Chemist jobs in Kentucky - 34 jobs

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

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

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

We are looking to fill a **Scientist 3 -** **Third Shift** **Analytical Chemist Pilot Plant** position working as **a full-time employee of Parexel FSP on long-term assignment** onsite at one of our clients located in **Rahway, NJ** . This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **Description** The Scientist III **Third Shift** - Analytical Chemist Pilot Plant operates and maintains a myriad of analytical instrumentation and other duties as assigned by the client. **Responsibilities** + Experience in routine and real-time testing for high-performance liquid chromatography (HPLC), gas chromatography (GC), ultraviolet (UV) spectroscopy, infrared (IR) spectroscopy, titrations, Karl Fischer (KF) testing, and other wet chemistry methods + Experience in HPLC and GC is required with an interest in expanding the knowledge and background in method development and optimization, validation, data analysis, and sample preparation techniques + Routine use of modern analytical techniques such as HPLC, GC, KF, ultraviolet-visible spectroscopy (UV-VIS), and IR spectroscopy + Comfortable working in a cGMP environment; knowledgeable in various GMP analytical activities, such as documentation procedures, abiding by relevant department SOPs and generation and second scientist review of GMP data + Experience with automated liquid handling systems (Tecan) for high throughput testing + Experience with a myriad of software platforms used in the compilation, processing, and reporting of data, such as Waters Empower, Relational Laboratory Information Management System (RLIMS), Lab X, etc. **Qualifications** + BA/BS (3-5 yrs.) of relevant experience in n chemistry or a related discipline testing lab + MS (1-2 yrs.) of relevant experience in chemistry or a related discipline testing lab **Desired Skills and Experience** + Effective organizational, multi-tasking, and oral/written communications skills + Ability to work under pressure and provide reliable results with quick turnarounds + Consistently deliver high quality and fully compliant results and interact with a diverse customer base daily + Proficient in written and spoken English, is required **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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

Role Description Lab Tech 1 - Chemistry SHIFT: Monday-Friday 10:00 pm - 6:30 am The Lab Technician 1 is responsible for performing routine laboratory tests to support the diagnosis and treatment of animal health conditions. Key responsibilities include preparing samples, operating laboratory equipment, and maintaining accurate records. This role supports the Global Diagnostics division at Zoetis and will work closely with internal veterinarians or medical team, and other lab personnel to ensure the highest standards of quality and accuracy in our diagnostic services. Job Duties: · Prepare biological specimens for testing in various departments, including but not limited to, hematology, urinalysis, serology, chemistry, endocrinology, parasitology, cytology, and coagulation · Use high-throughput automated analyzers, microscopes, and other diagnostic equipment to test various sample types, including but not limited to, whole blood, serum, urine, and feces · Set up and execute laboratory tests, review results, and release findings in accordance with ZRL Standard Operating Procedures (SOPs) · Perform routine and non-routine maintenance on analyzers, including but not limited to, daily, weekly, monthly, and as needed maintenance · Perform basic analyzer troubleshooting techniques on one major department analyzer · Review and accept daily Quality Control reports and weekly Levey-Jennings charts · Handle and store all biological specimens in accordance with ZRL Standard Operating Procedures (SOP) · Maintain a clean and organized laboratory workspace · Properly handle and dispose of medical and biohazardous waste while adhering to all applicable regulatory guidelines · Consistently and properly fill out laboratory logs, including but not limited to maintenance logs, environmental logs, and cleaning logs · Maintain several types of records, including but not limited to medical records, courier logs and manifests · Prepare biological specimens for shipment to offsite testing facilities, adhering to all standards set forth by regulatory bodies including the Department of Transportation (DOT) · Receive, store, and log all laboratory and office supplies into designated locations · Operate and maintain secondary laboratory equipment, including but not limited to centrifuges, pipettes, heating blocks, and slide stainers · Understand and follow SOPs and training modules set forth by Zoetis Reference Laboratories Education/Experience: · High School Diploma or equivalent required. · Associate or Bachelor's degree preferred. · Requires 1-2 years of experience in a clinical laboratory setting and experience in performing basic laboratory testing or operations · Proficient knowledge in one of the following preferred: Hematology, Chemistry, Urinalysis, Endocrinology, Parasitology, and Cytology Technical Skills Required: · Strong attention to detail · Proficiency in using laboratory equipment and software. · IT and LIS (laboratory information systems) experience and general comfort level with computer systems, technology, and equipment interfaces. · Team-oriented with excellent collaboration skills · Ability to work independently and as part of a team · Robust organizational and time management abilities · Excellent data entry skills · Strong written and oral communication skills · Ability to complete tasks with minimal supervision · Fluency in English language Physical Position Requirements: · Ability to lift up to 50 pounds · Ability to bend, kneel, stoop, crouch · Ability to walk, sit, or stand for extended periods Full time RegularColleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

