Offres Science à Chicago, IllinoisCréer des alertes d'emploi

Job Description Job Title: Production Chemist (3rd Shift Weekends) Job Description This role is a hands-on Production Chemist position supporting multi-kilo scale chemical synthesis and active pharmaceutical ingredient (API) production. The position offers the opportunity to grow within both the chemistry and production tracks as the site expands its API manufacturing capabilities. Responsibilities • Perform chemical synthesis on a multi-kilo scale and execute all steps in accordance with approved batch records., • Maintain documentation to meet Good Manufacturing Practice (GMP) standards, including accurate recording of material charges and transfers, acknowledging actions as they are performed, and documenting key observations for each operation., • Set up, operate, monitor, and clean plant equipment such as reactors, centrifuges, filter dryers, shelf dryers, milling equipment, and related production systems., • Stage raw materials for production, including verifying identification and quantities prior to use., • Load raw materials into equipment and unload intermediates and finished products from dryers and other processing equipment., • Follow written procedures, batch records, and standard operating procedures (SOPs) to ensure consistent product quality and regulatory compliance., • Work closely with chemical engineers and other technical staff to produce research and development (R&D) APIs and support scale-up activities., • Apply wet chemistry techniques and basic chromatography where required in support of production activities., • Use computer systems, including Microsoft Office and other plant software, to complete production documentation, reports, and communications., • Write routine reports and correspondence to document production runs, deviations, and observations., • Communicate effectively in group settings to coordinate tasks, share status updates, and participate in shift handovers., • Handle chemicals safely using appropriate engineering controls, personal protective equipment, and established safety procedures., • Adhere to Good Laboratory Practice (GLP) and GMP requirements throughout all production activities., • Perform manual compounding and blending operations in accordance with batch records and quality standards., • Support compounding of pharmaceutical products, including weighing, mixing, and blending ingredients., • Assist with equipment troubleshooting and basic mechanical tasks related to production processes., • Follow all health, safety, and environmental policies, including proper use of respirators and other protective equipment., • Maintain a clean, organized, and compliant production area, including participation in routine housekeeping and 5S activities., • Prioritize and multitask across multiple production activities while adapting to changing priorities and schedules. Essential Skills • Ability to perform chemical synthesis on a multi-kilo scale and follow detailed batch records., • Strong understanding of Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) principles., • Ability to read and interpret batch records, standard operating procedures, and other technical documents., • Ability to write routine reports and correspondence in a clear and accurate manner., • Ability to speak effectively in a group setting to share information and coordinate work., • Hands-on experience with production equipment such as reactors, centrifuges, filter dryers, shelf dryers, and milling equipment., • Experience with compounding pharmaceuticals, including manual compounding and blending., • Proficiency with Microsoft Office and general computer skills., • Mechanical aptitude and basic math proficiency to support equipment operation, measurements, and calculations., • Ability and willingness to handle chemicals safely with engineering and safety controls in place., • Ability to lift up to 50 pounds and perform moderate physical activity., • Ability to stand for extended periods (more than 6 hours per day)., • Ability to multitask, prioritize work, and adapt to changing production needs., • Willingness to undergo annual physical and drug screening as part of ongoing employment requirements., • Ability to use a respirator in accordance with safety and health guidelines. Additional Skills & Qualifications • Associate or bachelor’s degree in chemistry or engineering preferred., • High school diploma considered with relevant industry experience as a chemical operator, batch mixer, or compounder., • Experience in a production environment such as chemical, pharmaceutical, or food manufacturing preferred., • Experience with SAP or similar enterprise resource planning systems is a plus., • Previous experience in pharmaceutical manufacturing is a plus., • Experience working with reactors in a manufacturing setting is a plus., • Experience with chromatography and wet chemistry techniques is beneficial., • Familiarity with API production, batch record documentation, and transfers is advantageous., • Demonstrated flexibility, adaptability, and willingness to learn in a growing production environment. Job Type & Location This is a Contract to Hire position based out of Niles, IL. Pay and Benefits The pay range for this position is $23.00 - $30.00/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 Niles,IL. Application Deadline This position is anticipated to close on Jul 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: 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. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionJob Title: Production Chemist (3rd Shift Weekends) Job Description This role is a hands-on Production Chemist position supporting multi-kilo scale chemical synthesis and active pharmaceutical ingredient (API) production on 3rd shift weekends. You will train on 1st shift Monday through Friday and then transition to a weekend schedule working four 10-hour shifts from 10:00 p.m. to 8:00 a.m. on Friday, Saturday, Sunday, and Monday. The position offers the opportunity to grow within both the chemistry and production tracks as the site expands its API manufacturing capabilities. Responsibilities • Perform chemical synthesis on a multi-kilo scale and execute all steps in accordance with approved batch records., • Maintain documentation to meet Good Manufacturing Practice (GMP) standards, including accurate recording of material charges and transfers, acknowledging actions as they are performed, and documenting key observations for each operation., • Set up, operate, monitor, and clean plant equipment such as reactors, centrifuges, filter dryers, shelf dryers, milling equipment, and related production systems., • Stage raw materials for production, including verifying identification and quantities prior to use., • Load raw materials into equipment and unload intermediates and finished products from dryers and other processing equipment., • Follow written procedures, batch records, and standard operating procedures (SOPs) to ensure consistent product quality and regulatory compliance., • Work closely with chemical engineers and other technical staff to produce research and development (R&D) APIs and support scale-up activities., • Apply wet chemistry techniques and basic chromatography where required in support of production activities., • Use computer systems, including Microsoft Office and other plant software, to complete production documentation, reports, and communications., • Write routine reports and correspondence to document production runs, deviations, and observations., • Communicate effectively in group settings to coordinate tasks, share status updates, and participate in shift handovers., • Handle chemicals safely using appropriate engineering controls, personal protective equipment, and established safety procedures., • Adhere to Good Laboratory Practice (GLP) and GMP requirements throughout all production activities., • Perform manual compounding and blending operations in accordance with batch records and quality standards., • Support compounding of pharmaceutical products, including weighing, mixing, and blending ingredients., • Assist with equipment troubleshooting and basic mechanical tasks related to production processes., • Follow all health, safety, and environmental policies, including proper use of respirators and other protective equipment., • Maintain a clean, organized, and compliant production area, including participation in routine housekeeping and 5S activities., • Prioritize and multitask across multiple production activities while adapting to changing priorities and schedules.Essential Skills, • Ability to perform chemical synthesis on a multi-kilo scale and follow detailed batch records., • Strong understanding of Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) principles., • Ability to read and interpret batch records, standard operating procedures, and other technical documents., • Ability to write routine reports and correspondence in a clear and accurate manner., • Ability to speak effectively in a group setting to share information and coordinate work., • Hands-on experience with production equipment such as reactors, centrifuges, filter dryers, shelf dryers, and milling equipment., • Experience with compounding pharmaceuticals, including manual compounding and blending., • Proficiency with Microsoft Office and general computer skills., • Mechanical aptitude and basic math proficiency to support equipment operation, measurements, and calculations., • Ability and willingness to handle chemicals safely with engineering and safety controls in place., • Ability to lift up to 50 pounds and perform moderate physical activity., • Ability to stand for extended periods (more than 6 hours per day)., • Ability to multitask, prioritize work, and adapt to changing production needs., • Willingness to undergo annual physical and drug screening as part of ongoing employment requirements., • Ability to use a respirator in accordance with safety and health guidelines.Additional Skills & Qualifications, • Associate or bachelor’s degree in chemistry or engineering preferred., • High school diploma considered with relevant industry experience as a chemical operator, batch mixer, or compounder., • Experience in a production environment such as chemical, pharmaceutical, or food manufacturing preferred., • Experience with SAP or similar enterprise resource planning systems is a plus., • Previous experience in pharmaceutical manufacturing is a plus., • Experience working with reactors in a manufacturing setting is a plus., • Experience with chromatography and wet chemistry techniques is beneficial., • Familiarity with API production, batch record documentation, and transfers is advantageous., • Demonstrated