Chemist jobs in Indiana

Trelleborg is a world leader in engineered polymer solutions for almost every industry on the planet. And we are where we are because our talents brought us here. By specializing in the polymer engineering that makes innovation and application possible, Trelleborg works closely with leading industry brands to accelerate their performance, drive their business forward-and along the way, shape the industry and progress that will benefit humankind in the exciting years ahead. Our people are Shaping Industry from the Inside. Why don´t you join us? About the Role We are seeking a collaborative technical leader and subject matter expert in elastomer materials to help drive innovation and development in material selection, formulation, characterization, scale-up, and manufacturing. In this role, you will serve as the primary materials contact for cross-functional regional teams-including marketing, engineering, and manufacturing-and will be responsible for delivering innovative, technically differentiated solutions that meet regulatory standards and advance our material capabilities. In this role, you will serve as the primary materials contact for cross-functional regional teams-including marketing, engineering, and manufacturingand will be responsible for delivering innovative, technically differentiated solutions that meet regulatory standards and advance our material capabilities. Responsibilities Lead material-related initiatives that support strategic business segments and address diverse customer needs. Guide research and development (R&D) efforts in alignment with business strategies and technology roadmaps. Collaborate with customers and internal teams to translate requirements into material specifications; develop rubber formulations and conduct experiments to validate performance. Apply scientific principles to deliver innovative, high-value solutions. Formulate new materials, coatings, and polymers to address industry challenges and create new market opportunities. Analyze test data and provide recommendations on material selection, compounding, molding, testing, regulatory compliance, and vendor sourcing. Partner with manufacturing teams to support compounding, prototyping, and molding processes. Stay informed about global regulatory standards and work closely with compliance teams. Work collaboratively with vendors and customers to resolve technical material issues. Provide technical support across departments and manage projects effectively, fostering an inclusive and respectful team environment. Collaborate with global R&D teams across APAC, EMEA, and the Americas. Qualifications Bachelor's degree in chemistry, chemical engineering, polymer science, materials engineering, biochemical engineering, or related field. Strong background in rubber compounding and elastomeric materials. Familiarity with fillers and reinforced composites. Skilled in statistical design and experimental data analysis. Excellent problem-solving, communication, and documentation skills. Preferred Skills 10+ years of relevant experience in elastomer or advanced material development. MS or PhD in a related discipline. Deep expertise in rubber chemistry, thermoplastics, physics, DOE, and performance testing. Experience with elastomeric formulations for dynamic applications. Strong understanding of structure-property relationships in materials.

Job Title: Chemist Duration: 12 months contract with extensions Join a global leader in agricultural innovation, supporting the design and synthesis of novel organic compounds for crop protection and vegetation management. Key Responsibilities: Perform multi-step synthesis (mg-g scale) and purification using chromatography and crystallization. Collaborate with cross-functional teams to optimize lead compounds. Troubleshoot synthetic challenges and document experiments accurately. Maintain lab safety and organization. Qualifications: BS in Chemistry with 2+ years or MS in Chemistry with no experience of organic synthesis lab. Hands-on experience with NMR, LCMS, and other analytical tools. Strong planning, multitasking, and problem-solving skills. Preferred: Research experience in discovery-phase or agricultural chemistry. Passion for innovation and teamwork.

Job Responsibilities: Perform qualitative and quantitative chemical analyses using techniques such as HPLC, GC, UV-Vis, FTIR, and titrations. Prepare and standardize reagents, solutions, and buffers. Conduct testing on raw materials, intermediates, and finished products according to approved methods and SOPs. Document all testing activities clearly and accurately in compliance with cGMP and ALCOA+ principles. Interpret and evaluate analytical data, ensuring results meet established specifications. Participate in method validation, equipment calibration, and troubleshooting as needed. Maintain laboratory equipment and ensure proper functioning through routine maintenance and calibration. Assist in investigations of OOS (Out of Specification), OOT (Out of Trend), and deviations. Collaborate with QA, production, and R&D departments to support manufacturing and product release. Qualifications: Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field. Minimum 2 years of hands-on experience in a QC laboratory within the pharmaceutical or biotech industry. Proficient in analytical techniques (e.g., HPLC, GC) and good laboratory practices. Solid understanding of cGMP, USP/EP, and FDA regulatory requirements.

There is an opportunity for a scientist to serve as Analytical Lab Technician in the Regulatory Analytical Sciences Team within Global Regulatory Sciences R&D. Specifically, we are seeking a technician with strong analytical chemistry expertise. • Weekly Schedule : 40 hours • Shift Times: 8AM - 5PM Primary Responsibilities • Assists in the receiving, weighing and extraction of samples within a study to support product registration and to develop biologically active research chemicals. Supports laboratory testing and data generation as outlined by the principal investigators for the Regulatory Analytical Sciences residue studies. • Support experimental lab routine operations such as sample shipments, sample receiving, sample weighing, consumable ordering, etc. • Prioritize daily work activities to meet timelines. • Interact regularly with LIMS (Laboratory Information Management System) and with an assortment of automated equipment such as liquid handlers. • Follow specific protocols to perform routine lab support tasks including the following: o Solution preparation o Sample processing o Sample aliquotting o Sample extraction o Equipment and assay maintenance • Operate laboratory instrumentation, including balances, genogrinders, centrifuges, gas chromatographs, high performance liquid chromatographs, and mass spectrometers. Interface with instrument/equipment owners and the Lab Operations team to maintain system performance and minimize downtime. • Complies with all laboratory safety procedures, GLP Standards, and all other study-specific or pertinent regulatory agency requirements Documents activities in the required manner. Maintenance of neat, accurate, and complete records. • As needed, follow Good Laboratory Procedures (GLP) and prepare related support documentation. Required Qualifications: • Minimum of an Associate Degree in a science related field, BS preferred. • General knowledge of chemistry. • An understanding of computers and laboratory techniques is desirable. • Ability to conduct research and provide high-quality, finalized data in a fast-paced, time sensitive environment. Preferred Qualifications: • Experience with quantitative weighings, extractions and sample clean-up techniques from various complex agricultural matrices. • Quantitative LC-MS/MS analytical experience in small molecules. • An understanding of GLP regulations. • Excellent interpersonal skills. Must be able to effectively interact with a diverse group of customers, peers, and R&D regulatory and residue experts Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.

