant issues impacting sampling and safety • Ensure proper safety protocols are in place and in practice when performing duties • Identify issues that impact safety, environment and/or production Education / Professional Designations / Qualifications • Must be legally entitled to work in Canada • High school education, or equivalent • Valid driver's license with clean driving record • Laboratory and field experience • Ability to work long hours with physically demanding work, often outdoors and in the elements Work Schedule / Hours of work: 11hrs 26min per day, 7on / 7off schedule. 80hrs/rotatation

Outlier is the world's leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities. We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Chemistry. Develop and answer Chemistry-related questions to refine AI understanding. Assess and rank AI responses based on scientific rigor. Required expertise and qualifications: Education: Master's degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled) Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&D contributions English Proficiency: Ability to read and write with minimal errors Bonus Skills: AI model training experience is not required but helpful Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below) Opportunities for higher-paying research projects based on performance. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

Introduction Do you want to join an organization that invests in you as a Cardiac Cath Lab Tech? At Fairview Park Hospital, you come first. HCA Healthcare has committed up to $300 million in programs to support our incredible team members over the course of three years. Benefits Fairview Park Hospital, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include: Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more. Free counseling services and resources for emotional, physical and financial wellbeing 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service) Employee Stock Purchase Plan with 10% off HCA Healthcare stock Family support through fertility and family building benefits with Progyny and adoption assistance. Referral services for child, elder and pet care, home and auto repair, event planning and more Consumer discounts through Abenity and Consumer Discounts Retirement readiness, rollover assistance services and preferred banking partnerships Education assistance (tuition, student loan, certification support, dependent scholarships) Colleague recognition program Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence) Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income. Learn more about Employee Benefits Note: Eligibility for benefits may vary by location. You contribute to our success. Every role has an impact on our patients lives and you have the opportunity to make a difference. We are looking for a dedicated Cardiac Cath Lab Tech like you to be a part of our team. Job Summary and Qualifications OurCath Lab Technologistaccept the responsibility and accountability for the duties of a Radiology/Cardiac Technologist. Must be registered by the A.R.R.T. or Cardiovascular Credentialing (RCIS). Works in the Cardiac Cath Lab as a vital team member assisting the physician during invasive cardiovascular procedures such as angioplasty, catheterization, or electrophysiology. What qualifications you will need: Advanced Cardiac Life Spt must be obtained within 60 months of employment start date Basic Cardiac Life Support, or CPR must be obtained within 30 days of employment start date Registered Radiographer (ARRT), or Registered Cardiac Sonographer, or Registered Cardiovascular Invasive Specialist, or Cardiovascular Technologist (CV Tech) Certificate, or Vocational School Graduate Fairview Park Hospital is a 175+ bed acute-care hospital serving the City of Dublin, Laurens County, and the surrounding communities. Our hospital provides 24-hour emergency services, inpatient and outpatient surgery options, and rehabilitation therapy services. Other specialized programs include our Sleep Center at Fairview Park, the Same Day Surgery Center, the Heart Center at Fairview Park, the Womens Imaging Center and much more. We are committed to providing the best for our community. Our facility's stroke center scored A on Patient Safety Report Card. We have been named one of the nations top 100 hospitals by Truven Health Analytics, IBM Watson Health. At Fairview Park Hospital, our care like family culture extends to our patients, our people and our community. We are committed to each other because when we join together, our patients are cared for in the safest and most compassionate way. HCA Healthcare has been recognized as one of the Worlds Most Ethical Companies by the Ethisphere Institute more than ten times. In recent years, HCA Healthcare spent an estimated $3.7 billion in cost for the delivery of charitable care, uninsured discounts, and other uncompensated expenses. "Good people beget good people."- Dr. Thomas Frist, Sr. HCA Healthcare Co-Founder We are a family 270,000 dedicated professionals! Our Talent Acquisition team is reviewing applications for our Cardiac Cath Lab Tech opening. Qualified candidates will be contacted for interviews. Submit your resume today to join our community of caring! We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. RequiredPreferredJob Industries Other

