Chemist jobs in Calhoun, GA - 21 jobs

Actively Screening for Chemist to join global animal health company in Lithia Springs, GA! The candidate will be responsible for supporting analytical research and transfer activities for drug substances and drug products with a focus on small molecule substrates. The candidate will be responsible for supporting multiple projects and will work in close collaboration with partner groups across the organization. Job Responsibilities: * Conduct laboratory experiments supporting analytical method transfer. * Perform processes and operate equipment required for large-scale monoclonal antibody (mAb) production. * Utilize various modern analytical tools and technologies (e.g., U/HPLC, GC, MS, Karl Fischer, dissolution, particle size, etc.). * Maintain equipment and problem solve as needed. * Understand, follow, and accurately complete process documentation to maintain a high level of product quality. * Understand and follow safety policies. * Work collaboratively with members of other departments. Additional Skills & Qualifications * BS in Biological sciences or a related field * Previous experience in large-scale production or laboratory scale * 3-5+ years of relevant experience * In depth understanding and knowledge of applications of various modern analytical tools and technologies, including modern techniques for separation science (e.g., HPLC, NMR, GC, LC/MS, Dissolution etc.) * Experience with automation and ELISA. * Good understanding of quality requirements in analytical support for clinical supplies and manufacturing transfer work. * Good understanding of chemistry and formulation processes * Excellent documentation skills for recording research work and ability to summarize results and data. * Practical analytical experience working with active pharmaceutical ingredients and related dosage forms. * A track record of analytical problem solving and method development is desired. * Basic understanding of the pharmaceutical development process. Job Type & Location This is a Contract to Hire position based out of Lithia Springs, GA. Pay and Benefits The pay range for this position is $33.00 - $55.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Lithia Springs,GA. Application Deadline This position is anticipated to close on Jan 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

**NATURE & SCOPE** The Senior Chemist is responsible for ensuring samples from all phases of manufacturing or other handling process are prepared and tested according to specifications. This individual will employ a variety of methods and will require intermediate laboratory skills, as well as a thorough understanding of analytical testing equipment and processes. They will prepare and authorize documentation for the release of raw materials and finished goods and will play an active role in project implementation and documentation. He or she is also responsible for technician proficiency, training, interpretation of methods and results, and minor equipment troubleshooting and repair. They will play a role in preserving workplace safety and safe potentially hazardous materials handling. **MAJOR ACCOUNTABILITIES** The responsibilities of the Senior Chemist include but are not limited to, the following: **Testing and Reporting** + Test submitted samples under cGMP/GLP environment as per company's standard operating procedures and USP/FDA guidelines. + Assist Lab Administrator with scheduling analytical tests and/or experiments and ensure adequate coverage to meet commitment dates. + Provide expert opinions and interpretation of analytical assay results. + Provide expert opinions and interpretation of OOS results and guide the decision making and documentation process for Laboratory Error Investigations, nonconformances, and deviations. + Review and approve the interpretation and documentation of results generated by QC Chemists + Ensure analytical results are appropriately documented and reported in a timely basis. + Maintain up to date documentation. Enter all raw data directly into the notebook and promptly calculate all test results. + Peer review notebooks and test results generated by QC Chemists + Prepare and update COAs as needed **Inventory and Equipment** + Ensure reagents, substrates, and kits are prepared according to procedures and are readily available for testing. + Ensure adequate inventory of lab supplies to conduct analytical assays while working within the provided budget + Maintain laboratory equipment and instrumentation in good working order, following appropriate procedures for usage, clean-up and maintenance. + Ensure cleaning and use, verification, and maintenance logs are kept up to date and clearly represent the actual history and current status of each piece of equipment. + Provide input and feedback for design requirements for new and/or replacement equipment + Schedule and assist equipment repair technicians. + Assist Lab Manager with development of Capex requests. **Training and Proficiency** + Develop and execute training plan for QC Chemists on methods and technique. + Oversee and schedule laboratory proficiency testing as required by ISO 17025 standards. + Ensure QC Chemists are appropriately trained on all assays for which they are scheduled + Determine the proficiency status of QC Chemist. **Method Optimization and Validation** + Review validation results and investigate non-conforming values. + Optimize methods and investigate matrix interferences for documentation of exemptions + Oversee implementation of new methods + Conduct and determine uncertainty measurements as required by ISO 17025. + Submit change control requests for methods or procedures that need to be added, revised, or updated to ensure equipment and methods are performed in a manner to minimize uncertainty and variability. + Review and provide feedback on standard operating procedures, forms, and documents. **Management** + Lead chemistry department with effective mentoring, directing and coordination of development activities + Communicate and enforce laboratory quality requirements to personnel working in the lab and ensure that they are completed per GMP, GLP and ISO 17025 standards + Lead and facilitate initial and periodic training of QC Chemists to ensure standard laboratory practices, techniques, and adherence to cGxP and other applicable regulations and standards (21 CFR, §11, §111 and §117, ISO17025 and the requirements of TGA PIC/s) + Assist with preparation and delivery of personnel evaluations and competencies. + Assist with improvement plans/disciplinary action where necessary + Coordinate objectives with production procedures in cooperation with other managers to maximize product reliability and minimize costs **Education and Experience** + Minimum - Bachelor of Science in Chemistry, Biology or equivalent + Minimum - 2 years of experience in an Analytical Lab conducting assays **Specific Skills** + Strong attention to detail in order to produce accurate, precise, and reproducible data + Strong analytical, organizational, and time management skills + Task oriented and results driven + Strong work ethic and prioritization skills + Work collaboratively with various departments to compile, analyze, and interpret data + Manual dexterity + Ability to follow written protocols + Ability to work in a fast paced environment + Excellent written and oral communication skills - ability to make presentations and/or give presentations + Must be able to lift 25lbs + Must possess a valid US Driver's License Excited about this role but don't think you meet every requirement listed? We encourage you to apply anyway. You may be just the right candidate for this role or another one of our openings. ADM requires the successful completion of a background check. REF:101484BR **Req/Job ID:** 101484BR **City:** Kennesaw **State:** GA - Georgia **Ref ID:** \#LI-SC1 **:** **About ADM** At ADM, we unlock the power of nature to provide access to nutrition worldwide. With industry-advancing innovations, a complete portfolio of ingredients and solutions to meet any taste, and a commitment to sustainability, we give customers an edge in solving the nutritional challenges of today and tomorrow. We're a global leader in human and animal nutrition and the world's premier agricultural origination and processing company. Our breadth, depth, insights, facilities and logistical expertise give us unparalleled capabilities to meet needs for food, beverages, health and wellness, and more. From the seed of the idea to the outcome of the solution, we enrich the quality of life the world over. Learn more at ************ **:** \#LI-Onsite **\t:** **\#IncludingYou** Diversity, equity, inclusion and belonging are cornerstones of ADM's efforts to continue innovating, driving growth, and delivering outstanding performance. We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments - environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career. We respect and value the unique backgrounds and experiences that each person can bring to ADM because we know that diversity of perspectives makes us better, together. We welcome everyone to apply. We are committed to ensuring all qualified applicants receive consideration for employment regardless of race, color, ethnicity, disability, religion, national origin, language, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law **:** **Benefits and Perks** Enriching the quality of life for the world begins by taking care of our colleagues. In addition to competitive pay, we support your diverse needs with a comprehensive total rewards package to enhance your well-being, including: + **Physical wellness** - medical/Rx, dental, vision and on-site wellness center access or gym reimbursement (as applicable). + **Financial wellness** - flexible spending accounts, health savings account, 401(k) with matching contributions and cash balance plan, discounted employee stock purchasing program, life insurance, disability, workers' compensation, legal assistance, identity theft protection. + **Mental and social wellness** - Employee Assistance Program (EAP), Employee Resource Groups (ERGs) and Colleague Giving Programs (ADM Cares). Additional benefits include: + Paid time off including paid holidays. + Adoption assistance and paid maternity and parental leave. + Tuition assistance. + Company-sponsored training and development resources, such as LinkedIn Learning, language training and mentoring programs. *Benefits may vary for bargained locations, confirm benefit eligibility with your recruiter. **:** Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. If hired, employees will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. The pay range for this position is expected to be between: **:** $39,200.00 - $72,800.00

