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Research and development technician jobs in Lexington, KY

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  • Confections Formulation Scientist

    Curaleaf 4.1company rating

    Research and development technician job in Lexington, KY

    Job Description At Curaleaf, we're redefining the cannabis industry with a strong commitment to quality, expertise, and innovation. As a leading global cannabis provider, our brands-including Curaleaf, Select, and Grassroots-offer premium products and services in both medical and adult-use markets. Join us at Curaleaf to be part of a high-growth, purpose-driven company that champions corporate social responsibility through our Rooted in Good initiative, supporting community outreach and positive change. Here, you'll have the opportunity to make a meaningful impact, drive innovation, and help shape the future of cannabis. Job Title: Confections Formulation Scientist Location: Lexington, KY or Webster, MA (Relocation may be provided for the right candidate) Job Type: Full Time | Exempt Travel: Up to 50-75% to support our confection production facilities across the country Who You Are: You're a product development scientist with experience in confections, gummies, or candy formulation. You understand how hydrocolloids, pectin/gelatin systems, sugars, and emulsions work together to create consistent flavor, texture, and stability - and you know how to translate bench-top trials into scalable production. You bring deep knowledge of ingredient functionality, emulsions, and hydrocolloids, paired with the technical skill to scale formulations from the lab bench to full production. Whether running shelf-life studies, managing formulation data, or collaborating with cross-functional partners, you approach each challenge with precision, organization, and a problem-solving mindset. Above all, you're excited to push boundaries in the growing cannabis edibles space while upholding the highest standards of quality, safety, and compliance. What You'll Do: As a Confections Formulation Scientist, you'll play a central role in developing and scaling innovative cannabis-infused products. You'll conduct formulation trials, lead product testing, and support commercialization to bring new concepts to market. Your work will span from sensory evaluations to regulatory compliance, ensuring each product is safe, consistent, and high-quality. On any given day, you might be: Supporting the development, optimization, and scaling of cannabis-infused edibles through bench trials, pilot runs, and full-scale production Conducting sensory testing, shelf-life studies, and technical evaluations of texture, flavor, and stability using industry tools like viscometers and texture analyzers Maintaining SOPs, batch records, and technical documentation to streamline operations and support audits Ensuring compliance with GMP, food safety, labeling, and cannabis regulations, including coordinating third-party lab testing and interpreting results Managing formulation and ingredient data using MRP systems and formulation software for efficiency and accuracy Sharing data-driven insights that influence innovation, continuous improvement, and collaboration across the team What You'll Bring: 5-8 years of experience in confectionery formulation and/or food manufacturing A bachelor's degree in Food Science, Chemistry, Food Chemistry, or a related field Hands-on experience in confection formulation and scale-up, with knowledge of production equipment Strong understanding of ingredient functionality, food chemistry, emulsions, and hydrocolloids to design stable formulations Familiarity with GMPs, food safety, and regulatory requirements, with direct experience in sensory testing and shelf-life evaluations Excellent communication and documentation skills, paired with attention to detail and strong organizational abilities Proficiency with Microsoft Office and formulation software Willingness to travel for trials, production support, and industry events Even Better If: You have experience in the cannabis or hemp industry You're familiar with ERP/MRP systems for managing formulations and ingredient tracking You bring experience applying data science or analytics to product development You've supported R&D trials and helped scale products from concept to commercialization Physical Requirements: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this Job, the employee is regularly required to stand, walk, sit, talk or hear, use hands to finger or feel, reach with hands and arms, and lift up to 25 lbs. The employee is occasionally required to climb and balance, stoop, kneel, crouch, or crawl and lift up to 50 lbs. This position requires close vision, distance vision, peripheral vision, depth perception and the ability to adjust focus. Work Environment: This position has allergen warnings, potential exposure to dust, pollen, and plant pathogens, requires exposure to cleaning solvents, such as high volumes of isopropyl alcohol, requires daily use of provided PPE, such as masks, hair nets, beard covers, respirators, boot covers, scrubs, non-slip shoes, and Tyvek suits as necessary, requires the ability to work in confined spaces, has exposure to loud noises, including but not limited to air compressors, packaging equipment, and alarms, has exposure to CO2 manufacturing procedures at OSHA approved CO2 levels and requires a high stress tolerance, adaptability, and flexibility. Ability to work in an ever-changing environment. Curaleaf Pay Transparency$78,000-$87,000 USD What We Offer: Career Growth Opportunities Competitive Pay and Benefits Generous PTO and Parental Leave 401(K) Retirement Plan Life/ Disability Insurance Community Involvement Referral Bonuses and Product Discounts Benefits vary by state, role type, and eligibility. Follow us on Social Media: Instagram: @curaleaf.usa Twitter: @Curaleaf_Inc LinkedIn: Curaleaf LinkedIn Curaleaf Holdings, Inc. (TSX: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading international provider of consumer products in cannabis with a mission to enhance lives by cultivating, sharing, and celebrating the power of the plant. As a high-growth cannabis company known for quality, expertise and reliability, the Company, and its brands, including Curaleaf, Select, Grassroots, JAMS, Find and Zero Proof provide industry-leading service, product selection and accessibility across the medical and adult-use markets. Curaleaf International is the largest vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence Our Vision: To be the world's leading cannabis company by consistently delivering superior products and services and driving the global acceptance of cannabis. Our Values: Lead and Inspire. Commit to Win. ONE Curaleaf. Driven to Deliver Excellence. Curaleaf is an equal opportunity employer. Curaleaf recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, gender identity, sexual orientation, physical ability, age, veteran status, and other protected status as required by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Individuals adversely impacted by the war on drugs are encouraged to apply. Current Curaleaf employees should apply for open positions through our Internal Job Board, which can be accessed via the link on The Leaf.
    $78k-87k yearly 27d ago
  • Associate Scientist

    Catalent Pharma Solutions, Inc. 4.4company rating

    Research and development technician job in Winchester, KY

    Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. The Associate Scientist is responsible for performing analytical research and development work in the Analytical R&D Department. The Associate Scientist work/assist on method development, method transfer, method verification and method validation under appropriate guidance along with routine release and stability testing in support of clinical development and registration activities required for the regulatory submissions. This is a full-time on-site salaried position, Monday - Friday 8:00am - 5:00pm Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. The Role * Perform technical review of client's documents as required including but not limited to specification/validation reports/test methods/compliance reports etc. to perform gap analysis with respect to methods/instruments/procedures etc. for completing methods transfers from client's/or their third-party labs with guidance from supervisors/senior team members * Analysis of finished products, in-process materials, raw materials, according to the assigned specifications, methods, and protocols according to cGLP and cGMP. Document, process, report the data as applicable to support the team in timely fashion * Perform analysis as required to support assigned testing using KF titrations/Dissolutions/IR/UV spectrophotometers, LC to perform dissolutions/assays/BU/CU, impurities and data processing using Empower and document per applicable test methods/specification/protocols etc. with guidance from senior team members * Use Empower software- creating instrument/processing/report methods and performing online empower calculations for assay/dissolutions/impurities etc. Knowledge of Trackwise for managing deviations and investigations and ability to manage /handle with guidance from supervisors/senior team members * Troubleshoot and propose any method improvement requirements during the method feasibility work of client supplied methods and/or during compendial method evaluation for assay, impurities, dissolution etc. with guidance from supervisors/senior team members. Methods and/or during compendial method evaluation for assay, impurities, dissolution etc. with guidance from supervisors/senior team members * Perform/assist team members in method transfers, Compendial verifications or full method validations (forced degradation and calculating mass balance/peak purity to prove stability indicating nature of the method) per applicable guidances (USP , , ICH Q2 etc.) / SOPs with guidance from the supervisors/senior team members * Perform stability testing on developmental/clinical/registration batches as per approved test methods/stability protocols and report/document per applicable specification/stability protocols. Escalate any OOS/OOT/atypical/trending results with supervisors or concerned team members. * Other duties as assigned The Candidate * Bachelor's Degree in Chemistry, Pharmaceutical Sciences or Life Sciences is required, preferred major Analytical Chemistry * Must have at least one year of experience in pharmaceutical industry and 1+ years of experience in analytical testing/research experience using HPLC/GC/UV, etc * Understand analytical chemistry calculations such as concentrations (Area%, %w/w, ppm, µg/mL, etc.), molarity, Beer's Law, reference standard purity on as is, anhydrous, or dry basis etc. is required * Basic understanding and knowledge of analytical chemistry and chromatographic techniques (e.g., LC/GC/dissolutions) and spectroscopic (e.g., UV) analysis is required * Demonstrate Knowledge and ability to understand and follow ICH guidelines (ICH Q1, Q2, Q3 etc.) including other regulatory guidelines * Adhere and perform all lab job duties/responsibilities according to applicable SOP's related to DEA scheduled drugs, safety, waste management and housekeeping and work with the team in improvement of the processes and procedures is required * Assisting with other personnel with lifting of liquid containers and all objects of greater than 50 lbs. is required Why You Should Join Catalent * Several Employee Resource Groups focusing on D&I * Tuition Reimbursement - Let us help you finish your degree or earn a new one! * Generous 401K match * 152 hours accrued PTO + 8 paid holidays Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.
    $47k-67k yearly est. Auto-Apply 22d ago
  • Chemist I - Night Shift

