Scientist Jobs in Gladeview, 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.

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.

Actalent is Hiring a team of Scientists // First & Second Shift! Responsibilities * Perform routine tests of finished products, stability samples, raw materials, and CV samples, including assays, chromatographic purity, and content uniformity using UV and HPLC. * Conduct particle size distribution using different techniques and water determination by KF. * Evaluate test results and decide the acceptability of the samples based on the test results. * Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs. * Maintain the laboratories with good housekeeping practices and in compliance with cGMP. * Ensure notebooks are reviewed promptly in accordance with SOPs. * Analyze and interpret results in written and oral formats. * Assist in the training of new analysts. * Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. * Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Essential Skills * Proficiency with HPLC, UPLC, UV-Vis, and other analytical chemistry techniques. * Strong experience in analytical chemistry, not formulation. * Experience with fda and gmp regulations. * Ability to analyze and interpret complex data. * Excellent written and oral communication skills. Additional Skills & Qualifications * Bachelor's degree in Chemistry or a related scientific field with 1-2 years of related experience in pharmaceutical analysis. * Master's degree in Chemistry or a related scientific field with 1 year of related experience in pharmaceutical analysis. * Ability to deal with problems involving several concrete variables in standardized situations. * Proficiency in necessary computations and the ability to draw and interpret graphs. * Working knowledge of instrumentation software used in laboratories. Work Environment This position is based in a lab environment that is regulated by FDA and GMP standards. You will be working with various scientific instruments and software in a highly controlled and compliant setting. Pay and Benefits The pay range for this position is $28.00 - $32.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Pompano Beach,FL. Application Deadline This position is anticipated to close on Feb 14, 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.

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.

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

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

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.

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

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

At **APTIM** , we come to work each day knowing that we are making an impact on the world. Our work spans from safeguarding and maintaining critical infrastructure to helping communities recover from natural disasters, from empowering our armed forces and first responders to reducing carbon and energy use, and from making cities more resilient against the threats of climate change to restoring contaminated ecological systems. **Job overview** APTIM is seeking a Environmental Scientist (hydrogeologist, geologist or environmental scientist) to assist the retail petroleum new-store construction team. The qualified candidate will be a hands-on professional scientist, handling a wide-range of tasks both in the field and in the office, for small to large scale construction projects. **What you can expect from APTIM:** + Work that is worthy of your time and talent + Respect and flexibility to live a full life at work and at home + Dogged determination to deliver for our clients and communities + A voice in making our company better + Investment into your personal and professional development **Key Responsibilities/Accountabilities:** + Initial responsibilities will be in the office, to include permitting, project preparation, and report writing responsibilities for construction projects across the state of Florida. + Responsibilities will include: + Preparation of Best Management Practices and application submittals for dewatering permits, following through on permit approvals to completion. + Performing Phase I/II environmental assessment field activities, including the use of complex instrumentation or equipment, and overseeing subcontractors. + Report writing for Phase I/II environmental assessments, including interpretation and presentation of collected data in reports that include text, tables, and figures suitable for client and regulatory review. + Assist Project Managers with running projects including handling project-related tasks, such as setting up Purchase Orders, scheduling subcontractors, scheduling field personal, tracking deadlines for client submittals, etc. + Must be able to work as part of a team while at the same time taking ownership of your individual projects, managing time, effort, and duties within budgetary constraints and a timeline that shifts with client needs. + Uses best practices and knowledge of internal/external business issues to improve products or services in own discipline. + Applies knowledge and skills to a wide range of standard and nonstandard situations. **Basic Qualifications:** + Bachelor's degree in Geology / Environmental Science or related degree required + 3 years experience at a minumum + Working experience in the petroleum cleanup field + Working knowledge of Florida regulations related to environmental investigations and permits. + Must have good interpersonal skills, as you'll be interacting with clients and regulatory agencies on a regular basis. + Must have strong written communication skills and an attention to detail. + Proficiency in Microsoft Office and Excel required. + Able to work outside in typical Florida conditions, during all seasons, for up to 12 hours at a time. + Valid Driver's License. + OSHA 40 Hr HAZWOPER **Who we are and what we do:** APTIM is a global industry leader headquartered in Baton Rouge, Louisiana. With more than 4,000 employees worldwide, APTIM specializes in critical infrastructure, technical and data solutions, program management, environmental services, resilience, as well as sustainability and energy solutions. Our dedicated people have the proven experience and expertise to provide integrated services and solutions to government agencies, commercial, industrial, and energy customers. APTIM is committed to accelerating the transition toward a clean and efficient energy economy, building a sustainable future for our communities and the natural world, and creating an inclusive equitable environment that celebrates the diversity of our people. Watch our video: Aptim Making a Difference \#LI-BM1 Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled Applicants with a physical or mental disability who require a reasonable accommodation for any part of the application or hiring process may make their request known by e-mailing ********************************** or calling ************ for assistance. EOE/Vets/Disability

