Research and development technician jobs in Terre Haute, IN

Job Responsibilities: Develop, evaluate, and optimize the QC method transfer program for both analytical and microbiological assays. Assess incoming client methods and compendial test methods for raw materials, container/closures, APIs, in-process samples, and finished products, determining suitability with existing laboratory capabilities and identifying any additional instrumentation or reagents required. Collaborate with clients and internal teams to plan, review, approve, and execute method transfers into the laboratory. Work closely with the Quality team to maintain and enhance laboratory safety programs and promote a quality-driven culture. Maintain rigorous scientific and quality standards, ensuring accuracy, reproducibility, and compliance in all laboratory activities. Coordinate resources, scheduling, and logistics to support client testing needs, including microbiological sampling, laboratory instruments, and personnel availability. Ensure laboratory readiness for inspections, audits, and regulatory compliance by applying knowledge of cGMP, cGLP, and other regulatory standards. Lead and support investigations for out-of-specification (OOS), out-of-trend (OOT), and other non-conformance events using troubleshooting and corrective action processes. Manage laboratory documentation and technical records throughout their lifecycle, including authoring, reviewing, approving, and retiring procedures and reports, utilizing both manual and automated systems. Qualifications: Bachelor's degree in Biology, Microbiology, Biochemistry, or related field. 5+ years of experience in microbiology or related roles within GMP manufacturing or QC laboratory testing. Practical experience implementing FDA, EMA, and other regulatory authority expectations for QC, particularly regarding method development and method transfer. Proficiency with laboratory instrumentation and automated data management systems (e.g., LIMS, JMP, Minitab).

Ready to revolutionize flexible packaging technology with cutting-edge UV and EB liquid formulations? Pave Talent is hiring on behalf of our client - an established mid-size chemical manufacturer with multiple locations, known for their collaborative, innovation-driven, and safety-first culture. This industry leader is the third largest ink producer in North America, with 12+ years average employee tenure and tremendous growth in flexible packaging solutions. As an R&D Chemist - UV/EB Liquid Specialist, you'll drive breakthrough innovations in UV Flexographic and Screen Ink technologies while supporting a $100M+ business unit experiencing unprecedented growth. Your formulation expertise will directly impact cost-savings initiatives and customer satisfaction across commercial and packaging applications. Your Impact: Troubleshoot complex technical challenges with existing UV/EB technologies while providing rapid customer support solutions Develop next-generation UV Flexo and Screen Ink technologies tailored to evolving customer specifications and market demands Lead EB Liquid formulation projects and UV/EB Coatings development for emerging packaging applications Evaluate and optimize raw materials to achieve 15-20% cost-savings opportunities through strategic formulation improvements Provide critical technical manufacturing support, ensuring seamless scale-up from lab to production environment Author comprehensive project reports and technical documentation for sales teams and direct customer presentations Maintain state-of-the-art laboratory equipment and analytical instrumentation for optimal research productivity What You Bring: Required: Bachelor's degree in Chemistry, Chemical Engineering, or equivalent technical discipline 5+ years hands-on experience in ink and coating formulation with measurable product development success Proven UV/EB liquid ink formulation expertise with understanding of photopolymerization chemistry Advanced mathematical and analytical skills with proficiency in statistical analysis and data interpretation Exceptional technical writing abilities and strong verbal communication for customer-facing interactions Meticulous record-keeping skills with experience in regulated laboratory environments Preferred: Direct UV/EB Liquid Ink and Coatings application experience in packaging or commercial printing SAP or similar ERP system experience for materials management and project tracking Six Sigma or lean manufacturing methodology knowledge Why This Opportunity Stands Out: Market-competitive salary range $85K-$100K with performance bonus structure, comprehensive benefits from Day 1 including medical/dental/vision, 401(k) with company match, paid volunteer time off, and parental leave. Join a team where 1/3 of chemists have 15+ years experience, working in an autonomous environment with cutting-edge analytical equipment and significant opportunities for professional growth in sustainable chemistry innovation. Work alongside a close-knit R&D team that values creative problem-solving and celebrates breakthrough innovations in environmentally conscious ink technology. This is your chance to shape the future of flexible packaging while building a career with an industry leader committed to employee development and retention. Ready to make your mark in sustainable chemistry innovation? Apply via LinkedIn and Pave Talent will contact qualified candidates immediately. Confidential search - your application is fully private. Apply now!