    Piramal Group

    Research and development technician job in Lexington, KY

    Business: Pharma Solution Department: Analytical Quality Control (AQC) The Chemist I performs testing of raw materials, in-process and finished products, and maintains and calibrates analytical instruments in compliance with cGMP standards. Reporting Structure Directly reports to AQC Group Lead 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 Education Requirements • Bachelor of Science in Chemistry, Pharmaceutical Science, or other closely related scientific field Experience • 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 Competencies • 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
    $46k-67k yearly est. Auto-Apply 60d+ ago
  • Part-Time Wildlife Technician (Lexington, KY)

    Meridian Bird Removal

    Research and development technician job in Lexington, KY

    Job DescriptionDescription Meridian Wildlife Services is the fastest-growing bird capture company in the country! We are searching for our next Wildlife Technician to help us embrace new adventures daily. Why Join Us? Unforgettable Interactions: Each day offers new adventures and the chance to connect with new people, creating memorable experiences for both our technicians and the customers we serve. Local Impact, National Reach: Travel locally and nationally, enhancing your skills and broadening your horizons as you provide bird removal services to our customers. Become an Expert: Our comprehensive training program provides you with the skills needed to excel, covering everything from bird capture techniques to building positive customer relationships. Grow Fast: We provide clear career paths that require little to no prior experience. Grow with our dynamic team through continuous learning and opportunities for advancement. About Us:At Meridian, our goal is to provide safe and effective bird removal solutions to our customers in the commercial retail space. Role: As a Wildlife Technician, you will be the friendly face of Meridian. Our technicians uphold food safety standards for our customers while managing and mitigating potential bird-related nuisances in commercial spaces. Making a Difference for Our CustomersBecome a Trusted Advisor: Walk through customer facilities to identify bird activity and potential problems. Work closely with customers to understand their unique concerns and tailor effective solutions. Embrace the Challenge: No two jobs are the same and every job brings new challenges. You'll be resourceful and adaptable, tackling diverse bird-related issues to effectively address customer needs. Empower Our Customers: Share your knowledge of bird behavior and prevention techniques. This empowers customers to maintain bird-free spaces and achieve lasting results. Core Values: Uphold our core values to deliver exceptional service that builds trust and strengthens customer relationships. Eagerly Optimistic: We approach every assignment with a positive attitude. Humbly Confident: We're experts, but always open to learning more along the way. Adapt and Overcome: No bird challenge is too big! We find creative solutions that work. Commitment to Capture: We finish the job no matter what it takes and guarantee your satisfaction. Be Above the Bar: We strive to exceed our customers' expectations in every interaction. Help First: We're always willing to go the extra mile to assist our customers and teammates. Basic Qualifications and Job FunctionsBasic Qualifications: High School Diploma or GED. At least 21 years old. Valid Driver's License. Insured and reliable vehicle. Driving Record free from moving violations. Mobile smartphone. Lives within 50 miles of Lexington, KY. Job Functions: Lift and carry up to 50 lbs. Stand, walk, and sit for prolonged periods of time. Work exposed to outdoor elements. Frequent bending, kneeling, and reaching. Ability to work at heights, climb ladders, and use scissor lifts. Ability to see up close and at a distance. Ability to travel long distances to our customers' facilities. All technicians use their personal vehicles to travel to worksites. Learn MoreIf you want each workday to be a new adventure, apply now! About Us Frequently Asked Questions Our Services Part-Time Bird Removal Technicians (BRTs) typically earn between $1,000 - $2,200 per month. This role offers uncapped earning potential, which means your income can grow beyond this range. Actual earnings vary and are subjective to factors such as location, individual productivity, and seasonal demand.
    $1k-2.2k monthly 3d ago
  • Fire Scientist (Engineering Consultancy / Flexible Location)

    Gigantes Group

    Research and development technician job in Lexington, KY

    Fire Scientist Role Our client is actively seeking a highly skilled and scientifically oriented Fire Scientist to join their team. This role is ideal for an individual with a strong background in scientific research, a drive for innovation, and the ability to lead high-level technical projects. Key Responsibilities: - Conduct high-level scientific research in the field of fire science, focusing on innovative approaches and cutting-edge technologies. - Lead the creation of a state-of-the-art laboratory facility, driving the establishment of advanced research capabilities. - Pursue and secure grants and funding opportunities to support research initiatives and the development of the laboratory. - Advantage for candidates with experience in battery testing and fire research, particularly those with a track record of conducting research in renowned laboratories. Qualifications: - PhD in Fire Science, Engineering, or a related scientific field. - Proven experience in conducting scientific research, preferably in fire science or related disciplines. - Strong leadership skills with the ability to drive research initiatives and establish laboratory facilities. - Track record of securing grants and funding for research projects. - Familiarity with battery testing and fire research methodologies. - Excellent communication and collaboration abilities, essential for building partnerships with universities and industry peers. This role presents a unique opportunity for a driven and scientifically minded individual to lead groundbreaking research initiatives and shape the future of fire science. If you are passionate about pushing the boundaries of scientific knowledge and making a significant impact in the field, we encourage you to apply.
    $44k-66k yearly est. 60d+ ago
  • Applied Scientist 3

    Oracle 4.6company rating

    Research and development technician job in Frankfort, KY

    Invent, implement and deploy state-of-the-art machine learning and/or specific domain industry algorithms and systems. Build AI Agents on top of the latest reasoning LLMs (both frontier and open source) and analyze agent trajectories. Build prototypes and explore conceptually new solutions. Work collaboratively with science, engineering, and product teams to identify customer needs in order to create and implement solutions, promote innovation and drive model implementations. Applies data science capabilities and research findings to create and implement solutions to scale. Responsible for developing new intelligence around core products and services through applied research on behalf of our customers. Develops models, prototypes, and experiments that pave the way for innovative products and services. Build cloud services that work out of the box for enterprises, e.g. decision support, anomaly detection, forecasting and recommendations), natural language processing (NLP), Natural Language Understanding (NLU),Time Series etc. Design and run experiments, research new algorithms, and find new ways of optimizing risk, profitability, and customer experience. Conversant on ethical problems in consideration of sciences. **Responsibilities** Identify data science use cases and design scalable solutions that can be built as a feature of the product/service. Contributes to writing production model code. Work with Software Engineering teams to deploy them in production. Set up environment needed to run experiments for all projects. Set up distributed environments. Design and implement algorithms, train models, and deploy both to production to validate premises and achieve goals. Design and execute offline/online experiments and model performance testing. Work with large, complex data sets. Solve difficult, non-routine analysis problems, applying advanced analytical methods as needed. Address business/customer problems and questions using statistical and machine learning techniques to achieve business goals and KPI's. Come up with innovative solutions to address tradeoffs or challenges faced by team. Stay up-to date with research and trends regarding latest algorithms in ML or other industry/domain space. Perform research in emerging areas, which may include efficient neural network development including quantization, pruning, compression and neural architecture search, as well as novel differentiable compute primitives. May perform other duties as assigned. Disclaimer: **Certain US customer or client-facing roles may be required to comply with applicable requirements, such as immunization and occupational health mandates.** **Range and benefit information provided in this posting are specific to the stated locations only** US: Hiring Range in USD from: $97,500 to $199,500 per annum. May be eligible for bonus and equity. Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business. Candidates are typically placed into the range based on the preceding factors as well as internal peer equity. Oracle US offers a comprehensive benefits package which includes the following: 1. Medical, dental, and vision insurance, including expert medical opinion 2. Short term disability and long term disability 3. Life insurance and AD&D 4. Supplemental life insurance (Employee/Spouse/Child) 5. Health care and dependent care Flexible Spending Accounts 6. Pre-tax commuter and parking benefits 7. 401(k) Savings and Investment Plan with company match 8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation. 9. 11 paid holidays 10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours. 11. Paid parental leave 12. Adoption assistance 13. Employee Stock Purchase Plan 14. Financial planning and group legal 15. Voluntary benefits including auto, homeowner and pet insurance The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted. Career Level - IC3 **About Us** As a world leader in cloud solutions, Oracle uses tomorrow's technology to tackle today's challenges. We've partnered with industry-leaders in almost every sector-and continue to thrive after 40+ years of change by operating with integrity. We know that true innovation starts when everyone is empowered to contribute. That's why we're committed to growing an inclusive workforce that promotes opportunities for all. Oracle careers open the door to global opportunities where work-life balance flourishes. We offer competitive benefits based on parity and consistency and support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs. We're committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_************* or by calling *************** in the United States. Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans' status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.
    $55k-78k yearly est. 31d ago
  • Liquid Development Chemist

