Chemist jobs in Indianapolis, IN - 110 jobs

Indianapolis, IN $24/HR The Analytical R&D Team is seeking a detail-oriented and motivated Chemist. In this role, you will support scientists in day-to-day laboratory activities related to method development, non-GLP and GLP validations, and sample analysis. This position is ideal for someone who is eager to learn, values collaboration, and is committed to maintaining high standards of data quality and safety. Chemist Responsibilities: Assist ARD scientists with sample weighing, preparation, and analysis of active ingredients, intermediates, impurities, and formulated products for both quantitative and qualitative purposes Support laboratory experiments for non-GLP and GLP method validation as needed Learn and operate analytical instrumentation, including HPLC, GC, LC/GC/MS, and more. Perform routine instrument maintenance and troubleshoot issues when they arise Process analytical data and document experimental procedures and results in a timely and accurate manner to ensure data integrity Collaborate effectively with scientists and other stakeholders; adjust priorities to support urgent projects when necessary Work independently when appropriate and demonstrate strong problem-solving abilities Adhere to all Corteva EHS&S policies and demonstrate a strong commitment to laboratory safety Chemist Qualifications: Bachelor's degree in Chemistry or a related scientific field Familiarity or strong understanding of analytical chemistry techniques preferred Excellent written and verbal communication skills Willingness to learn continuously and follow all safety protocols

Responsibilities: Assist analytical scientists with routine laboratory activities, including sample weighing, preparation, and basic analysis. Support testing of active ingredients, intermediates, impurities, and formulated products for qualitative and quantitative evaluation. Learn to operate common analytical instrumentation such as HPLC, GC, LC/MS, GC/MS, Karl Fischer titration, and other wet chemistry techniques. Perform basic instrument setup, routine maintenance, and troubleshooting with guidance and training. Accurately record experimental data and results in laboratory notebooks or electronic systems to ensure data quality and traceability. Follow established laboratory procedures and safety practices while maintaining an organized and clean work environment. Collaborate with team members and communicate progress, issues, or questions effectively. Demonstrate flexibility and a willingness to support shifting priorities and time-sensitive laboratory tasks. Qualifications: Bachelor's degree in Chemistry, Biochemistry or a closely related scientific field. 1+ years of academic or internship laboratory experience is required. Familiarity with analytical techniques such as HPLC, GC, titration, or chromatography through hands-on lab experience. Basic understanding of analytical chemistry concepts and laboratory best practices. Strong attention to detail with the ability to follow written procedures and instructions. Effective written and verbal communication skills. Eagerness to learn new techniques and develop technical skills in a laboratory environment. Ability to work well in a collaborative, team-oriented setting while taking ownership of assigned tasks.

We have an exciting opportunity for a Bioanalytical Chemist to join the Metabolomics team in Crop Health Research and Development located in Indianapolis, IN. This role is focused on providing essential bioanalytical support to advance fermentation research goals. The candidate will conducts experiments and complex technical operations, recognize erroneous or unexpected results, interpret and analyze results, and makes suggestions based on their analyses and conclusions. Responsibilities: Execute established quantitative bioanalytical UPLC methods to support fermentation based programs by analyzing various small molecules. Handle and extract from varied biological matrices including microbial broths and extracts. Conduct basic data interpretation and processing of analytical results to ensure data quality and consistency. Maintain accurate records of instrument performance, results, and experimental procedures. Communicate technical results and instrument status clearly to team members and stakeholders in a dynamic environment. Requirements: B.S. in Chemistry, Biochemistry, Chemical or Biochemical Engineering, Biotechnology, or a related scientific field. Proven hands-on experience with HPLC or UPLC systems for analytical or bioanalytical chemistry applications. Strong work ethic and a proactive, collaborative approach to teamwork. Effective verbal and written communication skills. Preferred Qualifications: Previous research experience in an industrial or academic laboratory setting. Experience with Beckman-based automation or similar robotic liquid handling systems. Experience with Mass Spectrometry (MS) systems and software. Experience with Gas Chromatography (GC) based systems.

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. Organization Overview: The Lilly Industrial Hygiene (IH) Lab provides trace analytical services for the company's global Industrial Hygiene (IH) community. A primary mission of the IH Lab is to develop and validate monitoring methods for active pharmaceutical ingredients (APIs) coming from the clinical development pipeline. Lab staff work closely with site/location Industrial Hygienists to provide routine analysis of samples taken in the development and manufacturing space in support of employee exposure assessment, and they coordinate all 3rd party analytical needs including external data review and release. As well, lab staff provide creative technical solutions and project support for emerging needs as identified by the global IH community. This position reports through the Global Health, Safety, and Environment organization. Responsibilities: A primary mission of the IH Lab is to develop and validate monitoring methods for active pharmaceutical ingredients (APIs) coming from the clinical development pipeline. Monitoring methods typically include air sampling methods for personnel exposure characterization and swab methods for cleaning effectiveness after spills and decommissioning but may also include air and water monitoring methods and sample analysis for environmental evaluations. Key responsibilities of this position include: Partnering with internal customers and external lab vendors to efficiently meet business needs. Developing and validating air and surface monitoring methods, including sampling media. This may involve internal/external research and troubleshooting until an acceptable recovery is achieved. Conduct laboratory analysis of active pharmaceutical ingredient (API) samples collected globally. Coordinating sample analysis with third party laboratories and conducting a review of results before releasing to internal customers. Calculating, documenting, and reporting study results via established laboratory programs such as electronic notebooks and laboratory software application. Routinely monitoring the clinical development pipeline, connecting with site Industrial Hygienists to prioritize method development needs, and initiating requests when an occupational guideline limit is needed. Peer reviewing laboratory data to confirm it is accurate and in compliance with procedures, assuring data is stored as required for archival, and supporting laboratory data quality assessment. Researching and supporting the solution of key technical, operational, or business problems, as needed. Organizing and/or conducting laboratory inspections and supporting the resolution of observations or areas for improvements. Representing Lilly in the AIHA Pharma Round Robin and participating in external scientific forums, as appropriate. Maintaining awareness of analytical sciences, pharmaceutical industry trends and industrial hygiene issues to drive continuous improvement in laboratory services. Basic Requirements: B.S. with > 5 years of relevant experience or M.S. with >3 years of relevant experience in chemistry, biochemistry, or closely related field of study Mass spectrometry, liquid, and gas chromatography analytical method development experience. Additional Skills/Preferences: Proteomics experience strongly preferred. Experience in ISO 17025 accredited laboratory. Industrial Hygiene Chemist Certification. Experience in GMP lab operations and Lean. Coursework or experience in industrial hygiene or environmental sampling. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

