Research and development technician jobs in Kentucky - 71 jobs

Open your doors to a new possibility: Meijer is seeking candidates for our growing team. We're currently seeking Retail Team Members to join our family-owned company based in the Midwest. When you work retail with Meijer, you grow your customer service skills in a clean, safe environment with potential for career advancement. Our retail openings are available in all departments, including: Food Clerk Stocking Clerk General Merchandise Clerk Customer Service Meijer believes in efficiency, productivity, and growth. The following benefits are available to our retail staff: 10% team member discount Paid training Workplace diversity Flexible scheduling Weekly payroll Health coverage options Opportunities for promotion Required skills: Communicating with customers on a consistent basis in a friendly manner through positive eye contact and body language. Detail oriented and organized. Building rapport with customers through quality customer service. Providing assistance by responding to customer questions in an effective and efficient manner. Ability to stay calm while working in a fast paced environment. Ability to stand for long periods of time. Ability to lift, carry, push, pull, bend and twist while handling product.

Valeo is a tech global company, designing breakthrough solutions to reinvent the mobility. We are an automotive supplier partner to automakers and new mobility actors worldwide. Our vision? Invent a greener and more secured mobility, thanks to solutions focusing on intuitive driving and reducing CO2 emissions. We are leader on our businesses, and recognized as one of the largest global innovative companies. Together We Can Foster a More Sustainable Aftermarket, Join Valeo Service. Valeo is an automotive supplier and partner to automakers worldwide. As a technology company, we design innovative solutions for smart mobility, with a particular focus on intuitive driving and reducing CO2 emissions. Valeo's site located in Saint-Denis - 93 (330 employees) is Valeo Service Headquarters. Valeo Service, part of the Valeo Group, is the automotive aftermarket specialist worldwide. We provide a full array of services, of Original Equipment Spares to manufacturers and replacement parts and accessories to the Independent Aftermarket. Our commitments ? Reducing environmental impact and providing customers a safe, comfortable and unique driving experience. The teams at the Valeo Service Technical Center are currently looking to fill a vacancy for an Aftermarket Technical Development Engineer M/F, who will be responsible for managing and carrying out the technical development of after-sales products and services for distributors/repairers. Your responsibilities: * Identify customer needs * Write functional specifications for products (systems, electronics, electromechanics) * Monitor technical product development (quality, cost, deadlines) * Define functional validation tests and the test plan * Identify suitable suppliers * Specify reliability requirements for each supplier and analyze risks * Monitor the validation phase * Prepare for launch and monitor production * Work closely with the sales, marketing, purchasing, and quality teams * Present developments from the VS technical center to customers * Assist customers with specific technical issues * Identify benchmark services/products on the market What about you ? With a five-year degree (engineering, master's) in electronics, embedded systems, or electromechanics, you have at least five years of professional experience in the automotive sector. You have developed skills in product development, including a systems dimension, as well as in writing technical specifications. Recognized for your interpersonal skills and your ability to communicate effectively both orally and in writing, you thrive in a multicultural environment. You are proactive, have a positive attitude, and are proactive in finding solutions. You are fluent in English. A driver's license is required for this position, which involves conducting vehicle tests. Employee Benefits: * Profit-sharing * Company restaurant * Social and Economic Committee Why Valeo? * To join a top tech company shaping tomorrow's automotive industry * To explore national and international career mobility opportunities * To support the development of greener, safer and smarter mobility Valeo sees the diversity of its employees as a key asset across all of its businesses, in all its forms - including gender diversity, disability diversity, cultural diversity and intergenerational diversity. Job: Aftermarket Technical Support Organization: Technical Center Schedule: Full time Employee Status: Regular Job Type: Undefined term Job Posting Date: 2026-01-08 Join Us ! Being part of our team, you will join: * one of the largest global innovative companies, with more than 20,000 engineers working in Research & Development * a multi-cultural environment that values diversity and international collaboration * more than 100,000 colleagues in 31 countries... which make a lot of opportunity for career growth * a business highly committed to limiting the environmental impact if its activities and ranked by Corporate Knights as the number one company in the automotive sector in terms of sustainable development More information on Valeo: *********************

Build your career at Sazerac! With almost 400 years of rich history, Sazerac Company has thrived as an independent, American family-owned company with operations in the United States and around the world. Since the 2000s, Sazerac has averaged double digit growth every year! Sazerac Company produces and markets the most award-winning bourbons and whiskeys in the world, including Buffalo Trace, Pappy Van Winkle, Eagle Rare, Blanton's, and Sazerac Rye. Additionally, Sazerac owns many popular brands across a range of spirits, including Fireball, Southern Comfort, Seagram's V.O., Myers's, Goldschläger, Parrot Bay, 99 Brand, and Platinum Vodka. We're proud of our award-winning culture and distilleries. Our Louisville office has been named one of the “Best Places to Work in Kentucky” four times, and our Buffalo Trace Distillery has earned the title of “world's most award-winning distillery” through the dedication of our craftsmen for well over 200 years. Whether you're a recent graduate or an experienced professional, Sazerac provides extraordinary opportunities for growth with competitive salaries and benefits in an exciting, entrepreneurial industry. Job Description/Responsibilities The Product Development Scientist is responsible for new product development activities, reformulation of existing products, shelf life testing, conducting taste panels, and gathering information for formula submission to TTB; and assists in the QC laboratory as needed. Ensure the work environment is safe and practice safe work policies of the laboratory. Adhere to all OSHA, state and local regulations. Provide the best service to the entire customer base, both internal and external. Monitor and conduct taste panels. With knowledge of sensory evaluation techniques, conduct taste panels to determine the statistical difference between products through the use of Blind Triangle tests, Duo-Trio tests and/or Two-out-of-Five tests. Conduct taste panels to determine the acceptability of various product iterations through consumer preference. Develop and maintain a solid professional working relationship both inside and outside the company in a manner that's consistent with Sazerac values. Utilize company systems, such as CDS, the NBD System and Cognos, to be more efficient, effective and achieve goals. Engage in career development discussions with manager to communicate career aspirations and identify skill development needs to achieve career goals. Improve at least one skill each year as agreed with supervisor. Deliver on performance against outcomes, and record by commenting in the PDS system. Working with Brand Managers, through the use of creativity and the Brand Manager/PD Manager's direction, develop and create alcoholic beverages that meet or exceed demands of customers and consumer. Develop and prepare working formulas for all products developed or purchased by the company. Obtain all necessary documents for submission to the TTB for formula approval. Assist in the development, implementation and maintainance of the Sazerac Quality System as it relates to New Product Development and Formulation. Through testing and knowledge, ensure that there are minimal customer complaints due to formulation related issues. Ensure adherence to Personal Safety, Food Safety, Quality and Environmental Policies and Practices. Develop and maintain Sazerac product specifications and formulation with work instructions (SOP's) for the Processing Department in order to manufacture the product commercially. In addition, once a new product/ product reformulation is approved, test the final product for stability. This process will monitor and track changes in the product through the shelf life study. A regular report of new product shelf life will be completed and distributed. Assist in the documentation and auditing of the new product laboratory procedures, processes and systems to identify improvement opportunities and efficiencies. Ensure all lab practices and Sazerac product formulas meet company and regulatory requirements. Qualifications/Requirements MUST Bachelor's Degree (Food Science or related degree) 5-10 years relevant experience (minimum) Ability to communicate with all levels of an org Excellent oral & written communication skills Strong planning and organizational skills Physical Requirements Ability to pick up and/or move objects up to 50 pounds without assistance. Ability to work overtime if necessary Ability to work 8 hour shift In-person job attendance Strong communication skills Distinguish flavors through taste and smell Ability to read and write Ability to pay attention to detail Ability to work in fumes or airborne particles conditions Noise level at work station is moderate (business office with computer printers) Ability to identify and distinguish colors #LI-TH1 #LI-Onsite Culture and Benefits A career at Sazerac offers you the opportunity to reach your full potential as part of a creative, decisive, high-performance team. Sazerac values the needs and wants of our team members and offers inclusive benefits to attract and retain the best talent. Our culture is built upon the values of hard work, diligence and personal responsibility. Sazerac Team Members enjoy: Competitive Pay Comprehensive Benefits from Day One including medical, dental, vision, disability, and life insurance. Family Coverage: Options to cover family members, including domestic partners. 401(k) Plan: Immediate access to a matching 401(k) plan. Flexible Time Away: Enjoy paid time off (PTO), holidays, and parental leave. Mental Health and Wellness: Access to mental health care and wellness incentive programs. Educational Support: Benefit from tuition reimbursement and our scholarship program for dependents of Sazerac team members. Fun Extras: Enjoy branded apparel, fun events, and a team member bottle purchase program. Training and Development: Opportunities for professional growth and development. Benefits, salary range, and programs may vary by role or location. For roles within our commercial team - the Salary range refers to base salary only and does not include car allowance, annual bonus, fuel or cell phone reimbursement. Please ask your Talent Acquisition Partner for more information about our total rewards package. Sazerac is committed to equality of opportunity without regard to race, color, religion, national or ethnic origin, veteran status, age, gender, gender identity or expression, sexual orientation, genetic information, physical or mental disability or any other legally protected status. Min USD $85,661.60/Yr.

