Chemist jobs in Columbia, SC

Element is currently seeking an experienced Analytical Scientist for an amazing client in the nutraceuticals industry! This role requires a strong background in FDA-regulated cGMP laboratories. This is a permanent full-time salaried position with annual performance-based bonus and a robust benefits package. Summary of the Position: The Analytical Scientist will be expected to develop and validate new analytical methods with minimum to no supervision as well as to provide technical support to other corporate groups including Quality Control, Quality Assurance, and International Business. Roles and Responsibilities: Analytical Scientist reports to Analytical Chemistry (AC) Management. Performs Quality Control testing and data review to support timely release of product in weekly basis. Effective development, optimization, and validation of scientifically sound analytical methods to ensure analysis and prompt release of raw materials, finished products, and stability studies. Proficient in Empower Software and other laboratory software use in QC environment for chromatographic, spectroscopic methods as well as wet chemistry. Assess testing methodologies and their application to different sample matrix, instrumentation and will include evaluation of testing results from contract laboratories to be sure that the agreed methods and testing parameters were properly followed. Maintains current knowledge of latest technological and scientific trends and serves as an analytical science resource for the rest of the group. Mentor and train chemists in the proper execution, including interpretation of validation studies. Responsible for producing hazardous waste from it point of generation. Managing all produced in accordance with RCRA and SCDHEC regulations to include: proper containers, accumulation, labeling, marking, and storage. Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives. Communicate effectively with other departments within the organization and function within a team environment. Regular attendance is required. Minimum Requirements: Able to develop analytical methods for chromatographic, spectroscopic, titrimetric, and wet chemistry analyses. Must be proficient on laboratory instrument trouble shooting. In-depth knowledge of strategies of analytical method development and specification setting for raw materials and finished products. Knowledge in most of laboratory instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, HPTLC and test methods. Knowledge in the characterization and elucidation of botanical compound structures by study of the compound structure, spectroscopic methods, and Mass spectrometry. Proficient in the selection of analytical columns for chromatographic analyses, proper techniques or technologies and the selection for proper reagents to design effective analytical methods in timely manner. Experience in effective sample preparation techniques to support high number of samples for testing such as liquid-liquid extraction, derivatization, chemical manipulation, and mechanical manipulation. Knowledge of statistical techniques, such as data trend analysis and design of experiments, is highly desirable. Proficiency in reviewing and interpretation of laboratory data. Detailed knowledge of principles of routine laboratory operations. Thorough working knowledge of industry regulations, FDA and ICH guidelines; experience implementing and maintaining adherence to pharmaceutical and/or nutritional supplement GLP/GMP is strongly desired. Demonstrated aptitude to function in a dynamic fast-paced environment. Education and Experience A Bachelor's degree with 10 years of experience in validation and development of analytical methods for nutraceuticals and/or pharmaceutical samples in a GMP environment. A Master's degree and a minimum of 5 years of technical experience is preferred. Extensive experience may be accepted in lieu of an advanced degree. A degree in analytical chemistry, biochemistry, chemical engineering, or related fields is strongly preferred. A need to work on the bench to accomplish tasks along with the Analytical Chemistry team.

Job Description Mastech Digital provides digital and mainstream technology staff as well as Digital Transformation Services for all American Corporations. We are currently seeking an Analytical Scientist for our client in the Manufacturing domain. We value our professionals, providing comprehensive benefits and the opportunity for growth. This is a Permanent position, and the client is looking for someone to start immediately. Duration: Full-time Location: Lancaster, South Carolina Salary: $100,000/Annually Role: Analytical Scientist Primary Skills: Engineering Role Description: As an Analytical Scientist, you must have at least 6+ years of experience. Key Responsibilities: - Develop and validate analytical methods for chromatographic, spectroscopic, titrimetric, and wet chemistry analyses. - Troubleshoot and maintain laboratory instruments, including FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, and HPTLC. - Utilize expertise in method development, specification setting, and botanical compound characterization. - Select appropriate analytical columns, reagents, and techniques for effective method design. - Perform sample preparation techniques such as liquid-liquid extraction, derivatization, and chemical manipulation. - Analyze data using statistical techniques, and review laboratory data for accuracy. - Ensure adherence to FDA, ICH guidelines, and GMP/GLP standards. - Mentor and train junior staff and manage hazardous waste in compliance with regulations. Qualifications: - Bachelor’s degree in Analytical Chemistry, Biochemistry, Chemical Engineering, or related field with 10 years of relevant experience, or a Master’s degree with 5 years of experience. Extensive experience may be considered in lieu of an advanced degree. - Strong proficiency in analytical methods and instrument troubleshooting. - Knowledge of industry regulations and experience in a GMP environment is preferred. Education: Bachelor’s degree in Analytical Chemistry, Biochemistry, Chemical Engineering, or related field with 10 years of relevant experience, or a Master’s degree with 5 years of experience. Experience: Minimum 6+ years of experience Relocation: This position will not cover relocation expenses Travel: No Local Preferred: Yes Note: Must be able to work on a W2 basis (No C2C) Recruiter Name: Monika Soun Recruiter Phone: ************ Equal Employment Opportunity

