Quality control analyst jobs in Crown Point, IN

Adecco is hiring immediately for Quality Associates with a top local client in Joliet, IL. Be part of a team that's making a difference by preparing fresh meal kits for delivery- keeping our customers happy and satisfied! Starting Pay: $17.50/hr + Overtime Opportunities! Weekly Pay so you get your earnings fast! Comprehensive Benefits: medical, dental, vision, and 401(k) options available. Generous Referral Bonuses - Bring a friend and get rewarded! What You'll Do: Ensure food safety standards are met at all times Follow and enforce strict manufacturing policies and procedures involving allergen control, Organic and Gluten segregation Verify completeness and accuracy of daily production documentation Complete daily sanitation, facility, and quality documents as needed What We're Looking For: Entry level - no experience needed! Ability to read, write and speak English fluently Previous food, grocery, or restaurant experience preferred, but not required Basic computer skills required Must be able to stand for the entire shift. Ability to lift up to 50 lbs. and stay flexible as tasks may vary. Ready to Apply? Click "Apply Now" for immediate consideration and take the next step in your career with Adecco! Pay Details: $17.50 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: 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.

The Department of Physical Medicine and Rehabilitation at Northwestern University Feinberg School of Medicine, in collaboration Shirley Ryan AbilityLab, seeks a full-time non-tenure-eligible Team Scientist at the rank of Assistant Professor, Associate Professor, or Professor. The position is based at Shirley Ryan AbilityLab, with opportunities for collaboration with Northwestern University Departments of Biomedical Engineering, Mechanical Engineering, Physical Therapy & Human Movement Sciences, Neurology, Neurosurgery, Neuroscience, and Physical Medicine & Rehabilitation. Responsibilities include: * Develops and submits research proposals and grant applications to secure external research funding from agencies such as the NIH, VA, NIDILRR, DoD, NSF and private foundations. * Ensures that scientific and regulatory milestones of specific projects are met. * Publishes original studies in refereed journals that advance our understanding of motor control, and translation science linked to neurologic illness. * Demonstrates leadership activity in professional organizations such as the Society for Neuroscience, the International Society for Society for Neuroscience, Neural Control of Movement, Progress in Motor Control, etc. * Contributes to the educational of highly qualified personnel including graduate students, post-doctoral fellows, medical students, and residents. * Participate in and collaborate on Department activities, as requested by the Department Chair. Qualified candidates: * Knowledge of measurement and statistics principles acquired through a Ph.D. in a scientific discipline from an accredited school and successful completion of a postdoctoral fellowship. * Minimum 2 years of related experience with an expert knowledge of scientific principles and concepts. Reputation as emerging leader in field with sustained performance and accomplishment. * Uses professional concepts in accordance with institute objectives to solve complex problems in creative and effective ways. * Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought. * Works on complex problems and designs/conducts research projects in which analysis of situations or data requires an in-depth evaluation of various factors. * Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. * Requires proficiency in writing to prepare grant proposals, research reports and other publications, and explain complex results to a lay audience. * Interpersonal skills needed to communicate effectively with other staff members, fellow researchers. * May determine methods and procedures on new assignments and may provide guidance to other lower level personnel. * Commitment to teaching and teaching ability are requirements The start date is negotiable and the position will remain open until filled. When applying, please upload a CV and cover letter describing your interest and alignment with the position. Also upload a list of individuals who could write letters of reference on your behalf. Please read ALL instructions and make preparations before proceeding to the application page: * Applications will only be accepted via online submission (see link below). * Please prepare all documents in advance as Adobe PDF files, and please be sure all information is entered correctly and accurately (especially names and email addresses), as there will be no opportunity for online revision after your application has been submitted. * All required fields in the application form are marked with an asterisk and must be filled before clicking the "Submit" button. * Be aware that incomplete applications cannot be saved. Applications accepted here: Apply for Job Northwestern University is an Equal Opportunity Employer and does not discriminate on the basis of protected characteristics, including disability and veteran status. View Northwestern's non-discrimination statement. Job applicants who wish to request an accommodation in the application or hiring process should contact the Office of Civil Rights and Title IX Compliance. View additional information on the accommodations process.

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. This is Contract position with my direct client Job Description Understands and works within a broad range of guidelines, standard operating procedures and/ or technical methods that involve a variety of routine work procedures with a moderate degree of supervision. Perform analytical testing on raw materials, intermediate products, and finished goods adhering to GLPs, GMPs , and EHS requirements Performs laboratory activities in a timely manner to meet manufacturing and product delivery deadlines. Interpret analytical data relative to specifications, process controls, and other analytical references. Perform investigations on aberrant data and initiate deviation reports. Maintain and control quality records in compliance with regulatory requirements. Conducts laboratory support functions. Maintains supply levels to ensure availability. Understands the team organization and how the team cooperates with other teams in the area to jointly achieve objectives. Strong organizational skills with the ability to handle multiple conflicting resource requirements. Qualifications Excellent communication skills Strong computer skills including Excel and Access; Minitab a plus. Additional Information Regards, Sweta Verma IT Recruiter Integrated Resources, Inc. Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012 & 2013 (7th Year) Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70 Direct:- 732 549 5907 Tel: (732) 549 2030 x 210 Fax: (732) 549 5549 sweta(at)irionline.com http://www.irionline.com https://www.linkedin.com/nhome/?trk=nav_responsive_tab_home