This position is primarily responsible for the laboratory testing of raw materials, packaging materials, in-process, release and stability samples for developmental and pre-commercial drug products, including the evaluation of new raw materials, new packaging materials, reference standard qualifications, method transfers, and develop and validate methods within the framework of cGMP compliance guidelines. Responsibilities: Perform routine and non-routine physical and chemical tests and assays on raw materials, API's, in-process, finished products, experimental batches and associated stability studies Testing performed to include basic and complex lab equipment and procedures, such as pH, Loss on Drying, Residue on Ignition, Water Content by Karl Fischer, Assay/Impurities by HPLC, Dissolution, Residual Solvents by GC, and wet chemistry techniques such as titrations and sample derivatizations Conduct analytical research and develop analytical methods to test pharmaceutical products for conformance to established specifications with some supervision. Develop and validate analytical test methods for assay, dissolution, preservatives in drug products according to ICH/FDA/USP requirements with minimal to no supervision. Develop and validate test methods for residual solvents and impurities/degradation products in drug substances/excipients/drug products according to ICH/FDA/USP requirements under some supervision Develop and validate analytical Cleaning Validation methods and perform testing of cleaning validation samples and generate analytical report with minimum supervision. Multi-task by working on several simultaneous projects. Develop project timelines. Document all laboratory testing and maintain accurate and legible notebooks and records Perform peer review on other analysts' data. Provide regular update progress reports of projects Comply with all relevant regulatory requirements At all times strive to maintain the self-esteem of individual team members and the professionalism of the group as a whole Perform laboratory troubleshooting, propose solutions and implement Other projects and duties as required or assigned Provide technical input for purchase of new/updated laboratory instruments and software systems Train other laboratory chemists on analytical instrumentation and methods. Mentor/Train team members on new/revised skills and testing procedures Education/Qualifications: BS Degree in Chemistry or related field and 4 - 8 years of pharmaceutical product analysis experience in a cGMP-regulated lab environment Masters Degree preferred Experience working in the pharmaceutical industry and/or analytical laboratory Knowledge of cGMP, USP/NF, and FDA guidelines and regulations Expertise in analytical methods and lab instrumentation (e.g. HPLC, GC, dissolution, wet chemistry) Demonstrated ability to perform method development and validation in accordance with ICH regulations with minimal supervision Excellent oral and written communication skills Strong organization, time management, leadership and troubleshooting skills Demonstrated ability to work as part of a cross-functional team Basic knowledge in Microsoft Word and Excel Experience with software associated with a Laboratory Information Management System (LIMS) and a Chromatography Data System (CDS) Work mainly performed in lab Travel < 5%

Are you a creative and driven professional with a passion for developing innovative meat products? Join our team as a Food Scientist and lead the charge from concept ideation through commercialization. Be at the forefront of innovation, quality improvement, and cost savings while collaborating with cross-functional teams to bring exciting new products to market. Company At Land O'Frost, our brands of lunchmeat, hot dogs and specialty sausage products are recognized as one of the nation's best-selling and trusted brands. We have accomplished this through our incredible team of employees who are customer focused, motivated, achievers, developers, and purpose driven. How You Will Contribute Develop new meat products from concept ideation through commercialization. Lead and execute multiple projects concurrently, including innovation, quality improvement, product optimization, and cost savings. Develop manufacturing procedures, specifications, labels, and product costs. Collaborate with and lead cross-functional teams, both internal and external (co-manufacturers), in the execution of product launches. Influence business decisions by providing clear communication of results, technical hurdles with proposed solutions, and technical recommendations. Design and direct laboratory and production trials involving formulation, processing, packaging, and shelf life. Develop test plans with hypotheses and translate results to meet business objectives. Stay abreast of new developments in ingredient and process technologies, packaging, design, category trends, and related fields. Design and execute research to validate and implement new technologies to improve existing product performance or introduce new products. Collaborate with Regulatory partners on USDA requirements and regulations involving meat labeling, nutritional validation, GMO, allergen status, etc. Work with Operations and Business partners to identify opportunities to improve product performance or efficiencies. Develop strong relationships, both internally and externally (industry and academia), to execute projects and meet business objectives. Advise and mentor junior developers and cross-functional partners. About You 5+ years in meat product development, R&D, or a related field required. Bachelor's degree required (Master's degree a plus) in Meat Science, Food Science, or a related field. Proficient in Microsoft 365. ERP system experience preferred. Local and/or overnight travel required (approximately 25%).