IMMEDIATE OPENING: Analytical Chemist | ATKA Chromatography Scientist INTERVIEWS AVAILABLE THIS WEEK Interested in this role? Reach out directly to ***************************** or CALL ************ with an updated resume to apply (HIRING NOW) We are looking for an innovative and highly skilled Analytical Chemist - Chromatography Systems Scientist to join our Advanced Materials Purification Team. This position requires expertise in ATKA Chromatography, Fast Protein Liquid Chromatography (FPLC), and scale-up processes. In this role, you will operate and optimize automated chromatography platforms for the aqueous separation of high-value inorganic compounds. The ideal candidate will combine chemical analysis, process engineering, and automation to advance the development and scale-up of solvent-free purification workflows for specialty metals and oxides. Responsibilities * Operate, calibrate, and maintain systems and UNICORN control software for aqueous metal separation and purification. * Operate and maintain automated chromatography systems and control software for metal separation and purification. * Design and refine separation methods using ion-exchange, chelating, or size-based column technologies. * Prepare and condition columns for use with acidic, high-ionic-strength, or complex aqueous solutions. * Execute gradient and stepwise elution protocols while monitoring conductivity, pH, UV absorbance, and flow rates. * Collaborate with engineering and R&D teams to transition lab-scale methods to pilot and production environments. * Conduct mass balance assessments and generate recovery/purity profiles to support process validation. * Maintain detailed records of runs, chromatograms, and standard operating procedures. * Troubleshoot system components including fluidics, detectors, and valves to ensure consistent performance. * Train lab personnel on chromatography setup, operation, and maintenance best practices. * Support integration of analytical data with digital systems for automated reporting and process control. Qualifications Required * Bachelor's degree in Chemistry, Chemical Engineering, Materials Science, or a related field. * At least 1 year of hands-on experience with Cytiva AKTA Chromatography, automated chromatography systems, and control software. * Solid understanding of aqueous separation chemistry and metal purification techniques. * Experience with buffer preparation, column packing, and method optimization. * Strong documentation and troubleshooting capabilities. Preferred * Relevant field related to laboratory refining rare-earths, lithium, or other strategic metals. * Familiarity with chromatography scale-up and continuous separation systems. * Knowledge of trace analysis tools such as ICP-MS or ICP-OES. * Exposure to process analytical technology and automated fraction collection systems. Work Environment The position is based in a lab and pilot-scale setting focused on advanced separation technologies. Regular handling of aqueous solutions containing acids, salts, and chelating agents is required, alongside strict adherence to safety and contamination-control protocols. Frequent collaboration with multidisciplinary teams in R&D and process development is also part of the work environment. INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION: * I am scheduling interviews for this position ASAP and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Max Richey * HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to mrichey @actalentservices. com or CALL ************ Job Type & Location This is a Permanent position based out of Noblesville, IN. Pay and Benefits The pay range for this position is $80000.00 - $100000.00/yr. 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 Noblesville,IN. Application Deadline This position is anticipated to close on Jan 14, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