Corporate Statement Nephron Pharmaceuticals Corporation is a privately owned global leader in the manufacturing of generic drug products, over-the-counter (OTC) drug products and medical devices. Nephron's products are sterile, preservative and additive free and proudly made in the USA! We are headquartered in West Columbia, South Carolina. Our location provides the ability to develop new devices and medications including respiratory therapies, ophthalmics, and injectables, for in-house or contract manufacturing opportunities. The facility utilizes completely automated manufacturing, packaging, and distribution systems, in addition to high volume and redundant utility systems, to ensure production system availability. Nephron specializes in Blow-Fill-Seal (BFS) manufacturing, a niche technology that allows a vial of medication to be formed, filled and sealed in a continuous process, in a sterile, enclosed environment and without human intervention. As an industry leader in product safety and quality, Nephron produces a variety of inhalation solutions, and has distributed over 1 billion doses of respiratory medication per year since 2009. Nephron is currently working on research and development projects that include over 50 new products. The company's longstanding relationships with major drug wholesalers allow us to distribute our products to retail pharmacies, mail order pharmacies, hospitals, home care companies, and long-term care facilities. Nephron has a sales force that covers all fifty states and Puerto Rico, with additional sales channels throughout South America, the Middle East, and Europe. Nephron exists to provide top-quality, affordable medications to everyone. Position Summary: * Support quality control testing and research and development activities as needed. * Assists with additional work duties or responsibilities as evident or required. * Performs other duties as assigned or apparent. * Relies on instructions and pre-established guidelines to perform job functions. * Works under immediate supervision. NOTE: The Primary Accountabilities and Knowledge, Skills and Abilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed below. Specific tasks or responsibilities will be documented in the incumbents' performance objectives as outlined by the incumbents' immediate supervisor or manager. Primary Accountabilities: * Conduct routine laboratory testing for raw materials, in-process materials, finished product and stability samples in accordance with approved analytical methods. * To conduct laboratory work using best-practice analytical techniques, and to consistently follow laboratory GDP and cGMP requirements. * Perform calibration and routine maintenance of lab equipment as necessary and participate in troubleshooting and minor repair of instrumentation. * To skillfully and accurately verify notebooks and raw data and to enter this data into release forms. Knowledge, Skills & Abilities: * BS or MS in Chemistry, Biochemistry or a related field required with 0-3 years of pharmaceutical experience preferred. Experience outside of pharmaceuticals in chemistry quality control or R&D will be considered for the highly qualified candidate. * Experience with conducting analysis by HPLC, GC, FT-IR, UV/Vis spectroscopy as well as wet chemistry techniques. * Must possess strong analytical skills and problem solving ability, and show attention to detail, understanding of cGMP regulations pertaining to laboratory controls and knowledge of USP and compendia standards. * Ability to review and update standard operating procedures, forms and specifications and design new procedures as necessary under management guidance. * Ability to perform testing for laboratory investigations for 005 and atypical QC test results under management guidance. * Ability to effectively communicate within chemistry laboratory staff and management. * Must strive for continuous improvement in all work activities. * The ability to effectively use a multitude of resources and to be accurate and current with data and information. * Position requires, standing (40%), sitting (25%), talking, hearing, typing and walking (35%). * Position encounters the following environmental factors: hazardous materials including HPLC solvents, chemical reagents, acids and other non-specified hazardous materials that are project specific. * Position requires safety glasses, respiratory and other non-specified protective equipment to be worn as necessary. * Salary range: Based on experience EEO Statement: Nephron is an equal employment opportunity employer and does not discriminate against employees or job applicants on the basis of race, religion, color, sex, sexual orientation, age, national origin, mental or physical disability of a qualified individual, veteran or military status, pregnancy, marital status, familial status, genetic information, or any other consideration made unlawful by applicable federal, state or local law. Nephron Pharmaceuticals is a drug free workplace.