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: At MilliporeSigma, the Quality Control Scientist is responsible for performing multi-discipline analytical test methods for a variety of product lines to help achieve overall business objectives. This role is also responsible for maintaining the Product Stability, Product Retention, and Reverse Osmosis Water Quality Programs in accordance with the current regulatory guidelines. Additionally, this role supports Special Projects and Process Engineering analytical requirements to maintain existing, and future, business development. * Understands and works within a broad range of guidelines, standard operating procedures and/ or technical methods that involve a variety of routine work procedures with a moderate degree of supervision * Performs analytical testing on raw materials, intermediate products, and finished goods adhering to GLPs, GMPs, and EHS requirements * Performs laboratory activities in a timely manner to meet manufacturing and product delivery deadlines * Interprets analytical data relative to specifications, process controls, and other analytical references * Performs investigations on aberrant data and initiate out of specification reports * Maintains and control quality records in compliance with regulatory requirements * Conducts laboratory support functions. Maintains supply levels to ensure availability * Performs simple laboratory instrument upkeep including the cleaning, calibration, and the preventive maintenance of the instrument * Performs high-level instrument troubleshooting activities * Participates in audit readiness * May work a 2 week 12-hour shift cycle on either a day or night shift assignment Who You Are: Minimum Qualifications: * Bachelor's Degree in Biology, Chemistry, Microbiology, or other life science discipline OR * Associate's Degree in Biology, Chemistry, Microbiology, or other life science discipline AND 2+ years' work experience in a research or lab environment Preferred Qualifications * Knowledge of analytical chemistry, analytical microbiology, analytical biology, environmental monitoring, and plant hygiene processes and procedures * 1+ years of experience working in a cGMP Quality Control Laboratory * 1 + years of experience working with laboratory equipment such as (HPLC, GC, UV/Vis, TOC, AA, and KF) Pay Range for this position - $26-$44/hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

About Crown: CROWN Cork & Seal USA, Inc., a wholly owned company of Crown Holdings, Inc. is a global leader in the design, manufacture, and sale of packaging products for consumer goods. At Crown, we are passionate about helping our customers build their brands and connect with consumers around the world. We do this by delivering innovative packaging that offers significant value for brand owners, retailers, and consumers alike. With operations in 39 countries employing approximately 23,000 people and net sales of approximately $12 billion, we are uniquely positioned to bring the best practices in quality and manufacturing to our customers to drive their businesses locally and globally. Sustaining a leadership position requires us to build a team of highly talented, dedicated, and driven individuals. Division Overview: Crown's Beverage Division manufactures a variety of packaging solutions for soft drinks, craft beers, coffees and teas as well as new energy drinks. Crown Beverage leads the packaging industry with innovative technologies that redefine how the world looks at beverage cans. With a large printable surface area and a wide range of sizes, shapes and decorating options, our aluminum cans are the perfect packaging format to create compelling brand presence where it counts. Here is your chance to join the Crown Beverage Division. Location: 1035 E. North St. Bradley, IL. The Quality Control Technician works closely with Supervision and to ensure optimum levels in Quality Inspections, Testing, Package identification, and Final packaging. Duties And Responsibilities: Reporting directly to the Quality Assurance Manager and Production Supervisor, the Quality Control Technician responsibilities would include, but not be limited to, the following: Understand and follow verbal instructions to completion of assigned tasks. With focus on Safety and Spoilage, the responsibility of the Quality Control Technician will ensure a quality product is produced thru inspections and testing. Responsible for the quality of all operations of all process for the production of aluminum beverage cans. Ability to identify quality problems, and disposition. . Communicates all pertinent information between management, co-workers, and between shifts on changes to equipment, production problems or any other related information. Assists and trains and/or coaching of all new Technicians as needed or required. Applies skills, methods learned to improve plant production. Responsible in following JHA's, SOP's, Rules, 6S Housekeeping, maintaining gauging equipment and modifications of existing production standards to achieve optimal efficiencies Enter information into a computer to document data. Accurate and continuous quality checks and record keeping required. Complete and/or administer necessary documentation such as monthly SAFE cards, accident/near miss/hazard reporting, and data process control input. Performs other job-related duties as required or assigned. JOB REQUIREMENTS * In addition to the specific responsibilities listed above, the ideal candidate will possess the following: Minimum Requirements High School Education/GED 2-3 year(s) experience with computer skills in inspecting, testing, packaging and high speed manufacturing environment. Basic Computer skills required. Must be available to work various shifts if needed and be able to work nights, weekends, and overtime to cover absences or provide additional support. Preferred Requirements but not mandatory: Knowledge of all OSHA related training in a manufacturing environment. Beverage Packaging Quality industry experience Knowledge of AS400, QAS, and NWA 6S Training Competencies Problem solving skills through an individual and/or collaborative approach Ability to work independently or with a team. With consensus be able to look at new solutions and “think outside the box”. Effective leadership skills such as conflict resolution, communication, decision making, etc. Demonstrated good relations skills and the ability to motivate or team with people. Excellent time management skills and multi-tasking. Excellent oral and written communication skills. Computer skills and working knowledge of various Microsoft programs (Excel, Word, Access, etc.). Physical Requirements While performing the duties of this job, the associate is regularly required to sit, stand, walk, use hands, reach with hands and arms, and may be required to balance, stoop, kneel, crouch, or crawl. May be required to climb stairs to upper level at times. The associate may lift and/or move up to 50 pounds. Working Conditions Generally works in a manufacturing, office, packaging, and warehouse environment. While performing the duties of this job, the associate will be exposed to light lifting, warehouse forklift traffic. Production noise level is frequently loud. *Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Benefits: Crown offers competitive pay, comprehensive benefits including free company paid health insurance for employees as well as company matched 401(k). COMPENSATION: Actual salary will be determined based on skill and experience level. Pay rate $ 27.96- $ 28.57 per hour. Starting at $ 27.96 per hour. Interested: Take the next step in your career and apply online today at www.crowncork.com/careers. EEO/AA/Vets/Disabled