The QC Chemist will support all technical aspects related to quality control testing readiness, including QC reagents and materials management, equipment preparation and daily cleaning and maintenance activities, sample management and QC testing, and documentation completion and review in full compliance with GMP regulation, procedures, and product specifications Key Responsibilities: Finished Product testing, Environmental Monitoring and Sterility QC testing, and reporting of the QC results. Escalation in case of non-conformances and deviations and manage these quality incidents as per procedures. Support deviation investigations, OOS/OOT/OOE investigations, CAPA follow up and implementation, and Change Control management, including procedure and form revisions. Participation in assigned qualification/validation activities, as necessary. Responsible for successful on time completion of required training curricula comprising of the necessary Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications, Testing and specifications, and other relevant training including HSE for the specific role. Prepares applicable documents, forms, and records such as analytical batch records and follows Good Documentation Practices. Support internal and external Audits and Inspections, as required. Essential Requirements: Education: Bachelors' degree required in relevant Scientific discipline (e.g Chemistry, Microbiology). Minimum of 3-year experience in cGMP or aseptic environment required. Knowledge of cGMP regulations and FDA guidance applicable to Quality Control for product and Environmental Monitoring testing, as well as Aseptic techniques. Practical experience with Microbiology method verification and routine testing practices, EM Monitoring and basic knowledge of method/equipment validation principle and methodologies preferred HPLC knowledge is required. Ability to interpret analytical data and convert into technical documentation.

Kelly currently has an exciting opportunity available for a 2nd shift Analytical Technician in Kendallville, IN! The Analytical Technician performs both routine and non-routine analyses on process and product samples utilizing various techniques (Tensiometers, Rheometers, Durometers, etc.), and communicates results to customers using the proper media. Duties, projects, tasks, and activities you would be responsible for in this role: Characterizes sample composition (both process and product) accurately. Works closely with the Operations Team to aid in process troubleshooting and problem resolution. Performs basic calibration and preventative maintenance of analytical systems. Evaluates validity of data, applies basic statistics, interpret results and takes appropriate action. Monitors analytical systems, identifies problems, conducts first-line troubleshooting and escalates as appropriate. Documents, communicates and archives analytical results and calibration data. Follows EH&S and operating discipline management system (ODMS) procedures and practices for work tasks. Suggests improvements to lab work processes and tools. Escalates non-routine requests to appropriate team member for follow-up. Maintains inventory of laboratory supplies. Ensures accuracy of test results through the use of statistical techniques (SPC). Follow standard operating procedures to prepare samples for testing. Follow standard operating procedures/laboratory test method to perform characterization testing on various products. Adhere to all safety rules/regulations. Adhere to all environmental rules/regulations include the proper labeling and containers rules for hazardous and non-hazardous waste. Properly dispose of waste and move waste packs from lab to pallets. Proactively complete general housekeeping activities by 5S and maintain an organized lab environment. Conducts tests working with various hazardous samples, which includes chemicals and dusts. The equipment that this position interacts with is various analytical instrumentation and ancillary support equipment in a laboratory setting. Required Qualifications: A minimum of an Associate's Degree OR at 4 years or more of military training/experience. A minimum of 2 years of experience in working with analytical lab equipment. Basic knowledge of laboratory techniques (gravimetric, volumetric, and temperature measurements, etc.). Must be proficient with computers in order to perform testing, upload results, perform SPC charting, enter Work Notifications, enter Logbook notes, etc. (Outlook, Excel, SAP, Sample Manager, OPD, MOC). Must be proficient in issuing thorough and accurate Safe Work Permits. Must be willing and able to work the 2nd shift schedule (3PM-11PM) A minimum requirement for this U.S. based position is the ability to work legally in the United States. No visa sponsorship/support is available for this position, including for any type of U.S. permanent residency (green card) process. Preferred Skills: Proactive Problem Solving - The individual must have the ability to work in a fast-paced environment and react quickly to evolving and dynamic production scheduling situations, with minimum supervision. Time Management - Work independently with excellent time management and judgment in prioritization skills, as the requirements of the business may cause frequent interruptions and changing priorities. Multi-tasking - Complete multiple tasks and see them through completion. Troubleshooting - Ability to troubleshoot analytical equipment to drive resolution to unplanned equipment issues. Communication and Collaboration - Ability to properly communicate, work constructively and positively, with peers and co-workers, including working collaboratively and effectively in team, department, or other work group situations. Teamwork - Participate on Department Teams and have individual goal plan that aligns to Analytical Operations MI Plan. Attention to Detail - Must be able to follow written and oral instructions as this position requires the ability to learn multiple analytical techniques, work with close attention to detail, and multi-task effectively. Physical Requirements: Vision: Visual Acuity, Color Discrimination, Depth Perception, Peripheral. Constant standing, walking, hand movement, and repetition. Occasional carrying, push/pull, reaching, twisting/turning, and bending while utilizing proper ergonomic techniques. Physical requirements include long periods of standing or sitting with infrequent lifting requirements (up to 50 lbs.). Must be able to wear and use respirators.

