Total 2 job vacancies by Acm Global Central Laboratory (singapore) Pte. Ltd.

Job Description & Requirements

• Work closely with the local departments, and adapt to changing priorities with guidance from senior team members.
• Work with specimens maintained at varying temperatures (ranging from ambient to cryogenic), including the limited movement of shipper boxes filled with dry ice.
• Perform receipt, QC checks, labeling and onward processing of clinical trials specimens.
• Specimens Accessioning: Perform accurate data entry into various laboratory information management systems
• Specimen Storage: maintain full inventory and tracking of storage specimens while ensuring the integrity of the specimens at all times
• Specimen Shipping and Disposals: prepare specimens for real-time and scheduled onward shipment to other referral laboratories. Process specimens marked for disposal.
• Raise and resolve specimen management-related queries with other departments.
• Perform housekeeping to maintain a clean and tidy working environment, including basic freezer maintenance and disposition of waste.
• Support monitoring of cold storage units and environment.
• Utilise study documentation to aid in problem solving and escalate to senior staff as required.
• Manage specimen-related study documentation including archiving
• Monitor and maintain consumables inventory.
• Perform all processes in accordance with SOPs and appropriate regulatory guidelines including Good Clinical Practices (GCP) and IATA
• Perform other duties as assigned

Requirements:

• Minimum Higher Nitec or Diploma in arelated field
• Excellent communication skills
• Exceptional documentation and data entryskills
• 5-day work week including Saturday
• Willing to learn, positive attitude and mustbe a team player
• Trained in IATA Dangerous GoodsRegulations (DGR) would be advantageous
• Salary will commensurate with experience

ACM Global Laboratories is a Global organisation which has been established for over 15 years in the Asia-Pacific region. They have a clear vision and core values to ensure that they deliver actionable clinical insights that lead to therapies ad treatments that provide health, healing and hope to patients around the world.

This is an opportunity to join the Singapore team as their medical Technologist; a role includes a broad range of responsibilities. Team work is key to ensure the smooth, efficient running of the Singapore site and everyone has an important role within the organization.

SUMMARY

· Analysis & Reporting. Perform precise specimen analysis and report results accurately, following established procedures; recognize deviation from expected results, analyze and correct problems using scientific principles; complete QC Action Logs, preventative maintenance logs and pending lists daily.

· Training & Development. Assist with training new personnel on responsibilities in the laboratory; evaluate progress of training; make recommendations for training methods and content.

· Evaluation. Continuously assess work processes and make suggestions for improved work methods and ways to increase efficiency, reduce costs and solve operational problems; monitor departmental reagent inventories.

RESPONSIBILITIES

• Process the daily workload in close collaboration with colleagues.
• Perform and authorise maintenance, calibration and quality control as well as routine analysis.
• Be able to deal with interruption and be able to prioritise tasks appropriately.
• Be able to use the laboratory IT system to enter/validate results and to look up previous results, to generate worklists, and to enter data results.
• Participate in internal and external quality assessment as required.
• Assist in the testing and assessment of new equipment and introduction of new techniques and assays.
• Assist in other laboratory areas, including sample reception and sample storage as required.
• Participate fully in the general housekeeping of the laboratory, including counting stock, ordering supplies, and maintaining a clean and tidy working environment.
• Participate in all activities which seek to ensure compliance with GCP guidelines and CAP accreditation.
• Contribute to writing and reviewing of Standard Operating Procedures (SOP’s).
• Comply with policies for the safe, secure and con