Chemist jobs in Orlando, FL - 1,471 jobs

Chemistry Laboratory Technician We are a small family owned testing lab located in Punta Gorda, FL that provides product testing and certification services. We offer a full spectrum of consumer product testing accredited to ISO 17025 through A2LA and accepted by the CPSC. We are seeking an individual to assist in our chemical lab, who is hard working, has relevant lab/chemistry experience and enjoys learning new skills to join our team at AM Testing as a Laboratory Technician. Qualifications: -Prefer an associate or Bachelor degree in chemistry or relevant field or relevant work experience -Competent with basic computer skills -Ability to use basic hand tools, scales and other calibrated equipment -Previous lab or testing experience a plus, but not necessary -Must be able to lift 25 pounds easily, 50 pounds occasionally -Enjoys working with a team Responsibilities: -Prepare lab samples for testing including: prepping, digesting, sonicating -Conduct routine testing according to company SOP's and applicable methods -Assist with running samples on XRF, GC-MS, ICP, and other instruments -Occasionally assist other technicians and associates with tasks and technical support -Accurately record and maintain standardized test results. -Clean, Maintain and organize laboratory equipment -Calibrate and verify testing equipment -Keep customer jobs/samples organized -Perform other duties as needed Benefits: -Willing to train the right person -Ability to grow with the company -Competitive payment within the current market and based on experience -benefits -Paid Vacation Forward inquiries to: Heather Nolan ********************* AM Testing & Services, Inc 24451 Sandhill Blvd Unit A Punta Gorda, FL 33983

We are seeking a dedicated Technician to join our team. This role involves analyzing production and finished product samples to ensure quality and safety in a dynamic laboratory and manufacturing environment. Responsibilities + Analyze production and finished product samples to check for quality. + Record results and lab activities, including food safety and product quality. + Review data for accuracy and quality/food safety implications. + Communicate with other departments about lab activities, data, product quality, and food safety. + Perform lab testing, plating, and analysis of samples and finished products. + Test acids, flavors, and other physical components of the dairy cultures. Essential Skills + Proficiency in quality control, chemistry, and laboratory techniques. + Strong knowledge of biology, quality assurance, and microbiology. + Experience in laboratory settings with attention to detail. + Skills in wet chemistry and analytical chemistry. + Data entry proficiency. Additional Skills & Qualifications + Bachelor's degree in a science-related field. Work Environment Join a small, family-owned business with over 30 employees. Enjoy good benefits and holiday parties. The work environment is deadline-driven, involving both laboratory and manufacturing settings, including coolers and varied temperatures. The work schedule is Monday to Friday, from 11 AM to 7:30 PM, with overtime and weekends as required. Job Type & Location This is a Contract position based out of Tampa, FL. Pay and Benefits The pay range for this position is $17.00 - $19.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Tampa,FL. Application Deadline This position is anticipated to close on Jan 21, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

About AEL: Advanced Environmental Laboratories, Inc. (AEL) is Florida's largest environmental, chemical, analytical testing laboratory network. AEL has been in business for over 30 years and is a leader in the industry with modern instrumentation, computer technology, and opportunities of growth for our employees. Are you passionate about the environment? Join AEL! We are currently looking for senior and mid-level analysts for our AEL Gainesville, FL laboratory. This hire will join our growing team to support our mission of delivery high quality environmental data for our clients across Florida. Pay and Benefits: This is a full-time position with benefits including Health/Dental/Vision Insurance (60% paid by AEL), Floating Holiday, PTO, short and long term disability + life term insurance paid by AEL, and 401K retirement plan with up to 4% Company match. Salary based on experience. Job Description: Senior Analyst will be responsible for analyzing samples using manual and more complex instrumental and reporting techniques in accordance with prescribed methods, standard operating procedures, regulatory agency standards as well as client specifications. Aids in method development of new analyses and works on special projects as they arise. Provides extensive guidance for lower level analysts. Minimum Qualifications: Education: BS in Chemistry, Biology, Environmental Science, or equivalent Experience: 2 or more years as Analyst II or 5 years experience at another analytical laboratory High level reporting skills, Advanced instrument care and maintenance Ability to train others Continued Technical Skills, Knowledge, and Abilities: Analyze samples consisting of soil and water matrices using traditional laboratory technologies. Prepare samples for analysis while displaying good laboratory technique to avoid cross-contamination or misidentified samples. Accurately prepare calibration curves and quality control samples. Interpret and evaluate data in terms of accuracy, precision, trends, and quality control requirements. Maintain laboratory equipment by cleaning, and otherwise ensuring ongoing proper working order. Report equipment issues to Department Manager. Collaborate with the laboratory team to meet reporting deadlines. Ability to perform method validations, or verifications as needed. Manage inventory supplies and alert supervisor in advance when materials must be ordered May participate in root cause analysis for quality assurance. Assist with training, scheduling and supervision of lower level analysts and technicians on instrumentation and methodology. Participate in the development and updating of departmental SOPs. Other duties and special projects as assigned. Duties and Responsibilities: Adhere to Laboratory Standard Operation Procedures (SOPs), EPA methods, and Standard Methods Perform all duties associated with sample analysis of more complex laboratory tests. Analyze, interpret and review sample results, as well as, peer review of departmental data. Perform all quality control requirements associated with the methods and maintain appropriate records. Perform all work within established quality control parameters and within specified turnaround times. Troubleshoot and fix instruments as needed. Maintain high productivity, keen attention to detail, and consistent multi-tasking while yielding a low testing error rate. Strong agility, engagement, and flexibility in an ever-changing environment. Diligent commitment to organizing, analyzing and reporting data. Excellent communication skills and ability to effectively work, problem solve, and communicate with multiple levels of the organization. Provide department managers daily status information May be assigned duties to help manage Health and Safety and/or Hazardous Waste program

