R&D Scientist (Medical Devices)
- Global Medical Device MNC with HQ in Singapore
- In-depth knowledge of biocompatibility standards (ISO 10993 series)
- Base salary up to $108,000 + Bonus
Our client is a Japanese Medical Device and MedTech multinational company with the regional headquarter based in Singapore. The company comes with over 80 years of heritage and is a leading manufacturer of innovative, high-tech medical devices. Globally, they have a diversified workforce of over 30,000 employees across more than 30 countries.
Responsibilities
Reporting to the R&D Director (based in US), you will be chiefly responsible for the biocompatibility of Medical Devices (Ophthalmic) and to achieve business and R&D objectives. You will lead activities and assessments to ensure compliance with ISO 10993 series, ISO 11979-5, and ISO 11979-4 standards for several pipelines and existing devices. You will also conduct shelf-life studies to determine stability and safety of medical devices over time.
As the only R&D representative for APAC, you will work cross-functionally with global R&D, Quality, Regulatory Affairs, Clinical Affairs, and Manufacturing for successful product development and compliance.
Requirements
The ideal candidate is someone with minimum 3 years of biomedical research experience, particularly with Class 2B / Class 3 Medical Devices. Having Ophthalmology experience will be an added advantage. You will also need to be familiar with ISO 10993 series with excellent technical writing skills to prepare biocompatibility reports. You will ideally possess a Master of Science or PhD in related discipline.
To Apply
To apply, please submit your resume to Richard Tey at rt@kerryconsulting.com, quoting the job title RT32619. We regret that only successfully shortlisted applicants will be contacted.
Licence No: 16S8060
Registration No: R1653095