Our client, a leader in pharmaceutical manufacturing, is looking to hire an entry level Chemist to join their team! Pay Rate: $19-20/hr Hours: 1shift shift 8a-4:30p M-F Terms: contract-to-hire This candidate will be responsible for assisting with laboratory experiments, analyzing chemical compounds, preparing solutions, and maintaining equipment under the supervision of senior chemists. Key responsibilities include recording and interpreting data, ensuring quality control, and adhering to safety protocols. Core responsibilities Perform laboratory procedures: Conduct experiments, prepare chemical solutions and reagents, and analyze substances to determine their composition and concentration. Analyze data: Test materials to ensure they meet quality and safety standards and interpret experimental results. Maintain equipment: Set up, calibrate, and maintain laboratory equipment. Document findings: Record data, write technical reports, and maintain detailed lab notebooks. Ensure safety: Follow established procedures and safety protocols to maintain a safe laboratory environment. Support senior staff: Assist senior chemists and researchers with projects, which can include method development and quality control. Essential skills and qualifications A bachelor's or master's degree in chemistry. A strong foundation in chemistry principles and laboratory techniques. Proficiency in data analysis, including relevant software. Excellent attention to detail and problem-solving abilities. Strong communication skills for reporting and collaboration. Familiarity with common laboratory equipment and safety protocols.

• There is an opportunity at Client for a scientist to serve as Analytical Lab Technician in the Regulatory Analytical Sciences Team within Global Regulatory Sciences R&D. 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: Solution preparation Sample processing Sample aliquotting Sample extraction 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

We're looking for an Food R&D Scientist to join our team and help create the next generation of fully cooked USDA products. In this role, you'll be hands-on in the kitchen, pilot plant, and production floor-formulating recipes, running trials, and ensuring every product meets the highest standards for quality, taste, and safety. What you'll do: Support the development of new meat products from concept through launch Run product trials (batching, cooking, packaging) and evaluate taste, texture, and appearance Collaborate with production, QA, and marketing teams to bring ideas to life Document recipes, results, and improvements with accuracy Troubleshoot and refine formulations for scale-up Stay on top of industry trends, new ingredients, and processing technologies Present and showcase products to internal teams and customers What we're looking for: Culinary Arts degree/certification or related experience 3-5 years in food processing/manufacturing (meat/protein experience a big plus) Background in food product development and recipe scaling for production Strong knowledge of food science, ingredients, and processing equipment Comfortable tasting and evaluating meat products Organized, detail-oriented, and creative with strong problem-solving skills Team player who thrives in a fast-paced environment

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%).

Vacuum Systems Engineering Technician - Industrial Plasmas Hands-On Role Supporting PhD Engineers in Advanced Plasma R&D This company is developing next-generation plasma and vacuum technologies - and looking for a Vacuum Systems Engineering Technician who enjoys working directly with PhD engineers to bring research concepts into functional, production-ready systems. This is a hands-on, build-and-test position focused on assembling, troubleshooting, and improving high-vacuum systems used in plasma research and manufacturing. You'll be part of a team where theory meets real hardware - helping to turn R&D; breakthroughs into working prototypes and commercial products. Key Responsibilities • Assemble, test, and maintain high and ultra-high vacuum systems, chambers, and components. • Work closely with PhD engineers to execute experiments, prototype builds, and system upgrades. • Perform leak detection, troubleshooting, and repairs to ensure vacuum integrity and reliability. • Wire and integrate vacuum instrumentation, sensors, and digital control systems. • Maintain detailed build logs, test data, and equipment documentation. • Support transitions from R&D; prototypes to production-ready systems. Qualifications • A.S. or B.S. in Mechanical, Electrical, or related technical field. • 2+ years of hands-on experience with vacuum systems, instrumentation, or related technology. • Familiarity with pumps (rotary, turbo, cryo), gauges, fittings, and helium leak detection. • Comfortable using CAD software and data-logging or control interfaces. • Strong mechanical aptitude and attention to detail in precision assembly. • U.S. Citizenship required (due to projects and facility requirements). About The Company We design and manufacture advanced plasma and vacuum technologies where R&D; and production operate side-by-side. Our engineers and technicians collaborate daily - turning ideas into real systems that drive innovation from concept to commercialization. If you enjoy hands-on technical work, close collaboration with world-class scientists, and seeing your builds make an impact, this role is an excellent next step.