Job Description HiFyve is hiring a Senior R&D Chemist in the Personal Care/Cosmetics industry in Minneapolis, MN OR Miami, FL! Salary: $90K - $110K Shift: Days Job Summary: HiFyve is hiring a Senior R&D Chemist to lead formulation and development of personal care, cosmetic, and OTC products (including lip balms and sunscreens). This role owns projects end-to-end-from concept through scale-up-while collaborating cross-functionally and interfacing directly with customers. Key Responsibilities: Lead formulation projects from concept to commercialization Develop, optimize, and scale formulations; troubleshoot production issues Set product specifications and write compounding procedures Oversee pilot batches, stability testing, and documentation Partner with QC, Operations, Sales, and Regulatory Communicate technical, regulatory, and performance details to customers Identify cost-reduction opportunities and source raw materials Mentor and train lab staff; maintain compliant lab documentation Stay current on formulation trends, ingredients, and market gaps Knowledge, Skills, and Abilities: BS in Chemistry, Cosmetic Science, Chemical Engineering, or related field 8+ years of hands-on formulation experience in personal care/cosmetics OR - Advanced degree with 6+ years' experience Strong knowledge of FDA regulations and cGMPs Advanced formulation and scale-up expertise Excellent communication, leadership, and project management skills Master's degree (Prefered) 10+ years of formulation experience (Preferred) If you are interested, please apply.

About Us Kismet Technologies is a pioneering nanotechnology company revolutionizing antimicrobials with our mineral-based technologies. Our cutting-edge, patent-pending nanotechnology platform uses a potent antimicrobial response to eradicate harmful bacteria, viruses, and biofilms. Kismet antimicrobial technologies (KAT) are mediated cerium oxide nanoparticles that instantly generate hydrogen peroxide upon contact with pathogens, resulting in their destruction. The increasing regulatory headwinds for metal and quaternary ammonia compound antimicrobials present a unique opportunity for KAT to disrupt the antimicrobial additive market. About the Role We are seeking a highly motivated Product Development Chemist with strong expertise in coatings and formulation science. The ideal candidate will play a key role in developing, optimizing antimicrobial and antifouling coatings and integrating novel nanomaterial-based products into coatings. This position requires hands-on laboratory work, strong analytical skills, and close collaboration with cross-functional teams, including engineering, quality, and manufacturing. This position reports to the VP of Engineering. Key Responsibilities Develop and optimize coatings and formulations incorporating nanoparticles for targeted performance (e.g., durability, functionality, stability) Conduct product development and support scale-up activities, transitioning formulations from lab to pilot and manufacturing scale Assist in the Design, synthesize, and optimization of nanoparticles (e.g., inorganic, polymeric, hybrid) with controlled size, morphology, and surface chemistry Perform characterization of nanoparticles and formulations, including: Particle size and distribution (DLS, SEM/TEM) Surface chemistry (FTIR and UV-Vis Spectroscopy) Thermal, mechanical, and chemical performance testing Analyze experimental data and generate technical reports, protocols, and documentation Troubleshoot formulation and process challenges to improve product performance and reproducibility Collaborate with cross-functional teams to support product validation, customer requirements, and commercialization Maintain laboratory best practices, safety standards, and proper documentation Required Qualifications B.S. or M.S. in Chemistry, Polymer Science, Materials Science, Chemical Engineering, or a related field Strong background in functional coatings and formulation chemistry and integrating pigments or functional fillers into coatings Experience with material characterization techniques such as DLS, SEM, TEM, AFM, FTIR, XRD, or similar Proven ability to design experiments, interpret data, and solve complex technical problems Excellent written and verbal communication skills Preferred Qualifications Industry experience in product development or applied R&D Knowledge of polymer chemistry, surface chemistry, or colloidal science Familiarity with nanomaterial-based products Familiarity with quality systems, regulatory requirements, or ISO standards Experience working in multidisciplinary teams and fast-paced development environments What We Offer Opportunity to work on cutting-edge nanotechnology products Collaborative and innovation-driven work environment Competitive compensation and benefits H1B sponsorship is not available for this position.

