Scientist jobs in Coral Springs, FL

MUST HAVES: Bachelors Degree in Data Science, Masters or PhD preferred 1+ year of experience within data science Python and R Coding (different packages like ggplot2, dplyr, car, caret/xgboost) and machine learning experience Econometric and statistics modeling knowledge Plusses: Marketing experience Day to day: Our client is looking for a Data Scientist to join their Marketing Technology team in Miami! This role will be supporting the creating and maintenance of data analysis and predictive models to support marketing and sales efforts. This role will focus on various stages of the model development lifecycle, including data engineering, model design, testing, deployment, and monitoring, while collaborating with cross-functional teams. The role will be hybrid, 4 days on site in Doral and 6 months contract to hire.

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.

Job Description As an R&D Scientist at Sun Nutraceuticals, you will drive the formulation and development of dietary supplements across gummies, liquids, powders, and encapsulated products, with a focus on botanicals and functional ingredients. You will create product samples for client approval, develop appealing flavor profiles, conduct research to innovate delivery systems and optimize processes, and assist with regulatory compliance. This role offers the opportunity to innovate in a fast-paced, collaborative environment within a small, agile team. Key Responsibilities Product Formulation: Design and develop gummies, liquids, powders, and encapsulated supplements, incorporating functional ingredients to meet nutritional and sensory goals. Flavor Development: Create and refine flavor profiles to ensure consumer appeal, masking off-notes from functional ingredients using techniques like natural flavors or cyclodextrins. Sample Production: Prepare lab-scale product samples for client review, iterating based on feedback to ensure formulations are scalable and meet expectations. Research & Development: Conduct R&D to innovate new product concepts, enhance ingredient delivery, and streamline manufacturing processes to reduce costs as we scale. Regulatory Compliance: Assist with ensuring formulations comply with FDA regulations, including ingredient safety, labeling, and documentation for claims. Process Optimization: Experiment with production techniques to improve efficiency, such as optimizing gel strength and setting time with pectin or gelatin, to support cost-effective scaling. Collaboration: Work closely with internal teams and clients to align product development with market needs and stringent regulatory requirements. Requirements Education: Bachelor’s or Master’s degree in Food Science, Nutrition, Chemistry, Pharmaceutical Sciences, or a related field. Experience: 3–5 years of experience in dietary supplement, nutraceutical, or food product development, preferably with gummies, liquids, powders, or encapsulated products. Proven track record in formulation, flavor development, and sample creation. Familiarity with botanicals (e.g., cannabinoids, kratom, kava, mushrooms) and bitterness-masking techniques are a plus, but not required. Skills: Strong formulation and flavor development expertise for dietary supplements, including botanical-based products. Knowledge of delivery systems (e.g., solubility enhancement) and production processes for diverse product forms. Understanding of FDA regulations, cGMP, and NSF standards for dietary supplements, particularly for alternative botanicals. Ability to conduct independent R&D and troubleshoot formulation or process challenges. Excellent communication and collaboration skills for working with clients and a small team. Preferred: Experience with pectin-based gummies, liquid emulsions, powder blends, or encapsulation techniques. Experience with HPLC analysis of raw materials, in-process materials, and finished products to quantify and qualify ingredients. Hands-on experience with regulatory documentation or label compliance for dietary supplements. Benefits Health Care Plan (Medical, Dental & Vision) Paid Time Off (Vacation, Sick & Public Holidays) Training & Development Free Food & Snacks

