Chemist jobs in South Carolina - 57 jobs

**Our Mission** As the world's number 1 job site*, our mission is to help people get jobs. We strive to cultivate an inclusive and accessible workplace where all people feel comfortable being themselves. We're looking to grow our teams with more people who share our enthusiasm for innovation and creating the best experience for job seekers. (*Comscore, Total Visits, March 2025) **Day to Day** At Indeed, our mission is to _Help People Get Jobs_ . We are seeking a visionary Senior Marketing Data Scientist to define and drive our data science endeavors for Indeed's Marketing organization.The Marketing Data Science and Business Intelligence (MDSBI) organization partners with Marketing and collaborates across the SMB, Job Seeker, Brand, Enterprise, and Global Marketing teams. Your role will entail shaping and executing Indeed's AI strategy for Marketing measurement and driving optimal allocation and returns on our Marketing spend. You will guide our organization in pursuing the strategy and, through innovation, make a meaningful impact on the lives of millions of people who use Indeed every day. As AI technology, Marketing and job markets evolve rapidly, your role will be essential in shaping the future of acquisition for both job seekers and employers. **Responsibilities** + Build and improve all components of our Marketing measurement framework including Marketing Mix models, Multi-Touch attribution and Incrementality testing. + Mentor and grow other data scientists, data engineers and Machine Learning Engineers across teams. + Communicates how campaigns, campaign measurement and business outcomes can be transformed with Machine Learning (ML) and AI across the broad organization + Partner with cross-functional teams to implement data-driven solutions that enhance user and marketer experiences + Foster external partnerships, stay updated with industry trends, and ensure our data practices remain at the forefront of technological advancements **Skills/Competencies** + Bachelor's Degree in Computer Science, Mathematics, Statistics + 7+ years of experience in data science, analytics, Machine Learning or a related field + Prior success in deploying impactful Machine Learning solutions to large-scale production systems, while engaging across teams + A deep understanding of machine learning, statistical modelling, and predictive analytics. + Deep understanding of the complexities and tradeoffs of leveraging/deploying ML/AI at scale and experience using LLMs + Proven ability to translate complex data findings into actionable business strategies and experience in collaborating with marketing or product teams to drive business growth + Experience communicating and influencing marketing, technical, and business direction across all levels of a large organization + Knowledge and practical experience working on Deep Learning Libraries (like Torch, Tensorflow, etc.) **Salary Range Transparency** US Remote 154,000 - 224,000 USD per year Austin Metro Area 154,000 - 224,000 USD per year NYC Metro Area 171,000 - 247,000 USD per year Seattle Metro Area 164,000 - 239,000 USD per year San Francisco Bay Area 180,000 - 260,000 USD per year **Salary Range Disclaimer** The base salary range represents the low and high end of the Indeed salary range for this position in the given work location. 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We are committed to providing individuals with criminal records, including formerly incarcerated individuals, a fair chance at employment. Those with military experience are encouraged to apply. Equivalent expertise demonstrated through a combination of work experience, training, military experience, or education is welcome. **Indeed's Employee Recruiting Privacy Policy** Like other employers Indeed uses our own technologies to help us find and attract top talent from around the world. In addition to our site's user and privacy policy found at **************************** , we also want to make you aware of our recruitment specific privacy policy found at ****************************/indeed-jobs . **Agency Disclaimer** Indeed does not pay placement fees for unsolicited resumes or referrals from non-candidates, including search firms, staffing agencies, professional recruiters, fee-based referral services, and recruiting agencies (each individually, an "Agency"), subject to local laws. An Agency seeking a placement fee must obtain advance written approval from Indeed's internal Talent Acquisition team and execute a fee agreement with Indeed for each job opening before making a referral or submitting a resume for that opening. **Reference ID:** **46455** **The deadline to apply to this position is [1/16/2026]. Job postings may be extended at the hiring team's discretion based on applicant volume.** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Reference ID: 46455