Assoc Sci, R&D - Product Dev This is a Research and Development (R&D) role within the Portfolio Evolution team. The candidate will be an R&D resource for technical projects to meet business initiatives focused on beverage product formulation. This candidate should have experience developing and executing work plans and driving for results in a variety of settings. This role is responsible for the design and execution of product testing, analyzing data, drawing and documenting conclusions, communicating results, and product commercialization. Proven communication and teamwork skills are essential in this role, which operates in a dynamic cross-functional environment. This position requires an individual to manage multiple assignments/tasks and timelines concurrently. Responsibilities * Support and lead the commercialization of new and reformulated products and successful transition from development to production * Interact with Operations, Vendors, Quality, Regulatory, Finance and Marketing functions to drive for results * Conduct risk and feasibility assessments on all projects * Create and edit formulas, processing procedures and finished product specifications that deliver consistent, high-quality products * Interface with technical experts and category scientists to understand technologies and applications * Execute benchtop development, pilot plant and plant trials to support project goals * Coordinate with cross-functional teammates to organize product tastings and sensory evaluations * Manage multiple assignments/research projects concurrently with supervisor guidance and possess the ability to prioritize between a variety of business initiatives * Adapt and apply scientific principles to new situations/products, exhibit critical thinking and problem-solving skills Qualifications: * BS/MS degree in Food Science, Food Engineering, Chemical Engineering, Microbiology, Chemistry, Biochemistry, Life Sciences, or related field * Educational research & hands-on knowledge of consumer goods, food chemistry, analytical testing, formulations, and processing used in food manufacturing * Understanding of ingredient functionality and interrelationship of ingredients, process, and packaging - natural ingredients a plus * Clear communication, critical thinking, and problem-solving skills * Self-starter with attention to detail and a passion to learn * Self-motivated to drive projects forward * Willingness to travel around 30% pending business needs, including driving to production facilities for up to 3 hours Our Total Rewards philosophy is to provide a meaningful and flexible spectrum of programs that equitably support our diverse workforce and their families and complement Kraft Heinz' strategy and values. New Hire Base Salary Range: $68,900.00 - $86,100.00 Bonus: This position is eligible for a performance-based bonus as provided by the plan terms and governing documents. The compensation offered will take into account internal equity and may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors Benefits: Coverage for employees (and their eligible dependents) through affordable access to healthcare, protection, and saving for the future, we offer plans tailored to meet you and your family's needs. Coverage for benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. Wellbeing: We offer events, resources, and learning opportunities that inspire a physical, social, emotional, and financial well-being lifestyle for our employees and their families. You'll be able to participate in a variety of benefits and wellbeing programs that may vary by role, country, region, union status, and other employment status factors, for example: * Physical - Medical, Prescription Drug, Dental, Vision, Screenings/Assessments * Social - Paid Time Off, Company Holidays, Leave of Absence, Flexible Work Arrangements, Recognition, Training * Emotional - Employee Assistance Program , Wellbeing Programs, Family Support Programs * Financial - 401k, Life, Accidental Death & Dismemberment, Disability Location(s) Glenview R&D Center Kraft Heinz is an Equal Opportunity Employer - Underrepresented Ethnic Minority Groups/Women/Veterans/Individuals with Disabilities/Sexual Orientation/Gender Identity and other protected classes. In order to ensure reasonable accommodation for protected individuals, applicants that require accommodation in the job application process may contact *********************** for assistance.

