Chemist Jobs in Hialeah, FL

HealthTrust Workforce Solutions HCA is seeking a travel Cath Lab Technologist for a travel job in Aventura, Florida. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 04/14/2025 Duration: 13 weeks 36 hours per week Shift: 10 hours, days Employment Type: Travel Entrust Your Career to HealthTrust! At HealthTrust, we believe that healthcare is not defined by the four walls in which it is practiced; it's defined by its people. We pride ourselves on crafting opportunities that expand skill sets, broaden career horizons, provide economic stability, and cultivate personal growth. HealthTrust Offers: • Competitive Pay Packages • Guaranteed hours • Weekly direct deposit options • 401k with Company Match • Earn up to $750 for referrals • Free Private Furnished Housing or Tax-Free Subsidy To get started, you will need: • An adventurous spirit and fierce dedication • A degree from an accredited school of nursing • Minimum 1-year acute care experience in a hospital setting • Current State Nursing License • Appropriate certifications for the specific position HealthTrust Benefits: · Opportunities for a lifetime: When you become a part of the HCA family, you will have exclusive access to more opportunities than any other healthcare system in the nation. At HWS, we help open the door to a lifetime of lasting career opportunities. · A culture of care: Our clinicians have made HWS an industry leader for over 25 years. We are passionate about our mission that, above all else, we are committed to the care and improvement of human life. · Career Development: As a wholly owned subsidiary of HCA Healthcare, HWS is a preferred partner to thousands of top-performing hospitals. We provide our healthcare professionals with first-priority access to more than 200,000 jobs nationwide. We are uniquely positioned to offer you exclusive and direct access to HCA Healthcare's vast network of facilities. Let us open the door to nationwide opportunities that fit your lifestyle! We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Candidate Requirements State license requirements: Florida Preferred clinical experience: 1 year minimum experience Interview requirement: Phone interview HealthTrust Workforce Solutions HCA Job ID #911674. Posted job title: Travel Cath Lab Tech - General - Cath Lab Tech About HealthTrust Workforce Solutions HCA At HealthTrust Workforce Solutions, healthcare is not just about the four walls of a facility but about the people who provide and receive care. Our focus is on empowering healthcare professionals to deliver exceptional patient experiences by providing them with the necessary skills, tools, and support. We partner with healthcare facilities nationwide to ensure that the right professionals are in the right roles. We prioritize our clinicians by giving them a voice and access to opportunities to fulfill their mission of improving lives by providing quality patient care. We are committed to our core values of Trust, Innovation, Adaptability, Courage, and Accountability. We are dedicated to positively impacting the healthcare industry by providing first-priority access to more than 200,000 jobs nationwide to our healthcare professionals. Join us and be part of the HealthTrust family, where you can make a difference every day. We embrace our changing environment, and we maintain a culture that has a rich tradition of transforming itself to meet the challenges of the future. MISSION STATEMENT While putting great people in the right roles is essential, our mission is far greater. We want our clinicians to be part of the HealthTrust family, where healthcare professionals have a voice and are empowered with the right tools and opportunities to fulfill their personal mission of improving lives. Plus, as a preferred partner to thousands of top-performing hospitals, we provide our healthcare professionals with first-priority access to more than 200,000 jobs nationwide. Benefits Dental benefits Vision benefits Referral bonus Continuing Education Life insurance

Title: Analytical Scientist About the Company Are you passionate about groundbreaking science and innovative healthcare solutions? We are a rapidly growing, well-funded biotech company with a hybrid platform that combines both innovative and specialty products. Our mission is to revolutionize the biotech industry by developing cutting-edge therapies and specialty products that address unmet medical needs. Job Description As an Analytical Scientist, you will play a crucial role in our research and development efforts. You will be responsible for developing and validating analytical methods from scratch, ensuring compliance with Good Manufacturing Practices (GMP), and utilizing advanced analytical techniques to support our projects. Key Responsibilities Develop and validate analytical methods independently. Perform routine and non-routine analysis using techniques such as High-Performance Liquid Chromatography (HPLC), Mass Spectrometry (MS), and UV-Visible Spectroscopy (UV-Vis). Ensure all work complies with GMP regulations and standards. Troubleshoot and optimize analytical methods and instrumentation. Document and report analytical data accurately and promptly. Collaborate with cross-functional teams to support product development and quality control. Maintain and calibrate analytical instruments and equipment. Qualifications Bachelor's, Master's, or Ph.D. in Chemistry, Analytical Chemistry, or a related field with minimum 2 years GMP industry experience. Proven experience in developing analytical methods from scratch. Strong knowledge of GMP regulations and practices. Proficiency in using HPLC, MS, and UV-Vis techniques. Excellent problem-solving skills and attention to detail. Strong communication and teamwork abilities. Ability to work independently and manage multiple projects simultaneously. Benefits Competitive salary and benefits package. Opportunities for professional growth and development. Collaborative and inclusive enviornment