Research and Development ( R &D ) Chemist Tri-Pac, Inc. a contract development and manufacturing company (CDMO) specializing in liquid and aerosol filling for personal care and pharmaceutical marketers, is seeking an experienced Research and Development ( R &D ) Chemist for immediate addition to our fast growing team. Job Description: The R&D Chemist is responsible for all steps of formula development from ideation to final formulation. Primary responsibilities will be the innovation of new products, technology transfer and cost savings. He/she will demonstrate formulation and innovation skills in Personal Care, Cosmetics and Over-the-Counter products. The R&D Chemist will be proficient with analytical and numerical skills and able to perform basic mathematical calculations in various units of measurement and able to navigate concepts such as fractions, percentages, and ratios. He/she must have a strong attention to detail, capable of efficiently communicating verbally and through writing, produce and share reports, demonstrate excellent organizational skills be able to perform physically demanding activities such as moving and lifting equipment and standing for extended periods of time. Responsibilities: Formulate product prototypes and evaluate them for chemical and physical properties, performance, and stability. Develop new formulations for different personal care products, cosmetics, and OTC's. Improve current product formulations. Research product formulations and properties of raw materials. Provide and prepare samples for biological laboratory and field testing for efficacy and safety. Initiate, develop, and create innovative products to expand the R&D formulation library and enhance customer presentations. Establish product specifications and procedures as required for R & D projects. Support scale-ups from prototype to commercial manufacture and following Good Manufacturing Practices (GMP). Support technical service for operations and consumer relations. Conduct research and field evaluations on new products. Develop new products and improve functioning of existing products. Provide technical assistance and supervisory support within laboratory, and documentation to Compounding, Production, Documentation, and Scheduling Departments. Coordinate research and development activities within all organizational departments. Develop reports and documents detailing project processes, results, and conclusions. Maintain accurate records, notebooks of analysis and work performed. Comply with all Tri-Pac Safety requirements, GMP/GLP, and customer requirements. Support scheduling and testing of R&D stability samples. Support shipping samples to external lab for testing. Maintain laboratory paperwork system according to GMP. Education and/or Experience: BS or MS Degree in Chemistry or Biosciences or related degree Minimum 2 years' experience in cosmetic formulation/product development or related field. OTC/Drug formulation preferred. Must be familiar with basic cosmetic lab equipment including FTIR, viscometer, pH Meter, Moisture Analyzer, etc. HPLC and GC experience is desired. Benefits Competitive Salary/ Pay & Packages, Vacations, Insurance, 401K, Life Insurance, Disability (Long term/ Short term) and Continuous Training. Work where you are HAPPY! Tri-Pac, Inc. also recognizes the importance of continuing education and offers Education Assistance to our employees to encourage continued personal development and growth. ************** Thank you for your interest and consideration of a career with Tri-Pac, Inc. Tri-Pac, Inc. is an Equal Employment Opportunity / Affirmative Action Employer To Staffing & Recruitment Agencies: Our Company does not accept unsolicited CV's or applications from agencies. We are not responsible for any fees related to unsolicited CV's or applications and explicitly reserve its right to contact candidates presented in such unsolicited CV or application.

Summary of role: We are seeking a collaborative technical leader and subject matter expert in elastomer materials to help drive innovation and development in material selection, formulation, characterization, scale-up, and manufacturing. In this role, you will serve as the primary materials contact for cross-functional regional teams-including marketing, engineering, and manufacturing-and will be responsible for delivering innovative, technically differentiated solutions that meet regulatory standards and advance our material capabilities. Tasks and Responsibilities: Lead material-related initiatives that support strategic business segments and address diverse customer needs. Guide research and development (R&D) efforts in alignment with business strategies and technology roadmaps. Collaborate with customers and internal teams to translate requirements into material specifications; develop rubber formulations and conduct experiments to validate performance. Apply scientific principles to deliver innovative, high-value solutions. Formulate new materials, coatings, and polymers to address industry challenges and create new market opportunities. Analyze test data and provide recommendations on material selection, compounding, molding, testing, regulatory compliance, and vendor sourcing. Partner with manufacturing teams to support compounding, prototyping, and molding processes. Stay informed about global regulatory standards and work closely with compliance teams. Work collaboratively with vendors and customers to resolve technical material issues. Provide technical support across departments and manage projects effectively, fostering an inclusive and respectful team environment. Collaborate with global R&D teams across APAC, EMEA, and the Americas Education and Experience: Qualifications: Bachelor's degree in chemistry, chemical engineering, polymer science, materials engineering, biochemical engineering, or related field. Strong background in rubber compounding and elastomeric materials. Familiarity with fillers and reinforced composites. Skilled in statistical design and experimental data analysis. Excellent problem-solving, communication, and documentation skills. Preferred Qualifications: 10+ years of relevant experience in elastomer or advanced material development. MS or PhD in a related discipline. Deep expertise in rubber chemistry, thermoplastics, physics, DOE, and performance testing. Experience with elastomeric formulations for dynamic applications. Strong understanding of structure-property relationships in materials. Competencies: Ability to manage multiple priorities using effective prioritization to meet deadlines in a dynamic, fast-paced environment. Exceptional communication skills. Technology savvy and awareness Critical thinking Consensus building Effective consulting Agile, quick learner Application: Last application date: 2025-11-22 Apply Here Please right-click the link to open in a new tab

