Scientist Jobs in Ives Estates, FL

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Molecular Devices, 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. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Join Molecular Devices and help drive scientific discovery for life science customers in academia, biotech, pharma, and government. Our automated and AI-enabled technology empowers researchers to tackle complex questions and gain deep insights, accelerating the development of safer, more effective therapeutics. As part of our team-rooted in collaboration, authenticity, and innovation-you'll ultimately contribute to groundbreaking science that enhances lives globally and shapes a healthier future for all. Learn about the Danaher Business System which makes everything possible. We are seeking an experienced and innovative Data Scientist with a specialization in image analysis and a passion for leveraging artificial intelligence within the life sciences domain. In this role, you will be involved in the develop and implementation of advanced AI-driven image analysis solutions to drive breakthrough insights in areas such as drug discovery, diagnostics, and biomedical research. You will work closely with cross-functional teams, including biologists, data scientists, and software engineers, to transform complex image data into actionable insights that inform critical decision-making. This position reports to the Manager, Software Engineering and is part of the R&D-Team located in Bellevue, Seattle and will be an on-site role. In this role, you will have the opportunity to: Advanced Image Analysis & AI Integration: Develop and optimize AI algorithms for image analysis, collaborate with teams to solve biological challenges, and create innovative algorithms for feature extraction and pattern recognition. Data Management & Processing: Oversee the collection and preprocessing of large-scale image datasets, and develop scalable data pipelines for comprehensive analysis. Research & Development: Stay updated with the latest AI and computer vision advancements, lead research initiatives, and contribute to scientific publications and patents. Collaboration & Communication: Work with biologists and stakeholders to understand analytical needs, and present findings clearly to both technical and non-technical audiences. Project & Process Management: Manage projects to ensure timely delivery and quality, document methodologies, and evaluate emerging AI tools to enhance team capabilities. The essential requirements of the job include: Education: Bachelor's degree in Data Science, Computer Science, Bioinformatics, Life Sciences, or a related field. A Master's or Ph.D. is strongly preferred. Experience: Minimum of 7 years in data analysis, with at least 3 years focused on image analysis in the life science or biomedical research sector, and experience in applying AI and machine learning techniques to image data. Technical Skills: Proficiency in Python and/or R, experience with AI libraries (e.g., TensorFlow, PyTorch, Keras), and strong expertise in image processing tools (e.g., OpenCV, scikit-image, Matlab, ImageJ). Domain Knowledge: Understanding of biological imaging techniques (e.g., fluorescence microscopy, MRI, CT scans) and familiarity with life science research and clinical applications. Analytical & Problem-Solving Skills: Strong analytical mindset, ability to develop and implement complex data-driven solutions, and manage competing priorities effectively. It would be a plus if you also possess previous experience in: Experience with advanced topics such as GANs, video analysis, or 3D image reconstruction Experience in publishing research in peer-reviewed journals or presenting at scientific conferences. Experience in integrating multi-modal data sources (e.g., imaging data with genomic data). Contributions to computer vision open-source projects or competition rankings (e.g., Kaggle, ImageNet). Molecular Devices, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. The salary range for this role is $130K-$160K . This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. 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.