Responsible for product support investigations and improvements to existing products and procedures. Works independently to analyze and troubleshoot product issues and provide solutions. Responsible for leading smaller, independent, new product feasibility and product improvement efforts. Also works independently to help solve problems in other departments - primarily with the Production, Supply Chain, and Quality Control departments. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. • Learn and maintain a thorough understanding of all products by understanding how product performance is influenced by product designs, manufacturing, quality, and supplier processes. • Provide prompt and accurate investigation into product nonconformities and issues by evaluating, troubleshooting, conducting experiments, and drawing conclusions to drive suitable solutions. • Working with internal teams (Manufacturing, Quality, Supply Chain, Customer Care, etc,) to gather critical data as part of the investigation. • Design, plan and implement experiments to meet development and research goals • Evaluate and report experimental findings, interpret results and provide recommendations of action • Present project status, study results, and conclusions • Develop short-term plans for smaller projects to support, improve, and develop products • Provide ideas for creative, efficient problem solving SUPERVISORY RESPONSIBILITIES This job requires no supervisory responsibilities. EDUCATION and/or EXPERIENCE • Doctoral degree (Ph.D.) in Chemistry, Biochemistry or related technical discipline, with 1 or more years of product support and/or development experience • Master's Degree (M.S. or M.A.) in Chemistry, Biochemistry or related technical discipline plus 2 or more years of relevant industrial experience; -AND/OR- • Bachelor's degree (B.S or B.A.) in Chemistry, Biochemistry or related technical discipline plus 3 or more years of relevant industrial experience • Experience with chemical/biochemical testing is required. Direct experience with lab-bench work, formulation work, spectrophotometric assays, titration assays, microscopy and UV-vis spectrophotometry. • Experienced in biosensors and/or bioanalytical assay development and troubleshooting. Knowledge of electrochemistry is preferred, not required. KNOWLEDGE AND SKILLS Familiarity with 21 CFR 820, ISO 15197, and ISO 13485 QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. COMMUNICATION SKILLS Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to write procedures, specifications and SOPs that confirm to the company's prescribed style and format. Ability to effectively present information to senior management within and outside R&D. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability, validity and correlation techniques. REASONING ABILITY Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret a variety of technical instructions in mathematical or diagram form and deal with abstract and concrete variables. CERTIFICATES, LICENSES, REGISTRATIONS Minimum of Doctorial, Master's, and/or bachelor's degree in chemistry, biochemistry or related fields. PHYSICAL DEMANDS The physical demands described are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions While performing the duties of this job, the person in this position needs to move about inside the office and laboratory areas; must be able to remain in a stationary position for prolonged periods of time; frequently operate a computer and laboratory related equipment. Person in this position frequently communicates with others and must be able to exchange accurate information. Individual is required to have close visual acuity to perform activities such as documenting experimental results; preparing and analyzing data and figures; viewing a computer terminal; operating equipment and visual inspection of small parts. Individual must be able to frequently move objects (up to 10 lbs.) from one level to another and occasionally move objects (up to 25 lbs.) from one level to another. Travel requirements: ≤ 10% WORK ENVIRONMENT The work environment described is representative of that which an employee may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee in this position is expected to work regularly in a laboratory environment. While performing the duties of this job, the employee is required to work with biological samples which may expose him/her to bloodborne pathogens. The employee may be exposed to moving mechanical parts, fumes or airborne particles, and toxic or caustic chemicals. Appropriate use of Personal Protective Equipment (PPE) is required. Employee should fully understand applicable safety regulations and GLP/GMP/GCP guidelines and apply them appropriately. Employee will be expected to train other employees in relevant safety / compliance requirements and laboratory procedures. Trividia Health uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ******************** EQUAL OPPORTUNITY EMPLOYER: Trividia Health, Inc. is an Equal Opportunity, Affirmative Action, E-Verify employer. Employment decisions for all applicants and employees will be made without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, age, national origin, marital status, veteran status, disability or other characteristics protected under local, state or federal law.

