Laboratory Technologist

Vitrolife Group; Miami (FL); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Paid time off

401(k) with employer match

Medical, dental, vision

IVF coverage

Employee assistance program

Job summary

Vitrolife Group in Miami is seeking a Laboratory Technologist to support molecular testing workflows in reproductive health and genetics. The role emphasizes accuracy, compliance, and cross-functional collaboration in a fast-paced lab.

Ideal candidates have molecular biology skills, experience with PCR and related techniques, and a commitment to quality and safety in patient testing environments.

Qualifications

• Bachelor’s or higher degree in a laboratory science field or related area with supervised experience or training
• Experience in molecular skills incl. RNA/DNA extraction, PCR, and gel electrophoresis is a plus
• Florida CLT/Labtech licensure is preferred

Responsibilities

• Process specimens, perform tests, and review/report results as applicable
• Conduct high complexity tests authorized by supervisor or director
• Follow procedures for specimen handling, test analyses, and record-keeping
• Adhere to safety and quality control protocols
• Identify issues impacting test performance and notify supervisor immediately

Skills

Molecular biology techniques

RNA/DNA extraction

PCR

Gel electrophoresis

Real-time PCR

Education

Bachelor’s degree in laboratory science or medical laboratory technology

Tools

Centrifuges

Thermal cyclers

Real-time PCR analyzers

Job description

At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby.

Position Summary

We are currently seeking a Laboratory Technologist to join our Miami-based team. This individual will play a key role in molecular testing workflows that support our mission in reproductive health and genetic diagnostics. The ideal candidate is detail-oriented, highly skilled in molecular biology techniques, and committed to maintaining the highest standards of accuracy and compliance in a fast-paced laboratory environment.

Key Responsibilities

• Responsible for specimen processing, test performance, and for reviewing and reporting test results, if applicable.
• Performs high complexity tests that are authorized by the General Supervisor or Laboratory Director.
• Adhere to laboratory's procedures for specimen handling and processing, test analyses, reviewing and maintaining records of patient test results.
• Follow all safety and quality control protocols.
• Be capable of identifying problems that may adversely affect test performance or reporting of test results and immediately notify the General Supervisor or Laboratory Director.
• Document all non-conformities and corrective actions taken when test systems deviate from the laboratory's established performance specifications.
• Register samples in the designated system, witness the procedure, and ensure proper documentation is in place.
• Work flexible hours including overtime, weekends, and overnight shifts as dictated by operational needs.
• Collaborate effectively with cross-functional teams to ensure workflow efficiency and continuity.
• Maintain a high level of organization and accountability to support safe, accurate, and timely laboratory testing.
• Perform additional duties as assigned in support of laboratory operations.

Experience and Qualifications

• Bachelor’s, or higher, degree in a laboratory science, or medical laboratory technology from an accredited institution; OR a bachelor’s, or higher, degree in one of the chemical, or biological sciences from an accredited institution, and, in addition, at least 6 months of acceptable supervised experience and/or relevant training.
• Relevant molecular skill set consisting of the molecular fundamentals, RNA and DNA extraction, PCR, and gel electrophoresis will be plus.
• Experience with real time PCR, microarray or sequencing preferred.
• Possession of a Florida license for Clinical Laboratory Technologist is preferred.

Key knowledge, skills and abilities

• Highly organized and strong work ethic.
• Understanding of the equipment used daily, including, but not limited to centrifuges, thermal cyclers, and real-time PCR analyzers.
• Understanding of CLIA requirements and experience with CAP inspections for compliance with Checklist requirements.
• Demonstrate clear ability to explain experience with specific instrument platforms, including test principle(s), what controls were in place, and how results are interpreted and reported out.
• Ability to multi-task and work in a fast-past, deadline-driven environment.
• Communication - Proficient verbal and written communication skills, including ability to write clear reports and detailed laboratory procedures with correct grammar and spelling. Willingness to share and receive information and ideas from all levels of the organization in order to achieve the desired results.
• Teamwork - Commitment to the successful achievement of team and organizational goals through a desire to participate with and help other members of the team.
• Dependable; follow instructions, respond to management direction, complete tasks on time or notify appropriate person with an alternate plan.
• Visual acuity and analytical skills to distinguish fine detail.
• Manual dexterity to use common laboratory equipment and perform sterile techniques as required.
• Must possess ability to perform repetitive motion.

Benefits

• Paid Time Off and 10 Paid Holidays
• 401(k) with Employer Match
• Medical, Dental, Vision
• IVF Coverage to support family building needs
• GAP Insurance
• Basic Life and AD&D Coverage
• Short- and Long-Term Disability
• Optional AFLAC Supplemental Policies
• Employee Assistance Program (EAP)
• Flexible Spending & Health Savings Account

An offer of employment is contingent on the successful passing of a background check.In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment.

We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.