**The Chemist will direct, manage and oversee research, product development, quality control and regulatory requirements for products. Formulate and develop products through the combination of new and existing products, compounds, raw materials and other materials. Ability to reconstruct and deconstruct formulas and develop, plan and organize new product formulations and existing products ** ** **Essential Duties and Responsibilities **include the following; however, other duties may be assigned. ** ** • Conduct syntheses and analyses of both routine and developmental products at the direction of the Technical Director, commercial team, and/or other SLT members as needed • Perform literature searches and contribute to new product development within the Technology Department at Polyventive • Contribute to projects as an individual and as a team • Prepare products synthesized in the laboratory for pilot and full scale-up… take complete responsibility from commencement of the project to scale-up in the plant. Strive to become a technical leader within the group. • Perform technical support and plant support work as needed • Participate and lead in meetings regarding new product introductions and MOC's • Maintain a safe and clean laboratory workspace • Direct R&D technicians and QC technicians as needed • Prepare pertinent technical documentation as required **Essential Qualifications and Skills: ** To successfully perform this job, an individual must be able to perform each key responsibility in a satisfactory manner through individual effort or effective and appropriate collaboration. Additionally, the well-qualified candidate will have the following education and experience: • Bachelor's degree or equivalent combination of education and training • 3+ years of experience in surfactant and polymer synthesis/formulation/structure activity in at least two of the following: textiles, HI&I, O&G, adhesives, or coatings • Display excellent computer skills Display exc ellent interpersonal and communication skills • 3+ years of experience with the following analytical equipment: FTIR, GCMS, HPLC, etc ** ** **Work Environment: ** Work is typically performed in an inside, temperature-controlled environment. Work and travel throughout plant environment of varied temperatures and humidity, and wear personal protective equipment, as required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Various operations in the plant generate noise, dust, vapor and fumes in the normal course of production. The Company has been and is committed to eliminating these conditions to the extent possible through the application of design engineering. The Company also provides a variety of safety equipment to keep all associates safe and within OSHA standards. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.

Job Description **The Chemist will direct, manage and oversee research, product development, quality control and regulatory requirements for products. Formulate and develop products through the combination of new and existing products, compounds, raw materials and other materials. Ability to reconstruct and deconstruct formulas and develop, plan and organize new product formulations and existing products ** ** **Essential Duties and Responsibilities **include the following; however, other duties may be assigned. ** ** • Conduct syntheses and analyses of both routine and developmental products at the direction of the Technical Director, commercial team, and/or other SLT members as needed • Perform literature searches and contribute to new product development within the Technology Department at Polyventive • Contribute to projects as an individual and as a team • Prepare products synthesized in the laboratory for pilot and full scale-up… take complete responsibility from commencement of the project to scale-up in the plant. Strive to become a technical leader within the group. • Perform technical support and plant support work as needed • Participate and lead in meetings regarding new product introductions and MOC's • Maintain a safe and clean laboratory workspace • Direct R&D technicians and QC technicians as needed • Prepare pertinent technical documentation as required **Essential Qualifications and Skills: ** To successfully perform this job, an individual must be able to perform each key responsibility in a satisfactory manner through individual effort or effective and appropriate collaboration. Additionally, the well-qualified candidate will have the following education and experience: • Bachelor's degree or equivalent combination of education and training • 3+ years of experience in surfactant and polymer synthesis/formulation/structure activity in at least two of the following: textiles, HI&I, O&G, adhesives, or coatings • Display excellent computer skills Display exc ellent interpersonal and communication skills • 3+ years of experience with the following analytical equipment: FTIR, GCMS, HPLC, etc ** ** **Work Environment: ** Work is typically performed in an inside, temperature-controlled environment. Work and travel throughout plant environment of varied temperatures and humidity, and wear personal protective equipment, as required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Various operations in the plant generate noise, dust, vapor and fumes in the normal course of production. The Company has been and is committed to eliminating these conditions to the extent possible through the application of design engineering. The Company also provides a variety of safety equipment to keep all associates safe and within OSHA standards. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.

* Maintain the highest standards of scientific professionalism. When in doubt, get feedback from other R&D/Technical professionals. * Maintain detailed and comprehensive documentation of all work performed. * Stay current with the scientific literature, particularly in areas that may affect company's product line, existing processes or potential commercial opportunities. * Evaluate technology packages from external sources for chemical and cost-effective viability, as directed. * Perform literature searches for development work, potential projects, and to support QA/QC and Environmental/Health & Safety. * Provide ideas for investigation with an emphasis on commercialization, patent opportunity, or publication on a regular basis. * Provide support to QA/QC by writing analytical SOPs. * Communicate results by providing timely reports and project updates, to include technical reports and summaries for company business units and customers. * Provide monthly report on progress of work to the department head. * Provide help on preparation of quarterly/yearly R&D summaries of ongoing work to peers and senior management. * Plan and develop robust analytical methods including troubleshooting and validation, as appropriate. * Work closely with Synthesis group and support on routine analysis. * Work closely with Quality Assurance (QA) and Quality Control (QC) to identify project needs and to insure strict compliance with internal quality and/or cGMP/ICH guidelines. * Work closely with QA on validation efforts for new API processes to insure strict cGMP compliance, where appropriate. * Work closely with R&D team to answer DMF deficiencies and customer queries. * Maintain rigorous accountability and documentation of work related to controlled substances in accordance with established SOPs and requirements of federal regulations (21 CFR Part 1300-1399). * Adhere to all relevant company SOPs and guidelines, and provide input for correcting and changing existing procedures and processes. * Provide technical support as needed for company products, analytical methods and customer-driven issues, as needed. * Provide necessary information on cost-saving and time-saving alternatives to current analytical and laboratory practices whenever and wherever possible. * Assist in supervision of R&D laboratory operations in general, including troubleshooting of lab systems and instrumentation. * Work with Health, Safety and Environmental representative to identify waste stream data and possible hazards for potential products and processes. * Assist in the maintenance and cleaning of the R&D laboratory in general and in individual workspace in particular. * Seek out opportunities for professional development. * Select and purchase R&D chemicals, glassware and supplies, and track these orders using the established R&D purchase requisition system. * Execute R&D stability program, to include writing and following stability protocols, and packaging and testing APIs, as well as compiling and reporting stability results to R&D manager. * Facilitate the training system within the R&D department in coordination with the requirements set forth by QA. * Other duties as assigned. Position Requirements: * B.S. degree in Chemistry (preferable), Chemical Engineering, or related discipline. * Ability and attitude to assume a leadership role and work in a productive technical team within an industrial research environment. * Ability to communicate effectively through verbal, written, presentation and computer modes of expression. * Ability to confidently represent company on technical matters to customers, senior management, and at scientific venues (conferences and publications). The presently-anticipated base compensation pay range for this position is $102,500 to $125,000. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan, and may be eligible for the Long Term Incentive Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time. The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors. The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s). We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law. Nearest Major Market: Chattanooga