The Lab Assistant plays a key role in supporting daily operations in a manufacturing environment. This position involves a blend of administrative, logistical, and housekeeping tasks to ensure operational readiness, compliance with safety standards, and high-quality customer service. The Lab Assistant must be comfortable working independently, handling physical tasks such as lifting, and operating in a regulated environment with strict adherence to safety, quality, and environmental protocols. Key Responsibilities Read, interpret, and follow technical procedures, safety protocols, and operational policies Package and prepare radiopharmaceutical medication for shipment; perform necessary testing and documentation Load and unload materials; process returned shipments Assist with receiving, checking in materials, and maintaining accurate inventory records Communicate logistical updates and changes, including courier coordination Answer phones, provide basic customer service, and assist with tracking deliveries Clean and sanitize delivery cases, workspaces, and high-touch surfaces regularly Support production and pharmacy teams with clerical tasks as needed Follow radiation safety procedures and complete required training programs (GMP, EHS, etc.) within 30 days Perform general facility cleaning and additional duties as assigned by the supervisor Must-Have Skills Excellent organization and time management Strong attention to detail Effective verbal and written communication Ability to read, listen to, and understand technical instructions and documentation Capable of lifting up to 100 lbs (most items range from 65-75 lbs, with handles) Nice-to-Have Skills Experience in logistics, shipping/receiving, or material handling Customer service experience Comfortable answering phones and interacting with vendors or customers

Rockwell, NC Responsibilities Perform the receipt and logging of incoming pharmaceutical ingredients Perform the sampling of incoming pharmaceutical ingredients for internal laboratory testing and shipment to external contract laboratories for testing Perform internal laboratory testing (e.g., organoleptic tests, identification (FTIR), pH, viscosity, specific gravity, chemical assays (HPLC), etc.) on incoming pharmaceutical ingredients, in-process samples, finished products and stability samples Calculate adjustments for in-process bulk product Prepare and review internal laboratory testing and external contract testing laboratory reports for raw materials, in-process samples, finished products and stability samples Prepare and review Certificates of Analysis Notify manager immediately of non-conforming data or unexpected occurrences Conducts laboratory investigations under the supervision of the laboratory supervisor Prepare and/or review test procedures, SOPs and protocols as assigned. Prepare and review IQ/OQ/PQ Protocols for production and laboratory equipment Perform IQ/OQ/PQ testing on production and laboratory equipment Complies with all regulatory/in-house requirements which may include but not limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP documentation Requirements Combination of advanced degree (such as Bachelors in Chemistry or related science) and 3+ years of experience in high volume manufacturing preferred; extensive years of experience in lieu of advanced degree is acceptable Previous experience within a cGMP compliant facility, Quality Control and USP Standards preferred Ability to perform physical sampling/testing and instrumental chemical analysis in the chemical laboratory (e.g., chromatography, infra-red spectroscopy, titrations, etc.) Excellent analytical and problem-solving skills Excellent time management and organizational skills Ability to work effectively in a fast-paced, rapidly changing environment Excellent people skills, with demonstrated ability to communicate effectively across functional groups Proficiency with Microsoft (MS) Office

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 50,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. 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, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. Job Description Eurofins BPT-Columbia is looking for an Scientist to join our TASC (Trace Analytical Structural Chemistry) team located in Columbia, Missouri. The Associate Scientist position is an intermediate-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. * 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 and a minimum of two years of experience in a directly relevant or demonstrated comparable competency and skill attainment is required. * A Master's degree in a relevant field may be substituted for the bachelor's degree and experience. * Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information Position is full-time, Monday-Friday 8am-4:30pm, with overtime as