Offres Science à Indiana

Job Summary Supports Sustainability Services onsite program, including manual labor associated with chemical handling, lab pack duties, drum movements within the facility, drum bulking, drum crushing, assisting when extra personnel are needed and other duties as assigned. This is a support position focused on hazardous and non-hazardous waste related projects 7:00 a.m. - 4:00 p.m. M-F Essential Duties and Responsibilities To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Other minor duties may be assigned. • Ensure waste types are properly segregated, regulatory shipment windows are met, proper container labeling is adhered to, good housekeeping is maintained and accurate tracking logs are kept., • Identify best practices that assist customers in reducing waste volumes, increasing operational efficiencies, identifying optimal equipment usage and generating cost savings., • Segregate, label, mark and package waste materials in a safe and compliant manner., • Collect, pour, transfer, consolidate, repackage and package solid, liquid and sludge material., • Perform labor intensive activities such as container or drum collection, drum bulking, sorting trash for recyclables and loading of trucks., • Transfer waste into containers of different size., • Provide labor support at 90-Day Hazardous Waste Pad, when applicable., • May provide support or direction to less experienced Technicians., • Wears required personal protective equipment., • Participates and cooperates in safety process, including following written procedures, attending required training and scheduled meetings., • Immediately reports any unsafe conditions, incidents, injuries or property damage to supervisor., • Follows Environmental and Quality Management System (ISO 14001/9001) policy, procedures and operational controls related to job responsibilities. Qualifications The requirements listed below are representative of the qualifications necessary to perform the job. Education and Experience • Education: Bachelors Degree (accredited), • RCRA and DOT regulatory compliance experience preferred., • Ability to pass a respirator FIT test, • Valid Drivers License, • Ability to obtain a medical card & CDL within 6 months, • Labpacking experience preferred, • 40-hour HAZWOPER certification (or equivalent) or the ability to obtain such within 30 days of employment., • Manifesting hazardous and non-hazardous waste experience preferred., • Required to use motor coordination with finger dexterity (such as keyboarding, machine operation, etc.) most of the work day;, • Required to exert physical effort in handling objects up to 50 pounds most of the work day;, • Required to be exposed to physical occupational risks (such as cuts, burns, exposure to chemicals, etc.) most of the work day; If this sounds like the opportunity that you have been looking for, please click "Apply.

Production Chemist Schedule: Monday–Friday, 8:00 AM–4:30 PM (Overtime as needed) Position Summary The Senior Manufacturing Chemist is a key member of the production team responsible for manufacturing bulk radiopharmaceutical products in a highly regulated environment. This role supports production preparation, equipment maintenance, regulatory compliance, and continuous process improvement while ensuring safety, quality, and operational excellence. Key Responsibilities • Manufacture radiopharmaceutical products in compliance with SOPs, cGMP, and regulatory requirements., • Prepare production materials and supplies; manage production inventory., • Perform routine production equipment maintenance and troubleshooting, including complex technical issues., • Coordinate cross-functionally to meet manufacturing schedules and production targets., • Author and revise SOPs, batch records, protocols, and technical documentation., • Lead and support investigations including deviations, OOS events, CAPA, and Change Control activities., • Drive continuous process improvement initiatives to enhance reliability, output, and radiation safety., • Train and mentor Production Chemists as needed., • Support cost-savings initiatives and help achieve departmental safety, quality, and financial metrics., • Maintain regulatory compliance with U.S. and international agencies (FDA, NRC, EU, ISO, USP, etc.)., • Actively monitor and manage personal and team radiation exposure in accordance with established policies., • Maintain Class I Radiation Worker qualifications., • Assist with general laboratory housekeeping and support additional projects as assigned. Qualifications • Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or related field required., • Minimum 3 years of relevant manufacturing or production chemistry experience., • Experience working in a GMP-regulated environment., • Hands-on experience with chemistry-related production equipment., • Familiarity with radiation protection and handling radioactive materials preferred., • Experience with cyclotron solid targets, isotope dissolution, and separation preferred., • Ability to work independently in a fast-paced, deadline-driven manufacturing environment. Core Competencies • Strong problem-solving and technical troubleshooting skills, • Effective decision-making and leadership abilities, • Technical writing and documentation proficiency, • Attention to detail and organizational skills, • Collaborative, team-oriented mindset