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

Actual Job Title: Histology Technician II Pay Rate: $36/hr A Histology Tech II is responsible for performing routine laboratory tests to support the diagnosis and treatment of animal health conditions. Key responsibilities include working under minimal supervision on embedding tissue, cutting and staining of samples, operating laboratory equipment, and maintaining accurate records. This role supports the Global Diagnostics division at *** and will work closely with internal veterinary pathologists, and other lab personnel to ensure the highest standards of quality and accuracy in our diagnostic services. Position Responsibilities: •Under minimal supervison, prepare thin slices of tissue for analysis •Cut various tissue types using microtomes and operate the automated tissue stainer •Examine, adjust, and process the tissue for proper sample preservation •Independently perform tissue embedding of various tissue types •Mount the tissue sample on the slide and stain or dye the sample to emphasize abnormalities •Prepare and troubleshoot special stains and IHC slides •Recognize factors that affect procedures and quality results, and taking appropriate action when corrections are necessary •Review histology slides for quality and consistency •Perform special stains as requested by pathologists •Assist with using advanced techniques like molecular pathology or electron microscopy •Clean and operate all equipment within the anatomic pathology lab •Perform quality control checks on daily H&E stain •Complete other relevant tasks as required Education and Experience: •Bachelors degree preferred, Associates required •2+ years of experience in histology required •HT or HTL Certification in histology preferred •Proficiency in various staining techniques and equipment Technical Skills: •Strong attention to detail •Proficiency in using laboratory equipment and software •Team-oriented with excellent collaboration skills •Ability to work independently and as part of a team •Robust organizational and time management abilities •Excellent data entry skills •Strong written and oral communication skills •Ability to complete tasks with minimal supervision •Fluency in English language