Full-time Description ***NOTE: This opening is for a split shift position, Monday-Friday. Ideal schedule would be 10:30AM-7:00PM, but alternative schedules could be 11:30AM-8:00PM or 12:30-9:00PM. The Certifying Scientist is responsible for the quantitation of MS data and the final review of patient data and patient reports and interacting with clients to assist with report issues, such as issuing new reports, updating patient demographic information, and similar concerns. Ethos manages clinical samples for diagnostic drug and metabolite confirmation analysis, and this candidate will engage in professional work in conducting toxicological examinations to identify and quantify target compounds. In addition, they will participate in validation studies, proficiency testing programs, method development, and other programs at the direction of the Confirmation Supervisor. ESSENTIAL FUNCTIONS Final review and certification of patient reports following established protocols - specifically for urine and oral fluid testing - utilizing and reporting point of care testing, EIA screening, and LC-MS/MS confirmation testing results Transcribe data from first review onto final review list Review reports individually, checking for completion of all demographic information, all ordered tests, and that results correspond to established norms Identify and confirm prescribed medication vs. inconsistent reports - either due to the presence of non-prescribed medications or illicit drugs Add comments to reports as needed Document completed reports and items for further review Collaborate and communicate with other departments to maintain the highest quality standards for testing procedures Answer incoming phone calls to the Confirmation department from customers, including questions regarding basic toxicology, basic drug metabolism, assistance with report issues, and sending reports Complete internal and external rerun requests Final review of internal rerun requests Review calibration and quality control data for each batch of patient samples Perform data analysis on patient samples for multiple analytes using mass spec software programs Utilize established protocols to confirm retention time, precursor and product ions, and qualifier ions are within established ranges for peak qualification and note any discrepancies Identify patient samples requiring reinjections or re-extractions following established protocols Program reinjections to run on the mass spec instruments Document data analysis completed and items for further review Transmit completed data analysis to the Laboratory Information System (LIS) Assist in proficiency testing, monitoring of daily controls, and be responsible for operating within the established quality controls parameters; including the recognition of invalid data and bringing all errors to the supervisor's attention Complete updated reports as needed Ensure adherence to all regulatory requirements Other duties as assigned Requirements PROFESSIONAL REQUIREMENTS Regular and prompt attendance An advanced understanding of drug metabolism, toxicology, forensic testing, P450 enzymes, or testing principles specifically related to urine and oral fluid metabolism An advanced understanding of LC-MS/MS systems and data interpretation High level of attention to detail Proficient in operating complex laboratory instrumentation and computers with scientific software Ability to participate in method development, validation or research with Technical Supervision preferred Able and willing to follow established protocols employing acceptable forensic standards of analysis and the use of judgment in searching for solutions or new applications within one's own experience Must be able to work with limited supervision where the work assignments are subject to established procedures, practices, precedents, methods, techniques, standards, and/or well-defined policies Must be able to achieve superior results when work is reviewed in terms of quality, volume, timeliness, and adherence to established methods, standards and policies Participate in ongoing training and continuing education courses related to drug metabolism, toxicology, and LC-MS/MS systems Responsible for promoting a collaborative and entrepreneurial environment Must be able and willing to wear personal protective equipment (PPE) when required Proficient with Microsoft Office applications EDUCATION AND EXPERIENCE REQUIREMENTS Master's Degree in Life Science, Pharmacology, Toxicology, Biology, Physics, or similar analytical science field or Bachelor of Science in similar field with 1 year of related experience Preference for candidates with familiarity with LC-MS/MS instruments (other experience in instrumental analysis of HPLC or LC-MS/MS of drugs in biological tissues may be acceptable) Preference for candidates with familiarity with Agilent MS and LC systems - specifically MassHunter Acquisition and Quantitation programs Previous work with bodily fluids - such as urine and oral fluid is preferred KNOWLEDGE, SKILLS AND ABILITIES Ability to communicate effectively, orally and in writing Ability to coordinate laboratory functions and represent the toxicology laboratory professionally Excellent time management, documentation, and organizational skills Demonstrated troubleshooting abilities Must be flexible, innovative, and self-motivated Ability to plan and organize his/her work Ability to function independently and in a team environment Ability to listen, learn, and promote accountability and responsibility related to all processes PHYSICAL REQUIREMENTS Work is performed in a laboratory environment and exposes the incumbent to normal laboratory hazards and chemicals, including biohazard materials Work in varying degrees of temperature (heated or air conditioned) Position requires sitting, walking, reaching, bending, stooping, and handling objects with hands and/or fingers, talking and/or hearing, and seeing DIRECT REPORTS None