'We connect science to life for a better future.' With 50,000 patents, 20,000 employees and 58 locations worldwide, LG Chem is one of the largest science and chemical companies in the world. With its rapid growth, LG Chem endeavors to become a 'Global Top 5 Chemical Company' with a balanced business portfolio that has a competitive advantage across the globe, including business divisions in petrochemicals, advanced materials, life sciences, and a subsidiary specializing in batteries. LG Chem is a leading chemical company in Korea that has continuously achieved growth through relentless challenges and innovation since its establishment in 1947. From the infrangible facial cream lid to the world's most advanced batteries, LG Chem has turned dreams into reality and enriched our lives for 70 years. Building upon a balanced and globally competitive business portfolio, LG Chem manufactures a wide range of products from high-value added petrochemicals to renewable plastics, specializing in cutting-edge electronic and battery materials such as cathodes, as well as drugs and vaccines to deliver differentiated solutions for its customers. Beyond a chemical company, LG Chem will become a leading science-oriented corporation that creates value for our customers and is committed to reaching carbon-neutral growth by 2030 and net-zero emissions by 2050 by managing the impacts of climate change and making positive contributions to society through renewable energy and responsible supply chains. The Associate Chemist is responsible for analytical, environmental and physical testing. He or she also performs testing on raw materials and compounded products. This chemist will also participate in the development and formulation of new products under the direction of a Chemist or Senior Chemist. The Associate Chemist may provide any necessary technical support to various other departments. In addition, he or she is responsible for any other task the Chief Technology Officer deems necessary. Essential Functions: * Maintain and operate Analytical, Environmental and Physical test equipment including: * FTIR * Dual Plate Rheometer * DSC * DMA * TGA * Titration (Karl Fischer, Epoxy, NCO, Amine) * Brookfield * Particle Size Analysis * Corrosion Chambers * Long term weathering * Physical (Tensile, Impact, Vibration) * Formulate/ design new product * Prepare product submission * Takes test, experimental, product development or process research requests from supervisor, internal and external customers. Determines and performs routine testing/experiments and structured work assignments. * Collects, analyzes and interprets data using established methods and issues reports to supervisor or internal customer with minimum supervision. * Leads and coordinates implementation of assigned projects internal to own function with minimal supervision. * Monitors and maintains instruments, troubleshoots product issues using standard procedures. Maintains operating supply inventories. * Develop test methods * Test new supplies of raw materials * Submit new and/or reactivated gages and calibration standards to Gage Control * Ensure customer needs are represented during selection of significant characteristics and during product design and development. * Monthly review raw materials and samples to ensure items are properly identified * May be responsible for handling hazardous waste Skills / Competencies: * Superior communication skills * Excellent organizational skills * Strong analytical and interpersonal skills * Ability to demonstrate effective leadership skills * Excellent problem-solving skills * Proficiency with Microsoft Office (Word, Excel, PowerPoint, Outlook) * Strong training skills Education: Bachelor's Degree in Chemistry or Related Scientific Field required. Experience: 1+ years relevant chemistry or related scientific work experience Work Environment: The work environment characteristics described here are representative of those a team member encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Work requires exposure to manufacturing environment operations, such as moving equipment, noise, fumes, vibrations, dust, etc. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, gender, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any characteristic protected by applicable federal, state, or local law.

"We connect science to life for a better future." With 50,000 patents, 20,000 employees and 58 locations worldwide, LG Chem is one of the largest science and chemical companies in the world. With its rapid growth, LG Chem endeavors to become a 'Global Top 5 Chemical Company' with a balanced business portfolio that has a competitive advantage across the globe, including business divisions in petrochemicals, advanced materials, life sciences, and a subsidiary specializing in batteries. LG Chem is a leading chemical company in Korea that has continuously achieved growth through relentless challenges and innovation since its establishment in 1947. From the infrangible facial cream lid to the world's most advanced batteries, LG Chem has turned dreams into reality and enriched our lives for 70 years. Building upon a balanced and globally competitive business portfolio, LG Chem manufactures a wide range of products from high-value added petrochemicals to renewable plastics, specializing in cutting-edge electronic and battery materials such as cathodes, as well as drugs and vaccines to deliver differentiated solutions for its customers. Beyond a chemical company, LG Chem will become a leading science-oriented corporation that creates value for our customers and is committed to reaching carbon-neutral growth by 2030 and net-zero emissions by 2050 by managing the impacts of climate change and making positive contributions to society through renewable energy and responsible supply chains. The Associate Chemist is responsible for analytical, environmental and physical testing. He or she also performs testing on raw materials and compounded products. This chemist will also participate in the development and formulation of new products under the direction of a Chemist or Senior Chemist. The Associate Chemist may provide any necessary technical support to various other departments. In addition, he or she is responsible for any other task the Chief Technology Officer deems necessary. Essential Functions: Maintain and operate Analytical, Environmental and Physical test equipment including: FTIR Dual Plate Rheometer DSC DMA TGA Titration (Karl Fischer, Epoxy, NCO, Amine) Brookfield Particle Size Analysis Corrosion Chambers Long term weathering Physical (Tensile, Impact, Vibration) Formulate/ design new product Prepare product submission Takes test, experimental, product development or process research requests from supervisor, internal and external customers. Determines and performs routine testing/experiments and structured work assignments. Collects, analyzes and interprets data using established methods and issues reports to supervisor or internal customer with minimum supervision. Leads and coordinates implementation of assigned projects internal to own function with minimal supervision. Monitors and maintains instruments, troubleshoots product issues using standard procedures. Maintains operating supply inventories. Develop test methods Test new supplies of raw materials Submit new and/or reactivated gages and calibration standards to Gage Control Ensure customer needs are represented during selection of significant characteristics and during product design and development. Monthly review raw materials and samples to ensure items are properly identified May be responsible for handling hazardous waste Skills / Competencies: Superior communication skills Excellent organizational skills Strong analytical and interpersonal skills Ability to demonstrate effective leadership skills Excellent problem-solving skills Proficiency with Microsoft Office (Word, Excel, PowerPoint, Outlook) Strong training skills Education: Bachelor's Degree in Chemistry or Related Scientific Field required. Experience: 1+ years relevant chemistry or related scientific work experience Work Environment: The work environment characteristics described here are representative of those a team member encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Work requires exposure to manufacturing environment operations, such as moving equipment, noise, fumes, vibrations, dust, etc. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, gender, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any characteristic protected by applicable federal, state, or local law.