AirQuest Environmental, Inc. is an Environmental and Industrial Hygiene Consulting Firm that offers environmental services for both public and private sector clients at sites located throughout the United States and internationally. AirQuest is seeking an environmental field technician for a full-time position. Job Summary You will be an integral part of the industrial hygiene team by assisting in a variety of environmental and industrial hygiene field activities. AirQuest specializes in providing services to the following sectors: asbestos and lead-based paint detection and control, indoor air quality investigations, radon and/or mold detection and management services. You will be expected to take initiative in various projects assigned to you by your supervisor. After training and under supervision, you will perform a variety of specialized paraprofessional industrial hygiene, environmental or engineering field research, perform and document field observations report writing, file maintenance, basic scientific calculations, public relations and office administrative duties. Position Information: Full-Time (40-45 hours) Typical hours range from 8:00 AM to 5:00 PM Monday-Friday as well as rotational on-call weekends to meet client needs as necessary. Additional hours, including nights and non-on-call weekends, are occasionally required. Pay rates offered are contingent on experience Benefits:* 401(k) & 401(k) Matching Health Insurance - Humana Health Insurance - Vision, Dental Minimum 48 hours of PTO (Paid Time Off) Guaranteed after 90 days 7 Paid Holidays Professional Development Assistance Specific Responsibilities and Requirements: Conduct site inspections, material surveys and oversight activities for asbestos, lead, radon, mold, industrial hygiene and indoor air quality projects Input field project data in Microsoft Word and Excel and prepare and review technical reports Participate and pass required training and various required certification programs Daily travel throughout Miami-Dade, Broward and Palm Beach counties with occasional travel out of town for extended periods of times Communicate effectively and on a timely basis with clients in-person, via emails and phone conversations Required Skills & Qualifications: Must be able to read, understand, speak, and write in English Must be proficient in Microsoft Word and Excel A bachelor's degree or seeking a degree in an environmental science or industrial hygiene field, or other related fields is highly desirable. Preferred but not required: Experience in the following specialties: industrial hygiene, indoor air quality, asbestos inspections and air sampling, lead inspection and risk assessment. Preferred but not required: Current certifications for asbestos, lead-based paint or mold Requirements: Valid driver's license and a reliable means of transportation Ability to pass a comprehensive background check, physical examination and pre-employment drug test Ability to travel for out-of-town work. In most cases short durations 2-5 days. This includes required training programs. Ability to carry and use a ladder, use basic hand tools, lift heavy objects and equipment necessary for a given project and must be able to wear required personal protective equipment such as hard hats, hearing protection, safety glasses, respirators, protective footwear, and additional safety equipment such as fall protection harnesses and others as required by a given task This a physically demanding position. Must be able to be outdoors for extended period of times. Lift heavy objects and conduct work in not airconditioned environments. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.

Up to $5,000 Sign-On Bonus based on Experience Performs a variety of laboratory tests on blood, tissue and body fluids using both automated and manual methods. Ensures accurate, timely reporting of lab test results in order to assist medical staff in patient care. Serves as a technical resource and performs section supervisory functions. Interacts with a variety of persons such as nursing and medical staff, physician office staff, staff from other hospitals and clients, patients and family members, sales staff and repair representatives, etc. Represents the laboratory via telephone and fax communications to various clients, customers, etc. Assists in the administration of the laboratory department at West Boca Medical Center and/or off site at West Boca Emergency Center. Coordinates a wide variety of administrative, fiscal and technical activities to ensure efficient operation of all clinical laboratories. Ensures the delivery of quality laboratory services which meets the standards of practice, established policies and procedures, and applicable laws and regulations. ********** Employment practices will not be influenced or affected by an applicant's or employee's race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.

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.

