Chemist Jobs in Welby, CO

Employment Type: Full-time EFI Polymers is seeking an experienced Formulation Chemist to develop high-performance epoxy and polyurethane products for the electrical and electronics markets. This role involves formulating potting compounds, adhesives, sealants, and industrial coatings while providing technical support to customers. The ideal candidate will have extensive hands-on experience in epoxy and polyurethane formulation. Qualifications & Requirements: · Education: Bachelor's degree in Chemistry · Experience: 5-15 years of relevant epoxy and polyurethane formulation experience. · Compensation: Salary and title will be based on experience level. Key Responsibilities: 1. New Product Development & Technical Support · Lead the development of commercially viable new products · Formulate electrical potting compounds, adhesives, sealants, and industrial coatings (100% solids and waterborne). · Conduct testing and validation to ensure products meet customer specifications and industry standards. · Troubleshoot product issues and provide technical support to customers. · Expand EFI's product portfolio by exploring new technologies and chemistries. 2. Technical Expertise & Product Innovation · Work with epoxy, urethane, polyurea, and waterborne chemistries; including acrylic and urethane dispersions, and PVA. · Develop formulations that enhance thermal conductivity, flame resistance, stress relief, electrical insulation, and environmental/chemical resistance while meeting UL and third-party testing requirements. · Optimize formulations for performance and cost to maintain a competitive edge. 3. Cross-Department Collaboration · Work closely with Sales, Management, R&D Chemists, and Lab Technicians to align development efforts with business needs. · Provide technical information to support regulatory compliance. · Assist Production in improving processing capabilities and quality control. Additional Responsibilities · Evaluate new opportunities and recommend existing products when applicable. · Stay updated on emerging technologies relevant to EFI's industry. · Coordinate external testing and contract laboratories as needed. Required Skills & Competencies · Strong analytical and problem-solving abilities in a laboratory setting. · Proficiency with viscometers, TMA, DSC, TGA, Instron, FTIR, and other standard lab equipment. · Ability to prioritize multiple projects efficiently. · Excellent communication skills, with the ability to translate customer needs into actionable formulations. · Experience working with vendors and industry contacts to drive innovation. Work Environment & Company Overview EFI Polymers is a custom formulator and manufacturer of high-quality epoxy and polyurethane materials, industrial coatings, and latex adhesives. Since 1993, EFI has developed thousands of formulations for the electronics, electrical, coatings, and adhesives industries. Equal Opportunity Employer EFI Polymers is an Equal Opportunity Employer. We encourage all qualified applicants to apply, and we are committed to providing a workplace free from discrimination and harassment. All employment decisions will be made without regard to race, color, religion, national origin, age, citizenship, gender, marital status, pregnancy, sexual orientation, gender identity and expression, disability, or veteran status.

Outlier is the world's leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities. We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Chemistry. Develop and answer Chemistry-related questions to refine AI understanding. Assess and rank AI responses based on scientific rigor. Required expertise and qualifications: Education: Master's degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled) Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&D contributions English Proficiency: Ability to read and write with minimal errors Bonus Skills: AI model training experience is not required but helpful Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below) Opportunities for higher-paying research projects based on performance. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

Chemistry: - Design and execute multi-step organic syntheses to develop novel functional compounds (photochromic dyes). - Purify and characterize compounds using techniques such as NMR, GC-MS, and UV-Vis.- Conduct literature reviews to identify and evaluate synthetic methodologies and expected compound properties (e.g. color, absorption, intensity). - Optimize reaction conditions and troubleshoot challenges in the synthetic process. - Collaborate with the team to ensure the successful integration of organic compounds (photochromic dyes) into the final product (nanoparticle inks). General: - Design of experiments to test quality and functionality of novel compounds and delivery systems. - Coordination with contract manufacturers on process R&D and scale-up operations. - Maintenance of chemical inventory and relevant safety data. - Creation and maintenance of batch and quality records. Nice to have: - Ability to characterize nanoparticle inks using techniques such as: viscosity measurement, particle size distribution (DLS), color analysis (colorimetry and UV-Vis), analysis of particle morphology (SEM). - Familiarity with nanoparticle processing techniques such as: sonication, shear homogenization, centrifugation, tangential flow filtration, lyophilization. Job Type: Full-time Benefits: Health insurance Schedule: 8 hour shift Work Location: In person

Are you looking for an exciting job where you can put your skills and talents to work at a company you can feel proud to be a part of? Do you want a workplace that will challenge you and offer you opportunities to learn and grow? A position at Xcel Energy could be just what you're looking for. Position Summary Position supports laboratory, plant and field chemistry operations in all aspects of chemical, biological, and physical analysis and testing. Expertise is required in one of the five following systems: environmental, general water treatment, lubricants, fuel chemistry, and general analytical instrumentation. Position will work with Xcel facilities and/or customers to enhance availability, reliability, and help ensure low operating costs. This is a union represented position. The terms and conditions of employment for this position are currently being negotiated with the union. The terms and conditions that are initially offered for this position may change and be different once a contract with the union is finalized. Essential Responsibilities Uses advanced technical knowledge to develop and implement chemical treatment and/or analytical programs and related procedures, including chemical cleanings. Performs analysis, reviews and reports data. Maintains and troubleshoots instrumentation. Trains plant and/or analytical personnel. May include external training and presentations. Responsible for reviewing and assessing process parameters for compliance with control limits. Uses discretion and judgment to correct non-compliant parameters. Generate statistical control charts. Participate in the development of new technologies and writing of procedures utilizing appropriate improvements. Consult with internal and external customers to ensure compliance and optimize processes through inspections and data analysis, and provides recommendations based on analytical results/criteria. Interface with environmental services and governmental agencies to ensure compliance with regulations. Minimum Requirements for Chemist Bachelor's degree in chemistry or related science Five (5) years related experience in power plant, electric utility or laboratory settings. In lieu of a degree, candidates with at least 10 years of chemistry laboratory experience, along with some advanced college-level coursework in chemistry may be considered. Ability to obtain state certifications as applicable by the jurisdiction. Minimum Requirements for System Chemist Bachelor's degree in chemistry or related science 10 years related experience in power plant, electric utility or laboratory settings. Ability to obtain state certifications as applicable by the jurisdiction. As a leading combination electricity and natural gas energy company, Xcel Energy offers a comprehensive portfolio of energy-related products and services to 3.4 million electricity and 1.9 million natural gas customers across eight Western and Midwestern states. At Xcel Energy, we strive to be the preferred and trusted provider of the energy our customers need. If you're ready to be a part of something big, we invite you to join our team. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Individuals with a disability who need an accommodation to apply please contact us at *************************. Non-BargainingThe anticipated starting base pay for this position is: $62,500.00 to $102,100.00 per year This position is eligible for the following benefits: Annual Incentive Program, Medical/Pharmacy Plan, Dental, Vision, Life Insurance, Dependent Care Reimbursement Account, Health Care Reimbursement Account, Health Savings Account (HSA) (if enrolled in eligible health plan), Limited-Purpose FSA (if enrolled in eligible health plan and HSA), Transportation Reimbursement Account, Short-term disability (STD), Long-term disability (LTD), Employee Assistance Program (EAP), Fitness Center Reimbursement (if enrolled in eligible health plan), Tuition reimbursement, Transit programs, Employee recognition program, Pension, 401(k) plan, Paid time off (PTO), Holidays, Volunteer Paid Time Off (VPTO), Parental Leave Benefit plans are subject to change and Xcel Energy has the right to end, suspend, or amend any of its plans, at any time, in whole or in part. In any materials you submit, you may redact or remove age-identifying information including but not limited to dates of school attendance and graduation. You will not be penalized for redacting or removing this information. Deadline to Apply: 04/29/25 EEO is the Law | EEO is the Law Supplement | Pay Transparency Nondiscrimination | Equal Opportunity Policy (PDF) | Employee Rights (PDF) ACCESSIBILITY STATEMENT Xcel Energy endeavors to make *************************** accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact Xcel Energy Talent Acquisition at *************************. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.

