Chemist jobs in Kentwood, MI

Michigan State University (MSU) operates the Facility for Rare Isotope Beams (FRIB) as a user facility for the U.S. Department of Energy Office of Science (DOE-SC), supporting the mission of the DOE-SC Office of Nuclear Physics. FRIB provides researchers with one of the most advanced tools of modern science to study rare isotopes, or short-lived nuclei not normally found on Earth. Hosting what is designed to be the most powerful heavy-ion accelerator, FRIB enables scientists to make discoveries about the properties of rare isotopes, nuclear astrophysics, fundamental interactions, and applications for society, including in medicine, homeland security, and industry. User facility operation is supported by the DOE-SC Office of Nuclear Physics as one of 28 DOE-SC user facilities. MSU's nuclear physics graduate program is a top-ranked program nationally, according to U.S. News & World Report . This position affords an exciting opportunity to become part of the world-class FRIB Laboratory that enables unique discovery opportunities in nuclear science. Position Summary The Accelerator Physicist will contribute to the development and operation of the FRIB accelerators by undertaking projects and activities to improve facility performance as measured by beam quality, intensity, power, purity, and variety. These activities will focus on enhancing the performance of FRIB and providing planned availability of primary beams on target and secondary beams for experiments, primarily by applying AI/ML techniques. Major Duties/Responsibilities Develop new techniques, software, and hardware to improve the performance of the driver- and re-accelerators based on AI/ML methods Assist with the design, prototype, development, implementation, and maintenance of high-level physics applications based on AI/ML techniques Validate the accuracy and reliability of the physics applications and algorithms; Create detailed documentation for the developed applications, including user guides and technical specifications; Train users and operators on how to use the new tools and applications effectively, Continuously monitor the performance of the re-accelerator and adjust applications as needed. Conceive and execute studies of beam dynamics and electrodynamics using major programming languages (C++, Python) and computer programs Organize the data flow for optimal use with AI/ML applications Keep FRIB physics application environment up to date by collaborating with EPICS community Complete other duties as assigned within the scope of the role Knowledge, Skills, and Abilities Highly skilled in developing software for high-level physics applications using C++ and Python Advanced knowledge of software development practices and techniques for computational and data-intensive science problems Knowledge and skillful ability with heavy-ion beam diagnostic equipment Skills and ability to gather, analyze, and present findings by communicating effectively (both orally and written) Ability to conduct interdisciplinary research combining physical sciences/engineering and computing Skillful ability to collaborate and work in a team environment Ability to analyze and resolve technical problems in a timely manner Ability to effectively work in a team Excellent communication skills to communicate effectively and credibly verbally and in writing with all audiences. Proficiency with Microsoft Office Suites. Required Degree Doctorate -Physics or computer science Minimum Requirements A Ph.D. in physics or computer science, or related field At least one year of experience in accelerator physics and technology or an equivalent combination of education and experience Published peer reviewed papers on AI/ML applications to support accelerator design and operation Desired Qualifications Experience in the development of computer programs on Python Experience with software development practices and techniques for computational and data-intensive science problems, including AI/ML tools Experience with distributed accelerator control systems and their underlying concepts Required Application Materials CV Cover Letter Contact information for at least three references

We are seeking an experienced 3DX Solutions Architect with deep expertise in architecting, integrating, and scaling enterprise-level 3DEXPERIENCE solutions. The ideal candidate will have strong experience in PLM/3DX architecture, BOM management, system integrations, and customer-facing solution leadership. Key Responsibilities: Define and drive end-to-end 3DEXPERIENCE solution architecture, including integrations with PLM and enterprise systems. Provide architectural direction and guide customers through digital transformation initiatives. Evaluate business requirements and design scalable, maintainable 3DX solutions. Oversee technical execution and validate design approaches through Proof of Concepts (PoCs). Mentor technical teams and ensure alignment with 3DX best practices. Act as a functional and technical leader during customer-facing interactions. Qualifications: Bachelor's degree in Engineering or related field (preferred). Strong expertise in 3DEXPERIENCE data model, BOM, structure management, and system integrations. Proven experience handling complex PLM/CAD/BOM integrations across enterprise environments. Strong communication, leadership, and analytical skills. Ability to simplify complex requirements and deliver clear, practical solutions.

contract( 6-12 months) with possible extension Pay Rate $26/hr on w2 with Benefits Working schedule - 2-2-3 working structure - (2 days on, 2 days off, 3 days on, 2 days off) Requirements: Associate degree or higher from an accredited college or university with a major in chemistry, engineering, or related science Valid Michigan Driver's License Responsibilities: Collect field samples of wastewater, sludge, polymer, etc. from various process areas of the Plant and the outfall, and perform chemical, microbiological, toxicological, and physical analyses that include reagent and media preparation, instrument operation, calibration, maintenance checks, and quality assurance/quality control (QA/QC) Become knowledgeable in laboratory analyses and treatment processes. Become proficient in training new hires in process analyses and sampling. Contribute to the record-keeping and reporting of laboratory data, regulatory reporting, operations reports, plant meetings, etc. Validate accurate readings from monitoring equipment, maintain analyzers and perform analyzer reagent change/replenishment. Work Night and Day shifts as assigned. Work in an industrial setting supporting 24-hour operations. Support a large team where needed with a high degree of flexibility. Precisely and diligently follow complex procedures and guidelines. Work overtime if needed to achieve compliance and support operations. Communicate frequently with team members and other units across the organization about the process, equipment, or potential problems. Physical Requirements: This position requires the ability to climb, bend, twist, carry, stack, push, pull and other efforts requiring considerable physical strength. This position also requires the ability to lift a minimum of fifty (50) pounds, walk, stand, or work for long periods of time, demonstrate normal color perception, hear audible alarms, detect abnormal equipment sounds, visually inspect equipment and processes at any time of the day or night.