We are looking to fill a **Scientist 3 -** **Third Shift** **Analytical Chemist Pilot Plant** 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. **Description** The Scientist III **Third Shift** - Analytical Chemist Pilot Plant operates and maintains a myriad of analytical instrumentation and other duties as assigned by the client. **Responsibilities** + Experience in routine and real-time testing for high-performance liquid chromatography (HPLC), gas chromatography (GC), ultraviolet (UV) spectroscopy, infrared (IR) spectroscopy, titrations, Karl Fischer (KF) testing, and other wet chemistry methods + Experience in HPLC and GC is required with an interest in expanding the knowledge and background in method development and optimization, validation, data analysis, and sample preparation techniques + Routine use of modern analytical techniques such as HPLC, GC, KF, ultraviolet-visible spectroscopy (UV-VIS), and IR spectroscopy + Comfortable working in a cGMP environment; knowledgeable in various GMP analytical activities, such as documentation procedures, abiding by relevant department SOPs and generation and second scientist review of GMP data + Experience with automated liquid handling systems (Tecan) for high throughput testing + Experience with a myriad of software platforms used in the compilation, processing, and reporting of data, such as Waters Empower, Relational Laboratory Information Management System (RLIMS), Lab X, etc. **Qualifications** + BA/BS (3-5 yrs.) of relevant experience in n chemistry or a related discipline testing lab + MS (1-2 yrs.) of relevant experience in chemistry or a related discipline testing lab **Desired Skills and Experience** + Effective organizational, multi-tasking, and oral/written communications skills + Ability to work under pressure and provide reliable results with quick turnarounds + Consistently deliver high quality and fully compliant results and interact with a diverse customer base daily + Proficient in written and spoken English, is required **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Job type: Full-Time Type of role: On-Site 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

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods. We are seeking a skilled and detail-oriented chemist with a strong background in analytical chemistry and laboratory operations to join our team. This role is ideal for a motivated individual with a passion for science, problem-solving, and collaboration in a dynamic laboratory setting. Work Schedule: Monday - Friday 8am-5pm JOB QUALIFICATIONS: Bachelor's degree in Chemistry or a related science from an accredited institution, with 2-4 years of relevant laboratory experience in the pharmaceutical industry, or 2+ years of experience as a Chemist I; or an equivalent combination of education and experience. Expertise of GLP, cGMP, FDA and other regulatory requirements. Proficiency in laboratory instrumentation, including UV/Vis, FTIR, HPLC, and GC. Strong foundation in analytical chemistry. Experience with laboratory software and applications such as HPLC, FTIR, UV, LIMS, Lab Calc, and GC. Knowledge of sampling methods and quality control systems. Proficiency in quantitative and qualitative analysis, including the application of statistical methods. Knowledge of sample preparation techniques. Excellent communication skills, both written and verbal. Ability to establish and maintain cooperative working relations. Ability to manage multiple projects, duties and assignments. POSITION RESPONSIBILITIES: Adhere to organizational policies and procedures, as well as state, federal, and local laws. Ensure compliance with current Good Laboratory Practices (cGLP), current Good Manufacturing Practices (cGMP), safety requirements, and laboratory Standard Operating Procedures (SOPs). Conduct scheduled preventive maintenance and calibration of laboratory instrumentation (i.e., pH meter, HPLC, dissolution equipment, etc.). Prepare standard and sample solutions as required by the test methods. Operate general analytical instruments for all routine testing (i.e., HPLC, GC, UV/Vis, automatic titrator, and FTIR). Perform wet chemistry tests on raw material (i.e., LOD, Assays, pH, titration, etc.). Perform analyses on intermediate and finished products. Maintain appropriate documentation (records and lab notebooks) as required by SOPs. Comply with good housekeeping and safety practices. Participate in troubleshooting of analytical test methods and laboratory instruments. Take part in the training program as a qualified trainer, as requested. Assist in troubleshooting and problem solving. Accurately and precisely perform testing. Perform related duties as assigned. PHYSICAL REQUIREMENTS: Employees in this class are subject to extended periods of sitting, standing, walking, lifting materials weighing up to 50 pounds, vision to monitor, moderate to loud noise levels. Incumbents may be exposed to or work with toxic materials, toxic gases, electrical hazards, and dangerous tools and equipment. Work is performed in an office or laboratory environment. Incumbents must be able to use personal protective equipment (e.g. respirators, gloves, etc.). BENEFITS: PLD is a proud equal opportunity employer offering many corporate benefits, including: Medical and Dental Benefits Vision 401K with employer match Group Life Insurance Flex Spending Accounts Paid Time Off and Paid Holidays Tuition Assistance Corporate Discount Program Opportunities to Flourish Within the Company The EEO statement needs to be included in the detailed description... PL Developments 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 veteran status. #HP1