The Opportunity The Institute of Simulation and Training (IST) at the University of Central Florida (UCF) is seeking applicants for a full-time, 12-month non-tenure earning, associate scholar/scientist/engineer position which reports to the director of IST. We are searching for a Research Scientist with expertise in software engineering, visualization, immersive technologies, artificial intelligence (AI), and computational science to support the design, development, and integration of next-generation visual simulations and intelligent systems. The successful candidate will join a multidisciplinary team conducting applied research in simulation-based training, modeling, data analytics, and intelligent decision-support systems. Key Responsibilities Design, develop, and implement software architectures, frameworks, and prototypes for high-fidelity visual simulations and AI-enabled environments and applications. Apply computational models, data-driven algorithms, and physics-based simulation methods to enhance realism and interactivity in diverse domain systems and applications. Work with interdisciplinary teams including engineers, cognitive scientists, and domain experts to define research objectives, design experiments, and analyze results. Provide technical guidance on software engineering best practices, simulation technologies, and computational frameworks. Contribute to architecture design, performance optimization, and software verification and validation. Create prototypes and capabilities demonstrators to showcase IST's expertise aligned with trends and opportunities. Manage the common labs and provide guidance on equipment and infrastructure acquisition and upgrades. Contribute to or lead the preparation of grant proposals and technical reports for federal, state, and industry sponsors. Publish research findings in peer-reviewed journals and conferences. Present technical results to sponsors, collaborators, and stakeholders. Design and execute hands-on demonstrations and exhibits at strategic events. Minimum Qualifications: Ph.D. degree from an accredited institution in Computer Science, M&S, Engineering, or a related discipline in modeling and simulation is required at time of application. Preferred Qualifications: Strong programming skills in one or more of the following: C++, Python, C#, with experience in modern software engineering practices (version control, CI/CD, modular design). Experience with distributed systems, GPU computing, or cloud-based simulation environments. Knowledge of human-in-the-loop simulation, training effectiveness evaluation, or synthetic environments. Experience in government or defense research environments. Record of successful proposal writing and sponsored research funding. Demonstrated experience in software development for simulation systems, high-performance computing, or AI-based applications. Familiarity with simulation frameworks (e.g., Unity, Unreal Engine, Paraview, Fluent, or similar visual simulation engines). Experience with AI/ML tools and frameworks (e.g., PyTorch, TensorFlow, scikit-learn). Ability to work effectively in multidisciplinary research teams and communicate complex concepts clearly. Additional Application Materials Required: UCF requires all applications and supporting documents be submitted electronically through the Human Resources employment opportunities website, ************************** In addition to the online application, interested candidates should upload the following: A curriculum vitae. A letter of interest describing qualifications for the position, such as research agenda and teaching experience/interest. NOTE: Please have all documents ready when applying so they can be attached at that time. Once the online submission process is finalized, the system does not allow applicants to submit additional documents later. The selected candidate will be required to submit official transcripts (and, as applicable, U.S. degree equivalency evaluations) documenting the conferral of their qualifying academic credentials. Questions regarding this search should be directed to: Nayade Ramirez, Search Manager at **********************. Special Instructions to the Applicants: Sponsorship for employment-based visas will only be considered under exceptional circumstances and is not guaranteed. Preference will be given to candidates who are currently authorized to work for any employer in the United States. This position is funded with E&G funds. Job Close Date: Open until filled. Are you ready to unleash YOUR potential? As a next-generation public research university and Forbes-ranked top employer in Florida, we are a community of thinkers, doers, creators, innovators, healers, and leaders striving to create broader prosperity and help shape a better future. No matter what your role is, when you join Knight Nation, you'll play an integral role at one of the most impactful universities in the country. You'll be met with opportunities to connect and collaborate with talented faculty, staff, and students across 13 colleges and multiple campuses, engaging in impactful work that makes a positive difference. Your time at UCF will provide you with many meaningful opportunities to grow, you'll work alongside talented colleagues on complex projects that will challenge you and help you gain new skills and you'll have countless rewarding experiences that go well beyond a paycheck. Working at UCF has its perks! UCF offers: Benefit packages, including Medical, Dental, Vision, Life Insurance, Flexible Spending, and Employee Assistance Program. Paid time off, including annual (12-month faculty) and sick time off and paid holidays. Retirement savings options. Employee discounts, including tickets to many Orlando attractions. Education assistance. Flexible work environment. And more…For more benefits information, view the UCF Employee Benefits Guide click here. Unless explicitly stated on the job posting, it is UCF's expectation that an employee of UCF will reside in Florida as of the date the employment begins. Additional Requirements related to Research Positions: Pursuant to Florida State Statute 1010.35, prior to offering employment to certain individuals in research-related positions, UCF is required to conduct additional screening. Applicants subject to additional screening include any citizen of a foreign country who is not a permanent resident of the U.S., or who is a citizen or permanent resident but is affiliated with or has had at least 1 year of education, employment, or training in China, Cuba, Iran, Russia, North Korea, Syria, or Venezuela. The additional screening requirements only apply to research-related positions, including, but not limited to faculty, graduate positions, individuals compensated by research grants or contract funds, post-doctoral positions, undergraduate positions, visiting assistant professors, and visiting research associates. Department Institute for Simulation and Training (IST)* Work Schedule Varies Type of Appointment Regular Expected Salary Negotiable As a Florida public university, the University of Central Florida makes all application materials and selection procedures available to the public upon request. UCF is proud to be a smoke-free campus and an E-Verify employer. If an accommodation due to a disability is needed to apply for this position, please call ************ or email ************. For general application or posting questions, please email **************.

Job Requisition Name Quality Analytical Chemist Job Requisition No VN8368 USA - Sarasota Worker Basis Full Time Worker Type Employee Contract Type Permanent Applications Close Date Mar 31, 2026 Purpose As a Quality Control Analytical Chemist, you will be responsible for performing analytical testing of incoming materials, in-process samples, and finished materials within a regulated medical device manufacturing environment. You will ensure that materials meet defined specifications and regulatory requirements through accurate chemical analysis, thorough documentation, and close collaboration with internal and external stakeholders. * Perform analytical testing of incoming, in-process, and finished materials using techniques such as HPLC, GC, FTIR, UV-Vis, pH, titration, and conductivity * Inspect materials visually and dimensionally and approve or reject them based on specifications and test results * Accurately document analytical results and quality data in quality systems and databases * Prepare and maintain Certificates of Analysis, Nonconformance Reports, and related quality documentation * Ensure compliance with GMP, ISO 13485, and FDA regulatory requirements * Support internal and external audits by providing analytical data and documentation * Collaborate with internal teams and suppliers on quality issues, root cause analysis, CAPA, and continuous improvement * Associate or Bachelor's degree in Chemistry, Chemical Engineering, or a related field * Minimum 3 years of experience in analytical testing or quality inspection within a regulated industry * Proficiency in analytical techniques and laboratory instruments such as HPLC, GC, FTIR, UV-Vis spectroscopy, pH measurement, titration, and conductivity testing * Strong understanding of GMP, ISO 13485, and FDA regulatory requirements * Ability to interpret technical drawings, specifications, and tolerances * High attention to detail with strong documentation and communication skills Preferred Skills * Knowledge of statistical process control (SPC) * Familiarity with risk management and validation protocols BVI is refocusing the future of vision. As one of the fastest-growing, diversified surgical ophthalmic businesses in the world, our purpose-built portfolio of trusted brands includes: Beaver (Knives and Blades), Visitec (Cannulas), Malosa (Single-Use Instruments), Vitreq (Vitreoretinal Surgical Products) and PhysIOL (Premium IOLs), and spans more than 90 countries. We've set our sights on touching the lives of millions of patients affected by conditions such as cataracts, refractive error, glaucoma, retinal disease, and dry eye. Unburdened by legacy or bureaucracy, we have developed our strategy around a simple concept - taking pride in delivering innovative solutions for our physicians and patients, based on their needs. We trust and empower our associates to make decisions and solve problems because collaboration drives us. Valuing agility, simplicity, and transparency, we stay committed to listening to our customers, delivering for our patients, and keeping the future in focus. Learn more at ******************