Kelly is hiring an Associate Laboratory Technician for a 6 -month Contract role with one of our prestigious clients based out in Troy, MI 48083. Job Title: Associate Laboratory Technician Employment Type: 6-month contract Pay rate: $21-23.50/hr. Shift: 7 am - 4 pm Qualifications: • Excellent safety record and fundamental knowledge of pilot plant and or laboratory safety • Experience in lab operations, including use of computer control • Mechanical aptitude for operating and troubleshooting lab equipment • Ability to run or learn to run analytical tests required to support pilot plant operations • Excellent teamwork with the ability to manage all aspects of executing test plans supporting required by run engineers/technical liaisons. • Commitment to data quality • Attention to details • Flexibility to adapt to changing priorities Responsibilities: • Safely operate and maintain Lab equipment • Provide support for third party vendors performing required equipment calibration • Conduct lab test according to lab testing procedures • Record test results on computerized SPC charts • Communicate with operators and business group representatives • Maintain lab supplies • Attend unit pre-trial meetings • Participate in equipment safety reviews • Work independently as the only testing technician in the lab Conduct polymer property testing using the following equipment: Hardness Gauges APA LCR Tensile Tester Moisture analyzer Mahr tester Run small extruder Color use Hunter Lab scan Die Cutter Density Tester Injection molding If you believe you are a good fit for this opportunity, please submit your application through the job posting link. We also encourage you to share references if you have them.

A Day in Your Life at MKS: As an Associate Chemist at MKS | Atotech in the GMF industry, your day begins by receiving and preparing samples for analysis, followed by conducting chemical tests using techniques like UV-Vis, FTIR, and HPLC. You'll spend most of your time at the lab bench or workstation, documenting results in digital systems and collaborating with production and quality teams to ensure materials meet specifications. You will be trained to safely operate a forklift, as part of your responsibilities will include moving chemical shipments and supplies within the facility. The work environment is fast-paced, safety-focused, and offers opportunities to contribute to process improvements and product quality. In this role, you will report to the Site Manager. You Will Make an Impact By: • Perform various laboratory tasks such as preparing chemical solutions, conducting experiments, and operating laboratory equipment safely and efficiently • Collect and analyze experimental data using various techniques and instrumentation. This may involve using software programs to process and interpret results accurately • Maintain detailed records of experiments, procedures, and results in laboratory notebooks or electronic databases. Ensuring that all documentation meets regulatory and quality standards • Assist in quality control procedures to ensure that products meet specifications and regulatory requirements. This may involve conducting tests on raw materials, intermediates, and finished products • Adhere to safety protocols and guidelines to ensure a safe working environment. Following standard operating procedures (SOPs) and regulatory requirements related to chemical handling, storage, and disposal • Perform warehouse functions - shipping and receiving chemical products Skills You Bring: • Bachelor of Science in Engineering degree or equivalent experience • Minimum of 0-1 year of related experience * Familiarity with instrumentation and chemical safety * Must either have hi-lo forklift experience or be willing to learn. This is a mandatory function of position. Physical Demands & Working Conditions: • Perform activities such as sitting, standing, for extended periods of time • Must be able to lift up to 50 lbs • Regularly requires good manual dexterity and coordination • Frequently positions self to perform tasks and positions objects below, at, and above shoulder level • Ability to remain in a stationary position for 60-80% of the time * Must be able to safely operate a forklift (training and certification within 30 days of hire) • Operates in a laboratory/manufacturing environment • Noise levels in the work environment are typically moderate • Occasional exposure to chemicals and fumes may occur; adherence to safety guidelines is mandatory #LI-AS1 Globally, our policy is to recruit individuals from wide and diverse backgrounds. However, certain positions require access to controlled goods and technologies subject to the International Traffic in Arms Regulations (ITAR) or Export Administration Regulations (EAR). Applicants for these positions may need to be “U.S. persons.” “U.S. persons” are generally defined as U.S. citizens, noncitizen nationals, lawful permanent residents (or, green card holders), individuals granted asylum, and individuals admitted as refugees. MKS Inc. and its affiliates and subsidiaries (“MKS”) is an affirmative action and equal opportunity employer: diverse candidates are encouraged to apply. We win as a team and are committed to recruiting and hiring qualified applicants regardless of race, color, national origin, sex (including pregnancy and pregnancy-related conditions), religion, age, ancestry, physical or mental disability or handicap, marital status, membership in the uniformed services, veteran status, sexual orientation, gender identity or expression, genetic information, or any other category protected by applicable law. Hiring decisions are based on merit, qualifications and business needs. We conduct background checks and drug screens, in accordance with applicable law and company policies. MKS is generally only hiring candidates who reside in states where we are registered to do business. MKS is committed to working with and providing reasonable accommodations to qualified individuals with disabilities. If you need a reasonable accommodation during the application or interview process due to a disability, please contact us at: accommodationsat *************** . If applying for a specific job, please include the requisition number (ex: RXXXX), the title and location of the role

