Cosmetic Chemist jobs at Estée Lauder - 284 jobs

Quality Control Chemist II At Country Life, we inspire greatness through our wholistic approach of supplement and personal care products. Our team of experts, innovators and dreamers is dedicated to bringing the power of nature and the promise of science to people at every life stage. Join our Hauppauge, NY team and share our passion for natural health and pride in our company's commitment to excellence and quality! Position Summary: Testing pharmaceuticals, vitamins and herbal products using HPLC, ICP, FTIT, NIR, UV-VIS and wet chemistry per USP, AOAC, FCC, BP (British Pharmacopeia) and internal procedures. Properly disposes of waste chemicals based on OSHA requirements. Position Scope: Handles approximately 15 - 35 analytical tests per week Position Responsibility: Works with lab instruments, e.g. HPLC, AA, PDA, RI detection methods, ICP and ICP-MS to perform analytical tests. Also works with chemicals and reagent solvents during the day. Records the raw data and results from scientific test results. Reports any lab instruments malfunction to Lab Manager. Prepares and files all Quality Control documents, e.g. Certificate of Analysis (COA) Deviations, Out of Specification (OOS) reports. Reviews testing and notebooks to prepare bulk product release. Conducts daily calibration of balances and Ph meter. Calibrates an expiration date for all product labels based on shelf life expectancy. Disposes of waste chemicals appropriately. Checks raw materials and finished product potencies. Proper disposal of expired raw materials, in-process and finished goods (final batches). Coordinates such activities with Safety Manager. Prepares samples for shipment to outside testing laboratory. Assists in the inventory of supplies and upkeep of laboratory and laboratory machinery. Preparation of purchase orders, receipt of supplies, and interfacing with other departments to expedite these functions. Chemist II: in additional to the above Qualification and maintenance of primary and secondary standards of raw material and finished products. Maintains R&D raw material inventory, laboratory notebooks, equipment logs and maintenance schedules. Prepares specification for raw materials and finished products. Conducts in process testing of manufactured samples. Conducts minor repairs of lab instruments and other apparatus. Supports the preparation, manufacture, evaluation and documentation of new or modified R&D in-process and finished products associated with Country Life formulations, e.g., tablets, capsules and powders. Writes detailed scientific instructions and lab procedures. Senior Chemist: in additional to the above Develops analytical methods and validations. Analyses, records and releases raw materials and conducts maintenance of raw material specifications. Maintains lab chemicals for consistency to standards (e.g. USP, GLP and OSHA). Performs analytical troubleshooting and updates SOPs, log books and lab solutions preparation book. Provides guidance and training for Chemists I and II. General Clean working space, desk, equipment/glassware and whole lab. Must wear Personal Protective Equipment (PPE) at all times as stipulated by SOPs. e.g. respirator, ear plugs, hair net, beard cover and lab coat. Lifting up to 20 lbs. may be required. Position requires considerable standing on lab floor. Maintains professional and technical knowledge by attending educational symposia; reviewing professional publications; establishing personal networks; participating in professional societies, etc. Satisfactory completion of appropriate corporate training as related to the position and/or department. Assures compliance by following Food and Drug Administration's Good Manufacturing Practices (FDA cGMPs / GLPs) as well as other regulatory standards as required by the department. Contributes to overall achievement by accomplishing related tasks and demonstrating characteristics that exemplify team building and support. The above is not intended to be an all-inclusive list of responsibilities. Other activities may be assigned as required by management. QUALIFICATIONS Experience and Skills: Chemist I will have one year Pharmaceutical laboratory or related experience as well as good mechanical aptitude. Training on specific laboratory equipment and instruments is preferred and may be provided if no work experience outside of classroom laboratory Chemist II will have three years of Pharmaceutical lab experience and good familiarity with HPLC, ICP and ICP-MS as well as good mechanical aptitude. Senior Chemist will have five years Pharmaceutical lab experience and strong experience with HPLC, ICP and ICP-MS as well as good mechanical aptitude. Good organizational skills. Good interpersonal skills. Excellent knowledge of PC software, MS Office, Word, Excel. Good written and verbal communication skills. Excellent Chemistry background as well as practical application of the technical knowledge. Excellent understanding and attitude towards cGMP and GLP, which will increase with job level. Education and Certifications: Undergraduate degree in Chemistry required for Chemist I and Chemist II positions. Masters of Chemistry, or equivalent, is preferred for Senior

Join Agilent Technologies and contribute to the advancement of liquid chromatography products at our Newport manufacturing facility. As part of a high-impact team within our growing Consumables and Supplies Division, you'll play a key role in driving innovation, improving product quality, and enhancing customer satisfaction. This is a dynamic opportunity to apply your expertise in analytical chemistry while collaborating across disciplines in a Lean and Six Sigma-driven environment. Key Responsibilities Serve as a technical expert to investigate and resolve customer issues related to LC column products. Analyze customer methods to generate insights and communicate product impact. Provide feedback to engineering and chemistry teams to reduce product variability. Develop and optimize HPLC testing methods to support product and process improvements. Apply experimental design to deepen understanding of process chemistries. Collaborate on cross-functional projects, including capital and continuous improvement initiatives. Support new product introductions and represent manufacturing in cross-team efforts. Contribute to quality testing of silica-based packing materials for HPLC columns. Lead or participate in Lean, Six Sigma, and safety improvement initiatives. Qualifications Bachelor's or Master's degree in Chemistry or Chemical Engineering. 4+ years of hands-on experience with HPLC. Strong analytical and problem-solving skills. Effective written and verbal communication abilities. Demonstrated leadership and strategic thinking in technical environments. Proficiency in digital tools and data analysis. Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least September 29, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $97,920.00 - $153,000.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: OccasionalShift: DayDuration: No End DateJob Function: Manufacturing

