Regulatory Affairs Specialist (427903/002) Mannheim, Germany

Job Type: Regulatory Affairs Specialist
Location: Mannheim
A global leader in the innovative medical device industry, paving the way in discovering treatments for patients within the Ophthalmology industry, the organisation is seeking for a Regulatory Affairs Specialist to join their team. You can have a positive impact on the lives of millions of people around the globe, with the market of ophthalmology looking to surpass £27 Billion by 2023; the growth of products seem to be endless.

Key Responsibilities:
Identifying requirements for registrations and approval processes.
Conducting regulatory approvals for medical devices and ensuring that current regulatory approvals are maintained.
Processing International approvals for EU and USA.
Creating and maintaining important materials within marketing documentation.
Able to establish and explain in details how documents are processed.

Key Requirements Include:
Bachelor/Master degree in sciences, life sciences, engineering, software development or equivalent education gained through work experiences.
3/5 years’ experience in Medical device.
Knowledge in marketing surveillance report.
Experience in writing product description.
Medical Device Background.
Experience within Technical Files.
Background knowledge in MDR Regulations.

Benefits:
Competitive benefits and great personal development opportunities.
Great atmosphere within a vibrant team.
Learning & Development Support.
 
Apply here if you are interested in this opportunity or if you would like a confidential discussion about your career opportunities please contact Evan Shamma on +44 203 758 8904 or via email on

mehr...

zur Vakanz

Weitere Jobs von Aplitrak