Job Title: Environmental Field Chemist (Entry Level) Location: Indianapolis, IN Starting Pay: Up to $24/hr Contact to Hire - 9 months or sooner • Extensive training and advancement program including pay raises, • Open to recent graduates with no experience Our Client is looking for a entry level Environmental Field Chemist. They will be responsible for sorting, and transporting materials and waste. Will ensure compatibility and safety processes at all time for each job and lab pack services provided to customers. Essential Functions and Responsibilities • Ensures Health & Safety is the number one goal by following policies, processes, and acting in a safe manner at all times., • Provide Lab Packing services at customer sites maintaining compliance with applicable RCRA and DOT regulations and with established company SOP’s, • Sample and characterize customer waste, when necessary, • Assist in the segregation of chemicals by class; packing compatible materials in appropriate containers and preparing for transportation; completing necessary paperwork per job., • Determines and loads supplies needed for job completion and travels to various industry, laboratory, and school sites to perform lab pack services., • Assists in characterizing materials at field project sites., • Follows proper placarding and load segregation requirements when transporting materials., • Develop good client relations by effectively communicating with Customers., • Directs Field Technicians/Drivers assisting with waste collection., • Introductory knowledge of high hazard materials management /assessment and cylinder handling. Education: Four-year college degree (Science or environmental majors preferred) or 2+years related experience required. Experience: Prior lab packing or environmental waste experience preferred. • Knowledge and Abilities: This is a safety sensitive position. The ability to work in a constant state of alertness and in a safe manner is an essential function. Good knowledge and understanding of all federal, state, and local laws and regulations pertaining to the Environmental Services Industry. Excellent interpersonal skills necessary to effectively communicate with internal and external contacts.

Yoh is hiring a Manufacturing Chemist for our Pharmaceutical Manufacturing client in Noblesville, Indiana. Job Functions: • Ensure a safe and quality working environment through training, awareness, and compliance to safety guidelines, SOP’s and cGMP., • Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.)., • Manufacture radiopharmaceutical products, prepare production materials and supplies, perform general production equipment maintenance, and production inventory management., • Ensure regulatory compliance., • Create and optimize SOPs as needed., • Create and execute protocols as needed., • Support and execute Continuous Process Improvement (CPI) initiatives through implementation of CAPA, protocols and Change Control., • Author Quality Events as needed (deviations, OOS, CAPA, CC)., • Develop and promote equipment and process improvements which serve to improve reliability, increase output, and reduce radiation exposure., • Must actively manage personal radiation exposure as well as exposures of shift personnel per prescribed policies, procedures, and guidelines. Requirements/Education:, • Bachelor degree in Chemistry, Biochemistry, Chemical Engineering, or a related field., • 3 or more years of relevant experience required., • Experience with Chemistry related equipment, • Experience working in a GMP environment, • Familiar with cyclotron solid targets along with the dissolution and separation of radioisotopes preferred., • Familiar with radiation protection and safe handling of radioactive materials preferred. #IND-SPG Estimated Min Rate: $50000.00 Estimated Max Rate: $55000.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week), • Health Savings Account (HSA) (for employees working 20+ hours per week), • Life & Disability Insurance (for employees working 20+ hours per week), • MetLife Voluntary Benefits, • Employee Assistance Program (EAP), • 401K Retirement Savings Plan, • Direct Deposit & weekly epayroll, • Referral Bonus Programs Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:

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.