About Debut Debut is the unconventional innovation lab spearheading the next generation of big business. Only Debut has a scalable, integrated, climate-positive creation model powered by biotechnology that puts human wellbeing at the center of everything we do-setting the new standard for profitable business and a new pace for an ever-changing world. Our hybrid biotechnology approaches unlock latent markets, providing access to sustainably produced, natural ingredients with health benefits that cannot be obtained through other methods. We are committed to traversing the entire process, from ingredient discovery to the scaling of these products, for consumer markets. If you are passionate, enjoy fast-paced innovation and collaborative teams, then Debut is for you. Formulation Chemist Summary As a member of the Innovation team, you will work as a Formulation Chemist to support the development of skincare and color cosmetic products. This position is for an individual who enjoys working at the bench in a fast-paced environment looking to develop innovative formulas with novel raw materials. The successful candidate will have experience in skincare and color cosmetics with a working knowledge of raw materials and processing techniques for each of these categories. Essential Functions Designing and conducting experiments to develop new products or improve existing products Creating prototypes for further research, testing and application Assessing rheology, viscosity, stability, and compatibility of prototype formulas Maintaining awareness of relevant regulatory and safety requirements Supporting the scale-up of product to manufacturing scale Providing technical support to internal/ external teams Ability to work at the bench in a fast-paced environment Education and Experience BA or BS in chemistry, chemical engineering, biochemistry, or related field At least 3 years of previous skincare formulation experience Knowledge of color cosmetics and ability to color match is a plus Experience working on product development briefs and communicating project milestones with customers Experience with technology transfer from bench scale to full production Understanding of testing requirements necessary for product launch Essential Physical Characteristics The physical characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis. Continuous upward and downward flexion of the neck. Frequent: sitting, repetitive use of hands to operate computers, printers and copiers. Frequently uses hands to feel objects or control tools (e.g. pipetting). Laboratory operations require dexterity and care to perform studies as required. Occasional: walking, standing, climbing stairs, bending and twisting of neck, bending and twisting of waist, squatting, simple grasping, reaching above and below shoulder level, and occasional lifting and carrying of files or material weighing up to 50 pounds. Must be willing to work with biohazardous agents (up to BSL2) and chemicals. The R&D laboratory will result in exposure to hot and cold temperatures, noise, fumes, limited dust, and oily coolants. The performance of this position will present exposure to an industrial environment and requires support and compliance with the published Company PPE policy including but not limited to the use of personal protective equipment such as safety glasses with side shields, appropriate attire, safety shoes, hard hat, hearing protection, etc. Condition of Employment As part of Debut's pre-employment process, prospective candidates will undergo a background check prior to beginning employment. Additional types of background investigations may be conducted based on the job-related activities of the position. Debut is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. Salary: $90,000 - $120,000

About Debut Debut is the unconventional innovation lab spearheading the next generation of big business. Only Debut has a scalable, integrated, climate-positive creation model powered by biotechnology that puts human wellbeing at the center of everything we do-setting the new standard for profitable business and a new pace for an ever-changing world. Our hybrid biotechnology approaches unlock latent markets, providing access to sustainably produced, natural ingredients with health benefits that cannot be obtained through other methods. We are committed to traversing the entire process, from ingredient discovery to the scaling of these products, for consumer markets. If you are passionate, enjoy fast-paced innovation and collaborative teams, then Debut is for you. Formulation Chemist Summary As a member of the Innovation team, you will work as a Formulation Chemist to support the development of skincare and color cosmetic products. This position is for an individual who enjoys working at the bench in a fast-paced environment looking to develop innovative formulas with novel raw materials. The successful candidate will have experience in skincare and color cosmetics with a working knowledge of raw materials and processing techniques for each of these categories. Essential Functions * Designing and conducting experiments to develop new products or improve existing products * Creating prototypes for further research, testing and application * Assessing rheology, viscosity, stability, and compatibility of prototype formulas * Maintaining awareness of relevant regulatory and safety requirements * Supporting the scale-up of product to manufacturing scale * Providing technical support to internal/ external teams * Ability to work at the bench in a fast-paced environment Education and Experience * BA or BS in chemistry, chemical engineering, biochemistry, or related field * At least 3 years of previous skincare formulation experience * Knowledge of color cosmetics and ability to color match is a plus * Experience working on product development briefs and communicating project milestones with customers * Experience with technology transfer from bench scale to full production * Understanding of testing requirements necessary for product launch Essential Physical Characteristics The physical characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis. * Continuous upward and downward flexion of the neck. * Frequent: sitting, repetitive use of hands to operate computers, printers and copiers. * Frequently uses hands to feel objects or control tools (e.g. pipetting). Laboratory operations require dexterity and care to perform studies as required. * Occasional: walking, standing, climbing stairs, bending and twisting of neck, bending and twisting of waist, squatting, simple grasping, reaching above and below shoulder level, and occasional lifting and carrying of files or material weighing up to 50 pounds. * Must be willing to work with biohazardous agents (up to BSL2) and chemicals. * The R&D laboratory will result in exposure to hot and cold temperatures, noise, fumes, limited dust, and oily coolants. * The performance of this position will present exposure to an industrial environment and requires support and compliance with the published Company PPE policy including but not limited to the use of personal protective equipment such as safety glasses with side shields, appropriate attire, safety shoes, hard hat, hearing protection, etc. Condition of Employment As part of Debut's pre-employment process, prospective candidates will undergo a background check prior to beginning employment. Additional types of background investigations may be conducted based on the job-related activities of the position. Debut is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. Salary: $90,000 - $120,000

FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa, AZ facility for an Associate Research Chemist! With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. The Role The Associate Research Chemist will be responsible for design, develop and commercialization of new semiconductor etchants, post etch selective cleaners and strippers for advanced technology. Company Overview FUJIFILM Electronic Materials, U.S.A. fuels innovation in the semiconductor industry-where chemistry meets technology. Our advanced materials and formulations enable manufacturers to build the microchips that power Artificial Intelligence, computers, electric vehicles, smartphones, and more. We're a global business-to-business supplier of chemical formulations and advanced materials used for manufacturing and packaging semiconductors. Our chemical formulations allow top manufacturers to produce microchips that both power and connect our digital world. Think you've got what it takes to build a more connected world? Then connect with us today and challenge the boundaries of what's possible-for the world and your future. We have six U.S. manufacturing and Research & Development facilities, located in: Mesa, Arizona; Castroville, California; Hollister, California; Carrollton, Texas; and North Kingstown, Rhode Island-each offering unique local experiences, from vibrant cultural scenes to historic charm. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: *************************************************** Job Description Key responsibilities for this role include: Responsible for applied research & development and commercialization of new post etch cleaners and selective etchants for advanced IC technologies. Responsibilities include designing, lab testing and managing new chemical products under rigorous business and customer timelines. Specific activities include: Investigate and develop new chemical formulations for cleaning integrated circuit wafers with awareness of the status of the intellectual property field. Perform wet bench formulation and testing of new chemicals to meet customer requirements. Manage existing product testing and qualification using customer wafers. Support thin film surface analysis using tools including Ellipsometer, 4-Point probe, XRR, XPS, TOF-SIMS, SEM. Assist with IP searches and initial patent drafts. Assist in pilot line builds of successful beaker formulations. Generating and communicating product data and technical reports internally and to customers Write and present internal presentation updating technical and business groups on project status. REQUIREMENTS PhD in Chemistry with 1 to 5 years of experience in formulation. Prior industrial research experience in product development in semiconductor technology is highly prefered. Experience in developing and applying inorganic or organic solution chemistry to meeting customer requirements. Must be comfortable working safely with hazardous chemicals. Understanding Si wafer device processing in wet processing tool operation and process implementation. Experience with thin film surface analysis tools such as Ellipsometer, 4-Point probe, XRR, XPS, TOF_SIMS, SEM Must have a strong comprehension of surface cleaning methods and chemicals. Must be proficient in design of experiments, technical writing, literature search processes and methods and Intellectual property processes and methods. Must be a team player and collaborator. Must be able to communicate and work effectively with peers and customers. Organizational skills and prior project management experience desired. This is a safety-sensitive position that requires candidates to successfully pass a post-offer drug screening prior to employment. One of the essential job functions is the ability to work in a constant state of alertness and in a safe manner. ADDITIONAL REQUIREMENTS We value a professional, adaptable, and collaborative work environment. The following competencies are essential for success in any role and reflect our commitment to effective teamwork, problem solving, and workplace communication. Resilience -Ability to adapt to workplace challenges, maintain professionalism, and manage responsibilities effectively. Communication -Capacity to clearly and professionally exchange ideas, interact respectfully with colleagues and customers, and foster positive workplace relationships. Reasoning & Decision Making -Ability to analyze information, follow verbal and written instructions, and make logical, sound decisions. Comprehension -Capability to understand and complete tasks as assigned and solve problems effectively. Organizational Skills - Competence in managing multiple priorities, maintaining accuracy, and staying focused despite potential workplace distractions. To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (********************************).

Certified Group is a leading North American food testing and analytical services company with a mission to deliver food quality, safety, security, and sustainability. We are putting together a team of our next-generation R&D Center of Excellence, designed to transform Certified into a technical partner for high-growth, innovation-driven clients. This role is pivotal to our vision-unlocking new revenue streams, accelerating method development, and positioning Certified as a problem-solving collaborator in the food and nutraceutical industries. KEY RESPONSIBILITIES * Lead method development and validation for complex analytical targets (e.g., pesticides, PFAS, veterinary residues, vitamins, allergens, preservatives) in diverse food matrices. * Design and execute studies using LC-MS/MS, GC-MS/MS, ICP-MS, automated sample preparation platforms; and AI-powered process optimization * Act as the technical bridge between operations, R&D, and client innovation teams-consulting on custom analytical challenges. * Develop and implement rapid, high-ROI methods aligned with Certified Group's strategic focus (e.g., plant-based food, pet foods, dairy, clean-label products, sustainability analytics). * Contribute to regulatory compliance (FDA, USDA, ISO 17025) through SOP authorship, method transfer documentation, and validation reports. * Collaborate cross-functionally with QA, marketing, and business development to define service offerings. * Support the incubation and transfer of new methods to operational labs (Aurora, Melville, San Antonio, etc.) with hands-on training and handover protocols. * Evaluate and pilot new technologies (e.g., microwave extraction, CEM/NMR, AI-powered data tools). QUALIFICATIONS Required: * Ph.D. in Analytical Chemistry, Food Chemistry, or related discipline * 10+ years of experience in R&D or applied analytical chemistry (food, pharma, or biotech) * Deep expertise in LC-MS/MS and GC-MS/MS method development and troubleshooting * Proven experience with regulatory methods (FDA, USDA, AOAC, ISO) and quality systems (GLP/GMP/GDP) * Demonstrated ability to work across diverse matrices (fats/oils, proteins, supplements, plant-based foods) * Strong track record of scientific publications, presentations, or patents * Ability to lead cross-functional R&D projects with internal and external stakeholders Preferred: * Experience with automated sample prep platforms (SPE, QuEChERS, MW digestion, CEM, ANKOM, etc.) * Familiarity with IRR, ROI, EBITDA concepts and how analytical methods impact business KPIs * Ability to mentor junior scientists and lead training during method transfer Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off * Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Monday through Friday, 9:00 AM to 5:30 PM, evenings and weekends as needed.

