Associate Scientist Jobs in Coral Springs, FL

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.

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

This position will be responsible for the development of new roofing and waterproofing products for residential and commercial applications. He/She will be responsible for development of new products, improvement of existing products, advance laboratory testing, competitive analysis as well as value engineering initiatives intended for existing product lines. Responsibilities: Generate ideas that will enhance existing products and lead to the development of new products, test procedures and protocols. Manage research projects and work in teams towards executing the initiatives of the Manager of R&D and the research team Develop investigative work resolving associated technical issues on products and projects Use sound scientific principles such as statistical analysis, material science, rheology and solid mechanics. Cross-functional interaction with Product Management, Operations, Supply Chain, Engineering, Marketing, Technical Services and external vendors Design and conduct hands on experimentation using standard test methods and advanced analytical equipment Manage multiple short and long-term projects Use advanced material characterization techniques to establish structure property relationships of materials and final product performance Execute plant trials by transferring technology from small scale lab models to large scale plant production. Conduct and design testing internally and externally adhering to regional and third party code agencies and guidelines. Work closely with partner companies and key raw material suppliers to advance the development of products or processes. Represent Polyglass USA at key industry meetings and technical conferences. Manage technical business support for current products including raw material qualification, benchmarking of competitive materials and product/system testing internally and at external laboratories. Publish reports and conduct technical presentations at regular intervals on key projects. Advance the technology in building products & systems to improve performance, reduce total installed cost and established sustained competitive advantage. Assist in training new R&D scientists Requirements: Masters in Material Science, Civil Engineering ,Mechanical Engineering, Polymer Science, Building Science, or related fields with minimum 4 years of experience in one or more of these fields: asphalt, polymer modified asphalt, polymers, adhesives, concrete, and or waterproofing membranes for commercial or residential applications or similar endeavors. Bachelors of Science /Arts in Material Science, Civil Engineering ,Mechanical Engineering, Polymer Science, Organic Chemistry or related fields with minimum 6 years of experience in one or more of these fields: asphalt, polymer modified asphalt, polymers, and or waterproofing membranes for commercial or residential applications or similar endeavors Ph.D. in Material Science, Civil Engineering ,Mechanical Engineering, Polymer Science, Organic Chemistry, Chemical Engineering or related fields with minimum 2 years of experience in one or more of these fields: asphalt, polymer modified asphalt, polymers, adhesives, building materials, concrete, and or waterproofing membranes for commercial or residential applications or similar endeavors is preferred. Minimum of 10 years industrial experience in asphaltic products, polymer modified asphalt, polymers, and/ or roofing and waterproofing membranes for commercial or residential applications or similar endeavors Experience in the development of new products for roofing and waterproofing applications, as membranes, underlayment, above and below grade waterproofing membranes, air and vapor barriers, and synthetic adhesives Working knowledge of roofing and waterproofing membrane systems codes and industry standards Experience developing product from the lab, through scale-up and to the final launch Knowledge of material science, rheology, viscoelasticity and solid mechanics. Lab experience working with analytical and mechanical instruments for polymers and membranes characterization like: DMA, TMA, DSC, DSR, FTIR, TGA, Universal testing machine, etc. Ability to use analytical lab tools and data to generate correlations that predict ultimate material performance and durability Strong analytical problem-solving skills Ability to identify novel new approaches that establish sustained competitive advantage This position is located on-site in Deerfield Beach, FL. Polyglass will provide relocation assistance.

About Outlier 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.

The Cell Therapy Associate Scientist exercises extreme accuracy and attention to detail, as well as the ability to adjust to a flexible and sometimes unpredictable work schedule. Knowledge of cell culture, flow cytometry, and research in cell and gene therapy is required. This position is focused on a research project based on the expansion of Hematopoietic Stem Cells (HSC) from mobilized blood. The associate scientist will also assist the manufacturing team as needed and reports to the Chief Scientific Officer (CSO). Responsibilities * Adhere to GDP/GTP guidelines. * Work with the CSO on developing the research project. * Execute experiments needed for the expansion of HSCs (cell culture, etc.). * Perform flow cytometry (Cytoflex) to assess cell viability and phenotype. * Perform isolation of CD34+ cells using CliniMACS Prodigy or magnetic beads. * Culture CD34+ cells. * Perform Colony Forming Unit (CFU) assays. * Analyze data and present findings at seminars and conferences when required. * Use aseptic techniques while performing cell processing/culture procedures. * Investigate and resolve problems with procedures or processes. * Work on assigned research projects. * Maintain open communications with the CSO to coordinate, schedule, and perform experiments required by the project. * Maintain an accurate inventory of cryopreserved products (CD34+). * Ensure documentation is accurate, complete, comprehensive, and maintained. * Practice proper safety techniques and report any unsafe conditions to management. * Assist the manufacturing team as needed. * Perform other duties and procedures as assigned. Essential Skills * Cell culture * Flow cytometry * Research in cell and gene therapy * Aseptic techniques * Data analysis * Master's degree in Biology (or equivalent) * 5 years' professional laboratory experience * 3 years' experience in cell therapy Additional Skills & Qualifications * Experience in gene therapy strongly preferred Work Environment The role is based in a team environment within a clean room/lab setting. The work schedule may be flexible and sometimes unpredictable. Pay and Benefits The pay range for this position is $33.65 - $40.87/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 Boca Raton,FL. Application Deadline This position is anticipated to close on Mar 7, 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.