Job Title: Senior Formulating Chemist Company: Cosmetic Solutions Innovation Labs Employment Type: Full-Time Experience Level: Senior (7+ Years) Cosmetic Solutions Innovation Labs is a cutting-edge, full-scale cosmetics and OTC manufacturing company specializing in advanced formulation, clean beauty, and custom turnkey product development. We bring innovation, science, and speed to market for some of the most forward-thinking skincare and beauty brands in the industry. We are seeking a highly technical, experienced, and innovative Senior Cosmetic Chemist to join our R&D team. This is a high-impact role focused on leading new product development, troubleshooting complex formulations, and working closely with manufacturing to scale concepts into commercial success. Responsibilities will include, but are not limited to: Lead end-to-end development of skincare, OTC, and cosmetic formulations-from concept through scale-up. Design, test, and optimize formulations for performance, safety, sensory profile, and stability. Troubleshoot formulation issues, both in the lab and during manufacturing, applying deep technical knowledge to solve challenges efficiently. Collaborate with manufacturing teams during pilot batches and scale-up to ensure product consistency and process viability. Conduct raw material research and apply advanced formulation principles to support innovation goals. Maintain accurate and detailed documentation of all formulation processes, including batch records, lab notebooks, and experimental notes. Apply and enforce Good Laboratory Practices (GLP) in daily lab activities. Work cross-functionally with regulatory, marketing, and quality teams to align technical objectives with business needs. Utilize Coptis software for formulation tracking and documentation (proficiency is a plus). Ensure compliance with FDA, OTC, EU, and international cosmetic regulations. Qualifications: Bachelor's or Master's in Chemistry, Cosmetic Science, Chemical Engineering, or a related field. 7+ years of hands-on formulation experience in cosmetics, personal care, or OTC products. In-depth knowledge of emulsion systems, surfactants, active ingredients, thickeners, and preservative systems. Strong ability to troubleshoot, adjust, and optimize formulas under varying lab and production conditions. Experience with manufacturing scale-up and pilot batches in a GMP environment. Proficient in Microsoft Word and Excel; Experience with Coptis software a plus. Excellent communication and documentation skills. Detail-oriented with strong organizational abilities. Passion for innovation and staying current with industry trends and raw material technologies. What we Offer: The opportunity to work with a leading innovator in cosmetic and OTC manufacturing. Competitive salary and comprehensive benefits package. A collaborative, fast-paced environment that fosters creativity and innovation. Access to modern lab facilities, technologies, and ingredients. The chance to directly influence the success of top-tier beauty and wellness brands. Cosmetic Solutions LLC is committed to equal employment opportunities for all employees and applicants for employment without regard to age, color, disability status, gender, national origin, race, religion, sexual orientation or veteran status, or any other legally protected status. Ready to help us formulate the future of beauty? Please submit your resume.

It is the primary responsibility of the Analytical Chemist to maintain the instrumentation and analytical methods in the Analytical Sciences laboratory in a state of readiness for the analysis of essential oils and isolates for agricultural residues and other trace contaminants. DUTIES & RESPONSIBILITIES: Preparation, dilution and extraction, where appropriate, of samples for trace analysis Calibration of analytical balances and pipettes Instrument preparation including creation of sequences (GLC, GC-MS, GC-MSMS, GC-XSD and UHPLC) Data analysis, interpretation and reporting of trace analytical results (GLC, GC-MS, GC-MSMS, GC-XSD and UHPLC) Maintenance of the analytical calibration and verification spreadsheets (GC; GC-MS; GC-MSMS, GC-XSD and UHPLC) Advanced instrument maintenance & troubleshooting (GC; GC-MS; GC-MSMS, GC-XSD and UHPLC) Maintenance of the equipment down time log Method development and maintenance of advanced quantitative methods Preparation and appropriate storage of calibration standards for trace analysis Assist and contribute to Global Technical projects Maintain the supply of gas to the instrumentation by changing gas cylinders when required Monitor and log the ordering, receipt and return of gas cylinders on site including maintenance of the gas usage log Perform classical and/or instrumental analysis on any QC samples as and when requested by the Global Analytical Innovation Manager or the Quality Control Manager. Raise purchase orders where appropriate to replenish consumables and reagents. Report and address any deficiencies in equipment or analytical practices to Global Analytical Innovation Manager Undergo training in areas specific to Treatt PLC business Statistical data evaluation of new and existing analytical methods Write Quality Policies, Procedures and Operating Instructions. Ensure that the working area in the laboratory is maintained in a clean and orderly condition and that any hazard or potential hazard is reported to the Line Manager or H&S Officer Act in the best interest of Treatt PLC at all times Employees have a legal duty to take reasonable care of their own health and safety and that of others who may be affected by what they do at work. EDUCAION & TRAINING: Bachelor of Science Degree with Science Major or Master of Science Degree KNOWLEDGE & EXPERIENCE: Strong analytical skills with a minimum of 3 years' laboratory experience. Significant experience in working with GC-FID, HPLC, GC/MS Some experience in working with GC/MSMS and LC/MSMS preferred Knowledge of analytical disciplines, methods, developments and troubleshooting. Significant experience in data collection, extraction and analysis with strong analytical, problem-solving and research skills. Passionate about keeping up to date with relevant scientific and technological developments. The capability to organize and prioritize with a strong eye for detail. Excellent interpersonal and relationship skills with the ability to support teams and colleagues. Intermediate classical analytical skills. Exposure to hazardous Chemical WORKING CONDITIONS: Exposure to hazardous Chemical Open Office - typical spacious room, desks close together Shop floor, including some time inside and outside production

