Chemist jobs in Ohio

Job Description PharmaLogic is the fastest-growing SPECT & PET radiopharmaceutical solutions provider and contract development and manufacturing organization (CDMO) with radiopharmacies across North America. We are passionate about expanding the power of radiopharmaceutical technology to provide transformative diagnostic and therapeutic agents to patients from bench to bedside. PharmaLogic offers you an exceptional opportunity to join our dynamic team as a PET Chemist! As the Quality Assurance Specialist, you will play a vital role in the PharmaLogic quality program to assure compliance with cGMP and other standards for the manufacture of drugs for administration to patients. Responsible for completion of required quality assurance tasks of finished drug product as directed by cGMP SOPs and serves as site expert on PET quality assurance. The position involves a hands-on role in all quality assurance duties for the site, including materials acceptance and quarantine, batch release & record review, drug quality control, sterility, environmental monitoring, equipment maintenance / qualification/ calibration, investigation (IR, OOS, deviation, etc.) and corrective actions (CAPA), SOP writing, maintenance and review, inspection readiness, data quality and integrity, ANDA documentation and other routine QA functions. The QA Specialist is responsible for assisting in FDA inspections at the site. Ideally, there will be separation of QA functions from production and QC functions. However, depending on the size of the facility, these activities may be performed by the same person if there is the ability to segregate batch release from production through appropriate cross-training for batch release. For smaller facilities, the site QA Specialist may assume other duties which may include production activities, operation of the facility's cyclotron and associated chemistry modules and analytical equipment for production and QC of PET radiopharmaceuticals. The position may be required to perform various radiation safety and quality related tasks as directed by management. Job Responsibilities and Duties: Ensure compliance with all regulatory commitments and company policies and SOPs including cGMP and radiation safety. Actively promote adherence to SOPs, as well as safety rules and awareness. Report and take initiative to correct safety & environmental hazards. Provide immediate notification of quality related issues to site Manager, PET Operations Management and Q&R as necessary. Oversee production operations to assure that PET drugs meet requirements for identity, strength, quality and purity. May Perform PET radiopharmaceutical Quality Control (QC) in cGMP environment May perform aseptic processing related tasks Responsible for quality assurance oversight of routine production, packaging and shipping of radioisotopes. Examine and approve/reject components, closures, in-process materials, packaging materials, labeling and finished dosage forms to assure that all meet specification; manage onsite inventory quarantine and control process according to SOPs to assure specifications are met. Assure approved vendors used and maintain documents and records, including COA. Review batch, laboratory and production records to assure completeness, accuracy and conformance before batch release; authorize or reject batch according to SOPs or oversee batch release by other qualified team members. Perform batch trending analysis. Notify facility manager if any recall necessary to assure that recalled materials are not administered to patients. Initiate change to SOPs, participate in authoring and review of SOPs, maintain documents under control in QMS. Assure SOPs match processes and procedures in PET manufacturing operation and report concerns to Management. Document and Trend deviations, IRs, events and initiate investigation and assure documentation of corrective actions and retraining as applicable. Initiate and complete CAPA investigation as deemed necessary, and report results and trends. Maintain facility compliance with environmental monitoring and aseptic control, Review and trend environmental monitoring results and all testing records. Maintain records for inspection. Perform annual retraining upkeep of training files. Assure aseptic processing of samples and products, as per SOP. Assure aseptic processing area suitably cleaned, maintained, controlled to prevent mix-ups or contamination; assure personnel qualified in aseptic technique and cleaning of the area and that approved cleaning agents and processes used according to SOP. Assure environmental monitoring records are complete and readily available, including annual personnel media fill qualifications. Assure equipment is functional, within calibration, suitable for use, maintained and documented per SOP. Assure equipment qualified and operated under specified conditions; maintain vendor IQ/OQ and site PQ documents. Assure master production, laboratory controls/analytical tests and other control records are consistent with actual work procedures and any discrepancies reported to PharmaLogic Quality and Regulatory. Assist in maintaining records to comply with FDA and SOP requirements. Maintain, monitor, and report out on the location QA program to management. Support the site lead for FDA and other agency, vendor and internal quality audits, as directed. Maintain site audit readiness by thorough records, personnel, and facility review. Maintain site copy of ANDA and all related filing documentation up to date, available and organized for review. Draft ANDA related documents for submission including annual reports and other updates as required. Assists in conducting periodic and annual quality audits, training, SOP review and other activities as directed Job Requirements │ Skills │Education: BS/BA degree in a relevant scientific discipline (chemistry, physics, nuclear pharmacy, nuclear medicine, engineering, etc.) and a minimum of 1-3 years Quality experience in the pharmaceutical industry, or an equivalent combination of education and experience preferred. Pharmacy tech certification a plus; experience with aseptic technique a plus Experience working with ionizing radiation and laboratory equipment desirable including troubleshooting and repairs. Strong analytical, critical thinking and customer service skills. Experience working on a cross-functional team in fast-paced environment. Strong knowledge of cGMP environment and regulations. Knowledge of CFR21 Part 212 preferred. Strong attention to detail and experience with managing multiple projects and priorities. Come join our winning team and begin a fulfilling career with us by applying today. PharmaLogic is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other protected class. Benefits Include: 401(k) retirement benefit program Medical Dental care Disability insurance Employee assistance program Life insurance On-site parking Paid time off Vision care