Barentz is a leading global life science and specialty performance ingredients distributor. We source branded specialty ingredients from leading manufacturers worldwide and our ingredient experts provide value-added technical support which includes pre-mixing, blending, ingredient formulation, and ingredient testing from our state-of-the-art, customized formulation centers and application laboratories. Established in 1953, Barentz has operations in more than 70 countries with a strong presence in Europe and North America and a rapidly growing network in Latin America and Asia-Pacific. With a turnover of $2.5 billion, the company employs over 2,600 people worldwide and serves more than 25,000 customers. For more information, visit: **************** About this role What will you do? The Lab Chemist is responsible for overall quality control of toll manufactured materials, testing, data management, sample oversight and guidance in a laboratory/office setting. Critical results Perform preventative and corrective maintenance on instrumentation as needed. • Responsible for updating QC documentation, recording analysis and calibration results. • General lab duties including clean-up, maintenance of equipment, track and order chemicals and disposables used in the lab. • Data processing and documentation using common software tools such as Excel, PowerPoint as well as internal systems • Support and lead by example Barentz's culture, values and fundamentals. • Participate in ongoing personal development opportunities including, but not limited to, formal as well as informal training. Responsibilities • Responsible for ensuring quality control measures are in place, understood and followed at all times. • Responsible for approving, generating and maintaining Certificates of Analysis and USMCA Certificates. • Data management - responsible for acquiring, validating, and maintaining data for the lab. • Provide sample department oversight and guidance as necessary. • Perform biological testing (counts for wet and dry biological products). • Set up and troubleshoot laboratory equipment and instrumentation required for tests, research, or process control. • Ensure safety procedures and housekeeping are maintained to protect yourself, co-workers, and the environment. • Perform, interpret, and record quality About You Education / Experience • University or College degree, preferably in Chemistry, Biology, Engineering, Etc., or equivalent combination of education and experience required. • Minimum 1 year of previous experience in a laboratory setting. Skills • Demonstrated organizational, complex problem-solving, and analytical skills. • Must be self-motivated, high energy, and engaging level of enthusiasm and positive outlook. • Effective written and verbal communication skills, and ability to adapt communication style to the audience as needed. • Software knowledge of Microsoft Office including Outlook, Word, Excel and Power Point. • Act legally and ethically in all professional relationships in adherence with Barentz' culture, values and fundamentals. • Fluent in English, a second language would be considered an asset Why Barentz? Barentz is a fast-growing organization with an open culture and short lines of communication. We offer you the freedom and opportunity to operate independently within the set objectives and frameworks. Barentz is looking for employees who are creative, independent, and energetic and like to take on challenges. You like to work in a dynamic and rapidly changing environment, which requires a high degree of flexibility. • Competitive benefits package • 401K with matching • An inspiring multinational company in a fast-growing and innovative business Interested? Looking for an exciting position? Then join us. We're investing in our future, starting by adding talented people (like you) to our rapidly expanding team. Please apply using our apply button below.

Outlier is the world's leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities. We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Chemistry. Develop and answer Chemistry-related questions to refine AI understanding. Assess and rank AI responses based on scientific rigor. Required expertise and qualifications: Education: Master's degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled) Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&D contributions English Proficiency: Ability to read and write with minimal errors Bonus Skills: AI model training experience is not required but helpful Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below) Opportunities for higher-paying research projects based on performance. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

$26.88/hr + benefits on W2 Onsite in Miami, FL. 12+ month contract with likely extension/conversion. If you thrive in a multi-faceted role and want to work to build a world-class Package Engineering organization with us-read on. In this role, you will have the opportunity to: Assisting engineers with daily testing tasks and documenting test results to assist with Distribution Test Reports. Coordinate incoming and outgoing shipments of products and be responsible for the Lab Housekeeping and organization of supplies and materials. You will Execute packing instructions. Conduct test sequences. Download and manage data files. Provide input to the other engineers. Assist engineers with daily testing tasks and documenting test results to assist with Distribution Test Reports. Manage the Lab schedules and participate in weekly status report out of all projects coming in and out of the Labs. Assist engineers with coordinating incoming and outgoing shipments of products. Lab Housekeeping and organization of supplies and materials. Attention to detail is critical to this position. Qualifications: Ability to lift 50lbs. You are detail oriented. Follow processes and procedures. Timely Nice to have: College education in Packaging, or Material Sciences, or like programs. Experience or knowledge with Packaging Standards such as ASTM D series and/or ISTA. Other Engineering course work, such as Mechanical or Electrical. Packing or Warehouse experience. CAD or drafting and design experience. Interested? Apply today!