At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits. Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries-from food and water to pharmaceuticals and advanced materials. We help the world's top companies ensure their products are safe, authentic, and accurately labeled. Job Description Laboratory Operations Operate analytical instruments (plate readers, microplate washers, automated workstations) Handle liquid samples with micropipettes Prepare analytical samples and assay reagents per SOPs Perform biological assays (qPCR, ELISAs) Measure protein levels (host cell protein, protein A) in monoclonal antibody samples Assist as secondary operator during assay transfers Analytical Methods Run methods such as HPLC, UPLC, SEC, gel electrophoresis, capillary electrophoresis Conduct total protein and amino acid analyses Manage sample storage and handling Data & Documentation Analyze data using instrument software and MS Office (Word, PowerPoint, Excel) Independently interpret experimental results Contribute to SOPs, study reports, and protocols Maintain compliant laboratory notebooks Qualifications Preferred Qualifications Skilled in protein and macromolecule handling/analysis Proficiency with low-volume liquid handling equipment (e.g., micropipettes) Strong computer literacy; able to quickly learn and adapt to new software Minimum Qualifications Bachelor's degree in Chemistry or related field plus 2-3 years industry experience OR Master's degree with academic research experience Hands-on technical laboratory experience in analytical chemistry (academic, internship, or industrial) Demonstrated HPLC experience Authorization to work in the U.S. indefinitely without restriction or sponsorship Additional Information What we offer: 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 Career Development and continuing education opportunities Position is full-time, 8am - 5pm with occasional overtime required. #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits. Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries-from food and water to pharmaceuticals and advanced materials. We help the world's top companies ensure their products are safe, authentic, and accurately labeled. Job Description Laboratory Operations Operate analytical instruments (plate readers, microplate washers, automated workstations) Handle liquid samples with micropipettes Prepare analytical samples and assay reagents per SOPs Perform biological assays (qPCR, ELISAs) Measure protein levels (host cell protein, protein A) in monoclonal antibody samples Assist as secondary operator during assay transfers Analytical Methods Run methods such as HPLC, UPLC, SEC, gel electrophoresis, capillary electrophoresis Conduct total protein and amino acid analyses Manage sample storage and handling Data & Documentation Analyze data using instrument software and MS Office (Word, PowerPoint, Excel) Independently interpret experimental results Contribute to SOPs, study reports, and protocols Maintain compliant laboratory notebooks Qualifications Preferred Qualifications Skilled in protein and macromolecule handling/analysis Proficiency with low-volume liquid handling equipment (e.g., micropipettes) Strong computer literacy; able to quickly learn and adapt to new software Minimum Qualifications Bachelor's degree in Chemistry or related field plus 2-3 years industry experience OR Master's degree with academic research experience Hands-on technical laboratory experience in analytical chemistry (academic, internship, or industrial) Demonstrated HPLC experience Authorization to work in the U.S. indefinitely without restriction or sponsorship Additional Information What we offer: 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 Career Development and continuing education opportunities Position is full-time, 8am - 5pm with occasional overtime required. #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Analytical Chemist needs 4 years experience Analytical Chemist requires: Bachelor or Master degree in chemistry with prior laboratory experience preferred. Previous experience in an Analytical laboratory highly desirable. Good wet chemistry skills: titration, filtration, dilution, extraction, gravimetric determinations. Knowledge and experience with GC-FID, ICP, IC, SEM/EDS and FTIR is desirable Prior use of pH and specific ion electrode meters. Able to work in a fast-paced environment. Excellent attention to detail. Strong chemical math skills. Strong PC skills. Solid interpersonal skills. Analytical Chemist needs: Operation and routine Maintenance of Analytical Equipment Upkeep of analytical methods/procedures Work efficiently & effectively on major project Henkel teams Preparation of quality customer reports & project portfolio management. Customer interfacing (Communication: Correspondence, Presentation, etc.) Compliance & Understanding of Corporate Standards (Safety, Housekeeping, Quality, etc.) Upkeep of Digital Programs (Microsoft, LIMS, Statistical Analysis etc.)

