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Apidel Technologies is seeking a local contract Medical Lab Scientist for a local contract job in Miami, Florida. Job Description & Requirements • Specialty: Medical Lab Scientist, • Discipline: Allied Health Professional, • Start Date: ASAP, • Duration: 13 weeks, • 40 hours per week, • Shift: 8 hours, • Employment Type: Local Contract Position: Medical Lab Scientist Speciality: Florida State License, Chemistry, Hematology, Urinalysis, Coagulation, Core Lab Duration: 13+ Weeks of Contract to FTE Location: Miami, FL Note: Candidates will be responsible for covering all relocation expenses independently, including travel (airfare), accommodation costs and any other costs. Required Skills: • Florida State License, • Bachelors in Science field, • Chemistry, Hematology, Urinalysis, Coagulation, • Core lab Job Description: • Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist., • Work environment/department will be listed in requirement. Determine the acceptability of specimens for testing according to established criteria., • Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures., • Monitor, operate and troubleshoot instrumentation to ensure proper functionality., • Demonstrate the ability to make technical decisions regarding testing and problem solving., • Prepare, test, and evaluate new reagents or controls. Report accurate and timely test results to deliver quality patient care., • Perform and document preventive maintenance and quality control procedures., • Identify and replenish testing bench supplies as necessary., • Assist with processing of specimens when needed. Maintain a safe work environment and wear appropriate personal protective equipment. Experience: • Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements., • State Medical Technologist license required., • ASCP or AMT certification is preferred., • Proficient with computers; Familiarity with laboratory information systems is a plus., • High level of attention detail along with strong communication and organizational skills., • Flexibility to work overtime or other shifts depending on business needs. Apidel Technologies Job ID #API4109. About Apidel Technologies At Apidel Technologies LLC, we specialize in delivering high-impact healthcare staffing solutions that empower organizations to maintain operational excellence and deliver exceptional patient care. With our headquarters in Illinois and regional offices in New Jersey, California, and Georgia, we offer both nationwide reach and local insight to support the dynamic workforce needs of healthcare providers across the U.S. We deliver unmatched expertise in placing top-tier healthcare professionals, including Registered Nurses, Licensed Practical Nurses/Licensed Vocational Nurses, Certified Nursing Assistant/Certified Medical Assistant, and Nurse Practitioners, Medical Laboratory Scientist, Phlebotomist, Histologists, across a diverse spectrum of care settings such as hospitals, clinics, rehabilitation centers, long-term care facilities, correctional institutions, and more. Our deep talent network and sector-specific understanding position us as a valuable partner to client platforms, enabling a scalable and seamless workforce experience for healthcare employers and job seekers. Since our founding in 2012, Apidel has earned the trust of Fortune 500 healthcare organizations, mid-sized providers, and government agencies at the county and state levels. We provide end-to-end staffing services, contingent workforce solutions, direct hire, temp-to-hire, and executive search, designed to align with your clinical and operational objectives. As a certified WBENC firm, we are committed to Diversity, Equity, Inclusion & Belonging (DEI&B) and take a client-centric approach that combines industry insight, agile delivery models, and culturally competent staffing to help our clients thrive in today’s fast-evolving healthcare Benefits • 401k retirement plan, • License and certification reimbursement, • Medical benefits, • Dental benefits, • Vision benefits, • Referral bonus, • Sick pay

