Position Description

Quality Assurance Manager, Medical devices (ISO13485, Start-up)
Job Code 19532
Job Placement Location Singapore
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  • Our Client is a Start-up in Med-Tech industry.
  • Must have experience in ISO13485.
  • Manage a team of 3-4.


  • Oversee Quality Assurance and compliance functions and ensure that services are implemented at the highest standards.
  • Establish and implement product Quality Assurance and control process.
  • Preparation and submission of regulatory filings with relevant authorities.
  • Facilitate internal and external audits to maintain a Quality Management System.
  • Monitor and update policies and procedures to include regulatory changes.


  • Bachelor's Degree in Engineering, Biomedical Science or Science related discipline.
  • At least more than 3 years of experience in the Medical device industry and knowledge of Quality Assurance.
  • Strong interpersonal, oral and written communication skills.
  • Ability to multi-task and comfortable working in a Start-up environment.

Other Information:

  • Working Location: East.
  • Working Hours: Mondays to Fridays, 8.30am to 5.30pm.
  • Critical: Due to the organization's affirmed support and commitment to developing a Singaporean core, this role is only available to Singaporeans.

To apply, please visit www.gmprecruit.com and search for Job Reference: 19532.
To learn more about this opportunity, please contact Novita Tan at novita.tan@gmprecruit.com
We regret that only shortlisted candidates will be notified.
GMP Recruitment Services (S) Pte Ltd | EA License: 09C3051 | EA Personnel: Novita Tan | Registration No: R1220374

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