Associate Scientist Jobs in Florida

Lead IV Formulation Scientist - Advanced Sterile Solutions (503B Outsourcing) About Assure Infusions Assure Infusions is a leader in domestic IV fluid production, operating a robotics-driven 503B outsourcing facility dedicated to resolving critical shortages of premixed sodium chloride, lactated Ringer's, and dextrose solutions. Our innovations directly support 92% of U.S. hospital IV therapy protocols. Join the newest and most advanced pharmaceutical fluid manufacturer in the country. Your Impact Design and scale life-saving IV therapies in a facility equipped with advanced automation and real-time analytics: Solve stability challenges in pH-sensitive electrolyte buffer systems Optimize 4,000L+ GMP batches for robotic filling lines (20M+ annual unit capacity) Develop terminal sterilization protocols compliant with USP Phase 3 standards Lead cross-functional technical teams in process validation Qualifications Education MS/PhD in Pharmaceutical Sciences, Chemical Engineering, or related field (Parenteral Specialization Preferred) Experience 5+ years formulating large-volume parenterals (LVPs) in 503B/cGMP environments Proven success stabilizing dextrose solutions or electrolyte buffers at scale Skills Statistical process control (SPC) for formulation scaling CTD documentation for ANDA/NDA submissions FDA audit leadership in sterile processing Compensation & Benefits Salary: $95,000 - $125,000 base + performance-based bonuses Relocation Assistance (if needed) Healthcare: Zero-premium medical/dental/vision plans for employee Retirement: 401(k) with 6% company match Growth: We actively promote and support bolstering your qualifications with continued education. Lifestyle: PTO + hybrid scheduling flexibility Why Bartow? Cost of Living: 12% below national average Facility: Robotic ISO-7 cleanrooms and 24/7 analytical lab access Industry Impact: Direct role in strengthening U.S. pharmaceutical supply chains

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

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.

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.

IV Formulation Scientist - Contract - Bartow, Florida Proclinical is seeking an IV Formulation Scientist to contribute to the design and scaling of innovative IV therapies. Primary Responsibilities: The successful candidate will work in a state-of-the-art facility, focusing on solving stability challenges in pH-sensitive electrolyte buffer systems and optimizing large-scale GMP batches for robotic filling lines. Your role will also involve developing sterilization protocols and leading technical teams in process validation. Skills & Requirements: Bachelor's degree in Pharmaceutical Sciences, Chemical, or related field. Experience in formulating large-volume parenteral solutions in GMP environments. Proven success in stabilizing dextrose solutions or electrolyte buffers. Expertise in conducting stability studies for product shelf life and safety. Knowledge of FDA cGMPs and ICH Guidelines. Proficiency in FDA-regulated sterile processing. The IV Formulation Scientist's responsibilities will be: Design and scale IV therapies using advanced automation and analytics. Address stability challenges in pH-sensitive electrolyte buffer systems. Optimize large GMP batches for high-capacity robotic filling lines. Develop terminal sterilization protocols compliant with USP standards. Lead cross-functional teams in process validation efforts. If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.briggs@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.

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 Biology experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Biology Develop and answer Biology-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 Biology 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 Biology 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.