    Four Roses Distillery LLC

    Research and development technician job in Lawrenceburg, KY

    INTRODUCTION The Liquid Development Chemist applies technical and scientific principles to conduct complex analysis on in-process, experimental, and final product samples to support the quality, improvement, and development of new and existing products as directed by the Master Distiller. Sensory and organizational skills are also necessary to manage the day-to-day approval of final product, allocation of matured Barrel inventory, and development of new products. SUMMARY/OBJECTIVES This role ensures quality and consistency across all Four Roses products by working with the entire liquid inventory. This role also supports the Master Distiller, Operations, and Quality departments through analytical and experimental projects aimed at improving product consistency and fostering liquid innovation. Close collaboration with Operations and Quality ensures the production of high-quality bourbon via sample analysis and technical support ESSENTIAL FUNCTIONS Major Responsibilities Analysis and method development - 35 % Develop necessary analytical methods for beer, distillate, and maturate analysis. Establish and document Standard Operating Procedures for all new analytical procedures and best practices using the approved SOP document template. Track analytical and sensory trends for fermented mash, unaged distillate, and matured liquid. Support GC-MS lab at Warehousing/Bottling facility. Obtain and maintain TTB distilled spirits certification. Manage Day to Day Operation of Sensory Lab - 35% Organoleptically evaluate/approve daily distillate tank product. Prepare daily samples for group organoleptic evaluations. Manage sampling, approvals and records for all single barrel products. Identify and initiate all necessary barrel sampling for general inventory and product formulation. Assist in product formulation development and maintenance. Maintain records for all product formulations. Maintain quality records for total liquid inventory. Participate in Distillate and Product Standard composition. Assist in inventory allocation to meet forecasting demand. Maintain library for retention samples of daily distillate, barrel samples, and experimental liquid. Liquid Development/Innovation - 30% Support Master Distiller, Operations, and Quality on liquid innovation projects. Contribute innovative ideas for new product innovations. Manage Sensory panel and track organoleptic results for laboratory, ageing, and distillery trials. Utilize current technology and identify potential technology for liquid trial analysis. Support execution of experimental fermentation trials. Collaborate with Senior Fermentation Scientist to optimize and synergize GC and LC analysis for laboratory and distillery trials. Minor Responsibilities Other Duties as Assigned Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. QUALIFICATIONS Required Competencies Must have excellent interpersonal skills with ability to communicate all levels of employees/staff/visitors. Strong organizational skills, the ability to handle multiple tasks simultaneously, maintain flexibility as necessary. Ability to build and maintain positive relationships, manage conflicts and encourage friendly working environment. Proficient computer literacy with ability to utilize the Microsoft Office Suite, including Word, Excel and Outlook; must have ability to adapt to bottling line software. Must be at least 21 years of age Required Education and Experience A Bachelor's degree in chemistry; or Bachelor's degree in any physical, chemical, or biological science preferably with at least 30 credits of chemistry. Strong background with GC-MS method development. Willingness to sample and critically evaluate alcohol samples. Must have ability to make decisions in a high pressure and fast paced environment. High level of problem solving skills/critical thinking and reasoning preferred. Preferred Education and Experience Experience in beverage alcohol analysis Proficiency with Agilent GC-MS Mass Hunter software. Experience with GC-MS analysis utilizing headspace, stir bar, and SPME techniques. 4+ Years GC-MS experience. JOB INFORMATION Supervisory Responsibility The Liquid Development Chemist does not have any direct reports. Work Environment This job operates 10% in a manufacturing environment and 90% in an office environment. This role routinely uses standard quality control equipment such as Density meter, balance, gas chromatograph (GC), liquid chromatograph (LC). Travel Will travel occasionally between the Lawrenceburg and Cox's Creek Facilities. May travel to suppliers, Industry trade shows, etc. Some travel may be outside of the state and possibly outside of the U.S. as necessary. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms. The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
    $54k-86k yearly est. Auto-Apply 60d+ ago
  • Liquid Development Chemist

    Four Roses Bourbon Company

    Research and development technician job in Lawrenceburg, KY

    INTRODUCTION The Liquid Development Chemist applies technical and scientific principles to conduct complex analysis on in-process, experimental, and final product samples to support the quality, improvement, and development of new and existing products as directed by the Master Distiller. Sensory and organizational skills are also necessary to manage the day-to-day approval of final product, allocation of matured Barrel inventory, and development of new products. SUMMARY/OBJECTIVES This role ensures quality and consistency across all Four Roses products by working with the entire liquid inventory. This role also supports the Master Distiller, Operations, and Quality departments through analytical and experimental projects aimed at improving product consistency and fostering liquid innovation. Close collaboration with Operations and Quality ensures the production of high-quality bourbon via sample analysis and technical support ESSENTIAL FUNCTIONS Major Responsibilities Analysis and method development - 35 % Develop necessary analytical methods for beer, distillate, and maturate analysis. Establish and document Standard Operating Procedures for all new analytical procedures and best practices using the approved SOP document template. Track analytical and sensory trends for fermented mash, unaged distillate, and matured liquid. Support GC-MS lab at Warehousing/Bottling facility. Obtain and maintain TTB distilled spirits certification. Manage Day to Day Operation of Sensory Lab - 35% Organoleptically evaluate/approve daily distillate tank product. Prepare daily samples for group organoleptic evaluations. Manage sampling, approvals and records for all single barrel products. Identify and initiate all necessary barrel sampling for general inventory and product formulation. Assist in product formulation development and maintenance. Maintain records for all product formulations. Maintain quality records for total liquid inventory. Participate in Distillate and Product Standard composition. Assist in inventory allocation to meet forecasting demand. Maintain library for retention samples of daily distillate, barrel samples, and experimental liquid. Liquid Development/Innovation - 30% Support Master Distiller, Operations, and Quality on liquid innovation projects. Contribute innovative ideas for new product innovations. Manage Sensory panel and track organoleptic results for laboratory, ageing, and distillery trials. Utilize current technology and identify potential technology for liquid trial analysis. Support execution of experimental fermentation trials. Collaborate with Senior Fermentation Scientist to optimize and synergize GC and LC analysis for laboratory and distillery trials. Minor Responsibilities Other Duties as Assigned Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. QUALIFICATIONS Required Competencies Must have excellent interpersonal skills with ability to communicate all levels of employees/staff/visitors. Strong organizational skills, the ability to handle multiple tasks simultaneously, maintain flexibility as necessary. Ability to build and maintain positive relationships, manage conflicts and encourage friendly working environment. Proficient computer literacy with ability to utilize the Microsoft Office Suite, including Word, Excel and Outlook; must have ability to adapt to bottling line software. Must be at least 21 years of age Required Education and Experience A Bachelor's degree in chemistry; or Bachelor's degree in any physical, chemical, or biological science preferably with at least 30 credits of chemistry. Strong background with GC-MS method development. Willingness to sample and critically evaluate alcohol samples. Must have ability to make decisions in a high pressure and fast paced environment. High level of problem solving skills/critical thinking and reasoning preferred. Preferred Education and Experience Experience in beverage alcohol analysis Proficiency with Agilent GC-MS Mass Hunter software. Experience with GC-MS analysis utilizing headspace, stir bar, and SPME techniques. 4+ Years GC-MS experience. JOB INFORMATION Supervisory Responsibility The Liquid Development Chemist does not have any direct reports. Work Environment This job operates 10% in a manufacturing environment and 90% in an office environment. This role routinely uses standard quality control equipment such as Density meter, balance, gas chromatograph (GC), liquid chromatograph (LC). Travel Will travel occasionally between the Lawrenceburg and Cox's Creek Facilities. May travel to suppliers, Industry trade shows, etc. Some travel may be outside of the state and possibly outside of the U.S. as necessary. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms. The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
    $54k-86k yearly est. Auto-Apply 60d+ ago
  • Scientist II- Antifreeze

