We are currently looking for a Medical Device Auditor to join our Medical and Health Service team! You will be performing the audit for active medical device manufacturers and ensuring that their Quality Management System (QMS) complies with Medical Devices – including the Medical Device Regulation (MDR) / In Vitro Diagnostic Medical Devices Regulation (IVDR) and other QMS certification scheme, where applicable.

We welcome experts from different medical device industries!

For example:

• Active devices: active non-implantable surgical devices (Cryoablation, High frequency surgery, High-frequency generator, High-frequency instruments, ablation generators, suction pumps for blood), standalone software, Active Endoscopes, and etc
• Ethylene Oxide Sterilisation or other related sterilization

Key Responsibilities:

• Perform onsite audits at manufacturer’s premises by evaluating their Quality Management Systems in accordance with the requirements of the MDR / IVDR, and other QMS certification schemes such as ISO 13485, ISO 9001 and MDSAP
• Maintain customer communication as project leader for the allocated customers regarding auditing and certification, deal with clients’ queries relating to certification process including application reviews within acceptable time frames. 
• Take charge of pre and post audit tasks including preparation of audit documentation and audit package submission
• Assist Sales personnel by providing technical advice to existing and prospective clients

Job Requirements:

• At least bachelor’s degree with diploma in active medical device related major (e.g. Biomedical Engineering, Electronic Engineering, Automatic Control);
• Have minimum 4 years of relevant experience in testing of medical device / design and development activities / process validation / application of process technology / service & maintenance in the medical device industry.
• Have at least 2 years’ experience in Quality Management Systems environment (e.g. manufacturing, quality control, or research)
• Qualified auditor for ISO 13485; experience with MDR / IVDR and/or MDSAP is a strong advantage
• Clear and articulate presentation ability with excellent communication skills
• High level of customer orientation and ability to manage challenging audit situations
• Frequent travelling will be required within ASEAN, with occasional travel to other regions