Kopernik Global Investors, LLC is an SEC registered investment adviser under the Investment Advisers Act of 1940. The Firm provides investment management services to individual and institutional investors. Kopernik is a client-centric, 100% employee-owned, global equity investment management specialist. Summary: The Research Associate position is a two-year program based in Tampa, Florida and reports primarily to the Director of Research (DOR). This individual will work closely with assigned Research Analysts, participate in hands-on training on global value investing with experienced investment professionals while assuming responsibilities that are appropriate to their demonstrated capabilities. Responsibilities: Assists Research Analysts in conducting investment research and analysis: Creates and maintains spreadsheets and financial models (company and industry/sector). Collects industry and company data through sources such as sell-side research firms, internal databases, trade publications, and regulatory filings. Reviews and organizes data, synthesizes information, and helps Research Analysts analyze and interpret company and industry data. Assists Research Analysts with the annual update of the Company Report. Stays up-to-date and informs Research Analysts on key company news, industry trends, and regulatory issues. Prepares internal presentations and files research-related documents. May work with investment analysts to write Company Reports, prepare research whitepapers, and prepare background pieces for investment reports. May draft investment notes or publish own writing. Works on special research projects as needed to help support the Research Analysts. Attends company sponsored events including but not limited to Research Offsite, annual Company Offsite, conferences, and seminars. May attend broker and company meetings, as needed. Performs additional responsibilities as assigned. Requirements: Demonstrates intellectual curiosity and analytical skills. Demonstrates sound judgment in resolving complex matters. Demonstrates initiative by identifying issues and recommending solutions on complex and broad matters. Demonstrates ability to influence groups and/or more senior members of the research team. Demonstrates effective written and oral communication skills. Demonstrates ability to collaborate and develop/maintain relationships inside and outside the firm to enable effective completion of business objectives. Works well under pressure and demonstrates ability to prioritize multiple tasks. Takes ownership for work, always ensuring standards and deadlines are met and keeping others informed and up to date. Demonstrates ability to contribute to a team-based environment. Demonstrates excellent attention to detail. BA/BS degree; coursework in Economics, Accounting, Finance is preferred. No prior work experience is required but past internships and professional references are preferred. Active pursuit of CFA designation is preferred. The two-year program is temporary and does not lead to a permanent position. Reports directly to DOR. Additional Requirements: This is not a remote position and will require relocation if not already local to the Tampa, FL area. Being authorized to work in the U.S. without employer sponsorship is a precondition of employment. Application Requirements: All submissions are to be submitted to **************************. A resume, cover letter, and two writing samples are required. In the cover letter, please state why you want to work at Kopernik. In addition, please submit two writing samples answering the following questions: (1) What are you passionate about and why? (2) Does better education lead to some countries being more successful economically than others? Please use evidence to back up statements. The Firm provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

THE COMPANY: Formulated Solutions is redefining the Pharmaceutical and Self-Directed Consumer Healthcare CDMO experience through creativity and invention; delivering our world class Marketing Partners unmatched formulations, innovative packaging and cost effective, reliable supply. Formulated Solutions is and shall always be a company of people with the knowledge and dedication to provide our Marketing Partners with a single source solution for delivering quality and innovative products to market. We shall embrace changes and new opportunities as a vehicle to continually develop and grow sustainable relationships. As a company we shall never accept anything less than a culture that fosters creativity, growth, and profitability for both our Partners and the company. PRIMARY PURPOSE: Develop, transfer and validation of HPLC, Gas Chromatography, ICP and AA methodology. Must have extensive cGMP experience and be able to provide leadership and mentoring to Chemist I and Chemist II in QC Laboratory. Must have thorough understanding of Good Laboratory Practices and Good Documentation Practices, as well as compendial methodology. Must have experience in writing Standard Operating Procedures, Protocols and Reports. MAJOR DUTIES AND RESPONSIBILITIES: Perform all the activities for development, transfer and validation of analytical methods. Revise and write Validation Protocols, Test Methods, Validation Reports and SOP's. Testing of incoming materials, using compendial test methods (USP, PhEUR, JP) Testing of stability samples, in process samples and finished product testing, using a variety of techniques, such as HPLC, GC, AA, ICP, UV/Vis, etc. Accurately records raw data and analyzes, as well as calculates and interprets the results. Occasional customer interaction in a professional environment. Responsible for out of specification test results, investigation, and implementation of corrective actions. Ensure testing is performed accurately and in compliance with GLP, cGMP, cUSP, SOP and other approved test methods and protocols. Maintain analytical reagents in laboratory including but not limited to: inventory, current MSDS, PPE required for handling, waste generation and disposal. Assist Validation teams in cleaning validation activities. Support laboratory troubleshooting needs by interacting with vendors, customers and other relevant SMEs. Promote GMP and safety throughout the facility. Promote continuous improvement and customer satisfaction. Follow-up on OOS's and CAPAs to verify compliance. Potential exists for exposure to potentially harmful chemicals. Participate in other activities as assigned by the Lab Manager or VP Quality. QUALIFICATIONS: Required Knowledge of Compendia testing. Knowledge of the chemical composition, structure, and properties of substances and of the chemical processes and transformations that they undergo. This includes uses of chemicals and their interactions, danger signs, production techniques, and disposal methods. Knowledge of raw materials, production processes, quality control, and other techniques for maximizing the effective manufacture of goods. Working knowledge of FDA regulations for laboratory testing and disposition. Ability to use a personal computer and peripheral equipment to accurately enter an analyze data and produce reports. Knowledge of chemical safety and protective equipment. Expertise in various analytical equipment and techniques utilized in an analytical laboratory including but not limited to pH, viscosity, specific gravity, infrared spectroscopy, HPLC, GC, ICP, UV/VIS, atomic absorption. Ability to establish priorities, work independently, productively, and proceed with objectives without supervision. Ability to handle and resolve recurring problems. Understanding the implications of new information for both current and future problem-solving and decision-making. Ability to troubleshoot HPLC, GC, ICP and AA analyses Ability to communicate effectively, concisely in a professional manner with clients and others. Ability to work in a dynamic fast paced environment-sometimes rapidly shifting priorities. Ability to concentrate in such an environment and perform quality work. Must be able to lift up to 15 pounds. EDUCATION AND TRAINING: Bachelor's degree in Chemistry or related discipline. Must have three or more years' experience working in an analytical laboratory in an FDA regulated industry

