In the first six months of being a Medical Device Auditor you’ll:
- Be given training in ISO 13485 Lead Auditor training, MDSAP (Medical Device Single Audit Programme) and MDR (Medical Device Regulation)
- Initially observe how audits are conducted but then grow to conduct them on an individual basis on site at medical device manufacturers and remotely from your home office
In a typical week after being fully trained you’ll:
- Conduct an audit on site or remotely
- Write up your reports and liaise with the planning team to manage your audit schedule.
- You’ll also continue your development of MDR and be an advocate for the ISO 13485 Delivery Team.
To Thrive In This Career, You Must
- Have 4 years or more being directly accountable for the design or test or manufacture of different medical devices
- Be degree educated with discipline relevant to Medical Devices e.g. chemistry, physical chemistry, molecular genetics, textiles, material science, biology, biotechnology or similar
- Have at least 2 years’ experience working in an environment with a Quality Management System established
- Be able to speak and write fluently in the English and Thai language
- Be resilient and able to meet audit delivery by travelling frequently across the region as required.
- We’re enthusiastic to receive applications from those based in Thailand excited by this career opportunity.
- Our Excellence Behaviours: Client-centric, Agile, Collaborative. These three behaviours represent how we do things at BSI. They help us ensure that BSI is a great place to work and a highly successful business.
- To protect our candidates and BSI employees during the Covid-19 outbreak, all interviews will take place remotely.