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Job Summary: Eurofins BPT-Columbia is looking for an Associate Scientist to join our Biochemistry Release and Stability team located in Columbia, Missouri. The Associate Scientist position is an entry-level professional position involved in day-to-day activities in a laboratory setting under prescribed procedures (protocols, standard operating procedures, methods, etc.) * Follow cGMP processes and procedures and adhere to all regulatory requirements * Run a variety of equipment including HPLC, CE, pH meter, analytical balance, and pipetting, among other techniques * Perform various tasks and analyses of bio/pharmaceutical ingredients and products * Review or prepare standards and samples for analysis * Ensure that clients receive quality data by reviewing laboratory data for accuracy * Other job duties as assigned Qualifications Minimum Qualifications: * Bachelor's degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas. * Authorization to work in the U.S. without restriction or sponsorship The Ideal Candidate Would Possess: * Hands-on experience with laboratory analytical instrumentation (HPLC, CE, pH meter, analytical balance, pipettes). * Interest in learning complex analytical procedures supporting bio-pharma product testing. * Familiarity and/or experience in a laboratory setting. * Good organizational skills; ability to follow direction and good communication skills are required. * Working knowledge of Microsoft Word and Excel. Additional Information Position is full-time position, Monday - Friday 8:00am - 4:30pm. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply. * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Job Responsibilities The South Carolina Elections Commission is seeking a quality control analyst to assist with compliance audits of county voter registration and election offices. This senior auditor-level analyst will perform a significant quality control function for the team of eight auditors. The analyst will conduct quantitative and qualitative verifications of audit work, including: * Review and verification of data to identify trends and areas for improvement. * Review of report material to ensure supporting information is documented, factual, easily understood, sufficient, and appropriate. The quality control analyst requires strong skills in the following: Attention to Detail: * Meticulousness in reviewing records, identifying errors, and ensuring accuracy. Problem-Solving: * Using quantitative skills to identify and resolve issues related to data and reporting. Critical Thinking: * Applying logical reasoning to evaluate data, identify potential risks, and assess the effectiveness of internal controls. Data analysis: * Collecting, analyzing, and interpreting numerical data to identify patterns, anomalies, and trends. Interpersonal: * Communicating effectively with others. Become a part of our dedicated team and help shape the future of elections in South Carolina! Minimum and Additional Requirements A bachelor's degree and professional experience in accounting, auditing, finance, insurance, or tax preparation and/or analysis. Preferred Qualifications Master's degree in public administration or related field or a Law degree and 4+ years of audit-related experience C.P.A. (Certified Public Accountant), C.I.A. (Certified Internal Auditor), or C.F.E. (Certified Financial Examiner) designation may be required. Additional Comments The South Carolina Election Commission is committed to providing equal employment opportunities to all applicants and does not discriminate on the basis of race, color, religion, sex (including pregnancy, childbirth, or related medical conditions including, but not limited, to lactation), national origin, age (40 or older), disability or genetic information. Supplemental questions are considered part of your official application. Any misrepresentation will result in your disqualification from employment. Please complete the state application to include all current and previous work history and education. A resume will not be accepted nor reviewed to determine if an applicant has met the qualifications for the position. The South Carolina State Elections Commission offers an exceptional benefits package for full time (FTE) employees: * Health, dental, vision, long-term disability, and life insurance for employees, spouse, and children. * 15 days annual (vacation) leave per year * 15 days sick leave per year * 13 paid holidays * Paid Parental Leave * S.C. Deferred Compensation Program available (S.C. Deferred Compensation) * Retirement benefit choices * * State Retirement Plan (SCRS) * State Optional Retirement Program (State ORP)