Mark Anthony Group is an entrepreneurial drinks company, built from the ground up by thinking differently, innovating and doing the unexpected. Our company is rooted in family values, a bold vision and relentless determination to continuously raise the bar and make a positive difference in consumers' lives. Founded in 1972, we've grown organically from a one-person import wine business into an international drinks company whose hallmarks include a portfolio of luxury wineries and iconic beverage brands, including White Claw Hard Seltzer, Mike's Hard Lemonade and Cayman Jack. The Role Are you ready to shape the future of beverage quality and innovation? We're seeking a passionate and driven Senior Chemist to join our team-based in either Columbia, South Carolina or Glendale, Arizona-who will play a pivotal role in elevating our laboratory standards across the US and beyond. As a Senior Chemist, you'll be at the forefront of developing and implementing cutting-edge analytical methods for routine testing and product development. You'll lead the charge in method development, ensure our instrumentation is performing at its best, and oversee critical lab operations. Your expertise will empower chemists across multiple sites, as you mentor and guide them to new heights of technical excellence. Key Responsibilities: * Analytical Method Development: Design, validate, and review methods for raw materials, in-process, and finished goods (GC/MS, HPLC, ICP/MS, etc.). * Instrumentation Leadership: Oversee maintenance, troubleshooting, and vendor partnerships (Agilent, Thermo Fisher); ensure instrument reliability and uptime. * Routine Analytical Testing: Deliver timely, accurate results for production and innovation projects. * Quality & Compliance: Support ISO/GFSI standards, food safety protocols, and process improvement initiatives. * Mentorship & Training: Lead SOP development and hands-on training for chemists; manage the Chemistry Working Group and cross-site alignment (Columbia, Glendale, Vancouver). * Cross-Functional Collaboration: Partner with R&D, Product Development, and Liquid Technology teams to drive innovation and process optimization. * Software Systems: Utilize ETQ, QAR, Starlims, and instrument-specific software for lab operations and data management. Who You Are: * Bachelor's Degree in Chemistry (or similar) with at least 8 years of relevant experience. * 5+ years in method development and 5+ years maintaining analytical instrumentation. * Sufficient academic credits to apply for TTB Chemist certification (does not need to be certified but must be eligible to apply). * Experience with Agilent and Thermo Fisher instrumentation. * Familiarity with ETQ, QAR, Starlims, and related lab software. * Strong problem-solving, critical thinking, and cross-functional collaboration skills. * Comprehensive knowledge of quality assurance and food safety in beverage manufacturing. * Process optimization techniques for product consistency. * Ability to multitask, prioritize, and escalate effectively. * Open, honest communication and feedback style. * Highly organized, humble, and dedicated to continuous improvement. * Experience mentoring or training junior staff * ------------------------------------------------------------------------------------------------------------------------------------- At Mark Anthony, we exist to Unearth the Extraordinary: Our Purpose is not just a statement; it is a call to action that binds us together and ignites our passion for making a difference. It is the driving force behind why we do what we do every single day, connecting our global organization across all business units, roles, and locations. We are: Best in Our Craft We set the standard with a pursuit of excellence that can be found in everything from our products and processes to our plants and people. Ambitiously Curious We stay curious, dreaming big and navigating the unknown with an enduring belief in better. Made With Humility We bring humility, authenticity, fun, and support to every collaboration and celebrate wins as a team. Daringly Disruptive We disrupt the status quo, moving fast to seize opportunities and acting scrappy to stay ahead of industry giants.

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

Job Description 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.