    Valvoline Inc. 4.2company rating

    Research and development technician job in Lexington, KY

    Why Valvoline Global Operations? At Valvoline Global Operations, we're proud to be The Original Motor Oil, but we've never rested on being first. Founded in 1866, we introduced the world's first branded motor oil, staking our claim as a pioneer in the automotive and industrial solutions industry. Today, as an affiliate of Aramco, one of the world's largest integrated energy and chemicals companies, we are driven by innovation and committed to creating sustainable solutions for a better future. With a global presence, we develop future-ready products and provide best-in-class services for our partners around the world. For us, originality isn't just about where we began; it's about where we're headed and how we'll lead the way. We are originality in motion. Our corporate values-Care, Integrity, Passion, Unity, and Excellence-are at the heart of everything we do. These values define how we operate, how we treat one another, and how we engage with our partners, customers, and the communities we serve. At Valvoline Global, we are united in our commitment to: * Treating everyone with care. * Acting with unwavering integrity. * Striving for excellence in all endeavors. * Delivering on our commitments with passion. * Collaborating as one unified team. When you join Valvoline Global, you'll become part of a culture that celebrates creativity, innovation, and excellence. Together, we're shaping the future of automotive and industrial solutions. Job Purpose The Scientist II embraces our safety driven culture in all tasks and demonstrates enthusiasm for the role. Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure compounds in a variety of formulations and/or rheological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs, and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol, and product specifications. Write reports summarizing data, suggests improvements to work processes and test procedures, proactively communicate with formulators, peers, and managers. How You Make an Impact * Runs laboratory equipment as trained and prepares product blends as guided. * Collects and evaluates data, utilizing lab notebooks and laboratory information management systems. Reviews, interprets, and analyzes the data for technical, quality, SOPs, client criteria, and Good Laboratory Practices (GLP) * Provides straightforward solutions to problems using readily available clear and direct references. * Assists the team on projects including projects with cross functional groups. * Write reports summarizing data and on the projects provided. * Maintain instruments through routine calibration, troubleshooting, and preventive maintenance. * Participate in continuous improvement initiatives for efficiency, accuracy, and method development. * Support daily housekeeping, chemical inventory management, and waste disposal in compliance with safety regulations. * Demonstrate a strong commitment to laboratory safety, including proper use of PPE, safe chemical handling, and adherence to OSHA/EPA regulations. * Ensure compliance with environmental, health, and safety (EHS) policies, maintaining a clean and hazard-free work environment. * Characterization of coolant samples using HPLC, ICP, pH probe, titration, IC, LC, GC, densitometer, refractometer, UV-Vis, and Karl Fisher. * Conducts necessary performance and quality tests to approve batch samples of antifreeze/coolant for third party blending facilities. * Support as a technical contact for Valvoline's third-party antifreeze blending plants, providing day to day support with oversite from the Team Lead. * Effectively communicate sample statuses to the group and management. * Additional duties as assigned. What You Bring to the Role * Minimum B.S. in Chemistry, Chemical Engineering, or related scientific field required. * 3+ years of experience in analyzing aqueous samples utilizing chromatography equipment and/or previous experience supporting manufacturing in professional laboratory environments. * Experience with development of analytical test methods, and laboratory methods a plus * Experience managing complex projects and working on tight deadlines. * Excellent oral and written communication skills required. * Multi-tasker and problem-solver. * Attention to detail and desire to complete quality work products. * Ability to work well with others and comprehend instruction quickly. * Ability to work independently and as part of a collaborative team. * Effective problem-solving and critical thinking skills. * Strong commitment to safety, quality, and laboratory best practices. * Proficiency in Microsoft Office Suite; experience with Laboratory Information Management Systems (LIMS) a plus. * Familiarity with Antifreeze/Coolant chemistries * Knowledge of ASTM * Familiarity with Engine/Cooling System hardware, operation, and design Benefits That Drive Themselves * Health insurance plans (medical, dental, vision) * Health Savings Account (with employer base deposit and match) * Flexible spending accounts * Competitive 401(k) with generous employer base deposit and match * Incentive opportunity* * Life insurance * Short and long-term disability insurance * Paid vacation and holidays* * Employee Assistance Program * Employee discounts * PTO Buy/Sell Options* * Tuition reimbursement* * Adoption assistance* * Terms and conditions apply, and benefits may differ depending on position or tenure Valvoline Global is an equal opportunity employer. We are dedicated to fostering an environment where every individual feels valued, respected, and empowered to contribute their unique perspectives and skills. We strictly prohibit discrimination and harassment of any kind, regardless of race, color, religion, age, sex, national origin, disability, genetics, veteran status, sexual orientation, gender identity, or any other legally protected characteristic. We are committed to ensuring accessibility throughout our recruitment process. If you require a reasonable accommodation to participate in any stage of the recruitment or selection process, please contact us at:. * Email: ****************************************** This contact information is solely for accommodation requests. For inquiries about application status, please use the appropriate channels listed in your application materials. Are You Ready to Make an Impact? At Valvoline Global, we're looking for passionate and talented individuals to join our journey of innovation and excellence. Are you ready to shape the future with us? Apply today. Requisition ID: 1853
    $51k-74k yearly est. Easy Apply 19d ago
  • Scientist II

    Piramal Glass USA Inc. 4.0company rating

    Research and development technician job in Lexington, KY

    Business: Pharma Solutions Department: Analytical R&D (ARD) The Analytical Scientist II conducts complex chemical and physical testing of pharmaceutical raw materials and finished products. Executes proficiency in development and transfer/verification/validation of test methods for pharmaceutical raw materials and finished products for strength, impurities, and identity. Reporting Structure Directly reports to Associate Director, Analytical R&D Key Responsibilities • Conducts complex chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and compendial test methods. • Executes proficiency in development and transfer/verification/validation of test methods for pharmaceutical raw materials and finished products for strength, impurities, identity, and dissolution by HPLC, GC, dissolution, KF, spectroscopy, and traditional quantitative analysis, utilizing HPLC, GC, dissolution, KF, spectroscopy, and/or traditional wet chemical testing under general supervision • Recognizes and reports out-of-specification or unexpected results and non-routine analytical and product problems; recommends solutions • Maintains and troubleshoots analytical instrumentation as needed • Clearly and accurately communicates the results of work by creating documentation of the testing/analysis and obtained results. Records and reports results of analysis in accordance with prescribed lab procedures and systems. May interact with clients. • Prepares and assists in filing regulatory documents in support of internal projects and may provide communications with outside departments, corporate sites, agencies, and clients. • Writes SOPs and other instructional documents • Cleans and organizes work area, instrumentation, and testing materials • Maintains the necessary compliance status required by company and facility standards Experience • BS, MS or PhD in Chemistry, Biochemistry or Pharmaceutical Science or related Work Experience • BS with 2+ years' Pharmaceutical industry experience or similar • Experience working with potent, cytotoxic materials and parenteral drug products preferred Competencies • Proficiency using chemistry and analytical instrumental technologies • Knowledge of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs and descriptive organic chemistry. • Demonstrated proficiency approaching in solving scientific problems • Proficiency with HPLC, GC, KF and dissolution techniques • Good interpersonal and communication skills (both oral and written) • Ability to respond to common inquiries or complaints from customers or regulatory agencies • Ability to apply mathematical operations, to such tasks as determination of test reliability, analysis of variance and correlation techniques Physical Demands • Must use hands to handle, feel, reach, type or operate objects or controls • Frequent sitting, talking, reading or hearing • Frequent walking or long periods of standing, bending, pushing and pulling • Long periods of sitting, typing, or working at a computer station
    $33k-52k yearly est. Auto-Apply 60d+ ago
  • Scientist II

    Sumitomo Pharma 4.6company rating

    Research and development technician job in Frankfort, KY

    Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn. **Job Overview** We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Scientist II. This position will be part of the Translational Research and Medicine-Oncology team, with a primary focus on advancing translational research to support oncology programs in clinical trial stages. This individual will be responsible for designing, oversighting, and interpretating translational studies to understand mechanism of action, resistance pathways, and potential new indications. The candidate may also be involved in biomarker analysis to support these translational objectives. **Job Duties and Responsibilities** + Develop hypotheses by integrating insights from scientific literature, preclinical and clinical data + Design experiments to support identification of mechanism of action, resistance mechanisms, and potential indications + Manage translational research and biomarker studies conducted with CROs and academic investigators to ensure high-quality, timely delivery of data + Maintain organized, detailed logs of studies and data to ensure accuracy, reproducibility, and compliance with regulatory standards + Present data and insights in internal meetings and cross-functional program team discussions **Key Core Competencies** + Scientific curiosity with ability to generate and test hypotheses that inform drug development + Excellent problem-solving and critical-thinking skills to interpret complex data + Strong organizational skills and attention to detail in managing studies, data, and documentation + Strong project management and vendor oversight skills + Adaptability and resilience in a fast-paced, evolving research environment **Education and Experience** + PhD degree in a related field of science (Biology, Biochemistry, Molecular & Cellular biology, Cancer Biology, Immunology) + 1-3 years of postdoctoral or industry research experience + Familiarity with oncology research preferred + Experience with common biomarker platforms (e.g. NGS, flow cytometry, IHC) preferred The base salary range for this role is $102,000 to $127,000. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed. **Confidential Data** : All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential. **Compliance** : Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the "best" industry practices and the highest ethical standards. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. **Mental/Physical Requirements** : Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time. **Sumitomo Pharma America (SMPA)** **is an Equal Employment Opportunity (EEO) employer** Qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn. Sumitomo Pharma America (SMPA) endeavors to make its application process accessible to all. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact SMPA at ********************************************** This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. At Sumitomo Pharma America, our work is guided by the Sumitomo Pharma mission, vision and values, which tie closely to our company's cultural pillars. **Our** **Mission** _To broadly contribute to society through value creation based on innovative research and development activities for the betterment of healthcare and fuller lives of people_ _worldwide_ **Our** **Vision** _For Longer and Healthier Lives, we unlock the future with cutting edge technology and_ _ideas_
    $102k-127k yearly 30d ago
  • QC Lab Analyst