Job DescriptionSalary: POSITION SUMMARY Service Technician capable of inspecting, removing, installing, troubleshooting, repairing and maintaining our clients fueling facilities (vehicular, emergency generator, boilers, etc.). ESSENTIAL FUNCTIONS Reasonable Accommodations Statement To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. Essential Functions: • Perform on-site maintenance at our clients fueling facilities throughout South Florida regularly; Occasional travel to remote sites to assist Project Personnel., • Assist in the diagnosis, analysis, and resolution of fuel/petroleum equipment problems., • Perform fuel facility/systems monthly/annual/pre-regulatory inspections and diagnosis on regular schedules. Self-schedule much of your own activities in coordination with the Service Project Manager., • Maintain a high level of customer satisfaction, with an excellent work ethic, neat appearance, and good communication skills., • Keep customers informed of job progress, parts availability, cost estimates, and job completion. Contracts may require rapid response (less than 4 hours), 24 hours a day, 7 days a week., • Read, write, and speak English with exceptional analytical and communication skills;, • Coordinate all required inspections with the site Foreman and maintain good working relationships with inspectors., • Reviews, analyzes, and updates Labor Hours/Job Costs Report information with project management regularly., • Assist Project Managers with schedule preparation., • Keep proper and complete documentation of the project., • Responsible for the care and maintenance of a stock of tools and fuel equipment inventory., • Attend required training with Fuel and Electrical control systems. Participation in company-provided training., • Ensure accurate and complete cost coding of all time cards and Work Orders on a daily basis. Review, sign off, and forward time cards to the corporate office as required., • Ensure efficient project closeout, including completion of all punch list work, owner training and instruction, transfer of spare parts, final cleanup, demobilization, and project records archiving., • Enforce and implement the dictates and recommendations of the EHS department., • Complete all documentation required in the Corporate Health and Safety plan. Environmental • Assist the Environmental Scientist in the performance of sampling., • Set up of sampling and monitoring equipment this includes calibration of field equipment, • Maintenance of equipment (cleaning and repair), • Conduct or assist with environmental sampling - may include groundwater, surface water, or soil, • Complete field logs with all required information, • Set up field screening equipment/instruments (OVA Meter, GPS Trimble Unit, etc.), collect field data, and document readings, • Read and interpret field/site maps, document site conditions/changes, • Document field activities with daily reports and pictures, • Properly pack samples and coordinate the delivery of samples to the laboratory, • Operate remediation/dewatering systems, maintain components (pumps, etc.), collect necessary samples for screening POSITION QUALIFICATIONS Competencies: • Strong background or equivalent training in heavy mechanics, hydraulics, and electrical systems., • Strong diagnosis, repair, and testing abilities., • Ability to interact with others, including customers and colleagues, professionally and courteously., • Demonstrate high standards for appearance, safety, and professionalism., • Ability to build rapport with clients and identify, define, and solve problems and satisfy customer needs., • Ability to lead without constant supervision and be a self-starter., • Strong Multi-tasking skills., • Attention to detail., • Must be a team player. SKILLS & ABILITIES Education: • High school graduation or equivalent required., • Trade School or Apprentice program strong plus. Experience: • Minimum 3 years of previous experience in this position. Computer Skills: • Must have familiarity with computer operations and an aptitude for learning computer skills., • Complete Daily reports / JSAs / Toolbox meetings, • Ability to send and receive email., • Ability to complete online time reporting, including preparation of Certified Payroll sign-in., • Submit Project Photos on a scheduled basis., • Ability to complete online training Certificates & Licenses: • Currently or ability to obtain:, • NCCER accreditation desired, • OSHA 40-HOUR HAZWOPER, • OSHA 30-HOUR CONSTRUCTION, • Veeder Root Certification, • Pneumercator Certification, • Fuelmaster Certification, • Red Jacket Certification, • Others as the Market dictates Other Requirements: • Drivers License, • Competent Person lockout/Tagout, Confined space and trenching, and excavation procedures in a safe manner., • Identify safety hazards you or other employees may be subject to and take all necessary corrective action to eliminate or minimize hazards PHYSICAL DEMANDS • Hearing and vision within normal ranges are essential for normal conversations, to receive ordinary information, and prepare, inspect, or review documents., • Frequent walking and climbing (stairs, ladders, terrain), • Frequent lifting (up to and including 50 pounds), • Frequent bending, twisting, and standing, • Exposure to working outdoors in all-weather conditions, • Ability to work more than 40 hours in any given week, including weekend assignments as required Other Physical Requirements: Must wear steel-toed boots, must wear protective eye-wear, hearing protection, may work outdoors during inclement weather, ability to travel by car or plane, high frequency of computer keyboarding, high frequency of viewing a computer monitor, etc. WORK ENVIRONMENT Work is performed in outdoor settings and industrial settings, in all weather conditions, including temperature extremes, during day and night shifts. Work is often performed in emergency and stressful situations. This job description is subject to change at any time.