Novelis is one of the world leaders in aluminum recycling and rolling and a leading sustainable aluminum solutions provider. Driven by our purpose of shaping a sustainable world together, we work alongside our customers to provide innovative solutions to the aerospace, automotive, beverage packaging and specialty markets. Headquartered in Atlanta, Georgia, Novelis has approximately 13,000 employees in 32 operating facilities on 4 continents. Responsibilities & Qualifications The Novelis Kennesaw team is seeking an Analytical Chemist in ECA lab. The person in this role will report to the Laboratory Leader. The ideal candidate will be responsible for operating XRD, XRF, ICP, FTIR and XPS. This position will bring its experience in handling different analytical experiments and handle them according to the Novelis safety guidelines. Responsibilities Demonstrate personal commitment to safety and good EHS awareness by following established safety rules and practices during all activities. Ensure all users and visitors are aligned with all Safety Absolutes and other EHS initiatives. Maintain the analytical equipment situated in the area of responsibility to ISO 17025 standards Operate and maintain ICP-OES instruments for elemental analysis of alloys and beverage matrices. Perform XRD analysis for phase identification and crystallographic characterization of metallic samples Conduct XRF testing for rapid compositional screening of solid samples. Use FTIR spectroscopy for organic compound identification and beverage quality assessment. Prepare samples using appropriate digestion, grinding, or dilution techniques. Interpret and report analytical data with accuracy and clarity. Develop and validate analytical methods in compliance with industry standards and regulatory guidelines. Collaborate with cross-functional teams including R&D, Quality Assurance, and Manufacturing. Maintain laboratory documentation, calibration records, and safety protocols. Run qualitative and quantitative analysis of elements, coatings and lubricants using different spectroscopic techniques such as FTIR, NIR and GDOES. Communicate the research findings to the project managers and collaborators on routine basis Minimum Qualifications 3-5 years of progressive experience in analytical chemistry and a BS in chemistry, metallurgy, metallurgical engineering, material science, physics or equivalent. Minimum 3 years of experience in an analytical laboratory setting. Proficiency in operating and troubleshooting ICP-OES, XRD, XRF, and FTIR instruments. Experience with sample preparation techniques for metals and beverages. Strong understanding of analytical chemistry principles and data interpretation. Familiarity with laboratory information management systems (LIMS) is a plus. Excellent communication and organizational skills. Willing to collaborate with other Novelis R&D labs by undergoing training in other areas where resources are necessary for high priority testing Hands on experience working with wet chemistry techniques with an emphasis on material science. Desire and ability to collaborate and communicate across functions are essential to this position. Knowledgeable about overall chemical safety. Preferred Qualifications Master's in Chemistry with 3 years of experience in handling different analytical equipment Experience in metallurgical analysis and food/beverage testing. Knowledge of ISO, ASTM, or FDA standards relevant to analytical testing. Ability to work independently and manage multiple projects simultaneously. What We Offer: Novelis benefits say a lot about how we care for each other. Our employees and their families have many different needs. As a result, our benefits offer choices on many levels and are high in quality, competitive in the marketplace, and affordable. These are a few of the benefits we offer to support you and your family's well-being: Medical, dental and vision insurance Health savings accounts - Company Funded Health Savings Account (HSA) and Health Reimbursement Account (HRA) Company-paid basic life insurance and Additional voluntary life coverage Paid vacation and competitive personal time off 401(k) savings plan with company match Retirement savings plans - medical and prescription drug coverage through private exchange Employee assistance programs - available 24/7 to you and your family Wellness and Work Life Support - career development and educational assistance #LI-NT1 Location Profile Novelis' Global Research and Technology Center located in Kennesaw Georgia within the greater Atlanta metropolitan area is a cutting-edge full-service research and technology hub that employs approximately 200 people including world-class engineers metallurgists chemists scientists technologists and technicians. The facility includes state-of-the-art lab equipment and a diverse mix of product pilot lines that bring innovative solutions to customers in the automotive beverage can and specialty markets. Kennesaw provides a diverse and family-friendly place to live with countless museums cultural opportunities and educational institutions. Novelis is committed to the Kennesaw community and supports a number of local charitable organizations including Habitat for Humanity as well as FIRST Robotics aimed at encouraging young people to pursue the Science Technology Engineering and Mathematics (STEM) fields in order to spur the next generation of scientists and innovators. Novelis recognizes its talented and diverse workforce as a key competitive advantage. Novelis provides equal employment opportunities to all employees and applicants. All terms and conditions of employment at Novelis including recruiting hiring placement promotion termination layoffs recalls transfers leaves of absence compensation and training are without regard to race color religion age sex national origin disability status genetics protected veteran status sexual orientation gender identity or expression or any other characteristic protected by federal provincial or local laws. Disclaimer We encourage all potential candidates to follow the protocols below and to be diligent when sharing any personal information: 1. Check the job posting is live and valid via our careers page: Careers - Novelis 2. Verify any communication with us by contacting our talent team at Careers - Novelis

Provide technical and analytical support to Sales, Operations, and Quality Control Laboratory. Understand and conduct all activities required of a Quality Assurance Chemist. Become knowledgeable in product formulation, chemistry, and technology. Perform hands on analytical work for assigned projects. Coordinate outside analyses of products and projects as required. Develop reprocessing procedures for non-conforming inventories. Manage laboratory instrument calibration and maintenance. Maintain expertise in the operation and capabilities of analytical instrumentation. Provide oversight for instrument calibration and preventative maintenance schedule. Manage new instrument implementation and installation. Conduct research and development to compliment agriculture, construction, oil field, and surfactant portfolio. Develop and introduce new products, formulations, and analytical methods as requested. Communicate activities and findings routinely. Prepare formal reports on activities and goals. Process and analytical optimization. Develop improved analytical methods. Conduct accuracy and reproducibility studies. Prepare formal method documentation. Provide laboratory personnel training. Assist in resolving discrepancies in process and procedure adjustments. Recommend actions for continuous improvement. Indirect supervision of plant and laboratory personnel will be required during routine execution of job functions. Position can include work duties on evenings, nights and weekends to support production efforts. Maintain active certification in first-aid techniques and administer as needed in site emergencies. All Arclin Personnel are required to participate in all Safety Programs and any site-specific safety training and policies.

