Associate Scientist Jobs in Tampa, FL

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

Your Tasks: The Imaging Field Application Scientist (FAS) role is part of the Miltenyi Commercial Sales team and supports our Imaging portfolio from pre-sales to post-sales for both UltraMicroscope II/Blaze (Lightsheet Microscope) and MACSima (Spatial Biology). The FAS is responsible for coordinating pre-sales demonstrations with the Sales team (Blaze Lightsheet only), leading initial customer training, and continued support post-training which includes workflow support and troubleshooting, account management for their assigned territory, and re-trainings when needed. Imaging FASs regularly provide technical seminars for both prospective and current customers. Additionally, you will assist in the adoption of Miltenyi Biotec reagents and consumables by promoting products to customers when relevant. The ideal candidate has a background in confocal microscopy, light sheet microscopy and/or spatial biology, is a self-starter, enjoys teaching, and is an effective communicator, both written and verbally. They are able to manage customers with varying levels of knowledge/scientific background who study a variety of applications. The candidate must be able to work in a matrix organization with multiple teams involved in the management of the same territory. The candidate will travel up to 70% of their time within their territory, nationally, and internationally, depending on the team's needs. Essential Duties and Responsibilities: Act as the primary field support for the UMII/Blaze and MACSima install base providing onsite training. Provide ongoing technical/application support of existing customers with UMII/Blaze and MACSima, including onsite visits and remote support. Coordinate on site UltraMicroscope Blaze demonstrations with Spatial Biology Specialists and leads technical on-site demonstration. Conduct routine follow up post installation/training for existing UMII/Blaze and MACSima customers. Plan and manage time and accounts to ensure adequate coverage across the territory Prepare and deliver presentations and/or seminars for both pre-sales and post-sales customers. Attend conferences as needed. Travel domestically and internationally as required 70%. Requirements: Master's Degree in related scientific field or Ph.D. preferred in related scientific field, with preference for candidates savvy in confocal microscopy and/or spatial biology. Confocal microscopy experience preferred over spatial biology experience; 3 years' experience in biological sciences, microscopy, immunology and molecular biology with at least 2 years of confocal/spatial biology experience; or equivalent combination of education and experience. Must possess a valid driver's license, evidence of insurance/ insurability, and ability to receive appropriate clearance to access restricted government accounts. Preference given to candidates with customer facing experience. Physical Demands: The physical demands described here 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 employee is regularly required to walk; use hands to finger, handle, or feel; reach with hands and arms, talk, and hear. The employee is required to stand; climb or balance and stoop, kneel, crouch. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception and ability to adjust focus. Must have ability to handle more than one task at a time and must work at a rapid pace while maintaining attention to detail. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. This job is performed in a variety of facilities. Each person performing this job must have a home office environment, which is temperature controlled. This job requires the person to be mobile to visit customer sites. Due to the travel requirements, this position may be exposed to natural elements of nature. Miltenyi Biotec, Inc. is an EO Employer - M/F/Veteran/Disability/Sexual Orientation/Gender Identity. Miltenyi Biotec, Inc. participates in E-Verify. Are you ready to start revolutionizing biomedical research? When you join Miltenyi Biotec, you join a family that is passionate about making a real impact - one breakthrough at a time. For over 30 years, we have played a pivotal role in the design, development, manufacture, and integration of products for sample preparation, cell separation, cell analysis, imaging, and cell culture needs. These developments have led to cutting-edge cell and gene therapies - transformative methods that mobilize the body's own cells and genetic blueprint to tackle diseases such as cancer and autoimmune conditions. Today, our more than 18,000 solutions play a vital role in paving the way for the medicine of tomorrow. RequiredPreferredJob Industries Other

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

Allied Search Partners Molecular Flow Cytometry Scientist A healing presence in the communities we serve. Benefits Medical, Dental and Vision Insurance Prescription Plan Preventative Care Covered at 100% LRH Home Network Providers Paid at 100% Wellness Program Annual Biometric Health Screenings Tier Health Plan Premiums based on Income Tobacco Free Credit on Medical Insurance Disease Based & Chronic Care Program Diabetes Prevention Program Health & Wellness Coaching Tobacco Cessation Program Free Life and AD&D Insurance Dependent Life and Supplemental Life Free Short-Term Disability Supplemental AD&D Long Term Disability Healthcare Flexible Spending Account Dependent Care Flexible Spending Account 401(a) Retirement Plan & 403(b) Retirement Plan On-Site Retirement Consultation Legal Services Earned Time Off Relocation Assistance Job Description Molecular Flow Cytometry Scientist (Healthcare Sciences) Job Responsibilities Position Title: Molecular Flow Cytometry Scientist Shift: Monday-Friday, 8 hour Day Shift Location: Just outside of Tampa, FL area (30 Miles) and 1 Hour from Orlando, FL Skills and abilities of a Molecular Flow Cytometry Scientist include: Responsible for performing test procedures authorized by the medical laboratory director; with the degree of skill commensurate with individual education, training, experience and technical abilities. Insure that all laboratory testing is performed according to established protocols or procedures. Exercise professional judgment in evaluation and assessment of test performance, sample integrity, result accuracy and validity. He/she follows all safety practices and maintains ongoing competency to ensure high quality testing services. He/she also supports professional development. Molecular Flow Cytometry Scientist (Healthcare Sciences) Job Requirements Successful candidates for the Molecular Flow Cytometry Scientist: Bachelor's Degree Degree as Medical Laboratory Technician (ASCP) or equivalent with laboratory internship as required by CLIA '88 and State of Florida qualifications for licensure Licenses Essential: Maintains an active status for licensure as a Clinical Laboratory Scientist under the rules of the Board of Clinical Laboratory Personnel (Department of Health/Division of Medical Quality Assurance) for the disciplines of practice that are performed. Completes required continuing education credits to maintain licensure. Certifications Essential: Maintains an active status for licensure either as Clinical Laboratory Scientist (CLS) under the rules of the Board of Clinical Personnel (Department of Health/Division of Medical Quality Assurance) for the disciplines of practice that are performed. Certifications Preferred: National Registry (ASCP, NCA, etc.) at a Technologist level or higher. Completion of an approved MLS program Molecular Flow Cytometry Scientist (Healthcare Sciences) For a complete list of current Allied Search Partners openings Nationwide please go to: ******************************************* To apply: Please send resume to ****************************** To Schedule a meeting: ********************************* Connecting the Right Talent to the Right Organization!