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description · Develop ad qualify highly precise analytical methods for analysis of large molecule products. Support global transfer and trouble shooting of methods. Analyze data, prepare reports and presentations · Essential: Experience in cell culture, immunoassay and bioassay development are required. · Excellent documentation skills. · Preferred: Flow cytometry, Biacore, cell signaling, laboratory automation and DOE experience is preferred · Develop and qualify precise ELISA, CRBA and cell-based potency methods for analysis of large molecule products. Support global transfer, validation and trouble shooting of bioassays. Perform characterization sample testing, statistical data analysis and summarize assay results, prepare e-notebooks and reports. · Experience & Knowledge Essential: · Experience in cell culture, immunoassay and bioassay development are required. Excellent documentation skills. Preferred: Flow cytometry, Biacore, SDS-Page, laboratory automation are preferred. · Develop and qualify precise ELISA, CRBA and cell-based potency methods for analysis of large molecule products . · Support global transfer, validation and trouble shooting of bioassays . · Perform characterization sample testing, statistical data analysis and summarize assay results, prepare e-notebooks and reports . · Experience in cell culture, immunoassay and bioassay development are required. Excellent documentation skills. Preferred: Flow cytometry, Biacore, SDS-Page, laboratory automation are preferred Qualifications · Develop and qualify precise ELISA, CRBA and cell-based potency methods for analysis of large molecule products . · Support global transfer, validation and trouble shooting of bioassays . · Perform characterization sample testing, statistical data analysis and summarize assay results, prepare e-notebooks and reports . · Experience in cell culture, immunoassay and bioassay development are required. Excellent documentation skills. Preferred: Flow cytometry, Biacore, SDS-Page, laboratory automation are preferred Additional Information Regards, Sneha Shrivastava ************

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job-you will find purpose and pride. Your Role at Baxter As a Technologist, R&D at Baxter Healthcare Corporation, you'll have a meaningful role in our mission to Save and Sustain Lives. Located in Batesville, this opportunity allows you to be part of a world-class team dedicated to redefining healthcare delivery. You will perform technical analysis and delivery in diverse environments, with the mentorship of experienced Technicians, Engineers, or Managers. What you'll do Successfully implement assigned tasks with mentorship and support. Apply technical proficiencies to solve problems efficiently. Gain hands-on experience through exposure, observation, and delivering under close supervision. Document status and results flawlessly using good documentation practices. Use handheld and bench test equipment to acquire detailed test data. Contribute positively to team decisions and actions. Work primarily within your technical field. Provide clear and accurate data regarding product and process measurements. Apply new technical tools and concepts under direction. Seek input from experienced colleagues to improve the quality of deliverables. What you'll bring AS Degree (preferably in Electronics Technician field), or equivalent work experience required. 2+ years of technical experience, or comparable experience. Strong organizational and communication skills. Proven ability to work collaboratively in a team environment. Proficient problem-solving skills. Adaptable to change. Working knowledge of Microsoft Office. Displays curiosity about technology, industry, and competitive benchmarks. Join us and become part of a driven group where your efforts have an impact every day! We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $64,000-$88,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. #LI-TV1 US Benefits at Baxter (except for Puerto Rico) This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Job Posting: R&D Chemist III (Cosmetic Formulator) Schedule: 8 AM - 4:15 PM Status: Salaried, Exempt About the Role: The R&D Chemist lll is responsible for the research, development, and testing of new OTC Drug or Cosmetic products, technologies, packaging, and product improvements. This role will work with minimal guidance to incorporate the technical, regulatory, competitive, cost, operational, project timing, work prioritization and strategic considerations to support a successful product development. The R&D Chemist III will write technical updates and reports, memos, regulatory documents, operating procedures, protocols, experimental design, data analysis, and other communication as needed. Collaborates with internal or external partners involved with clinical testing, claims substantiation, formulation development, raw materials, manufacturing, or contract manufacturing with minimal guidance. Key Job Responsibilities Successfully formulate and scale up a variety of formulation types including but not limited to face creams, lotions, soaps, shampoos, cleansers, lip balms, SPF creams, oral creams, body sprays etc. Consistently maintains accurate documentation of formulation, procedures, results, data, and conclusions. Apply Blistex quality standards and consumer product usage trends during product development and raw material selection. Assesses stability of OTC drug and consumer products. Applies physical/sensory and technical test data for formulation development. Proposes investigative testing when troubleshooting formulation issues. Can independently make recommendations based upon analysis. Propose solutions when working with vendors to address raw material issues. Applies a strong understanding of raw materials and chemical compatibility to predict the overall final product's physical and chemical properties. Understands and follows appropriate lab safety practices. Effectively communicates with laboratory colleagues, project managers, and colleagues from numerous functional areas. Supports the R&D team achieve both individual and team goals and consistently treats people with respect. Basic Qualifications Bachelor's degree in chemistry, biology, or related scientific discipline with 7-10 years of applicable laboratory experience preferably in the cosmetics or pharmaceutical OTC industry. Proficient understanding of formulation laboratory equipment (e.g., mixers, hotplates, balances, pH meters, viscometers, filling equipment, lipstick molds, etc) Has a good understanding of the physical, chemical, biological, microbiological, engineering, and regulatory requirements involved in the assessment of OTC drug and consumer products. Deep understanding of the production equipment capabilities and its impact on the formulation for the formulation types mastered. Established experience in electronic forms of data analysis techniques and communication. Understands and adheres to Good Laboratory Practices, cGMP, safety regulations, and confidential procedures. Ability to work on simultaneous projects effectively and within allotted timelines and works with integrity. Constantly and effectively employs ingenuity and creativity in addressing opportunities and challenges. Able to deliver effective presentations to a variety of audiences. Additional Qualifications Strong mathematical ability and analytical skills. Accurately calculates percentages, formula costs, and applies basic statistics. Applies concepts of basic algebra and geometry. Performs spreadsheet mathematical and graphical analysis. Proficient with computers and in Microsoft programs including Outlook, Word, Power Point and Excel. Ability to learn new software such as ELN and Regulatory Documentation programs. Suggests or performs special projects, as assigned, or agreed by the Manager or Director, R&D. Performs and assumes other duties and responsibilities, as may be required by the Manager or Supervisor, R&D. M-F 8 AM - 4:15 PM