Why are we proud of what we do at allnex? We create coatings, products which help protect the world for all nex>t generations - and that's exactly what you can do joining us! Imagine how fast your smartphone would become scratched-up, ugly and unusable without a coating. Or an e-bike, the cabin of a train, a beautiful wooden floor, and countless other things in life. Making objects and their surfaces more attractive and longer-lasting means making them more sustainable, and that's a huge part of what working at allnex is about. No matter which role you step into, you'll become part of a global team of passionate people who care deeply about the chemistry, quality, and global impact of coatings. You'll also join a highly multicultural and diverse team of more than 4,000 employees in four regions who - as part of one of the world's leading coating resins companies - serve customers in over 100 countries across the globe. Click here to see why we are proud of what we do in allnex! For a sneak peek into life at allnex site, don't miss our manufacturing Operator Movie! Position overview Are you passionate about hands-on support for customers and helping them find innovative solutions that make a real impact? We are seeking a Technical Service & Business Development Chemist to serve the printing and packaging markets, specializing in inks and coatings based on energy curable, waterborne, and solventborne chemistries. In this role, you will work directly with customers to solve technical challenges, influence product selection, and support new product introductions that drive commercial success. You'll spend significant time in the lab preparing formulations, conducting application testing, and benchmarking performance, while also traveling to customer sites and industry events to provide on-site technical support and build strong relationships. If you thrive on making a difference through both laboratory work and customer engagement-and want to be part of a collaborative, innovative team-we want to hear from you! Responsibilities * Provide hands-on technical service and formulation support for printing and packaging applications (inks and coatings), focusing on energy curable, waterborne, and solventborne technologies. * Plan and execute laboratory work, including formulation development, application testing, and performance benchmarking to address customer and market needs. * Engage directly with customers through on-site visits, technical discussions, and virtual meetings to understand challenges and deliver solutions. * Travel to customer sites, industry events, and internal meetings (up to 30%) to provide in-person technical support and strengthen customer relationships. * Collaborate with Sales, Marketing, and R&D teams to support product selection, troubleshooting, and new product introductions for printing and packaging markets. * Translate customer requirements into actionable development briefs and contribute to technical value propositions and launch materials. * Monitor market and technology trends in printing and packaging to identify innovation opportunities and guide portfolio development. * Represent allnex as a technical expert at conferences, trade shows, and customer forums within the printing and packaging sector. Required skills and experience * Minimum 5 years of hands-on formulation experience in coatings or inks for printing and packaging applications. * Strong working knowledge of waterborne, energy curable, and/or solventborne chemistries. * Proven ability to work independently in a laboratory setting, including formulation development, application testing, and performance benchmarking. * Demonstrated success in engaging with customers to understand technical needs, troubleshoot issues, and deliver effective solutions. * Willingness and ability to travel up to 30% for customer visits, technical support, and industry events. * Strong communication skills, with the ability to clearly present technical information to both technical and non-technical audiences. * Proficiency in experimental design, data analysis, and technical documentation. * Team-oriented mindset with the ability to collaborate across functions (Sales, Marketing, R&D) and influence outcomes. * Fluent English skills, both written and verbal, required Qualifications * Bachelor's degree in Chemistry, Chemical Engineering, or a related scientific field required; Master's degree preferred. * Strong foundation in formulation science and application testing for coatings and/or inks. * Knowledge of polymer chemistry, surface chemistry, or radiation-curable systems is a plus. * Experience with printing and packaging technologies or materials is highly desirable. * Equivalent technical experience in lieu of formal education may be considered. We offer We are proud to offer an international working experience with a tight-knit network of employees, making it easy to connect and learn from people all across our different functions. On top of that we are a truly innovative company with a strong team spirit, openness to new ideas, and great opportunities to grow and develop your career. Equal Employment Opportunity allnex is proud to be an equal opportunity employer. We celebrate diversity and are committed to an environment where all colleagues contribute for the benefit of our employees, our products, and our communities. Find out how you can make an impact! Check out our careers page for available opportunities. We look forward to hearing from you. ************** Nearest Major Market: Alpharetta Nearest Secondary Market: Atlanta Job Segment: Research Scientist, Sustainability, Technical Support, Business Development, Science, Energy, Technology, Sales

Title: Process and Product Development Scientist Industry: Pharmaceutical Hours: M-F, 8am-5pm Salary: Competitive within industry Employment Type: Direct hire Environment: Client is a fully integrated biopharmaceutical company focused on developing, manufacturing and commercializing specialty products. Our diversified product portfolio in the specialty neurology and women's health space, together with our non-promoted complex formulations of generic drugs, form the foundation of our unwavering commitment to improve patients' lives. Description: The incumbent is responsible for supporting Technology Transfer and Product Development of pharmaceutical dosage forms and drug delivery systems for new and existing chemical entities according to approved plans/protocols. The Process and Development Scientist is responsible for developing, organizing, and leading development activities in the manufacturing area and performing developmental activities. The Process and Development Scientist also performs related technical writing functions, including Standard Operating Procedures (SOPs). The incumbent is also responsible for operating the laboratory process and testing related equipment in the Pharmaceutical Sciences Laboratory. Essential Responsibilities: Operate complex scientific instruments, mix and assemble compound drugs, and perform tests that determine whether liquids, powders or tablets contain the right amount of each ingredient and meet other requirements. Record production statistics, monitor equipment operations and assign tasks to production staff. Supervise manufacturing and/or packaging operations in full cGMP conditions. Assist with preparing laboratory experiments and critically analyzing results. Leads and assists all phases of formulation and process development. With minimal supervision, evaluates projects for development requirements, determines project timelines and priorities, develops protocols, and completes approval, execution and reporting. Provides guidance and technical information to manufacturing technicians and validation scientists. Supports project scope development activities with various related departments, and coordinates with testing participants during all development activities. Writes SOP s as new processes are developed and serves as subject matter expert in the assigned areas. Write, review, and approve cGMP documentation including batch records, protocols, SOPS, pharmaceutical development reports, investigation SME statements, and outcomes for development problems, etc. Participate in validation activities for projects that can encompass multiple protocols. Authors and reviews new procedures or incorporates changes to existing standard operating procedures describing validation principles, activities and training. Writes and conducts shipping studies at the vendor s site. Subject Matter Expert (SME) to all validation and manufacturing activities. Works with other departments (QA, Laboratory and Validation) to support site projects. Reviews engineering drawings (P&IDs, construction, as-built, flow diagrams) for accuracy and compliance with cGMP/Validation principles and provides feedback to engineering for any noted deficiencies or improvements. Performs and reviews development testing and presents results to various departments in team meetings. Writes and reviews development protocols and reports for completeness and accuracy, sound rationale, compliance with policies and procedures, and accurate data analysis. Compares results against acceptance criteria and brings exceptions and deviations to management's attention. Initiates Exception or Incident Reports and resolves discrepancies. Willing to travel to CMOs and vendor sites including internationally. Core Competencies Strong interpersonal and leadership skills are necessary to communicate clearly and effectively and coordinate with qualification/validation activities with all levels of personnel from various disciplines including Manufacturing Operations, Quality Assurance, Analytical Sciences, Engineering, Validation, Facilities, and Regulatory Affairs. Adept at using personal computers and various software programs (e.g., Word, Excel, Project & Minitab), for data acquisition, statistical analysis of validation data and word processing. Proficient in batch record and protocol development, data analysis and report writing. Understanding of basic statistics and their use in qualification and analysis. Minimum Qualifications: Bachelor s degree in chemistry, engineering, pharmacy or a related scientific discipline. Minimum 0-5 years experience in the pharmaceutical or biotechnology industry. Master s degree in chemical engineering or scientific equivalent preferred. Minimum 0-3 years experience in the pharmaceutical or biotechnology industry. Experience in manufacturing and packaging operation in a solid dose environment. Expertise in the principles of equipment design/operations and validation of at least 4 of the following: Facilities (including design, material and personal flow analysis, HVAC/HEPA), utilities (including WFI & purified water, clean steam, compressed air), Clean-In- Place system, solid dosage equipment, process and cleaning validation. Physical and Mental Demands and Work Environment The physical and mental demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodation will be made to enable individuals with disabilities to perform essential functions. Physical Demands While performing the duties of this job, the employee is regularly required to stand. The employee is frequently required to walk, sit, climb or balance and stoop, kneel, crouch or crawl. The employee is occasionally required to use hands to handle or feel. The employee must regularly lift and/or move up to 25 pounds, frequently lift and/or move up to 50 pounds, and occasionally lift and/or move more than 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Mental Demands While performing the duties of this job, the employee is regularly required to use English written and oral communication skills; read and interpret data, information and documents; analyze and solve non-routine office administrative problems; use math and mathematical reasoning; observe and interpret situations; learn and apply new information skills; perform detailed work on multiple, concurrent tasks; work under deadlines with frequent interruptions; and interact with the department staff and others outside the department. Work Environment The employee works under typical office conditions. The noise level in the work environment is usually quiet to moderate. The noise level on the shop floor may require the use of hearing protection. The use of PPE in manufacturing operations may be required. ADA/EOE IND123 SRG4 Life Sciences delivers flexible staffing solutions nationwide, specializing in pharmaceutical, CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors. We provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. SRG4 Life Sciences operates on a relationship-driven model partnering closely with clients to understand not only the role, but the company s culture, goals, and vision. Our mission is to match purpose-driven professionals with organizations committed to advancing human health, building long-term partnerships that drive innovation, quality, and performance.