PLZ is committed to product stewardship and innovation, strong ethical standards, sustainable operations and most importantly, the development of our people. Whether at our manufacturing facilities or corporate headquarters, PLZ prioritizes health and safety, and offers you the support you need to create the career you want, through engagement, equity and inclusion, and opportunity. From household cleaning solutions to personal care products, and food to automotive lubricants, PLZ produces more than 2,500 different aerosol and liquid products in our facilities across the continent. We know that being the partner of choice for our clients starts with being the partner of choice for our employees. Learn more at *********************** or visit **************************** We are currently seeking a Formulation Chemist II to join our team at Indy PLZ. As a cosmetic chemist working on primarily hair care products, you will be responsible for formulating, testing, and improving the performance of hair pomades, styling gels, shampoos, and conditioners. You will work with raw materials to create effective and safe formulas that meet consumer needs and demands. Additionally, you will collaborate with other teams to ensure the quality and safety of the products. Key Responsibility: * With guidance from the Manager of R&D, conduct research and development to formulate new cosmetic products. * Test and analyze the effectiveness of new formulations. Ensure they meet client guidelines. * Collaborate with other departments to ensure the quality and safety of the products. * Evaluate raw materials and choose the best options for formulations. * Develop bulk product specifications and evaluate formula compatibility. * Conduct stability testing on new formulations. * Ensure accurate and well-organized documentation of formulations. * Monitor industry trends and developments to ensure products remain competitive. * Troubleshoot formulation problems and identify solutions. * Continuously improve and optimize product formulations. Qualifications: * Bachelor's degree in chemistry, cosmetic science, or a related field. * Minimum of 3 - 5 years formulation experience in R&D (preferred) * Familiarity with FDA regulations for cosmetic products (preferred). * Proficiency in Microsoft Office and lab software. * Strong organizational and time management skills. * Excellent verbal and written communication skills. * Ability to work independently and as part of a team. * Attention to detail and accuracy. * Experience with lab techniques and equipment. * A passion for the cosmetic industry and staying up-to-date with new developments and trends. PLZ Corp offers a robust suite of benefits including: * Medical, Dental & Vision benefits. * Company paid Life and Short-Term disability. * Voluntary benefits including additional life, disability, and hospital/accident insurance. * 401k & company provided match. * Paid Time Off * Bonus incentive programs (Note, bonuses are subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance.) All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status or other protected status. EEOE/M/F/Vet/Disabled. All your information will be kept confidential according to EEO guidelines.

Linde Advanced Material Technologies Inc. Analytical Chemist Indianapolis, IN, United States | req25923 What you will enjoy doing* * As your top priority, you will ensure compliance with company safety and environmental standards in all areas of your work * You will conduct experiments, analyze data, and provide technical expertise to support ongoing production related needs * Further, you will work with a team of scientists to develop innovative solutions and drive advancements in material testing technology across Linde Advanced Materials Technologies * You will perform and develop testing method procedures required to maintain quality assurance of products and compliance with internal and regulatory standards * You will play an active role in leading and planning for customer audits and material testing accreditation bodies * You will provide technical leadership and expertise to the quality control and production staff What makes you great * Bachelor's degree in Chemistry, Chemical Engineering, or related field required * Master's degree in relative field is preferred but not required * You have at least 3 years of relative work experience with sample preparation, operating and maintaining ICP, ICP-MS equipment * It is preferred that you show familiarity with aerospace testing and industrial quality system requirements * You have strong analytical, statistical, and problem-solving skills * You should be proficient in Microsoft Office Suite Why you will love working with us Linde Advanced Material Technologies, formerly Praxair Surface Technologies, is a company that revolutionizes industries through innovative materials and surface coatings. We are leaders in advanced materials and offer metal powders, sputtering targets, and surface coatings that enhance performance across various sectors. Our strong focus on innovation is evident in our superior technologies for the aerospace, energy, semiconductor, automotive, and industrial industries. Linde employees learn and abide the Linde Code of Ethics and Code of Conduct by demonstrating honesty, integrity, professionalism in all communications, actions, and decisions. What we offer you! At Linde, the sky is not the limit. If you're looking to build a career where your work reaches beyond your job description and betters the people with whom you work, the communities we serve, and the world in which we all live, at Linde, your opportunities are limitless. Be Linde. Be Limitless. Linde offers competitive compensation and an outstanding benefits package. Enjoy access to health, dental, disability, and life insurance, paid holidays and vacation, 401(k) matching, pension benefits, an employee discount program, and opportunities for educational and professional growth. Additional compensation may vary depending on the position and organizational level. Build your future with us while making an impact every day! Have we inspired you? Let´s talk about it We are looking forward to receiving your complete application. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, pregnancy, sexual orientation, gender identity or expression, or any other reason prohibited by applicable law. Linde Advanced Material Technologies Inc. abides by applicable export control laws including the Export Administration Regulations (EAR) and the International Traffic in Arms Regulations (ITAR) in accordance with the company's export control procedures. As such, persons considered for this position must be either a U.S. Citizen, Permanent Resident (green card holder) or otherwise classifiable as a U.S. person under relevant regulations. Linde Advanced Material Technologies Inc. acts responsibly towards its shareholders, business partners, employees, society and the environment in every one of its business areas, regions and locations across the globe. The company is committed to technologies and products that unite the goals of customer value and sustainable development. * The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Therefore employees assigned may be required to perform additional job tasks required by the manager. #LI-AD1

Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. 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 (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment. We aim to recruit the best people who stand out among their peers and embody our Core Values: C lient Focused: We only succeed when our clients succeed. O utstanding: We deliver meticulous results through outstanding performance. G ood: We act ethically and morally. E mployee-Centric: We honor and support our employees. N imble: We are prepared to adapt in an ever-changing industry. T eam-Oriented: We collaborate with each other and with our clients. We currently have a role available for an Analytical Chemist in a pharmaceutical research lab setting. Job duties include, but are not limited to, the following: Performing chromatographic method analysis on individual sample and development of methods with quick turnaround times (1 - 2 days). Analyzing high throughput experimentally (HTE) generated samples using standard reverse-phase HPLC and UPLC methods. Documenting laboratory work appropriately in laboratory notebooks and/or reports. Supporting minor instrument repairs, setup, software troubleshooting, and/or routine maintenance of LC, LC/MS, SFC, and UPLC/MS equipment. Preparing laboratory reagents. Analyzing/triaging data from a variety of software. Maintaining a safe, organized, and productive lab. Job requirements include, but are not limited to: BS - Chemistry or related field with 1-3 years of industry experience (preferably pharma). Strong time management skills and flexibility to handle urgent projects within given timelines. Excellent communication skills - verbal and written. Very strong attention to detail and safety as well as problem-solving skills. Demonstration of excellent team player 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. This job posting will close by 2/1/2026 or when a candidate is identified, whichever comes first.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Raw Materials Analytical testing could include: compendial testing, HPLC/UPLC, generic testing (e.g., solvents, water, ash, titrations, heavy metals) and compound specific methods Ability to investigate and troubleshoot equipment related issues Work with a balance for weighing, pH, pipettes Preparation of buffer and media UV Smart Lab and Trackwise software experience a plus Qualifications Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Bachelor's degree in physical science (chemistry, physics, etc.), or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) Additional Information The position is full-time, Monday through Friday, 8 a.m. to 5 p.m., with overtime as needed. Candidates currently living within a commutable distance of Indianapolis, IN, are encouraged to apply. Ability to work overtime as required. Tasks require repetitive motion and standing for long periods of time. May be required to respond to off-shift operational issues. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Shift: Monday through Friday, 8:00AM - 5:00PM Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. Overview Seeking an Analytical Chemist to support our client's lab testing needs with 2+ years of experience. Compensation: $22.00 - 24.00 per hour Responsibilities Organizes and conducts routine analyses independently and in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines Documents work and maintains study documentation and laboratory records Independently able to use and perform basic troubleshooting of laboratory equipment and software appropriate for assigned tasks, while learning to perform routine and non-routine maintenance Provides input and participates in project meetings Performs assigned workload on a daily basis and effectively completes multiple assignments. Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members. Maintains a safe and clean laboratory work environment Understands data generated, and history of methods. Recognizes deviations from normal results and inform lab lead and/or management of any problems and/or deviations that may affect the integrity of the data and participates in corrective action of problems. Identifies problems, determines appropriate actions, and implements solutions with support or independently as appropriate. Able to adapt to new procedures or particular needs as directed. Able to identify critical steps in an assay. Knowledge of departmental procedures and policies Viewed as a resource within their team Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications BS Degree in Chemistry or related science field with 2+ years experience Experience with ELISA Microsoft Excel Proficient Independent and flexible/adaptable individual to manage multiple ongoing projects Preferred: Experience with chromatographic techniques including HPLC/UHPLC utilizing various detection techniques including UV, PDA, MS and FL (some combination of these) Experience with ELISA method development and techniques Experience with PCR Familiarity with statistical data analysis Experience troubleshooting equipment would be beneficial Experience with electronic notebook upkeep Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work. Benefits When you join Pace , you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

We are seeking a self-motivated Chemistry Lab Technician to join our Lab Operations team. In this role you will assist in laboratory confirmatory analysis of biological fluids including urine, oral fluid (saliva) or hair specimens. This role is also responsible for operating, maintaining and troubleshooting various Auto Chemistry instrumentation. Shift: PM Shift M-F 6pm-230am Salary:$20.00 Plus $2.00 Shift Differential for hours worked between 6pm-6am Primary Responsibilities * Loads, prepares and extracts specimens using various Auto-Chem Instrumentation. * Assist in instrument calibration, QC review, and initial analytical review. * Prepare reagents and buffers as needed. * Assists with maintaining an adequate inventory of laboratory supplies. * Responsible for all record keeping associated with specimen preparation, including following chain of custody handling guidelines and storage requirements. * Conducts safe work practices according to safety protocols, PPE requirements and decontamination procedures. * Responsible to maintain all safeguards as it pertains to Protected health information (PHI). Qualifications * Bachelor?s degree in a science field (Chemistry, Biochemistry, Biology, Microbiology, Pre-med (Biomed), Forensics & Toxicology), REQUIRED. * Experience as a lab technician, preferred. * Data entry skills via a keyboard (alpha and numeric) required. * Strong eye-hand coordination. * Ability to handle a high-volume environment while maintaining the highest level of quality, required. * Physical demands required to perform critical tasks in this role include standing for long periods of time, lifting up to 25lbs, bending and carrying. Benefits Cordant supports our employees by providing a comprehensive benefits package to eligible staff (per state regulations) that includes: Medical, Dental, Vision Insurance, Flexible Spending Accounts (FSA), Health Savings Accounts (HSA) Paid Time Off (PTO) accruing on day 1, Volunteer Time Off (VTO), Paid Holidays, 401(k) with Company Match, Employee Assistance Program (EAP), Short Term and Long-Term Disability (STD/LTD) and Company Paid Basic Life Insurance. #LAB123