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

The **Branch Quality Control Analyst** is responsible for performing independent, quality control reviews of retail branch locations to identify operational and compliance risk within the retail branch. This associate works closely with the Compliance and Oversight Program Manager and reports to the Director of Compliance & Oversight for Consumer Banking. The Compliance & Oversight team is comprised of a group of associates that are very hard working and are passionate about protecting the bank while providing support to our branches. At UMB, we want to be everything to our clients and the Compliance and Oversight Specialist team does just that by ensuring UMB's consumer operations function seamlessly and in a way that protects our client's financial needs. **_How you'll spend your time:_** + Ensuring each review includes, at a minimum: an assessment of branch documentation, certification of cash on hand at the branch, observation of associate behavior and interviews with branch associates to assess the associate's understanding of applicable regulatory requirements. + Issuing a summary memorandum of each retail branch quality control review performed, including an overall risk rating articulating the level of risk observed in the branch review. + Maintaining an ongoing risk rating guide accurately depicting the amount of risk within each retail branch. + Assisting in operations related projects, as needed. + Cultivate working partnerships with the Consumer Operations teammates and the Consumer Delivery Team. + Collaborate with partners and support Consumer Banking to respond to requests from and timely resolve issues identified by regulatory bodies, internal audits or compliance engagements, or self-assessments. + Evaluate operational documentation for monthly operational reporting of branch performance. + Act as a supportive resource regarding Consumer Banking operations matters. + Support Director of Compliance & Oversight in the aggregation and communication of Compliance & Oversight activities including data aggregation, analysis, and reporting. **_We're excited to talk with you if:_** + 5-7 years of branch / bank operations experience. + High school diploma or equivalent. + Must live within a major metropolitan area of the UMB footprint. + Have the ability to work independently with minimal supervision. + Have the ability to build relationships and inspire trust across the organization. + Have the ability to present and convey information in a way that is easily understandable to associates at varying levels within the organization. + Have the proficient writing ability and strong experience with Microsoft Suite software and related banking applications. + Ability to travel up to 75% of a scheduled work week. **Compensation Range:** $44,790.00 - $86,510.00 _The posted compensation range on this listing represents UMB's standard for this role, but the actual compensation may vary by geographic location, experience level, and other job-related factors. In addition, this range does not encompass the full earning potential for this role. Please see the description of benefits included with this job posting for additional information._ UMB offers competitive and varied benefits to eligible associates, such as Paid Time Off; a 401(k) matching program; annual incentive pay; paid holidays; a comprehensive company sponsored benefit plan including medical, dental, vision, and other insurance coverage; health savings, flexible spending, and dependent care accounts; adoption assistance; an employee assistance program; fitness reimbursement; tuition reimbursement; an associate wellbeing program; an associate emergency fund; and various associate banking benefits. Benefit offerings and eligibility requirements vary. **Are you ready to be part of something more?** You're more than a means to an end-a way to help us meet the bottom line. UMB isn't comprised of workers, but of people who care about their work, one another, and their community. Expect more than the status quo. At UMB, you can expect more heart. You'll be valued for exactly who you are and encouraged to support causes you care about. Expect more trust. We want you to do the right thing, no matter what. And, expect more opportunities. UMBers are known for having multiple careers here and having their voices heard. _UMB and its affiliates are committed to inclusion and diversity and provide employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex (including gender, pregnancy, sexual orientation, and gender identity), national origin, age, disability, military service, veteran status, genetic information, or any other status protected by applicable federal, state, or local law. If you need accommodation for any part of the employment process because of a disability, please send an e-mail to_ _*************************_ _to let us know the nature of your request._ _If you are a California resident, please visit our_ Privacy Notice for California Job Candidates (*********************************************************************************************************************************** _to understand how we collect and use your personal information when you apply for employment with UMB._ **_Who we are_** We are more than a company. We are advisors, consultants, problem solvers, friends, community members, experts, and we are here to help you make the best of every moment with a financial foundation that can help you succeed. Learn more about UMB's vision (****************************************************************************************************** Check out the road to a career at UMB

Responsible for the efficient and effective performance of testing in conformance with regulations and standards. Responsibilities include inspection, analysis of results, determining final disposition of some product and detecting nonconforming conditions. Works within clearly defined SOPs and/or scientific methods. Adheres to quality guidelines. Complies with regulations and standards. Identifies basic non-compliance within regulations and standards. Maintains appropriate licenses / training / certifications, as needed. One (1) to two (2)years experience. Demonstrated understanding in the use of calibrated equipment and ability to follow equipment maintenance repair procedures.