Job DescriptionSenior Analytical Chemist - Method DevelopmentHubot Tri-Pac, Inc. in South Bend, Indiana, United States (On-site) Hubot Tri-Pac, Inc. a contract development and manufacturing company (CDMO) specializing in liquid and aerosol filling for personal care and pharmaceutical marketers, is seeking an experienced Senior Analytical Chemist for immediate addition to our fast-growing team. Job Description The Analytical Chemist maintains a working knowledge of all Tri-Pac procedures, customer procedures and requirements, and follows Good Manufacturing Processes (GMP) and GLP. This individual must have good interpersonal skills with a collaborative team attitude that is customer focused, and quality driven. Responsibilities • Independently perform routine and complex testing for chromatographic and spectrophotometric methods (HPLC, GC, UV, IR, titration) of analysis for excipients, new chemical entities, drug products and stability samples, • Independently perform method evaluation/development/validation/verification and troubleshooting instruments and improvement of processes, • Support Cleaning Validation method development and sample testing., • Interpret data and make recommendations to management for improvement or potential concerns, • Compare laboratory data against specifications, prepare reports, and trend data where applicable to determine if results meet requirements, • Ensure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentation, • Ensure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigations, • Independently author standard operating procedures, analytical testing procedures, batch release testing forms, and create document templates for use by junior team members, • Create report templates and/or enter data into established reports/templates or software-based systems, • Review routine laboratory experiments for accuracy and provide guidance to junior team members to ensure future compliance, • Identify and recommend opportunities for improved efficiencies, internal/external client service and teamwork within the analytical group, • Serve as a point of contact for laboratory testing support and provide updates to laboratory supervision and/or client, • With supervision, support the scheduling and planning of internal/external client project work to ensure the highest levels of efficiency and quality standards are met, • Support the development of a quality environment by driving and monitoring quality standards within the team, • Become resident expert in the use of LIMS (perform supervisory sign-off for electronic reports) and other software-based systems, • Serve as a method troubleshooting resource to identify and document critical factors that affect method performance and assist peers in resolving method issues in a timely, cost-effective manner, • Assist laboratory management with the preparation and execution of laboratory investigations/deviations and CAPA., • Mentor and train new laboratory team membersEducation And/or Experience, • Experience with Medical Devices and/or OTC consumer products, • Lab Instrumentation including GC, HPLC, FTIR, • GMP, GLP, LIMS Thank you for your interest and consideration of a career with Tri-Pac, Inc. Tri-Pac, Inc. is an Equal Employment Opportunity / Affirmative Action Employer Powered by JazzHR KdAgVnJnar

Job Description Description: Aerospace Instructor for Aerospace client. Must have teaching/instruction/training experience. (Experience does not have to be in aerospace industry) 1. Electrical Instructor • Electrical Aircraft installations and assemble work, • Electrical Functional Test troubleshooting, • Electrical crimping, • Electrical soldering, • Basic mechanical skills 2. Aerospace Mechanical Skills Instructor • Electrical installations, Bonding & Grounding, • Aircraft assembly, Heavy Structure Drilling, and/or Maintenance, • Blueprints, productions standards, and/or Functional Test, • Aircraft systems operations, familiarization, and troubleshooting 3. Aerospace Seal Instructor • Experience in the application of Aircraft Sealant application, • Clean and apply a sealant to aircraft components 4. Environmental Health and Safety (EHS) Instructor Founded in 1998 on the idea that industry leaders needed a professional service, and workforce management expert, to fuel the development and execution of core business and technology strategies, BCforward is a Black-owned firm providing unique solutions supporting value capture and digital product delivery needs for organizations around the world. Headquartered in Indianapolis, IN with an Offshore Development Center in Hyderabad, India, BCforward’s 6,000 consultants support more than 225 clients globally. BCforward champions the power of human potential to help companies transform, accelerate, and scale. Guided by our core values of People-Centric, Optimism, Excellence, Diversity, and Accountability, our professionals have helped our clients achieve their strategic goals for more than 25 years. Our strong culture and clear values have enabled BCforward to become a market leader and best in class places to work. BCforward is an equal opportunity employer.About BCforward:\r\n\r\nFounded in 1998 on the idea that industry leaders needed a professional service, and workforce management expert, to fuel the development and execution of core business and technology strategies, BCforward is a Black-owned firm providing unique solutions supporting value capture and digital product delivery needs for organizations around the world. Headquartered in Indianapolis, IN with an Offshore Development Center in Hyderabad, India, BCforward’s 6,000 consultants support more than 225 clients globally.\r\n\r\nBCforward champions the power of human potential to help companies transform, accelerate, and scale. Guided by our core values of People-Centric, Optimism, Excellence, Diversity, and Accountability, our professionals have helped our clients achieve their strategic goals for more than 25 years. Our strong culture and clear values have enabled BCforward to become a market leader and best in class places to work.\r\n\r\nBCforward is an equal opportunity employer.