Job Description Chemical Mixer / Blender is responsible for mixing raw materials to create finished products according to batch tickets. Duties and Responsibilities: · Set up and start all mixing tanks and blenders. · Obtains and understands all documentation for making batches. Ensures correct ingredients are used for each batch. · Pumping and pouring chemicals into blend tanks in predetermined quantities. · Properly storing all chemicals, materials, and finished products. · Pumping and pouring finished product into containers for resale. · Operates equipment (mixers, scales, meters, pumps, forklifts, etc.) safely. · Monitors raw material usage on each blend are added correctly with right weights. · Ensures all raw materials returned to inventory have the right quantity and information on containers and containers are in good condition. · Follows lab instructions regarding batch approval, adjustments, and any additional requirements. · Cleans equipment and containers when needed. · Refers issues/problems to supervisor person(s). · Communicates with vendors/suppliers when materials are needed. · Complete all paperwork and batch documentation in a timely manner. · Maintain inventory counts on all supplies, products, materials. · Communicate with branch managers, chemist, accounting and truck drivers. · Observes safety requirements set forth by company. · Performs other related duties as required. · Ensure facility and equipment is secure. Position Requirements: · High School Diploma or GED equivalent. · Must be able to read/comprehend written and oral instructions in English, including safety rules, operating procedures, product recipes, material identification, etc. · Able to manipulate 55-gallon drums of chemicals. · Must have mathematical skills to add, subtract, multiply, and divide. Able to perform these operations using weight and volume measurements. · Able to manipulate powder bags up to 55 lbs.

Job Description We are adding to our Pharmaceutical Quality Control Chemistry Staff. We are currently seeking entry level individuals to: • Perform analytical testing of raw material, in-process product, final product release and stability testing., • Clear documentation of test activities in approved worksheets and laboratory notebooks., • Execute mathematical calculations as outlined in test methods., • Assess data to determine if the material tested meets specifications., • Peer review of quality control data., • Participate in investigational testing and assist with root cause analysis., • Create and review SOP’s and author Change Controls., • Bachelor's degree in Chemistry, Biochemistry, Biology, or related field, • One to two years' experience with hands on testing such as pH, titrations, determination of physical appearance, UV, IR and other wet chemistry tests. Instrumentation work with KF, HPLC, and GC, including instrumentation software a plus., • Hands-on analytical chemistry experience, • Prior success working with regulatory, USP, GLP, GDP, and cGMP requirements., • Ability to use Microsoft Suite of tools., • Pharmaceutical experience a plus.