! Weee! is the largest and fastest-growing ethnic e-grocer in the United States, operating in one of the largest underserved categories in retail with affordable access to exciting ethnic food. By partnering with local suppliers, redesigning the value chain and leveraging social buying, Weee! is reshaping the grocery business entirely. You can read more about us on Business Insider, Reuters and TechCrunch. Weee! is headquartered in Fremont, CA, and is currently available coast to coast with exceptional growth (5x YoY) across geographies, categories and ethnicities. We have raised $800M+ in funding to date from leading investors including Softbank Vision Funds, DST, Blackstone, Tiger Global, Lightspeed Ventures, Goodwater Capital, XVC and iFly. The opportunity now is to join a rocketship as we prepare for the next stage of growth, and an eventual public listing. This role is onsite 5 days a week in Hodgkin, IL About the Role The ICQA Specialist II will be responsible for overall inventory accuracy and managing shrinkage , including investigating customer complaint cases related to the inventory issues within the Fulfillment Centers. The location will be in Hodgkins, IL. Roles & Responsibilities Lead day-to-day work direction for ICQA Cycle Counters and Specialist I associates, including task assignment, productivity monitoring, and coaching Conduct advanced inventory discrepancy research and root cause analysis; develop and implement corrective action plans Analyze operational trends and build reporting tools using advanced Excel capabilities and tableau capabilities Supervise execution of cycle counts, bin audits, and quality checks to ensure operational accuracy and compliance Facilitate training for warehouse associates on operational SOPs to improve inventory related metrics Plan physical inventory events including planning, execution, and reconciliation Improve inventory-related processes and collaborate with department leaders to enhance KPI performance Ensure safety, food-safety, and compliance standards are upheld at all times Communicate performance results and systemic issues to leadership with clear documentation and recommendations Qualifications Bachelor's Degree required; Masters's degree preferred 5+ years of warehouse or operations experience, with at least 2 years focused in inventory management Demonstrated experience providing task leadership, mentorship, or people-focused supervision Advanced proficiency in spreadsheet and data analytics and visualization Strong investigative and analytical skills with the ability to interpret complex data Excellent verbal and written communication skills Proven ability to work effectively under pressure, handle multiple priorities, and meet deadlines in a fast-paced environment Experience supporting process improvement or continuous improvement initiatives preferred Requirements Ability to work 5 days onsite Ability to work shift schedules, including nights, weekends and holidays as business needs Must be able to work in freezer (-10°F to 32°F), refrigerated, and ambient warehouse environments for extended periods Must be able to lift and move up to 50lbs and perform physically active work throughout the shift Ability to stand, walk, bend, and reach for extended durations Must demonstrate reliability, adaptability, and resilience in high-volume operational settings Ability to reach above shoulder level at 72 inches (6 feet) without assistance Ability to work at elevated heights up to 30 feet Benefits Comprehensive health insurance package, including medical, dental, and vision. PPO/HMO packages 401k, 4% company match Equity and Bonus Vacation, sick and holiday time off Monthly mobile stipend Monthly Weee! Points credits Compensation Range The US base salary range for this full-time position is $53,000 - $63,000 This role may be eligible to discretionary bonus, incentives and benefits Our salary ranges are determined by role, level, and location The range displayed on each job posting reflects the minimum and maximum base salary for new hires for the position across all US locations. Within the range, individual pay is determined by multiple factors like job-related skills, experience and work locations. Your recruiter can share more about the specific salary range during the hiring process. Please note that the compensation details listed in US role postings reflect the base salary only, and do not include any variable compensation elements. Weee! is an equal opportunity employer welcoming all qualified applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status or any other basis prohibited by law. Discrimination or harassment of any kind is not tolerated at Weee!. If you need to inquire about an accommodation or need assistance with completing the application, please email us at applicantaccommodation@sayweee.com . For more jobs and to find out more about Weee!, visit our career page: ********************************* Softbank Vision Funds

Quality Control Associate (Entry Level) * Inspect and document vehicles for carrier damage * Verify reported vehicle damage on and off rail cars * Help manage facility access until repairs are completed * Transmit damage document to the OEM reporting sites (Data Entry) * Report damages in the BNSF system * Training Provided Areas of Responsibility: * Comply with all industry, client, and company safety regulations and operating procedures * Work independently and with a team * Other tasks as assigned What's Required: * High School Diploma or GED * Safety first mentality * Able to meet attendance requirements * Basic knowledge of Microsoft Office Suite * Able to work on rail cars in all elements (outside position) * Valid driver's license Type: F/T Pay: $20/ hr Hours: Wed-Sun 8:30AM-5:00PM We Offer: * A Full Benefits package including Medical, Dental, 401K * Paid Holidays and Vacations * An annual Steel Toe Boot allowance * All Personal Protective Equipment (PPE) provided * Veteran Friendly * We love to promote hard workers Company Overview: Established in 1987, Road & Rail Services has grown and diversified to become a leading provider of rail-related services in North America. Our network of skilled associates provides plant and terminal operating expertise as well as field maintenance of rail assets for railroads, rail shippers, and owners of rail related equipment and facilities. Visit us online at ******************* for more information!