    VWR, Part of Avantor 4.8company rating

    Research and development technician job in Paris, KY

    The Opportunity: Avantor is looking for a Quality Control (QC) Lab Analyst to join our Quality Control Laboratory team. The Analyst will be responsible for testing of raw materials and finished products in our Quality Control laboratory. This will be an onsite, Monday - Friday 3pm - 11:30pm shift, position at our Paris, KY chemical manufacturing facility. What we're looking for Education: Bachelor's degree in a science discipline with knowledge and experience in one of the following areas: Biology, Chemistry, or Microbiology Experience: 1-3 years of laboratory experience in a related field Collaboration Tool: Microsoft Office (Word, Excel, Access) experience preferred Preferred Qualifications: Wet chemistry experience preferred (ex. Acid/Base Titrations, water content) Laboratory Information Management System (LIMS) experience How you will thrive and create an impact Conducts routine and non-routine chemistry and microbiological analysis of raw materials, in-process formulations and final products to established specifications. Utilized and operates laboratory equipment and instruments according to laboratory work instruction or laboratory procedures such as pH, conductivity, UV, KF, FTIR and titrations. Ability to understand and follow Quality Control test methods or compendia methods (USP, EP, BP, JP or ACS) and EXCIPACT standard. Calculates and generates data for compliance to specifications and reports results. Performs technical review of lab data forms such as water, environmental monitoring and direct measure analysis. Calibrates and maintains lab equipment. Enters final results and raw data for tested materials or products in LIMS (Laboratory Information Management System) as needed. May perform investigative analysis to support investigations, complaints or instrument troubleshooting. Performs Environmental Monitoring duties, which requires gowning into cleanroom and collection of air and surface samples while in the cleanrooms. Reviews for discrepancies in data, manufacture COA, COC, and performs data verification in accordance with company procedures. Applies appropriate disposition labels to materials (accepted, rejected, etc). Handles hazardous materials using all appropriate or mandatory safety PPE and safety equipment. Completes documentation in a legible manner and reviews for accuracy. Performs other duties as assigned. KNOWLEDGE SKILLS AND ABILITIES (Those necessary to perform the job competently) Must have applied working knowledge of various laboratory instrumentation Must be able to work independently with limited direct supervision, have demonstrated ability to follow through on multiple projects, and be goal oriented with a strong desire for achievement Strong interpersonal and organizational skills ENVIRONMENTAL WORKING CONDITIONS & PHYSICAL EFFORT (Under Typical Positions) Typically works in an office environment with adequate lighting and ventilation and a normal range of temperature and noise level. At times, may be exposed to a variety of different chemicals including flammables, corrosives, oxidizers and others. Work assignments are diversified. Examples of past precedent are used to resolve work problems. New alternatives may be developed to resolve problems. A frequent volume of work and deadlines impose strain on routine basis. Minimal physical effort is required. Work is mostly sedentary but does require walking, standing, bending, reaching, lifting or carrying objects that typically weigh less than 10 lbs. #LI-Onsite Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at ****************************** and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. For more information about equal employment opportunity protections, please view the Know Your Rights poster. 3rd Party Non-Solicitation Policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.
    $44k-69k yearly est. Auto-Apply 14d ago
  • QC Lab Analyst

    Avantor 4.6company rating

    Research and development technician job in Paris, KY

    The Opportunity: Avantor is looking for a Quality Control (QC) Lab Analyst to join our Quality Control Laboratory team. The Analyst will be responsible for testing of raw materials and finished products in our Quality Control laboratory. This will be an onsite, Monday - Friday 3pm - 11:30pm shift, position at our Paris, KY chemical manufacturing facility. What we're looking for Education: Bachelor's degree in a science discipline with knowledge and experience in one of the following areas: Biology, Chemistry, or Microbiology Experience: 1-3 years of laboratory experience in a related field Collaboration Tool: Microsoft Office (Word, Excel, Access) experience preferred Preferred Qualifications: Wet chemistry experience preferred (ex. Acid/Base Titrations, water content) Laboratory Information Management System (LIMS) experience How you will thrive and create an impact Conducts routine and non-routine chemistry and microbiological analysis of raw materials, in-process formulations and final products to established specifications. Utilized and operates laboratory equipment and instruments according to laboratory work instruction or laboratory procedures such as pH, conductivity, UV, KF, FTIR and titrations. Ability to understand and follow Quality Control test methods or compendia methods (USP, EP, BP, JP or ACS) and EXCIPACT standard. Calculates and generates data for compliance to specifications and reports results. Performs technical review of lab data forms such as water, environmental monitoring and direct measure analysis. Calibrates and maintains lab equipment. Enters final results and raw data for tested materials or products in LIMS (Laboratory Information Management System) as needed. May perform investigative analysis to support investigations, complaints or instrument troubleshooting. Performs Environmental Monitoring duties, which requires gowning into cleanroom and collection of air and surface samples while in the cleanrooms. Reviews for discrepancies in data, manufacture COA, COC, and performs data verification in accordance with company procedures. Applies appropriate disposition labels to materials (accepted, rejected, etc). Handles hazardous materials using all appropriate or mandatory safety PPE and safety equipment. Completes documentation in a legible manner and reviews for accuracy. Performs other duties as assigned. KNOWLEDGE SKILLS AND ABILITIES (Those necessary to perform the job competently) Must have applied working knowledge of various laboratory instrumentation Must be able to work independently with limited direct supervision, have demonstrated ability to follow through on multiple projects, and be goal oriented with a strong desire for achievement Strong interpersonal and organizational skills ENVIRONMENTAL WORKING CONDITIONS & PHYSICAL EFFORT (Under Typical Positions) Typically works in an office environment with adequate lighting and ventilation and a normal range of temperature and noise level. At times, may be exposed to a variety of different chemicals including flammables, corrosives, oxidizers and others. Work assignments are diversified. Examples of past precedent are used to resolve work problems. New alternatives may be developed to resolve problems. A frequent volume of work and deadlines impose strain on routine basis. Minimal physical effort is required. Work is mostly sedentary but does require walking, standing, bending, reaching, lifting or carrying objects that typically weigh less than 10 lbs. #LI-Onsite Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at ****************************** and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. For more information about equal employment opportunity protections, please view the Know Your Rights poster. 3rd Party Non-Solicitation Policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.
    $51k-71k yearly est. Auto-Apply 14d ago
  • Scientist I

    University of Kentucky 4.2company rating

    Research and development technician job in Lexington, KY

    Unlock the Secrets of the Gut Microbiome - Join Our Research Team! The Corbin Lab within the Martin-Gatton College of Agriculture is actively seeking a passionate individual well-versed in gut microbiome research to join our dynamic team. We're in search of a dedicated Scientist I to spearhead groundbreaking research initiatives exploring the intricate dynamics of the gut microbiome, particularly focusing on the digestion of compounds within the human digestive tract and their subsequent effects on gut microbial communities. Primary Responsibilities: * Research Leadership: Lead innovative research projects employing in-vitro models, including the SHIME (Simulator of Human Intestinal Microbial Ecosystem), to study the behavior of compounds/food products in the gastrointestinal tract and its impact on the gut microbiome. * Specialized Expertise: Prior experience in testing the ability of plant-derived compounds, probiotics, synbiotics, or prebiotics to modulate the gut microbiome and/or conducting clinical trials in gut health is highly valued. * Bioethics and Project Management: Assist in the development of bioethics applications, oversee project management tasks, and contribute to publications and reports. * Lab Operations: Manage day-to-day laboratory operations including purchasing, reagent preparation, and ensuring adherence to safety standards. * Experimental Work: Conduct a range of laboratory tasks such as managing in vitro colon model systems, nucleic acid extractions, sequencing library preparation, microorganism isolation, and data analysis. * Training and Collaboration: Mentor students, staff, and visitors, collaborate with peers, and foster a positive team environment. Desired Qualifications: * Research Experience: Proven track record in investigating the diet-gut health nexus. * Bioinformatics Proficiency: Familiarity with bioinformatics and -omics data integration is advantageous. * Communication Skills: Excellent verbal and written communication skills are essential. * Reliability: Must exhibit reliability, respectfulness, and professionalism in all aspects of work. This research requires someone with a passion for studying gut health! Equipment Oversight: The Scientist I will oversee the operation and maintenance of specialized equipment including biosafety cabinets, anaerobic chambers, gas monitoring systems, and the SHIME. If you're an ambitious researcher eager to delve into the fascinating world of gut microbiome research and contribute to cutting-edge projects, we encourage you to apply. Join us in unraveling the mysteries of the gut microbiome and its profound impact on human health! This role does not entail supervisory responsibilities, allowing for focused contributions to research endeavors. Skills / Knowledge / Abilities Does this position have supervisory responsibilities? No Preferred Education/Experience Deadline to Apply 12/08/2025 Our University Community We value the well-being of each of our employees and are dedicated to creating a healthy place for everyone to work, learn and live. In the interest of maintaining a safe and healthy environment for our students, employees, patients and visitors, the University of Kentucky is a Tobacco & Drug Free campus. The University follows both the federal and state Constitutions as well as all applicable federal and state laws on nondiscrimination. The University provides equal opportunities for qualified persons in all aspects of institutional operations and does not discriminate on the basis of race, color, national origin, ethnic origin, religion, creed, age, physical or mental disability, veteran status, uniformed service, political belief, sex, sexual orientation, gender identity, gender expression, pregnancy, marital status, genetic information or social or economic status. Any candidate offered a position may be required to pass pre-employment screenings as mandated by University of Kentucky Human Resources. These screenings may include a national background check and/or drug screen.
    $34k-46k yearly est. 18d ago
  • Confections Formulation Scientist