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

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: At Viral Vector Services (VVS) a division of Thermo Fisher Scientific, we deliver from process development through commercial supply, we offer the expertise and resources necessary to help clients deliver innovative gene therapies. Placed in the forefront of our leading and ground breaking Cell and Gene Therapy business, our mission is to enable clients to cure genetic, rare, and otherwise untreatable diseases. How Will You Make an Impact? The Formulation Technician I is an associate with little to moderate level of technical expertise and experience. A Formulation Technician I may independently perform routine operations commensurate with their experience and training. The Formulation Technician I participates in the day-to-day operation of a cGMP compliant Manufacturing facility. A Day in the Life: Optimally complete work instructions while following procedures and cGMP regulations. Acquire job skills and learns company policies and procedures to complete routine tasks. Achieve full training status associated with the department. Work on assignments that are routine in nature, requiring limited judgment. Has little or no role in decision-making. Stay up to date on required job training. Operate automated and manual equipment and conduct associated activities such as sampling, material handling, cleaning and maintenance in accordance with Standard Operating Procedures, current Good Manufacturing Procedures and Safety guidelines. Perform in-process tests (weight, pH) to ensure that batches meet specifications. Execution of manufacturing batch records with focus on "right first time" Adhere to the Quality Management Systems by living the Quality values every day and holds peers across the site accountable as well. Assist in the completion and identification of PPI initiatives and continuous improvements. Bring up problems instead of trying to fix them independently. Maintain a clean and safe work environment. Maintain a culture of safety by identification of near misses, safety walkthroughs and assisting with resolution of safety observations. Ensure chemicals are properly stored and labeled. Follow all company policies including safety, training, GDP (Good Documentation Practices), clean room gowning, attendance, and PTO (Paid Time Off). Spend 90% of time in the manufacturing suites. Education: High school diploma or equivalent required. Experience: Required: No previous work experience required. Preferred: Previous work experience in manufacturing, operations, production or lab setting or related field. Preferred: Experience in a cGMP environment. Knowledge, Skills, Abilities: Technically capable with a basic theoretical comprehension of general biopharmaceutical manufacturing equipment, principles and processes and have a basic understanding of current GMP and safety standards. Ability to function in a dynamic environment and balance multiple priorities simultaneously. Ability to learn new software and tools quickly. Ability to make decisions and work with minimal to moderate supervision. Physical Requirements / Work Environment Ability to aseptically gown and/or sterile gown as needed. Required to write, read/review written documentation for extended periods of time. Specific vision requirements for this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Is regularly required to talk and hear. The employee frequently is required to sit and stand for extended periods. The employee is occasionally required to lift, stand; walk; use hands to finger, handle, or feel; reach with hands and arms; and stoop, kneel, or crouch. Required to wear Personal Protective Equipment (PPE) Daily computer use. May include working with dry ice, liquid nitrogen cryogenics, hazardous and infectious agents, as well as marked changes in temperature. Flexibility to be reassigned to other business unit locations within Massachusetts as business needs dictate. What We Offer Compensation Competitive Hourly Pay Rate Additional shift differential for 2nd shift and 3rd shift positions Annual performance-based bonus Annual merit performance-based increase Excellent Benefits Benefits & Total Rewards | Thermo Fisher Scientific Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Designated Paid Holidays Retirement Savings Plan Tuition Reimbursement Employee Referral Bonus Career Advancement Opportunities

Shift: Monday through Friday, 8:00 AM - 5:00 PM; times may vary based on business needs Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. SUMMARY: Looking for an experienced ICP/MS or OES metals specialist to join our Environmental lab. This role is vital to ensure that the lab is able to analyze water and soil samples for metal concentrations. The person chosen for this role will provide guidance in method development, instrument trouble shooting and maintenance. This facility houses a significant number of instruments allowing for high volume analysis. Responsible for being a technical specialist to serve the needs of the metals department to help achieve department goals. ESSENTIAL FUNCTIONS: Serves as a technical lead to staff to include providing analytical training and maintenance training. Troubleshoots instrument problems and works with instrument manufacturers to revolve problems. Develops methods as needed to achieve evolving regulatory limits or to meet needs of new methods. Sets up equipment and methods for use by analytical staff Overseeing or reviewing, completing and processing comprehensive types of SOPs and related materials. Provides analysis, interpretation and counsel to staff and management Performs data review or analysis as needed to meet customer needs Interprets and applies department policies and procedures and assists with applicable laws, rules, and regulations; receives guidance within these areas as needed. Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment. QUALIFICATIONS: Education and Experience: Bachelors Degree in Chemistry, Environmental Science, Biochemistry or related field, Required At least 5 years of experience, Required Experience operating and maintaining ICP-OES and/or ICP-MS, Required Instrument and method troubleshooting experience, Required Instrument maintenance experience, Required Training others on instrumentation, Preferred Method Development experience, Preferred Mercury analyzer experience, Preferred Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work. Benefits When you join Pace , you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