This position provides a strong technical expertise to develop new products, renovate the existing products and drive the innovation per the customer and business needs. This person plays an integral role within the company, working directly with the customers, and internal cross functional teams to drive the highest customer satisfaction and the value. ESSENTIAL DUTIES AND RESPONSIBILITIES: Develops new products working closely with the sales team and the customers that are commercially feasible based on the project scope. Partners closely with corporate research chefs to confirm and calibrate that developed products meet finished product applications and culinary gold standards. Scope includes products manufactured at Paradise's own manufacturing facilities and/or at co-manufacturing partners. Works on reformulations, product renovations, and cost optimization projects by revising the product formulations in a cross functional collaborative environment to ensure it would meet the current manufacturing capabilities. Works closely with Project Manager to commercialize the products and ensures that the finished product meets customer's analytical and sensory expectations. Formulates seasoning blends to reduce individual herbs and spices to match ingredient statements, nutritional profile, and sensory attributes of existing products to reduce manufacturing complexity. Makes prototypes to confirm that the finished product meets analytical and sensory specifications. Supports Procurement Team with regards to the ingredient substitutions, replacements, and formula modifications by making prototypes and testing it for the analytical and sensory compliance per the needs driven by internal and external threats, challenges and opportunities. Identifies areas of cost optimization through strategic raw material procurement, ingredient substitutions, or processing efficiencies. Reduces introduction and removal of unique raw materials from the product portfolio to reduce ingredient management complexities. Reviews batching data, analytical data, financial standard, and customer specifications to update the formula standards for all the products on an annual basis. Partners with Quality Assurance to gather and analyze formula deviations, product yield, and processing modifications/improvements/innovations prior to updating the standards. Work closely with the Processing team to propose changes and recommendations to the manufacturing process should any deviations be found in not meeting the standards. Supports culinary ideation sessions for the customers by developing commercially feasible products. Assists the chefs and/or sales to conduct the culinary meetings and/or product presentations in-house and off-site as per the business needs. Scouts for new ingredients and processing technologies for innovation partnering with internal partners (procurement, engineering), and external suppliers. Support forward thinking growth strategies laid out by the sales team analyzing consumer insights, and flavors trends in collaboration with the chefs to propose new product platforms and growth channels. Maintain R&I lab to support day-to-day functioning. Duties include but are not limited to ingredient management (ingredient stocking, disposal of expired materials, ingredient ordering, technical paperwork), packaging inventory management (packaging stocking, disposal of old materials), lab supplies management, organized storage of competitor products, Paradise's finished products, and trial run products, lab cleaning and garbage disposal, etc. Develops technical training documentation such as Tomato 101, Hot Sauce 101, Ingredient 101, etc. to drive technical awareness, knowledge, and training for the customers and internal cross functional teams. Generates and maintains technical documentation, reports, case studies, and other pertinent information to have robust knowledge transfer capabilities for the internal teams. Other duties as assigned QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. BS in Food Science/Food Technology 4 years of experience in product development with a minimum of 3 years of developing tomato-based and/or hot sauces preferred. Experience with thermal processing technologies. Excellent collaboration skills and able to excel in a team environment Sensory evaluation experience and skills Experience with a wide variety of equipment, kitchen set-up, cooking techniques and operator execution; or in-depth knowledge of key applicable equipment or processes Ability to read, analyze, and interpret common scientific and technical journals, and ingredient spec sheets Ability to flex schedule to support 24-hour production scheduling requirements for test products Ability to travel and work at California plant during In-Season (July -Sept) Ability to communicate and interact effectively with various sales, marketing, and technical services personnel Computer and software skills Ability to recognize, analyze, and develop solutions and initiate problem-solving actions Must have proven formulation and commercialization experience. 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. Ability to stand at bench routinely for hours at a time. Lifting can be accommodated; cases of goods can weigh up to 45 lbs. Capable of hand-mixing thick products, as required.

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

Job DescriptionOverview We are seeking a dedicated and detail-oriented Quality Control Welding professional to join our team in Louisville, KY. In this role, you will play a crucial part in ensuring that our welding processes meet the highest standards of quality and safety. If you have a passion for precision and a keen eye for detail, we want to hear from you! Responsibilities Conduct thorough inspections of welded components to ensure compliance with specifications and standards. Identify and document any defects or non-conformities in welding processes. Collaborate with welding teams to implement corrective actions and improve quality processes. Perform routine audits of welding procedures and equipment to maintain quality assurance. Maintain accurate records of inspections, tests, and quality control activities. Provide training and guidance to welding personnel on quality standards and best practices. Stay updated on industry standards and regulations related to welding quality control. Qualifications High school diploma or equivalent; relevant certifications in welding or quality control preferred. Proven experience in quality control within a welding environment. Strong understanding of welding processes, techniques, and materials. Familiarity with industry standards such as AWS, ASME, or ISO. Excellent attention to detail and problem-solving skills. Ability to work independently and as part of a team. Effective communication skills, both written and verbal. You should be proficient in: Quality Inspection Experience Quality Control Experience Welding Setups for Production Quality Control Data Analysis Blueprint Reading Machines & technologies you'll use: Measurement Gauges Calipers and Micrometers Salary info: $24 - $28 / hr