Biochemist Biophysicist needs 2+ years hands-on experience in biophysics, bioconjugation, protein labeling, or a combination thereof. Biochemist Biophysicist requires: BS, MS, or PhD in Biochemistry, Chemical Biology, or related field. 2+ years hands-on experience in biophysics, bioconjugation, protein labeling, or a combination thereof. Direct knowledge in assay development and utilizing SPR/BLI (e.g. Biacore or Octet) or LCMS technologies (e.g. QTOF or Orbitrap) Experience in method or assay development utilizing a variety of LCMS technology (e.g. QTOF or Orbitrap). Working knowledge of fluorescent based method or assay development (e.g. FP, FRET, etc). Working knowledge in assay development and utilizing SPR/BLI (e.g. Biacore or Octet). Excellent interpersonal skills with the ability to communicate and interact well with colleagues at all levels. Committed to staying current with the latest scientific breakthroughs in structure-based drug design and biophysical analysis. Biochemist Biophysicist duties: Work closely with senior scientists to accomplish team objectives and research milestones. Contribute to the development and optimization of conjugation schemes to achieve the required product specifications. Commit to producing and maintaining the highest standard of quality in antibody-conjugate productions. Perform the following bioconjugation procedures; 1) Antibody and recombinant protein isolation and purification, 2) Purification of antibodies and conjugates using various liquid chromatography methods (IEX, SEC, HIC); 3) Antibody and conjugate validation via various functional tests, 4) Biophysical characterization of proteins and conjugates (e.g., UV/VIS spectrophotometry, DLS, SEC-MALS, native mass-spectrometry Tm or Tagg determination). Characterize protein-ligand and protein-protein interactions by a variety of methods including but not limited to; Intact protein and peptide-based mass spectrometry, native mass spectrometry, fluorescence spectroscopy, SPR, BLI, and DSF.

Copperhead Environmental Consulting is expanding its team with Seasonal Wildlife Technicians. Wildlife Technicians assist Copperhead's Scientists with collecting data, conducting research and routine equipment maintenance/testing, and performing basic data entry while working in the field on multiple types of projects; however the technician will predominately be involved in projects involving the study of endangered bat species. These positions are seasonal/temporary, non-exempt, hourly (number of weekly hours not guaranteed but eligible for overtime). Positions will begin in May 2026 and end in August 2026. The number of seasonal positions and seasonal timeframes are approximate and are based on business need. Opportunity for regular employment at the end of the season is possible but not guaranteed. These positions are entry level, physically demanding and require travel to project sites including multiple day/week overnight stays and opportunity for overtime compensation. Travel expenses including transportation from the Copperhead office to the project site, meals and lodging are paid for by Copperhead. On-the-job, paid training is also provided. Cost of transportation to the Copperhead office prior to initiation of the project is not paid for. Amount of Travel: Estimated between 80% - 95% Requirements General Basic understanding of scientific principles. Assist with collection of data and basic data entry. Assist Scientists with the maintenance and care of field data, specimens, and samples. Assist with routine equipment maintenance and testing. Assist with transporting equipment to job sites including setting up and breaking down equipment. Learn and adhere to the corporate safety program and expectations. Utilize proper Personal Protective Equipment (PPE) when working in the field. Assist with ensuring all proper PPE and field gear is available for projects. Prepared to be away for up to two weeks at a time including over holidays as needed. Comfortable with working primarily at night in potentially adverse conditions and remote areas. Willing to work with a variety of personality types and people. Adapt easily to rapid changes in scheduling due to field work, project, and business needs. Willing to take direction and receive constructive criticism from team members and supervisor. Excellent communication skills including auditory, verbal, and written. Other duties as assigned. Project Management Understand the scope of services as it relates to assigned tasks and projects. Complete tasks within expected deadlines and with adherence to quality standards. Take initiative to ask questions, request help, and provide status updates on assigned tasks. Client Service Interact professionally both internally and externally at all times. Advance a conservation ethic, inspire biological curiosity, and drive environmental change. Physical Demands and Work Environment The physical demands described here are representative of those that must be met by an individual to safely and successfully perform the essential functions of this position. The individual is required to: Communicate effectively using auditory, verbal, and written skills Use hands and fingers to handle or feel objects, tools, or controls. Stand, walk, sit - often for long periods of time and on uneven surfaces; reach with hands and arms; climb or balance; and stoop, kneel, crouch, or crawl. Lift up to 30 pounds. Have excellent vision to include close vision, distance vision, color vision, peripheral vision, and the ability to adjust focus. Tolerate moderate noise levels in the work environment. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions and will be considered on a case-by-case basis. Other information to consider: The functions listed above, including physical demands, are only a summary and are not meant to serve as an exhaustive or comprehensive list of all possible job responsibilities, tasks, and duties and requirements. Candidates must be able to pass a pre-employment background check and future drug tests as applicable based on specific project requirements. Must hold a valid driver's license (REAL ID preferred in the event air travel and access to military bases is needed) and have a clean driving record to meet insurance requirements. Seasonal on-site room and board may be available for those who need it. One year experience or working towards or hold an associate's degree or higher in a related field of study required. Previous field experience with bats, mist-netting, and/or acoustic monitoring preferred. Pre-exposure rabies vaccination preferred - No one will be permitted to handle bats without the pre-exposure vaccination. Salary Description $15-$17/hour

NorthKey Community Care is seeking full-time Adult Development Technicians to work with individuals with intellectual and developmental disabilities (IDD) who attend NorthKey's Adult Day Training program in Williamstown, KY. The program provides services to adults with disabilities, assisting them with becoming more independent and involved in their community. PERKS & PAY Salary: $14 an hour Up to 12% annual contingency bonus Flexible schedule opportunities Generous plan for paid time off (PTO) (Up to 16 days first year) 10 Paid Holidays Individual and family insurance coverage: Various medical, vision, and dental plans to choose from HSA Employer match up to $1000, depending on plan 401(k) with employer match Professional Development Potential eligibility for Student Loan Forgiveness through the Public Service Loan Forgiveness program. QUALIFICATIONS High school diploma or equivalent is required. Relevant knowledge, training, and experience with adults with intellectual and developmental disabilities preferred. Ability to drive a motor vehicle and a valid driver's license. RESPONSIBILITIES Engage clients with intellectual and developmental disabilities (IDD) in a structured collaborative relationship which empowers them to gain necessary skills in a variety of areas related to personal skills development across the vocational spectrum. Promote environmental and developmental independence to improve and maintain lifelong well-being and highest level of functional status. Provide evidence based care in the area of skills development. Address functional challenges of individuals served. Provide education to clients to promote improved functioning and skills development. Participate in the development of an individualized plan for clients needing additional social and occupational skills. Prevent unnecessary functional deterioration that could result in loss of social and occupational skills. Provide job assistance, supervision, training, and direction to facilitate the development and maintenance of social and occupational skills. Maintain HIPAA compliance and appropriate client confidentiality. Complete initial and/or annual and other mandatory trainings as assigned related to position. Transport clients to community events when needed. NORTHKEY COMMUNITY CARE - COMPANY OVERVIEW Since 1966, NorthKey Community Care (NorthKey) has provided effective and efficient mental health, substance use, and developmental disabilities services to the Northern Kentucky region with the commitment to providing the right service, at the right time, and in the right place. NorthKey's commitment to providing a continuum of services for individuals and families seeking assistance for mental health, substance use, and developmental disabilities means that NorthKey employs staff with a wide variety of education, experience, and licensure. With multiple convenient locations throughout the Northern Kentucky region (Kenton, Boone, Campbell, Grant, Carroll, Gallatin, Pendleton, and Owen counties), NorthKey offers a wide array of mental health, substance use, and developmental disabilities services unparalleled in the region. Come join our team to help us Transform Lives and Communities through Excellent Service ! Benefits: 401(k) 401(k) matching Dental insurance Employee assistance program Employee discount Flexible schedule Health insurance Life insurance Paid time off Tuition reimbursement Vision insurance