Associate Scientist II Kelly Services has been providing outstanding employment opportunities to the most talented individuals in the marketplace. We are proud to offer a multiple direct hire opportunities to work as an Associate Scientist II located near the Ft. Lauderdale/Miami, FL area. Shift: Monday-Friday, 2nd shift, 4pm-12am Function: Chemistry, Manufacturing, and Control (CMC) Relocation offered Salary: Associate Scientist II : $65,000-85,000 plus 10% target bonus Job Summary: We are seeking a highly motivated Scientist (multiple levels) to join our Analytical Sciences team. The successful candidate will be responsible for conducting laboratory activities related to the development, optimization, transfer, and validation of analytical methods for drug products. The role involves using a variety of analytical techniques, such as liquid chromatography (LC), spectroscopy, and aerosol performance techniques for orally inhaled and nasal drug products (OINDP). The Scientist will also be responsible for conducting physico-chemical characterization studies, performing data analysis, and drafting scientific documents to meet global regulatory standards, including those from the US FDA and EMA. Key Responsibilities: Independently conduct standard and advanced laboratory activities, including liquid chromatography (LC), spectroscopy, and aerosol performance characterization studies for OINDPs. Perform physico-chemical and aerosol analytical characterization of OINDPs, including the evaluation and selection of raw materials such as APIs, excipients, and packaging materials. Develop, verify, optimize, transfer, and validate analytical methods in accordance with cGMPs, EH&S guidelines, and other regulatory requirements. Conduct in-depth data analysis using advanced statistical tools and techniques, identifying trends and making data-driven recommendations. Draft protocols, reports, SOPs, and regulatory submission documents regularly. Present data analysis and recommendations to senior management and communicate findings effectively with team members and external stakeholders. Troubleshoot technical issues and implement solutions in a timely manner. Ensure compliance with safety rules and corporate guidelines in all lab activities. Qualifications: Associate Scientist II: BSc in Chemistry, Pharmacy, or related fields with at least 3 years of experience in Pharmaceutical R&D, or MSc in Chemistry, Pharmacy, or related fields with 0-2 years of experience in Pharmaceutical R&D. Scientist I: Ph.D. in Analytical Chemistry, Organic Chemistry, Pharmaceutics, or related fields with at least 3 years of experience, OR MSc with at least 5 years of experience, OR BSc with at least 8 years of relevant experience. Scientist II: Similar qualifications with additional experience Extensive knowledge and hands-on experience with chromatography (HPLC, GC), spectroscopy (UV, FTIR), and other analytical techniques. Must have at least 2 years of experience in method development and validation using HPLC and Empower software for pharmaceutical products Proven experience in analytical method development, verification, and validation. Strong technical writing skills with the ability to draft high-quality documents, including protocols, reports, and regulatory submission sections. Experience with orally inhaled and nasal drug products (DPI, MDI, or nasal drug products) is a plus. Familiarity with USP methodologies, ICH guidelines, FDA, and cGMP regulations. Strong English language communication skills, both written and oral. This position offers competitive salary and benefits, and the opportunity to contribute to cutting-edge pharmaceutical research and development.