I have a Special Chemistry Med Tech role available near Cane Ridge, Tennessee! Details - Full-time and permanent - Shift: Days - Opportunities for growth - Full, comprehensive benefits package (PTO, health insurance, etc.) Requirements - College degree - ASCP cert - Prior experience, including special chemistry Click apply or email your resume to leah@ka-recruiting.com/call or text 617-746-2751! You can also schedule a time to chat here -https://calendly.com/leahkarecruiting/10min. REF#LM5029

Job Title: Chemical Technician II Department: Dalton Manufacturing FLSA Status: Non- Exempt At Harcros Chemicals Inc., an employee-owned company with a rich legacy in specialty chemical manufacturing and distribution, we're continuously expanding. With 2 manufacturing plants and 27 distribution facilities across 20 states, we're seeking a dedicated Chemical Technician II professional to join our team to assist with opportunities. This person will be responsible for: Job Description As A Quality Control Technician / R&D Chemist you will be expected to maintain product quality, develop and implement new processes, encourage process improvement, uphold safety standards, maintain all instruments, promote open lines of communication, work as a team, and always maintain professional integrity. Job Duties Proficiency in performing chemical, physical, and visual testing using standard laboratory equipment. Possible instruments include but are not limited to GC, GC Headspace, pH, Metrohm Auto-Titrators, KF, UV-Vis, HPLC, etc. Proficiency in setting up, running, and troubleshooting chemical reactions. Help develop, implement, and validate testing procedures. Maintain laboratory instrument(s) by performing calibrations, preventive maintenance, and routine inspections. Maintain quality records / databases and prepare required quality documents. Maintain a clean, organized, and safe laboratory environment in compliance with company and regulatory standards. Collaborate with production, maintenance, and distribution teams to troubleshoot quality issues and implement corrective actions. Help collect and prepare samples for shipment to customers. Help set up, run, problem solve, test, and clean up R&D reactions. Perform shipments of non-hazardous and hazardous chemicals domestically and internationally in compliance with company and regulatory standards. Education and/or Experience: Degree in Biology, Chemistry, or another related field. Experience in a manufacturing or laboratory environment preferred. Strong analytical skills with experience in data analysis, interpretation, critical thinking, and reporting. The Required Skills We Are Looking For: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical Capabilities & Requirements: Be able to pass a background check. Be able to work a 4 on 3 off 3 on 4 off work schedule. Working in an onsite setting. Authorized to work in the United States. Be able to lift or carry object(s) weighing up to 40 lbs. Be able to be on your feet for long periods of time. Be able to work in an outdoor environment with temperatures below 32degrees and above 100 degrees for a limited time. Being able to work holidays and overtime as needed or scheduled (Plant runs 24 hr./day 365 days a year). Work Environment: Potential air contaminated below established exposure levels that may affect the respiratory system or skin, (i.e., fumes, odors, dust, mist, etc.) but which may or may not require specific personal protective equipment. Outdoor environment and subject to temperatures below 32 degrees for periods of less than one hour and temperatures above 100 degrees for periods of less than one hour. Loud work environment requiring hearing protection in certain areas. Vibration The Benefits- Harcros Chemicals is 100% Employee-Owned Employee Stock Ownership Plan (ESOP)* * Qualifying period must be met. * Profit Share Program* * Qualifying period must be met. * Safe Harbor Contribution* * 401(k) Match* * Medical, Vision & Dental Insurance Coverage * Employer Paid Life Insurance * Parental Leave * Employer Paid Accidental Death & Dismemberment * Employer Paid Short Term & Long-Term Disability* * Employee Assistance Program * Inquire about additional benefits The information on this Benefit leaflet is presented for illustrative purposes and is based on information provided by the employer. The text contained in this was taken from various summary plan descriptions and benefit information. While every effort was taken to accurately report benefits, discrepancies, or errors are always possible. In case of discrepancy between this and the actual plan documents the actual plan, documents will prevail. All information is confidential, pursuant to the Health Insurance Portability and Accountability Act of 1996. If you have any questions about your Guide, please refer to the Employee Manual for additional information or contact benefits manager. Harcros Chemicals is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against based on their race, gender, sexual orientation, religion, national origin, age, disability, veteran status, or other protect classification.