    Curaleaf 4.1company rating

    Research and development technician job in Lexington, KY

    At Curaleaf, we're redefining the cannabis industry with a strong commitment to quality, expertise, and innovation. As a leading global cannabis provider, our brands-including Curaleaf, Select, and Grassroots-offer premium products and services in both medical and adult-use markets. Join us at Curaleaf to be part of a high-growth, purpose-driven company that champions corporate social responsibility through our Rooted in Good initiative, supporting community outreach and positive change. Here, you'll have the opportunity to make a meaningful impact, drive innovation, and help shape the future of cannabis. Job Title: Confections Formulation Scientist Location: Lexington, KY or Webster, MA (Relocation may be provided for the right candidate) Job Type: Full Time | Exempt Travel: Up to 50-75% to support our confection production facilities across the country Who You Are: You're a product development scientist with experience in confections, gummies, or candy formulation. You understand how hydrocolloids, pectin/gelatin systems, sugars, and emulsions work together to create consistent flavor, texture, and stability - and you know how to translate bench-top trials into scalable production. You bring deep knowledge of ingredient functionality, emulsions, and hydrocolloids, paired with the technical skill to scale formulations from the lab bench to full production. Whether running shelf-life studies, managing formulation data, or collaborating with cross-functional partners, you approach each challenge with precision, organization, and a problem-solving mindset. Above all, you're excited to push boundaries in the growing cannabis edibles space while upholding the highest standards of quality, safety, and compliance. What You'll Do: As a Confections Formulation Scientist, you'll play a central role in developing and scaling innovative cannabis-infused products. You'll conduct formulation trials, lead product testing, and support commercialization to bring new concepts to market. Your work will span from sensory evaluations to regulatory compliance, ensuring each product is safe, consistent, and high-quality. On any given day, you might be: Supporting the development, optimization, and scaling of cannabis-infused edibles through bench trials, pilot runs, and full-scale production Conducting sensory testing, shelf-life studies, and technical evaluations of texture, flavor, and stability using industry tools like viscometers and texture analyzers Maintaining SOPs, batch records, and technical documentation to streamline operations and support audits Ensuring compliance with GMP, food safety, labeling, and cannabis regulations, including coordinating third-party lab testing and interpreting results Managing formulation and ingredient data using MRP systems and formulation software for efficiency and accuracy Sharing data-driven insights that influence innovation, continuous improvement, and collaboration across the team What You'll Bring: 5-8 years of experience in confectionery formulation and/or food manufacturing A bachelor's degree in Food Science, Chemistry, Food Chemistry, or a related field Hands-on experience in confection formulation and scale-up, with knowledge of production equipment Strong understanding of ingredient functionality, food chemistry, emulsions, and hydrocolloids to design stable formulations Familiarity with GMPs, food safety, and regulatory requirements, with direct experience in sensory testing and shelf-life evaluations Excellent communication and documentation skills, paired with attention to detail and strong organizational abilities Proficiency with Microsoft Office and formulation software Willingness to travel for trials, production support, and industry events Even Better If: You have experience in the cannabis or hemp industry You're familiar with ERP/MRP systems for managing formulations and ingredient tracking You bring experience applying data science or analytics to product development You've supported R&D trials and helped scale products from concept to commercialization Physical Requirements: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this Job, the employee is regularly required to stand, walk, sit, talk or hear, use hands to finger or feel, reach with hands and arms, and lift up to 25 lbs. The employee is occasionally required to climb and balance, stoop, kneel, crouch, or crawl and lift up to 50 lbs. This position requires close vision, distance vision, peripheral vision, depth perception and the ability to adjust focus. Work Environment: This position has allergen warnings, potential exposure to dust, pollen, and plant pathogens, requires exposure to cleaning solvents, such as high volumes of isopropyl alcohol, requires daily use of provided PPE, such as masks, hair nets, beard covers, respirators, boot covers, scrubs, non-slip shoes, and Tyvek suits as necessary, requires the ability to work in confined spaces, has exposure to loud noises, including but not limited to air compressors, packaging equipment, and alarms, has exposure to CO2 manufacturing procedures at OSHA approved CO2 levels and requires a high stress tolerance, adaptability, and flexibility. Ability to work in an ever-changing environment. Curaleaf Pay Transparency $78,000 - $87,000 USD What We Offer: Career Growth Opportunities Competitive Pay and Benefits Generous PTO and Parental Leave 401(K) Retirement Plan Life/ Disability Insurance Community Involvement Referral Bonuses and Product Discounts Benefits vary by state, role type, and eligibility. Follow us on Social Media: Instagram: @curaleaf.usa Twitter: @Curaleaf_Inc LinkedIn: Curaleaf LinkedIn Curaleaf Holdings, Inc. (TSX: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading international provider of consumer products in cannabis with a mission to enhance lives by cultivating, sharing, and celebrating the power of the plant. As a high-growth cannabis company known for quality, expertise and reliability, the Company, and its brands, including Curaleaf, Select, Grassroots, JAMS, Find and Zero Proof provide industry-leading service, product selection and accessibility across the medical and adult-use markets. Curaleaf International is the largest vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence Our Vision: To be the world's leading cannabis company by consistently delivering superior products and services and driving the global acceptance of cannabis. Our Values: Lead and Inspire. Commit to Win. ONE Curaleaf. Driven to Deliver Excellence. Curaleaf is an equal opportunity employer. Curaleaf recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, gender identity, sexual orientation, physical ability, age, veteran status, and other protected status as required by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Individuals adversely impacted by the war on drugs are encouraged to apply. Current Curaleaf employees should apply for open positions through our Internal Job Board, which can be accessed via the link on The Leaf.
    $78k-87k yearly Auto-Apply 25d ago
  • Associate Scientist