We Are Accenture is helping companies use generative AI to reinvent their enterprise and optimize business functions for breakthrough innovation and competitive advantage. With over 1,600 professionals dedicated to generative AI, leveraging the depth and experience of more than 40,000 AI and data professionals across the company our Generative AI and LLM Center of Excellence brings together our Experienced Innovation, Strategic Investment, Exceptional Talent, and Power Ecosystem. You Are As an Advanced AI Research Scientist, you formulate real-world problems into practical, efficient, and scalable AI and Machine Learning problems. * You lead a team and provide guidance to explore and implement new methodologies, model building techniques, and cutting-edge algorithms, and applying these techniques with the right architecture to solve real-world problems. * You have a deep understanding and ability to remain at the forefront of generative AI, LLM, and multi-modal models (with a focus on driving innovation by applying these techniques to new business problems, use cases, and scenarios). * As needed by the specific problem, you train and/or fine-tune generative AI models and evaluate on the specific problem. * As a significant part of this role, you will be justifying the value of innovative generative AI or traditional Machine Learning approaches (or a combination of both) in the business problems, and you'll be expected to construct methodologies that clearly demonstrate their value. * You'll also work collaboratively with teams from both the business and technical side, including users, use case representatives, business owners, engineers, architects, and UI designers, to achieve end-to-end project development goals. The Work * Participate internal and external discussions to gather business use case requirements, provide on the spot AI expertise and AI solution options for business problems. * Design, develop and implement advanced AI/ML models, especially LLM and other Gen AI models from scratch or existing foundation models via self-supervised learning, transferred-learning, and fine-tuning techniques. * Design, develop and implement highly sophisticated Gen AI based applications including generative agent and similar architectures which support multiple Gen AI models to work together for complex tasks. * Lead technical teams and grow true AI expertise within broader team including offshore * Collaborate seamlessly with diverse, cross-functional teams to accurately identify and prioritize requirements, ensuring that the AI solutions meets the needs and expectations of various stakeholders. * Develop and execute an AI solution project plan with team, timeline, and infrastructure dependency. * Define and implement a value justification approach to the AI solutions; estimate solution cost with right technological choices; and calculate ROI. * Create and maintain comprehensive technical documentation that comprehensibly captures the intricate details of the solution, capture IP, facilitating seamless understanding, knowledge transfer and future development. * Collaborate with academia partners to stay on the cutting edge of AI, especially Gen AI technologies, provide through leadership on AI trend, AI use case innovation trend, new AI opportunities, or foreseeable limitation, risks, and concerns. Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements. This role is located in Mountain View, CA, so applicants must be local or able to relocate. Qualification Here's What You Need Minimum of 5 years of experience in the following: * Designing and developing neural network models, especially deep learning model, and Foundation models. * Experience in building, fine-tuning Foundation models including LLMs and multi-modal models. * Strong working knowledge of the different technologies, their differences, modalities in the Generate AI space. * Working knowledge and familiarity with different LLM driven application architecture patterns. * Experience in deep learning and neural networks, in particular training and large language models with popular libraries and GPUs. * Working knowledge of computer architecture, and familiarity with the fundamentals of GPU architecture. * Proven experience with processor and system-level performance modelling. Minimum of 3 years of experience of technical team management or team mentoring Bachelor's degree or equivalent (minimum 12 years) work experience. (If Associate's Degree, must have minimum 6 years work experience) Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired in California, Colorado, District of Columbia, Illinois, Maryland, Minnesota, New York or Washington as set forth below. We accept applications on an on-going basis and there is no fixed deadline to apply. Information on benefits is here. Role Location Annual Salary Range California $94,400 to $293,800 Colorado $94,400 to $253,800 District of Columbia $100,500 to $270,300 Illinois $87,400 to $253,800 Minnesota $94,400 to $253,800 Maryland $87,400 to $235,000 New York $87,400 to $293,800 Washington $100,500 to $270,300 #LI-NA-FY25 Locations