Job Description Position Overview Engineered Bonding Solutions, LLC seeks an experienced Chemist to lead product development, formulation, and materials testing. This salaried role involves creating and modifying adhesives, performing rigorous testing (including Instron or comparable equipment such as the Frank Bacon SSTM-20kN), and preparing technical reports. The Chemist will collaborate closely with sales, customers, and manufacturing to support commercialization, quality, and process improvements. Key Responsibilities Develop and modify adhesive formulations for targeted applications and markets. Conduct product testing and evaluation, including specimen preparation per ASTM standards. Operate and interpret data from mechanical testing equipment (Instron, Frank Bacon SSTM-20kN). Prepare clear, concise technical reports and visual presentations. Partner with sales and customers to provide input, technical service, and field support. Implement cost savings through formula optimization, raw material selection, and process improvements. Manage product scale-up from lab to full production. Oversee technical aspects of manufacturing and provide production support as needed. Perform quality control testing on products and incoming raw materials. Maintain ISO-compliant documentation and support internal/external audits. Ensure lab notebooks meet legal and intellectual property requirements. Promote safe laboratory practices and maintain organized, clean work areas. Qualifications Bachelor's degree or higher in Chemistry. Minimum 10 years' experience in adhesives development, technical service, or manufacturing. Strong knowledge of polymers (unsaturated polyesters, urethanes, epoxies) and reactive monomers. Experience with raw material analysis and mechanical testing of composites. Proficiency with ASTM testing methods for adhesives and composites (ASTM D1002, D5868, D638, etc.). Skilled in writing technical reports and documenting product testing. Familiarity with Quality Assurance, ISO procedures, and Good Manufacturing Practices. Physical Requirements Ability to perform light labor in varied indoor/outdoor conditions (including heat and humidity). Comfortable working around fumes, airborne particles, vibration, and noise with proper PPE. Ability to lift, push, or pull up to 25 lbs. and stand for extended periods. Strong vision requirements including color, depth perception, and focus adjustment. E04JI800t97s407tqe8

We are currently accepting applications for future Quality Control Chemists. WHY CORERX CoreRx, a dynamic pharmaceutical technology company that empowers its employees with responsibility and offers a supportive and highly progressive work environment. At CoreRx you will find a challenging career path directed towards growth and opportunity. We employ talented, motivated people - team players who are innovative thinkers. We offer our employees a comprehensive, competitive program of benefits and a corporate culture based on core values that include innovation, a results-oriented focus and ethical behavior. If we do not have any positions that fit your needs at this time; We invite you to join our talent network and stay informed about future opportunities by submitting your resume. Thank you for choosing CoreRx as your employer of choice. DESCRIPTION The Analytical Chemist II is an integral part of the team, contributing to our success by performing raw materials and clinical and commercial pharmaceutical products testing according to compendial method and/or methods provided by analytical development team or clients. ESSENTIAL DUTIES AND RESPONSIBILITIES Performs relevant QC testing, such as HPLC, GC, Dissolution, Malvern and wet chemistry testing as required in compliance with cGMP requirements, compendia standards, and internal procedures Ensures testing is properly conducted and documented for all performed activities with emphasis on data integrity Prepare test solutions, volumetric solutions, and samples used in analysis Performs assigned physical tests, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished, and stability products in an FDA regulated lab environment Perform analysis with a practical understanding of the test procedure and instrument operation Perform laboratory analysis right first time, contemporaneous documentation, analyze and document the results Conducts laboratory investigation under the supervision of laboratory manager. Complies with all regulatory/ in-house requirements may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, documentation Maintain required level of training needed to perform a GMP task Notify manager immediately of nonconforming data or unexpected occurrences Organize work schedule to complete assigned tasks efficiently and on schedule Work under direction provided by manager Conscientious with safety procedures and knowledgeable of hazardous waste procedures Performs other related duties as assigned by management EXPERIENCE AND EDUCATION REQUIREMENTS Experience in UPLC/HPLC GMP operations Knowledge with analytical equipment and Part 11 compliant software, such as Chemstation™, Chromeleon™, EMPOWER™, and Laboratory Information Management System. Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment Proficient in Microsoft Office Suite or similar software Minimum of 2 years experience preferred in an FDA-regulated pharmaceutical environment Experience in other highly regulated laboratory settings will be considered BS/BA in life science or chemistry required Equivalent experience may substitute for stated requirements PHYSICAL DEMANDS Regularly required to stand. Frequently required to sit, walk, talk, hear, handle or feel tools or controls Occasionally required to reach with hands and arms, stoop, crouch, climb or balance, kneel Vision suitable for performing detailed inspections May be required to move items weighing up to 25 lb Ability to communicate clearly in both written and verbal form We are an equal opportunity/equal access/affirmative action employer fully committed to achieving a diverse workforce and complies with all applicable Federal and State laws, regulations, and executive orders regarding nondiscrimination and affirmative action with our hiring activities. We do not discriminate based on race, color, religion, ethnic or national origin, gender, genetic information, age, disability, sexual orientation, gender identity, gender expression, and veteran's status. Notification to Agencies: Please note that CoreRx Inc. does not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Master Service Agreement, and specific approval to submit resumes to an approved requisition, CoreRx Inc. will not consider or approve payment regarding recruiter fees or referral compensation.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza Tampa is seeking a QC Chemist to join the Quality Control team. The incubment will be Conduct analysis of raw materials, In process items and finished products Key Accountabilities Analysis of dry product stability and finished product samples according to the assigned specifications, analytical methodology and protocols in a GMP laboratory setting with emphasis on attention to detail and accuracy of execution. Documentation of results in accordance with cGMP Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner. Reports lab testing data and completes documentation accurately and in accordance with laboratory procedures and regulatory requirements Reviews results for conformance to standards Perform analytical testing of pharmaceutical products following analytical methodology Read and interpret analytical methodology and the USP Supports method development and validation of new methods Performs investigations and completes CAPA in response to deviations. Develops and executes validation protocols for test methods and equipment qualification as requested. Meet fundamental cGMP requirements relating to conduct and work practices to ensure the SISPQ (Safety, Identity, Strength, Purity, and Quality) of the all products manufactured/tested at Lonza Tampa. Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to management and correct where possible Stop work where deemed necessary to maintain safety Key Requirement Associate's Degree in Science, preferably chemistry Minimum of 3 years experience in a GMP pharma environment Actively participates in customer and regulatory audits Demonstrated experience with peer review work and data of other analysts to ensure compliance with method and regulatory requirements Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