Machine Learning Applied Scientist - Permanent - Miami, FL - $150,000 - $200,000. The final salary or hourly wage, as applicable, paid to each candidate/applicant for this position is ultimately dependent on a variety of factors, including, but not limited to, the candidate's/applicant's qualifications, skills, and level of experience as well as the geographical location of the position. Applicants must be legally authorized to work in the United States. Visa sponsorship not available. Our client is seeking a Machine Learning Applied Scientist in Miami, FL. Role Description Job Description As an ML Applied Scientist you will play a pivotal role in supporting tech leadership through your work on critical path projects, core architectural design, and forward-thinking research initiatives. You will participate in the design of key ML initiatives by focusing on the design, development and deployment of ML models and systems to enhance our products and services. You will contribute to the architectural design and the technology that powers our core products, ensuring their successful integration into organizational infrastructure and applications. This role requires a strong foundation in machine learning models and algorithms tailored to real world applications. You'll collaborate with cross-functional teams to drive innovation and support the seamless operation of ML-powered applications. This role has the following responsibilities: Product Development Contribute as required to the development of machine learning products. Research and Innovation Conduct research and experiments to evaluate performance of different machine learning models and techniques to drive platform strategy, exploring new possibilities and identifying areas of opportunity for impact. Data Projects Work with large, complex datasets, leveraging both structured and unstructured data to drive insights and predictions. Early-Stage Concept Development Generate and evaluate ideas for potential new products and features, using both technical expertise and creative problem-solving skills. Architectural Design Assist in the architectural design of systems, working closely with data engineers and software developers to ensure scalability, reliability, and performance. Collaboration Partner with cross-functional teams, including data science, engineering, and product, to align research initiatives with business goals. Skills & Requirements • 2 - 5 years of Machine Learning / AI Engineering experience (if PhD education level) o 6 - 9 years of Machine Learning / AI Engineering experience (if Master's education level) • Must possess expertise architecting LLM models and improving existing models • Must possess extensive research background with demonstrable techniques and algorithms to enhance the capabilities of LLMs • Must possess expertise integrating ML models into production (inclusive of fine-tuning models) • Must possess strong proficiency designing and conducting experiments, with a strong understanding of A/B testing and evaluation metrics for computing intelligence model performance • Must possess strong proficiency in programming languages such as Python with extensive experience using ML frameworks (TensorFlow, PyTorch, Scikit-learn, Keras) • Must possess minimum Master's level education in related STEM discipline Benefits/Other Compensation: Medical, Dental, Life Insurance, 401K. Why Hays? You will be working with a professional recruiter who has intimate knowledge of the industry and market trends. Your Hays recruiter will lead you through a thorough screening process in order to understand your skills, experience, needs, and drivers. You will also get support on resume writing, interview tips, and career planning, so when there's a position you really want, you're fully prepared to get it. Nervous about an upcoming interview? Unsure how to write a new resume? Visit the Hays Career Advice section to learn top tips to help you stand out from the crowd when job hunting. Hays is committed to building a thriving culture of diversity that embraces people with different backgrounds, perspectives, and experiences. We believe that the more inclusive we are, the better we serve our candidates, clients, and employees. We are an equal employment opportunity employer, and we comply with all applicable laws prohibiting discrimination based on race, color, creed, sex (including pregnancy, sexual orientation, or gender identity), age, national origin or ancestry, physical or mental disability, veteran status, marital status, genetic information, HIV-positive status, as well as any other characteristic protected by federal, state, or local law. One of Hays' guiding principles is ‘do the right thing'. We also believe that actions speak louder than words. In that regard, we train our staff on ensuring inclusivity throughout the entire recruitment process and counsel our clients on these principles. If you have any questions about Hays or any of our processes, please contact us. In accordance with applicable federal, state, and local law protecting qualified individuals with known disabilities, Hays will attempt to reasonably accommodate those individuals unless doing so would create an undue hardship on the company. Any qualified applicant or consultant with a disability who requires an accommodation in order to perform the essential functions of the job should call or text ************. Drug testing may be required; please contact a recruiter for more information.

About Us: Come join a rapidly growing biotechnology company dedicated to advancing scientific research and developing innovative solutions. We are committed to excellence and are seeking a highly skilled Analytical Scientist to join our dynamic team. Job Summary: The Analytical Scientist will play a crucial role in our research and development efforts, focusing on method development, analytical techniques, and documentation within a GMP (Good Manufacturing Practice) environment. The ideal candidate will have extensive experience in developing methods from scratch, drafting Standard Operating Procedures (SOPs), and utilizing various analytical techniques such as HPLC, UPLC, GC, and Empower. Key Responsibilities: Develop and validate analytical methods from scratch to support product development and quality control. Draft and revise SOP documentation to ensure compliance with GMP regulations. Perform routine and non-routine analysis using HPLC, UPLC, GC, and Empower software. Troubleshoot and optimize analytical methods to improve accuracy and efficiency. Maintain accurate and detailed records of all analytical activities and results. Collaborate with cross-functional teams to support research and development projects. Ensure all laboratory activities comply with GMP, GLP (Good Laboratory Practice), and other regulatory requirements. Participate in internal and external audits and inspections. Stay current with industry trends and advancements in analytical techniques and technologies. Qualifications: Ph.D. or Master's degree in Chemistry, Biochemistry, Analytical Chemistry, or a related field. Minimum of 2 years of experience in analytical method development and validation in a GMP environment. Proficiency in HPLC, UPLC, GC, and Empower software. Strong knowledge of GMP regulations and SOP documentation. Excellent problem-solving skills and attention to detail. Ability to work independently and as part of a team. Strong written and verbal communication skills. Experience with statistical analysis and data interpretation is a plus. Benefits: Competitive salary and benefits package. Opportunities for professional growth and development. Collaborative and innovative work environment.