Empower, Innovate, Impact! At Team A-TEK, we EMPOWER people to drive INNOVATION that impacts MISSION! A-TEK operates at the intersection of mission and innovation by applying our deep domain expertise across the federal markets. Embracing our digital-first strategy, A-TEK provides enhanced capabilities in application development, digital transformation, enterprise IT, and scientific services. Our solutions are designed to modernize, automate, secure, protect, and enhance the operations of our federal clients, ensuring they stay ahead in a rapidly evolving digital landscape. Our work is fueled by a passion to serve our clients' needs and to protect the safety and welfare of Americans. That passion shapes how we nurture our most valuable asset - Our Employees. A-TEK actively cultivates the talent that drives our success and fosters a creative, challenging, and mission-driven work environment for current and future employees. This position will be responsible for performing non-research molecular testing to rapidly identify and characterize potential pathogenic bacterial and viral threat agents. Ensures incoming biological samples are processed and triaged maintaining chain of custody. Performs and interprets a variety of specialized tests and strains, detection, and identification of pathogenic microorganisms. Prepares written and oral reports, answers questions, troubleshoot and makes recommendations to the supervisor for inclusion in comprehensive reports on test findings. Maintains and operates equipment including performing calibrations, adjustments, and to operate equipment and instruments properly and in a safe manner. Participates in cross training related to bioterrorism and other public health emergencies. Additionally, will be responsible for maintaining knowledge and skills related to position and program and to carry out all procedures in accordance with proper handling and storage of various biological materials. Must be available 24/7/365 to respond in case of emergency. Rotating weekends and some holidays are required. Kindly be aware that drug screening is a mandatory condition of employment for this position. REQUIRED QUALIFICATIONS: Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences. REQUIRES at least one year of laboratory bench experience, utilizing PCR, aseptic techniques and experience with biological assays. Laboratory training that is assigned or accompanies an associated course is not considered applicable training. Biological Safety Level (BSL)-3 experience is highly desirable. This position supports a federal contract which requires that all employees and job applicants hold a valid Green Card or US Citizenship at the time of application. #LI-OnSite A-TEK, Inc. 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, or status as a qualified individual with a disability, or Vietnam era or other protected Veteran status.

RES is looking for a Scientist with up to two (2) years of relevant work experience based out of our Fort Lauderdale, FL office. The mission: Our Florida operation is growing exponentially and is in sharp need of an entry-level Scientist to do the groundwork. You will have the opportunity to expand your knowledge of natural resource evaluations and environmental permitting, whil e learning from the experienced team of senior biologists, scientists, and ecologists! The final product of your work is a result of tight collaboration between several team members and different teams, who all might speak different technical languages and be located in different geographies. We therefore are looking for a skillful Communicator, who will be able to navigate through this complexity. While you will be properly trained, the team is expecting you to be a Self-Starter who enjoys solving problems and independently working on solutions for clients. What your day-to-day might look like? Assisting in several projects for both private clients and municipal clients, at least 70% of the time you will be working in the field. Tasks you will be accomplishing include: Groundwater and soil sampling using Florida Department of Environmental Protection (FDEP) Chapter 62-160 F.A.C sampling protocols. Construction compliance: Health and Safety Plan compliance, soil management, dust monitoring and air quality sampling. Landfill Monitoring Engineering Control inspections Note that we perform these tasks in Florida's hot, humid environment for extend periods of time, in natural and disturbed land settings with potential exposure to biting and stinging insects, venomous snakes and spiders, wild animals and other hazards. Work can also been in urbanized settings, high traffic areas, landfills, scrap metal yards, and parks. Being a person who is well versed in multiple environments is essential for this job 30% of the time you will be in the office, assisting in the preparation of reports and permitting documents for submittal to clients and state, federal and local regulatory agencies. Technical Writing skills are paramount, so be ready to showcase them during the interview. We would love to talk to you if you have many of the following: B.S. in an environmental science-related field (such as but not limited to ecology, soils, hydrology, environmental engineering, environmental science, etc.) Experience conducting and soil sampling using FDEP Standard Operation Procedures Experience Phase I and Phase II Environmental Site Assessments using ASTM standards Knowledge of FDEP or Miami Dade County Environmental (DERM) assessment regulations Contaminated Site Assessment Report Writing Experience in using Survey123, Field Maps, GPS and ArcGIS Pro for collecting data, and knowledge of field sampling procedures, equipment, and safety protocols. Qualifications What will make you stand out? HAZWOPER 40 certification or OSHA 10 or 30 for construction or Part 46 New Miner Training Certificate-MSHA FDEP SOP Sampling Certification Certification including professional geologist, professional engineer or the ability or obtain them in one to two years. FAA 107 drone pilot license Spotter Training for Solid Waste Facilities FDEP Stormwater Erosion and Sedimentation Control Inspector Boating Experience Who is RES: We are the nation's largest and most experienced provider of ecological restoration and water resource solutions. To date, we have restored over 294 stream miles and 58,000 wetland acres, in addition to conserving and preserving 9,100 acres of endangered species habitats. RES operations include planting over 14,000,000 restorative trees and reducing over 250 tons of polluting nutrients. RES ecological solutions enable a balance of economic development and ecological sustainability. Our culture: Working for RES means having a career that truly makes an impact and a job that helps make nature and communities better. Our people share a deep interest and passion for sustainability and ecological restoration. As an ever-growing company, we cultivate entrepreneurship, flexibility, and collaboration while taking a bold approach to project development. We foster a team environment while enriching individual growth. VEVRAA Federal Contractor RES is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Job Details Experienced ADMA Biologics FL - Boca Raton, FL Full Time 4 Year DegreeDescription 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 Scientist II, Analytical Development located in Boca Raton, FL! The Scientist II, Analytical Development demonstrates success in technical proficiency, scientific creativity, collaboration with others and independent thought. Works on complex problems in which analysis of data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Qualifications Develop, qualify, validate analytical and bioanalytical test methods and assays with minimum supervision, write SOPs and transfer methods to QC department as needed. Be familiar with regulatory guidelines pertaining to assay development/qualification/validation and support regulatory submissions. Design experiments and write protocols for assay qualification and development. Perform assays or supervise other analysts for assay qualification and validation work. Frequently write technical reports and present findings internally to management or to external clients. Analyze experimental data with appropriate statistical tools and report scientific results. Interpret data and adhere to strict guidelines on documentation when recording data. Review and/or approve cGMP documentation generated by other analysts in the laboratory if necessary. Analyze samples from various sources to provide information on compounds or quantities of compounds present. Use analytical techniques and instrumentation, such as gas and high-performance liquid chromatography (HPLC), ion chromatography, spectroscopy (infrared and ultraviolet amongst others), ELISA, and potentiometry. Use a range of analytical techniques, instrumentation and software and serve as a subject matter expert. Develop new techniques for the analysis of drug products and chemicals. Work collaboratively in cross-functional teams. Liaise with customers, staff and suppliers. Comply with all safety requirements in all aspects of the work undertaken. Use judgment, creativity and sound technical knowledge to obtain and recommend solutions to problems as directed by AD management. Interact with contract labs in a method development/qualification/validation if necessary. Constantly observe current QC methods and propose areas for improvement. Maintain current knowledge in field of expertise through reading articles and attending technical courses. Perform risk and gap assessment and life cycle of the existing methods/systems in support of FDA's requirement for continuous improvement. Propose efficiencies to existing processes and be familiar with laboratory automation. Education Requirements: A minimum of a Master's degree in a scientific discipline such as Chemistry, Analytical Chemistry, Biochemistry, Biological Sciences, Engineering or equivalent is required. Experience Requirements: A minimum of five years of related employment experience is required with a Master's degree. Three years of experience (may include post-doctoral experience) is required for a PhD. Expert knowledge of scientific principles and concepts is 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.