We are seeking a part-time, Chemical Lab Technician to support our R&D and manufacturing laboratory operations. This role is ideal for a recent graduate or current student looking to gain hands-on laboratory experience in a professional engineering and research environment. The Chemical Lab Technician will assist with maintaining a safe, organized, and compliant laboratory while supporting routine testing and applied research activities. Key Responsibilities As a part-time Chemical Lab Technician, you will: Assist in maintaining Safety Data Sheet (SDS) records for laboratory chemicals Support proper handling, labeling, storage, and disposal of chemicals and chemical waste Help maintain laboratory cleanliness, organization, and safety standards Assist with chemical inventory tracking and ordering under supervision Operate and support routine use of laboratory instrumentation under guidance, including: Gas Chromatography (GC) High-Performance Liquid Chromatography (HPLC) UV-Vis Spectroscopy FTIR Spectroscopy Thermogravimetric Analysis (TGA) Differential Scanning Calorimetry (DSC) Assist with experimental setup, data collection, and basic documentation Follow established laboratory procedures, safety protocols, and training requirements Education Pursuing or recently completed an AS or BS in Chemistry or a closely related field Experience & Skills Coursework or academic laboratory experience required Strong interest in laboratory work, safety, and chemical handling Ability to follow written procedures and maintain accurate records Good organizational skills and attention to detail Willingness to learn laboratory instrumentation and safety practices Additional Requirements U.S. Citizenship (required by ITAR regulations GPA greater than 3.3 at all degree levels Mainstream Engineering Corporation is an equal opportunity employer. Qualified candidates will be considered without regard to legally protected characteristics. Job Posted by ApplicantPro

Job Title: QC Chemist Ready to make an impact? Join Lonza Tampa as a QC Chemist and help ensure the quality and safety of life-changing medicines. In this role, you'll work in a cutting-edge GMP laboratory, collaborating with passionate professionals to deliver products that improve lives worldwide. What you will get * An agile career and dynamic working culture. * An inclusive and ethical workplace. * Compensation programs that recognize high performance. * Medical, dental, and vision insurance. * Our full list of global benefits can be found here: *************************************** What you will do * Perform analytical testing of raw materials, in-process items, and finished products in a GMP laboratory setting. * Document results accurately in compliance with cGMP and regulatory standards. * Review data for conformance to specifications and report findings promptly. * Support method development, validation, and equipment qualification activities. * Investigate deviations and implement corrective and preventive actions (CAPA). * Ensure adherence to FDA, EPA, and OSHA regulations while maintaining safety and sustainability standards. * Contribute to maintaining product Safety, Identity, Strength, Purity, and Quality (SISPQ). What we are looking for * Associate's Degree in Science, preferably Chemistry required. * Minimum of 3 years' experience in a GMP pharmaceutical environment required. * Proficient in HPLC techniques, including hands-on experience with Empower software required. * Familiarity with Solutia systems or similar platforms required. * Strong knowledge of analytical methodologies and USP standards. * Ability to review peer data for compliance with regulatory requirements. * Experience supporting audits and regulatory inspections. * Detail-oriented with strong documentation and problem-solving skills. * Commitment to safety and quality in all work practices. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now

Analyzes Products and Materials and the composition of their ingredients. Includes the following. Other duties may be assigned. Following approved procedures and under general direction: Develops formulas, processes, and methods for solution of technical problems. - Provides input to the development of procedures. - Follows established procedures and documents all findings and results timely, concisely, clearly and accurately. - Analyzes compounds to determine chemical and physical properties. - Conducts research on manufactured products to develop and improve products. - Conducts research into composition, structure, properties, relationships, and reactions of matter. - Prepares standards and specifications for processes, facilities, products, and tests. - Measures products for compliance to standards and specifications and reports same. - Contributes to a continuous improvement process to lower product costing and/or add product value. - Follow Prime Enterprises, Inc. SOPs, STPs and cGMP. - Keeps records updated, distributed, and filed. Job Performance Standards: Neither suffers nor contributes to any injury or accident. Maintains an exemplary attendance and punctuality performance record. Adheres to all Prime Personnel Policies as established by the company. Performs all tasks and assignments in a safe and timely manner. Strives toward continuous self-improvement in personal productivity. Skills: requires a combination of technical skills, analytical capabilities, and attention to detail. Candidate should have a solid working knowledge of laboratory instrumentation such as FTIR, HPLC. Candidate must have a demonstrated proficiency in laboratory instrument troubleshooting and knowledge of statistical techniques. Education: Minimum of a BS in Chemistry, Chemical Engineering or Biochemistry. Degrees in other scientific disciplines will be considered.