Job Description Responsible for product support investigations and improvements to existing products and procedures. Works independently to analyze and troubleshoot product issues and provide solutions. Responsible for leading smaller, independent, new product feasibility and product improvement efforts. Also works independently to help solve problems in other departments – primarily with the Production, Supply Chain, and Quality Control departments. **ESSENTIAL DUTIES AND RESPONSIBILITIES ** include the following. Other duties may be assigned. Learn and maintain a thorough understanding of all products by understanding how product performance is influenced by product designs, manufacturing, quality, and supplier processes. Provide prompt and accurate investigation into product nonconformities and issues by evaluating, troubleshooting, conducting experiments, and drawing conclusions to drive suitable solutions. Working with internal teams (Manufacturing, Quality, Supply Chain, Customer Care, etc,) to gather critical data as part of the investigation. Design, plan and implement experiments to meet development and research goals Evaluate and report experimental findings, interpret results and provide recommendations of action Present project status, study results, and conclusions Develop short-term plans for smaller projects to support, improve, and develop products Provide ideas for creative, efficient problem solving SUPERVISORY RESPONSIBILITIES This job requires no supervisory responsibilities. EDUCATION and/or EXPERIENCE Doctoral degree (Ph.D.) in Chemistry, Biochemistry or related technical discipline, with 1 or more years of product support and/or development experience Master’s Degree (M.S. or M.A.) in Chemistry, Biochemistry or related technical discipline plus 2 or more years of relevant industrial experience; -AND/OR- B ac h e lor’s degree (B.S or B.A.) in Chemistry, Biochemistry or related technical discipline plus 3 or more years of relevant industrial experience Experience with chemical/biochemical testing is required. Direct experience with lab-bench work, formulation work, spectrophotometric assays, titration assays, microscopy and UV-vis spectrophotometry. Experienced in biosensors and/or bioanalytical assay development and troubleshooting. Knowledge of electrochemistry is preferred, not required. KNOWLEDGE AND SKILLS Familiarity with 21 CFR 820, ISO 15197, and ISO 13485 QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. COMMUNICATION SKILLS Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to write procedures, specifications and SOPs that confirm to the company’s prescribed style and format. Ability to effectively present information to senior management within and outside R&D. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability, validity and correlation techniques. REASONING ABILITY Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret a variety of technical instructions in mathematical or diagram form and deal with abstract and concrete variables. CERTIFICATES, LICENSES, REGISTRATIONS Minimum of Doctorial, Master’s, and/or bachelor’s degree in chemistry, biochemistry or related fields. PHYSICAL DEMANDS T he physical demands described are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions While performing the duties of this job, the person in this position needs to move about inside the office and laboratory areas; must be able to remain in a stationary position for prolonged periods of time; frequently operate a computer and laboratory related equipment. Person in this position frequently communicates with others and must be able to exchange accurate information. Individual is required to have close visual acuity to perform activities such as documenting experimental results; preparing and analyzing data and figures; viewing a computer terminal; operating equipment and visual inspection of small parts. Individual must be able to frequently move objects (up to 10 lbs.) from one level to another and occasionally move objects (up to 25 lbs.) from one level to another. Travel requirements: ≤ 10% WORK ENVIRONMENT The work environment described is representative of that which an employee may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee in this position is expected to work regularly in a laboratory environment. While performing the duties of this job, the employee is required to work with biological samples which may expose him/her to bloodborne pathogens. The employee may be exposed to moving mechanical parts, fumes or airborne particles, and toxic or caustic chemicals. Appropriate use of Personal Protective Equipment (PPE) is required. Employee should fully understand applicable safety regulations and GLP/GMP/GCP guidelines and apply them appropriately. Employee will be expected to train other employees in relevant safety / compliance requirements and laboratory procedures. EQUAL OPPORTUNITY EMPLOYER: Trividia Health, Inc. is an Equal Opportunity, Affirmative Action, E-Verify employer. Employment decisions for all applicants and employees will be made without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, age, national origin, marital status, veteran status, disability or other characteristics protected under local, state or federal law.

Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on women's health. Our first Research and Development facility in the US is located in Coral Springs, Florida which focuses on generic and branded orally inhaled and nasal drug products. Somerset, New Jersey is home to one of Fifteen commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, as well as additional Research and Development teams. Lupin is prided on being people-focused and centered around how impactful we are with our customers. Dollars are not a measure of success but rather the people we help along the way. Responsibilities Role Summary Conducts laboratory activities following Standard Operating Procedures (SOPs). Assures that quality standards are met. Documents activities following cGMP rules. Essential Duties and Responsibilities Conduct laboratory activities with limited supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Lupin, FDA and other governing bodies. Independently set up and operate lab equipment, prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all testing performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine calculations. Support the manufacture of Dry Powder Inhaler and Metered Dose Inhaler drug products. Perform equipment qualification and calibrations as directed Execute approved method transfer protocols Assist in the training of other chemists Perform other tasks as assigned Participate in project activities and support project timelines and proactively contribute to meeting the team objectives. Communicates effectively with team members. Establish and maintain effective relationships with team members Conduct lab work in accordance with SOPs; follow corporate safety rules and procedures. Comply with all Corporate guidelines and policies Qualifications Education & Experience BS Degree preferably in chemistry, pharmacy or related fields. 0-2 years' experience with a BS. Familiarity with analytical methodology, laboratory practices, wet-chemistry, manufacturing or process equipment used in laboratories such as HPLS/UPLC, UV-Vis, powder blender, etc. Computer literacy (MS-Word, Excel and Powerpoint). Effective English written and oral communication skills. Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion, age, disability, veteran's status, or any other classification as required by applicable law. Physical Requirements The physical requirements of the position generally include: standing, walking, sitting, using hands and fingers, reaching with hands and arms, talking and hearing. In some circumstances, bending, kneeling, crouching, stooping, and crawling may apply. This position may require lifting up to 15 pounds occasionally. Generally work is performed in an office environment. Search Firm Representatives Please Read Carefully Lupin USA, and its Affiliates does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms for any current openings at our company without a valid written search agreement in place will be deemed the sole property of Lupin. No fee will be paid in the event a candidate is hired by Lupin as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, No phone calls or emails

Job Description 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.

