Hobson Prior currently have an exciting new opportunity for a Regulatory Affairs Specialist to join one of the world's leading specialised medical diagnostic companies on a permanent basis where you will be working from home.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• You will be responsible for assisting with key development projects to meet strategic business objectives.
• You will be supporting vigilance and post market surveillance activities.
• Regulatory review-controlled documents.
• Assist in global submissions including EU, FDA.
• Support regulatory compliance for QMS to meet requirements, including MDSAP and IVDR.
• Support 3rd party audits.
• To assist in regulatory affairs projects for invitro diagnostics manufacturer for global markets including EU, USA, Asia Pac, LATAM.

Requirements:

• The ideal candidate will require a relevant scientific degree B.Sc. in Life sciences or M.Sc. or higher in life sciences or equivalent.
• Several years in QA/RA roles in healthcare industry (pharma, medical devices, or diagnostics.
• IVD industry experience.
• Global registration.
• R&D clinical, production research & development.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.