JUMP TO CONTENT

Medical Technologist I

040777_2

About the role

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

Medical Technologist I

Dublin

Summary

To ensure the Central Laboratory is meeting the highest quality standards. To perform the general technical assignments and testing in the Laboratory Department in accordance with current procedures and quality standards.

Assists with the daily management and operation of the department ensuring that turnaround times agreed in each contract are met and as assigned by the management team.

JOB FUNCTIONS/RESPONSIBILITIES

        Assist with the teaching and development of staff currently in the department; to maintain at all times the required high standards and quality.

        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.

SUPERVISION

        Provides mentorship for training of: Technicians I & II/BMS I & II and Lab Assistants

        A minimum of 1 year experience successfully performing as a Technologists

        in depth proven experience successfully performing as a Technologist or a significant proven experience supporting development activities.

        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 behaviour 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.

EXPERIENCE, SKILLS, KNOWLEDGE REQUIREMENTS

        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.

        *An alternative combination of experience, education, and training determined by management to be equivalent to the foregoing.

EDUCATION REQUIREMENTS

        Bachelors’ degree in Medical Technology or equivalent. OR

        A Medical Laboratory Technician's diploma in Biomedical Science a significant component of which involved the study of Chemistry, Haematology, Immunology, and/or Infectious Diseases. OR

        A BSc degree in Medical Laboratory Science/Biomedical Science majoring in Chemistry, Haematology, Immunology, and/or Infectious Diseases. OR

        A degree in Biological Science equivalent* with relevant experience in the field.

        A postgraduate qualification such as FIBMS/FAMLS/ASCP or MSc while highly desirable is not essential.

·         An alternative combination of experience, education, and training determined by management to be equivalent to the foregoing.

 

List #1

Day in the life

Ovarian cancer knot being held in woman's hands
Standing Strong on Ovarian Cancer Day

Teaser label

Inside ICON

Content type

Blogs

Publish date

05/08/2025

Summary

Standing Strong on Ovarian Cancer Day:    ICON's Commitment to Advancing Care Ovarian cancer remains one of the most challenging gynaecologic malignancies, both in terms of detection and treatmen

Teaser label

Martin Lachs, VP, Oncology Project Management at ICON discusses ICON’s role in advancing ovarian cancer research.

Read more
Nurse and patient
Patient Centricity in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

05/07/2025

Summary

Patient Centricity in Clinical Research: What it is and Why it Matters In the past, clinical research was designed around the needs of sponsors, researchers, and regulatory bodies. Patients were of

Teaser label

Discover how patient centricity is reshaping clinical research by placing participants at the heart of study design and execution.

Read more
Liquid capsules
Navigating Regulatory Landscapes - FDA, EMA, & MHRA

Teaser label

Industry

Content type

Blogs

Publish date

05/05/2025

Summary

Navigating Regulatory Landscapes:     Comparing FDA, EMA, & MHRA in Clinical Trials In clinical research, no matter how promising a new therapy may be, it will go nowhere without regulatory appro

Teaser label

Compare FDA, EMA, and MHRA regulatory frameworks for clinical trials, and why this knowledge matters.

Read more
View all

Similar jobs at ICON

Senior CRA

Salary

Location

France, Paris

Department

Clinical Monitoring

Real World Solutions

Location

Paris

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team within ICON Biotech. ICON Biotech develop transformative therapies with small & mid-sized bioph

Reference

JR130384

Expiry date

01/01/0001

Read more Shortlist Save this role
Senior CRA

Salary

Location

France, Paris

Location

Paris

Lyon

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team in France. As a Senior CRA for ICON, you will play a critical role in overseeing and managing c

Reference

JR129352

Expiry date

01/01/0001

Read more Shortlist Save this role
CRA II

Salary

Location

France, Paris

Location

Paris

Lyon

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team in France. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal rol

Reference

JR129356

Expiry date

01/01/0001

Read more Shortlist Save this role
Senior Lead Clinical Data Science Programmer

Salary

Location

India

Department

Biometrics Roles

Location

India

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Biometrics Portfolio

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us

Reference

2025-118592

Expiry date

01/01/0001

Kalpana Kulasekaran Read more Shortlist Save this role
CTM

Salary

Location

Netherlands

Department

Clinical Trial Management

Location

Netherlands

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

The CTM in general, is responsible for the maintenance and further development, and the communication of high-quality standards in the delivery of clinical studies. This includes a key role in ensurin

Reference

2025-119327

Expiry date

01/01/0001

Iris Brouwer

Author

Iris Brouwer
Read more Shortlist Save this role
Clinical Research Associate I

Salary

Location

Changchun

Department

Clinical Monitoring

Location

Changchun

Remote Working

Office Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRAI you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2025-118401

Expiry date

01/01/0001

Irena Guo

Author

Irena Guo
Irena Guo

Author

Irena Guo
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above