Minimum Job Requirements Ph.D. in epidemiology or related field 4-7 years of experience in a University or academic medical center environment 2-4 years of work experience leading and contributing to multi-site research protocols, grant and manuscript writing, and implementing science initiatives Knowledge, Skills, and Abilities Experience in healthcare research setting to include management responsibility Experience coordinating, implementing and supervising live recruitment studies, including the preparation of clinical protocols and correspondence with the IRB, authoring consent forms, designing data collection tools and creating study tracking databases, preferred Knowledge of research principles, design and strategies, and data interpretation methods Able to work independently in accordance with established objectives Detail oriented, highly motivated, and committed to achieving excellence in the form of productivity and publications Able to negotiate and manage time commitments and resources Able to acquire and maintain knowledge of systems and databases Able to develop and present professional reports and presentations to senior-level audiences Able to develop and implement research instruments Ability to function in a team environment Job Summary Serves as a key collaborator to investigators, providing clinical and behavioral research expertise. Participates in ongoing implementation science, quantitative and qualitative research, and pursues independent and collaborative research. Focuses on implementation science and also broadly contributes to a variety of activities including health outcomes, quality of life, and population health initiatives. Job Specific Duties Designs and conducts research studies, such as personalized medicine, quality of life, implementation science, and other priority areas. Collaborates with other investigators in developing and executing interdisciplinary clinical research. Provides consultation to investigators and project coordinators on clinical study design and development of research questions. Leads or supports the preparation of extramural grant applications and contracts. Analyzes and interprets complex data for reporting, presentations and publications. Contributes to high level discussions with funding agencies and research teams within organization and with collaborating organizations. Makes decisions for day-to-day operations of projects including the resolution of technical problems and questions from project staff. Monitors progress of study activities (e.g. data collection and validation, recruitment, pilot studies, focus groups, etc.) and ensures that study objectives are met. Collaborates with researchers, biostatisticians, data scientists, graduate students, residents and clinical fellows to ensure progress of studies. Oversees data collection and direct data analysis by staff. As a subject matter expert, trains and mentors researchers and trainees in scientific writing including grantsmanship and manuscript development.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: To be part of a team of Scientists & Engineers providing dedicated technical expertise to customers to ensure robust, reliable, and sustainable support to their processing needs using MilliporeSigma technologies at all stages of drug development and manufacturing. * Provide sound technical recommendations and consultations after appropriate internal discussions; able to set project commitments and follow through in a timely fashion. * Communicates on project status or issues with manager and concerned support team members in a timely fashion. Proactively works to propose and discuss solution options and approaches for various technical or problem-solving needs; Has a reputation for trustworthiness * Works effectively in cross-functional teams; actively participates and leads team discussions and brings potential conflicts to management attention in a timely fashion. * Brings new ideas and ways of solutions to technical managers' and teams' attention. Actively proposes new ways and methods to add value to what TSS group does. * Promote your position and services among our customers and potential customers. * Passionate about science & technology * Being Curious with eagerness to learn & develop * Motivated by making positive impact on society * Possessing a Collaborative mindset and Empowering others' success * Being a Self-starter * Travel 30% domestically & internationally (Cost Rica, Panama, Guatemala, El Salvador, Dominican Republic, Nicaragua, Burlington MA & Argentina Physical Attributes: Ability to lift small equipment up to15 pounds Location: A field-based role located in San Juan Puerto Rico area Who You Are: Minimum Qualifications * Bachelor´s degree in the Life Sciences or in Biology, Mechanical engineering or Chemical Engineering (some examples: Bioprocessing Engineering or Biotechnology, Bioengineering, Biochemistry, Bioscience, Biology) * 5+ years of experience in the pharmaceutical industry. * Fluent in Spanish and English (written and oral) Preferred Qualifications: * Sound knowledge of engineering fundamentals- especially fluid dynamics. * Practical sensibility of engineering design and system operation with a hands-on approach. * Strong time management and verbal and written communication skills. * Strong interpersonal and teamwork skills. * Sound knowledge of the application of engineering fundamentals to bioprocess separations. A current and high level of technical competency in our markets, applications, and products. Recognized as an internal expert on application of customer processes to Millipore technologies. * Hands-on experience with operating and troubleshooting separation systems at lab, pilot, and industrial scale. Also possess excellent hand-on skills with membrane and media technologies. * Excellent time management and verbal and written technical communication and presentation skills. Produce solid, defensible, and publishable data. * Excellent interpersonal skills. Active participant as the TSS representative on complex projects involving diverse groups. RSREMD Base pay range for this position is 76,100 - 121,700/year Our ranges are derived from several sources, and largely reliant on relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors. This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k)-matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