Animal Health Corporation Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals. Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro's revenues are in excess of $1 billion and are supported by over 2,400 employees worldwide. At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be. If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions. The Laboratory Analyst III is an integral part of our Quality team based out of our US - Chicago Heights, IL site. Hourly rate range for this position is $25.00 - $25.00 Position Details The Laboratory Analyst position supports the Medicated Feed Additives (MFA) business of Phibro in Chicago Heights, IL. The Quality Control laboratory provides testing and release support for multiple sites in the MFA network, in addition to analytical support for contract manufacturing. The preferred candidate will meet the criteria for an Analyst III, IV, or V level, as described below. Key Responsibilities Receives and prepares samples for analytical testing and initiation of stability studies. Performs physical testing of routine and non-routine samples with little supervision including but not limited to raw materials, in process testing, API & finished good release and stability testing. Supports the site quality, safety and production needs and goals compliantly. Works within cross-functional teams. Coordinates own work assisting the lab to complete priority projects. Completes all activities following site cGMP, Safety requirements and Phibro Standards. Conducts laboratory activities related to experiments, studies, and projects in support of production, laboratory, or other Phibro groups: Understands and follows GMP/GLP regulations. Data maintenance and record keeping are in accord with GMP and SOPs Participates in projects and follows through to completion. Supports laboratory operations using technical ability to run routine samples independently. Recognizes abnormal results and/or instrument problems and reports them to supervision providing input to cause and possible solutions. Key Responsibilities Continued Performs routine tests and experiments following compendial or standard procedures Has an understanding and has applied skills related to Lean & 5-S. Sets up, adjusts and operates laboratory basic equipment such as balances, pH meter, sieves, ovens and has an understanding and has used advanced laboratory equipment such as Viscosity, Karl Fischer, UV/VIS, HPLC, GC. Maintains and follows Standard Operating Procedures dealing with their work area and can apply knowledge to assist in other work areas. Generation of protocols and execution of projects with little oversight. May lead a project and be responsible for completion. May assist with the writing and revising of procedures. May be assigned to projects dealing with special samples needing method modifications, with close supervision. Records tests results on standardized forms and prepares reports describing procedures used. Prepares charts and graphs to assist in evaluation and interpretation of data. Key Responsibilities Continued Completes investigations into aberrant data and generation of summary reports for their own work, can apply problem solving techniques in a team environment. Considered a Subject Matter Expert in Procedures for their area, providing training in and out of their department. Maintains a safe and clean working area and assists others in same. Will work with Analysts, Scientists and Management staff on a routine basis for the receipt and preparation of QC Test Samples and Stability study samples. Follows good documentation practices. Adheres and demonstrates exemplary behaviors. Identifying EHS hazards and propose solutions to improve lab/safety compliance. Key Competencies AccountableAccepting DirectionAttendance and PunctualityAttentive ListeningCollaborativeCommunicating EffectivelyCritical ThinkingDelivering High Quality WorkDemonstrating InitiativeDetailed OrientedDisplaying Technical ExpertiseFollowing Policies and ProceduresInteracting with People at Different LevelsManaging TimePrioritizing and Organizing WorkProblem SolvingWorking SafelyTechnical Skills Requirements Excellent attention to detail. Ability to use and perform HPLC, UV, GC and other instrumental techniques. Ability to generate protocols and summarize data. Ability to communicate within and outside immediate department. May contact vendors and/or external customers for administrative and technical information. Ability to work weekends and off shifts, as needed. Computer literate with the following applications: MS Excel, Word, Access Ability to utilize application software such as: Empower, Trackwise, JDE. Familiarity with Lean concepts and 5-S. Skills High degree of time management skills and ability to handle multiple priorities and projects at once.Prioritizes and plans work activities, uses time efficiently and develops realistic action plans.Excellent Written and Verbal Communication SkillsProven ability to work effectively in a team environment.Education & Experience ANALYST III High School degree or equivalent with approximately 10 years lab experience, preferably in an FDA regulated environment; or 2-year degree with approximately 3 years' experience or B.S. degree in a related scientific field with approximately 1.5 years of experience. ANALYST IV High School degree or equivalent with approximately 15 years lab experience, preferably in an FDA regulated environment; or 2-year degree with approximately 5 years' experience or B.S. degree in a related scientific field with approximately 3 years of experience. ANALYST V High School degree or equivalent with approximately 20 years lab experience, preferably in an FDA regulated environment; or 2-year degree with approximately 10 years' experience or B.S. degree in a related scientific field with approximately 5 years of experience. Physical Requirements Operations of laboratory equipment Required to bend frequently Required to sit frequently Required to stand frequently Required to talk or hear constantly Required to use hands constantly Required to walk frequently Specific vision abilities include ability to adjust focus Specific vision abilities include close vision Specific vision abilities include depth perception Specific vision abilities include distance vision Specific vision abilities include perpheral vision To learn more about Phibro Animal Health's competitive benefits package, please click here: Phibro Benefits. Phibro is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law. Business Unit: Animal Health & Mineral Nutrition Division: Animal Health & Nutrition Department: Quality Location: US - Chicago Heights, IL Work Schedule: Monday - Friday (Standard Work hours)