St. Petersburg, FL/Remote Salary Range: $55,000 - $70,000 Crawford, Murphy & Tilly, Inc. (CMT), is seeking an experienced Aviation Noise Scientist to support our growing Aviation Noise Practice. CMT is a nationally recognized leader in aviation noise. CMT staff are experienced in providing noise analysis for Master Plans, NEPA Actions, and FAR Part 150 Studies. Staff include environmental data analysts, aviation noise scientists, airport planners/forecasters, and professional engineers who are at the forefront of aviation-related applications. Responsibilities include: * Applying state and federal environmental policies and regulations as they relate to aviation noise * Preparing aviation noise analysis for Master Plans, NEPA Actions, and FAR Part 150s * Providing internal input on airport operations/aircraft fleet mix for Master Plans * Assisting airports with the management of their noise abatement office * Respond to noise complaints and speak with members of the community * Preparing reports that describe the relevant analysis policies and regulations and the methodologies and results of the aviation noise analysis * Interacting with clients and the public to present analysis results * Managing multiple projects and clients * Assisting with the pursuit of aviation noise contracts (may require travel) Minimum requirements: * B.S. degree in Environmental Science, Aviation, Acoustics, or related discipline; M.S. degree preferred. * Minimum 3 years of experience in a direct or related field * Experience as an aviation consultant, working at an airport or with Part 91, 121, or 135 operators (preferably in aviation noise) * Knowledge of aviation operations, ATC procedures, and FAA regulations * Experience using AEDT, NOMS systems and related flight data is a plus * Proficient in Microsoft Office products * Strong communication skills (written and verbal reports) * Acceptable driving record and valid driver's license with access to transportation About CMT: Our tagline "Centered in Value" is more than a promise to clients; it's the commitment we make to staff that their careers will be valued and championed. CMT's environmental professionals work collaboratively with our clients and internal with CMT's engineers, planners, GIS analysts, and other experts to provide smarter and integrated environmental solutions. Our success begins with an intimate understanding of our client's project goals as well as those of corresponding agencies and affected stakeholders. We have the state-of-the-art collection processes and computer software suites required to assess existing and potential future conditions while navigating our clients' projects through applicable regulatory processes and approvals. CMT is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. CMT does not discriminate in employment opportunities or practices on the basis of age, color, disability, gender identity, national origin, race, religion, sex, sexual orientation, veteran status, or any other characteristic protected by country, regional or local law. ADDITIONAL INFORMATION Please visit *************************************** to learn more about some of the benefits CMT offers! Equal Employer Opportunity including individuals with disability and protected veterans Visa sponsorship is available for this position.