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. Lilly is currently constructing a cutting edge facility for the manufacture of new modalities including Gene Therapy. At Lebanon, Indiana, this facility will be Lilly's most technically advanced manufacturing site focused on the delivery of the next wave of innovative products at Lilly. It will include next-generation manufacturing technologies and advanced data collection and analysis platforms that will deliver improvements in safety and quality, and process performance. This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing site, and the successful candidate will help to design, commission and start up the facility for both clinical and commercial supply. This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up. The TS/MS team will own all areas of technology transfer, process validation, and process stewardship. Position Description: Bioprocess - Technical Services/Manufacturing Scientist (TS/MS) role is responsible for providing technical support for the development, implementation, and technical transfer of compliant manufacturing of gene therapy drug substance for clinical and commercial manufacture. The successful candidate will be required to build deep technical expertise in their area of responsibility (including in-depth knowledge of the science behind the molecule and the process), have strong working skills on the manufacturing equipment set and control systems, and consistently demonstrate strong data-driven decision-making and problem-solving capabilities. They may also work to ensure that the process is in-control, capable, compliant, and maintained in a validated state through continual monitoring and may play a role in by implementing new technologies and process improvements in the manufacturing environment. Key Objectives/Deliverables Have an in-depth knowledge of the science behind the molecule and the processes. Understand the process control strategy for gene therapy products Provide technical support for all start-up TS/MS activities (e.g., NPI, tech transfer, process validation, process stewardship and improvement) Ownership and technical stewardship of bioprocess and provide technical expertise during Root Cause Analysis for deviations and Impact Assessments for changes Work as part of cross-functional teams, and establish partnerships with applicable functions, operations, and development to understand interface between the science/engineering with the operations on the floor and bring deep technical expertise to the team Be able to assess whether the process is in control and capable of meeting its stated purpose and is in a constant state of validation Identify process improvements and participate in implementation of Lean manufacturing initiatives Prepare, review, approve, and provide technical support for preparation of relevant technical documents, as required, such as: change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, process description documents and annual reports Support and/or lead TS/MS technical projects to ensure a successful start-up, improve process control, yield, product quality and/or productivity. Implement process changes and improvements through the technical agenda Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess process variability and capability Serve as technical interface external to the Lebanon site Provide audit support, as needed Work within or lead cross-functional teams in a positive fashion to implement TS/MS objectives and deliver on business plan and quality objectives. Ensure a safe working environment through compliance with safety rules and improve safety culture by actively participating in safety-related activities Basic Requirements: Bachelor's in Biochemical Engineering, Chemical Engineering, Biotechnology, Biochemistry or related quantitative field 3+ years of experience in cGMP manufacturing, specifically within Operations, Validation, TS/MS, or Engineering Additional Preferences: Have an in-depth knowledge of the science behind the molecule and the processes on mRNA/LNP drug substance manufacturing. Understand the process control strategy for mRNA/LNP mediated gene therapy products Experience and understanding of technical challenges with mRNA as a therapeutic modality is required Experience with mRNA/LNP formulation Experience with QC assays in line with product CQAs including variability Strong interpersonal and teamwork skills Strong self-management and organizational skills Strong oral and written communication skills that demonstrate an ability to effectively (clearly, succinctly) communicate with all levels of the organization Experience with data trending and analysis Ability to analyze complex data and solve problems Demonstrated successful membership/leadership of cross-functional teams 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 $66,000 - $171,600 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

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.