Engineered Bonding Solutions, LLC is an industry-leading structural adhesive manufacturer. In our 14th year of business, we are looking for long-term career-minded individuals to grow with us. After successful completion of the probationary period, EBS, LLC offers 100% EMPLOYER PAID Health Insurance, 50% paid dental insurance, 100% paid life and AD&D insurance, as well as a matching 401k plan. If you have a strong adhesives chemistry background, excellent track record, and are looking to be a part of a quality-driven team, you are encouraged to apply. Engineered Bonding Solutions, LLC, located in Titusville, FL, is seeking a full-time adhesives chemist. Prior adhesives chemistry experience is required. The Chemist is a salaried position which is responsible for the following: · Product evaluation and development to create new products and modify existing products for specific applications and markets. · Interact with sales personnel and customers, including field visits, to gain required input and feedback on development projects and to assist, as needed, in the commercialization of new products. · Provide technical service for EBS adhesives and other related products. · Implementation of cost savings and justification (formulas, raw materials, processes) · Change existing formulations to improve product cost. · Support and maintain the integrity of EBS products through interaction with sales, marketing, and manufacturing quality personnel. · Coordinate and manage the scale-up of new products from laboratory through pilot scale up to full production and commercial status. · Oversee technical aspects of manufacturing process and assist as needed in production management. · Achieve quality objectives by contributing information and analysis to operational plans and reviews · Perform quality testing and reporting on products and incoming materials. · Maintain the Document and Change Control processes using ISO Quality Procedures · Obtain a thorough knowledge of products, Manufacturing and Quality processes · Keep an organized lab notebook compliant to legal requirements for protection of intellectual property. · Daily housekeeping and attentiveness to safety of self and others are absolute requirements Job Requirements include but are not limited to: · Bachelor's degree or higher in Chemistry · Minimum 10 years' experience in developing, technical service, mixing experience, manufacturing of adhesives with general knowledge of mostly polymer industry, including unsaturated polyesters, urethanes and epoxies. · Experience in adhesives, paints, coatings, sealants. · General knowledge of reactive organic monomers. · General knowledge of raw material analysis and mechanical testing of composites · General knowledge in the writing of technical reports related to product development and product testing. · Understanding of Quality Assurance and Good Manufacturing Practices Physical Requirements may include: · Able to perform light labor in hot/humid conditions, both indoor and outdoor in all conditions · Able to work while exposed to fumes, airborne particles, vibration, moving parts, noise, and other conditions while wearing proper personal protective equipment for the hazards. · Physically able to lift, push, pull up to 25 lbs. · Able to work standing up for long periods of time · Must be able to read small print, color vision, have good peripheral vision, depth perception, and ability to adjust focus. Salary range is $100,000 - $150,000; commensurate with experience. Email cover letter and resume to ******************** for consideration.