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

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. By harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making-we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible. The Scientist I Reagent Manufacturing for Beckman Coulter Diagnostics is responsible for manufacturing products per Manufacturing Batch Records (Paper and/or electronic) using various system and equipment Standard Operating Procedures (SOPs). Maintaining accurate records of work performed according to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Quality System Regulations (QSRs). Schedule and perform Preventive Maintenance of equipment. Perform Indirect Labor tasks such as Inventory counting, Material transactions, process verifications, and troubleshooting malfunctions. This position is part of the Cytometry Department located in Beckman Coulter, Hialeah FL and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. In this role, you will have the opportunity to: Perform In-Process testing by following experimental protocols and analyze results by means of a variety of Lab Instrumentation (pH, Osmometer, Spectrophotometer, Fluorometer, wet chemistry methods, etc.) Maintain accurate records of work performed according to GLP, GMP, and QSRs and equipment under a maintenance schedule and/or calibration Fulfill indirect labor tasks such as inventory, material transactions, process verifications, daily management of the lab, layered audits in a rotational cadence, and general instrument troubleshooting. Drives Continuous Process Improvement and contributes technical expertise and direction for root-cause analysis, implementation and sustainment Collaborates with departments and colleagues within and outside of Production, including, but not limited to, Manufacturing Technical Operations, QC, QA, Development, Engineering, etc. The essential requirements of the job include: Bachelor's Degree in a Biology, Chemistry, or related scientific field Ability to operate in a fast-paced environment. Proficient in Excel is a MUST, Microsoft Word, and general Microsoft software Physical/Environment Requirements: Ability to lift 50 pounds with or without assistance Ability to stand 6 to 7 hours a day. It would be a plus if you also possess previous experience: Experience working in an FDA regulated environment laboratory, and using aseptic techniques Basic troubleshooting skills to identify minor issues with machinery and ability to read and interpret technical documents. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.

Atlantic Pacific Companies is a dynamic industry leader, with a growing and diverse portfolio of properties throughout Florida, Georgia, Texas, California, North Carolina, and Washington, D.C. We are looking for passionate people who enjoy challenges and helping others. Does this sound like you? Join us! Want to be a part of a dynamic real estate team? We are looking for an Acquisitions Research Associate ready to take their career to the next level. Our Acquisitions Research Associates are involved in identifying land and securing financing for affordable housing developments that make a lasting difference at Atlantic Pacific Companies and the communities we serve. Atlantic Pacific Companies strives to bring out the best in our people and empowers them to provide excellence to the communities we serve. We mentor our staff, give them as much responsibility as they can handle, and award autonomy and career growth as merited. We enjoy working smart and hard: the best ideas win, and your contribution to our team's performance is the only constraint to your growth. Be a part of our fast-paced, growing team! Using research and analytical skills, the Acquisitions Research Associate will support the Acquisitions/Applications team in researching real estate opportunities and providing support for applications to federal, state, and local governments for affordable and workforce housing. They will act as a key support person in identifying, researching and presenting potential development sites to the executive acquisitions team. Your role will include maintaining and enhancing the quality of our GIS datasets to support ongoing and future projects. Any prior knowledge of, and experience with the Low-Income Housing Tax Credit (LIHTC) program, GIS, or grant writing is beneficial. Responsibilities include, but are not limited to: Research, analyze and interpret Qualified Allocation Plans and federal, state, and local government affordable housing program rules and regulations Search for development opportunities, such as Request for Qualifications and Request for Proposals, conduct preliminary screening, analyze opportunities, and assist in the preparation of the submission Identifying land acquisition opportunities that align with strategic goals Conducting zoning and planning research Assist with preparation and submitting funding applications to federal, state, and local government finance agencies Assist in research and data collection and updating databases for mapping projects using GIS, Google Earth, Google Maps Assist the team with acquisition and underwriting due diligence Attend meetings and workshops as necessary Maintain pertinent paper and electronic files and records by naming conventions, ensuring complete, accurate, and organized files Perform related duties as required Requirements: Bachelor's degree High proficiency with computer software, including Microsoft Outlook, Word, Excel, PowerPoint, Adobe Acrobat, and Google Earth. Experience with ESRI products and Python programming language is a strong plus. Demonstrated attention to detail, interpersonal skills, and ability to work both independently and as part of a team Strong writing skills Ability to multi-task and prioritize Experience with grant writing, State or federal housing programs, particularly the LIHTC program is a strong plus. Some travel (overnight) and the ability to work flexible hours to meet deadlines required. What We Offer: 100% Employer-Paid Health Insurance options (after 30 days of employment). Flexible Spending Accounts, Life Insurance, Long-Term Disability, and other supplemental insurance benefits Paid Time-Off/Holidays - New Year's Day, Memorial Day, Juneteeth, Independence Day, Labor Day. Thanksgiving Day, Day after Thanksgiving, Christmas Day, and a Personal Floating Holiday to use as you see fit 401(k) Retirement Plan Employee Referral Program Employee Assistance Program Employee Discounts Program on Rental cars, Movie Tickets, Disney Tickets, and Gym memberships, to name a few Yearly Recognition Gifts For more information, please visit Our Website Follow Us: Facebook LinkedIn Twitter Atlantic Pacific Companies is a drug-free workplace. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Disclaimer: The tasks and responsibilities listed are not the only ones applicable to the positions

