Chemist jobs in South Carolina

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

We are seeking a detail-oriented Staff Chemist/Scientist to join our team in Massachusetts. Our ideal candidate has a B.S. in Chemistry to support our growing chemistry practice (functions listed below) and will also appreciate participating in field work to help during surges in field work and/or if the chemistry practice workload is light. The selected candidate will work both independently and as part of a larger team to execute environmental investigation and remediation projects. This position is remote while performing office duties, and daily travel to job sites in Middlesex County, Massachusetts required while conducting field work. Infrequent overnight travel to support field work may be needed, but is negotiable. Key Responsibilities: - Support the development of UFP-QAPPs and other technical reports. - Assist in the preparation of laboratory and data validation scopes of work and bid sheets. - Evaluate and interpret laboratory data, regulations, and other relevant information. - Coordinate with laboratory and field teams for bottle ware orders and resolve issues during field investigations. - Respond to laboratory inquiries during sample analysis. - Track field samples and manage laboratory and data validation processes for field investigations. - Set up and manage FUDSchem or similar event management systems, including approvals and exports. - Support environmental fieldwork, including groundwater and soil sampling. Skills: - Strong analytical and problem-solving skills. - Excellent communication and coordination abilities. - Proficiency in data evaluation and interpretation. - Familiarity with environmental regulations and laboratory procedures. - Experience in field sampling techniques and data management. - Ability to work collaboratively in a team-oriented environment. We encourage candidates with diverse backgrounds to apply and join our commitment to environmental excellence. Job Type: Full-time Benefits: · 401(k) · 401(k) matching · Dental insurance · Flexible spending account · Health insurance · Life insurance · Paid time off · Vision insurance Schedule: Monday to Friday Requirements: Position Requirements: · Bachelor's degree in chemistry · 2-5 years' relevant experience · Detail oriented · Excellent written and verbal communication skills · Ability to pass a background check in order to access military bases · Valid driver's license · PFAS experience a plus · US Department of Defense experience a plus

Job type: Full-Time Type of role: On-Site About Lubrizol The Lubrizol Corporation, a Berkshire Hathaway company, is a specialty chemical company whose science delivers sustainable solutions to advance mobility, improve wellbeing and enhance modern life. Founded in 1928, Lubrizol owns and operates more than 100 manufacturing facilities, sales, and technical offices around the world and has about 8,000 employees. For more information, visit ***************** We value diversity in professional backgrounds and life experiences. By enabling a consistent, unbiased, and transparent recruitment process, Lubrizol seeks to create a positive experience for candidates so we can get to know them at their best. We recognize unique work and life situations and offer flexibility, ensuring our employees feel engaged and fulfilled in every aspect of life. Join Our Thriving Team as a Quality Control Chemist! Unleash Your Potential. At Lubrizol we're transforming the specialty chemical industry and looking for exceptional talent to join us on this journey. If you are ready to join an international company with talent around the world, and want to make a real impact, we want you on our team. What You'll Do: Lubrizol's QC Chemists are responsible for supporting manufacturing operations through the application of chemical expertise, quality assurance practices, analytical instrumentation knowledge, and oversight of the facility's Quality Management System. This role ensures product integrity and regulatory compliance with our ISO9001, RSPO and Halal certifications by overseeing chemical processes, maintaining laboratory equipment, and implementing quality control procedures. The incumbent will collaborate with cross-functional teams to resolve process issues, support continuous improvement initiatives, and uphold safety and environmental standards. What We're Looking For: * Oversee chemical processes within the plant to ensure product quality, safety, and regulatory compliance. * Support and maintain analytical instrumentation (e.g., GC, ICP, FTIR, spectrophotometers) used in quality control and process monitoring. * Manages the site's ISO 9001, RSPO, and Halal standards. * Maintains KPI's for QC targets. * Maintains Quality Management System to retain certification, including documents control system, preventative and corrective action systems and internal auditing function. * Develop and implement quality assurance protocols to ensure consistent product performance. * Conduct routine and non-routine chemical analyses to support production and resolve process deviations. * Collaborate and partner with Process Engineers and operations to identify and address process and quality issues to optimize plant performance & capability. * Lead investigations into non-conformances and implement corrective and preventive actions (CAPAs). * Maintain accurate documentation of analytical results, calibration records, and quality reports. * Provide and document training for laboratory staff on quality procedures and process changes. * Lead and support continuous improvement initiatives focused on process optimization and quality enhancement. * Ensure compliance with environmental, health, and safety regulations related to chemical handling and laboratory operations. * Apply Statistical Process Control (SPC) and Statistical Quality Control (SQC) methodologies to support production and quality control operations. * Manage Out of Specification (OOS) results and process deviations from a quality perspective. * Ensure adherence to Standard Work Processes (SWP), Management System protocols, and analytical standards. * Provide technical guidance and analytical support to Production Units and the Quality Control Laboratory. * Collaborate with cross-functional teams to achieve quality and capacity goals, with a focus on reducing Non-Conforming Materials (NCMs). * Ensure reliability of analytical data and instrumentation used in process and quality monitoring. * Assist in developing and implementing continuous improvement initiatives related to quality and process performance. * Support documentation, reporting, and compliance with internal and external quality standards Skills That Make a Difference: * Bachelor's degree in chemistry or related field. * 5years+ Quality Control experience in chemical manufacturing, chemical processing, or related industrial experience. * Knowledge of ISO 9001, RSPO, and Halal standards is preferred * Experience in chemical manufacturing with Esters, Emulsifiers, Phosphations and Aminations * Proven experience in project management or working on projects * Experience with Agilent Gas Chromatographs, ChemStation software and ICP are pluses. * Ability to effectively & efficiently communicate both verbally & written in English * Ability to problem-solve by trouble shooting & critically thinking. * Experience working as a team and cross-functionally. * Strong attention to detail / detailed oriented * Ability to multi-task and prioritize task by urgency * Self-Motivation (takes initiative & works independently) * Interpersonal skill+ Physical, Regulatory, & Safety Requirements * Ability to lift and handle objects weighing up to 40 lbs * Ability to discern colors, read burettes, and has physical capability to operate instrumental analysis equipment. * Ability to successfully complete and maintain safety training requirements Ready for your next career step? Apply today and let's shape the future together! It's an exciting time to be part of Lubrizol. Lubrizol is not staying put. We are continually learning and evolving. Our passion delivers our success - not only for Lubrizol but for those who count on us every day: our employees, customers and communities. We work with a relentless commitment to operate safely and responsibly, keeping safety, sustainability, ethics, and compliance at the forefront of everything we do. The well-being of our employees, customers and communities is paramount to our culture and in the way we approach our work. As a diverse, global team, we work together to solve some of the world's most pressing challenges. We impact everyday lives through science only Lubrizol can deliver, and we never stop pushing to do it better. One of the founding principles of The Lubrizol Corporation more than 90 years ago was treating every employee with dignity and respect. That same commitment is only stronger today. More than that, we are committed to providing an environment where every employee can be the best they can be, no matter their race, color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status or any other characteristic. #LI-LT1 #LBZUS