Business: Pharma Solutions Department: Analytical Quality Control (AQC) REPORTING STRUCTURE: reports to the AQC Group Lead. Reporting to the AQC Group Lead, the Chemist I performs testing of raw materials, in-process and finished products, and maintains and calibrates analytical instruments in compliance with cGMP standards. KEY RESPONSIBILITIES: • Perform routine/non-routine testing, both wet chemistry and instrumental analysis, according to SOPs, testing methods, protocols, compendia (USP EP/JP) etc. with minimum supervision • Testing of raw materials, APIs, finished products, stability samples, and cleaning verification samples, etc. • Document laboratory work according to, GDP, cGMPs, and SOPs • Troubleshoot, calibrate and maintain instruments as required • Prepare and label laboratory reagents, reference standards, or solutions according to SOPs. • Write SOP's, laboratory protocols and reports, memos and/or other interdepartmental correspondence • Participate in laboratory investigations • Perform peer review of analytical documentation • Follow safety procedures when working in laboratory. • Understand and comply with cGMPs and other regulations • Maintain the laboratory in an organized and neat manner • Act as backup for Material sampling activities. • Purchasing of laboratory reagents and consumables QUALIFICATIONS: • Bachelor of Science in Chemistry, Pharmaceutical Science, or other closely related scientific field • Minimum 1-year hands-on experience performing quality control work within a laboratory, proficiency with HPLC/GC analysis strongly preferred • Experience working with potent, cytotoxic materials and parenteral drug products preferred • High level of proficiency operating all Microsoft Office applications • Excellent communication skills, both verbally and in writing • Detail oriented and organized • Demonstrated ability to work within a team environment, supporting a continuous operation manufacturing facility • Excellent problem solving, communication, and interpersonal skills • Ability to follow written instructions

Business: Pharma Solutions Department: Analytical Quality Control (AQC) REPORTING STRUCTURE: reports to the AQC Group Lead. Reporting to the AQC Group Lead, the Chemist I performs testing of raw materials, in-process and finished products, and maintains and calibrates analytical instruments in compliance with cGMP standards. KEY RESPONSIBILITIES: * Perform routine/non-routine testing, both wet chemistry and instrumental analysis, according to SOPs, testing methods, protocols, compendia (USP EP/JP) etc. with minimum supervision * Testing of raw materials, APIs, finished products, stability samples, and cleaning verification samples, etc. * Document laboratory work according to, GDP, cGMPs, and SOPs * Troubleshoot, calibrate and maintain instruments as required * Prepare and label laboratory reagents, reference standards, or solutions according to SOPs. * Write SOP's, laboratory protocols and reports, memos and/or other interdepartmental correspondence * Participate in laboratory investigations * Perform peer review of analytical documentation * Follow safety procedures when working in laboratory. * Understand and comply with cGMPs and other regulations * Maintain the laboratory in an organized and neat manner * Act as backup for Material sampling activities. * Purchasing of laboratory reagents and consumables QUALIFICATIONS: * Bachelor of Science in Chemistry, Pharmaceutical Science, or other closely related scientific field * Minimum 1-year hands-on experience performing quality control work within a laboratory, proficiency with HPLC/GC analysis strongly preferred * Experience working with potent, cytotoxic materials and parenteral drug products preferred * High level of proficiency operating all Microsoft Office applications * Excellent communication skills, both verbally and in writing * Detail oriented and organized * Demonstrated ability to work within a team environment, supporting a continuous operation manufacturing facility * Excellent problem solving, communication, and interpersonal skills * Ability to follow written instructions

Job Title: Plant Chemist Why consider a career at MLC? MLC was recognized by Newsweek as one of America's Greatest Workplaces in 2024. * Highly collaborative work environment focused on growth and innovation * Safety and sustainability are top priorities * Excellent compensation, benefits, generous perks; focused on employee wellbeing * Great development and advancement opportunities * Bring your real self to work, come grow with us! MLC operates the largest lime facility in the Americas and mines some of the purest limestone reserves in the world…and we are global! The company is committed to development and employee satisfaction. Join our outstanding team! About the Job The Plant Chemist is responsible for all aspects of the Verona laboratory. This includes lab equipment setup and periodic preventative maintenance and calibration of such equipment. The Plant Chemist is responsible for stocking the lab with all necessary consumables for normal lab operation. They are responsible for routine analysis of production samples and outbound customer samples. The Plant Chemist is responsible for continued development and implementation of the Quality Control / Quality Assurance (QCQA) program in collaboration with the Quality Team Leader and Senior Chemist. This position uses collected sample data to generate certificate of analysis reports for outbound truck shipments. * Operation and routine calibration / maintenance of standard laboratory equipment including the LECO Carbon Sulfur, XRF, Reactivity testing equipment, Muffle Furnace, various Lab Crushers, Splitters, and Sieve Analysis devices * General housekeeping of the main laboratory and prep laboratory * Ensuring the laboratory is well-stocked and resourced with the necessary materials * Collect and analyze production samples at required intervals or as directed by Operations Manager or Team Lead position. * Enter the resulting quality data into the LIMS software and inform the appropriate supervisor or manager of the results. * Analyze required customer loadout samples. * Create Certificate of Analysis documentation for all outbound truck shipments * Supervises, schedules, and organizes the daily work of the Lab Technicians * Keeps attendance records on all laboratory personnel and submits biweekly reports for laboratory personnel to the payroll department * Maintains employee evaluations, goals, and objectives * Assures that all employees under their supervision are provided with a safe, clean work area and that they know and follow all Company policies and normal industrial practices pertaining to safety. * Employees are expected to perform other responsibilities as needed. Required Qualifications * Education: Bachelor of Science or Associates Degree in Chemistry or other relevant field of study preferred. * Experience: 1-2 years of laboratory experience required. * Knowledge: Must have an understanding of laboratory analytical procedures, customer specifications, and certification reporting requirements. Special consideration will go to candidates that have experience with XRF. Must have a working knowledge of statistics including statistical process control and the use of control charts. * Skills: The individual must have good time management skills to perform sample preparation and analysis in a timely fashion to keep the kiln operators and operations manager aware of the status of the kiln. Must be able to troubleshoot, maintain, and calibrate various lab instruments. * Abilities: The individual must have the ability to observe the work environment, collect data and independently solve problems or make recommendations for correcting identified deficiencies. * Behaviors: Strong communication and able to work under minimal supervision. * Schedule: Must be willing to be on call on off shifts and/or weekends when needed to assist with issues. The Fine Print Benefits and perquisites may vary based on the nature and location of each job. Click here for MLC EEO information About MLC MLC, headquartered in St. Louis, Mo., is a leading global supplier of high-calcium lime products and technical solutions. These offerings bring essential performance and value to a broad range of market applications, including metals, construction, chemical synthesis, water and emissions treatment, glass, textiles, plastics, rubber, agriculture, foods and beverages. With over a century in business, MLC has built a reputation on the quality of its products and services, as well as an unwavering commitment to safety, sustainability and service. The company's expanding global footprint includes a diversified, reliable network of production and distribution facilities in the U.S., as well as in the UK through our Singleton Birch business. For more information, visit *********************