Working Title: FISHERIES & WILDLIFE BIO SCIENTIST III - 77073282 Pay Plan: Career Service 77073282 Salary: $1,730.77 biweekly + benefits Posting Closing Date: 03/31/2025 Total Compensation Estimator Tool Employment is contingent upon successful completion of a background check. FWC Mission Statement: Managing fish and wildlife resources for their long-term well-being and the benefit of people. Working Title: Fisheries and Wildlife Biological Scientist III Section : Wildlife and Habitat Management Position number: 77073282 Salary: $1,730.77 biweekly Address: 3365 Taylor Creek Road, Christmas, FL 32709 Phone: ************** Supervisor: Melanie Mancuso Description of duties: The FWC's Northeast Region is seeking a highly motivated candidate for an exciting and challenging opportunity to lead management on the Split Oak Forest Wildlife and Environmental Area (WEA) in Orange and Osceola Counties, Florida. Split Oak Forest WEA, located just outside of metropolitan Orlando in an increasingly urbanized region, serves as an important link in the Florida wildlife corridor as an area where visitors can experience the natural landscape of central Florida and observe many of the native plant and wildlife species. This position serves as the Lead Area Biologist responsible for habitat management on over 1,650 acres of natural communities including scrubby, mesic, and wet flatwoods, basin marsh, and hammocks to benefit non-game and imperiled wildlife and plant species including the gopher tortoise, gopher frog, Bachman's sparrow, and wild turkey. The successful candidate will be responsible for coordinating and implementing habitat management and restoration activities including the application of prescribed fire on approximately 450 acres per year as well as conducting various mechanical and chemical treatments, and invasive species management. The incumbent will also assist with management on various other WMAs in the NE region. Incumbent is responsible for all aspects of running the WEA including assisting with periodic revision of the management plan; infrastructure management, development and maintenance as required by area management plans; wildlife monitoring and data entry; managing public access; reporting; purchasing; and budget management; and GIS. The incumbent will interact professionally with the public and partners, including other state and federal agencies as well as non-governmental organizations to provide information concerning wildlife, area management, and rules and regulations. Occasionally the incumbent will be required to travel to attend regional and divisional meetings as well as various trainings as needed. Preference will be given to candidates that have hands on prescribed burn experience and candidates that are Florida Certified Prescribed Burn Managers. Knowledge, Skills, and Abilities: Incumbent must have excellent verbal and written communication skills and leadership skills, be able to work well with team members and interact positively with stakeholders and cooperators. Other knowledge, skills and abilities include: Knowledge of principles of ecology and wildlife management Knowledge of the common and imperiled species of Florida Knowledge of the principles of fire ecology and experience with the application of prescribed fire Knowledge of wildlife and land management practices including mechanical and chemical vegetation control Knowledge and experience in supervising multiple team members Knowledge of outdoor recreational activities including hunting and fishing Ability to work as part of a team and independently Experience conducting wildlife surveys and summarizing biological data Knowledge of and experience in ArcGIS and GPS and its application to land management and surveys Proficient with Windows and Microsoft Office applications Ability to identify common and imperiled wildlife species Ability to operate outdoors under harsh weather conditions Ability to write technical reports Ability to plan and prioritize work assignments and multi-task Ability to operate vehicles, ATVs, trailers and heavy equipment Broadband code: 19-1023-03 Class code: 5074 Region: Northeast Title: Fisheries and Wildlife Biological Scientist III County: Orange and Osceola Working hours: 8:00am - 5:00pm, Monday - Friday, occasional weekend work and atypical hours expected. Occasional overnight travel required. List of any subordinates supervised: 1 OPS Fish and Wildlife Technician Residency requirement: Required to live within 25-miles of the entrance of Split Oak Forest WEA. Level of Education: Preferred Bachelor of Science degree in a life or physical science. A bachelor's degree can substitute for four years of direct, relevant experience. Benefits: Participate in Group health insurance and included in the Florida Retirement System (FRS). Other Requirements: This position is designated as a home-is-office position. Incumbent will be required to complete prescribed burning training to obtain and maintain a FL certified prescribed burn manager certificate within 18 months of hire date. Will be required to obtain and maintain a current and valid Florida Driver's license. Employment is contingent upon successful completion of a background check. The criminal history check must be completed prior to or within the first three days of employment. 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.