Title: QC Analyst Shift: SAT, SUN, MON 6AM-6PM & EVERY OTHER TUES 6AM - 2:30PM. Pay rate: $27.76/hr Start: ASAP thru July 2026 Education: - Bachelor's degree in Chemistry, Biology, Chemical Engineering or Life Sciences with no work experience OR any other Bachelor's degree Requirements: *Entry Level (0-1 years of experience) - General knowledge of the use and operation of basic laboratory equipment. - Basic knowledge of lab safety and the ability to work safely with chemicals of varying potency. - General computer literacy including use of Microsoft Word and Excel. - Ability to perform analytical testing while standing for long periods of time - Accurate testing on the first attempt under pressure of production details. Responsibilities: - Perform efficient/reliable/high quality analytical testing in accordance with USP/NF/EP/JP/FCC/etc. or customer supplied guidelines. Typical testing may include Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metal Content, FTIR, HPLC, and GC, etc. - Maintain accurate written records of all analysis performed. - Accurately interpret and effectively communicate analytical results and issues. - Schedule daily tasks in an organized and efficient manner. - Calibrate and maintain lab equipment and instrumentation. - Responsible for operating in a safe manner using laboratory and chemical hygiene practices #m3 Ref: #558-Scientific System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Chemical Analyst - Owensboro KY Be a part of a revolutionary change! At Philip Morris International (PMI), we've chosen to do something incredible. We're totally transforming our business and building our future on one clear purpose - to deliver a smoke-free future. With huge change, comes huge opportunity. So, if you join us, you'll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. Our success depends on people who are committed to our purpose and have an appetite for progress. This position sits with our Swedish Match affiliate. Your 'day to day' * Performs analyses utilizing gas chromatography, ultra high pressure chromatography, and ion chromatography. * Responsible to maintain cleanliness and orderly arrangement of Analytical laboratory. * Provides support to Sr Analytical Chemist, Analytical Chemist, Sr Chemical Analyst, and Chemical Analyst. * Responsible for accurate records of assigned projects. * Knowledgeable in ISO 17025 Standard requirements. * May be required to work additional/different shifts. * Provides support to Production, Research and Development, Quality Assurance, and Leaf Operations. * Knowledgeable of method validation procedures. * Performs special projects as directed by Chemical Analysis Supervisor/Manager. * Responsible for sample preparation and extraction as indicated by written SOP. * Responsible for written SOPs of validated methods and procedures. * Responsible for routine and non-routine Microbiology testing. * Ability to review, interpret, and report analytical results using LIMS. Who we're looking for: * Minimum Bachelor's degree in scientific discipline such as Chemistry, Biology, related discipline or equivalent experience. * Minimum one year as a Laboratory Technician or comparable position/experience. * Knowledgeable in chemical laboratory safety and analytical procedures and methodologies. * Knowledgeable of Microbiological procedures and equipment. Must be able to prepare concise and accurate reports. * Must be able to work 3rd shift (12:00am - 8:30am) Annual Base Salary $ 64,300 What's 'nice to have' Legally authorized to work in the U.S. (required) What we offer * We offer a competitive base salary, annual bonus (applicable based on level of position), great medical, dental and vision coverage, 401k with a generous company match, incredible wellness benefits, and much more! * Seize the freedom to define your future and ours. We'll empower you to take risks, experiment and explore. * Be part of an inclusive, diverse culture where everyone's contribution is respected; Collaborate with some of the world's best people and feel like you belong. * Pursue your ambitions and develop your skills with a global business - our staggering size and scale provides endless opportunities to progress. * Take pride in delivering our promise to society: To improve the lives of millions of smokers. PMI is an Equal Opportunity Employer. PMI is headquartered in Stamford, Conn., and its U.S. affiliates have more than 2,300 employees. PMI has been an entirely separate company from Altria and Philip Morris USA since 2008. PMI's affiliates first entered the U.S. market following the company's acquisition of Swedish Match in late 2022.Philip Morris International and its U.S. affiliates are working to deliver a smoke-free future. Since 2008, PMI has invested $12.5 billion globally to develop, scientifically substantiate and commercialize innovative smoke-free products for adults who would otherwise continue to smoke with the goal of transitioning legal-age consumers who smoke to better alternatives. In 2022, PMI acquired Swedish Match - a leader in oral nicotine delivery - creating a global smoke-free champion led by the IQOS and ZYN brands. The U.S. Food and Drug Administration has authorized versions of PMI's IQOS electronically heated tobacco devices and Swedish Match's General snus as Modified Risk Tobacco Products and renewal applications for these products are presently pending before the FDA. For more information, please visit ************** and ******************* #PMIUS #LI-DH1

Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments - creating exceptional outcomes for our clients and the millions of people who count on them. You have an opportunity to personally thrive, make a difference and be part of a culture where individuality is noticed and valued every day. **Mailroom Quality Associate** Onsite - Lexington, KY **Training Hours:** Monday - Friday 8:00am - 4:30pm (4-6 weeks) **Work Hours:** Monday - Friday 8:00am - 4:30pm **Pay Rate:** $16.00/hour, which may be below your state's minimum wage. Please take this into consideration when applying. **Job Summary:** As a Mailroom Quality Associate at Conduent, you'll be on-site working hands-on. You will be sorting incoming and outgoing mail efficiently and accurately. You'll be responsible for monitoring and verifying the quality of work performed in both the inbound and outbound mailrooms, as well as completing **and grading** various data‑entry tasks for onshore and offshore processes. **Key Responsibilities:** + Reviews approximately 5% of each mailroom operator's work daily + Delivering errors in person and in real time to the production operator + Correcting the issue and returns the item to the rescan desk for completion **Qualifications and Skills:** To be successful in this role you will: + High School Diploma required + Basic computer knowledge (Microsoft Outlook, Excel, and Word) + Must be able to lift recycle bins that can weigh up to 20lbs + Must be dependable, organized and able to stay focused + Strong verbal communication skills + Must have high attention to detail + Must have effective time management skills + Must have problem solving ability + Must be able to work mandatory overtime + Live in one of the following states AL, AR, AZ, CO, CT, DE, FL, GA, ID, IN, IA, KS, KY, LA, ME, MI, MS, MO, NE, NV, NH, NJ, NM, NC, ND, OH, OK, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY **Working with Us** Join a rapidly growing organization that can support your career goals. **Working for Us** What you get: + Paid Training + Career Growth Opportunities + Full Benefit Options + Great Work Environment Pay Transparency Laws in some locations require disclosure of compensation and/or benefits-related information. For this position, actual salaries will vary and may be above or below the range based on various factors including but not limited to location, experience, and performance. In addition to base pay, this position, based on business need, may be eligible for a bonus or incentive. In addition, Conduent provides a variety of benefits to employees including health insurance coverage, voluntary dental and vision programs, life and disability insurance, a retirement savings plan, paid holidays, and paid time off (PTO) or vacation and/or sick time. The estimated salary range for this role is $26,600 - $33,250. _We are currently NOT hiring in the following geographies,_ including but not limited to: _States: AK, CA, HI, MA, IL, MT & NY_ _Metro Areas: MN - Minneapolis, IL - Chicago, NY - New York City, OR - Portland, MD - Montgomery County, WA - Seattle, Washington, DC_ Conduent is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, creed, religion, ancestry, national origin, age, gender identity, gender expression, sex/gender, marital status, sexual orientation, physical or mental disability, medical condition, use of a guide dog or service animal, military/veteran status, citizenship status, basis of genetic information, or any other group protected by law. For US applicants: People with disabilities who need a reasonable accommodation to apply for or compete for employment with Conduent may request such accommodation(s) by submitting their request through this form that must be downloaded: click here to access or download the form (********************************************************************************************** . Complete the form and then email it as an attachment to ******************** . You may also click here to access Conduent's ADAAA Accommodation Policy (***************************************************************************************** .