Clean Earth is a leading provider of environmental services in the United States providing remediation, disposal, recycling, and beneficial reuse solutions for hazardous and non-hazardous waste, contaminated soil, and dredged material. Our vast portfolio of technologies and services touches nearly every industry that generates waste including energy, infrastructure, commercial, industrial, retail, and healthcare markets. Every day our teams across the country take a hands-on, dedicated approach to recycling and beneficially reusing waste that would otherwise go into landfills. We value our employees as our most important asset, and this is reflected in many areas across our company including recently being named a 2024 Most Loved Workplace . We are committed to creating a positive work culture that fosters growth and development while ensuring the health and safety of our employees. Why join Clean Earth? In addition to competitive pay, we also offer: + Health benefits available Day 1 + 401k available Day 1 + 10+ paid holidays/year + Free HAZWOPER training and certification + Overtime opportunities + Ability to be cross-trained into different roles Performs various assigned tasks and physical labor to ensure proper off-site treatment and disposal of customers' hazardous waste materials in accordance with environmentally responsible and cost-effective practices and Clean Earth policies, practices, and procedures. The ability to oversee a small project/job with supervision of personnel. **Primary Responsibilities (Essential Functions):** - Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations. - Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract. - Assists other business groups, i.e., Depack, Retail and HHW, for both internally and onsite as needed. - Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle - Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR's), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures. - Maintain a Commercial Driver's License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers' job locations. - Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA's) procedures including development of on-site Health &Safety plans/JSA's as outlined in the procedures and policies. - Perform unknown field testing for classification and packaging for transportation and disposal. - Mentor and assist new employees in field work duties. - Complete site walks to inventory and assess requirements for potential and awarded work. - Assist sales in creating estimates for lab pack work. - Performs other duties as assigned. - Lead/coordinate field service/lab pack jobs requiring multiple personnel/days. - Associate College degree in area of General Science or equivalent experience - Commercial Driver's License (CDL) with Hazardous Material endorsement and a clear record - Moderate to extensive travel with 20% overnight travel - Physical ability to lift and move material of various weights frequently exceeding 55 lbs. - Basic understanding of chemistry through general chemistry or biology - Advanced knowledge of EPA and DOT - Minimum one (1) year lab pack experience 40-hour OSHA HAZWOPER (29 CFR 1910.120) - 40 hours Depack Experience - 8 hours DOT Training - PPE Training which includes Respirators **Preferred Qualifications:** **EDUCATION/CREDENTIALS:** - BS/BA in science related field. **MEASURES OF PERFORMANCE:** Completion of the following curriculum: - Clean Earth Lab Pack I Training - (24 hours) - RCRA/DOT refresher course - Department of Transportation - Lab Pack definitions and procedures - Lab pack Field Program - Introduction to High Hazardous Cylinder Assessment course - Customer Interactions - Waste Management Methods - On-Site Expectations - Manifest/ LDR Completion - Health & Safety course(s) - Customer Approach - Forklift Training - Local Facility Capabilities - CPR/First Aid/Blood-borne Pathogen training - State regulations (if applicable) - All required local training **DEMONSTRATED KNOWLEDGE, SKILLS, AND ABILITIES:** - Strong communication skills to interact with customer to provide information, explanations, and/or instructions - Team Player - Attention to detail - Ability to work independently using initiative and effective communication to solve challenges. - Demonstrate proficiency to operate a computer with Windows based programs (i.e., Microsoft excel and word) - Demonstrates extensive Lab Pack knowledge (i.e., US EPA, DOT, and chemical properties) **WORKING ENVIRONMENT:** - Customer sites, plant, labs - Indoor/Outdoor and associated weather conditions **This position requires a CDL B to be obtained within a 6-month period from your start date. Failure to obtain a CDL B within the 6-month period will mean you are no longer eligible for the Lab Pack Chemist position.** **This position is also contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements.** Clean Earth offers competitive benefits including health, dental, vision, life, and disability insurance plans starting on the first day of employment; paid time off, wellness benefits, employee discount program, tuition assistance, and a 401k with company matching. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, gender identity, or genetics. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. If you have a difficulty applying for any job posted on Harsco Clean Earth's website because a disability prevents you from using the online system, Clean Earth offers the following alternate application procedure: Call toll free ************** and leave your name, phone number, city and state of residence. Clean Earth will arrange for an alternate method of applying and will consider your application together with all other applications received for the job. This line is dedicated to disability applications only. No other inquiries will receive a response.