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

Seneca, SC, US, 29678 Leveraging its deep expertise as the global leader in catalysis and precious metals, BASF Environmental Catalyst and Metal Solutions (ECMS) serves customers in many industries including automotive, aerospace, indoor air quality, semiconductors and hydrogen economy, and provides full loop services with its precious metals trading and recycling offering. With a focus on circular solutions and sustainability, ECMS is committed to helping our customers create a cleaner, more sustainable world. Protecting our elements of life is our purpose and this inspires us to ever-new solutions. ECMS operates globally in 15 countries with approximately 20 production sites and over 4,000 employees. **As a Chemist you will LEAD by..........** We are seeking a professional like you to be a member of the Precious Metal Chemicals (PMC) and Refining Group based at our Seneca SC site. In this role, you will be responsible for leading and managing product and process optimization projects. Potential projects consist of new product introduction and process optimization, cost reduction efforts and process improvements to enhance operational excellence. A strong focus will be on laboratory skills and interfacing with operations and engineering personnel for chemical manufacturing support at scale. The PMC scope of these efforts can range from collaboration on initial lab development through scale up and plant scale support. The Refining scope will focus mainly on process trouble shooting and process optimization. **_In this role you will_** + Work on producing PMC products, new product introduction, process optimization and process troubleshooting. + Identify and evaluate best practices for both the PMC and Refinery operations. + Take ownership of and assist in leading best practices in the laboratory, while supporting best practices at scale + Generate ideas on how to achieve production targets through your familiarity with multiple related disciplines, technologies, and processes. + Address EHS requirements in your areas of responsibility with the goal of meeting standards for Zero Incident and Zero Loss of Containment Mindsets. + Collaborate to complete process optimization, plant trials requiring effective interaction with multiple groups including Production, Product Management, Process Technology and EHS for scale-up of new products, improved manufacturing processes of existing products or processes. + Maintain technical accountability, develop, and communicate detailed process improvement proposals, communicate, and present process trial results, and lead the completion of projects of responsibility. + Provide laboratory skills training to the site PMC and Refinery technical and operations resources as needed. + Collaborate with global precious metal and refining technical resources during plant trials and project meetings. This position is a BB4 and will report to Ana Barrios Sosa. **Your elements for success......** + _Bachelors degree in Chemistry or a related field required_ + _Experience in precious metals or inorganic chemistry preferred_ + _Familiarity in scale up concepts and chemical manufacturing support preferred_ + _The ability to self-lead and drive innovation_ + _Strong attention to detail and effective record keeping skills_ + _Strong communication skills_ + A commitment to quality and workplace health and safety **_You @ BASF ECMS_** At BASF ECMS you get more than just compensation, Medical & Dental. Our total offer includes a wide range of elements you need to be your best in every stage of your life. + Flexible Work Arrangements whenever possible + Retirement Benefits with company contributions + Competitive Medical and Dental Plan Options + Disability and Life Insurance Programs + Wellness Programs + Maternity/Paternity Leave, Infertility & Adoption reimbursement + Mentoring & Development Programs + Employee Discounts + Pet insurance **_What are you waiting for? Click Apply now to BELONG@BASF!!_** BASF takes security & data privacy very seriously. We will never request financial information of any kind via email, private text message or direct message on any social medial platform or job board. Furthermore, we will never send a candidate a check for equipment or request any type of payment during the job application process. If you have experienced any of the above, please contact ******************************** to report fraud. BASF is committed to pay transparency practices. The competitive Pay Range for thisrole is $80k-$95k annually. Actual pay will be determine based on education, certifications, experience, and other job-related factor permitted by law. **All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status.** **Nearest Major Market:** Greenville **Nearest Secondary Market:** South Carolina