Create agentic AI for industries where decisions matter: from healthcare to aerospace. Oh, and you'll have the compute power train large models to solve this challenge. Your role as Applied Scientist is to build next-generation AI agents solving real problems in regulated STEM fields. From Healthcare to Aerospace. You'll train large transformer models and work on reasoning and agentic ai to create secure, explainable agentic AI systems for regulated environments. You'll be joining a top team, ex-big tech and start-up execs and a founder who is a successful entrepreneur with billion-dollar+ exits. This company is tackling the significant architectural, security, and ethical challenges of current AI systems. They've also raised $ 20 million and are already working with companies in industries where standard AI approaches fall short. Your focus: Applied research from research to data to model fine-tuning & training and evals. Training (pre & post-training) and fine-tuning Large Language Models (text and multimodal) specifically for complex industry workflows. Creating systems with strong reasoning and explainability capabilities Working with complex datasets (proprietary, customer, and synthetic) Implementing supervised fine-tuning and reinforcement learning techniques Collaborating with engineering teams to pass off model deployment The ideal candidate has: Hands-on experience training LLMs from scratch Deep understanding of transformers Experienced in Applied Research Strong Python and PyTorch skills Experience with NLP or multimodal models (computer vision backgrounds considered if you've worked with large transformer models) Track record of building real AI products with measurable impact They offer: Abundant compute resources for training large models Salary ranges from $200k-$250k for experienced hires, plus up to 20% performance bonus Significant share package Healthcare (medical, dental, vision) 401k 20 vacation days and flexible working hours Relocation package. You'll join a team that values clear communication, hands-on building, and a no-ego culture. The research team is small now but growing to 15-20 members within the next year, giving you significant influence on direction and approach - giving the chance to put your stamp on truly Agentic systems. You'll need to be based in Miami or Fort Lauderdale, the work arrangement is hybrid. Generous relocation package on offer if you are relocating to Florida. You must have eligibility to work in the US and valid right to work. At this time, visas cannot be sponsored. If solving unique technical challenges in an ego-free environment with strong resources appeals to you, reach out for a confidential conversation. Everyone will receive a response.