Job DescriptionCompany Description 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 Job Description CDL Sign on Bonus $3,000.00 PRINCIPAL DUTIES AND RESPONSIBILITIES: • 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., • May require obtaining and maintaining 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., • Performs other duties as assigned.Qualifications Basic Requirements: • An associate’s degree in general science (BS preferred) is required for the Lab Pack Chemist., • Driver’s License with clear record, • Moderate to extensive travel with 20% overnight travel, • Physical ability to lift and move material of various weights frequently exceeding 55 lbs. This position is also contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements. Additional Information 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 (833) 209-2659 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

Job Description Job Title: Analytical Chemist Job Description We are seeking a dedicated Analytical Chemist who will be responsible for migrations, extractables and leachables, impurity isolation, identification, and structural characterization studies. The role requires proficiency in LC-MS/MS and GC-MS, as well as strong sample preparation skills. You will work in a GMP analytical laboratory involved with FDA testing and handle pharmaceuticals and food packaging. Reviewing data for technical content and regulatory compliance will be part of your core responsibilities. Responsibilities • Conduct migrations, extractables, and leachables studies., • Isolate, identify, and characterize impurities., • Operate and maintain LC-MS/MS and GC-MS instruments., • Prepare samples for analysis., • Work with pharmaceuticals and food packaging materials., • Proficiency in LC-MS/MS and GC-MS., • Strong knowledge in analytical chemistry., • Experience in a GMP laboratory., • Knowledge of FDA compliance., • Ph.D. in Chemistry or a related field., • 2-4 years of experience in an analytical laboratory., • Experience with HPLC, GC, HPLC MS/MS, semi-prep chromatography, and lyophilization., • Experience in the isolation and identification of impurities. The role is based in a lab environment where you will work with extractables and leachables, migrations, and utilize LC-MS/MS technology. You will be part of a high-level pharmaceutical company, providing an excellent opportunity to gain valuable experience in the pharma industry. Job Type & Location This is a Permanent position based out of Painesville, Ohio. Job Type & Location This is a Permanent position based out of Painesville, OH. Pay and Benefits The pay range for this position is $65000.00 - $85000.00/yr. 401K, medical, dental, vision, PTO, Vacation time Workplace Type This is a fully onsite position in Painesville,OH. Application Deadline This position is anticipated to close on Dec 24, 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 for other accommodation options.

Job Description Environmental Enterprises, Inc. is a specialty environmental management and disposal company. We are dedicated to protecting the environment by providing quality environmental services, recycling options, and waste disposal at competitive rates through innovative technologies and superior technical support. We strongly support improving the quality of life for our employees and the community. We are currently looking to fill the challenging and rewarding position of Lab Pack Chemist This is an entry level position that involves working both indoors and outdoors at our customer’s sites. This is NOT a laboratory position. The field chemist is responsible for preparing containers for pick up, including identification of chemicals, lab packing hazardous and non-hazardous chemicals at customer locations. Limited travel including overnight stays (~10%). DETAILS OF ASSIGNMENT: • Moving and preparing containers (pails, drums, viles) for transport, • Identification of chemicals, • Packing hazardous and non-hazardous chemicals at customer locations At times, the field technician may be required to wear a full or half face respirator, SCBA, or air lines. Ability to routinely lift 60 pounds, with occasional lifting in excess of 60 pounds. Insurable driving record. Willingness to obtain a class B CDL with hazmat endorsement within the first year preferred. High school graduate required. 2-year degree in chemistry or other natural sciences highly preferred. The field technician is OSHA HAZWOPER 24-Hour trained. Typically, the work is conducted in Level D but sometimes conditions warrant Level B or C personal protective equipment. Some travel may be necessary for this position. The field technician is capable of taking direction, working well with others, and decision-making. Additional skills required for this position are provided below. • Safety oriented, • Observant, • Resourceful Learn more about the great things we do at: Environmental Enterprises Inc. is an Equal Employment Opportunity (EEO) employer and does not discriminate on the basis of race, color, national origin, religion, gender, age, veteran status, political affiliation, sexual orientation, marital status or disability (in compliance with the Americans with Disabilities Act) with respect to employment opportunities. Full Time; Monday to Friday 8 AM to 4:30 PM 40 hours weekly