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: • Client Focused: We only succeed when our clients succeed., • Outstanding: We deliver meticulous results through outstanding performance., • Good: We act ethically and morally., • Employee-Centric: We honor and support our employees., • Nimble: We are prepared to adapt in an ever-changing industry., • Team-Oriented: We collaborate with each other and with our clients. We currently have a role available for a Pharma Bioanalytical Chemist. Job duties include, but are not limited to, the following: • Performing routine & non-routine LC/MS analyses., • Sciex/Analyst experience preferred., • Developing and optimizing LC/MS analytical methods., • Consistently producing standard curve and QC data that meet established validated assay criteria., • Operating and performing basic, routine maintenance and diagnostics on HPLC and mass spectrometers., • Using the LC/MS software to perform routine data processing., • Accurately preparing and labelling laboratory reagents, solutions and samples., • Consistently utilizing data file nomenclature and organizational conventions., • Tracking study submissions on the analyst/customer collaboration site. Job requirements include, but are not limited to: • BS-Chemistry (or related field) with 1-2 years of industrial experience., • Ability and willingness to adapt to changing project needs and timelines., • Works well both as a team and as an individual., • Excellent communication skills verbal and written. Ability to communicate issues as they occur., • Strong attention to detail., • Demonstration of excellent team player skills, very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions. The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery. This job posting will close by 4/1/2026 or when a candidate is identified, whichever comes first.

Job Description Entry-Level QA/QC Lab & Manufacturing Chemist Interested in this role? Apply directly today to Chaney Cornell at chcornell@actalentservices. com for immediate consideration Job Description We are seeking a motivated and detail-oriented Chemist to join our team in a dynamic industrial environment. This role offers excellent opportunities for professional growth and hands-on experience in chemical analysis, quality control, and process improvement. The team is responsible for all technical service work onsite at the client. While the position is largely lab-based, it also includes some responsibilities beyond the lab, such as maintenance of the product, cleaning out expired lubricants, and mechanical work on pumps. Responsibilities • Conduct quality control testing on production materials using techniques such as ICP, FTIR, pH, conductivity, and titrations., • Maintain and monitor chemical solutions used in industrial processes., • Perform microbiological and water treatment testing., • Troubleshoot issues on the production floor and support operational efficiency., • Collaborate with team members to identify and implement cost-saving and safety-enhancing initiatives., • Maintain lab tools, equipment, and workspaces to ensure readiness and compliance., • Manage inventory, track usage, and coordinate supply orders., • Cross-train across lab functions to provide coverage during absences., • Assist in developing testing protocols and reporting results., • Strong understanding of basic chemistry principles and lab techniques., • 1+ years experience in a manufacturing lab or QA/QC setting., • Familiarity with Microsoft Excel and Office Suite, including the ability to use formulas and create documentation., • Strong communication and problem-solving skills., • Ability to work independently and manage time effectively., • Associates or Bachelor's degree required, preferably in applied sciences, chemistry, biology, or a related field., • Unrelated 2 or 4-year degrees will be considered with relevant GMP/Lab/Quality experience. The position is based onsite at a fluid management facility in an industrial blue-collar plant setting. The lab is smaller in size but well-equipped with analytical equipment such as FTIR and ICP. The environment is climate-controlled, providing a comfortable workspace. Available shifts: • M-W 5:00 PM to 5:00 AM The employee will work a 3-day workweek for a total of 36 hours but will be paid for a full-time 40-hour workweek. Job Type & Location This is a Contract to Hire position based out of Lafayette, IN. Pay and Benefits The pay range for this position is $24.00 - $26.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Lafayette,IN. Application Deadline This position is anticipated to close on Mar 6, 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 for other accommodation options.