Posting TitleResearcher III-Quantum Materials Chemist . . TypeRegular . Hours Per Week40 . Working at NREL Join the National Renewable Energy Laboratory (NREL), where world-class scientists, engineers, and experts are accelerating energy innovation through breakthrough research and systems integration. From our mission to our collaborative culture, NREL stands out in the research community for its commitment to an affordable and secure energy future. Spanning foundational science to applied systems engineering and analysis, we focus on solving complex challenges to deliver advanced, secure, reliable, and cost-effective energy solutions. Our work helps strengthen U.S. industries, support job creation, and promote national economic growth. At NREL, you'll find a mission-driven environment supported by state-of-the-art facilities, multidisciplinary research teams, and strong collaborations with industry, academia, and other national laboratories. We offer robust professional development opportunities, and a competitive benefits package designed to support your career and well-being. Learn about NREL's critical objectives: NREL's Mission and Vision. Job Description A regular term Researcher III position is available in NREL's Materials, Chemical and Computational Science Directorate on research efforts in quantum materials discovery. This position will focus on the synthesis and characterization of novel quantum materials and relevant device structures. Systems of interest include novel quantum dot chemistries and chiral materials exhibiting spin selectivity. The collaborative environment requires a candidate who can interface with researchers of different disciplines and learn topics outside their area of expertise. Candidates will be expected to communicate their results to internal stakeholders and in more traditional journal publications, and conference presentations. In general, candidates should have a demonstrated track record of success in technical activities associated with automation and be comfortable formulating value proposition automation use cases in a technologically relevant way while addressing key science questions to challenging problems as part of a team effort. The candidate will be required to work closely with the Environment, Health, & Safety team to follow safe work procedures, as well as to handle waste properly and keep a clean, well-organized work environment. . Basic QualificationsRelevant PhD . Or, relevant Master's Degree and 3 or more years of experience . Or, relevant Bachelor's Degree and 5 or more years of experience . Demonstrates complete understanding and wide application of scientific technical procedures, principles, theories and concepts in the field. General knowledge of other related disciplines. Demonstrates leadership in one or more areas of team, task or project lead responsibilities. Demonstrated experience in management of projects. Very good technical writing, interpersonal and communication skills. * Must meet educational requirements prior to employment start date. Additional Required Qualifications Candidates should have extensive experience with synthesis and characterization of quantum materials systems, demonstrated success in a collaborative environment, and a track record of high-impact publications. Candidate should show ambition to develop funding proposals with a new ideas and a knowledge of potential funding opportunities to grow programs at NREL. Demonstrates leadership in one or more areas of team, task or project lead responsibilities. Very good technical writing, interpersonal and communication skills. Preferred Qualifications Ability to formulate testable research hypotheses and independently lead experiments in the laboratory. Critically analyze results and present research updates, propose research experiments on a regular basis, draft manuscripts, and write research proposals. Candidate should be well versed in nanoscience materials of current interest, chirality in semiconductors, novel device platforms and fabrication and characterization of materials. . Job Application Submission Window The anticipated closing window for application submission is up to 30 days and may be extended as needed. Annual Salary Range (based on full-time 40 hours per week) Job Profile: Researcher III / Annual Salary Range: $81,500 - $146,700 NREL takes into consideration a candidate's education, training, and experience, expected quality and quantity of work, required travel (if any), external market and internal value, including seniority and merit systems, and internal pay alignment when determining the salary level for potential new employees. In compliance with the Colorado Equal Pay for Equal Work Act, a potential new employee's salary history will not be used in compensation decisions. Benefits SummaryBenefits include medical, dental, and vision insurance; short*- and long-term disability insurance; pension benefits*; 403(b) Employee Savings Plan with employer match*; life and accidental death and dismemberment (AD&D) insurance; personal time off (PTO) and sick leave; paid holidays; and tuition reimbursement*. NREL employees may be eligible for, but are not guaranteed, performance-, merit-, and achievement- based awards that include a monetary component. Some positions may be eligible for relocation expense reimbursement. Limited-term positions are not eligible for long-term disability or tuition reimbursement. * Based on eligibility rules Badging RequirementNREL is subject to Department of Energy (DOE) access restrictions. All employees must also be able to obtain and maintain a federal Personal Identity Verification (PIV) card as required by Homeland Security Presidential Directive 12 (HSPD-12), which includes a favorable background investigation.Drug Free Workplace NREL is committed to maintaining a drug-free workplace in accordance with the federal Drug-Free Workplace Act and complies with federal laws prohibiting the possession and use of illegal drugs. Under federal law, marijuana remains an illegal drug. If you are offered employment at NREL, you must pass a pre-employment drug test prior to commencing employment. Unless prohibited by state or local law, the pre-employment drug test will include marijuana. If you test positive on the pre-employment drug test, your offer of employment may be withdrawn. Submission Guidelines Please note that in order to be considered an applicant for any position at NREL you must submit an application form for each position for which you believe you are qualified. Applications are not kept on file for future positions. Please include a cover letter and resume with each position application. . Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard basis of age (40 and over), color, disability, gender identity, genetic information, marital status, domestic partner status, military or veteran status, national origin/ancestry, race, religion, creed, sex (including pregnancy, childbirth, breastfeeding), sexual orientation, and any other applicable status protected by federal, state, or local laws. Reasonable Accommodations E-Verify ******************** For information about right to work, click here for English or here for Spanish. E-Verify is a registered trademark of the U.S. Department of Homeland Security. This business uses E-Verify in its hiring practices to achieve a lawful workforce.

Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to partner in the global effort to improve lives through innovative science with an experienced workforce. We can offer you the chance to build on your skills and knowledge while working among experts in their fields and with cutting-edge instrumentation. Cogent Scientific offers competitive pay, attractive benefits, and an exciting work environment. We aim to recruit the best people who stand out among their peers and embody our Core Values: Client Focused: We only succeed when our clients succeed. Outstanding: We deliver meticulous results through outstanding performance. Good: We act ethically and morally. Employee-Centric: We honor and support our employees. Nimble: We are prepared to adapt in an ever-changing industry. Team-Oriented: We collaborate with each other and with our clients. We currently have a role available for a Pharma NMR Chemist. Job Duties include, but are not limited to: Processing and high-level interpretation of NMR spectra using 1D and 2D techniques Quantitative NMR (qNMR) analysis Accurate preparation of buffers and samples Calibrating and maintaining instrumentation to assure good quality spectra. Familiarity with gradient shimming preferred Creating worklists and SOP's Maintaining and ordering NMR lab consumables Maintaining a safe, organized, and productive lab. Job Requirements include, but are not limited to: BS - Chemistry or related field with 3-5 years of industry experience (pharma preferred) in analytical, bioanalytical or biological laboratories. Excellent communication skills - verbal and written. Works well both as a team and as an individual. Demonstration of very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions. The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery.