INCOG is seeking a Quality Control (QC) Chemist with a passion for working within a team, a desire to drive Quality processes in a regulated setting, and a commitment to upholding the integrity of data generated for clients. The QC Chemist will work closely with the QC Chemistry Manager and Quality Control Method Transfer Scientists, as well as Project Management and Supply Chain teams, to support development, readiness, and routine testing activities for the Quality Control Chemistry laboratory. This role is crucial in generating ALCOA+ data and upholding our Quality Mindset through attention to detail, on-time delivery, and commitment to Quality excellence. Strict adherence to Good Documentation Practices (GDP) is required as Good Manufacturing Practice (GMP) testing is performed. Excellent written and oral communication skills with the ability to clearly and concisely articulate complex issues to a range of target audiences is critical in this role. The QC Chemist will exemplify excellent interpersonal skills and be capable of developing productive, customer-centric working relationships with colleagues, clients, suppliers, and partners. The QC Chemist will thrive in a team environment but can also work autonomously with strong self-management and organizational skills. Essential Job Functions: Perform routine and batch-related testing on incoming components, raw materials, in-process samples, finished product, and stability samples according to validated methods as well as special testing deemed necessary by protocols Assist in sampling and testing of incoming materials requiring QC testing as needed Create/revise SOPs and other relevant documents related to laboratory equipment and/or processes Participate in the completion of laboratory investigations/deviations and provide SME support where needed Perform basic troubleshooting activities with respect to methods/assays, equipment malfunctions, and investigations (Deviations and OOS) Execute routine laboratory work orders for maintenance and non-critical calibrations Perform minor preventative maintenance on QC laboratory instrumentation as needed using written SOPs or assist vendors with access to systems/materials when vendor performs maintenance Execute day-to-day tasks within the laboratory including sample inventory disposition/disposal, consumables ordering/inventory, preparing instruments for testing, and laboratory waste management Assist in the control and management of laboratory waste in cooperation with relevant EH&S standards Assist in the development and execution of protocols for method transfers, method validations, stability studies, cleaning validations, and any other special testing required from the Quality Control Chemistry laboratory Support internal and external customers to ensure proper and timely execution of all aspects of the clinical/commercial analytical method life cycle across clients Conduct periodic reviews of analytical test procedures and SOPs as required Review and approve analytical testing procedures and protocols as needed Assist in training fellow QC and Development personnel on instruments and assays when cross-training is needed Assist in the professional support and development of QC Chemistry Technician staff within the QC laboratory Be team-oriented and willing to act as both a facilitator of special projects and a contributor to special projects when needed Set deadlines and prioritize work for self, group members, and support groups involved Review/approve work performed by coworkers for accuracy and alignment with procedures Collaborate with internal departments and teams to resolve quality issues regarding facility, products manufactured, and released Identify, evaluate, and implement continuous business process improvements Special Job Requirements: This position will support primarily third shift (11:00pm-7:30am) Bachelor's Degree in Science (Chemistry or Biochemistry) Minimum of 3+ years of biopharma industry experience, with at least 2 years of hands-on experience in a GMP environment/Quality Control testing in a regulated environment or other related experience High proficiency level in operating UHPLC/HPLC, GC, SoloVPE, UV-VIS, TOC, particulate matter analyses, method validation/transfer, and relevant laboratory computer systems with associated data integrity requirements Excellent working knowledge, understanding, and experience with practical implementation of FDA, EMA, and other regulatory authority expectations for Quality Control Exceptional computer skills evidenced by hands-on work with automated data management and/or data analysis systems (LIMS, JMP, Minitab, etc.) Additional Preferences: Experience with Continuous Improvement, Six Sigma, and/or Lean principles Experience with building processes and procedures Experience in performing testing and/or characterization of biologic (monoclonal antibody, enzyme) and small molecule (peptide, mRNA) products Experience performing container closure integrity testing (CCIT) Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

INCOG is seeking a Quality Control (QC) Chemist with a passion for working within a team, a desire to drive Quality processes in a regulated setting, and a commitment to upholding the integrity of data generated for clients. The QC Chemist will work closely with the QC Chemistry Manager and Quality Control Method Transfer Scientists, as well as Project Management and Supply Chain teams, to support development, readiness, and routine testing activities for the Quality Control Chemistry laboratory. This role is crucial in generating ALCOA+ data and upholding our Quality Mindset through attention to detail, on-time delivery, and commitment to Quality excellence. Strict adherence to Good Documentation Practices (GDP) is required as Good Manufacturing Practice (GMP) testing is performed. Excellent written and oral communication skills with the ability to clearly and concisely articulate complex issues to a range of target audiences is critical in this role. The QC Chemist will exemplify excellent interpersonal skills and be capable of developing productive, customer-centric working relationships with colleagues, clients, suppliers, and partners. The QC Chemist will thrive in a team environment but can also work autonomously with strong self-management and organizational skills. Essential Job Functions: * Perform routine and batch-related testing on incoming components, raw materials, in-process samples, finished product, and stability samples according to validated methods as well as special testing deemed necessary by protocols * Assist in sampling and testing of incoming materials requiring QC testing as needed * Create/revise SOPs and other relevant documents related to laboratory equipment and/or processes * Participate in the completion of laboratory investigations/deviations and provide SME support where needed * Perform basic troubleshooting activities with respect to methods/assays, equipment malfunctions, and investigations (Deviations and OOS) * Execute routine laboratory work orders for maintenance and non-critical calibrations * Perform minor preventative maintenance on QC laboratory instrumentation as needed using written SOPs or assist vendors with access to systems/materials when vendor performs maintenance * Execute day-to-day tasks within the laboratory including sample inventory disposition/disposal, consumables ordering/inventory, preparing instruments for testing, and laboratory waste management * Assist in the control and management of laboratory waste in cooperation with relevant EH&S standards * Assist in the development and execution of protocols for method transfers, method validations, stability studies, cleaning validations, and any other special testing required from the Quality Control Chemistry laboratory * Support internal and external customers to ensure proper and timely execution of all aspects of the clinical/commercial analytical method life cycle across clients * Conduct periodic reviews of analytical test procedures and SOPs as required * Review and approve analytical testing procedures and protocols as needed * Assist in training fellow QC and Development personnel on instruments and assays when cross-training is needed * Assist in the professional support and development of QC Chemistry Technician staff within the QC laboratory * Be team-oriented and willing to act as both a facilitator of special projects and a contributor to special projects when needed * Set deadlines and prioritize work for self, group members, and support groups involved * Review/approve work performed by coworkers for accuracy and alignment with procedures * Collaborate with internal departments and teams to resolve quality issues regarding facility, products manufactured, and released * Identify, evaluate, and implement continuous business process improvements Special Job Requirements: * This position will support primarily third shift (11:00pm-7:30am) * Bachelor's Degree in Science (Chemistry or Biochemistry) * Minimum of 3+ years of biopharma industry experience, with at least 2 years of hands-on experience in a GMP environment/Quality Control testing in a regulated environment or other related experience * High proficiency level in operating UHPLC/HPLC, GC, SoloVPE, UV-VIS, TOC, particulate matter analyses, method validation/transfer, and relevant laboratory computer systems with associated data integrity requirements * Excellent working knowledge, understanding, and experience with practical implementation of FDA, EMA, and other regulatory authority expectations for Quality Control * Exceptional computer skills evidenced by hands-on work with automated data management and/or data analysis systems (LIMS, JMP, Minitab, etc.) Additional Preferences: * Experience with Continuous Improvement, Six Sigma, and/or Lean principles * Experience with building processes and procedures * Experience in performing testing and/or characterization of biologic (monoclonal antibody, enzyme) and small molecule (peptide, mRNA) products * Experience performing container closure integrity testing (CCIT) Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