Arvida Labs is seeking an analytical technician to join our team and support our in-house hemp cannabinoid testing efforts in our processing facility located in Fort Lauderdale, FL . The successful candidate will be responsible for carrying out chemical analysis using an HPLC & GC. The technician will be responsible for maintaining and calibrating the equipment, as well as preparing samples and analyzing data. The technician will also be responsible for ensuring that all lab procedures are followed according to established protocols and safety guidelines, and will play a key role in helping to ensure the quality and safety of our hemp products. The technician will be responsible for managing the Certificate of Analysis (COA) process and ensure that all products comply with the FDA and 2018 Farm Bill regulations. This role involves managing COA databases, coordinating product sampling and testing, and monitoring regulatory compliance for Alpha Brands LLC and Arvida Labs products in our processing facility located in Fort Lauderdale, FL Responsibilities: Conduct cannabinoid analysis using Shimadzu LC-2030, Agilent 1200 HPLC, Agilent GC Daily operation and maintenance of LC and/or GC systems Generate quality system-compliant data Work with team members to execute analysis conforming to SOPs and to maintain good record keeping practices Identify instrument problems and perform routine troubleshooting Participate in and promote continuous improvement efforts within the laboratory Prepare samples for analysis Analyze data and report results Follow established lab procedures and safety guidelines Requirements: 1 or more years experience in an analytical laboratory preferred Experience with the operation and maintenance of chromatographic instrumentation preferred Experience operating analytical instrumentation, specifically Shimadzu LC-2030, Agilent 1200, and Agilent GC Strong problem-solving and analytical skills Ability to maintain and troubleshoot analytical equipment Laboratory experience performing method development, qualification, and validation activities Ability to work independently and as part of a team Attention to detail and strong organizational skills Motivated self starter Preferred Qualifications: Bachelor's degree in chemistry or related field Experience working in a cGMP environment Familiarity with regulatory guidelines for the hemp industry Strong verbal and written communication skills Benefits: Arvida Labs offers a competitive and comprehensive benefits package including health and paid time off Job Type: Full-time Pay: Starting at $20+ per hour Benefits: 401(k) 401(k) matching Dental insurance Flexible spending account Life insurance Paid time off Vision insurance Schedule: 8 hour shift Work Location: In person

ZEO ScientifiX is looking for a Laboratory Technician ZEO ScientifiX is a clinical stage biotechnology company developing tissue-derived and extracellular vesicle based therapeutics. ZEO ScientifiX is seeking a Laboratory Technician to work within our biologics manufacturing laboratory Responsibilities of the Laboratory Technician include a variety of supportive activities involved with biologic manufacturing and processing. The laboratory technician will work within a cGMP-compliant, clean room environment and will assist with manufacturing tasks. Other responsibilities will include inventory and material management, proper documentation practices and reviews, and the participation with general laboratory operations. Qualifications: Must have prior experience in a biomedical research environment B.S. or M.S. in Biomedical Sciences or related sciences are encouraged to apply Must be highly motivated with professional etiquette Must be a skilled writer Must demonstrate self-initiative Have excellent organizational skills Have strong attention to detail Strong communication skills with internal and external individuals Must be comfortable working with computers and digital communication Job Type: Full Time Education: Bachelor of Science (BS) degree or Higher (required) Benefits: 401K Program Health Insurance, Dental, Vision

Piper Companies is currently seeking an experienced Chemist to support a highly reputable Pharmaceutical company in Miami, FL. Responsibilities for the Chemist * Conduct analytical testing along with perform qualitative and qualitative chemical and physical testing * Operates laboratory equipment which includes balances, pH meters, HPLC, GC, UV, IR, Dissolution equipment * Draft proper laboratory records in accordance with cGMP and company SOPs and policies * Ensure materials meet compliance standards and specifications Qualifications for the Chemist * 1-5 years of experience in a regulated/cGMP environment * Previous experiences performing HPLC, GC, UV, IR is preferred * Current knowledge of SCM concept and principles * Bachelor's degree in related field Compensation for the Chemist * Salary Range: $50,000 - $75,000 * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays This job opens for applications on 3/24/2025. Applications for this job will be accepted for at least 30 days from the posting date." Keywords: Chemistry, Chemist, HPLC, GC, Gas Chromatography, Mass Spectrometry, Karl Fischer, cGMP, GMP, GLP, LIMS, Laboratory Technician, Quality Control, Pharmaceutical, SCM, pH, Dissolution, Disintegration, Compendial, #LI-JM1 #LI-ONSITE