Job DescriptionSalary: $50,000-$60,000/year JOB TITLE: CHEMIST REPORTS TO: Laboratory Manager STATUS: Full-time, exempt LOCATION: Avon Lake, OH (onsite) SALARY RANGE: $50,000-$60,000/year depending on experience and interview outcome BENEFITS: Medical, dental, and vision insurance, optional FSA/HSA, 401k with 6% employer match, life and AD&D insurance, Employee Assistance Program, short & long term disability, tuition reimbursement, 21.67 days of paid time off + 10 holidays About Tidal Vision: We believe that sustainability should not require customers to compromise on price, convenience, or performance. Our mission is to create positive and systemic environmental impact by making our biopolymer solutions cost competitive, more convenient, and better performing than the synthetic chemicals we displace. We value innovation and take pride in challenging the status-quo; we choose to view obstacles as opportunities. We value new ideas and encourage the team to apply creativity and invent new solutions to meet challenging demands. We foster open, direct communication, and a collaborative working environment through our unique approach to work culture. We value our employees and demonstrate that through our compensation and benefits programs and opportunities for growth and development. Applied Specialties Innovations. (ASI): Applied Specialties, LLC. was founded in 1981 as a water treatment company that specialized in providing heavy industry clients with service and technology geared to individual needs. The founding concept was, and remains today, concentrated on solving client problems with as little chemicals as possible. ASI was acquired by Tidal Vision in 2024, and both work towards providing valuable solutions to our customers while serving our mission. About Tidal Visions Unique Work Culture: Tidal Vision strives to build and invest in the highest performing and most innovative team. We put our people and customers above process, avoid company-wide rules as much as possible, and have the courage to take unusual approaches to advance our mission. With this approach, we believe we can create a more flexible, fun, stimulating, creative, collaborative, and innovative organization. Our commitment to developing, practicing and promoting direct and open communication, responsibility and freedom, and leading with and seeking context is a responsibility for every role at Tidal Vision. JOB SUMMARY: The Chemist in Quality Control and Applications is responsible for the instrumental and wet chemistry techniques for testing materials, finished products, customer samples, and components. The testing includes, for example, ICP-OES, IC, and wet chemistry. The Chemist will work in the laboratory in a safe and effective manner. ESSENTIAL JOB FUNCTIONS: • Analytical testing of materials, finished products, customer samples, and components. This testing will primarily be instrumental ICP-OES, IC, along with wet chemistry techniques., • Performs QC testing, generates C of As, and maintains documentation for QA/QC program., • Will train lab personnel on ICP, IC and other lab equipment and procedures., • Becomes familiar with the appropriate specifications and methods for testing., • Execution of mathematical calculations outlined in the test methods., • Analysis of data to determine if material tested meets specifications., • Determines mathematically what is necessary for and advises production on the blending of final products to meet specifications., • Assists with development of test methods, writing and validating procedures for customers., • Assists with product development including formulating, prototypes, reliability, safety, and environmental testing., • Maintains meticulous records and assists with laboratory audits., • Learn aspects of the water treatment industry from colleagues., • Prepares data summaries and reports for salesmen and customers., • Assist with the development of a laboratory and company-wide quality management plan., • Assists with preparation and shipping of samples to customers and field agents., • Assists with preparation of safety data and product data sheets., • Maintains material inventory in the lab, maintains laboratory safety data sheet files., • Maintains a clean and orderly work area. Cleans counters and storage areas and maintains records of samples. Consolidates samples for disposal as directed., • Maintains and further assists lab manager with NSF documentation., • Maintains the organization and operational efficiency of the laboratory working towards continuous improvement., • Complies with all ANSI, EPA, DOT, and OSHA regulations and company policy including hazardous wastes., • Reports all accidents, injuries/illnesses, spills to supervisor., • Adhere to ISO documents and meet company / department quality, environmental & safety objectives., • Other duties as assigned. BASIC QUALIFICATIONS: • Bachelors degree in Chemistry, Chemical Engineering, or related field., • 1 + years experience in laboratory work must include preparation of samples, following written procedures, record keeping and excellent interpersonal skills., • Ability to work for extended periods of time without direct supervision., • 1+years of experience including practical experience with ICP, IC, and wet chemistry techniques. Use of Microsoft Office products, especially Microsoft Excel is a must. Licensing & Special Requirements • Incumbent is subject to a criminal background check., • Incumbent is subject to drug screening. WORKING CONDITIONS & PHYSICAL REQUIREMENTS: The incumbent must be able to lift 50+ lbs, carry, twist, walk, bend, rotate, and stand. Must be able to be visually and spatially aware of surroundings and be able to hear. Must be able to work in varying temperatures and in environments such as the laboratory, production floor, and general office settings. Proper PPE is required at all times. Tidal Vision and ASI provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. The statements contained herein reflect general details as necessary to describe the principal functions of this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Individuals may perform other duties as assigned including work in other functional areas to cover absences or relief, to equalize peak work periods, or otherwise to balance the workload. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the employer.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ABOUT ABBOTT: Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Abbott’s Nutrition Division develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, Glucerna® – to help get the nutrients they need to live their healthiest life. WORKING AT ABBOTT: At Abbott, you can have a good job that can grow into a great career. We offer: * Fast paced work environment where your safety is our priority * Production areas that are clean, well-lit and temperature-controlled * Training and career development, with onboarding programs for new employees and tuition assistance * Financial security through competitive compensation, incentives and retirement plan with company match * Health care and well-being programs including medical, dental, vision, wellness and occupational health programs, Medical Benefits start Day 1 * Vacation – 3 weeks accrued vacation (1st year is prorated) + vacation buy program + 3 personal days + 10 paid holidays * Company Paid Pension Plan * Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. * A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. * A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. * The stability of a company with a record of strong financial performance and history of being actively involved in local communities Learn more about our benefits that add real value to your life to help you live fully: . THE OPPORTUNITY: The Analytical Chemist Laboratory Supervisor (Night Shift, 6:30pm - 7:00am EST – with alternating weekends) is responsible for implementing and maintaining the effectiveness of the quality system for our Tipp City, Ohio location. The position is based on-site (Tipp City, Ohio). This position reports directly to the Site Quality Assurance Manager or Compliance and Food Safety Manager. * Responsible for the overall results for a single shift of a multi-shift laboratory operation that is open 7-Days per week * Coordinate activities for the shift team to ensure delivery of all key performance metrics including those in Environmental, Health and Safety (EHS), Quality, Finance, Productivity and People * Lead efforts required to deliver quality and compliance performance for the shift. Initiate, manage, and make decisions which impact product quality. * Drive a culture of engagement through the team and department. Directly supervise a team of 3-6 employees and participate in staffing activities. Develop all line personnel by securing appropriate staffing, training, mentoring, performance reviews, and assigning progressively challenging stretch responsibilities within the scope of the team and department accountabilities. Maintain a safe lab environment. * Assure lab test results reflect compliance to plant, division, and corporate guidelines and procedures and that test methods are followed * Engage with employees and other key stakeholders to ensure all EHS requirements are met inclusive of internal and external regulatory objectives and direction * Promote behaviors that ensure delivery of high-quality products for our customers while maintaining compliance with Abbott policies and procedures, meeting all local and statutory requirements, and adhere to the regulatory requirements of countries to which products are shipped * Prepare and actively participate in internal and external Quality audits and incident investigation and reporting; coupled with timely implementation of CAPA activities * Model and promote a thorough understanding of what drives product costs, profitability, and cash flow for the shift and within the department, while operating within budget material utilization and Cost Improvement Program goals. Manage budget accountability for Headcount, Overtime, and direct expenses for a shift and/or line. Track, trend and continuously improve budgetary performance for direct expenses, headcount, overtime (OT), and Scrap and Cost Improvement Projects (CIP). * Manage and guide a team(s) of lab associates to improve quality and increase productivity of the lab * Coordinate activities related to shift starts and changes. Lead and coordinate daily activities of the shift team. Work with their direct manager, other Front Line Leaders and other management, and establish the right team culture where people feel empowered, are accountable for the business and continuously improve the shift and the lab. * Track, trend & report on established Key Performance Indicators (KPI) SHIFT: This is an onsite, salaried, night shift position (6:30pm - 7:00m EST) with an alternating 2, 2, 3 schedule. Example: Week 1: Monday: 12 hours, Tuesday: 12 hours, Wednesday: OFF, Thursday: OFF, Friday: 12 hours, Saturday: 12 hours, & Sunday: 12 hours Week 2: Monday: OFF, Tuesday: OFF, Wednesday: 12 hours, Thursday: 12 hours, Friday: OFF, Saturday: OFF, & Sunday: OFF Week 3: Monday: 12 hours, Tuesday: 12 hours, Wednesday: OFF, Thursday: OFF, Friday: 12 hours, Saturday: 12 hours, & Sunday: 12 hours REQUIRED QUALIFICATIONS: * Bachelor’s Degree in science, food technology, technical, or a related degree * 2 years or more of related experience PREFERRED QUALIFICATIONS: * 2 or more years of experience in a laboratory in a regulated industry with preference for experience in one or more of the following industries: food, pharmaceuticals, medical devices, cosmetics, or a related regulated industry * Laboratory Experience within a regulated manufacturing work environment with emphasis on infant formula manufacturing experience/high-volume manufacturing support laboratory * Experience using project planning and execution tools * Knowledge of FDA – 21 CFR and other regulatory requirements for Infant Formula * Microsoft Office computer skills * Leadership experience * Knowledge of project planning tools * Experience working with and implementing Continuous Improvement projects Apply Now • Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: . Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity and a Military/Veteran Friendly employer. Connect with us at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $60,000.00 – $120,000.00. In specific locations, the pay range may vary from the range posted.