Enjoy 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. If 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. 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 Tuesday – Saturday 8a-4:30p. Occasional holiday and weekends required. How You'll Contribute: We always do whatever it takes, even if it isn’t specifically our “job.” In general, the Embryologist is responsible for: Clinical and technical standards Perform the following aspects of Assisted Reproductive technology (ART) procedures including but not necessarily limited to: i. oocyte retrieval ii. sperm preparation for insemination iii. in-vitro fertilization (IVF) iv. fertilization check v. embryo evaluation vi. selection of embryos for transfer and vitrification vii. embryo vitrification viii. embryo thawing ix. embryo transfer x. surgical sperm retrieval and processing xi. cell to tube transfer of embryo biopsy material xii. micromanipulation (1) ICSI (2) Assisted hatching (3) Embryo biopsy Prepare embryo culture dishes and solutions required for ART procedures using sterile tissue culture techniques. Perform embryology and andrology proficiency testing required by CAP-approved agency (ABB, CAP). Assure proper sample collection, delivery and identification, including PGT samples for release. Perform safe handling of specimens by following the safety guidelines for biohazardous, infectious and toxic substances in the IVF laboratory. Document quality assurance activities including description of unusual incidents, problems, and appropriate corrective action. Perform daily/weekly quality control for procedures and equipment used in the IVF Laboratory. Prepare semen specimens for intrauterine inseminations (IUIs). Perform all aspects of reproductive tissue (sperm, oocyte and embryo) cryopreservation/vitrification including sample identification, inventories, checks of serology screening, freezing and thawing procedures. Maintain laboratory records, reports, quality assurance data and assist in preparation of SART, Artworks, and Cryomodule data. Assist in the preparation of data for clinical meetings Operate laboratory equipment including laminar flow hoods, microscopes, centrifuges, analytical balance, pH meter Set up, calibrate and clean laboratory equipment and glassware, and assure routine maintenance and repairs are performed and documented. Perform various office functions including photocopying, answering telephones, scheduling appointments, faxing and filing reports. Laboratory Services/Operations Attend monthly IVF laboratory meetings and periodic staff meetings. Assist in research projects under the IVF Laboratory Director’s supervision. Assist in training and assigning work to junior IVF support staff. Communicate with center personnel, medical staff, patients and outside resources to ensure high quality patient care. Assist laboratory personnel in performing laboratory services in accordance with Federal, State and local laws and guidelines to ensure laboratory maintains accreditation. Assist as required in maintaining laboratory operations in conformity with OSHA and CLIA ‘88 regulations. Must meet CLIA ‘88 requirements of education and experience for General Supervisor or Technical Supervisor. Must be thoroughly familiar with Laboratory Operations Manual. Must demonstrate skills and aptitude appropriate to the position. Must demonstrate an ability to function effectively without direct supervision and to perform laboratory services in accord with the Laboratory Philosophy and Operating Standards. 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. What You'll Bring: Bachelor’s degree in biological science required. 2-3 years minimum experience, 4-6 years preferred. Preferred Certification/License: American Board of Bioanalysis: Embryology and Andrology Florida CLS license with ASCP certification required only if performing diagnostic semen analysis Ability to access, input, and retrieve information from a computer. Knowledge of office procedures and office machines (i.e. computer, fax, copier, etc.). Ability to work as part of a multi-disciplinary team. Ability to communicate accurately and concisely. Excellent interpersonal skills Demonstrated expertise in continuous quality improvement, customer service, and team building. Ability to travel throughout the San Francisco Bay area. More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful. What We Offer: Competitive pay + bonus Comprehensive training Medical, dental, vision, and 401(k) matching Generous paid time off and holidays Retirement plan Tuition assistance Ability to make an impact in the communities we serve At IVF Florida, we promote and develop individual strengths in order to help staff grow personally and professionally. To learn more about our company and culture, visit here. How To Get Started: To 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.

DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an MD or DO for our clinical research site in Miami, FL to serve as a sub-investigator on clinical research trials. This medical professional will conduct clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes. Responsibilities Conduct physical exams per protocol Review labs and assess abnormalities for clinical significance per protocol Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies. Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site. Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants. Interprets protocols and IB and participates in initiatives to strategize for patient recruitment. Carries out clinical evaluation and assessment of participants to ensure eligible participants are enrolled onto studies. Ensures and protects the welfare and safety of participants through ethical conduct. Fulfills and comply with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations. Exercises meticulous attention to detail in documentation and patient care. Requirements Medical License (MD, DO) - Florida Spanish Bilingual a plus.