JBW Federal is a subsidiary company of the Kanaka Foundation - An NHO who's mission is to support Native Hawaiians. You will receive a comprehensive benefits package that includes: Health insurance Dental insurance Vision insurance Pet insurance Annual membership to Costco or Sam's 401K ...and much, much more! Job Description: The SSHO/QC shall be responsible for field execution of assigned projects, including site management, onsite construction operations and oversight of all work being installed for the duration of the Contract. Must have in-depth knowledge and experience as a general contractor for construction including pre-construction planning, scheduling, safety, quality control, equipment and workforce supervision. Must have the ability to lead and problem solve while working with all CSI trade divisions and the assigned self-performing work force. Responsibilities: Coordinate daily with Construction Project Manager Maintain and assist with updating project schedule and three week lookahead Coordinate subcontractors and support staff to accomplish onsite tasks Complete daily reporting requirements and catalog site photos Read/Understand Plans and Specifications Construct the work according to Plans/Specifications and Contract Documents Coordinate with Government stakeholders on status of field activities Monitor workmanship and maintain compliance with submittal requirements Maintain and Facilitate the Company Safety Program Review subcontractor materials and workmanship Facilitate the Company Quality Control Program Maintain RMS and other Govt reporting programs Track and complete punch list according to contract requirements Assist with gathering O&M Manuals and Closeout Documents Perform other position-related duties as assigned, depending on assignment setting Minimum Qualifications: Experience as a Quality Control Manager that has executed new construction and renovation type projects Experience working with RMS (Resident Management System) software Minimum of 5-years of experience working as a Superintendent/Quality Control Manager/Site Safety Officer on government construction projects. Proficient in Windows operating systems and associated software Experience working on smartphones and tablets Ability to work with numerous subcontractors and support staff in an efficient manner Ability to read Plans, Specifications, and Shop Drawings Ability to multi-task and establish priorities Strong communication and analytical skills CPR/First Aid and OSHA 30 certifications CQM (Construction Quality Management) Certificate Required Willing to travel to various job sites Secret Clearance, preferred not required Kanaka Family of Companies is an Equal Opportunity Employer, and all qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, marital status, sex (including pregnancy), gender identity or expression, age, disability, veteran status, sexual orientation, genetic information (family medical history), or any other status protected by federal, state or local laws. EEO/AA employer/Vet/Disabled. Job Posted by ApplicantPro

Mailroom Quality Associate Onsite - Lexington, KY Training Hours: Monday - Friday 8:00am - 4:30pm (4-6 weeks) Work Hours: Monday - Friday 8:00am - 4:30pm Pay Rate: $16.00/hour, which may be below your state's minimum wage. Please take this into consideration when applying. Job Summary: As a Mailroom Quality Associate at Conduent, you'll be on-site working hands-on. You will be sorting incoming and outgoing mail efficiently and accurately. You'll be responsible for monitoring and verifying the quality of work performed in both the inbound and outbound mailrooms, as well as completing and grading various data‑entry tasks for onshore and offshore processes. Key Responsibilities: Reviews approximately 5% of each mailroom operator's work daily Delivering errors in person and in real time to the production operator Correcting the issue and returns the item to the rescan desk for completion Qualifications and Skills: To be successful in this role you will: High School Diploma required Basic computer knowledge (Microsoft Outlook, Excel, and Word) Must be able to lift recycle bins that can weigh up to 20lbs Must be dependable, organized and able to stay focused Strong verbal communication skills Must have high attention to detail Must have effective time management skills Must have problem solving ability Must be able to work mandatory overtime Live in one of the following states AL, AR, AZ, CO, CT, DE, FL, GA, ID, IN, IA, KS, KY, LA, ME, MI, MS, MO, NE, NV, NH, NJ, NM, NC, ND, OH, OK, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY Working with Us Join a rapidly growing organization that can support your career goals. Working for Us What you get: Paid Training Career Growth Opportunities Full Benefit Options Great Work Environment Pay Transparency Laws in some locations require disclosure of compensation and/or benefits-related information. For this position, actual salaries will vary and may be above or below the range based on various factors including but not limited to location, experience, and performance. In addition to base pay, this position, based on business need, may be eligible for a bonus or incentive. In addition, Conduent provides a variety of benefits to employees including health insurance coverage, voluntary dental and vision programs, life and disability insurance, a retirement savings plan, paid holidays, and paid time off (PTO) or vacation and/or sick time. The estimated salary range for this role is $26,600 - $33,250. We are currently NOT hiring in the following geographies, including but not limited to: States: AK, CA, HI, MA, IL, MT & NY Metro Areas: MN - Minneapolis, IL - Chicago, NY - New York City, OR - Portland, MD - Montgomery County, WA - Seattle, Washington, DC