Job Description QC Compound Lab Associate I The QC Compound Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. This position generally works alongside chemists and other technicians, organizing the lab workspace, maintaining cleanliness of equipment, creating chemical solutions, and performing chemical experiments. Works with a team that is dedicated to the formulation, processing and evaluation of additives for use in rubber compounds for tire and has full access to state of the art, industry standard capabilities, located in a highly desirable working environment. Will also be responsible for supporting fundamental programs aimed at providing a sustainable competitive advantage in tire performance and/or cost Essential Duties & Functions Apply training to regularly isolate and prepare samples for chemical analysis Apply knowledge of various chemical analysis techniques to effectively use and calibrate instruments Manage time and resources to effectively meet expected completion dates for requests Document observations and conclusions in clear and concise notes and formal reports Participate in project updates each week Lab scale weighing, mixing and compounding of polymers with various additives for rubber formulations Curing and physical testing of compounds Documentation and reporting of experimental data Assistance with the development of new testing procedures and predictive capabilities for the assessment of tire tread performance properties, whose needs are constantly evolving Training of team members in newly developed test procedures Promote a safe work environment through work practices Under minimal supervision, employee will perform, coordinate, analyze and monitor quality control and product assurance tests and test results to ensure products meet or exceed quality and reliability, specifications and standards Employee will also generate certificate of analysis and approves all raw materials Enforce and follow company policies as required Resolves less complex problems immediately, while more complex problems are typically assigned to next level Perform other duties of equal or less complexity as assigned or directed by management Engage and retain high-performance standards and elevate level of responsibility and performance Skills/Qualifications High-level laboratory skills preferred Safe, careful work habits with attention to detail Must be able to prioritize and multi task Must be able to use Word, Excel, and Outlook Good communication, analytical and troubleshooting skills Good verbal and writing skills Strong interpersonal skills and the ability to work within a team environment recommended Education and/or Experience High School diploma or GED. Prefer Associates degree in Chemistry or laboratory science; or an equivalent combination of education and experience Minimum 1 year work experience in chemical analysis or relevant field preferred 2 years of manufacturing experience preferred Knowledge of laboratory analytical testing procedures and specific lab equipment required to perform quality testing Knowledge of common lab procedures Ability to learn quickly and to apply knowledge on practical problem solving Experience with precise measurements preferred Experience with various types of chromatography, spectroscopy and wet chemical analysis techniques preferred Experience in and/or willing to learn and apply a variety of sample isolation and preparation procedures

The QC Compound Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. This position generally works alongside chemists and other technicians, organizing the lab workspace, maintaining cleanliness of equipment, creating chemical solutions, and performing chemical experiments. Works with a team that is dedicated to the formulation, processing and evaluation of additives for use in rubber compounds for tire and has full access to state of the art, industry standard capabilities, located in a highly desirable working environment. Will also be responsible for supporting fundamental programs aimed at providing a sustainable competitive advantage in tire performance and/or cost Essential Duties & Functions Apply training to regularly isolate and prepare samples for chemical analysis Apply knowledge of various chemical analysis techniques to effectively use and calibrate instruments Manage time and resources to effectively meet expected completion dates for requests Document observations and conclusions in clear and concise notes and formal reports Participate in project updates each week Lab scale weighing, mixing and compounding of polymers with various additives for rubber formulations Curing and physical testing of compounds Documentation and reporting of experimental data Assistance with the development of new testing procedures and predictive capabilities for the assessment of tire tread performance properties, whose needs are constantly evolving Training of team members in newly developed test procedures Promote a safe work environment through work practices Under minimal supervision, employee will perform, coordinate, analyze and monitor quality control and product assurance tests and test results to ensure products meet or exceed quality and reliability, specifications and standards Employee will also generate certificate of analysis and approves all raw materials Enforce and follow company policies as required Resolves less complex problems immediately, while more complex problems are typically assigned to next level Perform other duties of equal or less complexity as assigned or directed by management Engage and retain high-performance standards and elevate level of responsibility and performance Skills/Qualifications High-level laboratory skills preferred Safe, careful work habits with attention to detail Must be able to prioritize and multi task Must be able to use Word, Excel, and Outlook Good communication, analytical and troubleshooting skills Good verbal and writing skills Strong interpersonal skills and the ability to work within a team environment recommended Education and/or Experience High School diploma or GED. Prefer Associates degree in Chemistry or laboratory science; or an equivalent combination of education and experience

This is a permanent, full-time, salaried position with an amazing nutraceutical manufacturing company! Apply today! Roles and Responsibilities: The Quality Control Chemist I (QCC) reports to Quality Control (QC) Management. Perform release, stability and special request testing of finished products and raw materials following Standard Operating Procedures (SOPs), in-house test methods, and/or compendial methods. 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. The QCC will stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control laboratory complies in the areas of analytical applications, release specifications, and documentation practices. The QCC will assist QC management and/or designee in resolving Out of Specification (OOS) results in the QC Laboratory. Communicate effectively with QC management and with the Out-of-Specification/Trend Coordinator when suspect results are generated as well as with the Stability Coordinator when needed. The QCC will assist in training new laboratory personnel and document training in accordance with established laboratory SOPs and the company training program. The QCC will follow Current Good Manufacturing Practice (cGMP) documentation guidelines to record all procedures in a timely fashion. Maintain a safe working environment and will ensure that all equipment used in the testing procedures is calibrated and properly maintained. The QCC will compete specific projects assigned by management and other necessary functions. 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 QCC will have 0 - 5 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), troubleshooting, generation and revision of operating procedures and test methods. Effective interpersonal, self-motivation skills, and the ability to interact with all levels of personnel are required. Education and Experience: A Bachelor of Science (B.S.) or Bachelor of Arts (B.A.) degree in a science-related field such as Chemistry, Biochemistry or Biology preferred.