    Catalent Pharma Solutions 4.4company rating

    Research and development technician job in Winchester, KY

    Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. The Associate Scientist is responsible for performing analytical research and development work in the Analytical R&D Department. The Associate Scientist work/assist on method development, method transfer, method verification and method validation under appropriate guidance along with routine release and stability testing in support of clinical development and registration activities required for the regulatory submissions. **This is a full-time on-site salaried position, Monday - Friday 8:00am - 5:00pm** Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. **The Role** + Perform technical review of client's documents as required including but not limited to specification/validation reports/test methods/compliance reports etc. to perform gap analysis with respect to methods/instruments/procedures etc. for completing methods transfers from client's/or their third-party labs with guidance from supervisors/senior team members + Analysis of finished products, in-process materials, raw materials, according to the assigned specifications, methods, and protocols according to cGLP and cGMP. Document, process, report the data as applicable to support the team in timely fashion + Perform analysis as required to support assigned testing using KF titrations/Dissolutions/IR/UV spectrophotometers, LC to perform dissolutions/assays/BU/CU, impurities and data processing using Empower and document per applicable test methods/specification/protocols etc. with guidance from senior team members + Use Empower software- creating instrument/processing/report methods and performing online empower calculations for assay/dissolutions/impurities etc. Knowledge of Trackwise for managing deviations and investigations and ability to manage /handle with guidance from supervisors/senior team members + Troubleshoot and propose any method improvement requirements during the method feasibility work of client supplied methods and/or during compendial method evaluation for assay, impurities, dissolution etc. with guidance from supervisors/senior team members. Methods and/or during compendial method evaluation for assay, impurities, dissolution etc. with guidance from supervisors/senior team members + Perform/assist team members in method transfers, Compendial verifications or full method validations (forced degradation and calculating mass balance/peak purity to prove stability indicating nature of the method) per applicable guidances (USP , , ICH Q2 etc.) / SOPs with guidance from the supervisors/senior team members + Perform stability testing on developmental/clinical/registration batches as per approved test methods/stability protocols and report/document per applicable specification/stability protocols. Escalate any OOS/OOT/atypical/trending results with supervisors or concerned team members. + Other duties as assigned **The Candidate** + Bachelor's Degree in Chemistry, Pharmaceutical Sciences or Life Sciences is required, preferred major Analytical Chemistry + Must have at least one year of experience in pharmaceutical industry and 1+ years of experience in analytical testing/research experience using HPLC/GC/UV, etc + Understand analytical chemistry calculations such as concentrations (Area%, %w/w, ppm, µg/mL, etc.), molarity, Beer's Law, reference standard purity on as is, anhydrous, or dry basis etc. is required + Basic understanding and knowledge of analytical chemistry and chromatographic techniques (e.g., LC/GC/dissolutions) and spectroscopic (e.g., UV) analysis is required + Demonstrate Knowledge and ability to understand and follow ICH guidelines (ICH Q1, Q2, Q3 etc.) including other regulatory guidelines + Adhere and perform all lab job duties/responsibilities according to applicable SOP's related to DEA scheduled drugs, safety, waste management and housekeeping and work with the team in improvement of the processes and procedures is required + Assisting with other personnel with lifting of liquid containers and all objects of greater than 50 lbs. is required **Why You Should Join Catalent** + Several Employee Resource Groups focusing on D&I + Tuition Reimbursement - Let us help you finish your degree or earn a new one! + Generous 401K match + 152 hours accrued PTO + 8 paid holidays **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers (*********************************** to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE (*************************************************************************************************************************** .
    $47k-67k yearly est. 60d+ ago
  • Applied Scientist 4

    Oracle 4.6company rating

    Research and development technician job in Frankfort, KY

    Invent, implement and deploy state-of-the-art machine learning and/or specific domain industry algorithms and systems. Build prototypes and explore conceptually new solutions. Work collaboratively with science, engineering, and product teams to identify customer needs in order to create and implement solutions, promote innovation and drive model implementations. Applies data science capabilities and research findings to create and implement solutions to scale. Responsible for developing new intelligence around core products and services through applied research on behalf of our customers. Develops models, prototypes, and experiments that pave the way for innovative products and services. Build cloud services that work out of the box for enterprises, e.g. decision support, anomaly detection, forecasting and recommendations), natural language processing (NLP), Natural Language Understanding (NLU),Time Series, Automatic Speech Recognition (ASR), Machine Learning (ML), and Computer Vision (CV). Design and run experiments, research new algorithms, and find new ways of optimizing risk, profitability, and customer experience. Conversant on ethical problems in consideration of sciences. **Responsibilities** Leading contributor providing guidance and mentorship to define, design and deliver product quality improvements from ideation stage to shipping to the customer. Write high quality code to power experiments and build models. Contributes to writing production model code. Work closely with product management and engineering to deliver products which solves the needs of our customers by building relevant, innovative results which strategically differentiates Oracle in the market. Set up environment needed to run experiments for all projects. Set up distributed environments. Engage with customers and help solve complex problems with the customer/partner. Directly impact our customers via innovation in products and services that make use of ML/AI technology. Clearly articulate technical work to audiences of all levels and across multiple functional areas. Keep track of the progress and ensure the team is following the best practices. Works on training data collection, feature engineering, model training, offline and online experimentation. Drives independent research and development. Advance the state-of-the-art machine learning and algorithms for real-world large-scale applications. Ensure solutions are designed with fairness and explainability in mind. May perform other duties as assigned. Disclaimer: **Certain US customer or client-facing roles may be required to comply with applicable requirements, such as immunization and occupational health mandates.** **Range and benefit information provided in this posting are specific to the stated locations only** US: Hiring Range in USD from: $120,100 to $251,600 per annum. May be eligible for bonus, equity, and compensation deferral. Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business. Candidates are typically placed into the range based on the preceding factors as well as internal peer equity. Oracle US offers a comprehensive benefits package which includes the following: 1. Medical, dental, and vision insurance, including expert medical opinion 2. Short term disability and long term disability 3. Life insurance and AD&D 4. Supplemental life insurance (Employee/Spouse/Child) 5. Health care and dependent care Flexible Spending Accounts 6. Pre-tax commuter and parking benefits 7. 401(k) Savings and Investment Plan with company match 8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation. 9. 11 paid holidays 10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours. 11. Paid parental leave 12. Adoption assistance 13. Employee Stock Purchase Plan 14. Financial planning and group legal 15. Voluntary benefits including auto, homeowner and pet insurance The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted. Career Level - IC4 **About Us** As a world leader in cloud solutions, Oracle uses tomorrow's technology to tackle today's challenges. We've partnered with industry-leaders in almost every sector-and continue to thrive after 40+ years of change by operating with integrity. We know that true innovation starts when everyone is empowered to contribute. That's why we're committed to growing an inclusive workforce that promotes opportunities for all. Oracle careers open the door to global opportunities where work-life balance flourishes. We offer competitive benefits based on parity and consistency and support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs. We're committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_************* or by calling *************** in the United States. Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans' status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.
    $55k-78k yearly est. 43d ago
  • Scientist II- Antifreeze

    Valvoline Global 4.2company rating

    Research and development technician job in Lexington, KY

    **Why Valvoline Global Operations?** At **Valvoline Global Operations** , we're proud to be **The Original Motor Oil** , but we've never rested on being first. Founded in 1866, we introduced the world's first branded motor oil, staking our claim as a pioneer in the automotive and industrial solutions industry. Today, as an affiliate of **Aramco** , one of the world's largest integrated energy and chemicals companies, we are driven by innovation and committed to creating sustainable solutions for a better future. With a global presence, we develop **future-ready products** and provide **best-in-class services** for our partners around the world. For us, originality isn't just about where we began; it's about where we're headed and how we'll lead the way. **We are originality in motion.** Our corporate values- **Care, Integrity, Passion, Unity, and Excellence** -are at the heart of everything we do. These values define how we operate, how we treat one another, and how we engage with our partners, customers, and the communities we serve. At Valvoline Global, we are united in our commitment to: - Treating everyone with care. - Acting with unwavering integrity. - Striving for excellence in all endeavors. - Delivering on our commitments with passion. - Collaborating as one unified team. When you join **Valvoline Global** , you'll become part of a culture that celebrates creativity, innovation, and excellence. Together, we're shaping the future of automotive and industrial solutions. **Job Purpose** The **Scientist II** embraces our safety driven culture in all tasks and demonstrates enthusiasm for the role. Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure compounds in a variety of formulations and/or rheological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs, and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol, and product specifications. Write reports summarizing data, suggests improvements to work processes and test procedures, proactively communicate with formulators, peers, and managers. **How You Make an Impact** + Runs laboratory equipment as trained and prepares product blends as guided. + Collects and evaluates data, utilizing lab notebooks and laboratory information management systems. Reviews, interprets, and analyzes the data for technical, quality, SOPs, client criteria, and Good Laboratory Practices (GLP) + Provides straightforward solutions to problems using readily available clear and direct references. + Assists the team on projects including projects with cross functional groups. + Write reports summarizing data and on the projects provided. + Maintain instruments through routine calibration, troubleshooting, and preventive maintenance. + Participate in continuous improvement initiatives for efficiency, accuracy, and method development. + Support daily housekeeping, chemical inventory management, and waste disposal in compliance with safety regulations. + Demonstrate a strong commitment to laboratory safety, including proper use of PPE, safe chemical handling, and adherence to OSHA/EPA regulations. + Ensure compliance with environmental, health, and safety (EHS) policies, maintaining a clean and hazard-free work environment. + Characterization of coolant samples using HPLC, ICP, pH probe, titration, IC, LC, GC, densitometer, refractometer, UV-Vis, and Karl Fisher. + Conducts necessary performance and quality tests to approve batch samples of antifreeze/coolant for third party blending facilities. + Support as a technical contact for Valvoline's third-party antifreeze blending plants, providing day to day support with oversite from the Team Lead. + Effectively communicate sample statuses to the group and management. + Additional duties as assigned. **What You Bring to the Role** + Minimum B.S. in Chemistry, Chemical Engineering, or related scientific field required. + 3+ years of experience in analyzing aqueous samples utilizing chromatography equipment and/or previous experience supporting manufacturing in professional laboratory environments. + Experience with development of analytical test methods, and laboratory methods a plus + Experience managing complex projects and working on tight deadlines. + Excellent oral and written communication skills required. + Multi-tasker and problem-solver. + Attention to detail and desire to complete quality work products. + Ability to work well with others and comprehend instruction quickly. + Ability to work independently and as part of a collaborative team. + Effective problem-solving and critical thinking skills. + Strong commitment to safety, quality, and laboratory best practices. + Proficiency in Microsoft Office Suite; experience with Laboratory Information Management Systems (LIMS) a plus. + Familiarity with Antifreeze/Coolant chemistries + Knowledge of ASTM + Familiarity with Engine/Cooling System hardware, operation, and design **Benefits That Drive Themselves** - Health insurance plans (medical, dental, vision) - Health Savings Account (with employer base deposit and match) - Flexible spending accounts - Competitive 401(k) with generous employer base deposit and match - Incentive opportunity* - Life insurance - Short and long-term disability insurance - Paid vacation and holidays* - Employee Assistance Program - Employee discounts - PTO Buy/Sell Options* - Tuition reimbursement* - Adoption assistance* _*Terms and conditions apply, and benefits may differ depending on position or tenure_ Valvoline Global is an **equal opportunity employer** . We are dedicated to fostering an environment where every individual feels valued, respected, and empowered to contribute their unique perspectives and skills. We strictly prohibit discrimination and harassment of any kind, regardless of race, color, religion, age, sex, national origin, disability, genetics, veteran status, sexual orientation, gender identity, or any other legally protected characteristic. We are committed to ensuring accessibility throughout our recruitment process. If you require a reasonable accommodation to participate in any stage of the recruitment or selection process, please contact us at:. - **Email** : ****************************************** This contact information is solely for accommodation requests. For inquiries about application status, please use the appropriate channels listed in your application materials. **Are You Ready to Make an Impact?** At Valvoline Global, we're looking for passionate and talented individuals to join our journey of innovation and excellence. **Are you ready to shape the future with us? Apply today.** Requisition ID: 1853
    $51k-74k yearly est. Easy Apply 37d ago
  • Implementation Scientist