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. Position reports directly to the Principal Scientist or Manager of R&D and may supervise other scientists and research technicians. Responsibilities: Work independently, manage research projects and work in teams towards executing the initiatives of the Manager of R&D and the research team Generate ideas that will enhance existing products and lead to the development of new products, test procedures and protocols. 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 and technicians as needed and as directed by the Manager of R&D. Promotes health, safety and environmental regulations by ensuring that standards, policies, and procedures are adhered to in compliance with corporate, federal, state, and local requirements. Performs other duties as required for the success of Polyglass USA, Inc. Requirements: 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 Able to multitask, and work effectively with internal and external partners at a technical and interpersonal level Masters in Material Science and Engineering, Chemical Engineering, 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 Engineering, Chemical Engineering, 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 roofing and waterproofing membranes for commercial or residential applications or similar endeavors 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 Preferred Background: Ph.D. in Material Science and Engineering, 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 roofing and waterproofing membranes for commercial or residential applications or similar endeavors. This position is located on-site in Deerfield Beach, FL. Polyglass will provide relocation assistance.

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. By applying, you consent to your information being transmitted by HourlyJobsNearMe to the Employer, as data controller, through the Employer's data processor SonicJobs. See SonicJobs Terms & Conditions at us/terms-conditions and Privacy Policy at us/privacy-policy and SonicJobs Privacy Policy at us/privacy-policy and Terms of Use at us/terms-conditions

NOTE: This role does NOT offer sponsorship for work authorization. External applicants must be eligible to work in the US. Candidates must have a minimum of 2-3 years pharmaceutical industry experience to be considered. In this role, the Associate Scientist I/II will provide hands-on formulation and process expertise during the development of clinical and commercial formulations for orally inhaled and nasal drug products (OINDPs). Conducts laboratory activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to product development team. Contribute towards the development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. Essential Duties and Responsibilities Conducts standard and advanced laboratory activities including formulation development and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. Conducts manufacture of lab scale R&D, pilot scale, pivotal scale and commercial scale batches by following written documentation. Works independently to determine methods and techniques on new or difficult assignments related to research, formulation and process development and manufacturing activities. Demonstrates technical proficiency, scientific creativity, collaboration with others and independent thought in suggesting experimental design and research strategy. Interfaces with Quality Assurance and Compliance, to ensure that work is being performed and documented according to established procedures. Plans and designs new testing methodologies to assess the performance of new product formulations. Contribute towards development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. Document and report all laboratory and manufacturing activities according to cGMPs and Transpire Bio's SOPs. Work and communicate effectively with other functional groups and across global respiratory R&D sites. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs; follow Transpire Bio safety rules and procedures. Comply with all Transpire Bio Corporate guidelines and policies. Qualification Requirements Degree in Chemistry, Chemical/Biochemical Engineering, Biochemistry or a related scientific discipline and relevant industry experience that demonstrates an expertise in formulation process development. BS degree with 2+years' experience in industry, OR a MS degree with 1-3 years' experience is required. Experience in the formulation, process development and/or manufacture of injectables, ophthalmic, other sterile products is preferred. The ability to embrace a highly multi-disciplinary collaborative approach and work independently is essential. Adaptable and flexible, readily adapts to change & new projects. Engineering/Science background with knowledge of product development processes Quick learner and ability to think critically Ability to pay special attention to detail with degree of accuracy. Excellent interpersonal, organizational and communication skills. Strong written and verbal communication skills are required.