Job Description Certified Group is a leading North American food testing and analytical services company with a mission to deliver food quality, safety, security, and sustainability. We are putting together a team of our next-generation R&D Center of Excellence, designed to transform Certified into a technical partner for high-growth, innovation-driven clients. This role is pivotal to our vision-unlocking new revenue streams, accelerating method development, and positioning Certified as a problem-solving collaborator in the food and nutraceutical industries. KEY RESPONSIBILITIES Lead method development and validation for complex analytical targets (e.g., pesticides, PFAS, veterinary residues, vitamins, allergens, preservatives) in diverse food matrices. Design and execute studies using LC-MS/MS, GC-MS/MS, ICP-MS, automated sample preparation platforms; and AI-powered process optimization Act as the technical bridge between operations, R&D, and client innovation teams-consulting on custom analytical challenges. Develop and implement rapid, high-ROI methods aligned with Certified Group's strategic focus (e.g., plant-based food, pet foods, dairy, clean-label products, sustainability analytics). Contribute to regulatory compliance (FDA, USDA, ISO 17025) through SOP authorship, method transfer documentation, and validation reports. Collaborate cross-functionally with QA, marketing, and business development to define service offerings. Support the incubation and transfer of new methods to operational labs (Aurora, Melville, San Antonio, etc.) with hands-on training and handover protocols. Evaluate and pilot new technologies (e.g., microwave extraction, CEM/NMR, AI-powered data tools). QUALIFICATIONS Required: Ph.D. in Analytical Chemistry, Food Chemistry, or related discipline 10+ years of experience in R&D or applied analytical chemistry (food, pharma, or biotech) Deep expertise in LC-MS/MS and GC-MS/MS method development and troubleshooting Proven experience with regulatory methods (FDA, USDA, AOAC, ISO) and quality systems (GLP/GMP/GDP) Demonstrated ability to work across diverse matrices (fats/oils, proteins, supplements, plant-based foods) Strong track record of scientific publications, presentations, or patents Ability to lead cross-functional R&D projects with internal and external stakeholders Preferred: Experience with automated sample prep platforms (SPE, QuEChERS, MW digestion, CEM, ANKOM, etc.) Familiarity with IRR, ROI, EBITDA concepts and how analytical methods impact business KPIs Ability to mentor junior scientists and lead training during method transfer Benefits: Progressive 401k Retirement Savings Plan Employer Paid Short- Term and Long-Term Disability, and Life Insurance Group Medical Tuition Reimbursement Flexible Spending Accounts Dental Paid Holidays and Time Off Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Monday through Friday, 9:00 AM to 5:30 PM, evenings and weekends as needed.

Conduct experimental studies to investigate nonconforming products, support new product development as well as product / process improvements. Ability to design experimental protocols and work independently is essential. ESSENTIAL DUTIES AND RESPONSIBILITIES • Conduct product root cause investigations for returned or nonconforming products or materials. • Design experimental protocols (reviewed and guided by supervisor) and conduct experimental studies to meet project goals • Able to carry out a series of experiments independently for a designed study • Maintain detailed laboratory notebook • Write detailed reports of experimental studies and draw conclusions from results • Interact with other functional departments (QC, QA, RA, Production, Supply Chain, etc.) as needed to get materials/processes required for product investigations or development. • Communicate experimental results and conclusions to supervisor and peers • Assist in general laboratory maintenance • Complete calculations and prepare solutions according to cGLP. Special skill such as phlebotomy is desirable, but not required. SUPERVISORY RESPONSIBILITIES This position has no supervisory responsibilities. EDUCATION and/or EXPERIENCE Master degree (M.S., M. Eng.) in Chemistry, Biochemistry or related technical discipline; Bachelor degree (B.S or B.A.) in Chemistry, Biochemistry or related technical discipline; Additional Experience listed below desired: • Work experience in a medical diagnostic company. • Work experience in product support, including investigations, and development. • Hands on experience in a clinical laboratory or with clinical diagnostic device. • Previous experience in verification and validation testing. • Working knowledge of MS Excel and Word. KNOWLEDGE AND SKILLS 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. The employee should have in-depth knowledge and experience working with common laboratory techniques and equipment. It is also desirable that employee has a full understanding of technologies employed for point-of-care testing, particularly blood glucose monitoring. Ability to apply advanced mathematical concepts such as quadratic equations, permutations, analysis of variance, correlation technique, sampling theory and factor analysis to solve practical problems is essential. Able to deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form is also required. Proficiency in using PC and common software including MS WORD, EXCEL, POWERPOINT and OUTLOOK is required. Additional KSA (knowledge, Skills and Ability) are as follows: • Analytical reasoning and data analysis skills • Root cause investigations • Ability to trouble-shoot formulations and instrumentation problems • Whole blood testing • Solution Preparation COMMUNICATION SKILLS Ability to read and comprehend scientific journals, technical procedures and governmental regulations is required. Ability to maintain detailed laboratory notebooks and write detailed reports with conclusions is also mandatory. The employee is also expected to communicate experimental results and conclusions to supervisor, peers and project teams orally or by writing. MATHEMATICAL SKILLS Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. REASONING ABILITY Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. CERTIFICATES, LICENSES, REGISTRATIONS N/A PHYSICAL DEMANDS Travel requirements: ≤ 10% The physical demands described 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 person in this position needs to move about inside the office and laboratory areas; must be able to remain in a stationary position for prolonged periods of time; frequently operate a computer and laboratory related equipment. Person in this position frequently communicates with others and must be able to exchange accurate information. Individual is required to have close visual acuity to perform activities such as documenting experimental results; preparing and analyzing data and figures; viewing a computer terminal; operating equipment and visual inspection of small parts. Individual must be able to frequently move objects (up to 10 lbs.) from one level to another and occasionally move objects (up to 25 lbs.) from one level to another. WORK ENVIRONMENT The work environment described is representative of that which an employee may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee in this position is expected to work regularly in a laboratory environment. While performing the duties of this job, the employee is required to work with biological samples which may expose him/her to bloodborne pathogens. The employee may be exposed to moving mechanical parts, fumes or airborne particles, and toxic or caustic chemicals. Appropriate use of Personal Protective Equipment (PPE) is required. Employee should fully understand applicable safety regulations and GLP/GMP/GCP guidelines and apply them appropriately. Employee may be expected to train other employees in relevant safety / compliance requirements and laboratory procedures. Trividia Health uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ******************** EQUAL OPPORTUNITY EMPLOYER: Trividia Health, Inc. is an Equal Opportunity, Affirmative Action, E-Verify employer. Employment decisions for all applicants and employees will be made without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, age, national origin, marital status, veteran status, disability, or other characteristics protected under local, state or federal law.