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 biological science work utilizing microbiological and molecular techniques, including, but not limited to, DNA extraction and real-time polymerase chain reaction (real-time PCR) to rapidly identify and characterize potential pathogenic bacterial and viral threat agents. Responsibilities: Handling, receipt, and processing of operational, Quality Assurance (QA), and proficiency test (PT) samples potentially containing biological threat agents. Preparing reagents and samples. Familiarity with Good Laboratory Practice (GLP). Decontamination of workspaces, including Biological Safety Cabinets (BSCs), hoods/air boxes, equipment, and other items associated with processing and analysis activities. Maintaining chain-of-custody (CoC). Interpretation of results. Data entry utilizing computerized or computer-linked systems. Performing routine equipment calibration, cleaning, assembly, and maintenance. Collecting, processing, and analyzing internal laboratory swipes/swabs for Quality Assurance/Quality Control (QA/QC) and contamination monitoring. Proper disposal of biohazardous waste. Restocking and maintaining proper inventory of necessary supplies. Supporting BW Program logistics in conducting and documenting annual inventory of DHS-procured durable equipment and property. QA/QC and acceptance testing of reagents in accordance with applicable Standard Operating Procedures (SOPs) and the Laboratory Operations Quality Assurance Program Plan (QAPP). Adhering to QA/QC requirements in accordance with the Public Health Laboratory quality management systems and the QAPP. Maintaining documentation of records demonstrating compliance with applicable training/retraining, competencies, and document reviews. Analyzing routine external QA samples in accordance with the BW SOP's and QA Program guidance. Proper archiving, storage, and shipping of samples. Follow and adhere to written procedures and accepted practices in accordance with federal, state, and local regulations, safety, security and dress code policies, procedures, and guidelines, including DHS Safeguarding Sensitive but Unclassified (For Official Use Only) Information (January 2005) when visiting or working at Government facilities. Preparing written and oral technical reports, answering questions, and making recommendations to the Lead Biological Scientist for inclusion in comprehensive reports. Accurately performing work with confidence. Demonstrate competency in various testing methodologies (e.g., multi-center studies), evaluate potential products and processes against unique environmental backgrounds, and meet established deadlines. Must be present for all hours of the workday and be available 24/7/365 to respond in case of emergency. Rotating weekends and some holidays are required. QUALIFICATIONS: Master's degree or Ph.D. from an accredited university in microbiology, molecular biology or related course work in biological sciences, and REQUIRES at least one (1) year of laboratory bench experience utilizing polymerase chain reaction (PCR), aseptic techniques and biological assays, and at least one (1) year of experience serving as a Senior Scientist or Team Leader of a laboratory team/project. Bachelor's degree from an accredited university requires four (4) years of laboratory bench experience to include one (1) year of utilizing polymerase chain reaction (PCR), aseptic techniques and biological assays, including at least one year of experience as a Team Leader/Senior Scientist. BSL-3 experience is highly desirable. #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.

This position is for an experienced Staff Level Environmental Scientist, Engineer, or Geologist responsible for undertaking project responsibilities associated with due diligence (Phase I Environmental Site Assessments (ESA)) projects, soil and groundwater field and sampling data during Phase II ESA and site assessment projects. The candidate will support and lead safety efforts on project sites, interpret results, and develop conclusions concerning environmental site conditions. With the oversight of Project Managers, the candidate will prepare reports to summarize findings, including soil and groundwater analytical data, distribution (mapping) of analytical results and groundwater flow direction, and develop additional necessary reports. This role involves developing plans and overseeing field monitoring and testing of soil and groundwater, preparing written reports related to site investigations, assessments, and remediation activities, conducting client interactions, preparing technical and cost proposals, and assisting with managing project budgets. Responsibilities * Conduct due diligence (Phase I Environmental Site Assessments (ESA)) projects. * Collect and analyze soil and groundwater field and sampling data during Phase II ESA and site assessment projects. * Support and lead safety efforts on project sites. * Interpret results and develop conclusions concerning environmental site conditions. * Prepare reports summarizing findings, including soil and groundwater analytical data, distribution of analytical results, and groundwater flow direction. * Develop additional reports necessary for projects. * Oversee field monitoring and testing of soil and groundwater for site assessment and remedial undertakings. * Prepare written reports related to site investigations, assessments, and remediation activities. * Conduct client interactions and prepare technical and cost proposals. * Assist with managing project budgets. * Follow safety rules, guidelines, and standards for all projects. * Participate in pre-task planning and report safety issues or concerns to management. * Maintain quality standards on all projects. * Sample appropriate materials (soil, vapor, groundwater) and review and interpret analytical data. * Provide recommendations for further assessment and/or remedial approach on medium-sized projects. * Participate with more Geologists or Environmental Engineers on large, more complex projects. * Perform site visits, field observations, and field data collection. * Install soil borings and monitoring wells. * Collect soil and groundwater samples, indoor air quality readings, and building material samples. * Prepare written field and final reports for clients. * Evaluate laboratory and field data and assemble in written reports. * Serve as a team member in meetings and communications with clients. * Serve as a client liaison with direct communication with clients. * Prepare technical and fee proposals. * Lead site safety on project sites. Essential Skills * Minimum 5 years of experience in environmental science, geology, or environmental engineering. * Strong knowledge of Florida soil and groundwater sampling protocols and federal, state, and local environmental regulations. * Excellent written and verbal communication skills. * Proficient in report writing and interpreting analytical data. * Experience with environmental compliance, testing, and permitting. Additional Skills & Qualifications * Degree in geology, chemistry, environmental engineering, or a related science field. * Experience working on Miami projects is a plus. Work Environment The position involves 80% office work and 20% fieldwork, typically from 8am-5pm. Occasional site visits in Fort Lauderdale (FLL) or Miami (MIA) may be required. Pay and Benefits The pay range for this position is $38.46 - $48.07/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 Fort Lauderdale,FL. Pay and Benefits The pay range for this position is $33.65 - $43.27/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 Fort Lauderdale,FL. Application Deadline This position is anticipated to close on Feb 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.