Enjoy 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. If 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. 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 Tuesday - Saturday 8a-4:30p. Occasional holiday and weekends required. How You'll Contribute: We always do whatever it takes, even if it isn't specifically our “job.” In general, the Embryologist is responsible for: Clinical and technical standards Perform the following aspects of Assisted Reproductive technology (ART) procedures including but not necessarily limited to: i. oocyte retrieval ii. sperm preparation for insemination iii. in-vitro fertilization (IVF) iv. fertilization check v. embryo evaluation vi. selection of embryos for transfer and vitrification vii. embryo vitrification viii. embryo thawing ix. embryo transfer x. surgical sperm retrieval and processing xi. cell to tube transfer of embryo biopsy material xii. micromanipulation (1) ICSI (2) Assisted hatching (3) Embryo biopsy Prepare embryo culture dishes and solutions required for ART procedures using sterile tissue culture techniques. Perform embryology and andrology proficiency testing required by CAP-approved agency (ABB, CAP). Assure proper sample collection, delivery and identification, including PGT samples for release. Perform safe handling of specimens by following the safety guidelines for biohazardous, infectious and toxic substances in the IVF laboratory. Document quality assurance activities including description of unusual incidents, problems, and appropriate corrective action. Perform daily/weekly quality control for procedures and equipment used in the IVF Laboratory. Prepare semen specimens for intrauterine inseminations (IUIs). Perform all aspects of reproductive tissue (sperm, oocyte and embryo) cryopreservation/vitrification including sample identification, inventories, checks of serology screening, freezing and thawing procedures. Maintain laboratory records, reports, quality assurance data and assist in preparation of SART, Artworks, and Cryomodule data. Assist in the preparation of data for clinical meetings Operate laboratory equipment including laminar flow hoods, microscopes, centrifuges, analytical balance, pH meter Set up, calibrate and clean laboratory equipment and glassware, and assure routine maintenance and repairs are performed and documented. Perform various office functions including photocopying, answering telephones, scheduling appointments, faxing and filing reports. Laboratory Services/Operations Attend monthly IVF laboratory meetings and periodic staff meetings. Assist in research projects under the IVF Laboratory Director's supervision. Assist in training and assigning work to junior IVF support staff. Communicate with center personnel, medical staff, patients and outside resources to ensure high quality patient care. Assist laboratory personnel in performing laboratory services in accordance with Federal, State and local laws and guidelines to ensure laboratory maintains accreditation. Assist as required in maintaining laboratory operations in conformity with OSHA and CLIA ‘88 regulations. Must meet CLIA ‘88 requirements of education and experience for General Supervisor or Technical Supervisor. Must be thoroughly familiar with Laboratory Operations Manual. Must demonstrate skills and aptitude appropriate to the position. Must demonstrate an ability to function effectively without direct supervision and to perform laboratory services in accord with the Laboratory Philosophy and Operating Standards. 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. What You'll Bring: Bachelor's degree in biological science required. 2-3 years minimum experience, 4-6 years preferred. Preferred Certification/License: American Board of Bioanalysis: Embryology and Andrology Florida CLS license with ASCP certification required only if performing diagnostic semen analysis Ability to access, input, and retrieve information from a computer. Knowledge of office procedures and office machines (i.e. computer, fax, copier, etc.). Ability to work as part of a multi-disciplinary team. Ability to communicate accurately and concisely. Excellent interpersonal skills Demonstrated expertise in continuous quality improvement, customer service, and team building. Ability to travel throughout the San Francisco Bay area. More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful. What We Offer: Competitive pay + bonus Comprehensive training Medical, dental, vision, and 401(k) matching Generous paid time off and holidays Retirement plan Tuition assistance Ability to make an impact in the communities we serve At IVF Florida, we promote and develop individual strengths in order to help staff grow personally and professionally. To learn more about our company and culture, visit here. How To Get Started: To 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.