Job Description Isotopia is a global biotech company manufacturing key ingredients for pharmaceutical cancer drugs. At our US headquarters in Indianapolis, we will be next door to our key customers, delivering our products just in time, each day, every day. We are seeking a highly motivated and detail-oriented Quality Control Chemist to join our dynamic team. You will play a crucial role in ensuring the safe and efficient production of our products. You will be part of a family, a team, dedicated to our mission to deliver on our covenant with our customers. Requirements Responsibilities: · Perform routine testing of raw materials, in process materials, and radiopharmaceutical products · Execute method validation protocols and generate reports · Execute stability protocols and generate reports · Assist with method development and implementation · Comply with cGMP requirements for recording of data · Perform routine inspections of laboratory notebooks and of the laboratory environment in accordance with written inspection procedures · Perform routine wipe and survey testing for radiation protection · Maintain inventory of materials required for analytical testing · Assist with analytical equipment IQ/OQ/PQ protocol execution · Coordinate with third party equipment vendors to schedule routine equipment requalification · Assist with drafting analytical equipment risk assessments · Assist with trending of data and report drafting as needed · Assist with environmental monitoring program as needed · Coordinate with production personnel to ensure timely testing and release of intermediate materials and final product · Coordinate sampling plans and shipment of samples to third party labs for any necessary third-party testing · Assist with technical review of routine test documents, method validation protocols / reports, and method development protocols / reports · Perform any other tasks related to analytical testing as necessary Education and Skills: · Bachelor's degree in Chemistry is strongly preferred · Previous experience with compendial USP test methods, ICP-MS / ICP-OES, radio-TLC, and/or direct inoculation sterility testing is strongly preferred · Previous experience in pharmaceutical / radiopharmaceutical quality control is preferred · Strong understanding of cGMP requirements and radiation safety practices is preferred · Detail-oriented mindset with excellent organizational and record-keeping skills · Effective communication and teamwork abilities, with a focus on collaborative problem-solving · Ability to work in a regulated and fast-paced environment while maintaining a high level of accuracy · Flexibility to work in shifts and handle time-sensitive processes · Strong commitment to safety, ethical conduct, and compliance with regulations · Physical ability to stand for extended periods, lift moderately heavy objects up to 50 pounds, and to handle frequent stooping and crouching, and wear appropriate PPE · Manual dexterity for manipulating small items Benefits · 401K Retirement Program with 3% of Salary Company Contribution · Individual and Dependent Health Insurance · Dental Insurance · Vision Insurance · Life Insurance · Short-term Disability Insurance · Long-term Disability Insurance