Role Description Lab Tech 1 - Chemistry SHIFT: Monday-Friday 10:00 pm - 6:30 am The Lab Technician 1 is responsible for performing routine laboratory tests to support the diagnosis and treatment of animal health conditions. Key responsibilities include preparing samples, operating laboratory equipment, and maintaining accurate records. This role supports the Global Diagnostics division at Zoetis and will work closely with internal veterinarians or medical team, and other lab personnel to ensure the highest standards of quality and accuracy in our diagnostic services. Job Duties: * Prepare biological specimens for testing in various departments, including but not limited to, hematology, urinalysis, serology, chemistry, endocrinology, parasitology, cytology, and coagulation * Use high-throughput automated analyzers, microscopes, and other diagnostic equipment to test various sample types, including but not limited to, whole blood, serum, urine, and feces * Set up and execute laboratory tests, review results, and release findings in accordance with ZRL Standard Operating Procedures (SOPs) * Perform routine and non-routine maintenance on analyzers, including but not limited to, daily, weekly, monthly, and as needed maintenance * Perform basic analyzer troubleshooting techniques on one major department analyzer * Review and accept daily Quality Control reports and weekly Levey-Jennings charts * Handle and store all biological specimens in accordance with ZRL Standard Operating Procedures (SOP) * Maintain a clean and organized laboratory workspace * Properly handle and dispose of medical and biohazardous waste while adhering to all applicable regulatory guidelines * Consistently and properly fill out laboratory logs, including but not limited to maintenance logs, environmental logs, and cleaning logs * Maintain several types of records, including but not limited to medical records, courier logs and manifests * Prepare biological specimens for shipment to offsite testing facilities, adhering to all standards set forth by regulatory bodies including the Department of Transportation (DOT) * Receive, store, and log all laboratory and office supplies into designated locations * Operate and maintain secondary laboratory equipment, including but not limited to centrifuges, pipettes, heating blocks, and slide stainers * Understand and follow SOPs and training modules set forth by Zoetis Reference Laboratories Education/Experience: * High School Diploma or equivalent required. * Associate or Bachelor's degree preferred. * Requires 1-2 years of experience in a clinical laboratory setting and experience in performing basic laboratory testing or operations * Proficient knowledge in one of the following preferred: Hematology, Chemistry, Urinalysis, Endocrinology, Parasitology, and Cytology Technical Skills Required: * Strong attention to detail * Proficiency in using laboratory equipment and software. * IT and LIS (laboratory information systems) experience and general comfort level with computer systems, technology, and equipment interfaces. * Team-oriented with excellent collaboration skills * Ability to work independently and as part of a team * Robust organizational and time management abilities * Excellent data entry skills * Strong written and oral communication skills * Ability to complete tasks with minimal supervision * Fluency in English language Physical Position Requirements: * Ability to lift up to 50 pounds * Ability to bend, kneel, stoop, crouch * Ability to walk, sit, or stand for extended periods Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

We are seeking a dedicated and detail-oriented Quality Control Welding professional to join our team in Louisville, KY. In this role, you will play a crucial part in ensuring that our welding processes meet the highest standards of quality and safety. If you have a passion for precision and a keen eye for detail, we want to hear from you! Responsibilities Conduct thorough inspections of welded components to ensure compliance with specifications and standards. Identify and document any defects or non-conformities in welding processes. Collaborate with welding teams to implement corrective actions and improve quality processes. Perform routine audits of welding procedures and equipment to maintain quality assurance. Maintain accurate records of inspections, tests, and quality control activities. Provide training and guidance to welding personnel on quality standards and best practices. Stay updated on industry standards and regulations related to welding quality control. Qualifications High school diploma or equivalent; relevant certifications in welding or quality control preferred. Proven experience in quality control within a welding environment. Strong understanding of welding processes, techniques, and materials. Familiarity with industry standards such as AWS, ASME, or ISO. Excellent attention to detail and problem-solving skills. Ability to work independently and as part of a team. Effective communication skills, both written and verbal. You should be proficient in: Quality Inspection Experience Quality Control Experience Welding Setups for Production Quality Control Data Analysis Blueprint Reading Machines & technologies you'll use: Measurement Gauges Calipers and Micrometers Salary info: $24 - $28 / hr

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