tdp The Sun Orchard Innovation team plays a critical role in driving company growth by developing and optimizing products and processes that deliver customer and consumer satisfaction while maximizing profitability./p pThe Product Scientist position will lead and support projects focused on the development and commercialization of new products and processes, and the enhancing of existing product and process efficiencies. The position will also collaborate with cross-functional team members and external partners to deliver high-quality, safe, and cost-effective products that deliver against customer and consumer needs. The position will involve working in laboratory, test kitchen and food manufacturing environments./p pLOCATION: Boca Raton, FL/p ul li Engage directly in product formulations and calculations, laboratory bench experiments and prototype development, sensory evaluations, process integration, shelf-life validations, and technical specifications development, through collaboration with a cross-functional team, from concept through commercialization and launch./li li Manages multiple projects involving product and process development and optimization, including manufacturing trials and scale-up./li li Represent the Innovation department in teams formed across company functions, including but not limited to Food Safety amp; Quality Assurance, Operations, Procurement, Finance and Sales./li li Evaluate ingredients and suppliers for suitability in new product applications, or as potential substitutes for existing products./li li Develop product prototypes that meet organoleptic, nutritional and cost targets./li li Conduct shelf-life studies to determine the stability and performance of finished products and raw ingredients through analytical and sensory testing./li li Conduct and participate in sensory tests and tastings, supports external consumer testing, and manages 3rd party laboratory testing./li li Ensure compliance of ingredients and products with applicable regulatory nutritional and labeling requirements./li li Partner with the Sales, Procurement, Operations and Finance teams to assess and determine the financial viability of assigned initiatives./li li Support the scale-up and optimization of new and existing products by creating production formulations, blending instructions, and process guidelines in collaboration./li li Develop recipes and product applications for food shows, sales, and media content./li li Write detailed amp; accurate reports of analyses, experiments, shelf-life studies, specifications, and standard operating procedures./li li Effectively communicates activity and project updates./li li Serve as a subject matter expert for internal and customer presentations and at industry events./li li Provide training to team members to develop product and applications expertise./li li Demonstrates adaptability and resourcefulness in responding to changing priorities./li li Excellent written, verbal, listening and presentation skills/li li Ability to effectively communicate and engage with fellow scientists, cross-functionally with Sales, Procurement, Operations, Finance and other associates, and externally with customers and suppliers./li li Self-starter, collaborative, with strong problem-solving and project management skills, with an ability to thrive in a fast-paced, dynamic environment./li li Domestic and international travel as required for project management and support./li li Other duties as assigned./li /ul p /p /td

Top aerospace company is looking to add an Aero Thermal Fluids Engineer level 4, 5, or 6 to their growing team in Jupiter, Florida. The ideal candidate will have experience with commercial and in-house developed software tools, and/or hand calculation methods to design and analyze bearings and seals related to pump fed liquid rocket engine systems. Will also have extensive knowledge of designing and analyzing a variety of bearings and seals such as: Bearings Rolling Elements: Ball, Roller, and Cylindrical bearings Fluid Film: Hydrostatic, annular, balance piston, and hydrodynamic Seals Dynamic, clearance, rubbing contact, and lift-off

The company is seeking a Senior Scientist, Formulated to join our product development team based in Miami, FL, reporting to the Director of Formulated & Assembled Products. The selected candidate will support the development of an innovative and robust product pipeline, including cosmetics, OTC drugs, medical devices, supplements and disposable hygiene products, from discovery to mass production. The ideal candidate has a passion and proven experience in designing a delightful consumer experience, developing claims, and troubleshooting different kinds of product performance and manufacturing challenges in a dynamic and fast-paced entrepreneurial environment. Additionally, the ideal candidate has strong organizational and prioritization skills, staying on top of multiple projects at the same time. Responsibilities to include: Product Development Transform technical, consumer, and competitive insights into product innovation while following the stage-gate design process Develop multiple projects from ideation through production start of the highest complexity within a fast-paced development environment Deliver key project milestones and make recommendations that drive efficiency and manage risk within cost, quality and timelines Identify unique product features and specifications and integrate into product designs Develop methods to test performance and claims Identify the best-in-class technologies, ingredients, and materials to meet the performance needs of the product requirements Establish manufacturing production specifications and performance requirements Develop claims and substantiation across new product categories, create claims support strategy and documentation to enable usage and commercialization in the marketplace Maintain good working knowledge of current global regulatory requirements (claims, actives, testing, etc.) for cosmetics, OTC drugs, medical device, supplements and disposable hygiene products Define and use technical standards, SOPs, best practices, and test methods to ensure products meet quality and regulatory compliance Support capability and process improvements to enable more efficient and rigorous product development Cross-Functional Leadership Ensure cross-functional teamwork and communication with internal and external contacts to drive the progress of projects to plan Collaborate with brand, packaging, industrial design, engineering, and the operations teams to identify challenges and offer solutions Partner with marketing, sales, and regulatory to develop and validate consumer stories Vendor Collaboration Develop and maintain professional relationships with suppliers, technical experts etc. Support the selection of product manufacturers, including overseeing first through final article verification Maintain regular communications supporting successful partnerships and manage project expectations and collaborative product designs Deliverables Unique and differentiated products that meet project objectives Product and/or material specifications Competitive product claims and substantiation Sustaining innovations to improve existing products to 4.5+ Stars Input for technical readiness, regulatory, and quality testing requirements What You Will Need BS/MS/PhD in Chemistry, Chemical Engineering, or equivalent relevant discipline 5+ years baby care, feminine care, beauty care, formulation, and / or claims validation Proven ability to use this knowledge to develop innovative products and work effectively with a global supplier network Passion for innovation and able to translate consumer insights and technical data into unique products and claims Ability to learn new concepts quickly Strong organizational and multi-tasking skills with high attention to detail Excellent interpersonal, written, and verbal communications skills Able to manage quality, efficacy, and clinical testing programs Experience developing products in highly regulated industries (juvenile products, medical) Strong leadership and influencing skills Ability to work in a fast-paced environment in which requirements & priorities constantly change A self-starter with an ability to complete tasks both independently and collaboratively as part of a team Who You Will Work With As the Senior Scientist, you will work closely with Product Development, Sourcing, and Brand Management teams.