The Product Development Scientist role: Responsible for developing and leading scaleup of new products to commercialization. Creative and self-motivated, the Product Development Scientist plays a key role in introducing novel ideas and techniques to the product development and commercialization process - leading directly to improved commercial results for the company. Duties & Responsibilities: Research and develop creative and novel products with a focus on extracts and distillates - bringing them to commercial fruition. Utilize and maintain a range of laboratory and pilot-plant equipment (introducing new equipment and techniques where necessary) during product development. Identify unique raw materials for the development of new products. Work with the Innovation, QC teams, VP of Innovation, and Category Managers in the planning of R&D project priorities. Provide Senior Innovation Manager-Coffee and Tea with ongoing and consistent communication of status of R&D efforts and commercial implications of R&D work. Lead in planning, monitoring and documentation of plant trials leading to successful commercialization of new products. Execute shelf life and stability studies of new product development. Support the Production Supervisor to determine, define and improve product tolerance limits of new and existing products. Lead projects relating to quality or cost improvement. Lead Continuous improvement projects as pertinent. Lead projects and evaluation of alternate raw material sources with detailed reports of findings Participate in sensory evaluation of R&D projects, new products, reformulations, ingredient substitutions, and competitive products. Maintain and share accurate records of lab work, and documentation of used ingredients, formulation modifications and provide statistical evaluations and reports. Develop product and raw material specifications suitable for QA, QC, Regulatory, and Customer Display understanding of HACCP, GMP, and Acidified Foods Filing Demonstrate proficient use of internal Systems (JDE, STARS, SharePoint, GICP etc.) Coordinate with Quality Control in scheduling the use of laboratory facilities and equipment to ensure the appropriate levels of R&D, application and QA testing are performed. Stay abreast of current, worldwide R&D efforts and transfer new knowledge to Treatt product lines. Continually explore and identify ways to tailor Treatt product lines to appeal to untapped markets. Provide/Support Capex planning by identifying and costing out potential solutions that may grow business. Provide both technical and non-technical articles and reports for internal publication. Cultivate sales opportunities with current customers and other industry contacts by building strong partnering relationships with key technical personnel in these organizations. Participate in customer call and/or product demonstrations as needed. Work with customers as needed on new product developments and reformulations. Partner with sales team members to identify and analyze consumer market trends that might provide increased sales and product development opportunities. Act in the best interest of Treatt at all times. All other duties as customary or as delegated. Work primarily independently or with minimal supervision to complete required tasks. Education & Traininig: A bachelor's degree in chemistry, Food Science or a related Scientific field, plus a minimum of 1 years lab and product development experience in a closely affiliated field. Knowledge & Experience: A proven independent worker with strong creativity and problem-solving skills. An in-depth understanding of fundamental chemistry principles. Demonstrate knowledge of regulations, policies, procedures and processes in food science and product development. Superior ability to research and analyze information and data to arrive at valid conclusions and plans of actions. Effective communication skills at all levels - both orally and in writing. Basic knowledge in the use of various laboratory equipment and methodologies. Including: Gas chromatography, mass spectrometry and other analytical measurement methods a plus Ability to use various spreadsheets, word-processing and database computer software. Environment: Normal laboratory and manufacturing working conditions.