About Phibro Animal Health Corporation Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals. Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro's revenues are in excess of $1 billion and are supported by over 2,400 employees worldwide. At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be. If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions. The Laboratory Analyst III is an integral part of our Quality team based out of our US - Chicago Heights, IL site. Hourly rate range for this position is $25.00 - $25.00 Position Details The Laboratory Analyst position supports the Medicated Feed Additives (MFA) business of Phibro in Chicago Heights, IL. The Quality Control laboratory provides testing and release support for multiple sites in the MFA network, in addition to analytical support for contract manufacturing. The preferred candidate will meet the criteria for an Analyst III, IV, or V level, as described below. Key Responsibilities * Receives and prepares samples for analytical testing and initiation of stability studies. * Performs physical testing of routine and non-routine samples with little supervision including but not limited to raw materials, in process testing, API & finished good release and stability testing. * Supports the site quality, safety and production needs and goals compliantly. * Works within cross-functional teams. * Coordinates own work assisting the lab to complete priority projects. * Completes all activities following site cGMP, Safety requirements and Phibro Standards. * Conducts laboratory activities related to experiments, studies, and projects in support of production, laboratory, or other Phibro groups: * Understands and follows GMP/GLP regulations. * Data maintenance and record keeping are in accord with GMP and SOPs * Participates in projects and follows through to completion. * Supports laboratory operations using technical ability to run routine samples independently. Recognizes abnormal results and/or instrument problems and reports them to supervision providing input to cause and possible solutions. Key Responsibilities Continued * Performs routine tests and experiments following compendial or standard procedures * Has an understanding and has applied skills related to Lean & 5-S. * Sets up, adjusts and operates laboratory basic equipment such as balances, pH meter, sieves, ovens and has an understanding and has used advanced laboratory equipment such as Viscosity, Karl Fischer, UV/VIS, HPLC, GC. * Maintains and follows Standard Operating Procedures dealing with their work area and can apply knowledge to assist in other work areas. * Generation of protocols and execution of projects with little oversight. May lead a project and be responsible for completion. * May assist with the writing and revising of procedures. * May be assigned to projects dealing with special samples needing method modifications, with close supervision. * Records tests results on standardized forms and prepares reports describing procedures used. Prepares charts and graphs to assist in evaluation and interpretation of data. Key Responsibilities Continued * Completes investigations into aberrant data and generation of summary reports for their own work, can apply problem solving techniques in a team environment. * Considered a Subject Matter Expert in Procedures for their area, providing training in and out of their department. * Maintains a safe and clean working area and assists others in same. * Will work with Analysts, Scientists and Management staff on a routine basis for the receipt and preparation of QC Test Samples and Stability study samples. * Follows good documentation practices. * Adheres and demonstrates exemplary behaviors. Identifying EHS hazards and propose solutions to improve lab/safety compliance. Key Competencies Accountable Accepting Direction Attendance and Punctuality Attentive Listening Collaborative Communicating Effectively Critical Thinking Delivering High Quality Work Demonstrating Initiative Detailed Oriented Displaying Technical Expertise Following Policies and Procedures Interacting with People at Different Levels Managing Time Prioritizing and Organizing Work Problem Solving Working Safely Technical Skills Requirements * Excellent attention to detail. * Ability to use and perform HPLC, UV, GC and other instrumental techniques. * Ability to generate protocols and summarize data. * Ability to communicate within and outside immediate department. May contact vendors and/or external customers for administrative and technical information. * Ability to work weekends and off shifts, as needed. * Computer literate with the following applications: MS Excel, Word, Access * Ability to utilize application software such as: Empower, Trackwise, JDE. * Familiarity with Lean concepts and 5-S. Skills High degree of time management skills and ability to handle multiple priorities and projects at once. Prioritizes and plans work activities, uses time efficiently and develops realistic action plans. Excellent Written and Verbal Communication Skills Proven ability to work effectively in a team environment. Education & Experience ANALYST III High School degree or equivalent with approximately 10 years lab experience, preferably in an FDA regulated environment; or 2-year degree with approximately 3 years' experience or B.S. degree in a related scientific field with approximately 1.5 years of experience. ANALYST IV High School degree or equivalent with approximately 15 years lab experience, preferably in an FDA regulated environment; or 2-year degree with approximately 5 years' experience or B.S. degree in a related scientific field with approximately 3 years of experience. ANALYST V High School degree or equivalent with approximately 20 years lab experience, preferably in an FDA regulated environment; or 2-year degree with approximately 10 years' experience or B.S. degree in a related scientific field with approximately 5 years of experience. Physical Requirements Operations of laboratory equipment Required to bend frequently Required to sit frequently Required to stand frequently Required to talk or hear constantly Required to use hands constantly Required to walk frequently Specific vision abilities include ability to adjust focus Specific vision abilities include close vision Specific vision abilities include depth perception Specific vision abilities include distance vision Specific vision abilities include perpheral vision To learn more about Phibro Animal Health's competitive benefits package, please click here: Phibro Benefits. Phibro is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law. Business Unit: Animal Health & Mineral Nutrition Division: Animal Health & Nutrition Department: Quality Location: US - Chicago Heights, IL Work Schedule: Monday - Friday (Standard Work hours)