Conduct experimental studies to investigate nonconforming products, support new product development as well as product / process improvements. Ability to design experimental protocols and work independently is essential. ESSENTIAL DUTIES AND RESPONSIBILITIES • Conduct product root cause investigations for returned or nonconforming products or materials. • Design experimental protocols (reviewed and guided by supervisor) and conduct experimental studies to meet project goals • Able to carry out a series of experiments independently for a designed study • Maintain detailed laboratory notebook • Write detailed reports of experimental studies and draw conclusions from results • Interact with other functional departments (QC, QA, RA, Production, Supply Chain, etc.) as needed to get materials/processes required for product investigations or development. • Communicate experimental results and conclusions to supervisor and peers • Assist in general laboratory maintenance • Complete calculations and prepare solutions according to cGLP. Special skill such as phlebotomy is desirable, but not required. SUPERVISORY RESPONSIBILITIES This position has no supervisory responsibilities. EDUCATION and/or EXPERIENCE Master degree (M.S., M. Eng.) in Chemistry, Biochemistry or related technical discipline; Bachelor degree (B.S or B.A.) in Chemistry, Biochemistry or related technical discipline; Additional Experience listed below desired: • Work experience in a medical diagnostic company. • Work experience in product support, including investigations, and development. • Hands on experience in a clinical laboratory or with clinical diagnostic device. • Previous experience in verification and validation testing. • Working knowledge of MS Excel and Word. KNOWLEDGE AND SKILLS 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. The employee should have in-depth knowledge and experience working with common laboratory techniques and equipment. It is also desirable that employee has a full understanding of technologies employed for point-of-care testing, particularly blood glucose monitoring. Ability to apply advanced mathematical concepts such as quadratic equations, permutations, analysis of variance, correlation technique, sampling theory and factor analysis to solve practical problems is essential. Able to deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form is also required. Proficiency in using PC and common software including MS WORD, EXCEL, POWERPOINT and OUTLOOK is required. Additional KSA (knowledge, Skills and Ability) are as follows: • Analytical reasoning and data analysis skills • Root cause investigations • Ability to trouble-shoot formulations and instrumentation problems • Whole blood testing • Solution Preparation COMMUNICATION SKILLS Ability to read and comprehend scientific journals, technical procedures and governmental regulations is required. Ability to maintain detailed laboratory notebooks and write detailed reports with conclusions is also mandatory. The employee is also expected to communicate experimental results and conclusions to supervisor, peers and project teams orally or by writing. MATHEMATICAL SKILLS Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. REASONING ABILITY Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. CERTIFICATES, LICENSES, REGISTRATIONS N/A PHYSICAL DEMANDS Travel requirements: ≤ 10% The physical demands described 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 person in this position needs to move about inside the office and laboratory areas; must be able to remain in a stationary position for prolonged periods of time; frequently operate a computer and laboratory related equipment. Person in this position frequently communicates with others and must be able to exchange accurate information. Individual is required to have close visual acuity to perform activities such as documenting experimental results; preparing and analyzing data and figures; viewing a computer terminal; operating equipment and visual inspection of small parts. Individual must be able to frequently move objects (up to 10 lbs.) from one level to another and occasionally move objects (up to 25 lbs.) from one level to another. WORK ENVIRONMENT The work environment described is representative of that which an employee may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee in this position is expected to work regularly in a laboratory environment. While performing the duties of this job, the employee is required to work with biological samples which may expose him/her to bloodborne pathogens. The employee may be exposed to moving mechanical parts, fumes or airborne particles, and toxic or caustic chemicals. Appropriate use of Personal Protective Equipment (PPE) is required. Employee should fully understand applicable safety regulations and GLP/GMP/GCP guidelines and apply them appropriately. Employee may be expected to train other employees in relevant safety / compliance requirements and laboratory procedures. Trividia Health uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ******************** EQUAL OPPORTUNITY EMPLOYER: Trividia Health, Inc. is an Equal Opportunity, Affirmative Action, E-Verify employer. Employment decisions for all applicants and employees will be made without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, age, national origin, marital status, veteran status, disability, or other characteristics protected under local, state or federal law.

SummaryYou will be responsible for in-process and release testing of Injectable pharmaceutical finished products produced on site. The chemist participates in the development of new procedures and is involved in validation studies as they pertain to analytical testing. Work is technical and specialized, requiring accuracy and attention to detail. Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world.Job DescriptionKey responsibilities/essential functions: Performs required analytical testing on in-process and final products. Testing using HPLC, FTIR, ICP-OES, UV/VIS, Liquid Scintillation, and Gamma Spectrometer. Participates in the performance of investigations of OOS results. Tracking and trending of analytical data. Participates in validation projects requiring analytical support. Contributes to process improvement through Lean and 5S. Assists in the stocking and supplying of the QC lab. Performs visual inspection of finished product. Quality Specific Goals: Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure the product conforms to its specification and out of specification items are properly handled. Basic knowledge and understanding of Stop Orders, Concessions, CAPA, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, Part 11 compliance as associated with this job type/position Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position Complete all planned Quality & Compliance training within the defined deadlines Identify and report any quality or compliance concerns and take immediate corrective action as required Required Qualifications: Bachelor's degree in chemistry (preferred) or related science field. Proficient with software applications applicable to the job. Must be available for nights and weekends as needed. Must have the ability to distinguish color. Ability to lift 25lbs Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening. Preferred Qualifications: Waters Empower Experience or similar software. Equipment experience with HPLC, ICP, UV/Vis, FT-IR. Experience working with radioactive material including the use of gamma spectrometers, Ion Chambers and liquid scintillation analyzers. Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment Background in Math or Chemistry We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support. We will not sponsor individuals for employment visas, now or in the future, for this job opening. For U.S. based positions only, the pay range for this position is $52,400.00-$78,600.00 Annual. It is not typical for an individual to be hired at or near the top of the pay range and compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate may be influenced by a variety of factors including skills, qualifications, experience and location. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). GE HealthCare offers a competitive benefits package, including not but limited to medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement.Additional Information GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees. Relocation Assistance Provided: No