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

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

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. As a Research Scientist at Lonza, you'll have the exciting opportunity to dive into hands-on scientific experiments while collaborating with a dynamic, cross-functional team. You'll play a key role in providing analytical and technical support, helping to drive solutions and bring projects to successful completion. If you thrive in a fast-paced environment, love problem-solving, and are passionate about innovative research, this is the role for you! Key Responsibilities * Perform scientific assignments on time to support Product Development projects. * Demonstrate accountability for project-level assignments with a strong technical foundation. * Operate and maintain analytical instruments (HPLC, dissolution, KF, DSC, TGA, VSA, FTIR, etc.). * Collect, analyze, and summarize scientific data for internal and external reporting. * Author and review study protocols, reports, SOPs, and other internal documents. * Identify atypical results, collect supporting data, and assist in resolving corrective actions. * Support investigations, documentation review, and approve results from team members. * Ensure compliance with safety standards, SOPs, and cGMP requirements. * Maintain a clean, safe, and inspection-ready laboratory environment. * Foster professional and confidential relationships with internal and external stakeholders. * Assist in training new team members and implementing new technologies. * Continuously improve laboratory practices and contribute to process optimization. * Enforce to all Safety and Sustainability policies, promptly addressing and reporting any issues. Responsibilities & Technical Expertise * Execute scientific and non-scientific assignments with minimal oversight. * Apply technical expertise to experimental activities, data interpretation, and reporting. * Improve and refine safety and compliance practices in alignment with SOPs. * Contribute to the development, implementation, and continuous improvement of laboratory processes. * Possess an understanding of the drug development process, particularly in pre-formulation and analytical settings. * Participate in scientific publications (posters, webinars, papers) by generating supporting data to showcase technical advancements or innovations. Environmental & Physical Requirements * Ability to lift, bend, and stand for periods in laboratory settings. * Accurate handling of hazardous materials while adhering to PPE requirements. Key Requirements: * Bachelors Degree In Chemistry or a related field * 3 years of relevant work experience Compensation for the role will depend on a number of factors, including the successful candidate's qualifications, skills, competencies, experience, and job-related knowledge. Full-time employees receive a comprehensive benefits package including performance-related bonus, medical and dental coverage, 401k plan, life insurance, short-term and long-term disability insurance, an employee assistance program, paid time off (PTO), and more. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. As a Research Scientist at Lonza, you'll have the exciting opportunity to dive into hands-on scientific experiments while collaborating with a dynamic, cross-functional team. You'll play a key role in providing analytical and technical support, helping to drive solutions and bring projects to successful completion. If you thrive in a fast-paced environment, love problem-solving, and are passionate about innovative research, this is the role for you! Key Responsibilities Perform scientific assignments on time to support Product Development projects. Demonstrate accountability for project-level assignments with a strong technical foundation. Operate and maintain analytical instruments (HPLC, dissolution, KF, DSC, TGA, VSA, FTIR, etc.). Collect, analyze, and summarize scientific data for internal and external reporting. Author and review study protocols, reports, SOPs, and other internal documents. Identify atypical results, collect supporting data, and assist in resolving corrective actions. Support investigations, documentation review, and approve results from team members. Ensure compliance with safety standards, SOPs, and cGMP requirements. Maintain a clean, safe, and inspection-ready laboratory environment. Foster professional and confidential relationships with internal and external stakeholders. Assist in training new team members and implementing new technologies. Continuously improve laboratory practices and contribute to process optimization. Enforce to all Safety and Sustainability policies, promptly addressing and reporting any issues. Responsibilities & Technical Expertise Execute scientific and non-scientific assignments with minimal oversight. Apply technical expertise to experimental activities, data interpretation, and reporting. Improve and refine safety and compliance practices in alignment with SOPs. Contribute to the development, implementation, and continuous improvement of laboratory processes. Possess an understanding of the drug development process, particularly in pre-formulation and analytical settings. Participate in scientific publications (posters, webinars, papers) by generating supporting data to showcase technical advancements or innovations. Environmental & Physical Requirements Ability to lift, bend, and stand for periods in laboratory settings. Accurate handling of hazardous materials while adhering to PPE requirements. Key Requirements: Bachelors Degree In Chemistry or a related field 3 years of relevant work experience Compensation for the role will depend on a number of factors, including the successful candidate's qualifications, skills, competencies, experience, and job-related knowledge. Full-time employees receive a comprehensive benefits package including performance-related bonus, medical and dental coverage, 401k plan, life insurance, short-term and long-term disability insurance, an employee assistance program, paid time off (PTO), and more. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