JOB QUALIFICATIONS: BS or MS in Chemistry with a minimum of 5+ years of pharmaceutical experience or equivalent combination of education and experience with testing Finished Products and Raw Materials Strong technical skills in HPLC, and GC required, including theoretical understanding of technique Demonstrated use of the analytical techniques in support of product development activities Comprehensive knowledge of current Good Manufacturing Practices (cGMP), FDA Guidance, and ICH Guidelines Familiar with requirements of various pharmacopeias (USP, EP, JP) and basic regulatory requirements and applies knowledge appropriately to activities Ability to successfully direct or manage various analytical projects and to contribute / facilitate team investigations Demonstrated ability to work well in a fast-paced setting. Demonstrate ability to take concepts and produce laboratory results Self-starter with a strong work ethic. Must be able to operate with minimal supervision Demonstrated ability to train and/or mentor new employees Excellent written and verbal communication skills. Problem solving skills POSITION RESPONSIBILITIES: Creates and executes new methods or procedures through appropriate research, development and validation stages Creates and executes project protocols and reports to support new product research and development as assigned by management Performs testing on raw material, in-process, & finished good samples when applicable Documents all data in corresponding laboratory notebook and files documentation according to approved SOP and data integrity guidelines Supports pilot scale manufacturing to scale up of new manufacturing processes Responsible for analytical method validation/verification/transfer from R&D or client site to QC when assigned Interface with contract labs regarding QC sample handling and reporting Evaluate and interpret the test results and other related technical documentation Document writing includes, but not limited to, preparation and review of SOPs, STMs, failure investigation and process deviation report, stability study protocol/report, method transfer protocol/report, method validation/verification protocol/report, instrument qualification protocol/report and analytical technical transfer protocol/report when assigned Other duties may be assigned as deemed appropriate by management PHYSICAL REQUIREMENTS: Employees are required to wear eye protection and lab coats while in the lab area Work safely and follow all OSHA regulations and company safety policies and procedures Ability to frequently lift and/or move up to 25 lb Ability to occasionally lift and/or move up to 35 lb Ability to regularly stand, sit and walk to perform task

About the Role: We are seeking a Senior Analyst, Research & Data Scientist to play a pivotal role in driving data-driven decision-making within the health care and social assistance sector. ILS, along with its affiliated health plans known as Florida Community Care and Florida Complete Care, is committed to promoting a higher quality of life and maximizing independence for all vulnerable populations. Under the guidance of the Director, Business Intelligence, the Senior Analyst, Research & Data Scientist is responsible for in-depth analysis to support operational functions to improve clinical, utilization, operational, and financial performance of the company's lines of business. This position is critical in measuring the impact of company solutions, identifying unusual variances in performance, conducting root cause analysis, and generating actionable insights to enable pertinent areas to make informed decisions. Minimum Qualifications: Master's degree in Data Science, Statistics, Public Health, or a related field. At least 5 years of experience working with claims data, risk models, statistical analysis and predictive modeling, preferably in the health insurance field. Proficient in SQL or other data query languages and in statistical software (e.g., R, Python, SAS) and data visualization tools (e.g., Tableau, Power BI). Relevant experience may substitute for the educational requirement on a year-for-year basis. Preferred Qualifications: PhD in a relevant field. Experience with machine learning techniques and predictive modeling. Familiarity with health care regulations and compliance standards. Responsibilities: Validate, transform, and model health care claims, enrollment, and operational data to improve decision making, using statistical analysis to identify patterns, correlations, and actionable results. Work closely with business stakeholders and source system owners to research data anomalies and provide recommendations for resolutions. Collaborate with other functional areas such as Finance, Care Management, Quality, Clinical Services, Claims Processing, Health Plan Operations. Maintain detailed documentation, including data issues and resolution, methodology employed, decisions made, and reports delivered. Communicate data-driven insights and recommendations to internal stakeholders, including executive leadership, soliciting and incorporating feedback as appropriate Skills: The required skills in statistical analysis and data visualization are essential for interpreting complex health care data and presenting it in a clear, actionable format. Proficiency in programming languages like R and Python allows the analyst to manipulate large datasets efficiently and apply advanced analytical techniques. Collaboration skills are crucial as the analyst will work closely with various teams to ensure that research aligns with organizational goals. Strong communication skills are necessary to convey findings effectively to both technical and non-technical stakeholders. Additionally, familiarity with health care regulations enhances the analyst's ability to conduct research that complies with industry standards.