Working Title: RESEARCH SCIENTIST-FWC - 77071893 Pay Plan: Career Service 77071893 Salary: $72,100 Annually Total Compensation Estimator Tool FWC Fish and Wildlife Research Institute (FWRI) Section/Subsection: Wildlife Research/Marine Mammal Research and Rescue Research Scientist-FWC - Career Service Position with Benefits $2,773.08 Biweekly, $72,100 Annually 100 Eighth Avenue SE St. Petersburg, FL Fish and Wildlife Research Institute/Marine Mammals Research Scientist- CS 77071893 Working Title: Senior Database Engineer St. Petersburg, Florida - $72,100 Annually Our organization: The FWC envisions a Florida where fish and wildlife are abundant and thriving in healthy and connected natural landscapes with vital working lands and waterways; where natural resources are valued and safely enjoyed by all; and wherein natural systems support vibrant human communities and a strong economy. Our Mission: Managing fish and wildlife resources for their long-term well-being and the benefit of people. Every organization has an identity that is forged not only by what it does, but by how it conducts itself. The values embedded in our mission and expressed in the vision of the FWC are to make quality decisions by being dynamic, science-informed, efficient, ethical, collaborative and committed to the vitality of the state and its environment. Minimum Qualifications: 9 years of professional experience relevant to the position is required or a bachelor's degree from an accredited college or university with major course of study in one of the physical or natural sciences, computer science, or mathematics and five years of professional experience in one of the physical or natural sciences, computer science, or mathematics; or A master's degree from an accredited college or university with major course of study in one of the physical or natural sciences, computer science, or mathematics and four years of professional experience as described above; or A doctorate from an accredited college or university with major course of study in one of the physical or natural sciences, computer science, or mathematics and two years of professional experience as described above can substitute for the required experience. Preferred Qualifications: Preference may be given to candidates who possess a master's degree from an accredited college or university with major course of study in natural, computer, or data sciences; candidates who have three or more years of professional experience in database design and management; or candidates who have experience with fish and wildlife data collection and analysis, relational database management, database and application programming, application development, project management, natural resource data management, and/or a doctorate from an accredited college or university in data science, computer science, or one of the natural sciences. Requirements: Employment in this position is contingent upon a satisfactory Level 1 background check at no cost to the candidate. Office hours are from 8:00 A.M. to 5:00 P.M. Eastern Standard Time, Monday through Friday. Not eligible for Telework. Responses to qualifying questions should be verifiable by skills and/or experience stated on the profile application/resume. Information should be provided regarding any gaps in employment. Candidates selected for an interview may be asked to provide documents demonstrating, describing, and/or diagramming a relational database or application they have developed and maintained. Position Overview and Responsibilities: The incumbent will lead the FWRI Marine Mammal program data management team that provides spatial and non-spatial data management and analysis support for multiple long-term marine mammal research projects. The program collects a wide range of biological and environmental data including for mortalities and rescues, photo-identification, satellite and VHF telemetry, aerial surveys, genetics, behavior, and habitat characteristics, including water temperature. Working with current data management and program staff, they will develop and implement a long-term, holistic, data management vision for the Marine Mammal program, based on current and projected needs/growth and to ensure that practices secure data and facilitate the scientific data life cycle to achieve program objectives. Furthermore, as program SQL database administrator, they will be responsible for technical database design, management, programming, documentation, and planning, and play a leading role in project management related to the ongoing migration and development of a suite of data management applications for SQL relational databases, including the restructuring of existing Access and SQL databases, the development of new SQL relational databases, and creating associated stored procedures and other tools. Key responsibilities include but are not limited to: Develop a strategic plan to address program database and application needs, streamline workflows, increase data accessibility, and provide novel insights to support marine mammal research and management decision making. Work closely with program staff to understand available data, workflows, and information needs; identify technical solutions and advise on workflow improvements; and then design, develop, and implement custom tools, workflows, programming scripts, or other innovative solutions to meet those needs. Serve as primary database architect and engineer and take a leading role in planning, managing, and advancing Marine Mammal program application and database development projects, including monitoring and coordinating the work of the development team and tracking and documenting work in Microsoft Azure DevOps. Implement agile development methods and collaborate with software developer(s), subject matter experts, and other technical staff to identify, define, and prioritize project-specific user needs; to develop and integrate data solutions into new and existing software applications, services, and platforms; and ensure seamless interoperability and data accessibility and the timely delivery of high-quality products. Develop and optimize SQL queries, scripts, and stored procedures for application CRUD functions and data import, validation, aggregation, transformation, summary, analysis, and distribution. Automate data workflows, data validation checks, data maintenance tasks, data integration, and data product creation using scripting languages, scheduling tools, etc. Create and maintain comprehensive database documentation and metadata including data architecture, data flows, data dictionaries, and database specifications, maintaining up-to-date documentation to support knowledge sharing and collaboration among team members. Serve as program liaison with Institute IT staff to manage Marine Mammal program network drives and file server cloud migration, including planning and approving user access group policies for network and application resources, and monitoring and managing program network usage to ensure data accessibility, efficient data storage, and adherence to agency data security, compliance, and data governance policies. Responsible for the supervision of assigned personnel in a coaching and mentoring manner to maintain a team-oriented approach to section goals. Other duties include but are not limited to: recruitment, training, planning and directing work, reviewing performance with employee, and ensuring compliance with FWRI rules, policies and procedures. Maintains a professional working environment that promotes teamwork within working units and with other sections in the Institute. Contribute to the writing of scientific papers, reports and grants, as assigned. The ideal candidate will have demonstrable experience in data management, SQL database design and programming, and project management experience related to software development, preferably with a master's degree in the ecological, data, or computer sciences. They will have created one or more back-end relational databases. They will have experience creating database documentation and metadata. They will have experience managing data through back-end systems and via front-end application tools. They will have a firm grasp on the scientific data life cycle and will be able to demonstrate experience supporting scientific data through all stages of the data life cycle. Candidates must have strong programming and project management skills Knowledge, Skills and Abilities: Proficient with SQL, MS Access, and Excel Possess strong organizational and project management skills Knowledge in using Microsoft SQL Server Management Studio, MS Azure DevOps, MS Azure Databases Knowledge in using Microsoft Office Word, Excel, Outlook, and Adobe Pro Knowledge of applied database and application development Knowledge of database & interface design principals, data standardization methodologies, relational database structures, and normalizing & optimization techniques Ability to organize and analyze data for database and software design Ability to communicate effectively both orally and in writing Ability to efficiently plan, organize, and coordinate work assignments Ability to work independently and as part of a team to multi-task, prioritize, and meet deadlines Ability to develop procedural documentation Ability to establish and maintain effective working relationships with others Ability to understand and appreciate natural resource problems from the perspective of a biologist or resource manager Ability to identify and define technical needs and assist with project prioritization to ensure priority project needs are met in a timely fashion Experience with fish and wildlife data collection and analysis techniques preferred Proficient writing SQL queries and programming including stored procedures and reverse engineering existing processes Analytical and problem-solving skills, with the ability to understand complex data requirements, analyze data quality issues, and implement effective solutions to ensure data accuracy, consistency, and reliability Why should I apply? The Benefits of Working for the State of Florida: State of Florida employees enjoy top-tier benefits offerings including comprehensive health coverage to meet the needs of you and your family while maintaining low deductibles and low monthly out-of-pocket contributions. State employees also enjoy the option of selecting between the FRS Pension Plan and the FRS Investment Plan for retirement. As an additional benefit, state employment affords you the opportunity to take part in the tuition waiver program within the state university and community college systems. Health Premiums $25.00- Single / $90.00- Family Biweekly No Cost $25,000 Life Insurance Nine Paid State Holidays, One Personal Holiday per year 4 hours Annual Leave and 4 hours Sick Leave accrued Biweekly Retirement Plan Options State University and College Tuition Waiver Program On the Job Trainings Support for family planning, including paid maternity leave, adoption benefits, Family and Medical Leave Act (FMLA), Family Supportive Work Program (FSWP), and paid leave for family and medical responsibilities for eligible employees. Paid administrative leave for mentoring, volunteering, voting, and other reasons because we understand the importance of giving back to the community. For a more complete list of benefits, visit ************************************** The State of Florida is an Equal Opportunity Employer/Affirmative Action Employer, and does not tolerate discrimination or violence in the workplace. Candidates requiring a reasonable accommodation, as defined by the Americans with Disabilities Act, must notify the agency hiring authority and/or People First Service Center (***************. Notification to the hiring authority must be made in advance to allow sufficient time to provide the accommodation. The State of Florida supports a Drug-Free workplace. All employees are subject to reasonable suspicion drug testing in accordance with Section 112.0455, F.S., Drug-Free Workplace Act. VETERANS' PREFERENCE. Pursuant to Chapter 295, Florida Statutes, candidates eligible for Veterans' Preference will receive preference in employment for Career Service vacancies and are encouraged to apply. Certain service members may be eligible to receive waivers for postsecondary educational requirements. Candidates claiming Veterans' Preference must attach supporting documentation with each submission that includes character of service (for example, DD Form 214 Member Copy #4) along with any other documentation as required by Rule 55A-7, Florida Administrative Code. Veterans' Preference documentation requirements are available by clicking here. All documentation is due by the close of the vacancy announcement. Location: ST PETERSBURG, FL, US, 33701