Job Title: Plant Chemist Why consider a career at MLC? MLC was recognized by Newsweek as one of America's Greatest Workplaces in 2024. + Highly collaborative work environment focused on growth and innovation + Safety and sustainability are top priorities + Excellent compensation, benefits, generous perks; focused on employee wellbeing + Great development and advancement opportunities + Bring your real self to work, come grow with us! MLC operates the largest lime facility in the Americas and mines some of the purest limestone reserves in the world...and we are global! The company is committed to development and employee satisfaction. Join our outstanding team! About the Job The Plant Chemist is responsible for all aspects of the Verona laboratory. This includes lab equipment setup and periodic preventative maintenance and calibration of such equipment. The Plant Chemist is responsible for stocking the lab with all necessary consumables for normal lab operation. They are responsible for routine analysis of production samples and outbound customer samples. The Plant Chemist is responsible for continued development and implementation of the Quality Control / Quality Assurance (QCQA) program in collaboration with the Quality Team Leader and Senior Chemist. This position uses collected sample data to generate certificate of analysis reports for outbound truck shipments. + Operation and routine calibration / maintenance of standard laboratory equipment including the LECO Carbon Sulfur, XRF, Reactivity testing equipment, Muffle Furnace, various Lab Crushers, Splitters, and Sieve Analysis devices + General housekeeping of the main laboratory and prep laboratory + Ensuring the laboratory is well-stocked and resourced with the necessary materials + Collect and analyze production samples at required intervals or as directed by Operations Manager or Team Lead position. + Enter the resulting quality data into the LIMS software and inform the appropriate supervisor or manager of the results. + Analyze required customer loadout samples. + Create Certificate of Analysis documentation for all outbound truck shipments + Supervises, schedules, and organizes the daily work of the Lab Technicians + Keeps attendance records on all laboratory personnel and submits biweekly reports for laboratory personnel to the payroll department + Maintains employee evaluations, goals, and objectives + Assures that all employees under their supervision are provided with a safe, clean work area and that they know and follow all Company policies and normal industrial practices pertaining to safety. + Employees are expected to perform other responsibilities as needed. Required Qualifications + Education: Bachelor of Science or Associates Degree in Chemistry or other relevant field of study preferred. + Experience: 1-2 years of laboratory experience required. + Knowledge: Must have an understanding of laboratory analytical procedures, customer specifications, and certification reporting requirements. Special consideration will go to candidates that have experience with XRF. Must have a working knowledge of statistics including statistical process control and the use of control charts. + Skills: The individual must have good time management skills to perform sample preparation and analysis in a timely fashion to keep the kiln operators and operations manager aware of the status of the kiln. Must be able to troubleshoot, maintain, and calibrate various lab instruments. + Abilities: The individual must have the ability to observe the work environment, collect data and independently solve problems or make recommendations for correcting identified deficiencies. + Behaviors: Strong communication and able to work under minimal supervision. + Schedule: Must be willing to be on call on off shifts and/or weekends when needed to assist with issues. The Fine Print Benefits and perquisites may vary based on the nature and location of each job. Click here for MLC EEO information (****************************************************************************** About MLC MLC, headquartered in St. Louis, Mo., is a leading global supplier of high-calcium lime products and technical solutions. These offerings bring essential performance and value to a broad range of market applications, including metals, construction, chemical synthesis, water and emissions treatment, glass, textiles, plastics, rubber, agriculture, foods and beverages. With over a century in business, MLC has built a reputation on the quality of its products and services, as well as an unwavering commitment to safety, sustainability and service. The company's expanding global footprint includes a diversified, reliable network of production and distribution facilities in the U.S., as well as in the UK through our Singleton Birch business. For more information, visit ******************** . Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled

Our Work MattersAt Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world. Why Kindeva? Purpose-driven work environment Significant growth potential Collaborative team culture Direct impact on patient care Industry-leading innovation At Kindeva - Lexington, KY, we're not just testing products - we're ensuring the safety and quality of nasal spray medications that make a difference. The Impact You Will Make: Transform Lives Through InnovationJoin a rapidly expanding pharmaceutical CDMO where your work directly impacts patient health outcomes worldwide. Kindeva offers a rewarding and fast-paced cGMP pharmaceutical environment where your work directly contributes to the safety, quality, and efficacy of life-saving drug products. As a Chemist II, you will independently perform laboratory testing, support method validation and instrument qualification, and conduct investigations while contributing to continuous improvement efforts alongside a dedicated and collaborative team. Growth Opportunity Our Lexington facility is experiencing exponential growth, offering exceptional opportunities for professional development and advancement. Join us during this exciting expansion phase and grow your career while contributing to meaningful healthcare solutions. Responsibilities: Work safely in accordance with site procedures Perform incoming raw material sampling and testing, component inspection, in-process analyses, finished product release testing, and stability testing Maintain the laboratory in accordance with SOPs Calibrate, operate, and maintain analytical instrumentation for product testing, including routine preventive maintenance and troubleshooting Write, revise, and review Standard Operating Procedures, Material Specifications, Forms, Protocols, and Reports Understand basic analytical techniques and execute tasks under supervision or under the direction of a test method, standard operating procedure, or a protocol, including: HPLC UV/Vis FTIR GC Nasal spray testing Develop method validation knowledge Develop instrument qualification knowledge Good understanding of cGMPsDevelop investigative skills for OOS, OOT, and aberrant result laboratory investigations Good oral and written communication skills Recommend and implement, as required, innovative approaches to problem-solving Qualifications: Bachelor's degree in Chemistry or related field with 3 years of pharmaceutical industry experience Master's degree in Chemistry or related field with 1 year of pharmaceutical industry experience, PhD in Chemistry or related field Qualified to work with controlled substances Able to multitask and adjust priorities in response to changing conditions and schedules Team player with well-developed interpersonal, organisational, and communication skills Maintain proper social etiquette and self-control when dealing with stressful situations Physical Demands/Qualifications: An employee is required to use their hands to handle materials and supplies regularly Employee is required to use computers for an extended period each day An employee is required to effectively use electronic communication Employee is required to stand and walk for extended periods of time regularly Employee must occasionally lift and/or move up to 20 pounds Ability to use proper PPE and be conscious of the work area hazards Employee is required to follow all site safety procedures Join our One Team mission of manufacturing more tomorrows. Your expertise will help ensure better health and well-being for patients worldwide.#LI-Onsite

