Description
This is a senior role; my client is looking for somebody to help with the full life cycle of their new Medical Device;Daily Responsibilities include;
- Leading Regulatory Strategies globally.
- Co-ordinating global team liaisons with local notified bodies.
- Over seeing a Regulatory team of 12.
- Managing deadlines for, technical file writing CE marking.
- Gaining Marketing Approval in all necessary territories.
- Post marketing surveillance and analysis.
Required skills;
- 8+ years in relevant field.
- Proven track record of gaining Marketing Approval for Medical Devices.
- Strong Technical File writing ability.
- Good working experience of post marketing surveillance.
- Project management experience.
- Strong interpersonal skills.
If you believe you fit the above requirements, or know someone who has, please contact Joseph on or apply below.
We have a £200 reward scheme for any referral given that goes on to be placed.
To find out more about Real please visit www.realstaffing.com