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

Job Details Tampa, FLDescription Title Research Scientist Clearance Level Required: Top Secret/SCI Responsibilities include (but are not limited to): Provide technical support in the areas of survivability and vulnerability research and analysis to inform USCENTCOM CCJ3 and CCJ5 continuing requirements to improve survivability capabilities through the enhancement of Force Protection (FP) and assessment concepts and techniques. Develop and implement new research objectives, establish project priorities, define methods of approach and execute the study. Provide scientific conclusions and interpretations. Responsible for innovative use of scientific research concepts, principles, and practices and contributes to advanced methods and techniques on Technical Area Tasks. Has expertise an outstanding knowledge and competence in one or more specific technical focus areas. Qualifications Minimum 5 years of Geographic Combatant Command (GCC) staff experience is required Experts on the functioning of a GCC, understand regional employment of national strategic objectives, and be knowledgeable on theater strategy, Combatant Command (COCOM) Campaign Plans (CCPs), COCOM Campaign Orders, Global Campaign Plans (GCPs), Annual Joint Assessment (AJA), and Chairman of the Joint Chiefs of Staff (CJCS) Joint Risk Assessment (CRAs), and Force Protection (FP) support to theater strategy, regional threats, security cooperation, advisory missions, phase zero operations, and the operations of a Joint Security Area. Experienced with the risk management process of the FP functions of the Service Components (i.e., ARCENT, AFCENT, MARCENT, NAVCENT, SPACECENT, and SOCCENT) Familiar with a variety of the field's concepts, practices, and procedures. Relies on extensive experience and judgment to plan and accomplish goals and independently performs a wide variety of complicated tasks. Provide consultation on complex projects and is considered to be the top level contributor/specialist. Master's degree and/or Ph.D.; at least 12 years of experience in the field or in a related area DoD secret clearance required, TS preferred with SCI eligibility

AMERICAN SYSTEMS is an employee-owned federal government contractor supporting national priority programs through our strategic solutions in the areas of Information Technology, Test & Evaluation, Program Mission Support, Engineering & Analysis, and Training. Responsibilities As a Research Scientist you will: * Provide technical support in the areas of survivability and vulnerability research and analysis to inform USCENTCOM CCJ3 and CCJ5 continuing requirements to improve survivability capabilities through the enhancement of Force Protection (FP) and assessment concepts and techniques. * Develop and implement new research objectives, establish project priorities, define methods of approach and execute the study. * Provide scientific conclusions and interpretations. * Responsible for innovative use of scientific research concepts, principles, and practices and contributes to advanced methods and techniques on Technical Area Tasks. * Has expertise an outstanding knowledge and competence in one or more specific technical focus areas. Qualifications * Minimum 5 years of Geographic Combatant Command (GCC) staff experience is required * Experts on the functioning of a GCC, understand regional employment of national strategic objectives, and be knowledgeable on theater strategy, Combatant Command (COCOM) Campaign Plans (CCPs), COCOM Campaign Orders, Global Campaign Plans (GCPs), Annual Joint Assessment (AJA), and Chairman of the Joint Chiefs of Staff (CJCS) Joint Risk Assessment (CRAs), and Force Protection (FP) support to theater strategy, regional threats, security cooperation, advisory missions, phase zero operations, and the operations of a Joint Security Area. * Experienced with the risk management process of the FP functions of the Service Components (i.e., ARCENT, AFCENT, MARCENT, NAVCENT, SPACECENT, and SOCCENT) * Familiar with a variety of the field's concepts, practices, and procedures. Relies on extensive experience and judgment to plan and accomplish goals and independently performs a wide variety of complicated tasks. * Provide consultation on complex projects and is considered to be the top level contributor/specialist. * Master's degree and/or Ph.D.; at least 12 years of experience in the field or in a related area * DoD secret clearance required, TS preferred with SCI eligibility Pay Transparency Statement AMERICAN SYSTEMS is committed to pay transparency for our applicants and employee-owners. The salary range for this position is USD $163,200.00/Yr. - USD $272,500.00/Yr. Actual compensation will be determined based on several factors permitted by law. AMERICAN SYSTEMS provides for the welfare of its employees and their dependents through a comprehensive benefits program by offering healthcare benefits, paid leave, retirement plans, insurance programs, and education and training assistance. EEO Statement EEO Race/Sex/Disability Status/Veteran Status Options