Piper Companies is seeking a Formulations Scientist to join a leading pharmaceutical manufacturing company located in Miami, Fl. This role is 100% onsite. The Formulations Scientist develops and optimizes liquid pharmaceutical formulations for diverse products. Responsibilities of the Formulations Scientist include: * Lead the development and optimization of liquid pharmaceutical formulations for a diverse and growing product line * Drive innovation by evaluating raw materials and refining manufacturing processes to enhance product quality * Collaborate with cross-functional teams, including regulatory and analytical departments to ensure successful product outcomes * Stay at the forefront of industry standards by reviewing and applying regulatory and compendial guidance * Own the full documentation process, from writing batch records to preparing development reports for final approval Qualifications for the Formulations Scientist include: * 2-4 years' experience in Drug Product Development for oral liquid dosage forms (4-6 years with a bachelor's degree) * Practical experience with pharmaceutical equipment and troubleshooting skills * Strong understanding of cGMP in pharmaceutical manufacturing * Proficient in formulation calculations, data analysis, and presenting findings effectively * Self-motivated, able to work under pressure, and open to occasional travel as needed * Master's degree in Pharmaceutics, Industrial Pharmacy, Chemistry, or related discipline Compensation for the Formulations Scientist include: * Salary Range: $85,000 - $90,000 Salary flexible on experience * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave if required by law, and Holidays This job opens for applications on 3/21/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords: Product development, liquid pharmaceutical, cGMP, GMP, Pharmaceutics, Industrial Pharmacy, chemistry, data analysis, pharmaceutical equipment, GLP, HPLC, SOP, manufacturing, pre-clinical trials, product development reports, designing, developing, compliance, validation, research and development, formulation, formulation development, analytic chemistry, delivery systems, clinical trials, creating, product, technical, experiment, innovation #LI-KT1 #LI-ONSITE

Clinical Diagnostic Solutions, Inc. (CDS) is a company that provides total hematology solutions for the physician office laboratory, clinic, small hospital, and veterinary office markets. At CDS, our mission is to provide the highest quality experience to our valued customers. Our employees achieve this through our cultural goals of working together through Teamwork, high Quality in the work we do, being Innovative and Courageous, always Results Oriented, and most importantly - being Customer Oriented. Under supervision, uses fundamental concepts, practices, and procedures of particular field of specialization to perform scientific, R&D tasks of some complexity requiring application and adaptation of established techniques, procedures, and criteria. Participates in new product development, optimization, validation, and transfer into production. Prioritizes work schedules to support team objectives. Job Responsibilities: Participates in method development and technical innovation within the research team and supports project timelines Performs method optimizations, validations and participates in technology transfer to production Performs routine operation, maintenance, calibration and troubleshooting of laboratory instruments such as pH, conductivity meters, osmometers, spectrnphotometers, hematology analyzers and nucroscopes Evaluates and selects methods, applies protocols and scientific techniques to accomplish study objectives Drafts and updates protocols, test methods and standard operating procedures as applicable Proactively collaborates and supports the team, communicates problems as they arise Provides solution/s to problem/ s of limited complexity, exercises judgment within defined policies to determine appropriate action Collects, analyzes and compiles data. Summarizes for interpretation and discussion Drafts statistical and narrative reports as applicable Recognizes and reports experimental variances Is able to coordinate a small project or a small component of a larger project according to set deliverables Maintains good laboratory records and documentation for experimental work and results Maintains workplace safety and environmental practices Maintains clean workplace including laboratory bench and glassware Supports the department with QC technical investigation activities as needed Works in the spirit of continuous improvement Engages in inter and intra-departmental activities/studies Performs other related duties as required or as directed. The omission of specific duties does not preclude the supervisor from assigning duties that are logically related to the position. Qualifications: Knowledge of scientific approach and methodologies. Ability to design small studies, gather, organize and analyze statistical data and generate reports Excellent oral and written communication skills Ability to investigate and analyze information and to draw conclusions Skill in the use of personal computers and related software applications such as Word/Excel/Powerpoint/Teams Knowledge of current technological developments/trends in area of expertise is desirable but not required Capable of adjusting to dynamic work environment and changing priorities Willing to take on new challenges and implement new ideas Must be Comfortable handling blood products Willing to embrace a learning environment, is open to suggestions, new ideas and innovation Ability to grasp methods fast and willingness to change course as applicable Familiar with GLP, GMP practices and capable of working in a regulated medical device company (ISO and FDA) Must have strong analytical skills Must be a team player and driven individual Must value innovation, accuracy and accountability Minimum Requirements: Bachelor's degree with 2-5 years or Associates degree with 5-8 years' experience that is directly related to the duties and responsibilities specified. EOE

