Accessability Links
Cookies on our website
By continuing to use this website we will assume you are happy to receive cookies as outlined in our cookie policy
Accept Policy

Medical Technologist I

Reference: JR062214
This vacancy has now expired.

At ICON, it's our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them? Suitable for persons looking for a career in clinical trials and laboratory testing

The Medical Technologist I will join the ICON Flow Cytometry team and process patient samples to deliver high quality Flow Cytometry data for cutting edge global clinical trials. Ensure the Central Laboratory is meeting the highest quality standards. 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 as assigned by the management team. Assist with the teaching and development of staff currently in the department; to maintain at all times the required high standards and quality.

The role

  • 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.
  • Provides mentorship for training of Technologists, Technicians and Lab Assistants

What you need

  • Basic working knowledge of and Compliance with all CAP and local agency regulatory requirements.
  • 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.
  • 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.
  • Basic working knowledge of LIMS with the desire to achieve the mathematical, computational and instrumentation skills necessary to work and progress in Biomedical Science.
  • Prior flow cytometry experience is not required but is strongly advantageous

Back to Top