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. St. Petersburg is our primary soft gel development and manufacturing facility in North America with capacity of 18 billion capsules per year. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve difficult development and manufacturing challenges. The Analytical Research and Development (AR&D) laboratory supports evaluation and testing of raw materials, excipients, APIs, in-process and finished product samples. AR&D also performs development and validation of methods used to support release and stability testing of non-commercial products and materials. The Associate Scientist II, Analytical Research & Development once trained will independently test raw materials to both compendial and non-compendial methods. Once trained, the Associate Scientist II, Analytical Research & Development independently test pre-capsulation, stability and finished product samples as per established methods. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. The Role * Perform compendial and non-compendial testing on raw materials, drug substances, in-process samples, cleaning samples and finished products as required. * Performs assay/CU/dissolution and other single analyte chromatographic testing. Prepares reagents, standards, media and mobile phase as needed for analyses. * Required to work with potent and teratogenic compounds with proper PPE equipment. Disposal of hazardous waste according to environmental regulations and company procedures. * Tabulation/ interpretation of results of analysis as recorded in notebooks, reports and logbooks. Assures right-first-time execution of departmental methods and SOPs. * Supports activities and services necessary to the operations of the department, as assigned. Writes/ reviews analytical methods, deviations, protocols, SOPs and other technical documents. * Supports Material Evaluation Process for new materials. Shares responsibility for the routine calibration of analytical equipment such as, but not limited to balances, pH meters, KF analyzers, AA, IR, etc. * Provides project support for new product development programs under the direction of the lead scientist or group leader. Assist with laboratory investigations using the appropriate Root Cause Analysis tools. * Participates in inter-departmental task teams. Interfaces with peers in other departments and management. Identifies/implements improvements that will reduce cycle time for testing/release products. * Other duties as assigned. The Candidate * Associate's in science with 10 plus years in an analytical lab, 5 in GMP environment OR * Bachelor's in science with 3 plus years in an GMP analytical lab * Experience with common pharmaceutical equipment: UV/VIS, IR, AA, and Dissolution required. * Expertise in wet chemistry techniques such as titrations, extractions as per compendia required. * Familiar with separation chromatographic instruments such as HPLC/UHPLC and GC required. * Familiar with pharmaceutical software such as LIMS, TrackWise, Empower, preferred. * Vision requirements include ability to differentiate color (Pass the Ishihara Color Vision Screening) and obtain 20/30 acuity in both far and near vision with or without corrective lenses. For Catalent's in-house screening, the acceptable score is to identify at least 4 of 6 numbers in the circles. Why you should join Catalent: * Tuition Reimbursement - Let us help you finish your degree or earn a new one! * WellHub program to promote overall physical wellness. * 152 hours of PTO + 8 paid holidays. * Medical, dental and vision benefits effective day one of employment. * Defined career path and annual performance review and feedback process. * Diverse, inclusive culture. Several Employee Resource Groups focusing on D&I. Community engagement and green initiatives. * Dynamic, fast-paced work environment. * Positive working environment focusing on continually improving processes to remain innovative. * Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives. * Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories. Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our diverse team of over 9,000 are dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. For this reason, Moffitt has been recognized on the 2023 Forbes list of America's Best Large Employers and America's Best Employers for Women, Computerworld magazine's list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems and continually named one of the Tampa Bay Time's Top Workplace. Additionally, Moffitt is proud to have earned the prestigious Magnet designation in recognition of its nursing excellence. Moffitt is a National Cancer Institute-designated Comprehensive Cancer Center based in Florida, and the leading cancer hospital in both Florida and the Southeast. We are a top 10 nationally ranked cancer center by Newsweek and have been nationally ranked by U.S. News & World Report since 1999. Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join our committed team and help shape the future we envision. Summary We are seeking a highly motivated and talented Research Scientist to join our team, focusing on the validation of observations from fragment-based drug discovery screens using CRISPR and RNA interference in cancer models. The Research Scientist will play a crucial role in advancing our understanding of potential cancer drug targets identified through fragment-based drug discovery screens and chemical proteomics. This position offers a unique opportunity to contribute to translational research and the development of novel therapies for cancer treatment. Responsibilities: * Validation of Drug Targets: * Design and execute CRISPR and RNA interference screening experiments to validate observations from fragment-based drug discovery screens. * Utilize molecular biology techniques to assess the impact of gene modulation on cancer cell behavior and response to potential drug candidates. * Utilize publicly available databases to provide additional data sets * Experimental Design and Optimization: * Develop and optimize protocols for CRISPR and RNA interference experiments tailored to specific drug targets. * Collaborate with oncologists, medicinal chemists and cancer biologists to ensure the relevance of screening assays. * Data Analysis and Interpretation: * Analyze and interpret screening data to validate the relevance of identified drug targets. * Collaborate with bioinformaticians to integrate screening results with other data sets for a comprehensive analysis. * Collaboration and Communication: * Work collaboratively with multidisciplinary teams, including medicinal chemistry, molecular biology, bioinformatics, and preclinical development. * Present findings at internal meetings, conferences, and contribute to publications. * Cell Line and Model Maintenance: * Maintain cancer cell lines and relevant in vivo models for validation experiments. * Instrumentation and Technology: * Operate and maintain cutting-edge laboratory equipment and technologies related to CRISPR and RNA interference. * Stay abreast of advancements in the field and recommend the integration of new technologies Qualifications: * Ph.D. in Molecular Biology, Cancer Biology, Genetics, or a related field with a minimum of two (2) years postdoctoral fellow or post PhD science experience in a relevant field is required. * Proven expertise in CRISPR and RNA interference screening, particularly in the context of cancer biology. * Strong molecular biology skills, including gene editing, nucleic acid isolation, and analysis. * Excellent organizational, analytical, and communication skills. * Ability to work collaboratively in a team-oriented environment. How to Apply: Interested candidates should submit a cover letter, curriculum vitae to **********************. Please include "Research Scientist - Validation of Drug Targets" in the subject line. Share:

Department Name: Pharmaceutical Science College/Division: USF Health- Taneja College of Pharmacy Salary Plan: 0015 Non-Student Temporary Hiring Salary/Salary Range: $43,000/yr 40hrs/wk is Grant Funded. Organizational Summary: The USF Health Taneja College of Pharmacy is managed by the Dean and an actively engaged administrative leadership team. The mission of the college is to Transform Health through educating students to be outstanding and successful practitioners and leaders in the profession; through leading in discovery and innovation of education and practice in pharmacy; and through delivering the highest quality care in diverse, interprofessional clinical and community settings. Job Summary: This position is pivotal to advancing the research goals of the Department of Pharmaceutical Sciences, involving a wide range of vital laboratory tasks such as precise sterile techniques, expert animal handling, histological slide preparation, and conducting assays for biological components. Supported by substantial grants funding, this role offers an exciting opportunity for the successful candidate to delve into cutting-edge research focused on retinal diseases. The primary focus involves evaluating the effectiveness of gene, drug, and nanoparticle treatments to slow or halt retinal degeneration, utilizing various experimental methods in cell culture and animal models. Job Description: The Research Scientist will help with ongoing research investigation in PI's lab on the following areas. * Executes and adapts laboratory research protocols involving biological materials, employing techniques such as mammalian tissue cultures, ELISA, Western blotting. Proficient in sterile techniques, the preparation of slides using staining methods, and the execution of assays for proteins (including western blotting), RNA, DNA, and other cellular components. * Responsible for the care and handling of laboratory animals, including performing behavior testing, in vivo procedures, surgical preparation, and post-operative care, as well as animal breeding, tissue collection, and genotyping. * Maintains meticulous records detailing the processes and results of laboratory analyses, potentially inputting data into databases. Also, adept at creating graphs, charts, and tables to illustrate experimental findings, ensuring their inclusion in presentations and publications. * Manages laboratory equipment, coordinates repairs as needed, oversees the ordering and inventory of laboratory supplies, and ensures compliance with lab safety standards, SOP records, and cleanliness protocols. Additionally, responsible for reagent preparation, autoclaving, and ensuring the availability of necessary standard supplies and reagents for experiments. * Collaborates closely with the principal investigator, lab manager, students, and fellow lab members to support the successful execution of research projects, aiding in tasks such as report and publication preparation under the guidance of the principal investigator. * Available for taking care of experimental procedures as required, and fulfills additional assigned duties as needed. Minimum Qualifications: This position requires a Bachelor's degree in a natural, physical or medical science. Preferred Qualifications: Bachelor's degree in the areas of Biology, Biochemistry, Biotechnology, Molecular Biology, Cell Biology, and should have prior knowledge & experience about Cell culture, Molecular Biology, lab maintenance, handling mice and conducting animal experiments. USF Health Information for Applicants This position is subject to a Level 1 criminal background check. Job Opening Number: 38832 Posting Date: 02/21/2025 Posting End Date: 03/31/2025 How To Apply Click on the Apply Now button. When applying to an opening you will have the opportunity to upload a cover letter and resume. Apply online by completing the required information and attaching your cover letter and resume. Please include your experience as it relates to the qualifications stated above. YOUR COVER LETTER AND RESUME, PLUS ANY OTHER REQUESTED MATERIAL, MUST BE IN ONE ATTACHMENT. Only online applications are accepted for this position. Click here for additional tutorial information. To request an accommodation with the application or interview process, please contact Central Human Resources by telephone: ************ or email **********************. Work Location Campus map and location overview: USF - Health USF - Tampa Campus About USF The University of South Florida is a high-impact global research university dedicated to student success. Over the past 10 years, no other public university in the country has risen faster in U.S. News and World Report's national university rankings than USF. Serving more than 50,000 students on campuses in Tampa, St. Petersburg and Sarasota-Manatee, USF is designated as a Preeminent State Research University by the Florida Board of Governors, placing it in the most elite category among the state's 12 public universities. USF is a member of the American Athletic Conference. Working at USF With more than 16,000 employees at USF, the University of South Florida is one of the largest employers in the Tampa Bay region. At USF you will find opportunities to excel in a rich academic environment that fosters the development and advancement of our employees. We believe in creating a talented, engaged and driven workforce through on-going development and career opportunities. We also offer a first class benefit package that includes medical, dental and life insurance plans, retirement plan options, tuition program and generous leave programs and more. To learn more about working at USF please visit: Work Here. Learn Here. Grow Here. Connect with us:

Under administrative supervision of the Director of Nursing Excellence, and in partnership and collaboration with the Tampa General Hospital Office of Clinical Research, the Nursing Research Scientist provides leadership, assistance, support and mentorship in the development, implementation, evaluation, enhancement, and maintenance of a comprehensive nursing research program which would enhance the quality and outcomes of nursing care at TGH. This role stimulates, promotes, and develops nursing research interests and develops a progressive strategic vision for nursing research with short- and long-term goals and engages others in that vision. The Nursing Research Scientist identifies nursing practice issues requiring investigation, collaborates with other health team members, secures research funding, and disseminates nursing research findings internally and externally. This role is accountable to facilitate nursing professional development in research activities through the support of various nursing initiatives and ongoing collaboration with clinical education, organizational and nursing leadership, and academic institutions. Graduated from a nursing credited program with an active RN license to practice in the State of Florida, Required. 3-5 years nursing research experience as an investigator and disseminating research findings 3-5 years of leadership experience Grant writing/management experience. Ability to disseminate scholarly works via publications and oral presentations Ability to write grants Proficiency in using computers, software, and web-based applications Leadership skills Effective verbal and written communication skills and ability to present information clearly and professionally to varying levels of individuals internal and external to the organization Develop, communicate, and monitor performance metrics for nursing research

is on site in Boulder, Colorado and requires relocation* We are seeking a skilled Analytical Chemist to join our team. The Analytical Chemist will be responsible for running HPLC, developing and validating new methods, and supporting manufacturing and regulatory needs through innovative analytical chemistry and methodology. We are looking for soft skills like strong communication, client communication, being able to work with a team, and the capacity for continuous learning, recognition of errors, and resilience in progressing forward Responsibilities * Participate in the development of new processes by applying analytical skills and training * Facilitate and support analytical technology transfers * Plan and formulate aspects of analytical research and development proposals, including objectives, applications, cost, equipment, and human resource requirements * Develop, implement, and validate analytical methods and procedures * Keep accurate records and document experiments * Support the Stability Program by understanding internal, corporate, and ICH stability guidelines * Engage in manufacturing site activities such as troubleshooting and resolving analytical problems * Develop an understanding of Quality, Environmental, Health, & Safety (QEH&S) principles and regulatory affairs * Analyze batches of drug substances, intermediates, and raw materials for clinical or registration programs * Properly manage the generation and accumulation of hazardous and non-hazardous waste Qualifications * 3 years of experience * HPLC * GMP regulations * Experience with samples like peptides, small molecules, potent or highly toxic materials, or lipids * We will consider candidates with advanced degrees (e.g., MS or PhD) with HPLC experience as part of their degree or other advanced analytics techniques such as Mass Spectrometry (MS) * Open to candidates with quality control experience (2-3 years) Work Environment The schedule is Monday to Friday 8-5pm with flexibility. No weekends required. 80% of the time will be working in the lab, so you must be onsite every day. Pay and Benefits The pay range for this position is $33.20 - $41.70/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 Tampa,FL. Application Deadline This position is anticipated to close on Mar 10, 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.

Outlier helps the world's most innovative companies improve their AI models by providing human feedback. Are you an experienced Biology who would like to lend your expertise to train AI models? About the opportunity: Outlier is looking for talented accounting and tax experts to help train generative artificial intelligence models This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you You may contribute your expertise by…Assessing the factuality and relevance of domain-specific text produced by AI models Crafting and answering questions related to BiologyEvaluating and ranking domain-specific responses generated by AI models Examples of desirable expertise:A bachelor's or higher degree in Biology or a related subject Experience working as an Biology professional Ability to write clearly about concepts related to Biology in fluent EnglishPayment:Currently, pay rates for core project work by Biology experts range from $30 to $50 per hour USD. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

Allied Search Partners Molecular Flow Cytometry Scientist A healing presence in the communities we serve. Benefits Medical, Dental and Vision Insurance Prescription Plan Preventative Care Covered at 100% LRH Home Network Providers Paid at 100% Wellness Program Annual Biometric Health Screenings Tier Health Plan Premiums based on Income Tobacco Free Credit on Medical Insurance Disease Based & Chronic Care Program Diabetes Prevention Program Health & Wellness Coaching Tobacco Cessation Program Free Life and AD&D Insurance Dependent Life and Supplemental Life Free Short-Term Disability Supplemental AD&D Long Term Disability Healthcare Flexible Spending Account Dependent Care Flexible Spending Account 401(a) Retirement Plan & 403(b) Retirement Plan On-Site Retirement Consultation Legal Services Earned Time Off Relocation Assistance Job Description Molecular Flow Cytometry Scientist (Healthcare Sciences) Job Responsibilities Position Title: Molecular Flow Cytometry Scientist Shift: Monday-Friday, 8 hour Day Shift Location: Just outside of Tampa, FL area (30 Miles) and 1 Hour from Orlando, FL Skills and abilities of a Molecular Flow Cytometry Scientist include: Responsible for performing test procedures authorized by the medical laboratory director; with the degree of skill commensurate with individual education, training, experience and technical abilities. Insure that all laboratory testing is performed according to established protocols or procedures. Exercise professional judgment in evaluation and assessment of test performance, sample integrity, result accuracy and validity. He/she follows all safety practices and maintains ongoing competency to ensure high quality testing services. He/she also supports professional development. Molecular Flow Cytometry Scientist (Healthcare Sciences) Job Requirements Successful candidates for the Molecular Flow Cytometry Scientist: Bachelor's Degree Degree as Medical Laboratory Technician (ASCP) or equivalent with laboratory internship as required by CLIA '88 and State of Florida qualifications for licensure Licenses Essential: Maintains an active status for licensure as a Clinical Laboratory Scientist under the rules of the Board of Clinical Laboratory Personnel (Department of Health/Division of Medical Quality Assurance) for the disciplines of practice that are performed. Completes required continuing education credits to maintain licensure. Certifications Essential: Maintains an active status for licensure either as Clinical Laboratory Scientist (CLS) under the rules of the Board of Clinical Personnel (Department of Health/Division of Medical Quality Assurance) for the disciplines of practice that are performed. Certifications Preferred: National Registry (ASCP, NCA, etc.) at a Technologist level or higher. Completion of an approved MLS program Molecular Flow Cytometry Scientist (Healthcare Sciences) To apply: Please send resume to ******************************** To Schedule a meeting: ********************************************************************** Connecting the Right Talent to the Right Organization!