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. Organization Overview: 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 motivated individuals who are determined to make life better for people around the world. The Bioproduct Research and Development (BR&D) organization delivers new medicines to patients through the development and commercialization of insulins, peptides, oligonucleotides, monoclonal antibodies, novel therapeutic proteins, and gene therapy systems. BR&D is a multidisciplinary group with deep technical expertise that works collaboratively with our discovery and manufacturing colleagues. Located in Indianapolis, IN, scientists have full access to Lilly's deep pharmaceutical development expertise and engineering capabilities. In this role, you will be part of a diverse team of analytical chemists, pharmaceutical scientists, and engineers delivering product and process understanding to deliver the antibody-drug conjugate portfolio. Ideal candidates will possess experience across multiple analytical techniques, demonstrate an aptitude in technical problem solving, and be motivated to work both independently and collaboratively in a dynamic environment. Top candidates for this position will be able to: Develop analytical methods to support progression of the antibody-drug conjugate portfolio. Evaluate and/or implement new analytical technologies/methods to advance Lilly's current analytical capabilities for bioproduct testing with a focus on state-of-the-art separation sciences capabilities. Generate key data and information applying HPLC, UHPLC, capillary electrophoresis, LCMS and/or other instrumental analysis techniques. The ideal candidate will demonstrate learning agility and be able to work with cross-functional teams. Position Responsibilities: Engage with scientists across Eli Lilly's Development and Manufacturing organizations to develop and validate robust analytical methods Identify and exploit new scientific concepts, strong problem-solving skills, and be self-motivated to contribute across multiple projects Strong written and verbal communication to speak to both technical and business-related implications of your work. Basic Qualifications: BS or MS in Analytical Chemistry, Biochemistry, Chemistry, or a related field. Additional Skills/Preferences: Experience with chromatographic separations and/or spectroscopic methods and methods for the analysis of antibody-drug conjugates. Experience with method validation and transfer. Demonstration of scientific and people leadership skills. Effective oral and written communication skills. The ability to work productively in an interdisciplinary team environment. Ability to balance multiple activities, prioritize and handle ambiguity. Additional Information: Potential exposure to chemicals, allergens, and loud noises Travel: 0 to 10% Position Local: Indianapolis, IN; Lilly Technology Center-North (LTC-N) Lilly is an EEO/Affirmative Action Employer and does not discriminate based on race, gender, protected veteran status, disability, or any other legally protected status Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

OPPORTUNITY: Analytical AKTA Chromatography Scientist INTERVIEWS AVAILABLE THIS WEEK Interested in this role? Reach out directly to ********************************* or CALL ************ with an updated resume to apply (HIRING NOW) We are looking for an innovative and highly skilled Analytical AKTA Chromatography Systems Scientist to join our Advanced Materials Purification Team. This position requires expertise in AKTA Chromatography, Fast Protein Liquid Chromatography (FPLC), ICP-OES / ICP-MS, and scale-up processes. In this role, you will operate and optimize automated chromatography platforms for the aqueous separation of high-value inorganic compounds. The ideal candidate will combine chemical analysis, process engineering, and automation to advance the development and scale-up of solvent-free purification workflows for specialty metals and oxides. Responsibilities * Operate, calibrate, and maintain systems and UNICORN control software for aqueous metal separation and purification. * Operate and maintain automated chromatography systems and control software for metal separation and purification. * Design and refine separation methods using ion-exchange, chelating, or size-based column technologies. * Prepare and condition columns for use with acidic, high-ionic-strength, or complex aqueous solutions. * Execute gradient and stepwise elution protocols while monitoring conductivity, pH, UV absorbance, and flow rates. * Collaborate with engineering and R&D teams to transition lab-scale methods to pilot and production environments. * Conduct mass balance assessments and generate recovery/purity profiles to support process validation. * Maintain detailed records of runs, chromatograms, and standard operating procedures. * Troubleshoot system components including fluidics, detectors, and valves to ensure consistent performance. * Train lab personnel on chromatography setup, operation, and maintenance best practices. * Support integration of analytical data with digital systems for automated reporting and process control. Qualifications Required * Bachelor's degree in Chemistry, Chemical Engineering, Materials Science, or a related field. * At least 1 year of hands-on experience with Cytiva AKTA Chromatography, automated chromatography systems, and control software. * Solid understanding of aqueous separation chemistry and metal purification techniques. * Experience with buffer preparation, column packing, and method optimization. * Strong documentation and troubleshooting capabilities. Preferred * Relevant field related to laboratory refining rare-earths, lithium, or other strategic metals. * Familiarity with chromatography scale-up and continuous separation systems. * Knowledge of trace analysis tools such as ICP-MS or ICP-OES. * Exposure to process analytical technology and automated fraction collection systems. Work Environment The position is based in a lab and pilot-scale setting focused on advanced separation technologies. Regular handling of aqueous solutions containing acids, salts, and chelating agents is required, alongside strict adherence to safety and contamination-control protocols. Frequent collaboration with multidisciplinary teams in R&D and process development is also part of the work environment. Interested in this role? SEE BELOW TO APPLY DIRECTLY FOR IMMEDIATE CONSIDERTATION: * I am scheduling interviews for this position TODAY and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Grace Williams * HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to grawilliams@actalentservices. com or CALL ************ Job Type & Location This is a Permanent position based out of Noblesville, IN. Pay and Benefits The pay range for this position is $80000.00 - $100000.00/yr. 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 Noblesville,IN. Application Deadline This position is anticipated to close on Jan 20, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job DescriptionSalary: $48K-$52K, depending upon experience Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. We can offer you the chance to build on your skills and knowledge while working among experts in their fieldsand with cutting-edge instrumentation. Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment.We aim to recruit the best people who stand out among their peers and embody our Core Values: C lient Focused: We only succeed when our clients succeed. O utstanding: We deliver meticulous results through outstanding performance. G ood: We act ethically and morally. E mployee-Centric: We honor and support our employees. N imble: We are prepared to adapt in an ever-changing industry. T eam-Oriented: We collaborate with each other and with our clients. We currently have a role available for an Analytical Chemist in a pharmaceutical research lab setting. Job duties include, but are not limited to, the following: Performing chromatographic method analysis on individual sample and development of methods with quick turnaround times (1 2 days). Analyzing high throughput experimentally (HTE) generated samples using standard reverse-phase HPLC and UPLC methods. Documenting laboratory work appropriately in laboratory notebooks and/or reports. Supporting minor instrument repairs, setup, software troubleshooting, and/or routine maintenance of LC, LC/MS, SFC, and UPLC/MS equipment. Preparing laboratory reagents. Analyzing/triaging data from a variety of software. Maintaining a safe, organized, and productive lab. Job requirements include, but are not limited to: BS - Chemistry or related field with 1-3 years of industry experience (preferably pharma). Strong time management skills and flexibility to handle urgent projects within given timelines. Excellent communication skills verbal and written. Very strong attention to detail and safety as well asproblem-solving skills. Demonstration of excellent team player 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. This job posting will close by 2/1/2026 or when a candidate is identified, whichever comes first.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Job Summary The position will be responsible for performing analytical testing on raw materials, intermediates, finished products, and to ensure compliance of all product quality attributes as defined in approved specifications. The incumbent will also participate in investigations (CAPA) and Deviation investigations when appropriate. This role will provide the opportunity to work within laboratory setting, giving exposure to different types of analysis. The successful candidate will have experience working within a GMP/GDP environment and possess excellent communication skills. Responsibilities: • Performing sample preparation and various analytical test procedures including chromatography (HPLC), spectroscopy (UV-Vis & IR), electrochemistry (pH, ORP, and conductivity), acid-base titrations, aliquoting, filtering, centrifuging, pipetting, and various other laboratory techniques. • Assisting in maintaining laboratory equipment, keeping accurate records, generating reports, and providing technical assistance to other departments. • Participating in Deviation investigations as needed. • Ensuring data integrity through good documentation practices. • Utilizing various software applications for data management and documentation purposes. • Other duties as assigned. Qualifications Minimum Qualifications: • Bachelor's degree in Chemistry or related field with at least 1 year of relevant industrial experience preferred. • Experience with HPLCs and basic wet chemistry • Knowledge of cGMPs and regulatory requirements. • Strong communication skills. • Ability to troubleshoot and problem-solve. • Ability to collaborate effectively across multiple disciplines. • Ability to generate reports and communicate results. • Basic computer skills. Preferred Qualifications: Experience with Empower Experience with Smartlab and Darwin Additional Information Position is Monday-Friday 8:00am - 5:00pm overtime as needed. Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