The Ion Source Group Leader Scientist will contribute to ion beam development projects and the advancement of new capabilities for the 28 GHz Superconducting ECR ion source, while also supporting beam delivery from multiple ECR ion sources to meet the needs of the nuclear science program. Major Duties/Responsibilities Research, test and develop beam production technique to extend the range of ions available for the FRIB science program Lead projects aimed at improving the ion source performances to support the facility power ramp up Lead the development of new ion sources for the FRIB accelerator and the Single Event Effect project, including their design, construction, assembly, and commissioning Develop and strengthen a preventive maintenance program for the ECR ion source and related equipment Responsible for the delivery of ion beams from two ECR ion sources to support FRIB mission with high availability and high reliability Collaborate, participate in conferences and publish results in peer review journals Lead development and operation of ECR ion source for the Single Event Effect Program Performs other duties as required or assigned which are reasonably within the scope of the duties in this job classification Knowledge/Skills/Abilities Knowledge and experience with high vacuum environment, high voltage, high magnetic field, superconducting magnet technology, RF power, mechanical engineering and thermal analysis Knowledge and experience in designing ion source or accelerator components and working in an accelerator environment are preferred Experienced in operating accelerator components Ability to comply with Environment, Safety and Health (ES&H) and QA requirements Excellent communication skills to communicate effectively and credibly, both verbally and in writing with all audiences. Proficiency with Microsoft Office Suites. Equal Employment Opportunity Statement All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, age, disability or protected veteran status. Required Degree Doctorate -Physics or Chemistry Minimum Requirements PhD with 5-7 years minimum experience with ion source, plasma physics, atomic physics, accelerator physics, and technology or related field Desired Qualifications Demonstrated experience in designing and operating ion source, plasma devices or accelerator components 10 + years Prior experience in accelerator physics and/or accelerator technology Nationally recognized leader in the field of expertise Record of publications in conference or peer reviewed journal related to ion source or accelerator technology Required Application Materials CV Cover Letter Contact information for three references Review of Applications Begins On 10/13/2025 Website https://frib.msu.edu/ MSU Statement Michigan State University has been advancing the common good with uncommon will for more than 160 years. One of the top research universities in the world, MSU pushes the boundaries of discovery and forges enduring partnerships to solve the most pressing global challenges while providing life-changing opportunities to a diverse and inclusive academic community through more than 200 programs of study in 17 degree-granting colleges.

Day Shift-- Vehicle Emissions Lab. Chemist The Chemist will perform liquid chromatograph analysis (carbonyl analysis from vehicle exhaust) and perform gas chromatograph analysis (hydrocarbon speciation, fuel dilution in engine oil, etc.). The Chemists responsibilities include but are not limited to: Conducting various fuel analysis (fuel composition, heating value, distillation points) Managing fuel inventory and fuel ordering Perform maintenance and calibration on various instruments (all kinds of instruments in emissions lab, not limited to chemical instruments) Support testing operation and trouble shoot instrument problems Develop new chemical analysis when there are new emissions testing needs Requirements: Bachelor's degree in Chemistry Minimum 3-5 years' experience in chemistry analysis with liquid chromatograph and gas chromatograph General understanding of vehicle powertrain and exhaust after treatment Experience with vehicle emissions testing and with conventional emission analyzers (HC, CO, CO2, NOx and CH4) Team player with good communication skills Dedicated and well organized Preferred Requirements: Master's degree in Chemistry Additional Notes: No driving a company vehicle required Location is Auburn Hills, MI - onsite - 7am-4pm Contract to hire opportunity

Lab Chemist needs Bachelor's degree in chemistry with prior laboratory experience Lab Chemist requires: Good wet chemistry skills: titration, filtration, dilution, extraction, gravimetric determinations. Knowledge and experience with GC-FID, ICP, IC, SEM/EDS and FTIR is desirable. Prior use of pH and specific ion electrode meters. Able to work in a fast-paced environment. Strong chemical math skills. PC savvy Quality control tech Expertise with microscopy, spectroscopy, chromatography, and x-ray related techniques as applied to analytical chemistry evaluation. Qualitative identification of materials, quantitative measure of chemical composition and general problem-solving skills Experience with oversight of high-volume lab processes with minimal supervision from senior technical staff. Knowledge and experience with software for statistical evaluation, presentation and report generation is mandatory Lab Chemist duties: Customer interfacing (Communication: Correspondence, Presentation, etc.) Compliance & Understanding of Corporate Standards (Safety, Housekeeping, Quality, etc.) Upkeep of Digital Programs (Microsoft, LIMS, Statistical Analysis etc.)