Job DescriptionDescription: 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:

Corporate Statement Nephron Pharmaceuticals Corporation is a privately owned global leader in the manufacturing of generic drug products, over-the-counter (OTC) drug products and medical devices. Nephron's products are sterile, preservative and additive free and proudly made in the USA! We are headquartered in West Columbia, South Carolina. Our location provides the ability to develop new devices and medications including respiratory therapies, ophthalmics, and injectables, for in-house or contract manufacturing opportunities. The facility utilizes completely automated manufacturing, packaging, and distribution systems, in addition to high volume and redundant utility systems, to ensure production system availability. Nephron specializes in Blow-Fill-Seal (BFS) manufacturing, a niche technology that allows a vial of medication to be formed, filled and sealed in a continuous process, in a sterile, enclosed environment and without human intervention. As an industry leader in product safety and quality, Nephron produces a variety of inhalation solutions, and has distributed over 1 billion doses of respiratory medication per year since 2009. Nephron is currently working on research and development projects that include over 50 new products. The company's longstanding relationships with major drug wholesalers allow us to distribute our products to retail pharmacies, mail order pharmacies, hospitals, home care companies, and long-term care facilities. Nephron has a sales force that covers all fifty states and Puerto Rico, with additional sales channels throughout South America, the Middle East, and Europe. Nephron exists to provide top-quality, affordable medications to everyone. Position Summary: • Support quality control testing and research and development activities as needed. • Assists with additional work duties or responsibilities as evident or required. • Performs other duties as assigned or apparent. • Relies on instructions and pre-established guidelines to perform job functions. • Works under immediate supervision. NOTE: The Primary Accountabilities and Knowledge, Skills and Abilities below are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or most of the primary accountabilities listed below. Specific tasks or responsibilities will be documented in the incumbents' performance objectives as outlined by the incumbents' immediate supervisor or manager. Primary Accountabilities: • Conduct routine laboratory testing for raw materials, in-process materials, finished product and stability samples in accordance with approved analytical methods. • To conduct laboratory work using best-practice analytical techniques, and to consistently follow laboratory GDP and cGMP requirements. • Perform calibration and routine maintenance of lab equipment as necessary and participate in troubleshooting and minor repair of instrumentation. • To skillfully and accurately verify notebooks and raw data and to enter this data into release forms. Knowledge, Skills & Abilities: • BS or MS in Chemistry, Biochemistry or a related field required with 0-3 years of pharmaceutical experience preferred. Experience outside of pharmaceuticals in chemistry quality control or R&D will be considered for the highly qualified candidate. • Experience with conducting analysis by HPLC, GC, FT-IR, UV/Vis spectroscopy as well as wet chemistry techniques. • Must possess strong analytical skills and problem solving ability, and show attention to detail, understanding of cGMP regulations pertaining to laboratory controls and knowledge of USP and compendia standards. • Ability to review and update standard operating procedures, forms and specifications and design new procedures as necessary under management guidance. • Ability to perform testing for laboratory investigations for 005 and atypical QC test results under management guidance. • Ability to effectively communicate within chemistry laboratory staff and management. • Must strive for continuous improvement in all work activities. • The ability to effectively use a multitude of resources and to be accurate and current with data and information. • Position requires, standing (40%), sitting (25%), talking, hearing, typing and walking (35%). • Position encounters the following environmental factors: hazardous materials including HPLC solvents, chemical reagents, acids and other non-specified hazardous materials that are project specific. • Position requires safety glasses, respiratory and other non-specified protective equipment to be worn as necessary. • Salary range: Based on experience EEO Statement: Nephron is an equal employment opportunity employer and does not discriminate against employees or job applicants on the basis of race, religion, color, sex, sexual orientation, age, national origin, mental or physical disability of a qualified individual, veteran or military status, pregnancy, marital status, familial status, genetic information, or any other consideration made unlawful by applicable federal, state or local law. Nephron Pharmaceuticals is a drug free workplace.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins BioPharma Product Testing Columbia, LLC (formerly EAG Laboratories) offers the pharmaceutical industry an analytically focused CRO with deep experience in method development, program design and complex study execution. A true development CRO, we deliver comprehensive CMC analytical support including multi-disciplinary, multi-technique analytical method development and validation, complete stability program management and in-depth extractables and leachables expertise-plus in-house custom synthesis and cGMP radiolabeling services. Eurofins BioPharma Product Testing Columbia also offers specialized materials testing to support supply chain and packaging initiatives, and the full range of environmental fate, metabolism and toxicology studies required to evaluate a pharmaceutical's potential environmental impact. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Eurofins BPT-Columbia is looking for an Associate Scientist to join our Stability and Batch Release team located in Columbia, Missouri. The Associate Scientist position is an entry-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments. The ideal candidate would possess: * Experience with GLP and/or GMP and hands-on experience with HPLC and/or GC desirable. * Experience with LIMS system desirable. * Familiarity and/or experience in a laboratory setting is required. * Good organizational skills; ability to follow direction and good communication skills are required. Qualifications Minimum Qualifications: * Bachelor's degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas is required. * Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information The position is full-time, Monday-Friday, 8am-4:30pm, with overtime as needed. Candidates within a commutable distance of Columbia, MO are encouraged to apply. * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Job Responsibilities Works under the supervision of the Lead Cook in a small to medium-sized food service unit; and assists with inspections, staff training, oversee staff job duties. Also helps as a backup in the preparation and cooking/baking of food products. As the Quality Control/Attendant Supervisor, you need to become familiar with headcount/cashier procedures, meal adjustment, and appearance of the serving line, posting meal requirements, and help with shift coverage. Minimum and Additional Requirements A high school diploma with 3 years of supervisor experience and or cooking experience in quantity and quality cooking or baking. Servsafe Certified. Ability to work in cohesion with Lead Cook with little to no supervision. Ability to read and prepare meals utilizing recipe cards and production sheets. Additional Comments Knowledge of the procurement, storage, preparation, distribution and serving of food products. Knowledge of dietetic principles involved in planning and reviewing menus for nutritional adequacy, dietary balance and attractiveness of prepared food products. Knowledge of principles and procedures of food service management. Knowledge of the methods, materials and appliances used in a dining facility. Knowledge of sanitary and safety procedures pertaining to dining operations and/or general food preparation and service. Ability to maintain food service records and prepare written reports. A resume will not be accepted in lieu of an online South Carolina State Employment Application. Only those applicants chosen for interview will be notified of job filled status. Note: Applicants indicating college credit, degree(s) or specialized training on the application shall provide an official copy of transcripts upon notification of selection for hire. This serves as verification of credentials listed on the application.