Stratfield Consulting is seeking an Food Scientist to play a pivotal role in bringing innovative beverage concepts to life from idea to market. This hands-on, entrepreneurial position bridges science, creativity, and execution-managing day-to-day product development activities such as lab work, ingredient sourcing, and prototype testing while driving broader project timelines and innovation goals. The ideal candidate combines technical expertise, curiosity, and organizational strength with a roll-up-your-sleeves attitude to balance strategic oversight and practical execution. This is an opportunity to make a tangible impact in a fast-paced, collaborative environment where ideas move quickly and innovation is celebrated. This is permanent role that will be fully onsite in the Roswell, Ga area. Sorry, sponsorship is not available for this position. Responsibilities New Product Development Process Management Execute the New Product Development roadmap, ensuring progress across all phases. Schedule and facilitate New Product Development meetings, document discussions, and track key decisions. Maintain project trackers, timelines, and phase status updates. Prepare gate review presentations and post-launch recaps summarizing insights and outcomes. Product Development Support Collaborate with R&D partners to develop and refine beverage formulas. Prepare and present product samples for tastings, sensory panels, and demonstrations. Coordinate tasting sessions, compile feedback, and summarize actionable insights. Oversee lab organization, equipment readiness, and inventory management. Support pilot production runs, stability tests, and line trials with accurate documentation. Supply Chain Coordination Manage logistics for shipping ingredients, samples, and materials to partners. Oversee purchasing and invoicing for R&D materials and services. Track inventory of samples, packaging, and test ingredients to ensure availability. Marketing & Customer Engagement Support Lead product tastings for internal teams and external stakeholders. Collaborate with Sales and Marketing on presentations, packaging evaluations, and product positioning. Collect and analyze competitive benchmarks and consumer insights to guide development strategy. Qualifications Bachelor's degree in Food Science, Chemistry, Biology, or related technical discipline. 3+ years of hands-on experience in product development (beverage preferred; food acceptable). Experience managing innovation or New Product Development projects from concept to launch. Strong communication and project management skills. Analytical thinker with curiosity for market trends and emerging technologies. Experience in small to mid-sized environments preferred. What We Offer Competitive salary and benefits package (including medical and 401K). Opportunities for professional growth and development. A dynamic and inclusive work environment. About Stratfield Stratfield Consulting is a trusted partner for organizations seeking innovative solutions and exceptional talent. We specialize in connecting top professionals with opportunities that drive impact and growth. Our team values collaboration, integrity, and excellence-helping clients and candidates achieve success through strategic partnerships.

Job Purpose As Product Development Analyst, you will be responsible for managing the reference data for ICE's energy, agriculture and financial derivatives markets and distributing that data across multiple systems to the trading and clearing platforms. You will be responsible for ongoing product maintenance as well as generating and executing deployment plans for new product launches, and you will serve as a subject matter expert and escalation contact for operations incident resolution. Additionally, the Product Development Analyst will draft functional requirements for software enhancements to improve daily productivity of the team and serve as a stakeholder representing the configuration team on new derivatives market initiatives. Responsibilities * Create and execute workflow processes for reference data management * Work within team to validate change promotion in production environment and configure change sets in non-production environments * Investigate inbound data inquiries from external and internal stakeholders and escalate as needed * Extract and analyze product reference data using different tools (SQL, Excel, etc.) * Construct customized methods to update product reference data according to business needs * Work with the project team and stakeholders to configure, test and deploy new products * Assist project management with prioritizing, tracking, and improving the deployment of new product initiatives * Assist operations with incident resolution * Develop requirements and analysis artifacts including use-cases, activity diagrams, user-interface schematics, business rules, technical specifications, and process flow for ICE's derivatives reference data systems. Knowledge and Experience * Bachelor's Degree in Finance, Economics, Business Analytics, CS, MIS or related discipline * Strong written and verbal communication skills * Must possess excellent communication skills, written and oral * General interest in markets. 2+ years of experience with banking, trading, clearing, or related industry highly preferred * Basic PL/SQL knowledge preferred. Moderate or advanced skills a plus * Microsoft Office (Word, Excel, PowerPoint, and Visio) - Strong Excel skills required, experience with VBA a plus * Ability to proactively identify, report, and attack risks to project delivery using principles of iterative management * Demonstrates strong technical aptitude and understanding of how technologies impact delivery * Must be results-oriented and self-motivated * Ability to work independently and as a part of a team * Ability to work effectively in a fast-paced, dynamic environment * Ability to effectively facilitate requirements gathering sessions, reviews and issue resolution involving multiple stakeholders * Ability to enforce change control procedures to ensure requirements changes aren't ad hoc and are realized by the release team and stakeholders * Experience with object-oriented applications and relational databases a plus * Experience with API development a plus * Experience working on systems with high transaction volume management a plus #LI-JW1 Intercontinental Exchange, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to legally protected characteristics.

WHO WE ARE Elliott Davis pairs forward-thinking tax, assurance and consulting services with industry-leading workplace culture. Our nine offices - located in the fastest growing cities in the US - are built on a foundation of inclusivity, collaboration, and collective growth. We work daily to provide exceptional service to our people, customers, and our communities. Audit and assurance services are provided by Elliott Davis, LLC (doing business in NC and D.C. as Elliott Davis, PLLC), a licensed CPA firm. As an Internal Controls Experienced Associate at Elliott Davis, you will be part of a dynamic and expanding team that helps clients enhance their internal control environments, comply with regulatory requirements, and improve operational efficiency. You will work across industries to assess risk, evaluate control design and effectiveness, and support clients in achieving sustainable compliance. You will be a champion for the Internal Controls program, work collaboratively to build a strong team, and deliver extraordinary client service. Key Responsibilities: * Execute internal control assessments, including SOX readiness and compliance engagements. * Conduct walkthroughs and testing of business process and IT controls. * Evaluate control design and operating effectiveness; identify gaps and recommend remediation. * Prepare high-quality workpapers and client deliverables in accordance with firm methodology. * Collaborate with audit and advisory teams to integrate internal control insights into broader engagements. * Support clients in remediation efforts and implementation of control improvements. * Contribute to the development of internal methodologies, templates, and best practices as the program scales. * Proficient in writing, grammar, and editing skills. * Familiarity with risk and controls assessments and controls testing project lifecycles. * Stay current on regulatory changes and industry best practices related to internal controls and risk management. Qualifications: * Bachelor's degree in Accounting, Finance, Business Administration, or related field. * 1-3 years of experience in internal controls, audit, or risk management. * Knowledge of internal control frameworks (e.g., COSO, COBIT). * Experience in scoping and controls testing under AICPA and PCAOB standards and SOX compliance, including identification of control gaps and deficiencies. * Experience with ERP systems (e.g., SAP, Oracle) and data analytics tools is a plus. * Strong understanding of financial reporting and operational processes. * Proficient in Microsoft Office (Word, Excel, PowerPoint, Visio). * CPA or CIA certification preferred or in progress. Preferred Attributes: * Excellent analytical, communication, and organizational skills. * Professionalism and professional curiosity. * Attention to detail and commitment to quality. * Team-oriented and able to manage multiple priorities. * Proactive mindset with a continuous improvement approach. * Positive attitude and integrity * Adaptable and flexible. #LI-RB1 #LI-HYBRID WHY YOU SHOULD JOIN US We believe that when our employees are able to thrive in all facets of life, their work and impact are that much greater. That's right - all aspects of life, not just your life as an employee, because we understand that there's life beyond your job. Here are some of the ways our work works for your life, your growth, and your well-being: * generous time away and paid firm holidays, including the week between Christmas and New Year's * flexible work schedules * 16 weeks of paid maternity and adoption leave, 8 weeks of paid parental leave, 4 weeks of paid and caregiver leave (once eligible) * first-class health and wellness benefits, including wellness coaching and mental health counseling * one-on-one professional coaching * Leadership and career development programs * access to Beyond: a one-of-a kind program with experiences that help you expand your life, personally and professionally NOTICE TO 3RD PARTY RECRUITERS Notice to Recruiters and Agencies regarding unsolicited resumes or candidate submissions without prior express written approval. Resumes submitted or candidates referred to any employee of Elliott Davis by any external recruiter or recruitment agency by any means (including but not limited to via Internet, e-mail, fax, U.S. mail, and/or verbal communications) without a properly executed written contract for a specified position by an authorized member of the Talent Acquisition team become the property of Elliott Davis. Elliott Davis will not be responsible for, or owe any fees associated with, referrals of those candidates and/or for submission of any information, including resumes, associated with individuals. ADA REQUIREMENTS The physical and cognitive/mental requirements and the work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical Requirements While performing the duties of this job, the employee is: * Regularly required to remain in a stationary position; use hands repetitively to operate standard office equipment; and to talk or hear, both in person and by telephone * Required to have specific vision abilities which include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus Cognitive/Mental Requirements While performing the duties of this job, the employee is regularly required to: * Use written and oral communication skills. * Read and interpret data, information, and documents. * Observe and interpret situations. * Work under deadlines with frequent interruptions; and * Interact with internal and external customers and others in the course of work.