EQUAL OPPORTUNITY EMPLOYER Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices. CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients, and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2,600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people's lives. Our network in Europe and the U.S. offers flexible and specialized solutions across six technology platforms: Peptides; Lipids & LNPs; Injectables; Highly Potent & Oncology; and Small Molecules; and Oligos. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients. SUMMARY Acts to drive and demonstrate the technology for the planning and execution of development and implementation of chemical processes. Ensures that the chemistry is sufficient to meet goals on process yields, throughputs, and QSHE requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned: * Familiarity with general TFF/ultra filtration setup, operation, and components * Experience with lab and/or mid-large scale TFF/ultra filtration processing * Knowledge of various types of TFF filtration methods and systems * Understanding of key operating/scalable parameters for TFF/ultra filtration and ability to determine such parameters during process familiarization/optimization * Provides technical support to lab or plant processes * Works effectively in a team-oriented environment * Presents work orally and in form of written development reports * Adheres to GDP and SOPs in all aspects of work * Independently plans and executes experiments, while working in a project team, toward development of viable commercial processes * Demonstrates a clear understanding of technical issues and the requirements of a viable manufacturing process * Executes procedures, processes, and methods for solutions to chemical and technical problems on a lab or plant scale * Ensures that the chemistry is capable of meeting cost, yield, throughput, and QSHE goals on assigned processes * Leads a team to accomplish the development, transfer, or implementation of technology at a lab or plant scale * Develops and supports scalable processes and provides technical expertise and support during lab or plant operations LEADERSHIP & BUDGET RESPONSIBILITIES Demonstrates a positive attitude. Supports a positive, healthy, and flexible work environment that encourages employees and coworkers to develop their full potential and expand their horizons. This position has no supervisory responsibilities. Provides technical expertise to manufacturing. SAFETY & ENVIRONMENTAL RESPONSIBILITIES Every individual is personally responsible for the safety and environmental aspects of their activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience. QUALITY RESPONSIBILITIES Corden Pharma Colorado (CPC) is a manufacturer of a variety of pharmaceutical products. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable. This is critical as it is our mission to not place patients at risk due to inadequate safety, quality, or efficacy. CPC's Quality Management System, which incorporates cGMP, is designed to deliver this quality objective. Attainment is produced through the requisite participation and commitment of all staff across departments and at all levels within the company. cGMP is the part of Quality Management System ensuring products are consistently produced to accurate quality standards. Adherence to clearly defined procedures, in compliance with the principles of cGMP, is required when performing operations across Corden Pharma Colorado. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Bachelor's Degree (BS) in Organic Chemistry and 5 years related experience and/or training; or equivalent combination of education and experience. TFF/Untra filtration experience is required; and Peptide and GMP experience is a plus. LANGUAGE SKILLS Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to develop bench scale laboratory procedures into step-by-step operating instructions for chemical operators. Ability to effectively present information to top management, public groups, and/or boards of directors. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. REASONING ABILITY Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables. Ability to apply scientific methods to experimentally prove cause and effect. CERTIFICATES, LICENSES, REGISTRATIONS Domestic and international travel required. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, and sit. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles and low levels of toxic or caustic chemicals. The noise level in the work environment is usually moderate. CORE COMPETENCIES These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity. * Demonstrates a positive attitude * Strong background in chemistry or a related scientific field * Working knowledge of regulatory issues in Pharmaceutical Manufacturing including cGMPs, GDP, FDA, PSM, OSHA, and EPA requirements * Communicates effectively in writing and verbally within the department * Computer skills, in the areas of: Microsoft Office Products (Word, Excel, PowerPoint), Chemdraw, and SciFinder * Ability to work interactively within a multi-functional team-oriented environment * Takes initiative in setting own goals and work plans * Hands-on organic chemistry laboratory experience * Has a broad technical knowledge in Organic Chemistry and Process Improvement Methodology * Maintains a well-documented record of work performed in a laboratory notebook, laboratory reports, and campaign reports * Experience in the synthesis and purification of peptides (desired) * Has working knowledge of all plant-scale unit operations, scale-up, and plant design considerations * Understanding of chemical reactivity, potential exotherms, cross reactivity, side products, and waste streams, especially for processes they support * Regularly seeks out new learning opportunities beyond basic skills that can result in innovative approaches to technical issues * Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple (not necessarily simultaneous) processes * Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements projects * Assumes reasonable risk in trying out new, self-generated ideas * Proactive approach to problem identification and resolution * Communicates effectively in writing and verbally within and across departments and to site management; updates are clear, selective, and effective * Ability to understand and apply statistical design of experiments and draw sound conclusions from the results; uses results when solving problems or when proposing improvements * Ability to provide leadership in all process chemistry aspects of manufacturing processes; leads teams in the development, transfer, troubleshooting, and improvement of chemical processes in interactive, interdisciplinary team environment * Seeks out opportunities to learn manufacturing needs and methods that facilitate substantial process improvements; acquires new skills in state-of-the art technology and applies it to their assignments * Demonstrates skills in negotiation and influencing others This posting will expire on 4/30/2025

EQUAL OPPORTUNITY EMPLOYER Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices. CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients, and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2,600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people's lives. Our network in Europe and the U.S. offers flexible and specialized solutions across six technology platforms: Peptides; Lipids & LNPs; Injectables; Highly Potent & Oncology; and Small Molecules; and Oligos. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients. SUMMARY Acts to drive and demonstrate the technology for the planning and execution of development and implementation of chemical processes. Ensures that the chemistry is sufficient to meet goals on process yields, throughputs, and QSHE requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned: Familiarity with general TFF/ultra filtration setup, operation, and components Experience with lab and/or mid-large scale TFF/ultra filtration processing Knowledge of various types of TFF filtration methods and systems Understanding of key operating/scalable parameters for TFF/ultra filtration and ability to determine such parameters during process familiarization/optimization Provides technical support to lab or plant processes Works effectively in a team-oriented environment Presents work orally and in form of written development reports Adheres to GDP and SOPs in all aspects of work Independently plans and executes experiments, while working in a project team, toward development of viable commercial processes Demonstrates a clear understanding of technical issues and the requirements of a viable manufacturing process Executes procedures, processes, and methods for solutions to chemical and technical problems on a lab or plant scale Ensures that the chemistry is capable of meeting cost, yield, throughput, and QSHE goals on assigned processes Leads a team to accomplish the development, transfer, or implementation of technology at a lab or plant scale Develops and supports scalable processes and provides technical expertise and support during lab or plant operations LEADERSHIP & BUDGET RESPONSIBILITIES Demonstrates a positive attitude. Supports a positive, healthy, and flexible work environment that encourages employees and coworkers to develop their full potential and expand their horizons. This position has no supervisory responsibilities. Provides technical expertise to manufacturing. SAFETY & ENVIRONMENTAL RESPONSIBILITIES Every individual is personally responsible for the safety and environmental aspects of their activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience. QUALITY RESPONSIBILITIES Corden Pharma Colorado (CPC) is a manufacturer of a variety of pharmaceutical products. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable. This is critical as it is our mission to not place patients at risk due to inadequate safety, quality, or efficacy. CPC's Quality Management System, which incorporates cGMP, is designed to deliver this quality objective. Attainment is produced through the requisite participation and commitment of all staff across departments and at all levels within the company. cGMP is the part of Quality Management System ensuring products are consistently produced to accurate quality standards. Adherence to clearly defined procedures, in compliance with the principles of cGMP, is required when performing operations across Corden Pharma Colorado. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Bachelor's Degree (BS) in Organic Chemistry and 5 years related experience and/or training; or equivalent combination of education and experience. TFF/Untra filtration experience is required; and Peptide and GMP experience is a plus. LANGUAGE SKILLS Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to develop bench scale laboratory procedures into step-by-step operating instructions for chemical operators. Ability to effectively present information to top management, public groups, and/or boards of directors. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. REASONING ABILITY Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables. Ability to apply scientific methods to experimentally prove cause and effect. CERTIFICATES, LICENSES, REGISTRATIONS Domestic and international travel required. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, and sit. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles and low levels of toxic or caustic chemicals. The noise level in the work environment is usually moderate. CORE COMPETENCIES These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity. Demonstrates a positive attitude Strong background in chemistry or a related scientific field Working knowledge of regulatory issues in Pharmaceutical Manufacturing including cGMPs, GDP, FDA, PSM, OSHA, and EPA requirements Communicates effectively in writing and verbally within the department Computer skills, in the areas of: Microsoft Office Products (Word, Excel, PowerPoint), Chemdraw, and SciFinder Ability to work interactively within a multi-functional team-oriented environment Takes initiative in setting own goals and work plans Hands-on organic chemistry laboratory experience Has a broad technical knowledge in Organic Chemistry and Process Improvement Methodology Maintains a well-documented record of work performed in a laboratory notebook, laboratory reports, and campaign reports Experience in the synthesis and purification of peptides (desired) Has working knowledge of all plant-scale unit operations, scale-up, and plant design considerations Understanding of chemical reactivity, potential exotherms, cross reactivity, side products, and waste streams, especially for processes they support Regularly seeks out new learning opportunities beyond basic skills that can result in innovative approaches to technical issues Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple (not necessarily simultaneous) processes Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements projects Assumes reasonable risk in trying out new, self-generated ideas Proactive approach to problem identification and resolution Communicates effectively in writing and verbally within and across departments and to site management; updates are clear, selective, and effective Ability to understand and apply statistical design of experiments and draw sound conclusions from the results; uses results when solving problems or when proposing improvements Ability to provide leadership in all process chemistry aspects of manufacturing processes; leads teams in the development, transfer, troubleshooting, and improvement of chemical processes in interactive, interdisciplinary team environment Seeks out opportunities to learn manufacturing needs and methods that facilitate substantial process improvements; acquires new skills in state-of-the art technology and applies it to their assignments Demonstrates skills in negotiation and influencing others This posting will expire on 4/30/2025