The QC Compound Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. This position generally works alongside chemists and other technicians, organizing the lab workspace, maintaining cleanliness of equipment, creating chemical solutions, and performing chemical experiments. Works with a team that is dedicated to the formulation, processing and evaluation of additives for use in rubber compounds for tire and has full access to state of the art, industry standard capabilities, located in a highly desirable working environment. Will also be responsible for supporting fundamental programs aimed at providing a sustainable competitive advantage in tire performance and/or cost Essential Duties & Functions Apply training to regularly isolate and prepare samples for chemical analysis Apply knowledge of various chemical analysis techniques to effectively use and calibrate instruments Manage time and resources to effectively meet expected completion dates for requests Document observations and conclusions in clear and concise notes and formal reports Participate in project updates each week Lab scale weighing, mixing and compounding of polymers with various additives for rubber formulations Curing and physical testing of compounds Documentation and reporting of experimental data Assistance with the development of new testing procedures and predictive capabilities for the assessment of tire tread performance properties, whose needs are constantly evolving Training of team members in newly developed test procedures Promote a safe work environment through work practices Under minimal supervision, employee will perform, coordinate, analyze and monitor quality control and product assurance tests and test results to ensure products meet or exceed quality and reliability, specifications and standards Employee will also generate certificate of analysis and approves all raw materials Enforce and follow company policies as required Resolves less complex problems immediately, while more complex problems are typically assigned to next level Perform other duties of equal or less complexity as assigned or directed by management Engage and retain high-performance standards and elevate level of responsibility and performance Skills/Qualifications High-level laboratory skills preferred Safe, careful work habits with attention to detail Must be able to prioritize and multi task Must be able to use Word, Excel, and Outlook Good communication, analytical and troubleshooting skills Good verbal and writing skills Strong interpersonal skills and the ability to work within a team environment recommended Education and/or Experience High School diploma or GED. Prefer Associates degree in Chemistry or laboratory science; or an equivalent combination of education and experience Minimum 1 year work experience in chemical analysis or relevant field preferred 2 years of manufacturing experience preferred Knowledge of laboratory analytical testing procedures and specific lab equipment required to perform quality testing Knowledge of common lab procedures Ability to learn quickly and to apply knowledge on practical problem solving Experience with precise measurements preferred Experience with various types of chromatography, spectroscopy and wet chemical analysis techniques preferred Experience in and/or willing to learn and apply a variety of sample isolation and preparation procedures