Job DescriptionChemist – Industrial Laboratory (3‑Day Workweek) Join a hands-on, fast‑paced industrial laboratory team providing full technical service support onsite at the client. This role is ideal for someone who enjoys both lab work and practical, in‑field problem solving. You’ll gain experience in chemical analysis, quality control testing, process troubleshooting, and cross-functional support—while benefiting from a compressed work schedule that offers excellent work–life balance. Position Overview The Chemist plays a key role in maintaining product quality, supporting production operations, and ensuring process efficiency. While primarily laboratory-based, this role also includes light mechanical work such as maintaining pumps, managing expired lubricants, and supporting chemical systems on the production floor. This is a great opportunity for someone who wants broad experience across analytical chemistry, quality testing, and industrial operations. Key ResponsibilitiesLaboratory Analysis & Testing • Conduct QC testing using ICP, FTIR, titrations, pH, conductivity, and other analytical methods, • Perform microbiological and water treatment testing, • Maintain and monitor process chemical solutions, • Assist in developing testing protocols and reporting findingsOperations & Troubleshooting, • Support production floor troubleshooting to resolve process or product issues, • Perform maintenance tasks related to product systems and pump equipment, • Participate in safety and cost‑reduction initiativesLaboratory Maintenance & Documentation, • Maintain lab equipment, tools, and workspaces to ensure compliance, • Manage chemical inventory, track usage, and coordinate ordering, • Cross‑train on multiple lab functions to provide coverage as needed, • Step into supervisory responsibilities when requiredEssential Skills & Experience, • Strong understanding of chemistry fundamentals and common lab techniques, • 1+ year experience in a manufacturing lab, QA/QC environment, or similar, • Proficiency with Excel and Microsoft Office (formulas, documentation, data entry), • Excellent communication, problem solving, and time management, • Ability to lift up to 70 lbs, • Comfortable working independently in a dynamic industrial settingAdditional Qualifications, • 2‑ or 4‑year degrees (including non‑science majors) considered with relevant lab/GMP experience, • Ability to commit to a long‑term 3‑day workweek (12‑hour shifts), • Experience in GMP, industrial chemistry, or production support is a plusWhy This Role Stands Out, • 3‑day workweek (36 hours), paid as a full 40‑hour week, • Options for day OR night shift, with 2–4 weeks of paid first‑shift training, • Exposure to a wide range of hands-on testing: ICP, FTIR, titrations, pH, conductivity, microbiology, water treatment, and more, • Cross-training across lab and operational functions, • Opportunities to support process improvement and safety initiatives, • Ability to step into supervisory responsibilities as you grow 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 Lafayette,IN. Application Deadline This position is anticipated to close on Mar 10, 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 for other accommodation options.

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

Job Description Earth Smart Environmental Solutions, LLC is seeking an Environmental Field Chemist to collect, identify, and package/lab pack various hazardous/non-hazardous waste and transport in accordance with EPA and DOT regulations. Other essential functions and responsibilities include: • Maintain knowledge and training of job aspects, • Undertake responsibility and compliance of jobsite, • Manage services and ensure client/customer needs are met or exceeded BS Degreed science curriculum (Chemistry, Environmental, Biology or other with General and Organic Chemistry) or industry related experience Preferred / Not Required Lab packing experience Preferred/Not Required Class A or B CDL with HAZMAT Endorsement considered a plus but Not Required Ideal candidate will be able to lift 50 pounds Clean Driving Record Veterans Preference - encouraged to apply Compensation based on experience Company DescriptionEarth Smart Environmental Solutions (ES2) is a Service-Disabled Veteran Owned Small Business that provides recycling, reuse and/or disposal of hazardous, universal, medical, pharmaceutical, non-hazardous, and solid waste while meeting or exceeding customer expectations for all of the United States. ES2 follows all local, state, and federal requirements and has maintained zero safety finding or notice of violations. ES2 is an equal opportunity employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity, or any other characteristic protected by law. Service members and veterans, and the spouses and family members of the service members and veterans are encouraged to apply.Earth Smart Environmental Solutions (ES2) is a Service-Disabled Veteran Owned Small Business that provides recycling, reuse and/or disposal of hazardous, universal, medical, pharmaceutical, non-hazardous, and solid waste while meeting or exceeding customer expectations for all of the United States. ES2 follows all local, state, and federal requirements and has maintained zero safety finding or notice of violations. ES2 is an equal opportunity employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity, or any other characteristic protected by law. Service members and veterans, and the spouses and family members of the service members and veterans are encouraged to apply.