Working Title: CHEMIST III - 42001526 Pay Plan: Career Service 42001526 Salary: $56,500.08 - $62,150.14 Total Compensation Estimator Tool CHEMIST III FLORIDA DEPARTMENT OF AGRICULTURE AND CONSUMER SERVICES DIVISION OF CONSUMER SERVICES BUREAU OF STANDARDS * OPEN COMPETIVE OPPORTUNITY * CONTACT: Matthew Christianson ************** MINIMUM REQUIREMENTS: A bachelor's degree from an accredited college or university with a major course of study in chemistry or biochemistry and two (2) years of professional chemical or biochemical experience; or A master's degree from an accredited college or university with a major course of study in chemistry or biochemistry and one (1) year of professional experience as described above; or A doctorate from an accredited college or university with a major course of study in chemistry or biochemistry. Certain positions within this class require individuals to meet specific federal or state regulations as identified by the employing agency. EDUCATIONAL NOTE: Graduates utilizing education attained in the United States to meet the minimum requirements of a position will not be appointed until verification of the applicable degree has been obtained. Foreign trained graduates utilizing a degree attained outside of the United States to meet the minimum requirements of a position must be prepared to provide a copy of a credential evaluation conducted by an Approved Credential Evaluation Agency. A list of approved agencies can be viewed at "Approved Credential Evaluation Agencies, Florida Department of Education." Approved Credential Evaluation Agencies (fldoe.org) * ATTENTION CANDIDATES* To be considered for a position with the Florida Department of Agriculture and Consumer Services: * All fields in the Candidate Profile must be completed (an attached resume is not a substitution for the information required on the candidate profile). * Work history, duties and responsibilities, hours worked, supervisor, and formal education fields, etc. must be filled out to determine qualifications for this position. * Responses to Qualifying Questions must be verifiable in the Candidate Profile. The Florida Department of Agriculture and Consumer Services values and supports employment of individuals with disabilities. Qualified individuals with disabilities are encouraged to apply. NOTES: Successful applicant must pass a background screening, including fingerprinting, as a condition of employment. JOB DUTIES: Analyze petroleum, antifreeze, and brake fluid products to verify compliance with the latest ASTM and/or State of Florida specifications using the appropriate methods and Standard Operating Procedures. Utilize the bureau's Laboratory Information Management System (LIMS) to aide in the collection, analysis, review and authorization of analytical results, quality control system and other associated laboratory information. Maintain, calibrate and operate analytical instrumentation with minimal supervision by senior chemists and/or laboratory manager, to facilitate accurate and timely sample analyses. Maintain inventory of supplies and parts required to ensure accurate and timely analyses of samples via assigned instrumentation. Under direction of laboratory manager, monitor the daily laboratory functions in assigned area and provide feedback to the laboratory manager to aide in efficient and accurate operation of the laboratory. This includes monitoring analyses, data recording, and reporting for all types of fuel samples and ensuring that all samples are properly analyzed according to the appropriate ASTM and/or screening methods. Reports substandard products in a timely manner to the laboratory manager. Be familiar with Florida law as it relates to fuel testing and specifications. Monitor the workflow of the laboratory and assist the manager with prioritizing the daily sample work load. Be thoroughly familiar with the latest test methods, procedures, equipment changes, and fuel specifications in order to act as an in-laboratory contact and technical resource for other Chemists and Technicians. Recommend and oversee maintenance, calibration, and repair of equipment. Assist in the training of any present or new employees. Maintain a safe, organized and clean environment throughout the areas of responsibility. Participate in and assist the Laboratory Manager in the monitoring and verfication of the locations implementation of the bureau's Quality Control Program. This includes proper and successful analyses of proficiency samples in addition to routine quality control procedures as dictated by the bureau's quality control plan. Assist other laboratories and management on needed specifications, ordering and set up of equipment. This will include writing of specifications and research to determine the maximum efficiency and requirements to perform a given task and to meet appropriate ASTM methods. Assist supervisor as requested to conduct daily work and fill in as the person-in-charge in their absence. This will require being familiar with the over all operation of the laboratory and coordinating laboratory operations with the Laboratory Administrator or designate in the absence of the laboratory manager. Perform other duties such as, but not limited to, administrative paperwork, shipping/receiving, sample custody and other non-technical duties as required by management. The Benefits of Working for the State of Florida Working for the State of Florida is more than a paycheck. The State's total compensation package for employees features a highly competitive set of employee benefits including: * Annual and Sick Leave benefits; * Nine paid holidays and one Personal holiday each year; * State Group Insurance coverage options, including health, life, dental, vision and other supplemental insurance options; * Retirement plan options, including employer contributions (For more information, please visit *************** * Flexible Spending Accounts; * Tuition waivers; * And more! For a complete list of benefits, visit ***************************** For an estimate of the total compensation package for this position, please visit the "Total Compensation Estimator Tool" located above under the "Posting Closing Date." SPECIAL NOTES: The State of Florida is an Equal Opportunity Employer/Affirmative Action Employer, and does not tolerate discrimination or violence in the workplace. Candidates requiring a reasonable accommodation, as defined by the Americans with Disabilities Act, must notify the agency hiring authority and/or People First Service Center (***************. Notification to the hiring authority must be made in advance to allow sufficient time to provide the accommodation. The State of Florida supports a Drug-Free workplace. All employees are subject to reasonable suspicion drug testing in accordance with Section 112.0455, F.S., Drug-Free Workplace Act. VETERANS' PREFERENCE. Pursuant to Chapter 295, Florida Statutes, candidates eligible for Veterans' Preference will receive preference in employment for Career Service vacancies and are encouraged to apply. Certain service members may be eligible to receive waivers for postsecondary educational requirements. Candidates claiming Veterans' Preference must attach supporting documentation with each submission that includes character of service (for example, DD Form 214 Member Copy #4) along with any other documentation as required by Rule 55A-7, Florida Administrative Code. Veterans' Preference documentation requirements are available by clicking here. All documentation is due by the close of the vacancy announcement. Location: POMPANO BEACH, FL, US, 33069 POMPANO BEACH, FL, US, 33060 POMPANO BEACH, FL, US, 33068 POMPANO BEACH, FL, US, 33064 POMPANO BEACH, FL, US, 33062 POMPANO BEACH, FL, US, 33073