Assistant Manager / Management Trainee (Fast Track Manager Program) - SpeedWash Car Wash | Louisville, KY Full-time | $18/hr + bonus | Promotion-focused training (3-6 months to Assistant Manager certification) Want a role that builds real leadership skills and sets you up to run a location? SpeedWash's Fast Track Manager Program trains high-potential teammates to lead daily operations, coach teams, and drive performance in a high-volume, customer-first environment. Quick facts Location: 6014 Bardstown Rd. Louisville, KY 40291 Pay: $18/hour + performance bonus (bonus based on site and individual performance) Hours: Full-time (~40 hours/week) Availability: Open availability required, including weekends on a rotating schedule Growth: Pay increases are tied to performance and certification milestones, including Assistant Manager certification (typically 3-6 months) What you'll do Lead day-to-day shift execution: customer experience, speed, safety, and cleanliness Coach, train, and motivate teammates using clear expectations and feedback Drive membership and retail performance through great service and sales leadership Learn operational fundamentals: preventative maintenance, checklist routines, quality checks, basic KPI tracking, and labor awareness Resolve customer concerns and model exceptional customer service standards in a fast-moving environment Work outdoors and stay active while maintaining a professional, positive attitude What you'll need Open availability including weekends; reliable attendance is a must Comfortable working outdoors in all seasons and being on your feet throughout the shift Strong communication skills and a team-first mindset Confidence taking ownership and leading by example Leadership/retail/service experience is a plus (not required-we train) Ability to lift up to 50-75 lbs and work around moving vehicles Valid driver's license Benefits Competitive pay + bonus opportunity Company health, dental, and vision insurance PTO after 1 year One floating holiday Regular performance reviews with clear coaching and growth expectations Free uniforms 2 employee washes per week Biweekly pay This role is for someone who's hungry to win, humble enough to be coached, and people smart enough to bring a team with them. If you want to lead from the front, take ownership, and earn rapid growth through performance, this is your shot. Apply today - let's build your leadership path!

Your Role & Responsibilities Ensure the following tasks are performed by the branch quality lab Perform Quality Control analysis on incoming bulk raw materials, in-process production as part of our process control, and out-going materials for final analysis Record all pertinent analytical data in accordance with our Quality Management System Generate and maintain Certificates of Analysis for blended and packaged product and for outgoing bulk loads Perform necessary calibration checks and inspections on all instrumentation Perform maintenance on all instrumentation as is reasonably possible in the Branch Laboratory Instrumentation: GC, Karl Fischer titrator, Densitometer, RI, Spectrophotometer Prepare and standardize analytical reagents and solutions for use in daily analysis Maintain control of retention samples for storage and disposal Operate our pre-treatment facility Package samples for shipment to customers Maintain manning of the lab to accommodate production activities on all shifts Actively participate in our safety program by attending monthly plant-wide safety meetings, conducting a monthly SBWA (Safety By Walking Around), and reporting Near Misses. Provide technical support to all production departments in order to achieve target values and verify that materials meet customer specifications Ensure adequate training of new employees and cross training of tenured employees to maximize efficiency Assist customer service with quality-related customer inquiries and document requests, including in-person audits. Your Profile Education & Experience Bachelor's degree in chemistry, Three to five years lab experience with ICP, Gas Chromatography, HPLC and Infrared Spectrometry. Must be receptive to growth and training. Must be able to be trained in all functions relating to government regulations. Must be able to use knowledge of the field to make decisions without supervision. Must be able to train personnel below them. Our Offer We aim to create an environment where the best people want to work, where they can turn their passion into their job and realize their full potential. Individual development, on-the-job training, and development programs designed to help our employees grow in their careers. Paid parental leave Education assistance program Employee assistance program Various healthcare plan options as well as 401(k) Brenntag and its subsidiary companies will provide equal employment opportunities to all applicants without regard to any category protected by federal, state or local law, including as applicable, applicant's actual or perceived race, color, religion, creed, sex, sexual orientation, gender identity or expression (including transgender status), gender (including pregnancy, childbirth, lactation and related medical condition), genetic information, military service, national origin, ancestry, citizenship status, age, veteran status, physical or mental disability, protected medical condition as defined by applicable federal, state or local law, political affiliation, marital status, membership in an employee organization, parental status, expunged juvenile record, or any other status protected by federal, state, or local law. Brenntag will provide reasonable accommodations to allow an applicant to participate in the hiring process (e.g., accommodations for a test or job interview) if so requested. When completing this application, you may exclude information that would disclose or otherwise reference your race, religion, age, sex, genetic, veteran status, disability or any other status protected by federal, state, or local law. This application is considered current for sixty (60) days only. At the end of this period, if you are still interested in employment, it will be necessary for you to reapply by completing a new application. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to access job openings or apply for a job on this site as a result of your disability. You can request reasonable accommodations by contacting Human Resources at accommodations@brenntag.com (phone, tty, fax, email, etc.). Brenntag North America, Inc. and its subsidiaries use E-Verify, a government-run, web-based system that allows employers to confirm the eligibility of their employees to work in the United States. For more information, please go to ********************************** or view the poster at ********************************************** Contents/E-Verify_Participation_Poster.pdf. Brenntag TA Team