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Position Title: QC Chemist (Raw Material) Work Location: Indianapolis, IN 46241 Assignment Duration: 12 months Work Schedule: 1st Shift Thursday–Sunday (8 am–6 pm) eventually Wednesday–Saturday Work Arrangement: 100% Onsite Position Summary: • The QC Chemist will support all technical aspect

This is a part-time 12-hours per week, 12 week, unpaid remote internship.

Job Description Senior Chemist - REQUIRES RELOCATION. Fully on site in Golden, Colorado Job Description This position is responsible for performing quality control laboratory testing for incoming, in-process, and finished products, while assisting in laboratory operations. The focus is on compliance with regulatory activities and company procedures, conducting analytical testing per Standard Operating Procedures (SOPs) and regulatory requirements including dissolution, material identification, and particulate analysis. Responsibilities • Purchase analytical chemistry equipment and consumables to support chemistry laboratory operations., • Maintain daily use, maintenance, and cleaning logs for laboratory areas and equipment., • Perform routine preventative maintenance of laboratory equipment to ensure accuracy of results., • Prepare Certificates of Analysis for review., • Perform data entry, trending, and record organization., • Support in drafting and reviewing procedures, change controls, risk assessments, deviations, and CAPA., • Design and conduct test method and equipment validations., • Bachelor’s degree in chemistry is preferred or equivalent experience in the field., • Five years of experience operating analytical laboratory equipment including UPLC, FTIR, UV-Vis, and Dissolution., • Experience in a cGMP-compliant facility., • Minimum 2 years experience with method transfer and method validation activities., • Good documentation skills and organizational skills to record lab procedures and results., • Critical thinking and decision-making skills., • Management experience., • General knowledge of qualitative and quantitative chemistry and mathematics principles., • Candidates with dissolution experience preferred., • Ability to work in a variety of positions such as sitting, standing, squatting, kneeling, reaching, and walking for prolonged periods of time., • Exposure to chemicals used during assay preparation with special safety precautions., • Must be able to use necessary equipment such as computers, scanners, or other technology devices as assigned. Here at Belmar, employees are the most valuable resource. The success of the company depends on your health and productivity. With this in mind, our goal is to deliver high-quality, competitive, and affordable benefits to promote the health and well-being of you and your family. Belmar Pharma Solutions provides employees with several benefits, and this document is designed to take you through a high-level overview of what this includes. As an employee, you will have access to additional information regarding Benefits and Perks with specific coverage details. Benefits Health, Dental, Vision + Voluntary Benefits Our comprehensive benefits package includes essential health, dental, and vision coverage designed to support employees and their families. We also offer voluntary benefits such as Critical Illness, Short Term – Long Term, and more. These benefits ensure access to high-quality care, enabling employees to stay healthy and proactively manage their wellness. One medical plan option offers company funded HSA contributions. 401(k) – Administered by Johnson Financial Group The 401(k) plan administered by Johnson Financial Group allows employees to save for retirement in a tax-advantaged account. With a straightforward contribution process, this plan helps employees prepare financially for the future. Belmar matches $1.00 for $1.00 on the first 3% for employee contributions and $0.50 on the $1.00 for the next 2% of employee contributions. If you contribute the full 5% you will get a 4% match. Employees are immediately vested. The 401k also allows ROTH contributions. Johnson Financial Group offers free one-on-one sessions with a Financial Advisor. Employee Assistance Program – Administered by NYLife The Employee Assistance Program (EAP), administered by NYLife, offers confidential support services to employees dealing with personal or work-related issues. From counseling to legal and financial advice, the EAP is a valuable resource to help employees navigate challenges. It’s FREE to use, and provides access and support 24 hours a day, 7 days a week for you and your family. This includes three face-to-face visits with a licensed counselor per issue per year. Whether your concerns relate to health, personal or family issues, work-related challenges, or legal/financial stressors, the staff of masters-level counselors, nurses, and therapist are available to help. Perks and Benefits of Working at Belmar Pharma Solutions Perks and Benefits 2 Time Off Paid Time Off (PTO) Belmar provides PTO to full- and part-time employees based on length of service. PTO is accrued and credited on a per pay period basis. When employees receive certain anniversary milestones, there are increases to the PTO accrual rate. All accrued and unused PTO carries over from year to year, but once an employee reaches the annual accrual maximums, no additional PTO is accrued and credited until amounts fall below those maximums. Maternity Leave Belmar values its employees and recognizes the importance of family. We offer a generous maternity leave policy with 12 weeks of paid leave to new mothers. This support reflects our commitment to employee well-being and work-life balance. All-In-One Wellness Subscription Wellhub is an all-in-one subscription service aimed at promoting overall well-being. Offering access to gyms, fitness studios, wellness apps, and more, Wellhub is designed to support both physical and mental health, helping employees feel their best. Employee Discount Programs Perks at Work is an employee discount platform offering exclusive savings on a wide range of products and services. From retail and travel to entertainment and wellness, this program helps employees save on everyday purchases and enjoy exclusive offers. Discounted Medications Belmar Pharma Solutions offers free medication for employees and their immediate family members for any compounded product on the master internal formulary from any of the Belmar family pharmacies. Compounds not on the master internal formulary or certain high-cost compounds are offered at a 50% discount of the patient-pay price. Over-the-counter (OTC) commercial products and supplements are offered at cost if regularly stocked by the pharmacy. Employees or family members are responsible for shipping costs if outside our free options. Perks and Benefits of Working at Belmar Pharma Solutions Perks and Benefits 3 Education Support Continuing Education Credits We offer continuing education credits for Pharmacists and Pharmacy Technicians to help you stay current with industry standards and enhance your professional skills. We offer multimedia courses that combine convenience with comprehensive learning, offering real-world scenarios, interactive exercises, and diverse content to suit different learning styles. These programs feature motivating simulations, flashcards, and self-paced online modules designed to enhance knowledge appl Workplace Type This is a fully onsite position in Bloomington,IN. Application Deadline This position is anticipated to close on Mar 12, 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 for other accommodation options.