Job Summary A well respected and leading specialty chemical company that supports a variety of industries is seeking a Chemist to join their team in Ohio. This role will be focused on QC testing of raw materials, in-process samples, and finished goods within a GXP environment. • Day Shift and Night Shift available, • Schedule is 3 days per week (12hr shifts) and 1 day every other weekend., • Pay: $28.00/hr Responsibilities • Conduct analytical testing (HPLC and GC) per SOPs using instrumentation and wet chemistry methods., • Provide in-process testing support and ensure clear shift handoffs., • Calibrate and maintain lab equipment., • Lead OOS investigations and monitor CAPA effectiveness., • Assist with method optimization, troubleshooting, and equipment upkeep., • Maintain and update product specifications in internal systems. Qualifications • Bachelor’s in Chemistry or related field and 2+ years industry lab experience., • Proficient with GC, GC-MS, HPLC, LC, titrations, spectroscopy, physical testing, and related techniques, • Comfortable with working a 12hr schedule This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you

Synthetic Chemist – Material Science | Ohio (On-site) We’re working with a global leader in advanced materials, seeking a hands-on chemist to drive innovation and performance breakthroughs in the rubbers space. This is a unique opportunity to join a high-impact team focused on pioneering new additives and sustainable solutions for next-generation products. About the Role: You’ll lead investigations into complex chemical systems, collaborating with multidisciplinary experts to engineer transformative products. Reporting directly to technical leadership, you’ll have the autonomy to shape research direction, influence product development, and see your innovations swiftly implemented in real-world applications. What You’ll Do: • Conduct detailed studies of reaction mechanisms, kinetics, and material properties in rubber and polymer systems., • Utilize advanced analytical techniques and computational methods to characterize and predict performance outcomes., • Develop mechanistic models and propose new pathways for superior material properties., • Collaborate with scientists, process experts, and industry partners to integrate insights into product design and manufacturing., • Scout and evaluate emerging technologies to drive sustainability and performance, including renewable materials and alternatives to conventional additives. What You Bring: • Ph.D. in Organic Chemistry, Physical Chemistry, Polymer Science, or related field., • Proficiency with analytical instrumentation and data interpretation., • Strong problem-solving skills and ability to apply chemical principles to practical innovations., • Excellent communication skills for technical documentation and team collaboration., • Prior experience in the rubber industry is a plus.