Job DescriptionActalent is Hiring for Associate Scientist! Job Description We are seeking a dedicated Associate Scientist to perform routine tests on various samples, including finished products, stability samples, and raw materials, using techniques such as UV and HPLC in a regulated laboratory environment. This role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards. Responsibilities • Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution., • Evaluate test results and determine the acceptability of samples based on the results., • Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs., • Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards., • Review notebooks promptly and ensure compliance with SOPs., • Analyze and interpret results in both written and oral formats., • Assist in training 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. Required Skills • Minimum 2 years of Experience in HPLC and Working in GMP Environment., • Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience., • Problem-solving skills involving several concrete variables in standardized situations., • Ability to perform necessary computations and interpret graphs., • Working knowledge of instrumentation software used in laboratories. INTERESTED IN THIS ROLE? SEE BELOW TO BE IMMEDIATELY CONSIDERED: • I am scheduling phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Fathima, • HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to fam@actalentservices.com or CALL- 904 530 5415 Job Type & Location This is a Contract to Hire position based out of Miami, FL. Pay and Benefits The pay range for this position is $29.00 - $39.00/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 Miami,FL. Application Deadline This position is anticipated to close on Jun 29, 2026. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionDescription: Under the direction of the Director of Research, the Research Scientist is responsible for designing, executing, and documenting research activities supporting human tissue-based product development, product characterization, and translational performance testing. This role contributes to the development and evaluation of tissue allografts through experimental design, biochemical and biomechanical characterization, ex-vivo model development, data analysis, and cross-functional collaboration with Research, Quality, Regulatory, Operations, and Marketing teams. Ideal candidate profile: Scientist with prior human tissue/allograft experience with the ability to develop testing (biomechanical, functional, or ex-vivo models) to evaluate tissue characteristics, handling and performance. Requirements: Duties and Responsibilities · Design, execute, and document research studies supporting the development, characterization, and performance evaluation of human tissue-based products, including literature review, experimental design, sample selection, test method development, complex laboratory testing, data analysis, and interpretation of results. · Develop, optimize, and execute biomechanical, functional, and ex-vivo test models to evaluate tissue properties, handling characteristics, structural performance, and product-use conditions. · Analyze and interpret research data using appropriate statistical and scientific methods, and prepare clear technical summaries, internal reports, protocols, presentations, and manuscripts as needed. · Support product development activities by identifying relevant critical material attributes, product performance attributes, and test methods for tissue-based products. · Collaborate cross-functionally with Quality, Regulatory, Manufacturing, and Commercial teams to support product claims, technical justifications, design inputs, risk assessments, and regulatory strategy. Required Qualifications • Advanced degree (Master’s, PhD) in Biochemistry, Chemical Biology, Bioengineering or life sciences/health related field., • Prior hands-on experience with human tissue, allografts, extracellular matrix-based materials, or biologically derived implants is strongly preferred., • Experience designing and executing independent laboratory experiments, including study planning, protocol development, data analysis, and technical reporting., • Experience with tissue characterization methods, which may include biochemical assays, histology, microscopy, ELISA, flow cytometry, cell-based assays, tissue culture, extracellular matrix analysis, or related techniques., • Experience with biomechanical testing, functional performance testing, or ex-vivo model development is strongly preferred., • Strong technical writing skills, including the ability to prepare protocols, study reports, technical summaries, literature reviews, and scientific presentations., • Strong organizational skills with the ability to manage multiple projects, timelines, and experimental priorities., • Ability to work effectively in a laboratory environment and collaborate with cross-functional teams., • CTBS certification or ability to obtain certification within two years of employment. Applicants must be legally authorized to work in the United States. Vivex will not provide sponsorship or employment for candidates who require the 24-month STEM Optional Practical Training (OPT) extension. Please note this is not an offer of immigration sponsorship Preferred Qualifications · Experience supporting regulated product development in an FDA-regulated environment, preferably involving human tissue products, HCT/Ps, biologics, medical devices, or combination products, including product characterization, verification testing, technical documentation, and cross-functional support for Quality and Regulatory activities. · Experience working with musculoskeletal, birth tissue, cartilage, intervertebral disc, bone, connective tissue, or other structural tissue matrices. · Experience developing or executing biomechanical assays such as compression, tensile, shear, swelling, hydration, viscoelastic, injectability, extrusion, retention, or handling-related testing. · Direct Reports This position may supervise one Research Associate and may be responsible for assigning work, providing technical guidance, supporting training, reviewing experimental documentation, and ensuring completion of research activities in alignment with project objectives and laboratory procedures. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job any time. VIVEX Biologics is an equal opportunity employer (EEO) and expressly prohibits any form of workplace discrimination and/or harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. 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. VIVEX Biologics complies with the Americans with Disability Act (ADA) which prohibits discrimination against qualified individuals with disabilities who, with or without reasonable accommodation, can perform the essential functions of a job.