Be a part of a global team where what we do matters! At Epredia, we recognize that our talented employees are vital to our success. Our team is dedicated, our work is rewarding - both personally and professionally - because what we do matters. We seek talented individuals who will contribute to and thrive in our collaborative, diverse, fast-paced environment while demonstrating a commitment to our core values, People, Customer, Results, Continuous Learning, and Innovation. People - We win as a team. Customer - We deliver customer-centric solutions. Continuous Learning - We learn and always aim to be better. Innovation - We innovate every day. Results - Results matter for all of us. Job Title: Quality Control Chemist Who you are: You have energy and drive in abundance, a passion for serving our customers and possess a growth mindset and love of continuous learning, with an appreciation for diverse perspectives and helping others win. Position Overview: Our values reinforce our culture of collaboration, growth mindset, and how we serve our customers. * You will perform routine testing and inspection of manufactured products, raw materials, in-process samples and finished products in our Quality Assurance Laboratory. This testing is is essential to ensure the quality of our products for customers' use in diagnosing cancer. * You will report directly to the QC Laboratory Manager and be a member of a top-notch team of highly-skilled, energetic analysts. Every phase of production depends on the accuracy and thoroughness of the testing and inspections performed by the QA Lab staff. Location: This is an on-site position based out of Kalamazoo, MI. What you will do: Performs routine testing on manufactured products, incoming raw materials, in-process products, and finished goods. Testing assays include: pH, water content (Karl Fischer titration), UV-Vis spectrophotometry, gas chromatography, formaldehyde titration, viscosity, refractive index, residue, and other routine chemical tests. Documents results with accuracy and adheres to current good manufacturing practices (cGMP, cGDP). Collaborates with Quality, Manufacturing, and R&D colleagues to troubleshoot issues, improve processes, assist with new instrument verification and validation, write work instructions, revise standard operating procedures, and develop/validate new testing assays. Works with colleagues in R&D, Regulatory, Marketing, and Manufacturing to review new raw materials, review product formulations, and adjust product formulations when necessary. * Inspect incoming products and raw materials for quality specifications. * Test samples for physical properties (pH, color, water content, residue, viscosity, specific gravity, RI, UV-Vis, FL-AA, GC assay, etc.). * Record data and test results following good manufacturing and documentation practices. * Calculate batch adjustments to meet specifications and approve batches for packaging. * Collaborate with Quality, Manufacturing and Engineering colleagues to troubleshoot issues, improve processes, validate equipment, write work instructions, and develop new tests. * Investigate non-conformances and write corrective action reports. Qualifications & Skills: * Bachelor's degree in Chemistry and a minimum of two years of experience in an analytical laboratory. * Experience with analytical equipment (pH, titrations, gravimetry, RI, FL-AA, GC, etc.). * Experience in proper data handling, documentation and recordkeeping (cGMP, cGDP). * Detailed-oriented, positive team attitude, able to handle a fast pace and shifting priorities. * Honesty, integrity, efficiency, punctuality, multitasking, and a good work ethic. The hiring range for this position is: $49,500 - $61,000, plus individuals may be eligible for an annual discretionary bonus. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. (Epredia Company) offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation and more. #LI-SJ1 TO ALL RECRUITMENT AGENCIES: Epredia does not accept unsolicited third-party resumes. Building an Inclusive Culture: We are a company that brings the best people together and leverages their varying backgrounds, ideas, and points of view to invent on behalf of all customers. We are committed to equal employment opportunity for all individuals, without regard to race, color, national origin, ancestry, sex, age, religion, physical or mental disability, medical condition, veteran status, marital status, pregnancy, sexual orientation, gender identity, genetic information or any other protected classes which may exist under applicable federal, state or local law.

Be a part of a global team where what we do matters! At Epredia, we recognize that our talented employees are vital to our success. Our team is dedicated, our work is rewarding - both personally and professionally - because what we do matters. We seek talented individuals who will contribute to and thrive in our collaborative, diverse, fast-paced environment while demonstrating a commitment to our core values, People, Customer, Results, Continuous Learning, and Innovation. People - We win as a team. Customer - We deliver customer-centric solutions. Continuous Learning - We learn and always aim to be better. Innovation - We innovate every day. Results - Results matter for all of us. Job Title: Quality Control Chemist Who you are: You have energy and drive in abundance, a passion for serving our customers and possess a growth mindset and love of continuous learning, with an appreciation for diverse perspectives and helping others win. Position Overview: Our values reinforce our culture of collaboration, growth mindset, and how we serve our customers. + You will perform routine testing and inspection of manufactured products, raw materials, in-process samples and finished products in our Quality Assurance Laboratory. This testing is is essential to ensure the quality of our products for customers' use in diagnosing cancer. + You will report directly to the QC Laboratory Manager and be a member of a top-notch team of highly-skilled, energetic analysts. Every phase of production depends on the accuracy and thoroughness of the testing and inspections performed by the QA Lab staff. Location: This is an on-site position based out of Kalamazoo, MI. What you will do: Performs routine testing on manufactured products, incoming raw materials, in-process products, and finished goods. Testing assays include: pH, water content (Karl Fischer titration), UV-Vis spectrophotometry, gas chromatography, formaldehyde titration, viscosity, refractive index, residue, and other routine chemical tests. Documents results with accuracy and adheres to current good manufacturing practices (cGMP, cGDP). Collaborates with Quality, Manufacturing, and R&D colleagues to troubleshoot issues, improve processes, assist with new instrument verification and validation, write work instructions, revise standard operating procedures, and develop/validate new testing assays. Works with colleagues in R&D, Regulatory, Marketing, and Manufacturing to review new raw materials, review product formulations, and adjust product formulations when necessary. + Inspect incoming products and raw materials for quality specifications. + Test samples for physical properties (pH, color, water content, residue, viscosity, specific gravity, RI, UV-Vis, FL-AA, GC assay, etc.). + Record data and test results following good manufacturing and documentation practices. + Calculate batch adjustments to meet specifications and approve batches for packaging. + Collaborate with Quality, Manufacturing and Engineering colleagues to troubleshoot issues, improve processes, validate equipment, write work instructions, and develop new tests. + Investigate non-conformances and write corrective action reports. Qualifications & Skills: + Bachelor's degree in Chemistry and a minimum of two years of experience in an analytical laboratory. + Experience with analytical equipment (pH, titrations, gravimetry, RI, FL-AA, GC, etc.). + Experience in proper data handling, documentation and recordkeeping (cGMP, cGDP). + Detailed-oriented, positive team attitude, able to handle a fast pace and shifting priorities. + Honesty, integrity, efficiency, punctuality, multitasking, and a good work ethic. The hiring range for this position is : $49,500 - $61,000, plus individuals may be eligible for an annual discretionary bonus. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. (Epredia Company) offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation and more. #LI-SJ1 TO ALL RECRUITMENT AGENCIES: Epredia does not accept unsolicited third-party resumes. Building an Inclusive Culture: We are a company that brings the best people together and leverages their varying backgrounds, ideas, and points of view to invent on behalf of all customers. We are committed to equal employment opportunity for all individuals, without regard to race, color, national origin, ancestry, sex, age, religion, physical or mental disability, medical condition, veteran status, marital status, pregnancy, sexual orientation, gender identity, genetic information or any other protected classes which may exist under applicable federal, state or local law. At Epredia, we improve lives by enabling better cancer diagnostics. We are a team of talented individuals with diverse backgrounds and expertise, working together to develop precision diagnostic solutions for our customers. We are a fast growing global company that drives innovation in diagnostics to create better outcomes for patients. Joining Epredia is much more than a job- it is an opportunity to be part of something with a purpose. Find out how you can improve lives while advancing your career.