OPPORTUNITY: Analytical AKTA Chromatography Scientist **INTERVIEWS AVAILABLE THIS WEEK** Interested in this role? Reach out directly to ********************************* or CALL ************ with an updated resume to apply (HIRING NOW) We are looking for an innovative and highly skilled Analytical AKTA Chromatography Systems Scientist to join our Advanced Materials Purification Team. This position requires expertise in AKTA Chromatography, Fast Protein Liquid Chromatography (FPLC), ICP-OES / ICP-MS, and scale-up processes. In this role, you will operate and optimize automated chromatography platforms for the aqueous separation of high-value inorganic compounds. The ideal candidate will combine chemical analysis, process engineering, and automation to advance the development and scale-up of solvent-free purification workflows for specialty metals and oxides. Responsibilities + Operate, calibrate, and maintain systems and UNICORN control software for aqueous metal separation and purification. + Operate and maintain automated chromatography systems and control software for metal separation and purification. + Design and refine separation methods using ion-exchange, chelating, or size-based column technologies. + Prepare and condition columns for use with acidic, high-ionic-strength, or complex aqueous solutions. + Execute gradient and stepwise elution protocols while monitoring conductivity, pH, UV absorbance, and flow rates. + Collaborate with engineering and R&D teams to transition lab-scale methods to pilot and production environments. + Conduct mass balance assessments and generate recovery/purity profiles to support process validation. + Maintain detailed records of runs, chromatograms, and standard operating procedures. + Troubleshoot system components including fluidics, detectors, and valves to ensure consistent performance. + Train lab personnel on chromatography setup, operation, and maintenance best practices. + Support integration of analytical data with digital systems for automated reporting and process control. Qualifications Required + Bachelor's degree in Chemistry, Chemical Engineering, Materials Science, or a related field. + At least 1 year of hands-on experience with Cytiva AKTA Chromatography, automated chromatography systems, and control software. + Solid understanding of aqueous separation chemistry and metal purification techniques. + Experience with buffer preparation, column packing, and method optimization. + Strong documentation and troubleshooting capabilities. Preferred + Relevant field related to laboratory refining rare-earths, lithium, or other strategic metals. + Familiarity with chromatography scale-up and continuous separation systems. + Knowledge of trace analysis tools such as ICP-MS or ICP-OES. + Exposure to process analytical technology and automated fraction collection systems. Work Environment The position is based in a lab and pilot-scale setting focused on advanced separation technologies. Regular handling of aqueous solutions containing acids, salts, and chelating agents is required, alongside strict adherence to safety and contamination-control protocols. Frequent collaboration with multidisciplinary teams in R&D and process development is also part of the work environment. Interested in this role? SEE BELOW TO APPLY DIRECTLY FOR IMMEDIATE CONSIDERTATION: + I am scheduling interviews for this position TODAY and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Grace Williams + HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to grawilliams@actalentservices. com or CALL ************ Job Type & Location This is a Permanent position based out of Noblesville, IN. Pay and Benefits The pay range for this position is $80000.00 - $100000.00/yr. 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 Noblesville,IN. Application Deadline This position is anticipated to close on Jan 20, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.