Job Details Experienced ADMA Biologics FL - Boca Raton, FL Full Time 4 Year Degree None PharmaceuticalDescription ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Chemist II, Bioanalytics in Boca Raton, FL! The Chemist II, Bioanalytics will perform quality control testing of raw materials, in-process, and final products with minimal supervision, with a concentration in immunoassays. Uses knowledge of corporate policies to resolve routine problems and ensure compliance with procedures. Qualifications ESSENTIALS OF THE JOB: Perform quality control testing for raw materials, in-process, and final product samples, according to approved Standard Operating Procedures (SOPs) and cGMP guidelines Complete testing documentation and data entry as required for procedures and tests performed Apply knowledge of analyzing issues and uses judgment to make decisions Knowledge of immunoassays, specifically plate-based assays and ELISAs Utilize cGMP practices in documentation and execution of job functions Perform instrument calibration or qualification according to written procedures Write and revise SOPs and/or participate in validation protocol execution, as needed Perform testing, as needed, to generate data for qualification/validation and special projects Fulfill requests from management for assistance in other matters, as needed Accountable for following SOPs and adhering to cGMP guidelines Review documentation on trained tasks as assigned by QC management Use technical and scientific knowledge to recommend solutions to problems as directed by QC management Mentor junior analysts and provide training as requested on QC assays Education Requirements: Bachelor's degree in Chemistry, Biochemistry, Molecular Biology, or related science discipline. Experience Requirements: At least three years of experience performing chemical/biochemical testing or developing immunoassays. Work in a regulated environment (FDA, EPA, etc.) is highly preferred. In addition to competitive compensation, we offer a comprehensive benefits package including: 401K plan with employer match and immediate vesting Medical, Vision, Life and Dental Insurance Pet Insurance Company paid STD and LTD Company Paid Holidays 3 Weeks' Paid Time Off (within the first year) Tuition Assistance (after the first year) Easily accessible to Tri-Rail Company paid shuttle to the Boca Tri-Rail station ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ********************* ADMA Biologics is an Equal Opportunity Employer.

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.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Eurofins EPK Built Environment Testing, LLC is searching for an experienced PLM Asbestos/Mold Analyst in Fort Lauderdale, FL. The Analyst performs analysis of bulk samples for asbestos using polarized light microscopy. Analysis of non-culturable surface and air samples for fungi is a plus but not required. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS and reports to clients. Schedules sample workload according to due dates and sample hold times and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. The Analyst's responsibilities include, but are not limited to, the following: Prepare and analyze aerobiological, environmental, and water samples for fungal, asbestos and bacteria analysis. Accurately enters and reports analytical data using the LIMS Performs independent data reviews for other analysts' work Performs analysis of reference materials, proficiency samples and other quality control samples as needed Performs confirmation of lab results as needed by client services personnel Performs and completes all analytical testing QA related tasks as needed Assists in pursuing, receiving, and maintaining necessary laboratory accreditations Maintains and updates all necessary Training and QA documents onsite as necessary Co-ordinates and manages projects according to their rush status and due time for timely delivery Follows company policies and procedures and ensures that coworkers are doing the same Qualifications Basic Minimum Qualifications: Bachelors degree in Microbiology, Biology, Geology or a closely related science. 2-3 years of laboratory work experience involving mold and/or asbestos microscopy analysis. 8 units of Microbiology courses PREFERRED Additional Information Requirements: Authorization to work in the United States indefinitely without restriction or sponsorship Professional working proficiency in English is a requirement, including the ability to read, write and speak in English Position is full-time, Monday - Friday 10 am - 6pm with overtime as needed. Candidates currently living within a commutable distance of Ft. Lauderdale, FL are encouraged to apply. Pay range: $21 - $24/hr depending on experience Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. To learn more about Eurofins, please explore our website ****************** . We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