Piramal Pharma Solutions' HPAPI Research and Manufacturing facility, located in Riverview, Michigan, is seeking a qualified Quality Control Chemist I to join our Quality Control team. The Quality Control Chemist II is responsible for providing analytical chemistry support for the facility. To perform this position 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: * Shall adhere to all applicable regulatory requirements, including FDA, EPA, OSHA, and related safety, health and environmental procedures, policies and practices. * Consistent support and practice of all Piramal Pharma Solutions mission, vision, and values. * Identify and protect the original technical information as part of the company property. Key responsibilities. * Support manufacturing operations through the testing of raw materials and starting materials as required to meet production timelines. * Perform cleaning verifications on multi-use equipment using approved methods. * Test reference standards and stability samples. * Document sample preparation, equipment set-up, and test results in laboratory notebooks or other appropriate test record forms. Verify data with second quality team member as required. Maintain all records as required to maintain compliance. * As required, test intermediates and final products to meet production timelines/client requirements. * Assist in the revision of documentation as required. * Participate in quality unit projects, including but not limited to supplier certification, methods development, methods validation and training of both quality unit members as appropriate. * Provide support in the maintenance and calibration of laboratory analytical instrumentation. * Assist in the maintenance of the QC laboratory through routine housekeeping, as well as keeping personal bench area and desk organized. * As required, perform routine testing on the water system (DI, ice, potable, and QC water), and prepare reports as needed. Education/Experience. * Bachelor's degree in Chemistry or Biochemistry or equivalent. * One (1) year of experience in pharmaceutical quality control or equivalent is preferred * Familiarity with analytical testing and instrumentation. Job Competencies. * Excellent organizational and planning skills. * Strong written, verbal, and interpersonal communication skills. * High attention to detail. * Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines. Job Conditions. The physical demands and work environment described here are representative of those that must be met by a team member to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Physical Demands: * Frequent lifting, bending, stooping, squatting, pushing and pulling can be expected. * Long periods of standing and walking can be expected in this position. * This position may require long periods of sitting, typing, computer entry or looking at a computer. * Work Environment: * Piramal Pharma Solutions is engaged in the business of pharmaceutical research and contract pharmaceutical manufacturing. As such, all PPS staff work in or nearby either chemical/pharmaceutical research or chemical/pharmaceutical manufacturing equipment and processes. * Potential limited exposure to hazardous chemicals. * Personal protective equipment including safety glasses, lab coats, gloves, specialized clothing including laboratory uniform and appropriate shoes may be required in areas associated with this position.

Responsive recruiter Benefits: Bonus based on performance Competitive salary Dental insurance Health insurance Opportunity for advancement Paid time off PEL Labs is looking for an environmental laboratory analyst to add to our rapidly growing firm. We are seeking an analyst ideally with experience in both flame AA lead paint analysis and PLM asbestos analysis, but will consider candidates with experience in one or the other who are willing to be cross-trained. Applicants must possess a minimum of 1-year of experience in lead paint analysis and/or PLM asbestos analysis in order to be considered. Primary duty will be as analyst in asbestos/lead, but will also be expected to assist with other general laboratory functions including sample accessioning, recordkeeping, supply ordering, phones, light janitorial, etc. Position is full time. Business hours are 9am - 5pm Monday to Friday, but there is some flexibility to work an earlier/later shift. Required weekend work is possible, although extremely rare. All full time employees are offered medical, dental, and vision insurance as well as a generous PTO plan. Benefits/Perks Flexible Scheduling Competitive Compensation Career Advancement Opportunities Job SummaryPreparing, identifying, and analyzing a variety of environmental samples. Responsibilities Preparation and analysis of bulk and paint chip samples for analysis using Atomic absorption spectrometry (AAS) and/or similar equipment. Preparation and analysis of bulk and solid materials for asbestos content using PLM (Polarized Light Microscopy) and all ancillary quality control procedures Determination of visual percentage and optical properties of asbestos and non-asbestos material Record data in a specified manner Sample and media preparation and inventory management Compensation: $45,000.00 - $60,000.00 per year PEL is a rapidly growing laboratory specializing in asbestos, mold, lead and smoke damage assessments. See our website, **************** for additional information on our growing company. We offer highly competitive pay, benefits, and room for anyone to grow within the company.