Job Description The Quality Control Chemist is responsible for daily lab testing with the purpose of accepting or rejecting test samples based on pre-determined specifications. The successful candidate will be able to work quickly and safely and will assist the Quality Control Manager with other tasks, as needed. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned. • Performs laboratory tests including pH, fluoride, viscosity, specific gravity, color, and appearance. • Tests raw materials, bulk intermediates, finished products and stability samples for specific quality attributes. • Uses and maintains HPLC, GC, FTIR, and other instruments. • Assists in performing method validations. • Performs a variety of wet lab techniques including but not limited to: titrations, pH, ISE, etc. • Writes and revises SOPs and tests methods as needed. • Follows documented procedures: SOPs, test methods, transfer protocols. • Prepares reports and reviews data. • Follows lab safety procedures. • Performs other tasks, as assigned. SUPERVISORY RESPONSIBILITIES None QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Bachelors of Science in Chemistry. LANGUAGE SKILLS Able to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. MATHEMATICAL SKILLS Able to calculate figures and amounts such as proportions, percentages, area, circumference and volume. Able to apply concepts of basic algebra and geometry. REASONING ABILITY Able to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Able to deal with problems involving several concrete variables in standardized situations. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Specific vision abilities required by this job include close vision and depth perception. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

We are seeking a skilled QC Chemist to perform wet chemistry testing on raw materials, including IR Spectroscopy, melting point temperature, and viscosity, while adhering to USP methodology. Responsibilities + Run identification tests like Thin Layer Chromatography and spectroscopic tests. + Perform limit tests for things like chlorides, sulfates, heavy metals, elemental impurities, and aluminum. + Carry out other tests and assays such as Karl Fischer, acid value, saponification value, iodine value, hydroxyl value, peroxide value, and oil-related assays. + Perform physical tests like viscosity, melting point, congealing temperature, and mid-IR and UV-Vis analysis. + Work with lab instruments like refractometers, densitometers, pH meters, auto-titrators, UV-Vis spectrophotometers, and FTIR. Essential Skills + Bachelor's Degree in Chemistry. + 1-3 years of experience in a GMP/regulated laboratory setting. + Familiarity with raw material testing. About Actalent Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021. Diversity, Equity & Inclusion At Actalent, Diversity And Inclusion Are a Bridge Towards The Equity And Success Of Our People. DE&I Are Embedded Into Our Culture Through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people Job Type & Location This is a Contract position based out of Oak Brook, IL. Pay and Benefits The pay range for this position is $25.00 - $25.00/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 Oak Brook,IL. Application Deadline This position is anticipated to close on Dec 19, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Founded in 1976, E K Industries, Inc. (EKI) manufactures high-purity chemical and reagent solutions used in laboratories, hospitals, and industrial applications nationwide. As an ISO 9001:2015 and ISO 13485:2016 certified manufacturer, EKI upholds rigorous standards for quality, traceability, and safety across all production operations. We're seeking a dependable, disciplined individual with real-world chemistry experience to join our production laboratory. The Laboratory Production Technician prepares and tests chemical batches, performs wet-chemistry QC (pH, titrations, spectrophotometric checks), and ensures every batch meets specification before packaging. This is a hands-on, production-focused laboratory role-mixing, measuring, cleaning, and documenting work in a regulated, team- oriented ISO environment under the supervision of the Quality & Regulatory Manager. Job Description Position Summary The Laboratory Production Technician plays an important role in EKI's batch production and quality control operations. This position involves preparing, blending, and testing batches of chemical and reagent solutions according to written formulations and laboratory procedures. Technicians are responsible for performing all tasks associated with laboratory production - from weighing and mixing raw materials to conducting quality control tests such as pH, spectrophotometric, and titration analysis. The role also includes maintaining accurate batch documentation, cleaning and calibrating laboratory equipment, and supporting general lab operations. This is a hands-on position that requires attention to detail, accuracy in measurement, and consistent adherence to laboratory safety, GMP, and ISO standards. Key Responsibilities ● Prepare and produce chemical batches according to established formulations and written batch instructions. ● Accurately weigh, measure, and blend components to meet required specifications. ● Filter, label, and package finished laboratory products. ● Perform in-process and final quality control testing (pH, titration, spectrophotometric checks). ● Document all test results and production data accurately within the laboratory record system. ● Calibrate and maintain laboratory instruments (pH meters, spectrophotometers, analytical balances, etc.). ● Maintain laboratory organization, cleanliness, and equipment readiness in accordance with Good Manufacturing Practices (GMP) and ISO 9001:2015 / ISO 13485:2016 requirements. ● Track and maintain inventory of lab materials, chemicals, and packaging supplies. ● Collaborate with the Laboratory Manager and Production team to align daily production with current orders and priorities. Qualifications ● High school diploma and a minimum of two years of hands-on experience in a chemical laboratory or chemical manufacturing environment required. ● Additional coursework or certification in chemistry, laboratory science, or a related field is preferred. ● Demonstrated proficiency in wet-chemistry testing methods, including but not limited to pH measurement, titration, and solution preparation. ● Experience using laboratory instruments such as balances, pH meters, and spectrophotometers. ● Strong understanding of safe chemical handling and personal protective equipment (PPE) use. ● Dependable, organized, and detail-oriented with strong record-keeping and documentation skills. ● Must be able to lift up to 50 lbs and stand for extended periods. ● Reliable transportation to workplace required. Additional Information Compensation and benefits ● Full-time, hourly position (40 hours per week). ● Paid time off (vacation, holiday pay, sick pay) ● Medical/Dental insurance benefit ● Retirement plan benefit Additional Information ● Employment is contingent upon successful completion of a background check and E- Verify confirmation. ● Due to the nature of our products, annual influenza and COVID-19 vaccinations (including boosters) are required and provided at no cost to employees. ● EKI is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, sexual NO IN-PERSON APPLICATIONS ACCEPTED - APPLY ONLINE ONLY

Founded in 1976, E K Industries, Inc. (EKI) manufactures high-purity chemical and reagent solutions used in laboratories, hospitals, and industrial applications nationwide. As an ISO 9001:2015 and ISO 13485:2016 certified manufacturer, EKI upholds rigorous standards for quality, traceability, and safety across all production operations. We're seeking a dependable, disciplined individual with real-world chemistry experience to join our production laboratory. The Laboratory Production Technician prepares and tests chemical batches, performs wet-chemistry QC (pH, titrations, spectrophotometric checks), and ensures every batch meets specification before packaging. This is a hands-on, production-focused laboratory role-mixing, measuring, cleaning, and documenting work in a regulated, team- oriented ISO environment under the supervision of the Quality & Regulatory Manager. Job Description Position Summary The Laboratory Production Technician plays an important role in EKI's batch production and quality control operations. This position involves preparing, blending, and testing batches of chemical and reagent solutions according to written formulations and laboratory procedures. Technicians are responsible for performing all tasks associated with laboratory production - from weighing and mixing raw materials to conducting quality control tests such as pH, spectrophotometric, and titration analysis. The role also includes maintaining accurate batch documentation, cleaning and calibrating laboratory equipment, and supporting general lab operations. This is a hands-on position that requires attention to detail, accuracy in measurement, and consistent adherence to laboratory safety, GMP, and ISO standards. Key Responsibilities ● Prepare and produce chemical batches according to established formulations and written batch instructions. ● Accurately weigh, measure, and blend components to meet required specifications. ● Filter, label, and package finished laboratory products. ● Perform in-process and final quality control testing (pH, titration, spectrophotometric checks). ● Document all test results and production data accurately within the laboratory record system. ● Calibrate and maintain laboratory instruments (pH meters, spectrophotometers, analytical balances, etc.). ● Maintain laboratory organization, cleanliness, and equipment readiness in accordance with Good Manufacturing Practices (GMP) and ISO 9001:2015 / ISO 13485:2016 requirements. ● Track and maintain inventory of lab materials, chemicals, and packaging supplies. ● Collaborate with the Laboratory Manager and Production team to align daily production with current orders and priorities. Qualifications ● High school diploma and a minimum of two years of hands-on experience in a chemical laboratory or chemical manufacturing environment required. ● Additional coursework or certification in chemistry, laboratory science, or a related field is preferred. ● Demonstrated proficiency in wet-chemistry testing methods, including but not limited to pH measurement, titration, and solution preparation. ● Experience using laboratory instruments such as balances, pH meters, and spectrophotometers. ● Strong understanding of safe chemical handling and personal protective equipment (PPE) use. ● Dependable, organized, and detail-oriented with strong record-keeping and documentation skills. ● Must be able to lift up to 50 lbs and stand for extended periods. ● Reliable transportation to workplace required. Additional Information Compensation and benefits ● Full-time, hourly position (40 hours per week). ● Paid time off (vacation, holiday pay, sick pay) ● Medical/Dental insurance benefit ● Retirement plan benefit Additional Information ● Employment is contingent upon successful completion of a background check and E- Verify confirmation. ● Due to the nature of our products, annual influenza and COVID-19 vaccinations (including boosters) are required and provided at no cost to employees. ● EKI is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, sexual NO IN-PERSON APPLICATIONS ACCEPTED - APPLY ONLINE ONLY

