Senior Manager – Regulatory Affairs
$130,000 – $150,000 + Executive Benefits
The successful candidate will have substantial Regulatory Affairs experience relating to the development and licensing of drug-device combinations. You will have worked on multiple projects and been integral in all aspects of the pre-approval process. A solid working knowledge of EMEA and APAC medical device submission regulations is highly desirable.
This organisation is at the forefront of the medical device industry, developing highly complex products. An opportunity not to be missed.
To discuss, please submit your resume to firstname.lastname@example.org.
If this opportunity isn’t quite right for you, we have a number of other MA based Regulatory roles – get in touch to discuss