Job Description We are seeking an Analytical Scientist to join an established pharmaceutical CDMO in the Bartholomew County, Indiana area! This person will support the company’s pharmaceutical and health-care product testing operations by performing routine and advanced chemical analyses, developing and validating analytical methods, and ensuring data integrity under current Good Manufacturing Practices (cGMP). Analytical Scientist (Temp- Hire), Monday- Friday 8am-5pm Responsibilities • Perform routine chemical analysis of raw materials, in-process samples, and finished products using wet chemistry and instrumental techniques., • Operate and maintain analytical instruments such as HPLC, GC, UV-Vis, FTIR, and other spectroscopy/chromatography tools (as applicable)., • Execute and troubleshoot analytical methods in accordance with established Standard Analytical Methods (SAMs)., • Record, compile, and interpret analytical data accurately in lab notebooks or electronic systems., • Prepare clear reports comparing results to specifications and escalate deviations as needed., • Follow cGMP and company quality standards in all laboratory activities., • Assist in developing, optimizing, and validating new analytical methods to support product development and quality monitoring., • Perform routine instrument calibration, preventive maintenance, and quality control checks Qualifications • Bachelor’s degree in Chemistry, Analytical Chemistry, or a related scientific discipline (higher degree preferred)., • Prior experience in analytical laboratory work — especially involving pharmaceutical quality testing — is a strong advantage., • Familiarity with wet chemistry, instrumental analysis, and data reporting in cGMP environments., • Experience with HPLC, GC, FTIR, UV/Vis, or related instrumentation. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! Company DescriptionSince 1995 Astrix has been delivering information technology consulting, regulatory advisory services and staffing solutions to the scientific community. We can assist in augmenting your internal resources to deliver optimum solutions on time and within budget. It is our goal to simply do it right. We work everyday to create value and build trust with our clients, employees, partners and vendors. Astrix provides scientists to a broad spectrum of scientific based industries including: Chemical, Biotech, Pharmaceutical, Cosmetics, Food Science, Flavors and Fragrances, Biomedical, Consumer Products, Environmental, Medical device, Petrochemical and Clinical Research.Since 1995 Astrix has been delivering information technology consulting, regulatory advisory services and staffing solutions to the scientific community. We can assist in augmenting your internal resources to deliver optimum solutions on time and within budget. It is our goal to simply do it right. We work everyday to create value and build trust with our clients, employees, partners and vendors.\r\n\r\nAstrix provides scientists to a broad spectrum of scientific based industries including: Chemical, Biotech, Pharmaceutical, Cosmetics, Food Science, Flavors and Fragrances, Biomedical, Consumer Products, Environmental, Medical device, Petrochemical and Clinical Research.