Job DescriptionBenefits: 401(k) matching Bonus based on performance Competitive salary Free uniforms At DreamScapes, we take pride in creating and maintaining healthy, vibrant landscapes for our clients. Our team of professionals is dedicated to providing high-quality lawn and plant care through responsible and effective treatments. Position Overview: We are seeking a knowledgeable and detail-oriented Chemical Technician to join our landscape maintenance team. The ideal candidate will have experience applying fertilizers, herbicides, and pesticides safely and effectively to promote healthy lawns, trees, and shrubs. Key Responsibilities: Mix and apply fertilizers, herbicides, and pesticides according to label and safety guidelines Identify turf and plant health issues, including weeds, diseases, and insects Maintain accurate records of chemical usage and service reports Calibrate and maintain spray equipment and other application tools Communicate effectively with clients and team members about treatments and results Follow all safety regulations and environmental standards Qualifications: 23 years of experience in lawn or landscape chemical applications preferred State pesticide applicators license (or ability to obtain one) Tree and shrub id of 20 plus grass type id Disease and insect id. Knowledge of fertilizers, herbicides, and pest management techniques Strong attention to safety and detail Ability to work outdoors in various weather conditions Valid drivers license and clean driving record required

ABOUT UA/UNIFORM ADVANTAGE BRANDS For over 35 years, UA Brands has been synonymous with fashion-forward specialty apparel for the medical and culinary professions. We are proud to support our valued customers - true heroes giving back with every shift. Our culture includes a long history of philanthropy and community support. Our strong values and unique culture are built on collaborating not merely as coworkers, but as family and friends. From the beginning, we provide candidates with an authentic look into how UA Brands embraces their skills and perspectives, all in ways that continue to set us apart. As a Quality Control Associate, Execute planned quality control inspections on goods in adherence to company quality standard requirements. This candidate will be responsible for the daily processes involved with the quality evaluation of inbound container shipment and quality callouts from returns, embroidery, customer service, retail and corporate. The team will be processing all quality evaluations within AQL standards established and within Inventory Control requirements. Report evaluations and works directly with third-party quality service providers when needed. HERE'S THE GOOD STUFF Earn $.75 more/hour for evening shifts Earn $2.00 more/hour for weekend shifts Must be able to work Saturdays and Sundays, as needed What you'll do Follows standards and methods for inspection, testing, and evaluation. Follows sampling procedures and designs. Completes forms and instructions for recording, evaluating, and reporting quality and reliability data. Interfaces with all departments to assist in the coordination and resolving of quality-related problems. Follows methods and procedures for disposition of non-conforming material. Provides computerized status report describing progress and concerns related to inspection activities, non-conforming items, and/or other items related to the quality of the process, material, or product. Maintains a working knowledge of the latest styles and specifications of products for examination methods. Must be willing to operate powered equipment. What you'll bring Identifies and resolves problems in a timely manner Basic PC skills include proficient typing, mouse usage, account navigation, Excel and Outlook. Writes clearly and informatively; Presents numerical data effectively; Able to read and interpret written information. Completes administrative tasks correctly and on time. Adapts to changes in the work environment; Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent changes, delays, or unexpected events. Priorities and plans for work activities; Uses time efficiently Meets productivity standards; Completes work in timely manner; Strives to increase productivity while maintaining accuracy and quality. It's a physical job Walk up to 5 miles a day Stand, walk or sit for long periods of time Crouch, kneel or crawl (occasionally) Lift, push or pull up to 40 pounds Be able to handle noisy conditions PLENTY OF BENEFITS TOO UA BRANDS offers a full range of benefits allowing you the opportunity to customize a benefits package that addresses both your health and financial needs. Flexible scheduling Medical, Dental, Vision, and Pharmacy Coverage Life/AD&D Insurance Employee Assistance Program - support for everyday challenges Extensive 401(k) plan with company matching - Save for your future Short & Long Term Disability - Company Paid Accident, Hospital Care and Critical Illness Insurance - Protect your Income Holiday Pay Paid Time Off - Life Balance Volunteer Time Off - Make an Impact Employee Discount Program Referral Program - Get paid to work with Friends Free work “uniform” tops provided Regular Social Activities and Events - Mandatory Fun See more of the benefits we offer Our distribution center is located at 777 Douglas Hill Road, Suite 100, Lithia Springs, GA 30122; we are NOT on the Marta line. UA is an Equal Opportunity Employer In order to provide equal employment and advancement opportunities to all individuals, employment decisions at UA Brands will be based on merit, qualifications, and abilities. UA Brands does not discriminate in employment opportunities or practices based on race, color, religion, sex, national origin, age, disability, or any other characteristic protected by law. UA Brands will make reasonable accommodations for qualified individuals with known disabilities unless doing so would result in an undue hardship. Last (but not least) UA is a drug-free workplace.

