Equipment Technician - #1096661

Quasar Medical (Singapore) Pte Ltd


Date: 4 days ago
District: Sembawang
Salary: $2,500 - $3,200 / month
Contract type: Full time
Work schedule: Full day
Quasar Medical (Singapore) Pte Ltd

Essential Duties and Responsibilities:

Include the following. Other duties may be assigned.

  • Work with Process and Manufacturing Engineering to develop and refine processes for production.

  • Work with Development or Manufacturing on the transfer of new products to manufacturing and define process capabilities.

  • Fixture development to improve throughput in manufacturing, this to include concept, refinement, evaluation, and implementation.

  • Support and run experiments to evaluate process improvement ideas.

  • Review and implement supporting documentation including DHR’s, MPI’s, SOP’s, & ECO’s.

  • Identify training requirements and train production personnel in accordance with company, department, ISO, and GMP guidelines.

  • Work “on-line” as the production schedule demands.

  • Design, specify, manufacture, test and document production equipment, changes and improvements.

  • Supports the scheduled and unscheduled maintenance activities to support manufacturing lines by conducting PM’s, documenting PM procedures and adhering to the PM scheduling for equipment under area of responsibility.

  • Assist in conducting IQ/OQ/PQ process of equipment. Assist in the creation and maintenance of up-to-date area SOPs.

  • Perform setup, troubleshooting and shut down of equipment.

  • Liaise with Global IT support desk to support the resolution of IT service equipment.  

  • Liaise with outside service support groups on the maintenance and installation of HVAC, Air Handling Units, and cleanroom and pressurised vessels and general electrical networks throughout the facility.

  • Support Environmental Health & Safety activities. Carrying out risk assessments of equipment / processes, contributing to the EH & S committee and its execution of tasks & carrying out ergonomic studies. 

  • Maintain and generate facility layout and cleanroom drawings.

  • Maintain and comply with ISO13485, GMP and FDA regulations.

  • Work as part of production support team to drive process improvements.

  • Take responsibility for preventative maintenance procedures with an assigned process or area.

·        Interface with a variety of personnel and with outside vendors when necessary while performing the above.

Education/Experience and Qualifications:

  • GCE “O” level or higher with 1-3 years assembly or technician experience preferably in medical device.

  • Able to work with a variety of equipment and to troubleshoot and correct mechanical/electrical problems as they arise.

  • Computer literacy required.  Familiar with Microsoft office software and AutoCAD a plus.

  • Knowledgeable in writing manufacturing procedures and GMP requirements.

  • Knowledgeable in GMP, ISO, cleanroom procedures, and documentation.

  • Good technical knowledge and understanding of broad scope of manufacturing processes.

  • Excellent communication skills.

  • Environmental Health & Safety Training is desired but not essential.

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