You will be responsible for in-process and release testing of Injectable pharmaceutical finished products produced on site. The chemist participates in the development of new procedures and is involved in validation studies as they pertain to analytical testing. Work is technical and specialized, requiring accuracy and attention to detail. Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world. **Job Description** **Key responsibilities/essential functions:** + Performs required analytical testing on in-process and final products. + Testing using HPLC, FTIR, ICP-OES, UV/VIS, Liquid Scintillation, and Gamma Spectrometer. + Participates in the performance of investigations of OOS results. + Tracking and trending of analytical data. + Participates in validation projects requiring analytical support. + Contributes to process improvement through Lean and 5S. + Assists in the stocking and supplying of the QC lab. + Performs visual inspection of finished product. **Quality Specific Goals:** + Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure the product conforms to its specification and out of specification items are properly handled. + Basic knowledge and understanding of Stop Orders, Concessions, CAPA, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, Part 11 compliance as associated with this job type/position + Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position + Complete all planned Quality & Compliance training within the defined deadlines + Identify and report any quality or compliance concerns and take immediate corrective action as required **Required Qualifications:** + Bachelor's degree in chemistry (preferred) or related science field. + Proficient with software applications applicable to the job. + Must be available for nights and weekends as needed. + Must have the ability to distinguish color. + Ability to lift 25lbs + Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening. **Preferred Qualifications:** + Waters Empower Experience or similar software. + Equipment experience with HPLC, ICP, UV/Vis, FT-IR. + Experience working with radioactive material including the use of gamma spectrometers, Ion Chambers and liquid scintillation analyzers. + Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment Background in Math or Chemistry We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support. We will not sponsor individuals for employment visas, now or in the future, for this job opening. For U.S. based positions only, the pay range for this position is $52,400.00-$78,600.00 Annual. It is not typical for an individual to be hired at or near the top of the pay range and compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate may be influenced by a variety of factors including skills, qualifications, experience and location. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). GE HealthCare offers a competitive benefits package, including not but limited to medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement. **Additional Information** GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer (****************************************************************************************** . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees. **Relocation Assistance Provided:** No

Job Description We are seeking an analytical chemist with broad experience in analytical chemisty including expertise in spectroscopy, solid-state characterization techniques, chromatography and mass spectrometry. This role will focus on supporting material characterization of energetic and related materials, and other novel materials of interest. Essential Duties and Reponsibilities: Develop and apply spectroscopy methods (e.g. Raman, FTIR, UV-Vis, fluorescence) for characterization of energetic materials and novel compounds. Develop and apply chromatographic and mass spectrometry methods (e.g. GC-MS, LC-MS, HRMS) for characterization of energetic materials and novel compounds. Perform thermal and crystallographic analyses (e.g. DSC, TGA) to evaluate material stability, polymorphism, and structure-property relationships. Collaborate with synthesis teams to identify and quantify trace impurities arising from benchtop chemical reaction experiments. Develop and validate analytical methods to detect unknown and known impurities at trace levels. Integrate spectroscopy data with chromatographic and mass spectrometric results for comprehensive material profiling. Contribute to expanding organizational capability into broader materials science (e.g., polymers, co-crystals, composites). Perform routine maintenance and troubleshooting for a variety of analytical instrumentation. Maintain rigorous safety practices appropriate for handling energetic and hazardous materials. Required Knowledge, Skills & Abilities: Demonstrated expertise in spectroscopy techniques (Raman, FTIR, UV-Vis). Demonstrated expertise in chromatographic and mass spectrometry techniques (GC-MS, LC-MS, HRMS). Experience with thermal analysis and crystallographic methods (emphasis on DSC/TGA). Familiarity with energetic materials, explosives, or hazardous chemical handling is highly desirable. Strong collaborative skills; ability to communicate across technical teams. Track record of method development and problem-solving in analytical chemistry. Advanced skills in maintenance of analytical chemistry equipment including spectroscopy and mass spectrometry instruments is desired. Education/Experience: Ph.D. in Chemistry, Materials Science, or related field; or MS in Chemistry, Materials Science, or related field with 2+ years relevant experience. BS in Chemistry, Materials Science, or related field with 5+ years relevant experience. Certificates & Licenses: None required Clearance: This position requires that the candidate be willing and able to complete a successful background screening for a security clearance. Candidates with an active security clearance will receive preference. Supervisory Responsibilities: None required. Working Conditions/Equipment: This is a full-time, fully on-site position. This position primarily operates during standard business hours, with occasional needs for extended workdays or weekend work to meet project timelines. A significant portion of this role (approximately 75%) involves hands-on laboratory work. You should be comfortable spending extended periods of time conducting experiments and working at a computer. The role may also require occasional domestic travel for conferences, trade shows, or research-related meetings. The ability to lift and carry light loads (under 25 lbs) without assistance is necessary. Powered by ExactHire:186047