Collaborate on multidisciplinary innovation, partnering with application scientists, synthetic chemists, process experts and tire manufacturers to integrate mechanistic insights into molecular design, next-generation tire formulations, evaluating environmental impacts, and support of pilot trials fo

Collaborate closely with internal technical, operations, commercial, and production support teams to understand the dispersion performance requirements in the coating, along with any manufacturing constraints and downstream process needs for the dispersion. Support and participate in manufacturing s

Collaborate with production and process engineer(s) to learn about processing of gums, HCR, LIMS.

Collaborate on multidisciplinary innovation, partnering with application scientists, synthetic chemists, process experts and tire manufacturers to integrate mechanistic insights into molecular design, next-generation tire formulations, evaluating environmental impacts, and support of pilot trials fo

The chemist supports basic business process and technical training for new hires. Participates in new business or internal business process improvement opportunities. Interact with internal technical and operations teams to gain understanding of coatings and manufacturing process requirements.

Collaborate on multidisciplinary innovation, partnering with application scientists, synthetic chemists, process experts and tire manufacturers to integrate mechanistic insights into molecular design, next-generation tire formulations, evaluating environmental impacts, and support of pilot trials fo

Prepares research proposals, technical specifications, reports and presentations, and specifies laboratory test equipment and processes.

Collaborate with scientists, process experts, and industry partners to integrate insights into product design and manufacturing.

We are seeking Quality Control Technician, to Conduct QC testing on raw materials, in-process samples, and finished products to deliver accurate, timely results aligned with ISO and cGXP requirements. Quality Control Chemist: $28-30 hour. Quality Control Lab Tech: $23-26 hour.

The Judge Group is seeking a Chemist for a manufacturing company located in the Cleveland area.MUST HAVE: Bachelors Degree, Chemistry.MUST HAVE: Chemical manufacturing experience.Prepare and validate prototype samples following company procedures.Interact with commercial and internal teams to meet c

PPG values your feedback on our recruiting process. Benefits will be discussed with you by your recruiter during the hiring process.

Job Summary A Research Analyst II supports the receipt, login, distribution, and disposal of materials utilizingthe appropriate software systems. About Charles River Charles River is an early-stage contract research organization (CRO).

An excellent opportunity to join a growing organization with great benefits! Duties: Assists QC Lab Technicians by testing and conducting routine and non-routine analysis of raw materials, in process, and finished products using a variety of testing devices and procedures to maintain product quali

Reducing overall material cost and waste through formulation and process improvements.

We are seeking QC Chemist, to Conduct QC testing on raw materials, in-process samples, and finished products to deliver accurate, timely results aligned with ISO and cGXP requirements. Support production with in-process testing and ensure smooth shift handoffs.