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 Advance Your Career with Eurofins PSS! Location of the position: Indianapolis, IN At Eurofins PSS, the work we do matters-from ensuring the safety of medicines to protecting the environment-and so do our employees. If you're ready to make a meaningful impact, we offer a place to learn, lead, and thrive. Why Join Eurofins? ✅ Career Growth - Expand your expertise and take on leadership roles ✅ Supportive Teams - A culture of collaboration and innovation ✅ Work-Life Balance - Flexible schedules + competitive benefits ✅ Industry Impact - Work with global leaders in biopharma Who We Are Eurofins Scientific is a global life sciences leader, providing analytical testing services that ensure the safety, authenticity, and quality of the food you eat and the medicines you rely on. Position: Analytical Chemist - QC Location: Indianapolis, IN Shift: Training on Day Shift (Mon-Fri, 8AM-5PM), then 3-2-2-3 rotation (6PM-6AM) Key Responsibilities: Perform analytical testing on proteins & antibodies using HPLC, CE, IC, SDS-PAGE, ELISA, UV Spectroscopy Document results in LIMS and lab notebooks Operate in a GMP-regulated environment and support continuous improvement initiatives Qualifications Bachelor's degree in Biology, Biochemistry, Chemistry, or related field Experience with HPLC, CE, IC, SDS-PAGE, ELISA preferred Must be authorized to work in the U.S. Additional Information Position is Monday-Friday 8:00am - 5:00pm overtime as needed. Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Quality Positions Available.

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. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Eurofins Built Environment Testing is proactively seeking an analyst to join our Naperville site. The Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP's, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. Analyst responsibilities include, but are not limited to, the following : Must be comfortable working with asbestos, mold and legionella samples Prepare and analyze environmental samples Accurately enters and reports analytical data using the LIMS Performs independent data reviews for other analysts' work Performs analysis of reference materials, proficiency samples and other quality control samples as needed Maintains client service and provides technical support as needed Assists the QA manager in development, implementation and data collection of QA processes for the different analytical tests Performs confirmation of lab results as needed by client services personnel Performs and completes all analytical testing QA related tasks as needed Assists in pursuing, receiving and maintaining necessary laboratory accreditations Maintains and updates all necessary Training and QA documents onsite as necessary Co-ordinates and manages projects according to their rush status and due time for timely delivery Assists co-workers on analytical questions, as necessary Participates in Lean initiatives and projects when called upon Follows company policies and procedures Manages and maintains the inventory of re-sale supply items and laboratory consumables and takes necessary steps to re-order supplies as needed Manages and disposes analyzed samples as needed Trains new mycology, asbestos or geology analytical testing analysts as needed Recommends and coordinates sample transfer as necessary Establishes and maintains laboratory stock culture and reference samples Performs root cause analysis and determines and implements corrective actions for errors and issues as necessary Maintains all equipment properly and co-ordinates servicing of all equipment used in the laboratory, as needed Routinely communicates available capacity to Regional Manager Other responsibilities as deemed necessary by the Supervisor/Manager Qualifications Qualifications Basic Minimum Qualifications : BS or BA in a closely related science 1- 2 years of previous experience with Asbestos, Mycology, Forensic Sciences or Geology testing services within a laboratory setting. Professional working proficiency in English is a requirement, including the ability to read, write and speak in English Authorization to work in the United States indefinitely without restriction or sponsorship The ideal candidate would possess : Environmental methodologies within Asbestos, Mycology, Forsensic Science or Geology General regulatory requirements Analytical laboratory techniques Laboratory QA requirements Knowledge of computers, spreadsheets, and databases Strong computer, scientific, and organizational skills Additional Information Position Pay Range starts at $17.75/hr based on experience Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business section, and geographic location As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins Environment Testing Businesses in the US are routinely engaged in Federal Contracts. Federal Government vaccination mandates may apply to staff working in these businesses. Successful applicants may be required to confirm vaccination status or demonstrate eligibility for medical or religious exemptions prior to commencing employment. In addition, certain positions require travel for which vaccination is required in accordance with Eurofins policy. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Sedron Technologies is hiring a talented Lab Analyst to work in Fair Oaks, IN! Founded in 2014 and headquartered in the Pacific Northwest, Sedron Technologies designs, manufactures, installs, and operates advanced water and waste upcycling technologies. With a focus on transforming the paradigm from waste processing to resource recovery, Sedron Technologies works with municipal, agricultural, and industrial customers to process their "waste" into climate-smart commodities through environmentally and financially sustainable methods. The Lab Analyst is responsible for performing a variety of laboratory tests and procedures to support the manufacturing process and ensure the highest quality standards. This role involves working closely with production teams to provide accurate and timely data, enabling informed decisions to maintain product integrity and safety. The ideal candidate will have a strong background in laboratory techniques, a keen eye for detail, and a commitment to maintaining a safe and compliant work environment. Because we design, build, commission, and operate our technologies, we are looking for individuals who can meet the following essential functions of the position: * Collect and analyze samples from various stages of the production process, including raw materials, in-process samples, and finished products * Accurately record test results and observations. Analyze data to identify trends, deviations, and potential issues, providing timely feedback to production teams * Perform routine and non-routine testing in accordance with established protocols and standard operating procedures (SOPs). Ensure all testing meets regulatory and company quality standards * Operate and maintain laboratory equipment, ensuring it is calibrated and functioning properly. Troubleshoot and resolve any equipment issues promptly * Adhere to all safety guidelines and regulatory requirements, including maintaining clean and organized workspaces. Participate in safety audits and training as required * Prepare and maintain detailed records, reports, and documentation to support quality assurance and regulatory compliance. Assist in the preparation of certificates of analysis (COAs) as needed * Work closely with cross-functional teams, including production, quality assurance, and R&D, to support continuous improvement initiatives and resolve quality issues This position allows for growth and career progression to be determined by performance, certifications, and supervisor discretion. BENEFITS * Multiple medical, dental, and vision insurance options to keep you feeling your best * 401(k) with employer matching - free money for future you * Generous paid time off and paid holidays (plus 2 floating holidays to use your way) * Disability, Life, and AD&D Insurance * FSA and HSA options with employer contributions * Tuition reimbursement - we invest in your growth * Casual work attire - no suits required (unless that's your thing) EDUCATION/EXPERIENCE * Bachelor's degree in Chemistry, Biology, or a related field. Equivalent experience may be considered * 2+ years of experience in a laboratory setting, preferably in a manufacturing or industrial environment * Proficient in laboratory techniques and equipment, including chromatography, spectroscopy, and titration * Strong analytical and problem-solving skills * Excellent attention to detail and accuracy * Ability to work independently and as part of a team * Strong communication skills, both written and verbal * Minimum requirement for all positions is a high school diploma or GED * Must have effective verbal, reading, and written communication skills in the English language PHYSICAL REQUIREMENTS * Ability to stand for extended periods. * Ability to lift and handle laboratory equipment or samples up to 30 lbs * Ability to work in environments with exposure to chemicals and varying temperatures ADDITIONAL INFORMATION * Compensation range for this role is between $55,000 to $75,000 annually * The range provided is Sedron's estimate of the base compensation for this role. Actual amount offered will be based on job-related and non-discriminatory factors such as experience, location, education, training, skills, and abilities. * Discretionary bonus Must be a US Citizen or legal permanent resident for this position. We are unable to sponsor any employment visas. We are committed to maintaining a drug and alcohol-free work environment, and our employees are expected to comply with all state and federal laws. Due to the nature of the work performed, this role is considered Safety Sensitive and as such all applicants will be subject to a pre-employment drug test, and background check after receiving a conditional offer of employment. Not sure you meet all the qualifications? We encourage you to still apply! We'll review your application and may have training opportunities or other positions available. Sedron Technologies is an Equal Opportunity Employer. Sedron Technologies does not discriminate on the basis of race, color, religion, sex, national origin, sexual orientation, marital or familial status, physical or mental disability, genetic information, age, retaliation, veteran/military service status, or any other legally protected status. Sedron Technologies is an EEO/AA/M/F/Disabled/Veteran/Drug-Free Employer.