MC Labs is growing and we have exciting opportunities available for analytical chemists! If you are a recent graduate in the chemical or biological sciences or have industrial experience already, we would love to hear from you. Due to large growth in the pharmaceutical testing sector, we are aggressively seeking new chemists wanting a challenge and a great place to learn and grow. Some of the advantages of working at MC Labs include: -Flexible Work Schedules (optional 4-day work weeks available) -Highly Competitive Pay -Sign-On and Retention Bonuses -Industry leading Paid-Time-Off Program -Paid holidays -Continued education in the Pharmaceutical Sciences -401K Savings with Company Match -Comprehensive Benefits Package (Health, Dental, Vision) -Energetic Work Environment with Excellent Flexibility and Opportunities for Advancement Here are the details of this exciting opportunity: Job Title: Analytical Chemist Job Description: Perform Chemical, Analysis on a variety of sample types (pharmaceutical intermediates and finished goods, raw materials, food additives, etc.) using the latest in laboratory and software technology. General responsibilities include maintaining a clean and safe working environment and adhering to laboratory procedures and policies in a cGMP laboratory. Essential Duties Include: Perform analysis utilizing a variety of laboratory equipment and procedures that may include Wet Chemistry, HPLC, GC, UV-VIS, KF, FTIR, pH, and TLC. Maintenance of a clean and safe working area. Execute Method Validation Protocols and Method Technical Transfer Protocols Document laboratory data using Good Documentation Practices utilizing an Electronic Laboratory Notebook Perform Data Analysis as Required by Analytical Method including data package write up and submission to Quality for approval. May author data reports for development studies as required. Must be motivated and able to work independently in a dynamic laboratory environment. Able to troubleshoot and maintain laboratory equipment as required. Good documentation skills are required. Must have a strong mathematic and analytical aptitude. B.S. in Chemistry/Biology 0 - 5 Years of experience in an industrial laboratory setting Skills Required: Must be motivated and able to work independently in a dynamic laboratory environment. Able to troubleshoot and maintain laboratory equipment as required. Good documentation skills are required. Must have a strong mathematic and analytical aptitude. Education and Experience Requirements: B.S. in Chemistry/Biology 0 - 5 Years of experience in an industrial laboratory setting