Job Description Description: Job Duties/Responsibilities: Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist. Work environment/department will be listed in requirement. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation to ensure proper functionality. Demonstrate the ability to make technical decisions regarding testing and problem solving. Prepare, test, and evaluate new reagents or controls. Report accurate and timely test results to deliver quality patient care. Perform and document preventive maintenance and quality control procedures. Identify and replenish testing bench supplies as necessary. Assist with processing of specimens when needed. Maintain a safe work environment and wear appropriate personal protective equipment Requirements: Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Minimum 2-4 years of clinical laboratory testing experience is required. State Medical Technologist license may be required (will be listed in requirement if its needed). ASCP or AMT certification is either preferred or required (will be listed in requirement if its required). Ability to work independently and within a team environment. Proficient with computers; Familiarity with laboratory information systems is a plus. High level of attention detail along with strong communication and organizational skills. Must be able to pass a standardized color vision screen. Flexibility to work overtime or other shifts depending on business needs

Description Job Summary The Clinical Research Scientist supports the scientific development, implementation, and analysis of early phase (Phase I/first in child) oncology clinical trials within the Clinical Trials Unit at Nicklaus Children's Health System (NCHS). The role partners closely with the Medical Director and Pediatric Clinician Scientists to advance innovative therapeutics for children and adolescents with high risk or refractory malignancies. The Clinical Research Scientist plays a critical role in protocol development, translational integration, data interpretation, regulatory documentation, and dissemination of research findings, strengthening the scientific rigor and operational success of early phase pediatric oncology trials. Job Specific Duties • Assists in the design and development of early phase oncology protocols. Contributes to study rationale, objectives, eligibility criteria, and correlative science components. Develops statistical analysis plans in collaboration with biostatistics teams. Contributes to study rationale, objectives, eligibility criteria, and correlative science components. Collaborates with investigators, regulatory staff, and research coordinators during study activation. Participate in dose-escalation meetings and safety review discussions. Supports DSMB reporting and pharmacovigilance documentation. Ensure scientific accuracy of consent forms, protocol amendments, and safety reports. Analyzes clinical and translational datasets, including PK/PD and biomarker data. Prepares interim reports, abstracts, and manuscripts. Contributes to regulatory safety updates and sponsor communications. Develops presentations for internal leadership and external stakeholders. Coordinates biospecimen collection and correlative science workflows. Partners with laboratory scientists to integrate molecular and genomic findings into trial design. Supports precision oncology and biomarker‑driven strategies within the Pediatric Early Phase Oncology Program. Contributes to grant applications and progress reports. Assists in the identification and development of grant opportunities including federal, state and foundation grants. Co-authors peer-reviewed publications. Presents findings at national scientific meetings. Qualifications Minimum Job Requirements • Doctoral Degree BPhD, PharmD, MD (non‑clinical track), or equivalent doctoral degree in biomedical sciences, clinical research, pharmacology, or a related field. Knowledge, Skills, and Abilities • Advanced scientific reasoning and clinical trials methodology knowledge. Strong understanding of regulatory and compliance principles in clinical research. Cross-disciplinary collaboration skills across clinical, regulatory, data, and laboratory teams. * High proficiency in data interpretation, PK/PD and biomarker analysis, and scientific communication. Job: Management Department: CANCER CENTER-2100-710000 Job Status: Professional

NEW Medical Technologist OR Laboratory Technologist Opening at an industry-leading laboratory located outside of Hollywood, Florida!. This laboratory is looking to add on a permanent and full time Laboratory Technologist to their team on day shift!. This laboratory has conducted 50 million tests sin

NEW Medical Technologist OR Medical Laboratory Scientist Opening available in the beautiful Southeast Florida! This hospital is an advanced medical center that offers cardiovascular care, oncology, women s health, orthopedics, emergency medicine and the neurosciences and more!. This hospital is look

This laboratory is looking to add on a permanent and full time Laboratory Technologist to their team! Ideally applicants with have experience in high volume laboratory settings - experience in either allergy testing laboratories or immunology preferred. NEW Medical Technologist OR Laboratory Technol

Medical Technologist/ Medical Laboratory Scientist to their team! There are day, evening and night shift openings! This facility requires a BS Degree in Medical Laboratory Technology as well as State of Florida License as a Medical Technologist (in any/all of the specialty areas). NEW Medical Techno

Ochsner Health System is seeking a Clinical/Medical Laboratory Scientist for the 7/7 Nightshift position.