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Medical Technologist I

  1. Singapore
JR104817
  1. Laboratory
  2. ICON Full Service & Corporate Support
  3. Office Based

About the role

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

Office location: 30 Loyang way, Unit 02/12-15, Singapore 508769 

Working schedule for this position:

Tuesday to Saturday fixed 5 day work week with below timeslots
•    830am - 530pm
•    9am - 6pm
•    10am - 7pm
•    11am - 8pm
(timing may change slightly from time to time to suit operational needs)

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The Role:

To be successful in the role, you will have:

• Recognize, exemplify and adhere to ICON's values which centers on 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. Personal Effectiveness: Operates independently with a willingness to make decisions; Projects credibility and makes a professional and positive impression on others; Monitors progress and holds self and others accountable. Robust Thinking: Identifies the key elements of a situation and makes sound decisions based on available information in order to contribute to the success of the laboratory.
• Accepts direction and instructions from the Laboratory Management Team and assists in overseeing work performed by staff in the Laboratory department and reporting the work performance to the 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.
• Directs and assists technical staff in the preparation quality control documentation, organization of proficiency testing and compliance with all appropriate regulatory procedures and quality requirements in testing area.
• Oversees the maintenance of regular inventory of all reagents and spare parts required in this section in order to ensure availability and future reagent usage prior to expiry dates. Also, ensure that reagents are maintained, prepared, stored and used in a manner suitable for testing and documentation is kept to ensure adequate records are available.
• Assists with the maintenance, calibration and validation of the instruments/assays assigned to the section according to written laboratory procedures.
• Establishes good relationships internally and externally. Interacts with other departments, such as Project Management, LIS, Global Validations, QA, Client Services and Global Labs. Also Interacts with clients and internal/external auditors.
• 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.
• Assists with Batch review and sign off in LIMS.
• Assists with Work flow assignments and section schedules.
• Assists with the writing of SOPs, quality documents and working procedures as required.
• Assists with the evaluation and validation of new procedures as required.
• Provide input to management about the performance of technical student trainees with the potential for future recruitment and/or assist in the recruitment and selection of staff in consultation with supervisor/manager.
• Responsible for training of employees in the section as well as maintaining training files. Performs continuing education of laboratory staff on new procedures, methodologies, etc. Perform advanced troubleshooting and continuing education.
• Assists in maintaining temperature monitoring system.
• 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

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs.  In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.


If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

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