We have partnered with one of the top-performing financial firms of all time, looking for an Equities Data Scientist/ Analyst with over 3 years of full-time experience, to join their successfully talented team in Miami. You must have experience within a hedge fund, large bulge bracket or private equities firm. Role Summary: You will be responsible for the processing, enhancement, and ongoing monitoring of priority alternative datasets for the Research Team. You will focus on understanding each dataset deeply while improving data integrity and quality through data visualisation, analysis, and anomaly detection. These datasets will then be used to enrich alpha signals across the Research Business. Our client is looking for individuals who are very detail-oriented and excited to solve unique and complex data problems on a world-class team and organisation. Skills and Qualifications Required: 3+ years of full-time experience in a fast-paced industry, research, or consulting setting Excellent analytical and problem-solving skills Demonstrated ability to ask the right questions and draw actionable conclusions from data Demonstrated ability to quickly learn new technologies, skills, and industries Experience visualising data in Tableau or another similar BI tool Expertise with SQL databases Bachelor's degree in a STEM field from a globally recognised university Profiles we are looking for: Data Scientist Experience with Alternative Data Working in a fast-paced environment Cross-asset class exposure

This physician-founded, Series A, venture capital-backed company offers ethically sourced, bovine colostrum concentrates for ultimate gut health, immunity, recovery, and metabolism-boosting benefits. They're a 200-person business that is looking for an internal AI consultant/ Director to leverage AI across business functions that had previously been siloed working with different tech stacks. The ideal person has built an AI solution that has optimized every vertical of a previous analog-based business. Whilst the PMF is defined, and ARR in the multi-digital millions, the infrastructure, data platforms, MLOps, governance, and compliance in AI systems are all there to be roadmapped and deployed from the ground up. Criteria design and implement a scalable AI infrastructure for a CPG company, (data from multiple sources like e-commerce, retail partners, supply chain, and marketing analytics). you've built an AI platform that optimized operations, demand forecasting, or marketing personalization in a CPG or related industry If no GPG, then a background in disruptive brands like Gymshark, Manscaped, Poppi etc You have chosen AI/ML frameworks, data platforms, and MLOps tools previously for a previously analog business and optimized them for AI evidence of approach data privacy, governance, and compliance in AI systems, especially when dealing with customer, sales, and retail data expert communicator, explaining AI strategy with business objectives and communicate its value to executives, marketing, and operations This is a remote-first company, with a distributed team across the US. We're happy for you to work anywhere across the US. Frequent offsites in Miami to keep connected.

The R&D Lab Chemist is responsible for working on various Technical Service and R&D Projects to support our Customers, Principals, Various product lines in our portfolio, and Sales Team in laboratory/office setting, resulting in making Barentz Always a better solution ESSENTIAL DUTIES AND RESPONSIBILITIES Position/Department Data management - acquiring, validating, and maintaining data for the lab projects. Perform, interpret, and record lab project data. Data processing and documentation using common software tools such as Excel, PowerPoint as well as Datacor/Chempax, eChempax, and BRM. Generation of various Lab Reports to summarize testing, results & conclusions. Ensure safety procedures and housekeeping are maintained to protect yourself, co-workers, and the environment. General lab duties including clean-up, maintenance of equipment, track and order chemicals and disposables used in the lab as needed. Leadership/ Teamwork Conduct necessary lab work to provide Technical Support to our Customers, Principals, Sales Team and Product Line Portfolio. Communicate with other Lab Technicians throughout the organization to stay up to date on processes, protocols and trends Provide additional documentation and supporting information cross-departmentally upon request Continuous Improvement/Problem Solving Ensure adherence to all applicable facility requirements, certifications and designations Contribute to and support continuous improvement of our processes and systems Seek opportunities to share best practices with the team, support staff and other divisions Barentz Culture/Fundamentals Support and lead by example, following Barentz' purpose, strategies, and values Act legally and ethically in all professional relationships in adherence with Barentz' culture, values and fundamentals Contribute to an environment of trust and mutual respect Maintain a strong commitment to teamwork and concern for others Maintain a high level of personal responsibility and ownership Use effective communication and listening skills Foster an inclusive and diverse workplace where every team member feels valued and respect Learning and Development Seek out and participate in ongoing growth and personal development opportunities Embrace and promote Barentz' learning and development culture Other Duties and Responsibilities: Duties and responsibilities may be amended at any time per business need Education Bachelor's degree in Chemistry, Biology, Engineering or other Sciences or equivalent of education and experience (required) Experience Minimum 3-5 years of previous experience in a laboratory setting (required) Certifications Any industry related certification (i.e., Laboratory Technician, Sales Techniques, Project Management, Regulatory, Quality Management, etc.) (preferred/encouraged) Position/Product/Industry Requirements Experience using industry related technologies and equipment Champion a safety-first mindset for yourself and others in the facility SKILLS AND KNOWLEDGE Self-motivated, high energy, and engaging level of enthusiasm and positive outlook Demonstrated organizational, complex problem-solving, and analytical skills. Effective written and verbal communication skills and the ability to adapt communication style to the audience as needed Software knowledge of Microsoft Office including Outlook, Word, Excel and Power Point Must be able to effectively prioritize work assignments for self and others Ability and desire to develop meaningful/productive business relationships