The NUFSM Department of Physical Medicine and Rehabilitation, in collaboration Shirley Ryan AbilityLab, seeks a full-time non-tenure-eligible Team Scientist at the rank of Assistant Professor, Associate Professor, or Professor. The position is based at Shirley Ryan AbilityLab, with opportunities for collaboration with Northwestern University Departments of Biomedical Engineering, Mechanical Engineering, Physical Therapy & Human Movement Sciences, Neurology, Neurosurgery, Neuroscience, and Physical Medicine & Rehabilitation. Responsibilities include: * Develops and submits research proposals and grant applications to secure external research funding from agencies such as the NIH, VA, NIDILRR, DoD, NSF and private foundations * Ensures that scientific and regulatory milestones of specific projects are met * Publishes original studies in refereed journals that advance our understanding of motor control, and translation science linked to neurologic illness. * Demonstrates leadership activity in professional organizations such as the Society for Neuroscience, the International Society for Society for Neuroscience, Neural Control of Movement, Progress in Motor Control, etc. * Contributes to the educational of highly qualified personnel including graduate students, post-doctoral fellows, medical students, and residents. * Participate in and collaborate on Department activities, as requested by the Department Chair. Qualified candidates: * Knowledge of measurement and statistics principles acquired through a Ph.D. in a scientific discipline from an accredited school and successful completion of a postdoctoral fellowship. * Minimum 2 years of related experience with an expert knowledge of scientific principles and concepts. Reputation as emerging leader in field with sustained performance and accomplishment. * Uses professional concepts in accordance with institute objectives to solve complex problems in creative and effective ways. * Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought. * Works on complex problems and designs/conducts research projects in which analysis of situations or data requires an in-depth evaluation of various factors. * Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. * Requires proficiency in writing to prepare grant proposals, research reports and other publications, and explain complex results to a lay audienc * Interpersonal skills needed to communicate effectively with other staff members, fellow researchers * May determine methods and procedures on new assignments and may provide guidance to other lower-level personnel. * Commitment to teaching and teaching ability are requirements The start date is negotiable and the position will remain open until filled. When applying, please upload a CV and cover letter describing your interest and alignment with the position. Also upload this completed list of references form to suggest the names of individuals who could write letters of reference on your behalf. Please read ALL instructions and make preparations before proceeding to the application page: * Applications will only be accepted via online submission (see link below). * Please prepare all documents in advance as Adobe PDF files, and please be sure all information is entered correctly and accurately (especially names and email addresses), as there will be no opportunity for online revision after your application has been submitted. * All required fields in the application form are marked with an asterisk and must be filled before clicking the "Submit" button. * Be aware that incomplete applications cannot be saved. Applications accepted here: Apply for Job Northwestern University is an Equal Opportunity Employer and does not discriminate on the basis of protected characteristics, including disability and veteran status. View Northwestern's non-discrimination statement. Job applicants who wish to request an accommodation in the application or hiring process should contact the Office of Civil Rights and Title IX Compliance. View additional information on the accommodations process.

We are seeking a skilled QC Chemist to perform wet chemistry testing on raw materials, including IR Spectroscopy, melting point temperature, and viscosity, while adhering to USP methodology. Responsibilities * Run identification tests like Thin Layer Chromatography and spectroscopic tests. * Perform limit tests for things like chlorides, sulfates, heavy metals, elemental impurities, and aluminum. * Carry out other tests and assays such as Karl Fischer, acid value, saponification value, iodine value, hydroxyl value, peroxide value, and oil-related assays. * Perform physical tests like viscosity, melting point, congealing temperature, and mid-IR and UV-Vis analysis. * Work with lab instruments like refractometers, densitometers, pH meters, auto-titrators, UV-Vis spectrophotometers, and FTIR. Essential Skills * Bachelor's Degree in Chemistry. * 1-3 years of experience in a GMP/regulated laboratory setting. * Familiarity with raw material testing. About Actalent Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021. Diversity, Equity & Inclusion At Actalent, Diversity And Inclusion Are a Bridge Towards The Equity And Success Of Our People. DE&I Are Embedded Into Our Culture Through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people Job Type & Location This is a Contract position based out of Oak Brook, IL. Pay and Benefits The pay range for this position is $25.00 - $25.00/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 Oak Brook,IL. Application Deadline This position is anticipated to close on Dec 19, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.