When you join Groundwater & Environmental Services, Inc. (GES), you are not a number - you become the reason for our success. You'll have the opportunity to carve your own career path while working shoulder-to-shoulder with some of the most talented and dedicated professionals in the industry. By combining our unique talents and expertise, we help the world's leading organizations solve their most complex environmental challenges. We work hard, and we have a lot of fun while we're at it. Our core values are centered on doing what's right - for our clients, our employees, and our community. Our employees benefit from a supportive, collaborative culture and an entrepreneurial spirit that promotes new ideas and shared learning. Groundwater & Environmental Services, Inc. (GES), an industry leader with a reputation for excellence in providing environmental consulting, engineering, compliance, and technical field services to clients in diverse market sectors, seeks an entry to mid-level Biologist or Environmental Scientist to support fieldwork and environmental remediation project activities. Position Description * Perform work associated with environmental permitting which may include natural resources inventory, wetland delineations, species assessments, and environmental sampling (chemical and biological). * Field work including completing wetland delineations and species surveys. * Stream Assessment (perennial/ intermittent/ ephemeral), Stream Reach Condition Studies and Benthic surveys. * 401/404 Permitting Documents and Agency Coordination, use of COE Regional Supplements for 404 wetland delineations. * Familiar with local, state and federal water quality laws (CWA, RHA Section 10, ESA, NHPA, NEPA, etc.). * Exposure to or use of Rosgen Natural Channel Design (Levels I, II, III or IV), a plus. * Field identification of flora and fauna including endangered and threatened species. * Perform Phase 1 and 2 environmental site assessments (soil, groundwater, soil gas, air, etc.), sampling, monitoring well installation, and related reporting. * Communicates with clients, third party and regulatory agents regarding project status, schedules and compliance issues. * Perform site investigations and develop SPCC Plans and SWPPP documents. * Ensures adherence to client and corporate contract specifications in all activities including Health, Safety, Security, and Environment. Skills & Requirements * A Bachelor of Science in Environmental Science, Biology, Ecology, Geology, Earth Sciences, Environmental Studies, Forestry, Wildlife Biology, or related field is required. Masters of Science a plus. * 0-5+ years of related experience. Experience must include hands on field and office project/task execution (preferably in a responsible position commensurate with employment level) based in environmental consulting field. Case management experience on retail petroleum and/or industrial projects preferred. * Must possess excellent communication and technical writing skills and be able to independently prepare a complete deliverable report with a focus on QA/QC. Proficient in the use of Microsoft Office suite software. * Experience using GPS equipment and developing data dictionaries for specific GPS data collection efforts to feed into GIS data display and map production. * Willingness to learn new skills and accept challenging task assignments. * Applicants must be eligible to work in the US and have a valid driver's license. Our comprehensive benefits program includes: Hybrid workforce, medical, dental, vision, prescription, 401k, FSA, STD, LTD, New Parent Leave, 529 College Bound Fund, Tuition Assistance, Bonus Plan, and more. Employee benefits are available to regular full-time and part-time employees in accordance with our company policy. Groundwater & Environmental Services, Inc. (GES) believes that diversity and inclusion among our staff is critical to our success, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool. At GES, we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and employees without regard to race, color, religion, gender, pregnancy, national origin, age, disability, marital status, sexual orientation, gender identity or expression, military and veteran status, and any other characteristic protected by law.

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.

Essential Duties and Responsibilities This role does NOT offer visa sponsorship or visa transfer for work authorization. External applicants must be eligible to work in the US. Conduct standard and advanced laboratory activities independently including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Independently set up and operate lab equipment, conduct instrument and analytical method troubleshooting; research and recommend corrective actions for out-of-specification and out-of-trend results. Execute approved method transfer protocols, develop and validate analytical methods Prepare and maintain accurate records in lab notebooks of all testing performed. Analyze data, identify trends and perform statistical analysis. Write protocols, methods, standard operation procedures, and submission documents independently. Design experimental studies and write reports with minimal supervision. Independently conduct manufacturing activities for inhalation drug products. Support the evaluation and introduction of new technologies; be capable of generating new practical ideas; possess good understanding of experimental design. Participate in project activities and support project timelines and proactively contribute to meeting the team objectives. Communicate effectively with team members and internal or external customers. Work and communicate effectively with other functional groups. Lead broad project tasks effectively, with minimal supervision. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate Health & Safety rules and procedures. Comply with all Corporate guidelines and policies. Qualification Requirements Sr. Scientist 1- PhD in Chemistry or Pharmacy or related fields with at least 6 years ; MSc with at least 8 years or BSc with at least 11 years of experience in pharmaceutical or related fields. Sr. Scientist 11- PhD in Chemistry or Pharmacy or related fields with at least 8 years ; MSc with at least 10 years or BSc with at least 14 years of experience in pharmaceutical or related fields. Experience in aerosol sciences preferred. Must possess broad analytical chemistry knowledge in HPLC, GC, UV, FTIR and other related analytical technologies and/or broad knowledge of development and manufacturing of inhalation drug products. Knowledge and broad understanding of FDA cGMP requirements as they apply to the Pharmaceutical industry. Good understanding of USP methodologies and ICH guidelines. Strong English language skills including writing ability and oral communication

Job Description 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