Introduction “Quality and safety above everything”. That is the unassailable theme that guides everything that we do, every day. We have an unwavering commitment to quality and the production of safe and effective products. Our science and risk-based compliant quality culture is innovative, and healthcare oriented. Whether you are involved in development, operations, maintenance, compliance or analysis, through research and manufacturing programs, your contribution will directly impact our success. Your Diligence Means Our Success At Pherros, we combine development and safety to improve the lives of those around us. Our employees bring life-changing medicines to people in need and improve the understanding and management of disease. We give our best to putting people first and we are looking for people who are determined to improve life for everyone. You will be a member of Pherros' dedicated and highly effective quality control operations team. Our aseptic manufacturing facility for parenteral pharmaceuticals presents an exciting opportunity to be an important part of a state-of-the-art facility and quality system. The Quality Control Laboratory assures patients worldwide that our drug products are safe and effective and of the highest quality and integrity. We exceed these standards through effective execution of process, environmental, supply and product testing. General Requirements As a Quality Control Chemist, you will perform accurate and timely testing of routine and non-routine samples in accordance with appropriate Good Manufacturing Practices (“GMP”), Good Laboratory Practices (“GLP”), and safety guidelines, to support site production and stability requirements. The Chemist and Chemistry Supervisor roles are focused on the quality control testing of the various pharmaceutical products manufactured at Pherros Biosciences. All testing performed is in accordance with the established drug product specifications. The candidate will participate in and perform development and validation of analytical test methods associated with finished dosage form (FDF) drug products as well as investigate, resolve, and mitigate deviations, non-conformances, and OOS (Out of Specification) events associated with products tested at the facility. The Quality Control Scientist utilizes technical skills to perform in-depth problem solving, proactively identify opportunities for continuous improvement, and assist in resolving laboratory investigations of atypical data and results. Additional key objectives and deliverables include the capability to: Be an inspirational part of a vibrant and growing group of professionals. Accurately and safely perform timely testing of routine and non-routine lab samples in accordance with appropriate GMP, GLP, and safety guidelines. Accurately record data in reports or Laboratory Information Management System (“LIMS”) in accordance with laboratory procedures, Good Laboratory Practices (“GLP”), standards, and GMP requirements. Recognize deviations from procedures, methods, etc., and initiate an investigation as required. Verify analytical data generated by other analysts within the lab as required. Adhere to all Environmental, Health, and Safety (“EH&S”) standards. Identify and communicate opportunities for improvement initiatives in daily work activities. Troubleshoot equipment and methods as required. Provide technical support for non-routine (e.g., deviation) investigations. Maintain inventory of all supplies and consumables for the laboratory. Gown for activities within aseptic manufacturing suites typical of a GMP environment. Engage in training exercises to fulfill compliance requirements associated with the position. Conduct chemical and physical testing of raw materials, API, in-process, finished products, and stability samples, and other in process samples, using established test methods to provide accurate and reliable data to assure their strength, identity and purity. Work with materials using safe protocols and participate in and contribute to the maintenance and calibration of analytical instruments within the quality control laboratories. Collaborate with other facility team members and regulatory colleagues to establish release and stability specifications for starting materials, intermediates, drug substances, and drug products. Work well in a fast-paced team environment. Collaborate with management to identify training needs and ensure appropriateness of training plans, creating and assigning curricula as required. Contribute to the training, education, guidance, and influence of operational and support areas on quality control policy and practices. Foster a culture of collaboration, partnership, teamwork, and a drive for change and continuous improvement. Take initiative and have the ability to work independently as well as collaboratively with exemplary enthusiasm amongst other team members. Perform other duties as assigned. Educational, Experience and Training Requirements Bachelors, Masters or Ph.D. degree in Chemistry with three (3) to seven (7) years of relevant experience in a GMP Chemistry Lab environment, including knowledge of analytical chemistry testing, excellent understanding and knowledge of analytical instrumentation technologies, chromatography methods, USP compendial test methods, ICH guidelines, and cGMP, experience with HPLC and LCMS analytical testing, method development, and method validation is required, experience with GCMS, FTIR and ICPMS is required for supervisors, strong communication and organizational skills, proficiency in Microsoft Office suite applications (Excel, Word, PowerPoint), ability to handle multiple tasks simultaneously while meeting deadlines, ability to investigate, collect data, and analyze trends investigations, ability to work as needed for off-hours stability timepoints and potential early start times, excellent communication (written and verbal), interpersonal, organizational and negotiation skills, project management skills, experience in process improvement, and the ability to be solution focused on the design and implementation of quality and process improvements. Additional Preferences: Experience with a LIMS system. Ability to lead and to inspire others. Experience with a Quality Management System (“QMS”) such as Master Control. Demonstrated problem solving and analytical thinking skills. Understanding of statistical tools and analysis. Excellent interpersonal skills and networking skills. Experience in a GMP QC Lab environment. Demonstrated written and verbal communications skills. Strong attention to detail. Ability to organize and prioritize multiple tasks. Experience with Root Cause Analysis. Demonstrated ability to work both independently and as a part of a team. Additional Information The position is full-time non-remote, Monday through Friday, with flexibility to support weekends. Applicants will work in various areas within the site. Some allergens may be present in the facility. Exposure to allergens should be considered when applying for this position. Tasks may require repetitive motion (e.g., keyboarding). Minimal travel required. Sunshine Act Pherros reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pherros to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pherros intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pherros that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative. EEO & Employment Eligibility Pherros is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pherros also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Quality Control About Us Careers at Pherros Biosciences are like no other. We believe in our ability to improve future healthcare, and potential to transform millions of lives. We're looking for new talent to join our global community in order to bring innovative therapies to market and to make the world a healthier place.

