JUMP TO CONTENT
Shortlist
search jobs Search
About the role ICON and you Application Process Day in the life Who we are

Medical Technologist II

059927_2

About the role

This vacancy has now expired. Please click here to view live vacancies.
Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance. As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. Accepts direction and instructions from the Laboratory Management Team Responsible for the quality and timelines of technical procedures, as well as their compliance with applicable company, CAP, and local regulatory agency testing requirements. Perform technical assignments and testing and issue reports in accordance with written procedures. These should be processed within agreed turnaround times. Enters and releases required information in the LIS, such as test results, comments, and quality control results in a timely manner with compliance to all regulatory requirements. Adheres to written internal and external quality control procedures in order to ensure the quality of the results and maintain Corrective action logs as appropriate. Consults with laboratory management staff prior to reporting grossly abnormal results and when OUT OF CONTROL test runs are encountered. Responsible for the preparation quality control documentation, instrument and equipment maintenance documentation, performance of proficiency testing and compliance with all appropriate regulatory procedures and quality requirements in testing area. Responsible for ensuring that reagents are maintained, prepared, stored and used in a manner suitable for testing and documentation is kept to ensure adequate records are available in test area. Performs the maintenance, calibration and validation of the instruments/assays assigned to the section according to written laboratory procedures. Responsible for maintaining all paperwork and ensuring all records are kept up to date and stored safely as per standard operating procedures Assists with responding to queries and quality issues, and participates in root cause analysis investigations as directed by laboratory management team. Assists with the evaluation and validation of new procedures as required. Assists in maintaining temperature monitoring system as required. Reports to and is responsible to Supervisor/Manager for daily operation and evaluation of work performance. Participates in required Continuous Professional Education Programs, including conferences, internal journal club and lectures, as required. To carry out specific tasks relevant to the general running of the laboratory as assigned by the Management team. Travel (approximately 0%) domestic and/or international Provides mentorship for training of: Technologists I/BMS III, Technicians I & II/BMS I & II and Lab Assistants To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. US/LATAM/CAN: A minimum of 5 years experience successfully performing as a Technologists EU/APAC: in depth proven experience successfully performing as a Technologist or a significant proven experience supporting development activities. For Farmingdale Lab: New York State License as a Clinical Laboratory Technologist. Compliance with all health and safety legislation and awareness of employee responsibilities in this context. Basic knowledge of immunization requirements for the role of occupational health professions. Basic working knowledge of and Compliance with all CAP and local agency regulatory requirements. Proficiency in Microsoft Office. Fluency in English both written and oral. Demonstrated ability to manage multiple tasks with good organization skills and good attention to detail. Ability to work as part of, and set the example of performance standards for a team. Ability to work in conformance with standard operating procedure and conditions with a systematic approach to tasks committed to seeing things through to completion. Demonstrated ability to keep accurate, legible records and recognize the need to handle these records and all other information in line with GCP/GLP/GDP. Familiar with the operation of laboratory equipment with a demonstrated ability to check that equipment is functioning within its specifications and to respond appropriately to abnormalities. Understands the basic principles of quality control, quality assurance and quality audits and outcomes. Customer Focused –providing timely, confident, reliable and friendly service to all our internal and external customers and inspiring the team to follow your example. Demonstrates a high level of personal integrity and ethical behavior with a responsible and mature approach to work duties. Action oriented demonstrating the ability to handle work load demands resulting in the generation of large amounts of data and to trouble shoot issues timely when required. Creative and enthusiastic with the ability to suggest and assists in implementing process improvement initiatives. Ability to confidently interact with all levels in the organization and provide senior management with valued feedback. Basic working knowledge of LIMS with the desire to achieve the mathematical, computational and instrumentation skills necessary to work and progress in Biomedical Science. Bachelors’ degree in Medical Technology or equivalent. OR A BSc degree in Medical Laboratory Science/Biomedical Science majoring in Chemistry, Haematology, Immunology, and/or Infectious Diseases. A postgraduate qualification such as FIBMS/FAMLS/ASCP or MSc while highly desirable is not essential.
List #1

Day in the life

Two medics at ICON clinical research clinic
The Strategic Role of Site Selection and Activation in Clinical Trials

Teaser label

Industry

Content type

Blogs

Publish date

10/28/2025

Summary

Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit

Teaser label

Explore the critical role of site selection and activation in clinical trials.