The Quality Control Chemist is responsible for preparing and verifying proper quantity of reference standards, calibrator, control material, and reagents under supervision. He or she will also track and replenish appropriate quality control and/or reagent materials to laboratory departments. He or she reviews and verifies proper calibration, maintenance, and cleanliness of all laboratory small equipment as necessary. Essential Duties & Responsibilities: Ensure proper documentation, use, and disposal of: Reference standards Calibrators Controls Reagents Blind Quality Control material Prepare and document the quality and assist in the verification of: Reagents Calibrators Quality Control materials Perform calibration, maintenance, and ensure cleanliness of: Pipettes Thermometers/Temperature Sensors Balances Timers Centrifuges Glassware And other small laboratory equipment as appropriate Participate in method validation and enhancement through preparation of QC standards Comply with all team and laboratory safety and quality procedures and requirements May perform hazardous waste activities such as handling, disposal, moving waste drums/containers, and signing hazardous waste manifests; initial and annual RCRA training is required to perform hazardous waste management tasks Education & Experience: Bachelor's degree in Chemistry or related field (with a minimum of 16 hours of chemistry and/or biological sciences coursework including at least 8 hours of general chemistry and/or upper level chemistry) required One (1) year of laboratory experience preferred Schedule: Monday, Tuesday, Wednesday, and Saturday - 8:00 am to 6:30 pm

You will be responsible for in-process and release testing of Injectable pharmaceutical finished products produced on site. The chemist participates in the development of new procedures and is involved in validation studies as they pertain to analytical testing. Work is technical and specialized, requiring accuracy and attention to detail. Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world. Job Description Key responsibilities/essential functions: * Performs required analytical testing on in-process and final products. * Testing using HPLC, FTIR, ICP-OES, UV/VIS, Liquid Scintillation, and Gamma Spectrometer. * Participates in the performance of investigations of OOS results. * Tracking and trending of analytical data. * Participates in validation projects requiring analytical support. * Contributes to process improvement through Lean and 5S. * Assists in the stocking and supplying of the QC lab. * Performs visual inspection of finished product. Quality Specific Goals: * Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure the product conforms to its specification and out of specification items are properly handled. * Basic knowledge and understanding of Stop Orders, Concessions, CAPA, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, Part 11 compliance as associated with this job type/position * Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position * Complete all planned Quality & Compliance training within the defined deadlines * Identify and report any quality or compliance concerns and take immediate corrective action as required Required Qualifications: * Bachelor's degree in chemistry (preferred) or related science field. * Proficient with software applications applicable to the job. * Must be available for nights and weekends as needed. * Must have the ability to distinguish color. * Ability to lift 25lbs * Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening. Preferred Qualifications: * Waters Empower Experience or similar software. * Equipment experience with HPLC, ICP, UV/Vis, FT-IR. * Experience working with radioactive material including the use of gamma spectrometers, Ion Chambers and liquid scintillation analyzers. * Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment Background in Math or Chemistry We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support. We will not sponsor individuals for employment visas, now or in the future, for this job opening. For U.S. based positions only, the pay range for this position is $52,400.00-$78,600.00 Annual. It is not typical for an individual to be hired at or near the top of the pay range and compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate may be influenced by a variety of factors including skills, qualifications, experience and location. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). GE HealthCare offers a competitive benefits package, including not but limited to medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement. Additional Information GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees. Relocation Assistance Provided: No

The purpose of this position is to provide analytical chemistry subject matter expertise to one or more chemistry-based applied research projects. Essential Duties and Responsibilities: Develops and validates analytical methods using thermal desorption (TD), gas chromatography (GC), liquid chromatography (LC), ion chromatography (IC), mass spectrometry (MS), and microscopy. Performs troubleshooting and non-routine maintenance on TD, GC, LC, IC, MS, and microscopy instrumentation. Ensures the readiness of TD, GC, LC, IC, MS, and microscopy instrumentation Facilitates the stand-up of new analytical instrumentation Leads meetings with company clients by preparing and presenting meeting materials in meetings Develops innovative solutions to complex problems Develops improvements to currently used processes and analysis methods Trains, leads, and mentors junior level scientists to execute analytical chemistry tasks Performs wet chemistry (dilutions, extractions, etc.) Composes, reviews, and executes test plans and standard operating procedures Composes and reviews technical reports Performs literature reviews Safely handles explosives and other hazardous materials Sources materials and submits purchase requests Other duties as assigned Required Knowledge, Skills & Abilities: Positive attitude with a willingness to learn new things Previous experience with TD, GC, LC, IC, or MS Excellent working knowledge of TD, GC, LC, IC, and MS Technical writing, presentation, verbal communication, and listening skills Education/Experience: Incumbent professional should have a minimum of a bachelor's degree in chemistry with five to ten years of analytical chemistry experience or a graduate degree (masters or PhD) chemistry with up to five years of experience. Certificates and Licenses: None Clearance: The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position. Supervisory Responsibilities: The incumbent professional has little to no supervisory responsibilities. Working Conditions/ Equipment: The incumbent professional is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor. Powered by ExactHire:160577

ARKANSAS CHILDREN'S IS A TOBACCO FREE WORKPLACE. FLU VACCINES ARE REQUIRED. ARKANSAS CHILDREN'S IS AN EQUAL OPPORTUNITY EMPLOYER. ALL QUALIFIED APPLICANTS WILL RECEIVE CONSIDERATION FOR EMPLOYMENT WITHOUT REGARD TO RACE, COLOR, RELIGION, SEX, SEXUAL ORIENTATION, GENDER IDENTITY OR EXPRESSION, NATIONAL ORIGIN, AGE, DISABILITY, PROTECTED VETERAN STATUS OR ANY OTHER CHARACTERISTIC PROTECTED BY FEDERAL, STATE, OR LOCAL LAWS. This position has been designated as safety sensitive and cannot be filled by a candidate who is a current user of medical marijuana. CURRENT EMPLOYEES: Please apply via the internal career site by logging into your Workday Account (****************************************** search the "Find Jobs" report. Work Shift: Please see job description for details. Time Type: Full time Department: CC038351 ACRI ACNC General SalarySummary:Provide laboratory and scientific support for chromatography based research projects, including conduct of laboratory analytical assays for the analysis of chemicals and metabolites in biological samples, evaluation of results, processing and reporting of data, and refinement of workflows to improve lab efficiency.Additional Information:Required Education:Bachelors Degree or Equivalent ExperienceRecommended Education:Master's degree in a related field of study.Required Work Experience:Related Field - 3 years of experience Recommended Work Experience:Required Certifications:Recommended Certifications:Description 1. Responsible for conduct and streamlining of sample preparation for liquid chromatography 2. Responsible for the operation of analytical equipment including UHPLC coupled mass spectrometers 3. Conduct of quantitative assays for various nutrients and metabolites 4. Participation in the evaluation of research results 5. Ensures data is generated and recorded according to procedures and protocols 6. Supports the development of new procedures and protocols 7. Maintains laboratory equipment to ensure it remains in proper working condition 8. Anticipates problems and corrects them and/or notifies the supervisor(s) in a timely manner 9. Maintains laboratory inventory, including chemical inventory and waste management 10. Maintains cleanly and safe laboratory working environment 11. All other duties as assigned.