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. At Lilly, we serve an extraordinary purpose. For more than 140 years, we have worked tirelessly to discover medicines that make life better. These discoveries start in Lilly Research Laboratories, where our scientists work to create new medicines that will help solve our world's greatest health challenges Responsibilities: This analytical position is in an early phase chemistry development and scale-up laboratory and entails developing analytical methods and analyzing for identity, potency and purity of starting materials, reaction conversions, work-up efficiency, crystallization productivity and endpoints, the purity, potency, polymorphism (API), and particle size (API) of isolated products, and overall mass balance tie up. The analyst is responsible for operating and maintaining analytical equipment in a pharmaceutical research and development laboratory. The analyst will be involved in receiving analytical methods from early phase process chemistry and medicinal chemistry labs and will be responsible for: receiving and establishing reference materials, evaluating the suitability of incoming analytical methods and modifying or developing new methods as needed, analyzing scale-up reactions to support early phase development and for demonstrations towards technical transfers to a GMP kilo-lab. In collaborations, the analyst will engage in reaction development by performing reaction characterization research to identify impurities and amounts and rates of formation to better understand competing mechanistic pathways. Understanding the stability of process streams and isolated materials will also be part of the analyst's responsibility. Basic Qualification MS/PhD level analytical chemist with experience developing methods and analyzing reactions and materials to support pharmaceutical process development. Additional Preferences: Expected to maintain a safe, clean, well-organized, and productive lab space. Experience with the development and use of a variety of analytical methods: HPLC/UPLC, GC, MS, NMR, KF, TGA, DSC, XRD, ICP etc. Process analysis and quantification, tying up mass balance, and material characterization. Familiarity with crystallization and physical/solid state characterization: experience with crystallization monitoring/analysis to understand kinetics and endpoints. Also expected to analyze for polymorphism and particle size and other solid-state characteristics in collaboration with partner analysts. Proficiency with the purification of chemicals via chromatography is a plus. Maintaining a well-organized and detailed lab notebook with accurate descriptions of method development and observations to enable the preparation of technical packages/technical transfers and accurate replication in receiving labs. Participate in training, mentoring, and supporting analytical chemists and chemists in the development and use of analytical methods for pharmaceutical process development. Analytical testing plans - Developing an analytical testing plan to ensure that all facets of a chemical process are understood and under control. This entails characterization of starting materials towards specification setting, establishing reaction end points, determining unit operation end points and optimal amounts of chemicals to use for reactions, work-ups/extractions, crystallizations, washes, etc. 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 $133,500 - $217,800 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

About Us At EA, you'll find yourself surrounded by dynamic professionals that embrace collaboration and curiosity to foster innovation and problem-solving. This culture forms the essence of our value proposition to apply high-quality, objective, and interdisciplinary services to complex environmental challenges. With a strong foundation in servant leadership and community service, EA employees are encouraged to pursue personal and professional passions. As a team, we empower each other to share ideas, believe in our common purpose, and value differing perspectives. Position Overview We are seeking a skilled and detail-oriented Mid-level Chemist to join our team, providing support for a variety of environmental projects with an emphasis on Department of Defense (DoD) and Environmental Protection Agency (EPA) projects. In this role, you will be responsible for assisting with the chemistry and laboratory analytical needs of these projects, ensuring that all analytical processes align with project data quality objectives. Responsibilities * Prepare analytical statements of work and assist with procurement activities for analytical laboratories and third-party data validators. * Coordinate with analytical laboratories, data validation firms, and field sampling teams throughout the project lifecycle. * Help prepare and review Quality Assurance Project Plans (QAPPs), working collaboratively with the project team to ensure the sampling and analytical approach and data reporting meet the project's data quality objectives. * Collaborate with Data Managers on the production, reporting, and submittal of analytical data tables to clients. * Review data validation reports for accuracy and prepare Data Quality and Data Usability reports. * Identify and communicate quality assurance/quality control issues with laboratory operations directly to the Project Manager. Required Qualifications * Bachelor of Science degree in Chemistry, Chemical Engineering, or a related field (Master's degree preferred). * 8 or more years of experience, including environmental consulting and/or environmental laboratory experience. * Familiarity with laboratory analytical methods and instruments. * Experience with environmental analytical needs and requirements for a variety of media, including soil, groundwater, surface water, sediment, and air. * Knowledge of environmental consulting activities, including the investigation, characterization, and remediation of various contaminants and media types (preferred). * Familiarity with emerging contaminants, such as PFAS, is highly preferred. * Excellent verbal and written communication skills with strong attention to detail. * Proficiency with Microsoft Office applications and Adobe Acrobat. Note: This position requires specific driving duties. You must be able to pass a motor vehicle records check required by our insurer. #LI-Hybrid Drug Screen Statement Offers of employment are contingent upon successful completion of a drug screen. Pay Range $75,000-$125,000 USD The EA pay range for this position is intended as a general guideline and does not guarantee specific compensation or salary. Factors considered when making an offer include job responsibilities, education, experience, knowledge, skills, abilities, internal equity, alignment with market data, and compliance with federal and state laws. Why Join EA? At EA, our core values are openness, balance, and challenge and we strive to improve the quality of the environment in which we live, one project at a time. Our professional, team-centric culture promotes collaboration and flexibility and allows employees to guide their own career development path. To that end, we provide training and coaching to support ongoing development for our project managers and consulting engineers. What We Provide: EA prides itself on servant leadership, career development for staff in all areas, and maintaining work-life balance including flexible schedules. We have a tremendous base of positive client relationships that has resulted in a stable backlog of projects and opportunities for growth. We offer paid volunteer time, tuition reimbursement, knowledge sharing, industry advancement, professional associations, and industry conferences. EA is proud to offer a fantastic benefits package that includes the following: * 401k with Employee Stock Ownership Plan (ESOP) * Competitive Salary * Low deductible health coverage for you and your family through Medical, Dental and Vision plans * Generous paid-time-off policy * Paid volunteer time * Tuition reimbursement * Professional Development * Healthcare and Dependent Care Flexible Spending Accounts * Employee wellness program Accommodation Information: If you are interested in applying for employment with EA and require special assistance or accommodation during any part of the pre-employment process, please contact the EA Talent Acquisition Office at ***********************. For TTY users, dial 711. Equal Opportunity Employer Statement: EA is dedicated to providing equal employment opportunities without regard to race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or veteran status. Recruiting Agency Disclaimer Recruiting agencies should not contact EA Engineering, Science and Technology, Inc., PBC directly with unsolicited resumes. Any unsolicited resumes submitted by a recruiting agency to EA via this website or email will be deemed the sole property of EA, and EA will not be responsible for any fee associated with such unsolicited resume.