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 1-2 years of experience in Pharmaceutical R&D. Extensive knowledge and hands-on experience with chromatography (HPLC, GC), spectroscopy (UV, FTIR), and other analytical techniques. Must have at least 3 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.

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.

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.

Perform routine tests of finished product and stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using different techniques including water determination by KF, and tests according to in-house monographs and USP in a regulated laboratory environment. 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 format. 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. Responsibilities * Perform routine tests of finished product and stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using different techniques including water determination by KF, and tests according to in-house monographs and USP in a regulated laboratory environment. * 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 format. * Assist in the training of new analysts. * Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. * Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Essential Skills * Proficiency in HPLC, UPLC, UV-Vis, and other analytical techniques. * Strong expe in chemistry and pharmaceutical analysis. * Experience in working in FDA and GMP regulated environments. * Ability to maintain accurate lab notebooks and documentation in compliance with SOPs. * Competence in analyzing and interpreting results in both written and oral formats. * Experience in training new analysts and conducting laboratory investigations. Additional Skills & Qualifications * Bachelor's degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis. * Master's degree in Chemistry or related scientific field with 1 year of related experience in pharmaceutical analysis. * Ability to deal with problems involving several concrete variables in standardized situations. * Ability to carry out necessary computations and to draw and interpret graphs. * Working knowledge of instrumentation software used in the laboratories. Work Environment Lab environment; FDA and GMP regulated. Hours are Monday-Friday: 8am-5pm OR 2pm-11pm 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 Coral Springs,FL. Application Deadline This position is anticipated to close on Apr 27, 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.

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

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 or Tuesday- Saturday 7am-4:00pm. 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.