Regulatory Affairs Specialist Medical Devices

Exciting multiple opportunities for experienced Regulatory specialists with experience in Regulatory Affairs and FDA to join a global medical device company. As a regulatory specialist you will be supporting all registration activities, CE marking and regulatory submissions as per project requirements.

What's the Offer?

• Salary: £45K-£60K
• Job Type: Permanent, Full-time
• Location: Leeds, UK
• Benefits: Healthcare, pension, bonus, holidays, Flexi-time, remote working until Dec 2020, education support ++++
• Opportunity to work for a world-class global medical device company and to be part of a highly collaborative team

Responsibilities

• Facilitating product registration activities by compiling appropriate dossiers, submissions, and responses to regulatory bodies globally.
• To maintain information on regulatory requirements and the status of product registrations.
• Review technical documentation created by teams to ensure their accuracy and completion.

Background Experience

• A graduate engineering/science degree.
• Good experience in Regulatory Affairs, preferably in Medical Devices.
• Knowledge and experience in EU and FDA regulations
• Strong knowledge in the application of MDD93/42/EEC

What Next?

To apply for these Regulatory Specialist Opportunities email CV or LinkedIn profile in the strictest of confidence to Som in Principle on som@principlehr.com or call 35316035075 | 443300526074

idence to Som in Principle on som@principlehr.ie or call 0035316035075 | 443300526074