Nightwing provides technically advanced full-spectrum cyber, data operations, systems integration and intelligence mission support services to meet our customers' most demanding challenges. Our capabilities include cyber space operations, cyber defense and resiliency, vulnerability research, ubiquitous technical surveillance, data intelligence, lifecycle mission enablement, and software modernization. Nightwing brings disruptive technologies, agility, and competitive offerings to customers in the intelligence community, defense, civil, and commercial markets. At Nightwing, we value collaboration and teamwork. You'll have the opportunity to work alongside talented individuals who are passionate about what they do. Together, we'll leverage our collective expertise to drive innovation, solve complex problems, and deliver exceptional results for our clients. About Cybersecurity, Intelligence and Services The Cybersecurity, Intelligence and Services (CIS) business provides technically advanced full-spectrum cyber, data operations, systems integration and intelligence mission support services to meet our customers' most demanding challenges. Our capabilities include cyber space operations, cyber defense and resiliency, vulnerability research, ubiquitous technical surveillance, data intelligence, lifecycle mission enablement, and software modernization. CIS brings disruptive technologies, agility, and competitive offerings to customers in the intelligence community, defense, civil, and commercial markets Job Summary Our team covers the full life cycle from emulation, reverse engineering, vulnerability research, and CNO/CNE tool development for various operating systems. Our mission covers a wide range of targets, anything from major consumer electronics to proprietary one-off systems. If it runs code, we have probably looked at it (or will soon.). In addition, the position will provide deliverables for real-world use in relatively short turn-around times. Projects will be undertaken in small teams with close coordination with customers to quickly enhance capabilities or resolve issues in existing tools for real-world applications. Working as part of a team you will also need to be familiar with source management tools such as GIT and team coordination tools like the Atlassian suite of work products. All candidates must be US citizens and be able to obtain and maintain a government security clearance. This position is an onsite role. Responsibilities to Anticipate We seek a qualified engineer that can perform as a team member on activities involved with research, reverse engineering, development, testing, maintenance, and modification of complex classified and unclassified software applications. Basic Qualifications TS/SCI Clearance Required Typically requires a Bachelor's in Science, Technology, Engineering, or Mathematics (STEM preferred) and a minimum of 5 years of prior engineering experience or equivalent experience unless prohibited by local laws/regulations Vulnerability research experience of public targets Reverse engineering utilizing any of IDA/Ghidra/BinaryNinja Utilizing full system emulation for research and analysis Understanding of network protocols (TCP/IP stacks, wire-level protocols, routing protocols, or others) Experience with source management tools Experience with assembly language (x86/64, ARM, PPC, Mips, etc.) Requires advanced knowledge of work area typically obtained through advanced education combined with experience May have practical knowledge of project management Practical to substantial knowledge of RTX projects, programs or systems with the ability to make enhancements and leverage in daily work Preferred Qualifications C/C++/Python Capture the Flag (CTF) experience Fuzzer development Understanding of network protocols (TCP/IP stacks, wire-level protocols, RF communications, BGP, routing protocols, or others) Linux or other OS reversing What We Offer Whether you're just starting out on your career journey or are an experienced professional, we offer a total rewards package that goes above and beyond with compensation; healthcare, wellness, retirement and work/life benefits; career development and recognition programs. Some of the benefits we offer include parental (including paternal) leave, flexible work schedules, achievement awards, educational assistance and child/adult backup care. In addition to competitive salaries, CODEX offers excellent benefits for you and your family: competitive medical, dental and vision plans, child, elderly and dependent-care programs, mental health resources, tuition assistance, employee discount programs, 401k matching, flexible work schedules (depending on program), a peer recognition and reward system and performance-based bonuses. Additional Information Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. ERIP Eligibility - This requisition is eligible for an employee referral award. ALL eligibility requirements must be met to receive the referral award. #CODEX At Nightwing, we value collaboration and teamwork. You'll have the opportunity to work alongside talented individuals who are passionate about what they do. Together, we'll leverage our collective expertise to drive innovation, solve complex problems, and deliver exceptional results for our clients. Thank you for considering joining us as we embark on this new journey and shape the future of cybersecurity and intelligence together as part of the Nightwing team. Nightwing is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.