Novelis is one of the world leaders in aluminum recycling and rolling and a leading sustainable aluminum solutions provider. Driven by our purpose of shaping a sustainable world together, we work alongside our customers to provide innovative solutions to the aerospace, automotive, beverage packaging and specialty markets. Headquartered in Atlanta, Georgia, Novelis has approximately 13,000 employees in 32 operating facilities on 4 continents. Responsibilities & Qualifications The Novelis Kennesaw team is seeking an Analytical Chemist in ECA lab. The person in this role will report to the Laboratory Leader. The ideal candidate will be responsible for operating XRD, XRF, ICP, FTIR and XPS. This position will bring its experience in handling different analytical experiments and handle them according to the Novelis safety guidelines. Responsibilities Demonstrate personal commitment to safety and good EHS awareness by following established safety rules and practices during all activities. Ensure all users and visitors are aligned with all Safety Absolutes and other EHS initiatives. Maintain the analytical equipment situated in the area of responsibility to ISO 17025 standards Operate and maintain ICP-OES instruments for elemental analysis of alloys and beverage matrices. Perform XRD analysis for phase identification and crystallographic characterization of metallic samples Conduct XRF testing for rapid compositional screening of solid samples. Use FTIR spectroscopy for organic compound identification and beverage quality assessment. Prepare samples using appropriate digestion, grinding, or dilution techniques. Interpret and report analytical data with accuracy and clarity. Develop and validate analytical methods in compliance with industry standards and regulatory guidelines. Collaborate with cross-functional teams including R&D, Quality Assurance, and Manufacturing. Maintain laboratory documentation, calibration records, and safety protocols. Run qualitative and quantitative analysis of elements, coatings and lubricants using different spectroscopic techniques such as FTIR, NIR and GDOES. Communicate the research findings to the project managers and collaborators on routine basis Minimum Qualifications 3-5 years of progressive experience in analytical chemistry and a BS in chemistry, metallurgy, metallurgical engineering, material science, physics or equivalent. Minimum 3 years of experience in an analytical laboratory setting. Proficiency in operating and troubleshooting ICP-OES, XRD, XRF, and FTIR instruments. Experience with sample preparation techniques for metals and beverages. Strong understanding of analytical chemistry principles and data interpretation. Familiarity with laboratory information management systems (LIMS) is a plus. Excellent communication and organizational skills. Willing to collaborate with other Novelis R&D labs by undergoing training in other areas where resources are necessary for high priority testing Hands on experience working with wet chemistry techniques with an emphasis on material science. Desire and ability to collaborate and communicate across functions are essential to this position. Knowledgeable about overall chemical safety. Preferred Qualifications Master's in Chemistry with 3 years of experience in handling different analytical equipment Experience in metallurgical analysis and food/beverage testing. Knowledge of ISO, ASTM, or FDA standards relevant to analytical testing. Ability to work independently and manage multiple projects simultaneously. What We Offer: Novelis benefits say a lot about how we care for each other. Our employees and their families have many different needs. As a result, our benefits offer choices on many levels and are high in quality, competitive in the marketplace, and affordable. These are a few of the benefits we offer to support you and your family's well-being: Medical, dental and vision insurance Health savings accounts - Company Funded Health Savings Account (HSA) and Health Reimbursement Account (HRA) Company-paid basic life insurance and Additional voluntary life coverage Paid vacation and competitive personal time off 401(k) savings plan with company match Retirement savings plans - medical and prescription drug coverage through private exchange Employee assistance programs - available 24/7 to you and your family Wellness and Work Life Support - career development and educational assistance #LI-NT1 Location Profile Novelis' Global Research and Technology Center located in Kennesaw Georgia within the greater Atlanta metropolitan area is a cutting-edge full-service research and technology hub that employs approximately 200 people including world-class engineers metallurgists chemists scientists technologists and technicians. The facility includes state-of-the-art lab equipment and a diverse mix of product pilot lines that bring innovative solutions to customers in the automotive beverage can and specialty markets. Kennesaw provides a diverse and family-friendly place to live with countless museums cultural opportunities and educational institutions. Novelis is committed to the Kennesaw community and supports a number of local charitable organizations including Habitat for Humanity as well as FIRST Robotics aimed at encouraging young people to pursue the Science Technology Engineering and Mathematics (STEM) fields in order to spur the next generation of scientists and innovators. Novelis recognizes its talented and diverse workforce as a key competitive advantage. Novelis provides equal employment opportunities to all employees and applicants. All terms and conditions of employment at Novelis including recruiting hiring placement promotion termination layoffs recalls transfers leaves of absence compensation and training are without regard to race color religion age sex national origin disability status genetics protected veteran status sexual orientation gender identity or expression or any other characteristic protected by federal provincial or local laws. Disclaimer We encourage all potential candidates to follow the protocols below and to be diligent when sharing any personal information: 1. Check the job posting is live and valid via our careers page: Careers - Novelis 2. Verify any communication with us by contacting our talent team at Careers - Novelis We can recommend jobs specifically for you! Click here to get started.

Sun Pharma is the world's fourth largest generics company with presence in Specialty, Generics and Consumer Healthcare products. Supported by more than 40 manufacturing facilities, we provide high-quality medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Over the last two decades, Sun Pharma has established itself as a leading player in the generics market in the U.S., and we are rapidly ramping up our presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology. Are you passionate about quality and precision in the lab? Join our team as a QC Chemist and play a key role in ensuring the highest standards across all departments. This is an exciting opportunity to contribute to method development, support critical QC activities, and drive continuous improvement in a dynamic environment. Schedule: 3rd Shift: Monday - Friday, 11:30pm - 8:00am Key Responsibilities * Provide analytical support to all departments. * Assist with regular QC activities as needed. * Lead method development, including validation and documentation. * Prepare concise and timely reports for management on projects and routine activities. * Investigate and resolve customer complaints. * Support technician training initiatives. * Perform other duties as assigned. Requirements * Associate or Bachelor's degree in Chemistry or a related field. * Hands-on laboratory experience. * Working knowledge of cGMP as it relates to lab activities. Why Join Us? * Be part of a collaborative team committed to excellence. * Opportunity to work on diverse projects and develop new methods. * Competitive compensation and benefits package. Ready to make an impact? Apply today and help us uphold the highest standards of quality! The presently-anticipated base compensation pay range for this position is $61,500 to $77,000. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan, and may be eligible for the Long Term Incentive Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time. The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors. The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s). We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law. Notice to Agency and Search Firm Representatives: Sun Pharmaceuticals (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Sun employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Sun. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Nearest Major Market: Chattanooga

Perform inspections on raw material, production, shipping, and developmental samples using standard methods. Inspections via physical test and Certificate of Analysis review. Approval of conforming materials to internal and customer requirements. Control non-conforming materials. Recommend any needed adjustments or actions to production based on sample test results, formula guidelines, experience, and other experts as necessary for efficient and timely completion of products meeting customer expectations. Experience and capability to operate a variety of laboratory analytical equipment; including set up, calibration, and maintenance. GC-FID (OpenLab CDS) HPLC (Empower 3) FTIR (Omnic) Flame AAS (Solaar) Auto Titrators (LabX) Viscometers Moisture Analyzers pH Meters Maintain accurate records of all data taken using the LIMS system, batch cards, notebooks, reports, and checklists necessary for the specific type of data being recorded. Capability of using statistical programs to evaluate results. Proficiency in Microsoft Office Suite and Microsoft 365. Ensure accurate and timely delivery of legally binding documents Certificates of Analysis Bills of Lading Collect and maintain samples for inspection, label properly, sort and store for all lots numbers, for required retain period. Participate in continuous improvement activities for laboratory, laboratory/production interactions, and production processes. Including recommending procedure changes, documenting non-conformance incidents, participating in root cause investigations, and actively learning/reviewing analytical test methods and quality protocols. Maintain the laboratory in safe, organized, neat, well stocked, functional condition; including cleaning up work areas, submitting purchase requests for depleted items, prepare replacement stock solutions, maintaining method calibrations, monitoring reagent shelf life, and repairing or notifying others of malfunctioning equipment. Participate in site safety and environmental programs. Perform various clerical duties relating to laboratory responsibilities. Perform laboratory activities as outlined in various ISO and work instruction documents including internal audit responsibilities. Train in and maintain active certification in first-aid techniques. Administer first-aid as needed in site emergencies. Communicate pertinent information to other shifts, staff, and plant personnel on a timely basis. Prepare weekly reports on progress toward yearly goals. Ability to interact and communicate with others effectively, written and oral.