Voyant Beauty believes our people are more than just employees; they're the driving force behind everything we achieve. Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual's contribution is valued and celebrated. We invest in their growth, providing opportunities for development and advancement within our dynamic team. Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products. We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs. This can include skincare, haircare, bath and body products, fragrances, and more. Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life. Safety is a core value at Voyant Beauty. We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel. If you're seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you. Come join us and be a part of our journey. A Brief OverviewEnsures accuracy and reliability in laboratory testing and analysis. The QC Analytical Chemist is responsible for conducting quantitative and qualitative analysis of raw materials and products, developing analytical methods, and ensuring compliance with industry standards.What you will do Conduct quantitative and qualitative analysis of raw materials and products. Collaborate with production teams to troubleshoot production issues. Ensure compliance with industry standards and regulations. Prepare technical documents and reports. Develop and validate analytical methods. Calibrate and maintain analytical instrumentation. Manage standard chemical inventory and safety protocols. Some duties may vary slightly by location. Education Qualifications Bachelor's Degree in Chemistry or related scientific discipline (Preferred) Experience Qualifications 1-3 years Analytical chemistry in a manufacturing environment (Preferred) 1-3 years Method development and validation (Preferred) Skills and Abilities Analytical Chemistry (High proficiency) Quality Control (Medium proficiency) Laboratory Safety (Medium proficiency) Technical Documentation (Medium proficiency) Regulatory Compliance (Medium proficiency) Data Analysis (Low proficiency) Instrumentation Calibration (Low proficiency) Method Validation (Low proficiency) Chemical Handling (Low proficiency) Collaboration (Low proficiency) To Staffing and Recruiting Agencies:Our company does not accept unsolicited curriculum vitae's or applications from agencies. We are not responsible for any fees related to unsolicited curriculum vitae's or applications and explicitly reserve its right to contact candidates presented in such unsolicited curriculum vitae's or application. Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, color, national origin, sexual orientation, age, disability or veteran status. Voyant Beauty will consider requests for accommodations due to a disability impacting a qualified employee's ability to perform the essential functions of their position consistent with applicable laws. In addition to federal law requirements, Voyant Beauty complies with applicable provincial and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Anticipated salary range: $68,500 - $97,800 Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. Medical, dental and vision coverage Paid time off plan Health savings account (HSA) 401k savings plan Access to wages before pay day with my FlexPay Flexible spending accounts (FSAs) Short- and long-term disability coverage Work-Life resources Paid parental leave Healthy lifestyle programs Application window anticipated to close: 12/20/2025 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. What Nuclear Manufacturing contributes to Cardinal Health Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. Shift/Schedule 40 hours weekly - Full Time 2nd shift hours Monday - Friday 3:00pm - 11:30pm Training will start on 1st shift Must be flexible to work other hours and days as needed Responsibilities Support the manufacturing activities from internal product development and external sponsors. Receive, sample, store and/or distribute all materials required for production. Safely receive, handle, and transfer radioactive isotopes and final products to end users. Facilitate day-to-day operation and maintenance of the facility, production equipment, radiation monitoring equipment, and testing instrumentation. Perform hands-on execution of manufacturing procedures, following standard operating procedures (SOPs), master batch records (MBRs), and protocols. Lead and/or support investigations and documentation of deviations and non-conformances. Clean and maintain all production equipment, including clean rooms and isolators. Record and maintain systems regarding cGMP compliance such as consumable inventory levels, area classification requirements, or site environmental monitoring. Communicate all issues related to safety, quality, and compliance to site leadership. Perform relevant documentation for maintenance activities, as well as modify and/or create SOPs. Provide input to the Product Development team regarding client drug manufacturing. Qualifications Bachelor's degree in life sciences or engineering with at least 2 years of experience working in a GMP manufacturing environment in the pharmaceutical or biotechnology industry preferred. Demonstrated familiarity with the operation, use, and cleaning of laboratory scale production equipment. Ability to work in a controlled environment requiring special attention to environmental, health, and safety regulation. Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements; ability to clearly document all work activities in a timely manner. Motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships. Flexibility to work periodic off-shift hours in support of routine production. Experience working in clean rooms/ISO5-8 environments/isolators not required, but is a plus. Experience working with radioactive isotopes not required, but is a plus. Must be able to lift up to fifty (50) pounds What is expected of you and others at this level Applies working knowledge in the application of concepts, principles and technical capabilities to perform varied tasks Works on projects of moderate scope and complexity Identifies possible solutions to a variety of technical problems and takes action to resolve Applies judgment within defined parameters Receives general guidance and may receive more detailed instruction on new projects Work reviewed for sound reasoning and accuracy Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here

Grow Your Scientific Career with Purpose at Eurofins PSS Insourcing Solutions At Eurofins PSS, the work we do matters-from ensuring the safety of medicines to protecting the environment-and so do our employees. If you're looking to advance your career and make a meaningful impact, we offer a place to learn, lead, and thrive. We believe in investing in your potential. Whether you're looking to deepen your expertise, take on new challenges, or expand your leadership skills, Eurofins provides the tools, support, and collaborative environment to help you grow. Why Join Eurofins? Career Development: Opportunities to expand your skillset and take on leadership roles Supportive Teams: A culture that values collaboration, innovation, and continuous improvement Work-Life Balance: Flexible schedules and a competitive benefits package Industry Impact: Work alongside global leaders in the biopharmaceutical space Who We Are Eurofins Scientific is a global life sciences company offering a unique range of analytical testing services across industries. From the food you eat to the medicines you rely on, we help ensure safety, authenticity, and quality. We're proud to be a leader in pharmaceutical, environmental, food, cosmetics, and genomics testing. Ready to Take the Next Step? If you're ready to grow your career in a mission-driven organization that values your contributions, apply today and discover what's possible at Eurofins. Job Description Key Responsibilities Biochemical Testing Perform analytical testing on proteins and antibodies using techniques such as: Capillary Electrophoresis (CE) Ion Chromatography (IC) HPLC, SEC, SDS-PAGE UV Spectroscopy Protein A Titer ELISA Particulate Analysis Lab Operations Work as part of a rotating day shift team (3-2-2-3 schedule), including weekends and holidays Enter and manage data in LIMS; experience with Empower is a plus Document results in lab notebooks and formal reports Compliance & Collaboration Operate independently and collaboratively in a GMP-regulated environment Participate in investigations and support continuous improvement initiatives Qualifications Qualifications Education: Bachelor's degree in biology, biochemistry, chemistry, or a related scientific field Technical Skills: Experience with one or more of the following is strongly preferred: HPLC Capillary Electrophoresis (CE) Ion Chromatography (IC) SDS-PAGE ELISA Work Authorization: Must be authorized to work in the United States indefinitely without restriction or sponsorship Additional Information Training will take place on day shift, Monday-Friday 8AM-5PM, for roughly 3 months. After the training period, the shift will be on a 3,2,2,3 rotation from 6PM-6AM. Candidates currently living within a commutable distance of Indianapolis, IN 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 #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Apply now " Tradebe Site: Tradebe East Chicago Department: Operations Business Line: Environmental Services & Global Functions Lab Chemist - 2nd Shift Description: Tradebe is a group of industrial businesses dedicated to creating a more sustainable planet and making a real impact on human wellbeing. In the US, we lead the way in recycling and the circular economy, managing diverse environmental challenges sustainably. Our East Chicago, IN facility is the heart of our operations and our largest processing hub, where innovation and teamwork drive meaningful environmental solutions. Join us in this dynamic location to be part of shaping a sustainable future. Opportunity Highlights * Location: East Chicago, IN * Schedule/Shift: Mon-Fri, 2nd shift, 3:00pm-11:30pm * Paid Weekly What will you do? Make an impact! As a Lab Chemist, you will perform routine laboratory duties including testing samples received at Tradebe's plants, primarily involving hazardous waste and chemicals. The ideal candidate will have a solid understanding of chemicals, hazardous materials, and general chemistry. Key Job Responsibilities * Follow all regulations, standards, and internal policies to ensure Environmental, Health, and Safety (EHS) compliance and promote a safe and environmentally responsible workplace. * Ensure compliance with all applicable EPA testing methods and requirements. * Conduct all analytical testing, including pH, moisture content, oxidation, and titration. * Process waste samples daily, including but not limited to fuel compatibility, bomb calorimetry, GC analysis, and metals analysis. * Perform daily calibration of laboratory equipment such as calorimeters, pH meters, GC-MS, and GC-FID. * Provide expertise in instrument maintenance, troubleshooting, and repair as needed. * Provide additional support in standards preparation, record-keeping, and other general laboratory duties as assigned. * Properly dispose of laboratory-generated wastes. * Maintain adequate laboratory supplies. * Keep the laboratory area clean, safe, and well-organized. Do you have what it takes? * HS Diploma or equivalent required. BS degree preferred * Willingness to work in an industrial setting with limited outdoor exposure and handle hazardous and non-hazardous wastes using appropriate PPE. * Ability to wear a face respirator when needed. Why Tradebe is Right for You * Competitive pay and benefits * Student loan repayment assistance * Generous vacation and sick plans * Medical (including telehealth), dental and vision * 401k Retirement match * Flexible spending accounts (FSA) * Health savings accounts (HSA) * Agency paid, basic life and AD&D insurance * Career ladders, professional development, and promotion opportunities * Leadership opportunities * Great work environment and culture * And MORE! Ready to make a difference? Apply now! #TeamTradebe #SustainableCareers #TradebeJobs If this offer does not match your expectations, but you would like to develop your career in a company that promotes circular economy and sustainability, register on our Career Page, and don't miss out on new job opportunities! Tradebe is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national origin, gender, sexual orientation, gender identity, age, physical or mental disability, genetic factors, military/veteran status or other characteristics protected by law . Nearest Major Market: Gary Nearest Secondary Market: Chicago