Hentzen is a unique company in today's world. Since our founding in 1923, we've remained an independent, privately held organization committed to being a leader in the development and manufacturing of high-performance coatings. Our success is built on a foundation of innovation, dedication, and service-to both our customers and our employees. With over 100 years of experience, Hentzen has earned recognition as a technology leader and trusted partner in the aerospace, defense, and industrial markets. Our ability to custom-engineer advanced coatings tailored to meet the specific and challenging requirements of our customers sets us apart. This innovation comes to life in our state-of-the-art facilities, where our talented employees are empowered to solve complex problems through creativity and collaboration. If you're looking to join a company known for its technical excellence, employee commitment, and customer focus, Hentzen offers a rewarding and challenging opportunity to learn, grow, and make a meaningful impact. DEVELOPMENT CHEMIST - LIQUID R&D 1st Shift M-F Batavia, IL Plant The Development Chemist - Liquid R&D is responsible for the formulation, research, and development of new products and colors as well as improvement of existing products. The successful candidates will have an acceptable score on the color matching and math tests. DESCRIPTION OF ESSENTIAL DUTIES: Develop new products for customers per their requirements. Develop products and solve technical issues with a relatively minor amount of direction. Exercise wide discretion when solving challenges. Provide technical assistance for existing accounts. Build knowledge of analytical methods for solving problems. Train production and quality control personnel. Work with production personnel to solve problems. Exhibit demonstrated decision-making abilities. Plan activities for support personnel. Reduce or rework distressed products on hand to reduce inventory. Ability to travel up to 10% of time. As part of the housekeeping procedures, the employee may be involved with the disposal of hazardous waste. The initial training of how to properly dispose of hazardous waste will be performed by the Environmental and Safety department or the department supervisor. Annual training of the same will be performed by the EHS department. Perform other miscellaneous duties as assigned. QUALIFICATION REQUIREMENTS: Education level strongly preferred: Bachelor's degree in chemistry or related field. Experience level preferred: One to three years in a manufacturing or industrial setting, preferably in coatings or chemical environment. Ability to receive and provide instructions in a positive manner. Ability to read, understand and apply complex mathematical calculations. Exemplify core values, i.e., Integrity, Loyalty, Passion, Commitment, and Respect. Must be a high energy, results driven individual with excellent communication, computer, and decision-making skills. Ability to work independently, in a fast-paced team environment, with the proactive problem-solving skills and work ethic necessary for timely completion of projects. Excellent computer skills (Microsoft Office - Word, Excel, Outlook), ERP system and other office machinery. WORK ENVIRONMENT: While performing the duties of this job, the employee is frequently required to talk and/or hear, stand, and/or walk, use hands to finger, handle or touch objects or controls, and move from place to place. The employee is regularly required to sit, balance, stoop, and occasionally reach above shoulders. The employee occasionally must use foot/feet to operate machinery, climb, or balance and reach above the shoulders. The employee may regularly lift and/or move up to 65 lbs. Personal Protection Equipment is required during various processes in the production facility. Safety shoes, glasses, respirators, fire retardant uniform, and earplugs may be required when performing certain functions. Please send your resume to: Hentzen Coatings, Inc. Attn: Human Resources 6937 W. Mill Road Milwaukee, WI 53218 or APPLY ONLINE AT: Hentzen Career Center Hentzen Coatings, Inc. is an Equal Opportunity Employer, including Veterans and Individuals with Disabilities. *************** All candidates are subject to post-offer testing: including a job-related pre-employment physical, drug screen, and background check.