Imagine yourself… * Contributing to cutting-edge innovations in water quality analysis that impact millions worldwide. * Expanding your expertise in electrochemical research and development while solving complex chemistry challenges. * Thriving in a collaborative, dynamic environment where your ideas drive meaningful change. At Hach (************** a Veralto company, we ensure water quality for people around the world, and every team member plays a vital role in that mission. Our founding vision is to make water analysis better-faster, simpler, greener, and more informative. We accomplish this through teamwork, customer partnerships, passionate experts, and reliable, easy-to-use solutions. As part of our team and the broader Veralto network, you'll work in an environment where purpose meets possibility, making an immediate, measurable impact on a global scale. Motivated by the highest stakes of climate change and global health, we are pioneering innovative technologies to safeguard our water and environment. This position is part of the Research & Development team, located in Loveland, CO, and will be on-site. Reporting to the R&D Manager, the Chemist II, Advanced Research is responsible for: * Developing and optimizing chemical methods for water analysis, focusing on Total Organic Carbon (TOC) measurements. * Designing, conducting, and troubleshooting laboratory experiments, including interference and stability studies, using statistical analysis and a "fail fast" approach. * Expanding product applications by identifying new uses for existing technologies and evaluating emerging water testing methods. * Collaborating with product management, marketing, and sales teams to support product commercialization and market applications. * Planning and managing research projects while maintaining accurate laboratory records and ensuring efficient lab operations. The Essential Requirements of the Job Include: * Bachelor's degree in chemistry or closely related field with 3 years industrial experience or * master's degree in chemistry. * Established lab experience outside of coursework. * Demonstrated knowledge in at least two areas of chemistry (e.g., analytical, organic, or inorganic). * Demonstrated ability in chemical design, characterization, function testing, problem solving. We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees. Hach is proud to be part of the Water Quality segment of Veralto (NYSE: VLTO), a $5B global leader dedicated to ensuring access to clean water, safe food and medicine, and trusted essential goods. When you join Veralto's global network of 16,000 associates, you become part of a culture where purpose meets possibility-where your work directly impacts vital global resources, and where career growth opportunities are abundant. Together, we're Safeguarding the World's Most Vital Resources while building rewarding careers. For Colorado roles only: This requisition will be open for a minimum of five days, though it may be open for a longer period. We encourage your prompt application. US ONLY: The below range reflects the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future. An associate's position within the salary range will be based on several factors, including, but not limited to, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, any collective bargaining agreements, and business or organizational needs. The compensation range for this role is $75,000 - $85,000 USD per year. This job is also eligible for Bonus Pay. We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. US residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Veralto Corporation and all Veralto Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@veralto.com to request accommodation. Unsolicited Assistance We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at any of the Veralto companies, in any form without a valid, signed search agreement in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Veralto and its companies. No fee will be paid in the event the candidate is hired by Veralto and its companies because of the unsolicited referral.

**Imagine yourself...** + Contributing to cutting-edge innovations in water quality analysis that impact millions worldwide. + Expanding your expertise in electrochemical research and development while solving complex chemistry challenges. + Thriving in a collaborative, dynamic environment where your ideas drive meaningful change. At **Hach (** **************** **), a** **Veralto** **company** , we ensure water quality for people around the world, and every team member plays a vital role in that mission. Our founding vision is to make water analysis better-faster, simpler, greener, and more informative. We accomplish this through teamwork, customer partnerships, passionate experts, and reliable, easy-to-use solutions. As part of our team and the broader Veralto network, you'll work in an environment where **purpose meets possibility** , making an immediate, measurable impact on a global scale. Motivated by the highest stakes of climate change and global health, we are pioneering innovative technologies to safeguard our water and environment. This position is part of the **Research & Development team** , located in **Loveland, CO,** and will be **on-site** . Reporting to the **R&D Manager** , the Chemist II, Advanced Research is responsible for: + Developing and optimizing chemical methods for water analysis, focusing on Total Organic Carbon (TOC) measurements. + Designing, conducting, and troubleshooting laboratory experiments, including interference and stability studies, using statistical analysis and a "fail fast" approach. + Expanding product applications by identifying new uses for existing technologies and evaluating emerging water testing methods. + Collaborating with product management, marketing, and sales teams to support product commercialization and market applications. + Planning and managing research projects while maintaining accurate laboratory records and ensuring efficient lab operations. **The Essential Requirements of the Job Include:** + Bachelor's degree in chemistry or closely related field with 3 years industrial experience or + master's degree in chemistry. + Established lab experience outside of coursework. + Demonstrated knowledge in at least two areas of chemistry (e.g., analytical, organic, orinorganic). + Demonstrated ability in chemical design, characterization, function testing, problem solving. We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees. **Hach is proud to be part of the** **Water Quality segment of** **Veralto** **(NYSE: VLTO)** **, a $5B global leader dedicated to ensuring access to clean water, safe food and medicine, and trusted essential goods. When you join** **Veralto's** **global network of 16,000 associates** **, you become part of a culture where purpose meets possibility-where your work directly impacts vital global resources, and where career growth opportunities are abundant. Together, we're** **Safeguarding the World's Most Vital Resources** **while building rewarding careers.** **For Colorado roles only: This requisition will be open for a minimum of five days, though it may be open for a longer period. We encourage your prompt application.** **US ONLY** **:** The below range reflects the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future. An associate's position within the salary range will be based on several factors, including, but not limited to, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, any collective bargaining agreements, and business or organizational needs. The compensation range for this role is $75,000 - $85,000 USD per year. This job is also eligible for Bonus Pay. We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. US residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Veralto Corporation and all Veralto Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available **here (********************************************* . We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@veralto.com to request accommodation. **Unsolicited Assistance** We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at any of the Veralto companies (*************************************** , in any form without a valid, signed search agreement in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Veralto and its companies. No fee will be paid in the event the candidate is hired by Veralto and its companies because of the unsolicited referral. Veralto and all Veralto Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Everyone on our Research & Innovation team shares a passion for innovation, new process, new formulations, new packaging and new ways of thinking. By joining this team, you will use your scientific and technologic expertise to bring health through food, meet the needs of consumers and nurture growth in the business. We are currently looking to hire a Food Scientist III based in Louisville, CO. In this role, you will be responsible for: * Supporting the Creamers businesses (International Delight, Silk, So Delicious, Dunkin', Land O' Lakes) with advanced understanding of R&I strategy, category/business strategy and the ability to leverage diverse methods for executing projects * Demonstrate ability to translate new business dynamics to product design * Deliver product productivity, renovation, and innovation programs, including complex programs (new platforms, high visibility programs) while anticipating challenges and building contingencies * Develop product formulas, processing procedures, product, and raw material specifications to deliver consistent, high-quality products that support business objectives * Independently plan and execute bench, pilot, and plant trials for new and improved products, analyze test results and effectively translate these into effective next steps that lead to project successes * Contribute to scoping of new ideas or technical solutions that contribute to R&I and product category strategy * Deliver fundamental training and information sharing to cross functional partners or junior team members; Optimize and/or champion new ways of working * Work closely with procurement, engineering, and our supplier base to identify potential innovation, renovation, and productivity opportunities The base compensation range for this position is $85,000 - $107,000 commensurate with experience. Danone North America additionally offers a performance-based bonus and has a strong benefits package including Medical, Dental, Vision, Prescription Drug Coverage, 401k Plan, Wellness Program, Life Insurance, Tuition Reimbursement, Flexible Time Off, and Paid Parental Bonding Leave, among other benefit plan options. * Degree in Food Science, Food Engineering, Chemical Engineering, or closely related field preferred (Masters or PhD preferred) with 6+ years of experience in product development in the food industry. Bachelor's degree in Food Science will be considered in combination with more work experience. * Strong technical skills on product formulation, industrial processes, ingredient functionality, and product-process interactions; preferred in-depth knowledge on dairy and non-dairy protein and functional ingredient technologies and/or coffee processing. * Knowledgeable in ingredient selection, formulation, processing equipment, and operating conditions for liquid-based oil-in-water emulsions. * Flexibility to travel * Strong project management/organization and the ability to influence key stakeholders on recommended courses of action. * Excellent communication skills (both written and oral) and the ability to interact with all company functions including R&D, Marketing, Purchasing and Operations. * Comfortable operating in the fuzzy front-end area of innovation and passionate about creating, rapid prototyping, development, and commercialization of ideas under tight timelines. /n At Danone North America, you'll work with some of the best-known food and beverage brands in the world like International Delight, Activia, Silk, Two Good, Oikos, Evian, and Happy Family. You'll be part of one of the largest Certified B Corps in the world, working together to make sure our brands create real benefits for people, communities, and the planet. We have 6,000+ employees across the U.S. and Canada. Come join our movement for a healthier world: One Planet. One Health BY YOU. Danone North America doesn't just welcome what makes you unique, we value it. We're proud to be an equal opportunity and affirmative action employer. All hires to our team are based on qualifications, merit and business needs. We recruit, employ, train and promote regardless of race, color, religion, disability, sex, sexual orientation, gender identity, national origin, age, veteran status, genetic characteristic or any other protected status. Faithful to our values of openness and humanism, all of our employees share in the commitment to engage one another with dignity and respect. #LI-NORAM #LI-ES3