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

Chemical Technician Greenwood Fabricating & Plating Greenwood, SC $21.00-$26.00 per hour, with opportunities for overtime. Full benefits package including health, dental, and retirement options. Paid training and all required PPE provided. Steady, year-round work in a growing industry. We are looking for a reliable and safety-focused Chemical Maintenance Technician to join our team in a metal plating facility. In this role, you will be responsible for cleaning chemical tanks, adding chemicals on schedule, and performing general maintenance and housekeeping to keep operations running smoothly. Key Responsibilities: Safely clean and maintain plating and process tanks. Add chemicals according to a set schedule and established procedures. Handle, label, and store chemicals safely. Maintain a clean and organized work area. Follow all safety rules, wear required PPE and participate in safety training. Support other maintenance and production tasks as needed. Education, Experience, Skills, & Abilities: High school diploma or equivalent. Experience working with chemicals or in a manufacturing/maintenance setting is a plus. Strong attention to safety and detail. Ability to follow written and verbal instructions. Comfortable wearing PPE and working in environments with chemicals and machinery. Ability to work in a non-climate-controlled environment. Must be able to lift to 70 lbs. at frequent intervals Requires standing, stooping, and bending more than 50% of the time. Basic computer or recordkeeping skills. Work Environment Industrial plating facility with chemical exposure. PPE (gloves, goggles, respirator, apron, etc.) provided and required. May require overtime or weekend shifts depending on business needs.