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Key Objectives /Deliverables: • Understand the scientific principles required for manufacturing and testing of intermediates and bulk drug substances, including the interaction of the chemistry and equipment. • Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess analytical vs. process variability and capability. • Provide technical support to non-routine (e .g., deviation ) investigations including the preparation as required of relevant technical documents, such as: Change Controls, Regulatory Submissions, Deviations, Validation Protocols, Tickets, Procedures, PFDs, Periodic Quality Evaluations, etc. • Support production floor operations through change proposals, investigations, and deviation root cause analysis. • Maintain and improve quality systems including method remediation. • Participate in self-assessments and regulatory agency inspections. • Ensure internal and external quality and supply commitments are met. • Manage the review and retention of cGMP documents. • Must follow data integrity practices and procedures. (ALCOA + principles ). Basic Requirements: • Bachelor's Degree in a science related field or 7-10 years of demonstrated relevant experience in a GMP laboratory. Additional Preferences: • Demonstrated strong problem solving and analytical thinking skills. • Understanding of statistical tools and analysis. • Excellent interpersonal skills and networking skills. • Experience in QA, QC, Manufacturing, Tech Services, or Regulatory Affairs. • Demonstrated strong written and verbal communications skills. • Strong attention to detail. • Ability to organize and prioritize multiple tasks. • Experience and knowledge of cGMP requirements. • Familiarity with wet chemistry techniques, HPLC, GC, FTIR, UV/Vis, Titrations Education Requirements: • Minimum of a Bachelor's Degree. Other Information: • Must complete applicable Learning Plan. • Tasks require entering manufacturing and laboratory areas which require wearing appropriate PPE. • Overtime or on-call hours may be required in order to meet business needs. • Unless approved by leadership, Chemist-QC-IAPI is considered an on-site position. • Must adhere to policies and guidelines outlined in the employee handbook and Red Book. The job specification is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job specification. As always, you should consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

We are seeking a self-motivated Chemistry Lab Technician to join our Lab Operations team. In this role you will assist in laboratory confirmatory analysis of biological fluids including urine, oral fluid (saliva) or hair specimens. This role is also responsible for operating, maintaining and troubleshooting various Auto Chemistry instrumentation. Shift: 03:00 - 11:30pm Salary: $20.00 per hour Primary Responsibilities Loads, prepares and extracts specimens using various Auto-Chem Instrumentation. Assist in instrument calibration, QC review, and initial analytical review. Prepare reagents and buffers as needed. Assists with maintaining an adequate inventory of laboratory supplies. Responsible for all record keeping associated with specimen preparation, including following chain of custody handling guidelines and storage requirements. Conducts safe work practices according to safety protocols, PPE requirements and decontamination procedures. Responsible to maintain all safeguards as it pertains to Protected health information (PHI). Qualifications Bachelor's degree in a science field (Chemistry, Biochemistry, Biology, Microbiology, Pre-med (Biomed), required. Experience as a lab technician, preferred utilizing LCMS equipment. Data entry skills via a keyboard (alpha and numeric) required. Strong eye-hand coordination. Ability to handle a high-volume environment while maintaining the highest level of quality, required. Physical demands required to perform critical tasks in this role include standing for long periods of time, lifting up to 25lbs, bending and carrying. Benefits Cordant supports our employees by providing a comprehensive benefits package to eligible staff (per state regulations) that includes: Medical, Dental, Vision Insurance, Flexible Spending Accounts (FSA), Health Savings Accounts (HSA) Paid Time Off (PTO) accruing on day 1, Volunteer Time Off (VTO), Paid Holidays, 401(k) with Company Match, Employee Assistance Program (EAP), Short Term and Long-Term Disability (STD/LTD) and Company Paid Basic Life Insurance. #LAB123