Full-time Description Laboratory Analyst will be responsible for conducting accurate and timely analyses of environmental samples, ensuring compliance with regulatory standards and supporting the company's mission to promote environmental health and sustainability. Job Responsibilities: Perform chemical, physical, and microbiological analyses on environmental samples, including water, soil, air, and waste. Prepare, calibrate, and maintain laboratory instruments such as spectrometers, chromatographs, and other analytical equipment. Follow standardized procedures and methodologies to ensure precise and reproducible results. Record, interpret, and report test results in accordance with established protocols and regulatory requirements. Assist in the development and validation of new analytical methods. Maintain detailed and accurate laboratory records, including sample logs, chain of custody, and quality control documentation. Monitor laboratory quality assurance/quality control (QA/QC) procedures to ensure adherence to accreditation standards (e.g., ISO 17025, NELAC). Troubleshoot equipment malfunctions and participate in preventive maintenance schedules. Collaborate with team members to ensure timely project completion and client satisfaction. Adhere to all safety guidelines, maintaining a clean and organized workspace. Perform all other duties as assigned. Requirements Education: Bachelor's degree in Chemistry, Environmental Science, Biology, or a related field. Experience/Qualifications: 1-3 years of experience in an environmental or analytical laboratory setting required; TO-15 experience preferred. License/Certification: Must have a valid driver's license. Knowledge/Skills/Abilities: Familiarity with standard laboratory techniques, such as gas chromatography (GC), liquid chromatography (LC), and inductively coupled plasma (ICP). Strong understanding of environmental regulations and testing standards. Excellent analytical and problem-solving skills. Proficiency with laboratory information management systems (LIMS) and Microsoft Office Suite. Strong attention to detail, organizational skills, and the ability to manage multiple tasks. Effective communication and teamwork skills. Work Environment: Laboratory environment with exposure to chemicals and testing equipment. Requires adherence to safety protocols, including the use of personal protective equipment (PPE). May involve occasional lifting of heavy equipment or materials (up to 25 lbs). Equal Employment Opportunity: Metiri Analytical Group, Inc. is an equal opportunity employer that celebrates diversity and is committed to an inclusive workplace for all employees. We prohibit discrimination based on race, color, sex, religion, age, national origin, disability, genetics, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Role Description The QO Lab Analyst position works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze finished product samples prior to commercial release. This is a dynamic, growing lab within a growing manufacturing site with opportunity to learn new skills and to work cross-functionally. Performs, documents and record checks qualitative and quantitative assays on samples. The primary technologies in this lab are HPLC and dissolution. Interprets and evaluates data for accuracy, precision, trends, and potential GMP impact. Recommends and executes process improvements to continually improve laboratory performance. High productivity and the ability to multi-task coupled with a low error rate and attention to detail are critical characteristics of this position. Demonstrates flexibility/agility and engagement in a changing environment. The candidate is expected to display good laboratory technique to avoid cross-contamination or misidentification of samples. Ability to follow written procedures. May train others as skills and knowledge allow. Troubleshoot instrumentation as skills and knowledge allow. Participates in laboratory investigations as required. May participate in manufacturing QC support such as cleaning verification. SHIFT HOURS: 2:00pm-10:30pm. Overtime may occasionally be required. EDUCATION AND EXPERIENCE AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred. Related experience in Quality Control is preferred but not required. Preferred experience includes GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS, HPLC, Dissolution, use of Empower3 Key characteristics of a successful candidate in this position: willingness and ability to learn, ability to work in a team environment, and attention to detail. Job duties involve occasional lifting (less than 35 lbs). Candidate must not be Cephalosporin/Penicillin sensitive. Full time RegularColleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

IEH Laboratories, a Leader in Food Safety, is now accepting applications for Laboratory Analyst - Day Shift at its facility in Muskegon, MI. Ideal candidates will possess the following skills: - A high school diploma or GED (required); a BS or BA in the biological sciences or related field (preferred) - Proficiency with data entry and computer applications - Strong attention to detail - Ability to multitask and work in a fast-paced environment - Strong written and verbal communication skills - Strong understanding of aseptic technique in the laboratory - A valid US driver's license and clean driving record (including, at minimum, no accidents in the last 5 years) that meets/continues to meet motor vehicle risk standards, as verified through ongoing MVR monitoring Laboratory Analyst duties include analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. Full-time employee will be eligible for standard benefits after a brief waiting period. Multiple shifts are available for this position including: (i) 12h hour rotating shift, from 10:00am - 10:00pm, and (ii) 8-hour Monday through Friday shift. Occasional weekend and holiday work may be required. Due to exposure to various food allergens in the laboratory environment, applicants with moderate to severe food allergies are discouraged from