needed. Candidates who live within a commutable distance of Columbia, MO are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Ergon Asphalt and Emulsions, Inc., Sumter Coatings is seeking a full-time Formulation Chemist 1 to join our team. The Formulation Chemist is responsible for planning and executing laboratory activities to support existing business and new product development. This position will lead the formulation and testing of new products from the lab bench to commercialization to drive innovation in coatings technology. Must have more than 2 years of direct, hands-on experience with formulating 1K and 2K protective coating systems. Skills Required: * Knowledge and expertise in advanced chemistry concepts is required * 2 years of direct, hands-on experience with formulating 1K and 2K protective coatings systems; solvent-based epoxy is preferred * Strong knowledge of coating formulation techniques and testing procedures for commercial and light industrial applications * Knowledge of structure-property relationships is required * Familiarity with multiple coating systems (solvent-based, water-based, 1K, 2K, epoxy, alkyd, polyurethane, acrylic, etc.) is desired. * Good communication (verbal and written), problem-solving, interpersonal, and computer skills Education and Experience Requirements: * B.S. Chemistry * 2 years or more of related experience. Duties and Responsibilities: * Formulate new products by utilizing knowledge of structure-property relationships * Reformulate based on raw material cost performance or availability of raw materials * Evaluate competitors' products to identify similar or identical products * Serve as a technical resource to Production, Quality, Customer Service, and Sales * Analyze rejected products from quality assurance or customers and develop root cause analyses to prevent ongoing problems * Oversee multiple projects simultaneously, prioritizing tasks based on evolving priorities and deadlines to ensure timely delivery * Manage and review all formula information, specifications, analytics, and procedures, including preliminary manufacturing instructions * Regularly communicate results of laboratory work to internal and external parties as required * Ensuring formula compliance with industry standards * Other duties as assigned Why Ergon Inc.? At Ergon, we are a relationship-driven, family-owned company that values each employee's growth and contributions. Headquarters in Flowood, Mississippi, we take pride in maintaining a close-knit, small-company atmosphere while offering exceptional career opportunities. Our comprehensive benefits package includes: * Competitive pay * 401(k) matching & profit sharing * Health, Dental, Vision, and Life Insurance * Short- and Long-Term Disability Plans * Additional voluntary benefits * Paid holidays, vacation, and sick leave * Tuition assistance At Ergon Inc., we live by our core values: * Empowered Service: Together, we're committed to delivering unparalleled service. We do what's right, provide solutions, and foster stronger relationships with our teams and customers. Employee safety is our top priority and the first consideration in all aspects of our service. That's empowered service. * Selfless Leadership: We lead with compassion and put those around us before ourselves. We don't say we're experts; we demonstrate it through technical expertise, category innovation, and care for what we do. We call this selfless leadership. * Purposeful Growth: We believe employee growth and company growth go hand in hand. We build our legacy together to ensure future success through purposeful growth. The company has always reinvested tremendously back into the business, not just growing for the sake of growing but growing in a careful and strategic way. * Respectful Relationships: Together, we foster a culture of respect, acceptance, and diversity of ideas and people. Our differences make us stronger. We're united by our shared values, always forging respectful relationships. Come and join the Ergon team! Must be able to pass a pre-employment drug screen and background check. A clean MVR is required. We are an EEO/AAP employer. Job Role: Formulation Chemist 1 Location: Sumter, South Carolina Pre-employment background, drug and MVR

**Physical Location:** **_Multiple Locations- Must be willing to relocate in the immediate future and eventually travel up to 50% as needed._** **Pay Rate** : $65,100 - $86,800 Multiple factors, including Individual experience, skills and abilities will determine where an employee is ultimately placed in the pay range. Variable pay may provide additional opportunities for financial awards. This job is eligible to participate in IP's annual incentive plan. **Category/Shift** : Salaried Full-Time **The Job You Will Perform:** - Work under the daily guidance of the site controller as part of a division-wide finance development program, gaining exposure to all aspects of the Container business through formal training, cross-site job rotations, special projects, and mentorship from NAC Finance leadership. - Generally, serve as one of two exempt