We are seeking a dedicated and detail-oriented Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples in a regulated laboratory environment. The ideal candidate will have experience with assays, chromatographic purity, content uniformity, particle size distribution, water determination, and other tests in compliance with in-house monographs and USP standards. Responsibilities * Perform routine tests of finished products, stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using various techniques, and water determination by KF. * Evaluate test results and decide on the acceptability of the samples based on the test results. * Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs. * Maintain the laboratories with good housekeeping practices and in compliance with cGMP. * Ensure notebooks are reviewed promptly in accordance with SOPs. * Analyze and interpret results in both written and oral formats. * Assist in the training of new analysts. * Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. * Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Essential Skills * Proficiency in HPLC, UPLC, UV-Vis, and other analytical techniques. * Strong chemistry experience. * Experience in a regulated laboratory environment. * Familiarity with FDA and GMP standards. * Ability to maintain accurate lab notebooks and documentation. * Experience in analyzing and interpreting test results. * Knowledge of instrumentation software used in laboratories. Additional Skills & Qualifications * Bachelor's degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis OR Master's degree in Chemistry or related scientific field with 1 year of related experience in pharmaceutical analysis. * Ability to deal with problems involving several concrete variables in standardized situations. * Ability to carry out necessary computations and to draw and interpret graphs. Work Environment This role is based in a lab environment regulated by FDA and GMP standards. The laboratory is equipped with advanced analytical instrumentation and follows strict compliance with safety guidelines and good housekeeping practices. Pay and Benefits The pay range for this position is $28.00 - $32.00/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 Pompano Beach,FL. Application Deadline This position is anticipated to close on Apr 10, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Outlier is the world's leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities. We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Chemistry. Develop and answer Chemistry-related questions to refine AI understanding. Assess and rank AI responses based on scientific rigor. Required expertise and qualifications: Education: Master's degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled) Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&D contributions English Proficiency: Ability to read and write with minimal errors Bonus Skills: AI model training experience is not required but helpful Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below) Opportunities for higher-paying research projects based on performance. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

Job Details Experienced ADMA Biologics FL - Boca Raton, FL Full Time 4 Year Degree None Day PharmaceuticalDescription ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Chemist II in Boca Raton, FL! The Chemist II will perform quality control testing of raw materials, in-process goods, and final products with minimal supervision. Uses knowledge of corporate policies to resolve routine problems. Qualifications Perform quality control testing for raw materials, in-process and final product sample testing according to approved Standard Operating Procedures. Complete testing documentation and data entry as required for procedures and tests performed. Apply knowledge of analyzes issues and uses judgment to make decisions. Utilize cGMP practices in documentation and execution of job functions. Perform instrument calibration or qualification according to written procedures. Write and revise SOPs and/or Validation Protocols. Perform testing as needed to generate data for Validation and Special Projects. Fulfill requests from management for assistance in other matters as needed. Accountable for following Standard Operating Procedures (SOPs) and adhering to cGMP guidelines. Review documentation on trained tasks as assigned by manager. Education Requirements: B.S. in Chemistry, Biochemistry, Molecular Biology, or related science discipline. Experience Requirements: At least three years of experience in a laboratory setting. Work in a regulated environment (FDA, EPA, etc). is preferred, but not required. In addition to competitive compensation, we offer a comprehensive benefits package including: 401K plan with employer match and immediate vesting Medical, Vision, Life and Dental Insurance Pet Insurance Company paid STD and LTD Company Paid Holidays 3 Weeks' Paid Time Off (within the first year) Tuition Assistance (after the first year) Easily accessible to Tri-Rail Company paid shuttle to the Boca Tri-Rail station ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ********************* ADMA Biologics is an Equal Opportunity Employer.