flexibility, adaptability, and willingness to learn in a growing production environment.Work Environment This position is based in a growing pharmaceutical production facility with a focus on API scale-up and manufacturing. The role operates on 3rd shift from 10:00 p.m. to 8:00 a.m. on Friday, Saturday, Sunday, and Monday, working four 10-hour shifts each week. New hires train on 1st shift, Monday through Friday, before transitioning to the weekend schedule. The site has recently received significant investment to expand its production capabilities, including construction to add additional production space. You will work in a small but expanding production area alongside a broader team that includes an R&D laboratory connected to a quality control (QC) lab. The environment is GMP- and GLP-regulated, with routine use of reactors, centrifuges, filter dryers, shelf dryers, milling equipment, and computer systems such as Microsoft Office and potentially SAP. Work involves extended periods of standing, moderate physical activity, and the use of respirators and other personal protective equipment in accordance with safety procedures. The culture supports growth and advancement within both chemistry and production functions as the site continues to expand its presence in the API and CDMO market. Job Type & Location This is a Contract to Hire position based out of Morton Grove, IL. Pay and Benefits The pay range for this position is $23.00 - $30.00/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 Morton Grove,IL. Application Deadline This position is anticipated to close on Jul 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: 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. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionProduction Chemist – 1st Shift (Weekend, 4x10s) Location: Onsite | Schedule: Friday–Monday, 8:00 AM – 6:00 PM Make an Impact in a Growing API Facility Join a rapidly expanding pharmaceutical manufacturing team where your work directly contributes to the development and production of active pharmaceutical ingredients (APIs). As a Production Chemist, you’ll play a hands-on role in multi-kilogram chemical synthesis within a GMP-regulated environment—working alongside engineering and technical experts to bring R&D processes to life at scale. This is an exciting time to join a facility investing heavily in new equipment, expanded production space, and future capabilities—offering strong career growth in both chemistry and manufacturing pathways. What You’ll Do • Execute chemical synthesis at scale following approved batch records and SOPs in a GMP environment, • Operate and maintain production equipment, including reactors, centrifuges, dryers, and milling systems, • Ensure high-quality documentation, recording material usage, process steps, and observations in real time, • Stage, verify, and handle raw materials safely and accurately, • Support API scale-up and tech transfer, collaborating closely with chemical engineers, • Perform compounding, blending, and processing activities while adhering to GLP/GMP standards, • Monitor processes and troubleshoot minor equipment issues to keep production running efficiently, • Maintain a strong safety mindset, using PPE and following all safety proceduresWhat You Bring, • Hands-on experience in chemical synthesis, compounding, or production operations (pharma, chemical, or food industries preferred), • Working knowledge of GMP/GLP environments and documentation practices, • Experience with process equipment such as reactors, dryers, or centrifuges, • Ability to read and follow batch records, SOPs, and technical documentation, • Strong attention to detail and commitment to quality and compliance, • Comfortable with physical work, including standing for extended periods and lifting up to 50 lbs, • Basic computer skills (Microsoft Office) and ability to document work accuratelyNice to Have, • Associate’s or Bachelor’s degree in Chemistry, Chemical Engineering, or related field, • Experience in pharmaceutical manufacturing or API production, • Familiarity with ERP systems (e.g., SAP), • Exposure to chromatography or wet chemistry techniquesWork Environment & Schedule, • 4-day workweek (Friday–Monday) with 3 days off during the week, • Modern, expanding production facility with major capital investment underway, • Collaborative but focused environment with close access to R&D and Quality teams, • Hands-on role involving production equipment, PPE use, and active floor workWhy Join Us?, • Be part of a high-growth API manufacturing site with significant expansion plans, • Gain exposure to process scale-up and advanced production technologies, • Clear opportunities to grow within both technical chemistry and operations leadership paths, • Work a unique weekend schedule that offers flexibility during the weekJob Type & Location This is a Contract to Hire position based out of Skokie, IL. Pay and Benefits The pay range for this position is $23.00 - $30.00/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 Skokie,IL. Application Deadline This position is anticipated to close on Jul 8, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: 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. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionJob Title: Production Chemist (2nd Shift Weekends) Job Description We are looking for a Production Chemist to join our team for the 2nd shift on weekends (Friday, Saturday, Sunday, and Monday) working from 1 or 2 pm to 11 pm or 12 am. This role involves working four 10-hour shifts. Initial training will be conducted on the 1st shift from Monday to Friday until the candidate is ready to transition to the weekend shift. Responsibilities • Perform chemical synthesis on a multi-kilo scale and execute tasks via batch records., • Maintain documentation standards to meet GMP requirements, including recording of charges/transfers and acknowledging actions as they are performed., • Document key observations related to specific operations., • Set up, operate, and clean all plant equipment such as reactors, centrifuges, filter dryers, shelf dryers, and milling equipment., • Participate in staging raw materials, loading raw materials into equipment, and unloading intermediates and products from dryers., • Read and interpret documents, write routine reports, and correspond effectively in a group setting., • Collaborate with Chemical Engineers to produce R&D Active Pharmaceutical Ingredients (API).Essential Skills, • Experience with chemical synthesis and multi-kilo scale operations., • Proficiency in maintaining GMP documentation standards., • Ability to operate and clean plant equipment., • Competence in reading and interpreting documents, writing reports, and speaking effectively., • Collaboration skills for working with Chemical Engineers.Additional Skills & Qualifications, • Associates or Bachelor’s degree in chemistry or engineering preferred; high school diploma with relevant industry experience accepted., • Computer proficiency required., • Experience in a chemical, pharmaceutical, or food production facility preferred., • Willingness to handle chemicals safely with engineering controls in place., • Mechanical aptitude and basic math proficiency., • Ability to lift up to 50 pounds and use a respirator., • Experience with SAP is a plus.Work Environment The role involves working on the 2nd shift during weekends, consisting of four 10-hour shifts from 1 or 2 pm to 11 pm or 12 am. Initial training will take place on the 1st shift from Monday to Friday. The company is small but growing, with recent investments enhancing production capabilities. The environment includes a small production area, with expansion underway. The R&D lab is connected to the QC lab, providing a unique opportunity for collaboration and growth. A 10% differential is offered for the 2nd shift after six months. Job Type & Location This is a Contract to Hire position based out of Morton Grove, IL. Pay and Benefits The pay range for this position is $23.00 - $30.00/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 Morton Grove,IL. Application Deadline This position is anticipated to close on Jul 3, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: 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. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Title: Quality Control Chemist 2 Department: Quality Control Reports To: Quality Control Supervisor Company Summary Dental Technologies, Inc. is a company specializing in the research, formulation, compounding and packaging of dental, orthodontic and oral pharmaceutical products. Our products include dental restoratives, core build-ups, bonding agents, orthodontic adhesives, prophylaxis paste, fluoride treatments, toothpastes, rinses, and varnishes. Dental Technologies maintains a quality system according to ISO 13485, FDA and MDR standards. Dental Technologies, Inc. is dedicated to excellence in research & development, manufacturing, in-depth testing, efficient packaging, and personalized service. We are committed to the highest level of integrity, quality, and service. Essential Duties and Responsibilities • Performs all required testing on drug products, cosmetics and medical devices according to product specifications, • Properly documents all calculations and results in a laboratory notebook as well as the company electronic laboratory testing database., • Communicates with production planners and compounders regarding statuses of incoming samples and ongoing testing., • Willingness to cross train to perform other roles within the lab and assist coworkers with testing as needed., • Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Participates in OOS investigations by providing data and supporting testing needs., • Writes Laboratory Investigation Reports (LIR) as required., • Identifies procedures that need to be updated and updates them with support as needed., • Performs basic troubleshooting of laboratory issues or quality issues in production, • Maintains a neat and orderly working environment., • Completes all training required per the Training Matrix for Quality Control Chemist 2., • Performs other tasks, as assigned. Required Qualifications • Bachelor of Sciencein Chemistry or related science and atleast 2 years of applicable laboratory experience, • Experience with wet chemistry techniques (including making standard solutions, titrations, using pH or other electrodes, etc.), • Experience with advanced laboratory techniques including analytical instrumentation (including at a minimum, HPLC, GC, and FTIR),, • Ability toapply concepts of basic algebra and geometryto lab related calculations, • Excellent attention to detail and organizational skills, • Multitasks, prioritizes, and meets deadlines intimelymanner, • Ability to work within a team and as an individual contributor in a fast-paced, changing environment Preferred Qualifications • Experience in a GLP/GMP environment inanFDA regulated manufacturing facility, • Familiarity with Out of Specification (OOS) investigationseither in a supporting capacity or writing capacity Pay Range The QC Chemist 2 is a non-exempt position that is paid hourly. Pay rate will be dependent on a number of factors including but not limited to knowledge, skills, and experience. EEO Statement Dental Technologies Inc. is proud to be an equal opportunity employer. Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Job DescriptionAnalytical Chemist Title: Analytical Chemist Location: Chicago, IL (on-site) Reports to: Director Laboratory Operations Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Our Chicago, IL site provides toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products. Position/Job Summary: The individual in this position is involved in studies that evaluate the safety and/or toxicity of various materials (e.g., pharmaceuticals, chemicals, etc.). This position involves formulating, developing and validating methodologies for dose formulation analysis. As needed, the Analytical Chemist supervises support personnel and reports to the Director of Laboratory Operations. This is a full-time on‑site position at our Chicago facility with no provisions for working remotely. Roles and Responsibilities: Frontage Laboratories is seeking a highly motivated and experienced Chemist/Scientist for the Dose Formulation Analysis (DFA) group supporting non-clinical toxicology studies conducted under GLP regulations. Key Responsibilities: • Develop, optimize, and validate analytical test methods for dose formulation analysis., • Preparation of formulations (e.g., solutions, suspensions, etc.) to be used in toxicology studies, • Perform analysis of dose formulation samples using HPLC/UPLC, • Analyze and interpret analytical data with high accuracy and scientific rigor, • Prepare and review Method Development/Validation and Dose Formulation Analysis (DFA) reports for GLP toxicology studies, • Function as Study Director on analytical validation studies, • Ensure compliance with GLP, SOPs, and regulatory guidelines, • Maintain analytical instruments and troubleshooting method/instrument-related issues, • Collaborate with toxicology, formulation, and study management teams to support study timelines, • Prepares SOPs and study specific methodologies, • Leads and coordinates activities of less experienced staff in specific assignments, • Interact with Study Directors and help define study priorities and schedules, • Implements and enforce the use of safety procedures, • Completes tasks within time and budget constraints, • Demonstrates the ability to contribute to the success of assignments, • Performs other duties as assigned Qualifications and Experience: • BS, MS, or PhD in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field., • Hands-on experience with HPLC and UPLC systems., • Experience with Mass Spectrometry will be preferred., • Strong experience in analytical method development and validation., • Experience supporting Non-GLP and GLP non-clinical toxicology studies is preferred., • Excellent scientific writing and documentation skills., • Ability to work independently and in a fast-paced CRO environment., • Experience in dose formulation analysis for toxicology studies., • Familiarity with FDA, OECD, and GLP regulatory requirements., • Experience with Agilent Open Lab software. Salary: $65-80k, negotiable based on experience. Benefits: • 401k Employer Match with immediate vesting, • Vision Insurance, • Medical and Dental Insurance with multiple coverage options, • FSA (Medical, Dependent Care, and Commuter), • Short Term Disability, • Long Term Disability, • Life Insurance, • Generous Paid Holidays and PTO Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Senior Environmental Geologist Hybrid Chicago, IL OR Glendale Heights, IL OR Lombard, IL Salary Range: $102,190 - $130,350 Provide geologic and consulting services for a broad array of environmental projects and clients. This may include performing and/or leading environmental site investigations, g

Stay connected: When projects need Chemistry expertise, we match you to opportunities based on your expertise and project needs. About Mercor’s talent network Join our Chemist Expert Network to connect with leading AI labs and companies seeking your expertise. About Mercor projects Experts in

The ideal candidate holds a Bachelor's degree in Chemistry and has at least 2 years of laboratory experience, particularly in wet chemistry techniques and analytical instrumentation. QC Chemist 2 in Lincolnwood, Illinois.

JD or MA in Political Science or closely related field. Applicants should provide a cover letter and curriculum vitae, which specifies undergraduate political sciences teaching experience and teaching training.

This Opportunity WSP is currently initiating a search for an Early Career Geologist for our Chicago, Illinois office.

TRC has long set the bar for clients who require more than just engineering, combining science with the latest technology to devise innovative solutions that stand the test of time.From pipelines to power plants, roadways to reservoirs, schoolyards to security solutions, clients look to TRC for brea