Weekend Chemical Analyst - Owensboro KY Be a part of a revolutionary change! At Philip Morris International (PMI), we've chosen to do something incredible. We're totally transforming our business and building our future on one clear purpose - to deliver a smoke-free future. With huge change, comes huge opportunity. So, if you join us, you'll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. Our success depends on people who are committed to our purpose and have an appetite for progress. This position sits with our Swedish Match affiliate. Your ‘day to day' Performs analyses utilizing gas chromatography, ultra high pressure chromatography, and ion chromatography. Responsible to maintain cleanliness and orderly arrangement of Analytical laboratory. Provides support to Sr Analytical Chemist, Analytical Chemist, Sr Chemical Analyst, and Chemical Analyst. Responsible for accurate records of assigned projects. Knowledgeable in ISO 17025 Standard requirements. May be required to work additional/different shifts. Provides support to Production, Research and Development, Quality Assurance, and Leaf Operations. Knowledgeable of method validation procedures. Performs special projects as directed by Chemical Analysis Supervisor/Manager. Responsible for sample preparation and extraction as indicated by written SOP. Responsible for written SOPs of validated methods and procedures. Responsible for routine and non-routine Microbiology testing. Ability to review, interpret, and report analytical results using LIMS. Who we're looking for: Minimum Bachelor's degree in scientific discipline such as Chemistry, Biology, related discipline or equivalent experience. Minimum one year as a Laboratory Technician or comparable position/experience. Knowledgeable in chemical laboratory safety and analytical procedures and methodologies. Knowledgeable of Microbiological procedures and equipment. Must be able to prepare concise and accurate reports. Must be able to work Saturday & Sunday (12:00am-12:30pm), Monday & Tuesday (12:00am-8:30am). Annual Base Salary $64,300 What's ‘nice to have' Legally authorized to work in the U.S. (required) What we offer We offer a competitive base salary, annual bonus (applicable based on level of position), great medical, dental and vision coverage, 401k with a generous company match, incredible wellness benefits, and much more! Seize the freedom to define your future and ours. We'll empower you to take risks, experiment and explore. Be part of an inclusive, diverse culture where everyone's contribution is respected; Collaborate with some of the world's best people and feel like you belong. Pursue your ambitions and develop your skills with a global business - our staggering size and scale provides endless opportunities to progress. Take pride in delivering our promise to society: To improve the lives of millions of smokers. PMI is an Equal Opportunity Employer. PMI is headquartered in Stamford, Conn., and its U.S. affiliates have more than 2,300 employees. PMI has been an entirely separate company from Altria and Philip Morris USA since 2008. PMI's affiliates first entered the U.S. market following the company's acquisition of Swedish Match in late 2022.Philip Morris International and its U.S. affiliates are working to deliver a smoke-free future. Since 2008, PMI has invested $12.5 billion globally to develop, scientifically substantiate and commercialize innovative smoke-free products for adults who would otherwise continue to smoke with the goal of transitioning legal-age consumers who smoke to better alternatives. In 2022, PMI acquired Swedish Match - a leader in oral nicotine delivery - creating a global smoke-free champion led by the IQOS and ZYN brands. The U.S. Food and Drug Administration has authorized versions of PMI's IQOS electronically heated tobacco devices and Swedish Match's General snus as Modified Risk Tobacco Products and renewal applications for these products are presently pending before the FDA. For more information, please visit ************** and ******************* #PMIUS #LI-DH1

Notes: Must have a degree Must be out of film converting. Our award-winning client is seeking an R & D Engineer to join their team. As a Product Development Engineer specializing in adhesive tapes, you will play a vital role in our innovation and product development initiatives. Adhering to established Design Control procedures, you will be responsible for developing new products and product variances. This dynamic role involves designing experiments, executing trials, and performing application testing to meet customer and market demands. Operating on pilot and production lines, you will work with various adhesive types, including solvent, emulsion, hot melt, and rubber-based pressure-sensitive adhesives and coatings. Responsibilities: Design Control Procedures: Follow established Design Control procedures for the development of new products and product variances. Experimentation and Trials: Design experiments, execute trials, develop and interpret data, and perform application testing to create new products aligned with customer and market demands. Pilot and Production Line Trials: Run trials on pilot and production lines using various adhesive types, including solvent, emulsion, hot melt, and rubber-based pressure-sensitive adhesives and coatings. Project Management: Implement product development projects consistent with corporate objectives, ensuring that project objectives are met and completed on schedule. Raw Material Sourcing: Source, analyze, and utilize new raw materials for product innovation and cost reductions. Issue Identification and Resolution: Identify equipment and processing issues affecting processing, quality, and performance. Collaborate with cross-functional teams on problem resolution and implementation. Tape Sample Preparation: Prepare finished tape samples, and operate various test equipment/methods, including application testing and data analysis for the evaluation and presentation of new tape designs. Technical Documentation: Implement technical documentation packages, including raw material specifications, product specifications, stability, and general technical data to support the introduction of new products. Standards and Testing: Know ASTM standards and PSTC methods to support product testing when required. Additional Duties: Perform additional duties as assigned by the Product Development Manager. Required Qualifications: Bachelor's degree in Chemical Engineering, Polymer Science, Chemistry, or related field. Three plus years of experience in pressure-sensitive adhesive tape, adhesive, or release liner design and manufacturing. Competence in the basic understanding of process control equipment and the interrelations of processing conditions versus final product performance. Competence in FTIR, DSC, peel adhesion, tack and shear testing, and other analytical techniques. Entrepreneurial and continuous innovation mindset.

Temporary Description Copperhead Environmental Consulting is expanding its team with Seasonal Wildlife Technicians. Wildlife Technicians assist Copperhead's Scientists with collecting data, conducting research and routine equipment maintenance/testing, and performing basic data entry while working in the field on multiple types of projects; however the technician will predominately be involved in projects involving the study of endangered bat species. These positions are seasonal/temporary, non-exempt, hourly (number of weekly hours not guaranteed but eligible for overtime). Positions will begin in May 2026 and end in August 2026. The number of seasonal positions and seasonal timeframes are approximate and are based on business need. Opportunity for regular employment at the end of the season is possible but not guaranteed. These positions are entry level, physically demanding and require travel to project sites including multiple day/week overnight stays and opportunity for overtime compensation. Travel expenses including transportation from the Copperhead office to the project site, meals and lodging are paid for by Copperhead. On-the-job, paid training is also provided. Cost of transportation to the Copperhead office prior to initiation of the project is not paid for. Amount of Travel: Estimated between 80% - 95% Requirements General Basic understanding of scientific principles. Assist with collection of data and basic data entry. Assist Scientists with the maintenance and care of field data, specimens, and samples. Assist with routine equipment maintenance and testing. Assist with transporting equipment to job sites including setting up and breaking down equipment. Learn and adhere to the corporate safety program and expectations. Utilize proper Personal Protective Equipment (PPE) when working in the field. Assist with ensuring all proper PPE and field gear is available for projects. Prepared to be away for up to two weeks at a time including over holidays as needed. Comfortable with working primarily at night in potentially adverse conditions and remote areas. Willing to work with a variety of personality types and people. Adapt easily to rapid changes in scheduling due to field work, project, and business needs. Willing to take direction and receive constructive criticism from team members and supervisor. Excellent communication skills including auditory, verbal, and written. Other duties as assigned. Project Management Understand the scope of services as it relates to assigned tasks and projects. Complete tasks within expected deadlines and with adherence to quality standards. Take initiative to ask questions, request help, and provide status updates on assigned tasks. Client Service Interact professionally both internally and externally at all times. Advance a conservation ethic, inspire biological curiosity, and drive environmental change. Physical Demands and Work Environment The physical demands described here are representative of those that must be met by an individual to safely and successfully perform the essential functions of this position. The individual is required to: Communicate effectively using auditory, verbal, and written skills Use hands and fingers to handle or feel objects, tools, or controls. Stand, walk, sit - often for long periods of time and on uneven surfaces; reach with hands and arms; climb or balance; and stoop, kneel, crouch, or crawl. Lift up to 30 pounds. Have excellent vision to include close vision, distance vision, color vision, peripheral vision, and the ability to adjust focus. Tolerate moderate noise levels in the work environment. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions and will be considered on a case-by-case basis. Other information to consider: The functions listed above, including physical demands, are only a summary and are not meant to serve as an exhaustive or comprehensive list of all possible job responsibilities, tasks, and duties and requirements. Candidates must be able to pass a pre-employment background check and future drug tests as applicable based on specific project requirements. Must hold a valid driver's license (REAL ID preferred in the event air travel and access to military bases is needed) and have a clean driving record to meet insurance requirements. Seasonal on-site room and board may be available for those who need it. One year experience or working towards or hold an associate's degree or higher in a related field of study required. Previous field experience with bats, mist-netting, and/or acoustic monitoring preferred. Pre-exposure rabies vaccination preferred - No one will be permitted to handle bats without the pre-exposure vaccination. Salary Description $15-$17/hour