As a Chemist level 1, you will be responsible for assisting and carrying out chemical analysis and designed experimental activities related to environmental testing. Your focus will be in wet chemistry where you will be preparing, extracting, and analyzing samples. You will be responsible for following SOPs, extracting samples, analyzing and entering data. You will be exposed to all of our instrumentation including IC, GCMS, GCFID, and ICPMS. You may be asked to prepare samples for other departments. Responsibilities * Follow SOPs * Perform multi-step procedures * Acquire and interpret analytical data from various meters, spectrophotometer, and other wet chemistry instruments * Summarize results, aid in writing technical reports and procedures, and present information to the technical team * Work collaboratively and effectively in a team environment * Critically think and problem solve * Reinforce safe work practices * Receive initial and annual training; handle and dispose of hazardous wastes Essential Skills * Experience with LIMS * Sample preparation * Knowledge in Chemistry and Analytical chemistry * Expertise in Wet chemistry * Proficiency in pH testing * Gas chromatography (GC) experience * Strong data review skills * Experience in digestion and EPA methods Additional Skills & Qualifications * ICPMS experience is a huge plus * Lab experience is required * Strong written and verbal communication skills * Relevant industrial experience * Experience in food, water, or regulated industries * Candidates from unregulated environments such as the cannabis industry are not suitable Work Environment This company has a total of 13 employees and is growing to keep up with the demand from their customers. The team is close-knit and likes to have fun together. They believe in 'work to live, not live to work' but are committed to their tasks. The team values candidates who are driven, have attention to detail, are self-motivated, and possess strong communication skills and initiative. Please apply for more details. Thank you! Pay and Benefits The pay range for this position is $24.04 - $28.85/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Aurora,CO. Application Deadline This position is anticipated to close on Apr 25, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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. At Lilly, we serve an extraordinary purpose. For more than 140 years, we have worked tirelessly to discover medicines that make life better. These discoveries start in Lilly Research Laboratories, where our scientists work to create new medicines that will help solve our world's greatest health challenges Responsibilities: This analytical position is in an early phase chemistry development and scale-up laboratory and entails developing analytical methods and analyzing for identity, potency and purity of starting materials, reaction conversions, work-up efficiency, crystallization productivity and endpoints, the purity, potency, polymorphism (API), and particle size (API) of isolated products, and overall mass balance tie up. The analyst is responsible for operating and maintaining analytical equipment in a pharmaceutical research and development laboratory. The analyst will be involved in receiving analytical methods from early phase process chemistry and medicinal chemistry labs and will be responsible for: receiving and establishing reference materials, evaluating the suitability of incoming analytical methods and modifying or developing new methods as needed, analyzing scale-up reactions to support early phase development and for demonstrations towards technical transfers to a GMP kilo-lab. In collaborations, the analyst will engage in reaction development by performing reaction characterization research to identify impurities and amounts and rates of formation to better understand competing mechanistic pathways. Understanding the stability of process streams and isolated materials will also be part of the analyst's responsibility. Basic Qualification + MS/PhD level analytical chemist with experience developing methods and analyzing reactions and materials to support pharmaceutical process development. Additional Preferences: + Expected to maintain a safe, clean, well-organized, and productive lab space. + Experience with the development and use of a variety of analytical methods: HPLC/UPLC, GC, MS, NMR, KF, TGA, DSC, XRD, ICP etc. Process analysis and quantification, tying up mass balance, and material characterization. + Familiarity with crystallization and physical/solid state characterization: experience with crystallization monitoring/analysis to understand kinetics and endpoints. Also expected to analyze for polymorphism and particle size and other solid-state characteristics in collaboration with partner analysts. + Proficiency with the purification of chemicals via chromatography is a plus. + Maintaining a well-organized and detailed lab notebook with accurate descriptions of method development and observations to enable the preparation of technical packages/technical transfers and accurate replication in receiving labs. + Participate in training, mentoring, and supporting analytical chemists and chemists in the development and use of analytical methods for pharmaceutical process development. + Analytical testing plans - Developing an analytical testing plan to ensure that all facets of a chemical process are understood and under control. This entails characterization of starting materials towards specification setting, establishing reaction end points, determining unit operation end points and optimal amounts of chemicals to use for reactions, work-ups/extractions, crystallizations, washes, etc. 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 $133,500 - $217,800 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

