• Our Client is a Start-up in Med-Tech industry.
• Must have experience in ISO13485.
• Manage a team of 3-4.

Responsibilities:

• 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.

Requirements:

• 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