We are seeking a skilled Thermal Chemist to conduct advanced thermal analysis and materials characterization in support of chemical formulation and materials development programs. This role requires strong knowledge of industrial chemical processes, thermal analysis techniques, and sophisticated analytical methods. The successful candidate will play a critical role in developing, testing, and characterizing chemical formulations while ensuring the highest standards of safety and analytical excellence. Essential Duties and Responsibilities: Advanced Thermal Analysis: Conduct detailed thermal analysis of materials using differential scanning calorimetry (DSC) Perform thermogravimetric analysis (TGA) to assess decomposition pathways and thermal stability Operate accelerating rate calorimetry (ARC) systems for comprehensive thermal hazard evaluation Analyze kinetic parameters and reaction mechanisms of material decomposition Develop thermal models and predictive capabilities for safety and performance assessment Data Analysis & Reporting: Analyze complex thermal and analytical data to extract meaningful insights about material properties Prepare comprehensive technical reports documenting experimental results and conclusions Present findings to technical teams, management, and external stakeholders Maintain detailed laboratory notebooks and ensure data integrity and traceability Support patent applications and technical publications Materials Characterization & Analysis: Perform comprehensive materials characterization using vibrational spectroscopy techniques (FTIR, Raman) Conduct particle size analysis to determine morphology and distribution characteristics Execute sensitivity testing protocols including electrostatic discharge (ESD), friction, and impact sensitivity assessments Analyze chemical composition, purity, and stability of energetic materials and intermediates Required Knowledge, Skills & Abilities: Advanced knowledge of chemical thermodynamics and materials science principles Proficiency with thermal analysis software and data interpretation Experience with statistical analysis and experimental design Understanding of chemical reaction mechanisms and kinetic modeling Education/Experience A bachelor's degree in chemistry with at least 12 years of experience OR a master's degree in chemistry with at least 6 years of experience OR a Ph.D. in chemistry with at least 1 year of experience. Certificates & Licenses: None Required Clearance: The ability to obtain a Department of Defense Secret clearance and Department of Homeland Security Fitness is required for this position. Supervisory Responsibilities: Supervision of the technical activities performed by the more junior staff members assigned to the project is required for this position. Working Conditions/Equipment: The incumbent professional is expected to be present at the work site and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor. Powered by ExactHire:179249

The primary purpose of this position is to serve as the lead synthetic chemist at the Transportation Security Laboratory (TSL). Essential Duties and Responsibilities: Follows currently established standard operating procedures (SOPs) to synthesize homemade explosives (HMEs). Performs research to develop syntheses for new HMEs of interest. Performs quality control of HMEs synthesized at the TSL. Works directly with federal client to achieve the goals of the HME laboratory at the TSL. Performs wet chemistry (dilutions, extractions, etc.). Composes and reviews technical reports and SOPs. Composes, reviews, and executes test plans. Performs literature reviews. Safely handles explosive and other hazardous materials. Sources materials and submits purchase requests. Other duties as assigned. Required Knowledge, Skills & Abilities: Previous experience synthesizing and handling energetic material. Good interpersonal, verbal, and written communication skills. Good listening skills. Team player with a positive attitude. Good working skills of software and tools necessary for job functions including Microsoft Office suite. Experience with measuring density and refractive index Experience with IR, RAMAN, or NMR Experience with using EasyMax for chemical syntheses Education/Experience: Incumbent professional should have: a bachelor's degree in chemistry with a minimum of five years relevant experience; or a master's degree in chemistry with at least two years of relevant experience; or a PhD in Chemistry with at least one year of relevant experience. Certificates and Licenses: None Clearance: The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position. Supervisory Responsibilities: The incumbent professional may oversee junior level chemists performing synthetic chemistry tasks. Working Conditions/ Equipment: The incumbent professional is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor. Powered by ExactHire:160567

The primary purpose of this position is to perform chemistry tasks at the Transportation Security Laboratory (TSL). Essential Duties and Responsibilities: Collects and analyzes data using gas chromatography (GC), liquid chromatography with mass spectrometry detection (LCMS), and ion chromatography (IC). Performs troubleshooting, maintenance, and method development on GC, LCMS, and IC instrumentation. Performs wet chemistry (dilutions, extractions, etc.). Collects and analyzes data using explosive trace detection (ETD) systems. Performs microscopy measurements using stereomicroscope or polarized light microscope. Composes and reviews technical reports and standard operating procedures. Composes, reviews, and executes test plans. Synthesizes homemade explosives. Performs literature reviews. Safely handles explosive and other hazardous materials. Sources materials and submits purchase requests. Other duties as assigned. Required Knowledge, Skills & Abilities: Positive attitude. Good working knowledge of trace analytical instrumentation (GC, LCMS, and IC). Good interpersonal, verbal, and written communication skills. Good listening skills. Good working skills of software and tools necessary for job functions including Microsoft Office suite. Previous experience handling energetic material. Previous experience with ETD systems. Education/Experience: Incumbent professional should have a minimum of a bachelor's degree in chemistry. Certificates and Licenses: None Clearance: The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position. Supervisory Responsibilities: The incumbent professional has little to no supervisory responsibilities. Working Conditions/ Equipment: The incumbent professional is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor. Powered by ExactHire:160581