financial professionals at the manufacturing site, typically working alongside a team that includes non-exempt staff-offering valuable leadership and managerial development opportunities as you progress. - While building the skills necessary for future leadership roles within the Finance organization, provide support to the plant controller, plant general manager, region controller, and NAC division staff. - Key responsibilities include ensuring strong internal controls to protect company assets, preparing financial statements in accordance with professional and corporate standards, delivering timely and actionable financial analysis, identifying and proposing solutions to business challenges, and mentoring and developing accounting staff. **The Skills You Will Bring:** - Bachelor's degree in Accounting, Finance, or Business Administration, with at least 12 credit hours in Accounting - Minimum of 2 years' experience in an Accounting or Finance role; experience in a converting facility is a plus - Geographic flexibility and willingness to travel up to 50% during the training period - Strong initiative and self-motivation, with excellent written, verbal, and active listening skills - Proven ability to collaborate effectively and contribute to team success - Comfortable working in a manufacturing environment - Strong knowledge of general and cost accounting, including month-end close processes and financial statement preparation - Experience with developing, maintaining, and assessing internal controls - Strong analytical and financial skills, including budgeting, forecasting, KPI tracking, working capital management, and supporting special projects - Familiarity with financial and operational information systems, preferably SAP, including system oversight and management - Understanding of sales, marketing, and distribution processes - Knowledge of quality improvement and manufacturing processes, including root cause analysis and implementation of corrective actions **The Benefits You Will Enjoy:** International Paper offers a benefits package that includes health, welfare and retirement plans including Medical, Dental, Life insurance, Flexible Spending Accounts, Short-term and Long-term Disability, 401(k), Company-funded retirement contributions, Paid Time Off, Education & Development (including Tuition Reimbursement), Student Loan Repayment Assistance, and Voluntary Benefits including insurance for home, auto, vision and pets. **The Impact You Will Make:** We continue to build a better future for people, the planet, and our company! IP has been a good steward of sustainable practices across communities around the world for more than 120 years. Join our team and you'll see why our team members say they're **Proud to be IP** . **The Culture You Will Experience:** International Paper promotes employee well-being by providing safe, caring and inclusive workplaces. We have team members all around the world with diverse backgrounds, experiences, and perspectives. These are our strengths. We are committed to creating a culture where all individuals are respected, valued, engaged and have an opportunity to do their best work every day. We invite you to bring your uniqueness, creativity, talents, experiences, and safety mindset to be a part of our increasingly inclusive and diverse culture. **The Company You Will Join:** International Paper (NYSE: IP) is the global leader in sustainable packaging solutions. With company headquarters in Memphis, Tennessee, USA, and EMEA (Europe, Middle East and Africa) headquarters in London, UK, we employ more than 65,000 team members and serve customers around the world with operations in more than 30 countries. Together with our customers, we make the world safer and more productive, one sustainable packaging solution at a time. Net sales for 2024 were $18.6 billion. In 2025, International Paper acquired DS Smith creating an industry leader focused on the attractive and growing North American and EMEA regions. Additional information can be found by visiting internationalpaper.com Share this job: Location: STATE WIDE, FL, US, #STATE WIDE, UT, US, #STATE WIDE, KY, US, #STATE WIDE, MI, US, #STATE WIDE, WA, US, #STATE WIDE, OR, US, #STATE WIDE, NH, US, #STATE WIDE, MA, US, #STATE WIDE, SC, US, #STATE WIDE, IL, US, #STATE WIDE, CT, US, #STATE WIDE, IA, US, #STATE WIDE, LA, US, #STATE WIDE, NC, US, #STATE WIDE, WI, US, #STATE WIDE, GA, US, #STATE WIDE, MN, US, #STATE WIDE, VA, US, #STATE WIDE, MD, US, #STATE WIDE, TN, US, #STATE WIDE, OK, US, #STATE WIDE, AR, US, #STATE WIDE, SD, US, #STATE WIDE, CA, US, #STATE WIDE, NJ, US, #STATE WIDE, AZ, US, #STATE WIDE, NE, US, #STATE WIDE, OH, US, #STATE WIDE, ME, US, #STATE WIDE, RI, US, #STATE WIDE, AL, US, #STATE WIDE, NM, US, #STATE WIDE, NY, US, #STATE WIDE, KS, US, #STATE WIDE, NV, US, #STATE WIDE, PA, US, #STATE WIDE, CO, US, #STATE WIDE, MO, US, #STATE WIDE, IN, US, #STATE WIDE, MS, US, #STATEWIDE, VT, US, #STATE WIDE, TX, US, # Category: Finance Date: Apr 2, 2025 If you are not finding suitable opportunities, please click below to join our talent community!