Job Description MANE is a 5th generation French family-owned business known for innovation and progress in the world of Flavor and Fragrance. As sensation enthusiasts, we strive to provide exceptional moments in people’s daily lives through the timeless flavors and fragrances we create. With our passion, creativity, and innovation, “We capture what moves”. Manage flavor development projects and provide project direction to R&D, Technology, Sales, Category Management, etc. as necessary. Formulate new flavor creations or modify existing flavors to meet customer requirements, internal testing needs or new technology development. The Flavor Chemist will effectively drive functional business growth in support of company goals and objectives while continuing to learn valuable techniques from Senior Flavor Chemists to advance knowledge, skills, techniques, and expertise. DUTIES AND RESPONSIBILITIES: • Create Savory flavors that meet the regulatory, cost, and performance guidelines outlined in R&D projects. Modify existing flavors and/or create new flavors as needed to meet internal as well as external customer project requirements., • Complete assigned projects and internal requests within the designated time frame and cost guidelines. Follows all procedures for documentation of flavor specifications and project completion., • Ensure that all flavors created adhere to manufacturing standards and internal technical and commercial aspects., • Provide technical flavor expertise and customer support (internal and external) for assigned market/project segments., • Lead technical presentations to customers and sales force as needed., • May manage a Flavor Technician’s daily work efforts., • Supports internal teams with issues or challenges as assigned., • Assist in the general up-keep, maintenance, and stocking of the Flavor Laboratory, e.g., lab cleanliness, raw material and flavor sample archival and inventory management., • Consistent with MANE’s environmental commitments, every employee shall actively participate in relevant education/training based upon corporate and local environmental objectives., • Other duties and responsibilities in support of company objectives, • Bachelor’s Degree in Science or related discipline, • 10+ years of experience creating winning flavors., • Thermally processed flavor formulation experience is considered an advantage. MANE is an equal opportunity employer.

Job Description The Senior Color Chemist is responsible for creating formulations to ensure our product matches our customers' color requirements for various applications. Responsibilities: • Create Color Matches at a high level of quality and efficiency., • Create formulations that meet customer specifications, cost parameters and manufacture capabilities at a high rate of efficiency., • Perform and excel at multiple color matching techniques, coloring systems, & color solutions., • Utilize strong knowledge and experience of formulating color and effects for multiple applications., • Maintain accurate & legible records that align with Ampacet’s ISO requirements, as well as good documentation practices (GDP)., • Be a mentor for other color chemists and assist in the development of the color chemists and color technicians., • Interface with and support internal & external customers where applicable., • Maintain lab and equipment in the highest standards for a clean working environment., • Adhere to all safety rules and regulations according to quality and safety policies., • Work at a high level of efficiency and productivity to support Ampacet service commitments., • Provide support to Color Lab Sample Department on the processing & color corrections when applicable., • Assisting Color Technicians as needed., • Assist production/QC in color corrections, • Perform additional projects or tasks as assigned by Color Lab Supervisor, • Communicate effectively and proactively with Sales. Requirements: • High School degree required, higher education in a related discipline preferred, but years of experience will be considered in lieu of a college degree., • Must have a minimum of 5 years’ of colormatching for masterbatch experience, with a focus on rigid packaging. Experience formulating for engineered resins applications is a plus., • Experience formulating for multiple applications, including but not limited to injection molding, blow molding, sheet extrusion, and thermoforming is required., • Strong formulating background with engineering grade resins, as well as knowledge of multiple extrusion processes, blow molding and injection molding., • Strong technical understanding and experience in all masterbatch formulating but with a specific focus on thermoplastics and engineered resins., • Experience utilizing various coloring methods and chemistries including pigments, dyes, and special effect type raw materials is expected., • Strong background in masterbatch as it relates to various color matching lab equipment types & processes, extrusion equipment, injection & blow molding, • Experience with X-Rite spectrophotometer and software., • Must pass Farnsworth-Munsell Color Discretion Test, • Excellent Color Vision and discretion, • Proficiency in MS Office (Outlook, Word & Excel), • Ability to work independently as well as on a team, • Excellent organizational and time management skills: ability to prioritize, • Able to communicate verbally and in writing with a high degree of professionalism.