Full-time Description 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

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Job Summary: Eurofins BPT-Columbia is looking for an Associate Scientist to join our Biochemistry Method Development and Validation team located in Columbia, Missouri. The Associate Scientist position is an entry-level professional position involved in day-to-day activities in a laboratory setting under prescribed procedures (protocols, standard operating procedures, methods, etc.) * Follow cGMP processes and procedures and adhere to all regulatory requirements * Run a variety of equipment including HPLC, CE, pH meter, analytical balance, and pipetting, among other techniques * Perform various tasks and analyses of bio/pharmaceutical ingredients and products * Review or prepare standards and samples for analysis * Ensure that clients receive quality data by reviewing laboratory data for accuracy * Other job duties as assigned Qualifications Minimum Qualifications: * Bachelor's degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas. * Authorization to work in the U.S. without restriction or sponsorship The Ideal Candidate Would Possess: * Hands-on experience with laboratory analytical instrumentation (HPLC, CE, pH meter, analytical balance, pipettes). * Interest in learning complex analytical procedures supporting bio-pharma product testing. * Familiarity and/or experience in a laboratory setting. * Good organizational skills; ability to follow direction and good communication skills are required. * Working knowledge of Microsoft Word and Excel. Additional Information Position is full-time, Monday-Friday 8am-4:30pm, with overtime as needed. Candidates who live within a commutable distance from Columbia, MO encourage to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

The QC Compound Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. This position generally works alongside chemists and other technicians, organizing the lab workspace, maintaining cleanliness of equipment, creating chemical solutions, and performing chemical experiments. Works with a team that is dedicated to the formulation, processing and evaluation of additives for use in rubber compounds for tire and has full access to state of the art, industry standard capabilities, located in a highly desirable working environment. Will also be responsible for supporting fundamental programs aimed at providing a sustainable competitive advantage in tire performance and/or cost Essential Duties & Functions Apply training to regularly isolate and prepare samples for chemical analysis Apply knowledge of various chemical analysis techniques to effectively use and calibrate instruments Manage time and resources to effectively meet expected completion dates for requests Document observations and conclusions in clear and concise notes and formal reports Participate in project updates each week Lab scale weighing, mixing and compounding of polymers with various additives for rubber formulations Curing and physical testing of compounds Documentation and reporting of experimental data Assistance with the development of new testing procedures and predictive capabilities for the assessment of tire tread performance properties, whose needs are constantly evolving Training of team members in newly developed test procedures Promote a safe work environment through work practices Under minimal supervision, employee will perform, coordinate, analyze and monitor quality control and product assurance tests and test results to ensure products meet or exceed quality and reliability, specifications and standards Employee will also generate certificate of analysis and approves all raw materials Enforce and follow company policies as required Resolves less complex problems immediately, while more complex problems are typically assigned to next level Perform other duties of equal or less complexity as assigned or directed by management Engage and retain high-performance standards and elevate level of responsibility and performance Skills/Qualifications High-level laboratory skills preferred Safe, careful work habits with attention to detail Must be able to prioritize and multi task Must be able to use Word, Excel, and Outlook Good communication, analytical and troubleshooting skills Good verbal and writing skills Strong interpersonal skills and the ability to work within a team environment recommended Education and/or Experience High School diploma or GED. Prefer Associates degree in Chemistry or laboratory science; or an equivalent combination of education and experience Minimum 1 year work experience in chemical analysis or relevant field preferred 2 years of manufacturing experience preferred Knowledge of laboratory analytical testing procedures and specific lab equipment required to perform quality testing Knowledge of common lab procedures Ability to learn quickly and to apply knowledge on practical problem solving Experience with precise measurements preferred Experience with various types of chromatography, spectroscopy and wet chemical analysis techniques preferred Experience in and/or willing to learn and apply a variety of sample isolation and preparation procedures