pEnjoy what you do while contributing to a company that makes a difference in people's lives. IVF Florida, is one of the premier fertility centers in the United States, continually seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward./p pIf you're an Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments. /p pstrong We currently have an opening for a full-time Embryologist to work in our fast paced, high volume, Embryology Lab located at our Margate, Florida lab. This is a full-time position working Sunday - Thursday 8a-4:30p. Occasional holiday and weekends required. /strongstrongspan /span/strong/p pstrong How You'll Contribute:/strong/p pWe always do whatever it takes, even if it isn't specifically our “job.” In general, the Embryologist is responsible for:/p pstrong Clinical and technical standards/strong/p ul li Perform the following aspects of Assisted Reproductive technology (ART) procedures including but not necessarily limited to:/li /ul pi. oocyte retrieval/p pii. sperm preparation for insemination/p piii. in-vitro fertilization (IVF)/p piv. fertilization check/p pv. embryo evaluation/p pvi. selection of embryos for transfer and vitrification/p pvii. embryo vitrification/p pviii. embryo thawing/p pix. embryo transfer/p px. surgical sperm retrieval and processing/p pxi. cell to tube transfer of embryo biopsy material/p pxii. micromanipulation/p p(1) ICSI/p p(2) Assisted hatching/p p(3) Embryo biopsy/p ul li Prepare embryo culture dishes and solutions required for ART procedures using sterile tissue culture techniques./li li Perform embryology and andrology proficiency testing required by CAP-approved agency (ABB, CAP)./li li Assure proper sample collection, delivery and identification, including PGT samples for release./li li Perform safe handling of specimens by following the safety guidelines for biohazardous, infectious and toxic substances in the IVF laboratory./li li Document quality assurance activities including description of unusual incidents, problems, and appropriate corrective action./li li Perform daily/weekly quality control for procedures and equipment used in the IVF Laboratory./li li Prepare semen specimens for intrauterine inseminations (IUIs)./li li Perform all aspects of reproductive tissue (sperm, oocyte and embryo) cryopreservation/vitrification including sample identification, inventories, checks of serology screening, freezing and thawing procedures./li li Maintain laboratory records, reports, quality assurance data and assist in preparation of SART, Artworks, and Cryomodule data./li li Assist in the preparation of data for clinical meetings/li li Operate laboratory equipment including laminar flow hoods, microscopes, centrifuges, analytical balance, pH meter/li li Set up, calibrate and clean laboratory equipment and glassware, and assure routine maintenance and repairs are performed and documented./li li Perform various office functions including photocopying, answering telephones, scheduling appointments, faxing and filing reports./li /ul p /p pstrong Laboratory Services/Operations/strong/p ul li Attend monthly IVF laboratory meetings and periodic staff meetings./li li Assist in research projects under the IVF Laboratory Director's supervision./li li Assist in training and assigning work to junior IVF support staff./li li Communicate with center personnel, medical staff, patients and outside resources to ensure high quality patient care./li li Assist laboratory personnel in performing laboratory services in accordance with Federal, State and local laws and guidelines to ensure laboratory maintains accreditation./li li Assist as required in maintaining laboratory operations in conformity with OSHA and CLIA ‘88 regulations./li li Must meet CLIA ‘88 requirements of education and experience for General Supervisor or Technical Supervisor./li li Must be thoroughly familiar with Laboratory Operations Manual./li li Must demonstrate skills and aptitude appropriate to the position./li li Must demonstrate an ability to function effectively without direct supervision and to perform laboratory services in accord with the Laboratory Philosophy and Operating Standards./li li Must demonstrate a good work ethic and commitment to participate in appropriate programs of continuing education and professional development to maintain up-to-date knowledge in the laboratory specialty./li /ul pstrong What You'll Bring:/strong/p ul li Bachelor's degree in biological science required. /li li2-3 years minimum experience, 3-5 years preferred./li li Preferred Certification/License: ul li American Board of Bioanalysis: Embryology and Andrology/li li Florida CLS license with ASCP certification required only if performing diagnostic semen analysis/li /ul /li li Ability to access, input, and retrieve information from a computer./li li Knowledge of office procedures and office machines (i.e. computer, fax, copier, etc.)./li li Ability to work as part of a multi-disciplinary team./li li Ability to communicate accurately and concisely./li li Excellent interpersonal skills/li li Demonstrated expertise in continuous quality improvement, customer service, and team building. /li li Ability to travel throughout the San Francisco Bay area./li /ul pstrong More important than the best skills, however, is the right person./strong Employees who embrace our mission, vision, and core values are highly successful. /p pstrong What We Offer:/strong/p ul li Competitive pay + bonus/li li Comprehensive training/li li Medical, dental, vision, and 401(k) matching/li li Generous paid time off and holidays/li li Retirement plan/li li Tuition assistance/li li Ability to make an impact in the communities we serve/li /ul pAt IVF Florida, we promote and develop individual strengths in order to help staff grow personally and professionally. /p pTo learn more about our company and culture, visit a href="************************************* rel="noopener" target="_blank"here/a./p pstrong How To Get Started:/strong/p pTo have your resume reviewed by someone on our Talent Acquisition team, click on the “Apply” button. Or if you happen to know of someone who might be interested in this position, please feel free to share the job description by clicking on an option under “Share This Job” at the top of the screen./p

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.