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

WHO WE ARE We are a company where people matter. We are family driven. We are financially strong. And we are looking for problem-solvers to join our growing team. BENEFITS Up to 10% Retirement Contribution $3,000 sign-on bonus! $600 per Year Wellness Incentive Two Weeks Starting Paid Time Off Medical, Dental, and Vision - Eligible f irst day of the month following hire date. JOIN A TOP WORKPLACE - ******************************************* QC Chemist The primary purpose of this position is to perform required quality control analysis of incoming, manufacturing and outgoing material with authority to make acceptance, production adjustment, and/or rejection decisions. This position may also provide technical support to operations and sales. Hours are for this position are Sunday-Monday 7am -7:30pm and Tuesday- Wednesday from 7am-3:30pm. As QC Chemist, primary responsibilities include: Perform required quality control analysis of incoming, manufacturing and outgoing material with authority to make acceptance, production adjustment, and/or rejection decisions. Record and maintain analysis/records accurately, neatly, legibly and completely. Prioritize daily laboratory activities to meet production schedules. Perform instrument maintenance, calibrations, quality control checks, solution preparations, and solution standardizations. Provide technical support and assistance to operations/production regarding manufacturing adjustment of non-conforming materials and quality issues. Maintain a clean and neat laboratory at all times. Adhere to all safety SOPPs. Initiate corrective actions on identified non-capable procedures or practices. Maintain and properly store sample retains. Communicate to supervisor concerns about standard laboratory procedures, operational problems, quality trends, etc. Maintain a professional attitude and demeanor at all times, treat others with courtesy and respect, and respond to all requests in a professional manner. Promote complete customer satisfaction through quality and service to both internal and external customers. All staff members are responsible for reporting food safety problems to their supervisor or the SQF Practitioner upon observation of a known or potential issue. Uphold Hydrite's Standard of Excellence through a continuous commitment to maintain quality facilities and provide quality products and services to internal and external customers Perform all duties outlined in relevant SOPs and all other duties to be assigned. Participate in RCRA, regulatory, health & safety and process training activities as required. Review changes/additions with your supervisor. Must be RCRA compliant. REPORTING STRUCTURE This position reports to the QC Lab Supervisor. EXPERIENCE AND EDUCATIONAL CRITERIA Bachelor's Degree in Chemistry or related field is required. Must have good communication and interpersonal skills, including the ability to read, write, and speak in English. Proficiency in computer skills and good working knowledge with all MS Office applications. Ability to accurately transfer written and verbal information and documentation and enter data into existing computer system. Must be self-motivated and able to work independently as well as in a group setting. Able to apply mathematical and problem solving skills for resolution. Must possess good laboratory analytical skills. JOB EXPECTATIONS: Uphold Hydrite's Standard of Excellence through a continuous commitment to maintain quality facilities and provide quality products and services to internal and external customers. Participate in RCRA, regulatory, health & safety and process training activities as required. Review changes/additions with your supervisor. Must be RCRA compliant. Regular attendance is essential. Perform all duties outlined in relevant SOPs and all other duties to be assigned. Work with other staff members to maintain workload balances. Provide back-up support as necessary. Support effective communication with all Hydrite departments where responsibilities overlap to ensure success of the branch team. REPORTING STRUCTURE This position reports to QC Lab Supervisor BENEFITS Benefits and perks include 401k and profit sharing, medical/dental/vision/life insurance, paid time off, tuition reimbursement, adoption assistance, legal services insurance, scholarship awards for children of employees, summer picnic, community giving events, free family wellness coaching including nutritionist and fitness coach. WHY HYDRITE? Watch this Why Hydrite video to find out: *************************** WANT TO STAY CONNECTED? FIND US ON SOCIAL MEDIA LinkedIn: linkedin.com/company/hydrite-chemical-co- Facebook: facebook.com/hydrite YouTube:******************************************* Learn more about Hydrite on our website: *********************** Privacy Notice for California Residents: **************************************************************

The QC Chemist will support all technical aspects related to quality control testing readiness, including QC reagents and materials management, equipment preparation and daily cleaning and maintenance activities, sample management and QC testing, and documentation completion and review in full compliance with GMP regulations, procedures, and product specifications. Key Responsibilities: Compendia experience (USP, EP, BP, JP, CP). Finished Product testing, Environmental Monitoring, Sterility QC testing, and reporting of the QC results. Escalation in case of non-conformances and deviations, and manage these quality incidents as per procedures. Support deviation investigations, OOS/OOT/OOE investigations, CAPA follow-up and implementation, and Change Control management, including procedure and form revisions. Participation in assigned qualification/validation activities, as necessary. Responsible for the successful on-time completion of required training curricula comprising the necessary Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications, Testing and specifications, and other relevant training, including HSE for the specific role. Prepares applicable documents, forms, and records such as analytical batch records, and follows Good Documentation Practices. Support internal and external Audits and Inspections, as required. Essential Requirements: Education: Bachelor's degree required in a relevant Scientific discipline (e.g, Chemistry, Microbiology). A minimum of 2-3 years of experience in a cGMP or aseptic environment is required. Knowledge of cGMP regulations and FDA guidance applicable to Quality Control for product and Environmental Monitoring testing, as well as Aseptic techniques. Practical experience with Microbiology method verification and routine testing practices, EM Monitoring, and basic knowledge of method/equipment validation principles and methodologies preferred; HPLC knowledge is required. Ability to interpret analytical data and convert it into technical documentation. Basic knowledge and understanding of aseptic principles and techniques, Quality Control Sampling, Quality Control (QC Testing), and General HSE knowledge.