MC Labs is growing and we have exciting opportunities available for analytical chemists! If you are a recent graduate in the chemical or biological sciences or have industrial experience already, we would love to hear from you. Due to large growth in the pharmaceutical testing sector, we are aggressively seeking new chemists wanting a challenge and a great place to learn and grow. Some of the advantages of working at MC Labs include: -Flexible Work Schedules (optional 4-day work weeks available) -Highly Competitive Pay -Sign-On and Retention Bonuses -Industry leading Paid-Time-Off Program -Paid holidays -Continued education in the Pharmaceutical Sciences -401K Savings with Company Match -Comprehensive Benefits Package (Health, Dental, Vision) -Energetic Work Environment with Excellent Flexibility and Opportunities for Advancement Here are the details of this exciting opportunity: Job Title: Analytical Chemist Job Description: Perform Chemical, Analysis on a variety of sample types (pharmaceutical intermediates and finished goods, raw materials, food additives, etc.) using the latest in laboratory and software technology. General responsibilities include maintaining a clean and safe working environment and adhering to laboratory procedures and policies in a cGMP laboratory. Essential Duties Include: Perform analysis utilizing a variety of laboratory equipment and procedures that may include Wet Chemistry, HPLC, GC, UV-VIS, KF, FTIR, pH, and TLC. Maintenance of a clean and safe working area. Execute Method Validation Protocols and Method Technical Transfer Protocols Document laboratory data using Good Documentation Practices utilizing an Electronic Laboratory Notebook Perform Data Analysis as Required by Analytical Method including data package write up and submission to Quality for approval. May author data reports for development studies as required. Must be motivated and able to work independently in a dynamic laboratory environment. Able to troubleshoot and maintain laboratory equipment as required. Good documentation skills are required. Must have a strong mathematic and analytical aptitude. B.S. in Chemistry/Biology 0 - 5 Years of experience in an industrial laboratory setting Skills Required: Must be motivated and able to work independently in a dynamic laboratory environment. Able to troubleshoot and maintain laboratory equipment as required. Good documentation skills are required. Must have a strong mathematic and analytical aptitude. Education and Experience Requirements: B.S. in Chemistry/Biology 0 - 5 Years of experience in an industrial laboratory setting

Anticipated salary range: $68,500 - $97,800 Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. * Medical, dental and vision coverage * Paid time off plan * Health savings account (HSA) * 401k savings plan * Access to wages before pay day with my FlexPay * Flexible spending accounts (FSAs) * Short- and long-term disability coverage * Work-Life resources * Paid parental leave * Healthy lifestyle programs Application window anticipated to close: 12/20/2025 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. What Nuclear Manufacturing contributes to Cardinal Health Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. Shift/Schedule * 40 hours weekly - Full Time * 2nd shift hours * Monday - Friday 3:00pm - 11:30pm * Training will start on 1st shift * Must be flexible to work other hours and days as needed Responsibilities * Support the manufacturing activities from internal product development and external sponsors. * Receive, sample, store and/or distribute all materials required for production. * Safely receive, handle, and transfer radioactive isotopes and final products to end users. * Facilitate day-to-day operation and maintenance of the facility, production equipment, radiation monitoring equipment, and testing instrumentation. * Perform hands-on execution of manufacturing procedures, following standard operating procedures (SOPs), master batch records (MBRs), and protocols. * Lead and/or support investigations and documentation of deviations and non-conformances. * Clean and maintain all production equipment, including clean rooms and isolators. * Record and maintain systems regarding cGMP compliance such as consumable inventory levels, area classification requirements, or site environmental monitoring. * Communicate all issues related to safety, quality, and compliance to site leadership. * Perform relevant documentation for maintenance activities, as well as modify and/or create SOPs. * Provide input to the Product Development team regarding client drug manufacturing. Qualifications * Bachelor's degree in life sciences or engineering with at least 2 years of experience working in a GMP manufacturing environment in the pharmaceutical or biotechnology industry preferred. * Demonstrated familiarity with the operation, use, and cleaning of laboratory scale production equipment. * Ability to work in a controlled environment requiring special attention to environmental, health, and safety regulation. * Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements; ability to clearly document all work activities in a timely manner. * Motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships. * Flexibility to work periodic off-shift hours in support of routine production. * Experience working in clean rooms/ISO5-8 environments/isolators not required, but is a plus. * Experience working with radioactive isotopes not required, but is a plus. * Must be able to lift up to fifty (50) pounds What is expected of you and others at this level * Applies working knowledge in the application of concepts, principles and technical capabilities to perform varied tasks * Works on projects of moderate scope and complexity * Identifies possible solutions to a variety of technical problems and takes action to resolve * Applies judgment within defined parameters * Receives general guidance and may receive more detailed instruction on new projects * Work reviewed for sound reasoning and accuracy Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.