At **APTIM** , we come to work each day knowing that we are making an impact on the world. Our work spans from safeguarding and maintaining critical infrastructure to helping communities recover from natural disasters, from empowering our armed forces and first responders to reducing carbon and energy use, and from making cities more resilient against the threats of climate change to restoring contaminated ecological systems. **Job overview** APTIM is seeking a Environmental Scientist (hydrogeologist, geologist or environmental scientist) to assist the retail petroleum new-store construction team. The qualified candidate will be a hands-on professional scientist, handling a wide-range of tasks both in the field and in the office, for small to large scale construction projects. **What you can expect from APTIM:** + Work that is worthy of your time and talent + Respect and flexibility to live a full life at work and at home + Dogged determination to deliver for our clients and communities + A voice in making our company better + Investment into your personal and professional development **Key Responsibilities/Accountabilities:** + Initial responsibilities will be in the office, to include permitting, project preparation, and report writing responsibilities for construction projects across the state of Florida. + Responsibilities will include: + Preparation of Best Management Practices and application submittals for dewatering permits, following through on permit approvals to completion. + Performing Phase I/II environmental assessment field activities, including the use of complex instrumentation or equipment, and overseeing subcontractors. + Report writing for Phase I/II environmental assessments, including interpretation and presentation of collected data in reports that include text, tables, and figures suitable for client and regulatory review. + Assist Project Managers with running projects including handling project-related tasks, such as setting up Purchase Orders, scheduling subcontractors, scheduling field personal, tracking deadlines for client submittals, etc. + Must be able to work as part of a team while at the same time taking ownership of your individual projects, managing time, effort, and duties within budgetary constraints and a timeline that shifts with client needs. + Uses best practices and knowledge of internal/external business issues to improve products or services in own discipline. + Applies knowledge and skills to a wide range of standard and nonstandard situations. **Basic Qualifications:** + Bachelor's degree in Geology / Environmental Science or related degree required + 3 years experience at a minumum + Working experience in the petroleum cleanup field + Working knowledge of Florida regulations related to environmental investigations and permits. + Must have good interpersonal skills, as you'll be interacting with clients and regulatory agencies on a regular basis. + Must have strong written communication skills and an attention to detail. + Proficiency in Microsoft Office and Excel required. + Able to work outside in typical Florida conditions, during all seasons, for up to 12 hours at a time. + Valid Driver's License. + OSHA 40 Hr HAZWOPER **Who we are and what we do:** APTIM is a global industry leader headquartered in Baton Rouge, Louisiana. With more than 4,000 employees worldwide, APTIM specializes in critical infrastructure, technical and data solutions, program management, environmental services, resilience, as well as sustainability and energy solutions. Our dedicated people have the proven experience and expertise to provide integrated services and solutions to government agencies, commercial, industrial, and energy customers. APTIM is committed to accelerating the transition toward a clean and efficient energy economy, building a sustainable future for our communities and the natural world, and creating an inclusive equitable environment that celebrates the diversity of our people. Watch our video: Aptim Making a Difference \#LI-BM1 Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled Applicants with a physical or mental disability who require a reasonable accommodation for any part of the application or hiring process may make their request known by e-mailing ********************************** or calling ************ for assistance. EOE/Vets/Disability