Working Title: FISHERIES & WILDLIFE BIO SCIENTIST II - 77000948 Pay Plan: Career Service 77000948 Salary: $1,538.46 biweekly + benefits Posting Closing Date: 04/10/2025 Total Compensation Estimator Tool Anticipated Vacancy Position Number: 77000948 Location: 663 Plantation Road, Perry, FL 32348 Salary: $1,538.46 bi-weekly + benefits Supervisor & Position Number: Mitch Haag (77000919) Broadband Code: 19-1023-02 Class Code: 5028 Region: North Central County: Taylor Working Hours: 8:00am - 5:00pm, with weekend and after-hours work occasionally required Residency Requirement: None List of Subordinates Supervised: Seasonal OPS employees and volunteers Requirements: Employment is contingent upon successful completion of a background check. Will be required to obtain and maintain a Florida Class E Driver's License and Florida Prescribed Burn Manager Certification. Occasional overnight travel. Minimum Qualifications: 5 years professional experience in a closely-related biological field or laboratory program is required. A Bachelor of Science degree in a relevant field can substitute for four of the 5 years of required experience. Preferred Qualifications: A Bachelor of Science degree with a major in one of the life/physical sciences, Preference will be given to applicants with experience in prescribed fire, native and non-native plant management, and wildlife monitoring. Our Organization: The FWC envisions a Florida where fish and wildlife are abundant and thriving in healthy and connected natural landscapes with vital working lands and waterways; where natural resources are valued and safely enjoyed by all; and wherein natural systems support vibrant human communities and a strong economy. Our Mission: Managing fish and wildlife resources for their long-term well-being and the benefit of people. Every organization has an identity that is forged not only by what it does, but by how it conducts itself. The values embedded in our mission and expressed in the vision of the FWC are to make quality decisions by being dynamic, science-informed, efficient, ethical, collaborative and committed to the vitality of the state and its environment. Description of Duties: An exciting opportunity exists for a Fisheries and Wildlife Biological Scientist II to join a team within the Wildlife and Habitat Management Section to assist with the management of Big Bend Wildlife Management Area (WMA) and other WMAs as needed. We are seeking a highly motivated applicant that is willing to assist a productive team with the challenge of managing wildlife habitat and public recreational opportunities on 90,000+ acres of conservation land in Taylor and Dixie Counties. Duties include, but are not limited to: Assisting lead area biologists in developing and implementing management programs for the Big Bend Wildlife Management Area. Assists with planning and implementing effective habitat management practices, such as prescribed burning, upland and wetland restoration, mechanical and chemical vegetation treatments, oversight of timber operations, water level manipulations, and other projects. Assists with planning, developing, and coordinating projects to facilitate public use, such as road construction and maintenance, culvert installation and repair, and construction and maintenance of boundary and interior fences and gates. Assists with developing bid specifications, overseeing contracts, and monitoring vendor compliance. Assists with the completion of annual work plans, budget proposals, accomplishment reports and other administrative tasks. Assists with public hunting and other recreational activities, including coordination and operation of check stations. Conducts wildlife population surveys using scientifically accepted techniques, including data analysis and report writing. Accurately and routinely submits reports of activity and accomplishments using online databases and ArcGIS. Surveys habitat types and monitors changes that take place in vegetative communities. Provides technical assistance to individuals, organizations and other agencies regarding wildlife biology and wildlife habitat management. Proposes regulations based on sound biological and sociological principles. Participates in seminars and workshops relating to wildlife resource management. Completes other duties or assists on other areas as assigned. Knowledge, Skills, and Abilities: Kowledge of prescribed burning Knowledge in conducting wildlife surveys, including game and nongame species, collecting and analyzing data, and summarizing results Knowledge of habitat restoration techniques, fire ecology, and plant succession Applied knowledge of chemical or mechanical control of invasive vegetation Ability to operate and maintain 4WD vehicles, farm tractors and implements, ATVs, and outboard motors Ability to work independently and in a variety of weather conditions Ability to work efficiently in a team of diverse people with differing backgrounds Ability to plan and prioritize multiple work assignments Ability to establish and maintain effective working relationships with internal and external partners Familiarity with common outdoor recreation activities Ability to write, edit, and produce scientific reports and summaries Ability to use hand tools, including chainsaws, power tools, auger, etc. Knowledge of GIS software (ArcMap, ArcPro) and handheld GPS units and their applications Skill in use of Microsoft Office software (e.g. Word, Excel, Access, etc.) 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.

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.