Selene Holdings is a multiple-lines business financial services firm with a mortgage servicing company, a loan diligence company, a title company, an insurance brokerage, and a real estate owned company. We have office locations in Dallas, TX, Jacksonville, FL, and Salt Lake City, UT. Founded in 2007 to address needs in the mortgage industry, Selene strives to provide amazing client and borrower experiences. A positive attitude coupled with proven creative thinking and actions are all attributes we seek in every one of our employees. If you want to make a difference, then Selene is the place for you! Position Summary: Our full-time Diligence Quality Control III is focused on controlling a high quality product, coaching and improving front to back knowledge and acting as go to subject matter expert for specialist topics. Essential Duties and Responsibilities include the following. Other duties may be assigned. Responsible for the Quality Control examination of loan reviews completed by Loan Review Analysts. Provide real time feedback to Loan Review Analysts pertaining to errors and determining corrective actions. Ensure regulatory compliance for loans reviewed. Identify trends of errors and escalate to management/legal. Develop deep understanding of specific client guidelines. Handle escalated and countered client conditions with minimal guidance. Assists with loan review system testing and enhancement. Acts as a subject matter expert on particular topics for Loan Review Analysts and other QCs, assisting with problem solving, issue resolution and loan review guidance. Provides guidance on daily matters, such as, questions regarding Underwriting Guidelines or Compliance questions relating to TRID, Reg X, TILA or others to QCs and LRAs. Maintains high level of confidentiality to protect privacy rights. Adheres to internal controls to reduce errors and customer complaints. Responsive to internal and external customers' needs in a timely, accurate and professional manner. Run QC the QC control checks in addition to Loan Review Analyst QC checks. Review and enhance procedures and address issues that may hinder accuracy, timeliness and or deadlines. Provides coaching and training to staff to ensure company and department goals and key performance indicators (KPIs) are met. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The qualified candidate must have: Maintains a current knowledge of underwriting guidelines, investor guidelines, regulatory compliance and TRID practices. Minimum 5-7 years mortgage underwriting and mortgage quality control within the origination or due diligence space. Strong understanding of condition clearing processes and their impact on loan grades. Good understanding of the credit rating agency requirements. Good knowledge of USPAP standards, supplemental valuation products and reconciliation. Ability to produce underwriting reports, analyze results, identify issues and take corrective actions. Experienced with reading, analyzing and understanding various loan servicer pay histories and servicing documentation. Developing leadership skills with the ability and experience to manage people. Effectiveness as a team player. Ability to easily prioritize job duties according to the needs of the company. Strong sense of professionalism and positivity. Excellent oral and written communication skills. Ability to develop rapport with all levels of associates and establish credibility. Excellent listening skills and the ability to use good judgment. Strong interpersonal/relationship building skills. Problem solving and decision making ability. Ability to produce quality work. Ability to think and solve problems strategically. Strong analytical and organizational skills. Excellent attention to detail. Ability to multi-task and consistently meet multiple deadlines. Education/Experience: Minimum 5-7 years' experience with emphasis on non-agency underwriting and QC desired. Experience in second level reviews; escalations and performance management required. Bachelor's degree preferred. Computer Skills: Working knowledge of and experience with Microsoft Office (Word, Excel, and Outlook). Previous experience with mortgage due diligence software, Andor, MSP, Black Knight/LPS and Fiserv preferred. Why Selene? Benefits Selene Finance LP is committed to the total wellbeing of its employees and therefore offers one of the best benefits packages available in the industry today, which includes: Paid Time Off (PTO) Medical, Dental &Vision Employee Assistance Program Flexible Spending Account Health Savings Account Paid Holidays Company paid Life Insurance Matching 401(k) Plan The job requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description is not an inclusive list of all duties and responsibilities of this position. Incumbents will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. Selene reserves the right to amend and change responsibilities to meet business and organizational needs. Privacy Policy - Selene (seleneadvantage.com)

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

Job Requirements TBC

This position works under minimal supervision and is primarily responsible for the understanding and development of basic to complex colors for specific applications and scaling up in any production facility with the purpose of advancing the growth of Oterra and FIS by Oterra. The position will have direct relationship with the commercial team, functioning as the technical advisor to the internal salesforce at FIS by Oterra. The successful applicant will have a strong background in food science, preferably food chemistry. The applicant should have experience with Project management, specifically within Product Development, and preferably experienced in interacting cross-functionally with Production, Quality and Sales acting as the technical expert. Experience with analytical chemistry, method development and validation is a plus. Principal Duties And Responsibilities: Handles simple to complex color formulation projects in a timely manner. Interacts with external customers, sales, applications scientists, and other departments internally as needed in defining specific parameters for projects. Serves as project manager for simple to complex development projects from conception through launch by following a defined launch excellence process. Develops simple to complex color formulation at a bench level in a timely manner aligned with customer needs. Scales up from bench to any global production facility. Conducts in-person consultation with customers from conception through commercialization in their facilities. Serves as local technical expert for color formulations for the local sales team. Supports production with upscaling and troubleshooting. Maintains safe working environment by practicing and coaching in established safety procedures. Learns and uses processing equipment in lab and pilot with minimal supervision. Provides training for QC and production personnel in new formulations and analytical methods. Knowledge, Skills & Abilities: B.Sc. or M.Sc. in Food chemistry, Food Science, Pharmaceutical Science or related field with 5+ years of relevant experience. Strong experience with Project and stakeholder management, preferably experience with managing development projects. Deep knowledge of food ingredients and processing. Experience with color ingredients is an advantage. Experience with customer interaction and driving customer projects. General understanding of analytical techniques and food quality and safety. Ability to read, collect data, analyze, and interpret technical information, as well as write and present reports and technical papers. Ability to distinguish colors in a wide variety of applications and media. Must have excellent color vision. (Color Vision Testing Required.) Working Conditions: Working environment is generally favorable. Lighting, temperature and noise levels are adequate with occasional exposure to cold temperatures. Personal Protective Equipment is required when working in the laboratory. This includes a lab coat, and if necessary, safety glasses, dust mask or gloves. When working in the production plant, a hair/beard net, safety glasses and safety shoes are required and GLP/GMP guidelines must be followed. The job is onsite in Mt. Pleasant, WI and Travel up to 25% of working time is required. Physical Demands: While performing the duties of this job, the employee is frequently required to stand, walk, talk and hear. The employee is regularly required to lift and/or move materials or equipment up to 25 lbs. and occasionally required to lift up to 50 lbs. Use of hands to handle or touch objects, tools or controls is frequently required. Specific vision abilities required by this job include vision, color vision, depth perception and the ability to adjust focus. Employee is occasionally exposed to moving mechanical parts, fumes or airborne particles and toxic or caustic chemicals. What We Offer: Comprehensive Health Coverage - Medical, Dental, and Vision Plans to support you and your family on your first day of employment 401(k) Retirement Plan with Employer Match - Plan for your future with company-supported retirement savings Paid Time Off - Enjoy a healthy work-life balance with PTO and 11 Paid Holidays Paid Parental Leave -Maternity and Paternity Leave so you can focus on what matters most Employee Engagement - Join our Engagement Team for fun events, volunteer opportunities, and ways to connect with colleagues across the company