Insight Global is seeking an experienced Senior Laboratory Systems Analyst to lead the implementation, Epic integration, and long-term sustainment of the Haemonetics SafeTrace TX Blood Bank application. This role is ideal for someone with a strong background in laboratory or Blood Bank information systems and hands-on experience configuring, fixing, and building backend solutions. The ideal candidate will have: - Experience with SafeTrace TX and Epic Beaker. - Familiarity with HL7 interfaces and middleware solutions like Data Innovations. - A solid understanding of Blood Bank workflows and regulatory compliance. - Previous experience as a Medical Technologist who now works on the technical side of Blood Bank systems. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements - Bachelor's degree in Computer Science, MIS, Information Sciences, or related discipline OR equivalent work experience. - 3-5 years of experience supporting or implementing laboratory or Blood Bank information systems in a hospital setting. - Familiarity with HL7 interfaces, data integration, and middleware solutions such as Data Innovations. - Understanding of Blood Bank workflows, including product management, crossmatching, transfusion documentation, and regulatory compliance. - Strong analytical, troubleshooting, and problem-solving skills. - Excellent communication and collaboration abilities to work with cross-functional clinical and IT teams. - Ability to manage multiple priorities in a fast-paced environment. - Local to South Florida Tri-County area (Miami-Dade, Broward, Palm Beach) or willing to relocate. Relocation will be compensated for. - Experience with Haemonetics SafeTrace TX (highly preferred). - Knowledge of Epic Beaker or prior Epic implementation experience. - Certification as an MT/MLS (ASCP) or equivalent. - Prior experience as a Medical Technologist who transitioned into backend system configuration, troubleshooting, and build.

Pay: $16.00/hour (Full-Time, Non-Exempt) Let's Be Blunt Cannabis isn't just an industry - it's a movement. At Mint Cannabis, innovation and precision drive everything we do - especially in our production labs. We're looking for a Formulation Technician to join our team and help create high-quality cannabis products by carefully blending distillates, terpenes, and other components. This hands-on role is perfect for someone who's detail-oriented, science-minded, and passionate about product consistency and safety. You'll work alongside our production and extraction teams to ensure every batch meets Mint's high standards for quality and compliance. Ready to mix things up and make an impact? 🌱 Let's make it happen. What You'll Do Accurately measure, mix, and blend cannabis distillates and terpenes according to established formulations and SOPs Operate and maintain laboratory equipment and mixing tools in a clean, safe, and compliant manner Assist in the preparation of raw materials and finished products for packaging and testing Follow safety and sanitation procedures to maintain a compliant work environment Conduct visual inspections and quality checks during formulation to ensure consistency and accuracy Collaborate with production leads and management to troubleshoot and optimize processes Maintain organization and cleanliness of the formulation lab and storage areas Support inventory tracking of ingredients, materials, and finished batches What You'll Bring 1+ year of experience in a production, laboratory, or food/pharmaceutical manufacturing environment (cannabis experience a plus) Strong attention to detail and ability to follow precise measurements and procedures Familiarity with basic lab or production equipment and safety protocols Strong organizational and record-keeping skills Ability to work efficiently in a fast-paced, high-volume environment Team player with good communication and collaboration skills Must be at least 21 years of age Must be able to obtain and maintain a Facility Agent Card in accordance with Florida state regulations Why You'll Love Mint Cannabis A work culture that's welcoming, passionate, and built on good vibes Opportunities for growth as we expand into new markets Employee discounts on Mint products and merch Health, dental, and vision benefits (for eligible roles) Paid time off to recharge and take care of you A chance to be part of something ama Zing 🌱 A Few Things You'll Need Ability to stand, bend, and perform repetitive tasks for extended periods Ability to lift up to 30 lbs Comfortable working around strong odors and raw cannabis materials Manual dexterity and visual acuity for precision measuring and mixing PPE required based on task or department policy About Mint Cannabis At Mint Cannabis, we're passionate about creating a premium cannabis experience - for everyone! Headquartered in Arizona, we're a national, multi-state operator proudly serving both medical patients and recreational customers. From state-of-the-art production facilities to dispensaries that redefine the retail experience, Mint is raising the bar in every market we enter. Our flagship location in Arizona - one of the largest dispensaries in the country - features a 24/7 storefront, the nation's first cannabis kitchen offering delicious infused foods, and a drive-thru for ultimate convenience. We're proud to offer a carefully curated menu of premium flower, concentrates, edibles, and more, designed to elevate the experience for seasoned consumers and newcomers alike. Named “Most Innovative Medical Cannabis Dispensary” by the International Commercial Cannabis Awards, Mint Cannabis continues to grow rapidly across Arizona, Michigan, Missouri, and beyond. Our team - from budtenders to leadership - is driven by passion, education, and a commitment to helping every guest feel welcome, informed, and supported. At Mint Cannabis, we're not just changing the cannabis industry - we're growing a community. Equal Opportunity Employer Statement Mint Cannabis is proud to be an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Verdant Specialty Solutions is a dynamic, innovation-driven specialty chemicals company with a global footprint. Born from the McIntyre Group of the 1970s and relaunched in 2021, Verdant combines the agility of a small business with the safety, reliability, and scale of a larger organization, offering personal attention backed by industry-leading manufacturing and technical capabilities. With over 375 product offerings, nine strategic sites across the U.S. and Europe, and a steadfast commitment to sustainability, compliance, and customer-centric solutions, Verdant brings functional chemistry to life safely, reliably, and responsively. Are you a hands-on chemist who loves ensuring quality, safety, and operational excellence? Verdant Specialty Solutions, a global specialty chemical company serving world-leading consumer, industrial, and energy brands, is looking for a Quality Control Chemist to join our University Park team. Why this role is exciting: * Play a key role in a fast-growing, start-up-like environment with global impact * Work with cutting-edge specialty surfactant chemistries for top-tier clients * Contribute directly to safety, quality, and operational excellence across multiple sites * Opportunities to grow professionally in a collaborative, innovative culture What you will do: * Perform in-process, final product, and raw material analyses * Certify products for shipment and maintain accurate lab records * Collaborate with operators, engineers, and QC colleagues to optimize processes * Participate in process improvements, investigations, and quality initiatives * Maintain compliance with ISO 9001, EFfCI, GMP, RSPO, and HSSE standards * Operate lab systems (SAP) to track data, generate certificates, and manage inventories