We are seeking a dedicated and detail-oriented Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples in a regulated laboratory environment. The ideal candidate will have experience with assays, chromatographic purity, content uniformity, particle size distribution, water determination, and other tests in compliance with in-house monographs and USP standards. Responsibilities * Perform routine tests of finished products, stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using various techniques, and water determination by KF. * Evaluate test results and decide on the acceptability of the samples based on the test results. * Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs. * Maintain the laboratories with good housekeeping practices and in compliance with cGMP. * Ensure notebooks are reviewed promptly in accordance with SOPs. * Analyze and interpret results in both written and oral formats. * Assist in the training of new analysts. * Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. * Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Essential Skills * Proficiency in HPLC, UPLC, UV-Vis, and other analytical techniques. * Strong chemistry experience. * Experience in a regulated laboratory environment. * Familiarity with FDA and GMP standards. * Ability to maintain accurate lab notebooks and documentation. * Experience in analyzing and interpreting test results. * Knowledge of instrumentation software used in laboratories. Additional Skills & Qualifications * Bachelor's degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis OR Master's degree in Chemistry or related scientific field with 1 year of related experience in pharmaceutical analysis. * Ability to deal with problems involving several concrete variables in standardized situations. * Ability to carry out necessary computations and to draw and interpret graphs. Work Environment This role is based in a lab environment regulated by FDA and GMP standards. The laboratory is equipped with advanced analytical instrumentation and follows strict compliance with safety guidelines and good housekeeping practices. Pay and Benefits The pay range for this position is $28.00 - $32.00/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 Pompano Beach,FL. Application Deadline This position is anticipated to close on Mar 18, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Details Entry ADMA Biologics FL - Boca Raton, FL Full Time 4 Year Degree PharmaceuticalDescription ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Chemist I in Boca Raton, Florida! The Chemist I will perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. Qualifications Second Shift 2pm-10pm Perform quality control chemistry and/or Immunoassays for raw materials, in-process and final products according to approved Standard Operating Procedures (SOPs). Perform instrument calibration or qualification according to written procedures. Perform testing as needed to generate data for method validations and other special projects, following general instructions on routine work and detailed instructions on new assignments. Fulfill requests from management for assistance in other matters as needed. Accountable for following Standard Operating Procedures (SOPs) and adhering to cGMP guidelines. Utilize cGMP practices in documentation and execution of job functions. Review documentation on trained tasks as assigned by manager Education Requirements: B.S. in Chemistry, Biochemistry, Molecular Biology or related science discipline is required. Experience Requirements: This position requires experience in a laboratory setting. Work experience in a regulated environment (FDA, EPA, etc.) is preferred. In addition to competitive compensation, we offer a comprehensive benefits package including: 401K plan with employer match and immediate vesting Medical, Vision, Life and Dental Insurance Pet Insurance Company paid STD and LTD Company Paid Holidays 3 Weeks' Paid Time Off (within the first year) Tuition Assistance (after the first year) Easily accessible to Tri-Rail Free shuttle to the Boca Tri-Rail station ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ********************* ADMA Biologics is an Equal Opportunity Employer.

Actalent is Hiring a Team of Associate Scientists!!Job Description We are seeking a dedicated and detail-oriented Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples in a regulated laboratory environment. The ideal candidate will have experience with assays, chromatographic purity, content uniformity, particle size distribution, water determination, and other tests in compliance with in-house monographs and USP standards. Responsibilities + Perform routine tests of finished products, stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using various techniques, and water determination by KF. + Evaluate test results and decide on the acceptability of the samples based on the test results. + Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs. + Maintain the laboratories with good housekeeping practices and in compliance with cGMP. + Ensure notebooks are reviewed promptly in accordance with SOPs. + Analyze and interpret results in both written and oral formats. + Assist in the training of new analysts. + Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. + Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Essential Skills + Proficiency in HPLC, UPLC, UV-Vis, and other analytical techniques. + Strong chemistry experience. + Experience in a regulated laboratory environment. + Familiarity with FDA and GMP standards. + Ability to maintain accurate lab notebooks and documentation. + Experience in analyzing and interpreting test results. + Knowledge of instrumentation software used in laboratories. Additional Skills & Qualifications + Bachelor's degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis OR Master's degree in Chemistry or related scientific field with 1 year of related experience in pharmaceutical analysis. + Ability to deal with problems involving several concrete variables in standardized situations. + Ability to carry out necessary computations and to draw and interpret graphs. Work Environment This role is based in a lab environment regulated by FDA and GMP standards. The laboratory is equipped with advanced analytical instrumentation and follows strict compliance with safety guidelines and good housekeeping practices. Pay and Benefits The pay range for this position is $28.00 - $32.00/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 Pompano Beach,FL. Application Deadline This position is anticipated to close on Apr 10, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people 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 process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.