Medical Technologist II job in

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.

Impactful work. Meaningful careers. Quality rewards.

At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential.
Learn more about Our Culture at ICON

List #1

Day in the life

Lydia's Journey Back to ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/24/2026

Summary

Career paths are rarely straightforward, especially in the fast moving world of clinical research. For many professionals, gaining experience across organisations can provide valuable perspectiv

Teaser label

Learn about Lydia's return to ICON and why she felt it was a natural choice.

Driving Trials Forward: Study Start-Up Leadership at ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/16/2026

Summary

Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl

Teaser label

Explore James Pereira's career in study start-up at ICON, leading global teams to accelerate patient access.

Who’s Who in a Clinical Trial Team

Teaser label

Inside ICON

Content type

Blogs

Publish date

03/15/2026

Summary

Who's Who In a Clinical Trial Team Clinical trials rely on large, cross functional teams working together across countries, time zones and specialisms. For those new to the industry, the number of

Teaser label

Understand the key roles in a clinical trial team, from study start up and site activation to data, safety and quality.

View all

Similar jobs at ICON

CRA - Germany

Salary

Location

Germany, Frankfurt

Location

Frankfurt

Mannheim

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate (CRA) to join our diverse and dynamic team. As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activit

Reference

JR146698

Expiry date

01/01/0001

Author

Dominic Brady

Author

Dominic Brady

Read more Shortlist Save this role

Senior Project Manager

Salary

Location

UK, Reading

Location

Reading

Warwickshire

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Project Management

Job Type

Permanent

Description

UK Clinical Study ManagerJoin our diverse and dynamic team as a Senior Local Trial Manager at ICON, where you will play a key role in driving the successful delivery of clinical studies across the UK.

Reference

JR145674

Expiry date

01/01/0001

Author

Dominic Brady

Author

Dominic Brady

Read more Shortlist Save this role

Site Management Associate I

Salary

Location

Mexico, Mexico City

Location

Sao Paulo

Mexico City

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Site Management Associate I to join our diverse and dynamic team. As a Site Management Associate I at ICON, you will play an important role in supporting the management of c

Reference

JR144316

Expiry date

01/01/0001

Author

Tulio Sanquiz

Author

Tulio Sanquiz

Read more Shortlist Save this role

Clinical Trial Specialist

Salary

Location

US, Blue Bell (ICON)

Location

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Senior Site Management Associate to join our diverse and dynamic team. As a Senior Site Management Associate at ICON, you will play a critical role in overseeing site manage

Reference

JR147575

Expiry date

01/01/0001

Author

Brendan Hoey

Author

Brendan Hoey

Read more Shortlist Save this role

Senior Program Manager - Clinical Data Review

Salary

Location

United States of America

Location

Canada

Multiple US Locations

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Data Management

Job Type

Permanent

Description

What You Will Be Doing:Lead clinical data review activities across assigned clinical studies or programs, ensuring medically meaningful interpretation of emerging efficacy and safety data.Perform comp

Reference

JR145961

Expiry date

01/01/0001

Author

Paula Cameron

Author

Paula Cameron

Read more Shortlist Save this role

Clinical Site Associate

Salary

Location

France, Paris

Department

Clinical Monitoring

Location

Paris

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Clinical Site Associate (CSA) We are currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team. As an CSA at ICON, you will play a pivotal role in supporting clinical tria

Reference

JR142456

Expiry date

01/01/0001

Author

Sophie Clarke

Author

Sophie Clarke

Read more Shortlist Save this role

About Icon

Overview of Service Lines

Full Service

ICON Strategic Solutions

Global Business Services

Global Office Locator

Inclusion & Belonging

ICON Cares - ESG

Building a Successful Clinical Research Resume

Landing Your First Job in Clinical Research

graduate What does full service mean for you?

Medical Technologist II

About the role

This vacancy has now expired. Please click here to view live vacancies.

ICON and you

About ICON

Career Pathways

Benefits & Rewards

Inclusion & Belonging

Environmental, Social & Governance

Global Office Locator

Impactful work. Meaningful careers. Quality rewards.