Job Description Purpose This position is responsible for assisting with research and development, validations of testing methods, and documentation. The primary focus of this role is transformer oil analysis, including method development. Essential Functions Weight of associated position responsibility, duty or task to successful performance: • 15%, • Complete activities associated with document management:, • Maintain current Material Safety Data Sheets (MSDS) in files for the organization and binder for the Indianapolis facility, • Maintain chemical inventories, • Create documentation, work instructions, forms, etc. as needed for new and existing procedures, • Create Excel spreadsheets to document research results, • 15%, • Enter data into various spreadsheets on a routine basis, • 25%, • Complete activities associated with supplies management:, • Assist in procuring materials for the department, • Assist in assessing potential equipment purchases, • Inspect, maintain and repair laboratory equipment, • 45%, • Provide Research Chemist Support, • Conduct test to validate analytical procedures, • Assist with PT process for all labs, • Assist with evaluation of apparatus and methods to determine feasibility of additional in-house testing, • Perform routine lab analysis as necessary The individual must possess the following knowledge, skills and abilities and be able to perform the essential functions of the job, with or without reasonable accommodation. • Ability to work autonomously, • Effective management of time and deadlines, • Intermediate knowledge Excel, • Chemistry degree or equivalent combination of education and related experience required The preferred qualifications desired in terms of education, course concentration, work experience, technical knowledge and desired advanced certifications. • Adherence and support of the POLARIS Employee Handbook inclusive of the Standards of Conduct, • Learn and support the Quality Management System, • Learn and support POLARIS Lean Initiatives, • OSHA laws require the use of the following Personal Protective Equipment (PPE) when performing work duties that have the potential of risk to your health or safety. At POLARIS Laboratories, when going through the Laboratory it is required that you wear eye protection., • To ensure safety throughout the facility, all employees are required to maintain up to date HAZMAT, OSHA, RCRA, Methylene Chloride, and General Laboratory Safety training as defined within the POLARIS Quality System.

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

Job DescriptionCompany Description 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 Responsibilities include, but are not limited to, the following: • Perform routine analytical testing of medium to high complexity drug substance/drug product and/or method verification/characterization using instrumentation including, but not limited to, HPLC, GC, UV spectrophotometer, dissolution apparatus, pH meter, water activity meter, Karl Fischer titrators., • Participate in conducting investigations, • Document test results in notebooks and reportsQualifications, • Bachelor's degree in biology, biochemistry, chemistry or other related degree concentration, • At least 10-15 years of related laboratory experience, • Authorization to work in the United States indefinitely without restriction or sponsorship, • 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 with internal and external clients, 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, • Proficiency in IT related skills such as Microsoft excel, word, PowerPoint, etc., • Candidates located within a commutable distance of Indianapolis, IN are encouraged to apply. Additional Information • The position is full-time, Monday through Friday, 8 a.m. to 5 p.m.,, • May be requested to work on weekends, overtime, and holidays based on business needs., • Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply., • Ability to work overtime as required., • 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