Serious inquiries only.
Eccolab Group is currently seeking qualified candidates that meet our criteria for this job opportunity. Please read the job description thoroughly — if you meet all criteria, please apply or send your resume to [email protected]
Schedule:
Full-time — Open availability. Morning, evening, or night shift. (40 hrs/week)
Part-time — Monday and Thursday 8:30 AM–4:30 PM, and Saturday 2:00 PM–10:00 PM. (25–32 hrs/week)
Licensure & Certification Requirements
Candidates must possess the following credentials (verification will be required during the interview process):
- Active Florida Clinical Laboratory Technologist License (non-negotiable)
- Current certification from one of the following:
- ASCP (American Society for Clinical Pathology)
- AMT (American Medical Technologists)
- AAB (American Association of Bioanalysts)
About us
Eccolab Group, Co. is a licensed, independent full-service clinical laboratory headquartered in Miami, Florida, with additional facilities in Tampa. Established in 2001, we provide comprehensive analytical services to a diverse clientele, including hospitals, skilled nursing facilities, assisted living centers, and research organizations. With a strong focus on accuracy, innovation, and client education, we are committed to improving patient outcomes through fast, reliable diagnostics and cutting-edge laboratory technologies. Our team upholds the highest standards in quality assurance, compliance, and customer service. Visit us at eccolabgroup.com for more information.
Job Summary
The Clinical Laboratory Medical Technologist – General Laboratory is responsible for performing moderate and high-complexity clinical laboratory testing with accuracy, efficiency, and strict adherence to regulatory and quality standards. This role supports continuous laboratory operations by ensuring timely and reliable test results across core disciplines, including chemistry, hematology, urinalysis, and immunology. The Clinical Laboratory Medical technologist plays a critical role in maintaining workflow efficiency, supporting clinical trials testing needs as applicable, and upholding Eccolab Group’s commitment to patient safety, regulatory compliance, and operational excellence.
Scope
This position provides dedicated second-shift coverage for the General Laboratory and is accountable for maintaining testing continuity, turnaround times, and operational stability during assigned hours. The role functions within established laboratory frameworks, following approved methodologies, instrumentation protocols, and quality systems. The Clinical Laboratory Technologist operates with a high level of technical accountability, contributing to workload distribution, shift-to-shift handoffs, and compliance readiness, while supporting departmental staffing balance and minimizing cross-departmental resource dependency.
Essential Duties/Responsibilities
- Perform moderate and high-complexity testing in the General Laboratory in accordance with approved methodologies, regulatory requirements, and laboratory policies.
- Perform clinical laboratory testing including hematology, coagulation, urinalysis, immunology, and clinical chemistry.
- Determine the acceptability of specimens for testing based on established criteria and testing requirements.
- ·Perform routine and complex technical procedures in compliance with departmental Standard Operating Procedures (SOPs)
- Operate, monitor, and troubleshoot laboratory instruments to ensure accurate and reliable performance.
- Demonstrate sound technical judgment when making testing decisions and resolving technical or procedural issues.
- Prepare, test, and evaluate reagents, calibrators, and quality control materials prior to use.
- Analyze, verify, and report accurate and timely test results through the laboratory information system.
- Perform and document quality control activities, calibrations, and preventive maintenance in accordance with laboratory standards.
- Identify, investigate, and document testing deviations, instrument issues, and quality variances, including corrective actions taken.
- Identify and promptly escalate critical values in accordance with laboratory policy and escalation protocols.
- Adhere to chain-of-custody, specimen handling, and documentation requirements throughout the testing process.
- Manage reagent and supply inventory to ensure adequate availability and uninterrupted testing operations.
- Maintain a safe work environment by complying with all laboratory safety policies, infection control procedures, and proper use of personal protective equipment (PPE).
- Support shift handoffs by communicating pending work, issues, and critical information to incoming staff.
- Participate in proficiency testing, competency assessments, inspections, audits, and corrective action initiatives as required.
- Maintain strict confidentiality of patient information in compliance with HIPAA and company policy.
- Maintain regulatory readiness by adhering to CLIA, COLA, OSHA, and internal quality management requirements.
Qualifications
- Associate or bachelor’s degree, or foreign equivalent, in Clinical Laboratory Science, Medical Technology, Biological Sciences, or a closely related scientific field.
- Active and unrestricted State of Florida Clinical Laboratory Technologist license, appropriate to the testing performed.
- Current ASCP, AMT, or AAB Medical Technologist / Medical Laboratory Scientist certification.
- Mid to Senior-level candidates meeting licensure and certification required.
- 3-6 years clinical laboratory experience.
- Prior experience in a high-volume or multi-discipline clinical laboratory environment is preferred.
- Must meet CLIA requirements to perform moderate and high-complexity testing.
- Ability to maintain all required licenses and certifications in good standing as a condition of employment.
Skills/Abilities
- Ability to work independently while effectively collaborating within a team-based laboratory environment.
- Strong analytical and problem-solving skills with the ability to exercise sound technical judgment.
- High level of attention to detail to ensure accuracy, quality, and regulatory compliance.
- Proficiency with computers and laboratory systems; experience with Laboratory Information Systems (LIS) preferred.
- Effective verbal and written communication skills for documenting results and communicating issues.
- Strong organizational and time-management skills to manage workload and meet turnaround times.
- Ability to adapt to changing priorities, workflows, and testing volumes.
- Commitment to safety, quality assurance, and adherence to laboratory policies and procedures.
Key Requirements
- Bilingual English and Spanish
- Authorized to work in the U.S. with valid I-9 documentation.
- Available for extended hours, weekends, or holidays as needed.
- Subject to background check and drug screening per Florida law.
- Completion of HIPAA and OSHA training upon hire; ongoing compliance required.
- Adherence to HIPAA, FIPA, and all confidentiality regulations.
- Compliance with Florida Department of Health and CDC safety protocols.
- Professional appearance and conduct required in a clinical setting.
- Willing to perform additional duties as assigned
Pay: $30.81 - $37.11 per hour
Benefits:
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Work Location: In person