Read more
Headshot of female
A Career Focused on Patients: Daniela's Journey at ICON

Teaser label

Our People

Content type

Blogs

Publish date

10/27/2025

Summary

Daniela’s Journey at ICON Daniela Gutierrez’s career at ICON has been a journey of transition, determination, and purpose. What began as a role in study start-up has evolved into a position deeply

Teaser label

Daniela shares insights into how collaboration, purpose, and innovation drive every part of her work.

Read more
Headshot of male
ICON Careers Spotlight: Chris Maguire, Director of Finance Business Partnering

Teaser label

Our People

Content type

Blogs

Publish date

10/15/2025

Summary

Chris Maguire’s Journey at ICON Over the past eight years at ICON, Chris Maguire has held six roles within the finance function, each expanding his expertise and sharpening his ability to support

Teaser label

Discover how Chris Maguire’s collaborative approach has shaped a rewarding career journey at ICON.

Read more
View all

Similar jobs at ICON

(Sr) Clinical Trial Manager

Salary

Location

Taiwan, Taipei

Location

Taipei

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Trial Manager to join our diverse and dynamic team. As the Senior Clinical Trial Manager, you will hold a crucial role in ensuring the successful delivery of

Reference

JR136990

Expiry date

01/01/0001

Sandy Tang

Author

Sandy Tang
Sandy Tang

Author

Sandy Tang
Read more Shortlist Save this role
Read more Shortlist Save this role
CTA 1

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a

Reference

JR138319

Expiry date

01/01/0001

Rita Villavicencio

Author

Rita Villavicencio
Rita Villavicencio

Author

Rita Villavicencio
Read more Shortlist Save this role
Read more Shortlist Save this role
Drug Safety associate

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Drug Safety

Job Type

Permanent

Description

We are currently seeking a Drug Safety Associate to join our diverse and dynamic team. As a Drug Safety Associate at ICON, you will play a pivotal role in ensuring the safety of investigational drugs

Reference

JR138519

Expiry date

01/01/0001

Rita Villavicencio

Author

Rita Villavicencio
Rita Villavicencio

Author

Rita Villavicencio
Read more Shortlist Save this role
Read more Shortlist Save this role
Drug Safety associate

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Drug Safety

Job Type

Permanent

Description

We are currently seeking a Drug Safety Associate to join our diverse and dynamic team. As a Drug Safety Associate at ICON, you will play a pivotal role in ensuring the safety of investigational drugs

Reference

JR138523

Expiry date

01/01/0001

Rita Villavicencio

Author

Rita Villavicencio
Rita Villavicencio

Author

Rita Villavicencio
Read more Shortlist Save this role
Read more Shortlist Save this role
Graduate Pharmacovigilance Associate

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Drug Safety

Job Type

Permanent

Description

We are currently seeking a Graduate Pharmacovigilance Associate to join our diverse and dynamic team. As a Graduate Pharmacovigilance Associate at ICON, you will play an essential role in supporting t

Reference

JR138518

Expiry date

01/01/0001

Rita Villavicencio

Author

Rita Villavicencio
Rita Villavicencio

Author

Rita Villavicencio
Read more Shortlist Save this role
Read more Shortlist Save this role
CSA

Salary

Location

Brazil, Sao Paulo

Department

Clinical Monitoring

Location

Sao Paulo

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own

Reference

JR136982

Expiry date

01/01/0001

Olivia Molina

Author

Olivia Molina
Olivia Molina

Author

Olivia Molina
Read more Shortlist Save this role
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above