Weekend Chemical Analyst - Owensboro KY Be a part of a revolutionary change! At Philip Morris International (PMI), we've chosen to do something incredible. We're totally transforming our business and building our future on one clear purpose - to deliver a smoke-free future. With huge change, comes huge opportunity. So, if you join us, you'll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. Our success depends on people who are committed to our purpose and have an appetite for progress. This position sits with our Swedish Match affiliate. Your 'day to day' * Performs analyses utilizing gas chromatography, ultra high pressure chromatography, and ion chromatography. * Responsible to maintain cleanliness and orderly arrangement of Analytical laboratory. * Provides support to Sr Analytical Chemist, Analytical Chemist, Sr Chemical Analyst, and Chemical Analyst. * Responsible for accurate records of assigned projects. * Knowledgeable in ISO 17025 Standard requirements. * May be required to work additional/different shifts. * Provides support to Production, Research and Development, Quality Assurance, and Leaf Operations. * Knowledgeable of method validation procedures. * Performs special projects as directed by Chemical Analysis Supervisor/Manager. * Responsible for sample preparation and extraction as indicated by written SOP. * Responsible for written SOPs of validated methods and procedures. * Responsible for routine and non-routine Microbiology testing. * Ability to review, interpret, and report analytical results using LIMS. Who we're looking for: * Minimum Bachelor's degree in scientific discipline such as Chemistry, Biology, related discipline or equivalent experience. * Minimum one year as a Laboratory Technician or comparable position/experience. * Knowledgeable in chemical laboratory safety and analytical procedures and methodologies. * Knowledgeable of Microbiological procedures and equipment. Must be able to prepare concise and accurate reports. * Must be able to work Saturday & Sunday (12:00am-12:30pm), Monday & Tuesday (12:00am-8:30am). Annual Base Salary $64,300 What's 'nice to have' Legally authorized to work in the U.S. (required) What we offer * We offer a competitive base salary, annual bonus (applicable based on level of position), great medical, dental and vision coverage, 401k with a generous company match, incredible wellness benefits, and much more! * Seize the freedom to define your future and ours. We'll empower you to take risks, experiment and explore. * Be part of an inclusive, diverse culture where everyone's contribution is respected; Collaborate with some of the world's best people and feel like you belong. * Pursue your ambitions and develop your skills with a global business - our staggering size and scale provides endless opportunities to progress. * Take pride in delivering our promise to society: To improve the lives of millions of smokers. PMI is an Equal Opportunity Employer. PMI is headquartered in Stamford, Conn., and its U.S. affiliates have more than 2,300 employees. PMI has been an entirely separate company from Altria and Philip Morris USA since 2008. PMI's affiliates first entered the U.S. market following the company's acquisition of Swedish Match in late 2022.Philip Morris International and its U.S. affiliates are working to deliver a smoke-free future. Since 2008, PMI has invested $12.5 billion globally to develop, scientifically substantiate and commercialize innovative smoke-free products for adults who would otherwise continue to smoke with the goal of transitioning legal-age consumers who smoke to better alternatives. In 2022, PMI acquired Swedish Match - a leader in oral nicotine delivery - creating a global smoke-free champion led by the IQOS and ZYN brands. The U.S. Food and Drug Administration has authorized versions of PMI's IQOS electronically heated tobacco devices and Swedish Match's General snus as Modified Risk Tobacco Products and renewal applications for these products are presently pending before the FDA. For more information, please visit ************** and ******************* #PMIUS #LI-DH1

NorthKey Community Care is seeking full-time Adult Development Technicians to work with individuals with intellectual and developmental disabilities (IDD) who attend NorthKey's Adult Day Training program in Williamstown, KY. The program provides services to adults with disabilities, assisting them with becoming more independent and involved in their community. PERKS & PAY Salary: $14 an hour Up to 12% annual contingency bonus Flexible schedule opportunities Generous plan for paid time off (PTO) (Up to 16 days first year) 10 Paid Holidays Individual and family insurance coverage: Various medical, vision, and dental plans to choose from HSA Employer match up to $1000, depending on plan 401(k) with employer match Professional Development Potential eligibility for Student Loan Forgiveness through the Public Service Loan Forgiveness program. QUALIFICATIONS High school diploma or equivalent is required. Relevant knowledge, training, and experience with adults with intellectual and developmental disabilities preferred. Ability to drive a motor vehicle and a valid driver's license. RESPONSIBILITIES Engage clients with intellectual and developmental disabilities (IDD) in a structured collaborative relationship which empowers them to gain necessary skills in a variety of areas related to personal skills development across the vocational spectrum. Promote environmental and developmental independence to improve and maintain lifelong well-being and the highest level of functional status. Provide evidence-based care in the area of skills development. Address functional challenges of individuals served. Provide education to clients to promote improved functioning and skills development. Participate in the development of an individualized plan for clients needing additional social and occupational skills. Prevent unnecessary functional deterioration that could result in loss of social and occupational skills. Provide job assistance, supervision, training, and direction to facilitate the development and maintenance of social and occupational skills. Maintain HIPAA compliance and appropriate client confidentiality. Complete initial and/or annual and other mandatory trainings as assigned related to the position. Transport clients to community events when needed. NORTHKEY COMMUNITY CARE - COMPANY OVERVIEW Since 1966, NorthKey Community Care (NorthKey) has provided effective and efficient mental health, substance use, and developmental disabilities services to the Northern Kentucky region with the commitment to providing the right service, at the right time, and in the right place. NorthKey's commitment to providing a continuum of services for individuals and families seeking assistance for mental health, substance use, and developmental disabilities means that NorthKey employs staff with a wide variety of education, experience, and licensure. With multiple convenient locations throughout the Northern Kentucky region (Kenton, Boone, Campbell, Grant, Carroll, Gallatin, Pendleton, and Owen counties), NorthKey offers a wide array of mental health, substance use, and developmental disabilities services unparalleled in the region. Come join our team to help us Transform Lives and Communities through Excellent Service ! Benefits: 401(k) 401(k) matching Dental insurance Employee assistance program Employee discount Flexible schedule Health insurance Life insurance Paid time off Tuition reimbursement Vision insurance