At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our diverse team of over 9,000 are dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. For this reason, Moffitt has been recognized on the 2023 Forbes list of America's Best Large Employers and America's Best Employers for Women, Computerworld magazine's list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems and continually named one of the Tampa Bay Time's Top Workplace. Additionally, Moffitt is proud to have earned the prestigious Magnet designation in recognition of its nursing excellence. Moffitt is a National Cancer Institute-designated Comprehensive Cancer Center based in Florida, and the leading cancer hospital in both Florida and the Southeast. We are a top 10 nationally ranked cancer center by Newsweek and have been nationally ranked by U.S. News & World Report since 1999. Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join our committed team and help shape the future we envision. Summary Melanoma Immunotherapy Development Research Scientist I The Markowitz lab seeks a Research Scientist whose skills and professional experience have prepared them to contribute to our commitment to diversity and excellence. The lab's research interest is in studying the role of nitric oxide in mediating responses to checkpoint blockade and other melanoma therapies. We are also developing tools to predict which patients will likely fail immune-based therapy via novel high dimensional flow cytometry, mass spectrometry, and informatics techniques, allowing those patients to be treated with other potentially more effective therapies. We are a translational laboratory striving to translate the knowledge gained in the laboratory via immune-based and traditional biochemical approaches to the clinic. Lab webpage: **************************************** Dr. Markowitz's webpage: *********************************************** Position Highlights: * The Research Scientist is a non-tenure track researcher who assumes the direct responsibility of conducting and performing experiments or directly overseeing experimentation as part of a research team under the general guidance of Dr. Markowitz * The Research Scientist only activity is research and related support activities, and the efforts of the Research Scientist are focused on goals of the laboratory they are part of. * The Research scientist will also assist in organizing the lab and day to day operations. * Study resistance mechanisms to immune checkpoint blockade * Translational research * Outstanding mentorship from Dr. Markowitz and expert faculty with wide-ranging funded research programs The Ideal Candidate: * Must possess good problem-solving and organizational skills, be self-driven and enthusiastic, and demonstrate the ability to conduct experiments independently and under supervision. * Proficiency in flow cytometry, murine experiments, IHC, immunoblot, cell culture techniques, immunoprecipitation, and general immunology. * General proficiency in computers with general familiarity with Bioinformatics and statistics preferred. * Team player * Excellent oral and written communication. Responsibilities: * Plans and performs experiments directed towards answering specific scientific questions with limited supervision under the general guidance of Dr. Markowitz. * Interacts closely with Dr. Markowitz and other researchers within the Markowitz Laboratory and conducts relevant background research including literature searches and reviews. * Assists in planning and developing research projects within the laboratory under the Dr. Markowitz's direction. * Position combines individual work and oversight over other less experienced research personnel. * Regularly present findings to the lab/Moffitt community and attend conferences to disseminate research findings in preparation for publication. * Write research papers and assist with grants. Credentials and Qualifications: * Minimum of two (2) years postdoctoral fellow or post PhD science experience in a relevant field is required (e.g., Immunology, Cancer Biology with a focus in immunology, Biochemistry with a focus in immunology). This lab is in the Immuno-Oncology program. Previous training in Immunology is required. To formally apply: Interested applicants should attach a single PDF file that includes a current CV and cover letter expressing interest in this position. You may be eligible for relocation assistance per policy. Reasons to relocate, aside from the sunshine, beaches and year-round outdoor recreation associated with the Gulf Coast of Florida, Tampa is a thriving metropolitan city, which has become a hub for ground-breaking research, welcoming individuals from around the globe. This diverse city is engulfed with rich culture, year-round activities for all, beautiful beaches, amazing cuisine and so much more. We strive for work/life balance. If you have the vision, passion, and dedication to contribute to our mission, then we have a place for you. Share:

Working Title: FISHERIES & WILDLIFE BIO SCIENTIST II - 77070462 Pay Plan: Career Service 77070462 Salary: $40,000.00 Annually Total Compensation Estimator Tool FWC - Fish and Wildlife Research Institute (FWRI) Marine Fisheries Research/Marine Fisheries Biology Fisheries and Wildlife Biological Scientist II-Career Service Position with Benefits $1,538.46 Biweekly, $40,0000 Annually 100 8th Avenue SE St. Petersburg, FL FWC - Fish and Wildlife Research Institute Fisheries and Wildlife Biological Scientist II- CS 770702462 St. Petersburg, Florida - $40,000 Annually Our organization: The FWC envisions a Florida where fish and wildlife are abundant and thriving in healthy and connected natural landscapes with vital working lands and waterways; where natural resources are valued and safely enjoyed by all; and wherein natural systems support vibrant human communities and a strong economy. Our Mission: Managing fish and wildlife resources for their long-term well-being and the benefit of people. Every organization has an identity that is forged not only by what it does, but by how it conducts itself. The values embedded in our mission and expressed in the vision of the FWC are to make quality decisions by being dynamic, science-informed, efficient, ethical, collaborative and committed to the vitality of the state and its environment. Minimum Qualifications: 5 years professional experience in a closely-related biological field or laboratory program is required. A bachelor's degree from an accredited college or university with a major in one of the biological sciences and one year of professional biological experience in a field or laboratory program; or A master's degree from an accredited college or university in one of the biological sciences can substitute for the required experience. Preferred Qualifications: Preference may be given to candidates who have demonstrated proficiency with fish otolith processing and ageing techniques. Requirements: Employment in this position is contingent upon a satisfactory Level 1 background check at no cost to the candidate. Office hours are from 8:00 A.M. to 5:00 P.M. Eastern Standard Time, Monday through Friday. Not eligible for Telework. Position Overview and Responsibilities: The incumbent will conduct age and growth laboratory research activities in support of marine fisheries research and stock assessments. Duties include, but are not limited to, sorting, entering, mounting, sectioning, filing, ageing and archiving otoliths and spines. Ensure all work activities are within compliance with the appropriate laboratory protocols, standards, procedures for maintaining high quality data. Participate in field sampling activities in inshore and offshore waters related to fish life history studies, including age and growth, movement patterns and reproductive biology. Duties include: trailering vessels, operating vessels in field sampling efforts, and helping maintain sampling fleet. Research includes both above water and underwater sampling techniques (may include participation in SCUBA dives). Assist in organizing and conducting outward-focused activities, including training visitors in age and growth research methodologies, fulfilling outreach and data requests and coordinating outreach events for the age and growth lab. Assists with Quality Control Workshops with internal and external State and Federal Partners. Perform other related work as required. Assist in producing scientific products for dissemination within the scientific community, including participation in project planning and meetings, report contributions, and presenting scientific content at conferences and meetings Knowledge, Skills and Abilities: Knowledge, ability, and skill in using scientific methods to solve problems. Knowledge of: the terminology, principles and techniques used in biological laboratory research and its application to fisheries management; laboratory techniques for ageing fishes; photo-microscopy hardware and software systems; image analysis software. Skill in: the use of personal computers, electronics and technology, including Microsoft Office suite; performing the techniques used in determining the age of fishes. Ability to: work in a laboratory setting conducting repetitive tasks; sustain a high level of organization in a scientific laboratory setting; to pay great attention to detail, including handling of microscopic structures; communicate effectively, both orally and in writing; to establish and maintain positive working relationships with others in a team environment; perform biological sampling activities under various field conditions, including heavy lifting; maintain a valid driver's license; work in excess of 40 hours per week Why should I apply? The Benefits of Working for the State of Florida: State of Florida employees enjoy top-tier benefits offerings including comprehensive health coverage to meet the needs of you and your family while maintaining low deductibles and low monthly out-of-pocket contributions. State employees also enjoy the option of selecting between the FRS Pension Plan and the FRS Investment Plan for retirement. As an additional benefit, state employment affords you the opportunity to take part in the tuition waiver program within the state university and community college systems. Biweekly Health Insurance Premiums: $7.50 or $25.00 for Single / $32.15 or $90.00 for Family No Cost $25,000 Life Insurance Nine Paid State Holidays, One Personal Holiday per year 4 hours Annual Leave and 4 hours Sick Leave accrued Biweekly Retirement Plan Options State University and College Tuition Waiver Program On the Job Trainings Support for family planning, including paid maternity leave, adoption benefits, Family and Medical Leave Act (FMLA), Family Supportive Work Program (FSWP), and paid leave for family and medical responsibilities for eligible employees. Paid administrative leave for mentoring, volunteering, voting, and other reasons because we understand the importance of giving back to the community. For a more complete list of benefits, visit ************************************** The State of Florida is an Equal Opportunity Employer/Affirmative Action Employer, and does not tolerate discrimination or violence in the workplace. Candidates requiring a reasonable accommodation, as defined by the Americans with Disabilities Act, must notify the agency hiring authority and/or People First Service Center (***************. Notification to the hiring authority must be made in advance to allow sufficient time to provide the accommodation. The State of Florida supports a Drug-Free workplace. All employees are subject to reasonable suspicion drug testing in accordance with Section 112.0455, F.S., Drug-Free Workplace Act. VETERANS' PREFERENCE. Pursuant to Chapter 295, Florida Statutes, candidates eligible for Veterans' Preference will receive preference in employment for Career Service vacancies and are encouraged to apply. Certain service members may be eligible to receive waivers for postsecondary educational requirements. Candidates claiming Veterans' Preference must attach supporting documentation with each submission that includes character of service (for example, DD Form 214 Member Copy #4) along with any other documentation as required by Rule 55A-7, Florida Administrative Code. Veterans' Preference documentation requirements are available by clicking here. All documentation is due by the close of the vacancy announcement. Location: ST PETERSBURG, FL, US, 33701

is on site in Boulder, Colorado and requires relocation*** We are seeking a skilled Analytical Chemist to join our team. The Analytical Chemist will be responsible for running HPLC, developing and validating new methods, and supporting manufacturing and regulatory needs through innovative analytical chemistry and methodology. We are looking for soft skills like strong communication, client communication, being able to work with a team, and the capacity for continuous learning, recognition of errors, and resilience in progressing forward Responsibilities + Participate in the development of new processes by applying analytical skills and training + Facilitate and support analytical technology transfers + Plan and formulate aspects of analytical research and development proposals, including objectives, applications, cost, equipment, and human resource requirements + Develop, implement, and validate analytical methods and procedures + Keep accurate records and document experiments + Support the Stability Program by understanding internal, corporate, and ICH stability guidelines + Engage in manufacturing site activities such as troubleshooting and resolving analytical problems + Develop an understanding of Quality, Environmental, Health, & Safety (QEH&S) principles and regulatory affairs + Analyze batches of drug substances, intermediates, and raw materials for clinical or registration programs + Properly manage the generation and accumulation of hazardous and non-hazardous waste Qualifications + 3 years of experience + HPLC + GMP regulations + Experience with samples like peptides, small molecules, potent or highly toxic materials, or lipids + We will consider candidates with advanced degrees (e.g., MS or PhD) with HPLC experience as part of their degree or other advanced analytics techniques such as Mass Spectrometry (MS) + Open to candidates with quality control experience (2-3 years) Work Environment The schedule is Monday to Friday 8-5pm with flexibility. No weekends required. 80% of the time will be working in the lab, so you must be onsite every day. Pay and Benefits The pay range for this position is $33.20 - $41.70/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 Tampa,FL. Application Deadline This position is anticipated to close on Mar 10, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.