Quandary is a full-service environmental consulting firm based in Denver, Colorado. Founded in 2016 Quandary has quickly become a top choice for clients in the construction, oil & gas, renewable energy, electric utility, and government sectors. We provide environmental permitting, regulatory compliance, air quality, remediation, weed management, stormwater management, and other environmental services to clients throughout the country. This position will support various new and existing air quality permitting and compliance Oil and Gas projects like preparation of emission inventories, permit application development, regulatory review, compliance recordkeeping, greenhouse gas reporting, air monitoring, etc. Duties and Responsibilities: Perform air compliance and permitting tasks. Conduct air emissions calculations for permitting, emissions inventories, annual compliance reporting, and greenhouse gas reports. Conduct peer review of teammates' calculations and reports, providing constructive feedback. Prepare and submit air permit applications to state and federal agencies. Utilize emissions modeling software. Become proficient in state, federal, tribal, and local air compliance and permitting regulations and assist clients in implementing operational and reporting requirements. Periodic short-duration day trips to client field sites to conduct site inspections and support air monitoring programs may be required. At times, overnight client work may be required, but is not expected. Assist in preparation, deployment, and all sampling aspects of air monitoring activities. Demonstrate commitment to safety and environmental compliance in all job aspects. Provide guidance to clients for site design/operations to ensure compliance with regulations. Act as a liaison between clients and regulatory agencies. Analytical and problem-solving abilities to identify safety risks, analyze data, and develop effective solutions. Key Capabilities/Skills: Professional demeanor and experience writing technical reports. Have strong attention to detail and able to follow specific directions on tasks. Must be a team player, receptive to feedback and open to constructive criticism. Capable of managing projects, meeting budgets, and being the main point of communication for client contact. Ability to manage multiple priorities and work in a fast-paced and challenging environment. Proficiency with Microsoft excel, including use of pivot tables. Valid driver's license and proven safe driving record. Strong understanding of air quality compliance requirements in Colorado for oil and gas, COGCC and CDPHE. Experience with clean air act (NSPS OOOO, OOOOa, KKKK, JJJJ, KKK, VV, VVa, GG). Familiarity with oil and gas equipment, operational practices, field environment and technical and engineering terms related to these practices. Ability to read complex state and federal regulations to determine applicability to varying client facilities and scenarios. Monitor federal, state, and local air quality regulations and rulemakings. Participate in trade and professional associations to support the above responsibilities. Demonstrates initiative by appropriately taking charge of situations. Strong verbal skills and ability to lead meetings with staff on air quality permitting and compliance. Education and Experience: Bachelor's degree in engineering, environmental science, or related field required. 3-8+ years of experience in air quality permitting and compliance, environmental consulting, or a related field. Working Conditions/Physical Requirements: Sitting or standing for prolonged periods of time Ability to lift a minimum of 50 lbs. Inclement weather conditions may exist during fieldwork. Occasional travel including overnight stay. Expected Salary: $80,000-$110,000 DOE. Job Type: Full-time Exempt Schedule: Monday - Friday, 40 hours a week average, schedule dictated by client needs Work Location: Denver, CO: Reliably commute to Denver office daily. Application Deadline: Will remain open until the position is filled. Benefits: Health Insurance (Medical, vision, dental) FSA and HSA options Employee Assistance Program (EAP) Short-Term and Long-Term Disability Life Insurance Paid time off Paid Holidays 401(k) matching If you have these skills and an environmental background and are interested in working for a dynamic environmental services company, we look forward to hearing from you! Quandary Consultants is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Ibotta is seeking a Decision Scientist, Client Analytics to join our innovative team and contribute to our mission to Make Every Purchase Rewarding. Ibotta captures billions of purchases annually, with over ten thousand brands and across hundreds of retailers, presenting the right candidate with the opportunity to work with one of the most comprehensive and unique (purchasing) data sets in the world. As a Decision Scientist of Client Analytics, you will be responsible for providing actionable and data-driven recommendations to internal stakeholders. You'll have the opportunity to work alongside talented individuals and understand the business in-depth, support and challenge strategic options, and build state-of-the-art tools to drive value throughout our business. This position will work cross functionally with the sales team to provide data and insights to our clients based around shopper behaviors to enable better decision making across the organization. This position is located in Denver, Colorado as a hybrid position requiring 3 days in office (Tuesday, Wednesday, and Thursday). Candidates must live in the United States What you will be doing: * Analyze large datasets to extract actionable insights to inform business decisions and understand consumer behavior to support the decision-making process * Use SQL, Excel and BI tools with some opportunity to partner with data scientists and other members of the Ibotta analytics community on projects needing the use of Python, R and other advanced analytics tools * Formulate solutions addressing major business challenges and innovation opportunities * Develop a deep understanding of Ibotta's data ecosystem and analytics tools * Bring proactive insights into our key business metrics through curiosity, dedication, and ongoing investment in understanding our products * Contribute to creating best practices and efficient processes for the team * Initiate and drive collaboration with stakeholders and cross-functional teams to define project scope, responsibilities, and expectations * Build and maintain dashboards, reports, and other analytics deliverables * Embrace and uphold Ibotta's Core Values: Integrity, Boldness, Ownership, Teamwork, Transparency & A good idea can come from anywhere What we are looking for: * 3+ years of experience in an analytical function * Bachelor's degree in Analytics, Statistics, Economics or related field * Experience and proficiency working with: * Data analysis tools (e.g., SQL (Databricks), Python/R, Excel, Powerpoint, Git/GitHub etc. Python or R preferred but not required) * BI & other analytics tools (e.g., Looker, Tableau, Mode, Power BI, etc.) * Exposure to Data pipelines and ETL/ELT processes * Solid experience in the collection, analysis, and delivery of large, multi‐dimensional data sets and building visualizations that turn data into meaningful business insights * Experience identifying, validating, documenting, and UATing events-based data for business utility in the data lake to help answer strategic questions Here are some of the traits that we seek in great decision scientists: You… * are proactive, collaborative and driven to deliver in a dynamic, fast-paced environment * are comfortable continually asking questions of our data and business * translate measurement outcomes into technical specifications and ambiguous business questions into structured data problems * use solid business sense to tie analytical outputs to actionable recommendations * are an intellectually curious, conceptual thinker who uses creative problem-solving skills to go beyond the symptoms of a problem and diagnose root causes * analyze, visualize, communicate and automate complex learnings, distilling them into digestible form for a broad set of stakeholders * have solid interpersonal skills, collaborate across functional areas, manage stakeholder expectations, and support key initiatives from start to finish under guidance of your manager * demonstrate empathy for stakeholders, functional partners, clients and users About Ibotta ("I bought a...") Ibotta (NYSE: IBTA) is a leading performance marketing platform allowing brands to deliver digital promotions to over 200 million consumers through a network of publishers called the Ibotta Performance Network (IPN). The IPN allows marketers to influence what people buy, and where and how often they shop - all while paying only when their campaigns directly result in a sale. American shoppers have earned over $1.8 billion through the IPN since 2012. The largest tech IPO in history to come out of Colorado, Ibotta is headquartered in Denver, and is continually listed as a top place to work by The Denver Post and Inc. Magazine. To learn more about what our Tech teams are doing day to day, visit Building Ibotta on Medium.com. Additional Details: * This position is located in Denver, CO and includes competitive pay, flexible time off, benefits package (including medical, dental, vision), Lifestyle Spending Account, Employee Stock Purchase Program, and 401k match. Denver office perks include paid parking, bagel Thursdays, snacks and occasional meals. * Base compensation range: $83,000- $99,000. Equity is included in overall compensation package. This compensation range is specific to the United States labor market and may be adjusted based on actual experience. * Ibotta is an Equal Opportunity Employer. Ibotta's employment decisions are made without regard of race, color, religion, national origin, age, sex, marital status, ancestry, physical or mental disability, veteran status, gender identity, sexual orientation, or any other legally protected status. * Applicants must be currently authorized to work in the United States on a full-time basis. * Applicants are accepted until the position is filled. * For the security of our employees and the business, all employees are responsible for the secure handling of data in accordance with our security policies, identifying and reporting phishing attempts, as well as reporting security incidents to the proper channels. Recruiting Agency Notice Ibotta does not accept agency resumes and is not responsible for any fees related to unsolicited resumes. Please do not forward resumes to any Ibotta employees. #LI-Hybrid #BI-Hybrid