    University of Kentucky 4.2company rating

    Research and development technician job in Lexington, KY

    We are seeking an Assistant, Associate, or Full Professor for tenure track, Regular Title Series, full time (12-month) positions in the Markey Cancer Center and the Department of Behavioral Science in the College of Medicine at the University of Kentucky. We seek a seasoned implementation scientist with a dynamic, productive research portfolio and active extramural grant support who aims to accelerate the dissemination and implementation of evidence-based practices in real world settings to reduce the burden of cancer and health disparities. The ideal candidate will have NIH-funded research or a very strong promise of such funding; maintain a focus on community-level factors that impact cancer vulnerability; aspire to engage in research mentorship, and contribute to a vibrant environment of scholars from the behavioral sciences, public health, social sciences, communication, health services research, biomedical informatics, health sciences (nursing, medicine, nutrition, etc.), and others. Special emphasis is placed on implementation science, patient and community engagement, quality of cancer care delivery, and health equity. All career stages are welcome. Attractive start up package, premium and contiguous space, and excellent benefits will be provided. The University of Kentucky is located in the beautiful, progressive, and accessible city of Lexington. Lexington, with over 250,000 residents, offers a high quality of life, affordability and a well-educated population. The Markey Cancer Center is an NCI-designated Comprehensive Cancer Center on the medical campus of the University of Kentucky. Situated on a campus with all six health profession colleges, the cancer center is located within a vibrant and expanding basic, clinical, and population research community with ample opportunities for collaboration within and across its research programs (see ********************************************************** for more information). Applications should include a curriculum vita, as well as a cover letter with description of cancer research interests, teaching philosophy, and a discussion of future research plans. Applications should be submitted online at the links below and will be reviewed by a faculty search committee as applications arrive. Job postings will remain open until the positions are filled. Competitive candidates will receive an invitation to visit the University of Kentucky for an interview. Skills / Knowledge / Abilities Oncology implementation science, grant/technical writing, supervision, excellent written & oral communication, teaching instruction, mentoring, leadership, creating thinking, collaboration Does this position have supervisory responsibilities? Yes Preferred Education/Experience PhD with demonstrated research experience in implementation science. Cancer-related interests may include any aspect of the cancer care continuum, including risk reduction/prevention (e.g., HPV vaccination, tobacco, obesity), screening, treatment, survivorship and/or end of life. Training and experience in cancer care delivery, patient/community engagement, and/or health equity is strongly desired. Deadline to Apply Open Until Filled Yes Our University Community We value the well-being of each of our employees and are dedicated to creating a healthy place for everyone to work, learn and live. In the interest of maintaining a safe and healthy environment for our students, employees, patients and visitors, the University of Kentucky is a Tobacco & Drug Free campus. The University follows both the federal and state Constitutions as well as all applicable federal and state laws on nondiscrimination. The University provides equal opportunities for qualified persons in all aspects of institutional operations and does not discriminate on the basis of race, color, national origin, ethnic origin, religion, creed, age, physical or mental disability, veteran status, uniformed service, political belief, sex, sexual orientation, gender identity, gender expression, pregnancy, marital status, genetic information or social or economic status. Any candidate offered a position may be required to pass pre-employment screenings as mandated by University of Kentucky Human Resources. These screenings may include a national background check and/or drug screen.
    $34k-46k yearly est. 52d ago
  • Applied Scientist 5

    Oracle 4.6company rating

    Research and development technician job in Frankfort, KY

    Invent, implement and deploy state-of-the-art machine learning and/or specific domain industry algorithms and systems. Build prototypes and explore conceptually new solutions. Work collaboratively with science, engineering, and product teams to identify customer needs in order to create and implement solutions, promote innovation and drive model implementations. Applies data science capabilities and research findings to create and implement solutions to scale. Responsible for developing new intelligence around core products and services through applied research on behalf of our customers. Develops models, prototypes, and experiments that pave the way for innovative products and services. Build cloud services that work out of the box for enterprises, e.g. decision support, anomaly detection, forecasting and recommendations), natural language processing (NLP), Natural Language Understanding (NLU),Time Series, Automatic Speech Recognition (ASR), Machine Learning (ML), and Computer Vision (CV). Design and run experiments, research new algorithms, and find new ways of optimizing risk, profitability, and customer experience. Conversant on ethical problems in consideration of sciences. **Responsibilities** Drives and plans implementation of company policy for achieving business goals. Defines the bar for science practices, and helps teams achieve those goals. Identifies and mitigates risks across full set of systems, particularly at the intersection of business and engineering. Innovate AI and ML powered solutions (rich APIs, ML models and end to end services) with strategic ISVs and customers. Develop deep product intuition to influence future product roadmaps and drive decision making. Clearly articulate technical work to audiences of all levels and across multiple functional areas in both internal and external settings. Engage in forward looking research both internal and with academic institutions globally. Hires and mentors across the org. Perform an active role in team planning, review and retrospective events. Ensures experiments are ready for hand-off to Software Developers ship into production. May perform other duties as assigned. Disclaimer: **Certain US customer or client-facing roles may be required to comply with applicable requirements, such as immunization and occupational health mandates.** **Range and benefit information provided in this posting are specific to the stated locations only** US: Hiring Range in USD from: $139,400 to $291,800 per annum. May be eligible for bonus, equity, and compensation deferral. Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business. Candidates are typically placed into the range based on the preceding factors as well as internal peer equity. Oracle US offers a comprehensive benefits package which includes the following: 1. Medical, dental, and vision insurance, including expert medical opinion 2. Short term disability and long term disability 3. Life insurance and AD&D 4. Supplemental life insurance (Employee/Spouse/Child) 5. Health care and dependent care Flexible Spending Accounts 6. Pre-tax commuter and parking benefits 7. 401(k) Savings and Investment Plan with company match 8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation. 9. 11 paid holidays 10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours. 11. Paid parental leave 12. Adoption assistance 13. Employee Stock Purchase Plan 14. Financial planning and group legal 15. Voluntary benefits including auto, homeowner and pet insurance The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted. Career Level - IC5 **About Us** As a world leader in cloud solutions, Oracle uses tomorrow's technology to tackle today's challenges. We've partnered with industry-leaders in almost every sector-and continue to thrive after 40+ years of change by operating with integrity. We know that true innovation starts when everyone is empowered to contribute. That's why we're committed to growing an inclusive workforce that promotes opportunities for all. Oracle careers open the door to global opportunities where work-life balance flourishes. We offer competitive benefits based on parity and consistency and support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs. We're committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_************* or by calling *************** in the United States. Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans' status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.
    $55k-78k yearly est. 43d ago

Learn more about research and development technician jobs

How much does a research and development technician earn in Lexington, KY?

The average research and development technician in Lexington, KY earns between $46,000 and $105,000 annually. This compares to the national average research and development technician range of $55,000 to $125,000.

Average research and development technician salary in Lexington, KY

$69,000
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