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

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

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 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 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

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

Who we are: Based in Lexington,SC, we are Sorinex Exercise Equipment. Leaders and innovators in the industry. We take pride in manufacturing some of the best exercise equipment there is to offer. Whether it's a personal home gym, athletic weight room or military contract, we provide top notch service to all. With 40+ years of experience, we are continuing to grow on a large scale. Visit Sorinex.com to see our catalog. If you're looking for a place to grow and excel, apply now! Who we are looking for: We are looking for a detail-oriented, conscientious individual to work in our Quality Control Department. This individual will be working Monday-Friday; 8am-5pm with a 1-hour lunch break. The ideal candidate will oversee quality control processes and ensure that products meet company standards. This position requires strong analytical skills and a keen eye for detail. As a member of Quality Control you will be responsible for tasks such as: Uphold stringent quality standards by thoroughly inspecting, testing, and measuring materials. Approve conforming parts and reject non-conforming items, ensuring only the highest quality products move forward. Promptly report any inspection failures or quality issues to the appropriate personnel for immediate resolution. Always strive for excellence, continually aiming to uphold and exceed quality standards. Maintain a deep understanding of product specifications and quality requirements. Efficiently stage completed jobs and assist with loading trucks to facilitate smooth operations. Perform all other duties as assigned. Physical Demands: Lift, carry, push and or pull 1 - 50 lbs. frequently. Squat/kneel, bend/stoop, crawl, twist/turn, grasp, and reach overhead and outward frequently. Sit, stand, and walk for 1 - 10 hours per day. Work in a fast-paced, industrial environment wearing hearing protection, eye protection, steel-toed shoes, and other appropriate protective clothing. Required Experience: Manufacturing: 2 years Quality Control: 2 years Tape Measuring: 2 years Schedule: 40 hours per week, Monday-Friday, 8am-5pm with 1 hour lunch break Pay: From $18.00 per hour Work Location: In-person, Lexington, SC 29073 Benefits: 401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Vision insurance

Job Description CompX is hiring a Chemical Technician on our 3rd shift Visit the following link to learn more about CompX National: CompX National - CompX Security Products Responsibilities: Support three electroplating lines and an onsite chemical physical wastewater treatment system with a safety-first mindset. Perform routine plating line including documentation of critical parameters (e.g., pH, temperature) Complete chemical adds to process tanks per instruction Support equipment upkeep Execute scheduled SROs on plating and waste treatment equipment (pumps, filters, transfer lines, chemical feed systems, tanks, meters/probes). Conduct basic troubleshooting of plating tanks and supporting equipment (e.g., low flow, poor filtration, out-of-range parameters, alarm response) Support operation of the waste treatment system by monitoring system performance with control points (pH adjustment, cyanide destruction, metal hydroxide precipitation, and flocculation), perform chemical feed adjustments, and maintain accurate logs. Maintain clean and safe work area, practice good housekeeping and safe chemical handling Work with a safety lead mindset and follow all safety procedures Qualifications: Required High school diploma or GED Ability to work independently or with a team on 3rd shift and maintain consistent documentation and communication Strong attention to detail and commitment to safety and procedural compliance Ability to lift 35 lbs, stand/walk for long periods, and work around wet/industrial environments Basic mechanical aptitude with pumps, valves, filters, hoses, meters Willing to obtain waste treatment license ASAP Preferred Experience in electroplating, metal finishing, or chemical process operations Experience operating or supporting chemical/physical wastewater treatment Familiarity with process testing and control South Carolina Class D or Trainee Chemical/Physical Wastewater Treatment License Be part of our CompX National team and enjoy our excellent benefits: Medical Insurance (FREE employee) Dental Insurance Vision Insurance LOW deductible and LOW out of pocket max Flexible Spending Accounts (FSA) 401k Retirement Plans Company paid Disability and Life Insurance Paid vacations and Holidays Tuition Reimbursement Referral Reward Program CompX National is an Equal Opportunity Employer. Please note: your application may not be considered if you do not provide your education and work history, either by 1) uploading a resume, or 2) entering the information in the application fields directly.

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