Savannah River National Laboratory (SRNL) is seeking a Scientist focused on Metal Additive Manufacturing Research and Development for the Advanced Engineering Division. In this position, the candidate will be expected to develop an externally funded project portfolio aligned with SRNL mission enablers of data-driven materials development and developing manufacturing solutions for Environmental Management, the NNSA, and energy security. This will include leading and partnering on proposal teams as well as managing both technical and programmatic aspects of successfully won projects responsibilities. Responsibilities SRNL is seeking a self-motivated, dynamic researcher willing to actively promote a collaborative, interdisciplinary research environment in Metal Additive Manufacturing Candidate should possess a background and working knowledge of additive manufacturing techniques as well as the fundamental concepts and behavior of metallic materials. They should exercise judgment with practical engineering or scientific principles to determine an appropriate action. Applicants should have experience in proposal development, publications, and networking within their field. The Researcher will be expected to interface with and develop an externally funded project portfolio aligned with SRNL mission enablers of data-driven materials development and developing manufacturing solutions for Environmental Management, the NNSA, and energy security. This will include leading and partnering on proposal teams as well as managing both technical and programmatic aspects of successfully won projects. Works safely with particular attention to quality. Complies with all policies and standards. Additive Manufacturing areas of interest may include, on-machine monitoring, machine learning, alloy development, materials synthesis, process modeling, etc. Specifically sought-after skills include using feedstock characterization and analysis, equipment toolpath and parameter development, and characterizing printed metallic parts. Works well in a collaborative, multi-disciplinary team environment. Generates original ideas and conveys them effectively through strong written and oral communication. Mentoring student interns and projects is expected in the course of work. Maintaining a national presence at technical meetings - both internal to DOE and through professional organizations - is expected in the course of work. Qualifications Minimum Qualifications: Ability to obtain and maintain a security clearance, US Citizenship is Legally Required Ph.D. in related field with 5 or more years of relevant experience Successful candidates will have completed at least one post-doctoral appointment or 2 years of relevant work experience since completing their PhD. Successful performance as a principal investigator (PI) on interdisciplinary research projects. Preferred Qualifications: Preferred degrees: Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, Metallurgical Engineering, and Material Science and Engineering. Successful customer/sponsor relationship management Strong interpersonal communications both oral and written, along with problem solving skills. Cross-discipline knowledge in advanced scientific or engineering concepts Active DOE Clearance

We offer: * Year-round Full time permanent work * Paid overtime * Medical and dental benefits * Competitive wages * Safety boot allowance * Bonus programs * Staff social events. * All this at a single location where we provide the tools, PPE and safety training needed for the job. THE ROLE The Quality Technician, reporting to the QA Supervisor, plays a crucial role in upholding product and raw material quality, adhering to approved standardized specifications outlined in either IFS or Procurement Documents. Key responsibilities include conducting product qualification tests for manufactured items, developing calibration procedures, and maintaining in-house calibration tools. Additionally, the Quality Technician is responsible for maintaining consistent and well-documented inspection methods in accordance with established templates and industry standards. DUTIES AND RESPONSIBILITIES * Foster a culture of safety, ensure adherence to corporate safety regulations, and serve as a safety role model within the organization, including mentoring and disciplining team members as needed. * Support the development of Hazard Analysis and Safety Operating Procedures (HAA and SOP) while maintaining a safe working environment. * Establish and maintain material inspection policies, perform raw material and purchased good inspections, manage tool calibration, and oversee quality reporting, communication, NCR process participation, and DMP contributions for comprehensive quality control. * Maintain quality testing policies, schedule, and reporting for outgoing products, including NCR support, RCA coordination, and NCR Performance Index management. * Assist in quality audits by coordinating issue corrections and ensuring conformance with work instructions and product specifications, including support for SMS and ISO audits. * Facilitate quality communications across the organization, updating the Quality Alert board, and informing stakeholders about NCRs, material deviations, corrective actions, process deviations, and other quality-related activities. * Generate and deliver necessary product certifications for customer requirements and provide quality documents to relevant departments and customers. * Document instances of product non-conformance, reporting them in writing and verbally to designated personnel, and provide comprehensive support for departmental documentation needs, including NCRs, CARs, SCARs, and work instructions. * Engage in data collection, continuous improvement activities, and Lean Enterprise initiatives, supporting best practices for SMS and contributing to corporate optimization efforts as necessary. * Provide cross-departmental support to address quality issues, mentor the production team on inspection methods, and maintain workspace safety and cleanliness through 5S duties. * Engage in cross-training, support manufacturing initiatives, and cultivate a reputation as a go-to resource for quality-related support while fulfilling any other assigned duties. REQUIRED QUALIFICATIONS * Completion of high school with 1-2 years of related experience. * Ability to work effectively both independently and as part of a team. * Strong teamwork, communication (verbal & written) and interpersonal skills. Applications will be accepted until the position is filled. We thank all applicants for their interest, but only those selected for an interview will be contacted. Nearest Major Market: Columbia Nearest Secondary Market: South Carolina