Be a part of a revolutionary change! At Philip Morris International (PMI), we've chosen to do something incredible. We're totally transforming our business and building our future on one clear purpose - to deliver a smoke-free future. With huge change, comes huge opportunity. So, if you join us, you'll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. Our success depends on people who are committed to our purpose and have an appetite for progress. We are hiring a quality Control Laboratory Analyst for our Aurora, CO factory! As a Quality Control Laboratory Analyst, you will apply validated methods and work instructions to perform routine analyses and technical activities, ensuring that all raw, semi-finished, and finished products are analyzed and monitored appropriately. You will also participate in method transfer and data evaluation reporting activities, ensure that instruments are calibrated for accuracy, precision, and reliability of the analysis, and participate in collaborative and proficiency testing. Your 'day to day': * Guarantee adherence to PMI and legal standards, policies, and environmental, health, safety, and sustainability guidelines. * Foster a proactive, safety-first culture using preventive and predictive approaches in line with our Integrated Operating System. * Plan and perform tests and analyses (physical, chemical, microbiological) on the quality of raw materials, tobacco, semi-finished, and finished products according to applicable procedures and analytical methods. * Ensure the integrity and timely reporting of analysis results in the laboratory management system for the execution of certificates of analysis. * Review and release testing results of other lab personnel. * Involve in method validation/transfer activities and the ISO 17025 accreditation process. * Participate in the creation and review of procedures, work instructions, and other quality documents as required. * Provide related support and training in accordance with the training management system. * Use, verify, and calibrate laboratory equipment as per PMI and ISO requirements in due time to ensure the accuracy of results. * Prepare and maintain logbooks according to QMS requirements. * Perform peer reviews for the data produced. * Perform tests and analyses to ensure the defined delivery KPIs. * Investigate out-of-specifications, resolve deviations, and contribute to defining appropriate corrective actions, leveraging problem-solving tools. * Provide timely and accurate information regarding products and testing activities. * Participate in interlaboratory collaborative and proficiency testing. * Participate in projects influencing product quality. * Ensure compliance with QMS requirements and follow standards for ISO 17025 accreditation. * Propose cost-efficiency initiatives and use resources responsibly to prevent instrument downtime. * Communicate all useful information to concerned colleagues and support teams to ensure the smooth flow of quality processes and meet quality and productivity goals. What we are looking for: * Bachelor's Degree with 5 years of laboratory experience or master's degree with 2 years of laboratory experience in Chemistry, Engineering, or a similar science field. * Bachelor's degree in science with 5+ years of quality and laboratory experience in tobacco, food, pharmaceutical, or a similar regulated industry. * Strong HPLC and GCMS knowledge and experience, including Agilent software and LabVantage LIMS System. * Advanced knowledge of quality tools, root cause analysis, analytical skills, and statistical tools. * Ability to transform data into information (reporting skills). * Ability to teach and share information with junior staff. * Knowledge of international standards (ISO 17025). Experience in FDA-regulated industries is a plus. What's 'nice to have': * Legally authorized to work in the U.S. Hourly Rate: $30-$33 / hour What we offer: We offer employees a competitive hourly salary. Employees (and their families) also have the option to enroll in our company's medical, dental, and vision plans. The company offers flexible spending accounts for health care and dependent care, as well as health savings accounts for those that choose to enroll in a high-deductible health plan (HDHP). Employees are auto-enrolled in our company's 401(k)/Deferred Profit Sharing (DPS) Plan, which provides for both an annual 5% employer matching contribution and an annual employer contribution. As a new hire, you will enjoy an allotment of paid vacation time, paid sick time, paid company holidays. We also provide our employees with paid parental leave for new parents, and short-term and long-term disability insurance, basic life insurance and accidental death & dismemberment (AD&D) insurance at no cost to the employee. Employees have the option to purchase supplemental life and AD&D coverage for themselves, spouse, and dependent children. PMI is an Equal Opportunity Employer. PMI is headquartered in Stamford, Conn., and its U.S. affiliates have more than 2,300 employees. PMI has been an entirely separate company from Altria and Philip Morris USA since 2008. PMI's affiliates first entered the U.S. market following the company's acquisition of Swedish Match in late 2022. Philip Morris International and its U.S. affiliates are working to deliver a smoke-free future. Since 2008, PMI has invested $12.5 billion globally to develop, scientifically substantiate and commercialize innovative smoke-free products for adults who would otherwise continue to smoke with the goal of transitioning legal-age consumers who smoke to better alternatives. In 2022, PMI acquired Swedish Match - a leader in oral nicotine delivery - creating a global smoke-free champion led by the IQOS and ZYN brands. The U.S. Food and Drug Administration has authorized versions of PMI's IQOS electronically heated tobacco devices and Swedish Match's General snus as Modified Risk Tobacco Products and renewal applications for these products are presently pending before the FDA. For more information, please visit ************** and *******************

The PhD Formulation Chemist plays a pivotal R&D role in developing the formulation and supporting integration of organic photoconductors by leveraging technical expertise, leading cross-functional collaboration, and driving innovation in material science to ensures that the photoconductors meet high-performance standards and are produced efficiently and reliably. Responsibilities and Duties: Technical Expertise: Possess broad knowledge of polymers, charge generation, charge transport, and nano metal oxides. Experience with nano dispersions, polymeric solutions, coating science and technology is preferred. Product Development: Lead the technical development of organic photoconductors to meet laser printer performance requirements. Ensure that photoconductors are optimized to meet stringent performance requirements, focusing on aspects like charge efficiency, durability, and print quality. Cross-Functional Collaboration: Collaborate with cross-functional teams, including supplies integration, product engineering, manufacturing, quality, and product support teams, to drive robust formulation, scale-up, reliable manufacturing, system integration and qualification of new products. Experimental Design and Analysis: Plan and execute designed experiments, utilize statistical software to analyze experimental results, identify relationships and trends, and make data-driven decisions. Develop actionable plans based on test outcomes to deliver photoconductors that meet product performance requirements. Communication: Communicate findings effectively through verbal updates and detailed written reports. Ensure that stakeholders are informed of progress, challenges, and achievements. Material Exploration: Identify and investigate new materials for photoconductor formulations. Work effectively with the material sourcing team on material supply risk mitigation. Lead technical interactions with raw material suppliers. Technical Support: Provide technical support to the manufacturing and quality teams. Assist in troubleshooting issues that arise during production, ensuring that products meet quality standards and performance specifications. Qualifications: PhD in Chemistry, Chemical Engineering, Material Science, or a related field. Extensive knowledge of and experience with polymers, charge generation, charge transport, and nano metal oxides. Strong analytical skills and proficiency with statistical design and analysis of experiments. Excellent communication and collaboration skills. Ability to lead cross-functional teams and manage multiple projects simultaneously. Salary Range: $90,000 - $189,000, based on relevant experience, training, and education. How to Apply ? Are you an innovator? Here is your chance to make your mark with a global technology leader. Apply now! We are proudly an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based on race, color, religion, gender, national origin, protected veteran status, disability status, sexual orientation, gender identity or expression. Global Privacy Notice Lexmark is committed to appropriately protecting and managing any personal information you share with us. Click here to view Lexmark's Privacy Notice.