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

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.

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

Job Details Rock Hill, SC Plant - Rock Hill, SC Full Time 2nd ShiftDescription 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

Job Description 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 Powered by JazzHR dc BFNICW51

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

We are seeking highly professional and skilled Spray Technicians. The Spray Technician will be responsible for delivering and maintaining a healthy dynamic appearance for a variety of turf, shrubs, and trees at different locations. What would my responsibilities be? Perform chemical and fertilizer applications on assigned high-profile properties. Scout properties beyond assigned needs for any issues. Report to Manager for direction to treat while on-site or future scheduling. Complete a pre-trip inspection report on vehicle, trailers, and equipment daily. Contribute to our safety culture by attending and actively participating in weekly safety trainings. Follow company safety protocols, identify, and communicate safety issues to the team. Why Join Yellowstone? Competitive hourly pay, paid weekly Benefits package including health, dental and vision insurance, 401k with a company match Industry-leading safety programs Company provided safety gear Equipped with optimal and most professional equipment High profile customers, worksites, and landscape results -A company that values and appreciates YOU Requirements Legal authorization to work in the United States Ability to diagnose insect, disease, and weed issues in the field. One year of experience in fertilization and chemicals Must have reliable transportation to the Branch or first job site Safe driving record and ability to successfully pass a Motor Vehicle Report (“MVR”) required Strong English communication skills. Spanish a plus Become part of the team dedicated to Excellence in Commercial Landscaping

Chemical Lab Technician Greenwood Fabricating & Plating Greenwood, SC $22.00-$26.00 per hour. Full benefits package including health, dental, and retirement options. Paid training and all required PPE provided. Steady, year-round work in a growing industry. We are seeking a meticulous and detail-oriented Chemical Laboratory Technician to join our team. In addition to performing standard laboratory duties, this role will take on the critical responsibility of ensuring compliance with chemical labeling regulations across the plant. The ideal candidate will have a strong understanding of laboratory procedures, chemical safety protocols, and regulatory standards. Key Responsibilities: Conduct laboratory tests and analyses to support scientific investigations. Prepare, test, and analyze chemical solutions, samples, and reagents. Maintain, calibrate, and troubleshoot laboratory equipment. Record and interpret test results, ensuring accuracy and reliability. Develop and implement a plant-wide chemical labeling compliance program. Ensure all chemical containers are properly labeled according to OSHA's Hazard Communication Standard (HCS) and the Globally Harmonized System (GHS). Conduct regular audits to verify compliance with labeling and safety data sheet (SDS) requirements. Train employees in chemical labeling protocols and hazard communication standards. Collaborate with safety personnel to address compliance issues. Maintain an inventory of chemicals and ensure proper storage and handling procedures. Assist Lead Lab Technician with other duties as assigned. Education, Experience, Skills, & Abilities: High school diploma or equivalent. Experience working with chemicals or in a manufacturing/maintenance setting is a plus. Strong attention to safety and detail. Ability to follow written and verbal instructions. Comfortable wearing PPE and working in environments with chemicals and machinery. Ability to work in a non-climate-controlled environment. Must be able to lift to 70 lbs. at frequent intervals Requires standing, stooping, and bending more than 50% of the time. Basic computer or recordkeeping skills. Work Environment Industrial plating facility with chemical exposure. PPE (gloves, goggles, respirator, apron, etc.) provided and required. May require overtime or weekend shifts depending on business needs.