Top aerospace company is looking to add an Aero Thermal Fluids Engineer level 4, 5, or 6 to their growing team in Jupiter, Florida. The ideal candidate will have experience with commercial and in-house developed software tools, and/or hand calculation methods to design and analyze bearings and seals related to pump fed liquid rocket engine systems. Will also have extensive knowledge of designing and analyzing a variety of bearings and seals such as: Bearings Rolling Elements: Ball, Roller, and Cylindrical bearings Fluid Film: Hydrostatic, annular, balance piston, and hydrodynamic Seals Dynamic, clearance, rubbing contact, and lift-off U.S. Citizenship only, no dual citizenship Will perform design and analysis tasks related to bearings and seals. The candidate shall be capable to work with minimal oversight. Responsible for utilizing a combination of commercial and in-house developed software tools, and/or hand calculation methods to correlate analysis models and review test data. Will strengthen the technical capacity of the company and facilitates transfer of technology by mentoring less experienced engineers and team members. Produce analysis reports and test reports. Present analysis to both internal and external customers. Skills:Candidate must have a Bachelor's Degree in Mechanical or Aerospace Engineering or the equivalent combination of education and a minimum of 7 years of experience Strong background in thermodynamics, heat transfer, and fluid dynamics, but Master's degree is desired. High proficiency in ANSYS Workbench and tools associated with turbomachinery analysis Familiarity with utilizing LINUX systems Experience programming in MATLAB, FORTRAN, Python Position is full time onsite but depending on candidate qualifications full time remote may be possible Level 4 $80 per hour Level 5 $95 per hour Level 6 $110 per hour #MCTA1

A new paradigm of computing Magic Leap is a pioneer in spatial computing, developing groundbreaking augmented reality technology that seamlessly blends digital content with the real world. As the creator of the next computing platform, our mixed reality devices unlock new possibilities for how people interact with and experience their surroundings. Magic Leap could be your place if you want to be part of a united team where everyone is empowered and trusted to make an impact. At Magic Leap, you can explore innovative solutions and use your talents to solve real-world problems. Working alongside industry experts, you can grow your skills and amplify human potential at the intersection of the physical and digital worlds. We know that successful change and progress accelerate diverse perspectives. As we shape our future, everyone's voice matters. Together, we can reimagine the world of work and, with our bold partners, make the impossible possible. The opportunity As a Staff Color Scientist within our Optical Engineering group, you will work closely with cross-functional teams to optimize existing color image processing algorithms, enhance calibration techniques, and develop new models of human color perception. The ideal candidate will apply their deep knowledge of color science and engineering to advise the team on mitigating issues of color uniformity and binocular color vision, making a direct impact on the development of cutting-edge augmented reality products. What you'll do Research, develop and facilitate integration of color calibration algorithms (including white balance correction, color mixing, etc.) Support and optimize existing colorimetry methods and color calibration algorithms Characterize, model, and analyze performance of displays and imaging systems on color metrics Develop and apply models of human color vision and verify models with empirical data Plan and conduct psychophysical studies with human observers Collaborate with internal/external stakeholders to bridge communication gaps, clarify requirements, identify risks, and support transparent exchange of data The experience you bring 8+ years of professional experience in color science in a technological or academic environment MS degree or higher in Color Science, Optical Engineering, Human Vision Science, or related fields Working knowledge of optics (including camera systems, projector systems, etc.) Scientific background on human color vision (including models of color adaptation, chromatic contrast sensitivity, etc.) Experience working with cross-functional teams and providing leadership and expertise for new projects Fluent in Matlab and/or Python and digital image processing Excellent communication, presentation, organization, and documentation skills It's exciting if you also have Hands-on experience with testing automation Experience with human subjects experiments Knowledge of C#/C++ Additional Information All your information will be kept confidential according to Equal Employment Opportunities guidelines Accommodations If you need an accommodation during the application, interviewing, or hiring process, you may request an accommodation by emailing ApplicantAccommodation@magicleap.com. Magic Leap will reasonably accommodate qualified individuals with disabilities to the extent required by applicable law. Please note that we do not accept any application documents via (e-)mail. Furthermore, we do not accept applications from recruitment agencies for this role. All legitimate Magic Leap email communications will end with "@magicleap.com". Please carefully review all emails you receive, to ensure you only engage with legitimate representatives of Magic Leap. For the protection of your Personal Information, do not click any links, open any attachments, or further engage with any suspicious communications. In the event you receive an unexpected or suspicious communication claiming to come from Magic Leap, please reach out directly to ******************************* for assistance. #LI-CP #LI-HYBRID Our salary ranges are determined by role, level and location. In addition to salary, Magic Leap offers a discretionary bonus, equity, and a fully comprehensive benefits package for eligible employees. US Base Salary Range$160,000—$180,000 USD