Regulatory Affairs Executive Job, Watford

Are you an ambitious regulatory affairs executive in medical devices looking for a career move?

A new opportunity has arisen for an ambitious regulatory affairs executive to join an established medical device company which specialises in manufacturing and distributing unique quality products within the healthcare industry.

Location

Hertfordshire, Watford

Job Responsibilities

* You will be responsible for the Creation and management of Technical Files for Class I, IIA and IIB Medical Devices(including but not limited to) (75% of the position)
* Management of ISO 13485 & ISO 9001 Quality Management System (including but not limited to) (25% of the position)

The Package

* £50K Basic
* Medical
* Annual Bonus
* Mobile Phone+ Laptop

The Person

* Must have experience with technical file writing
* Medical Device experience is essential
* Eye for detail and excellent written communication skills

Key Benefits

* Strong research and development of new products helping to develop an innovative portfolio
* Professional working environment with real hands on culture, you will be a key part of the team
* Opportunity to support the launch and development of market leading products

What Happens Next

If you would like to be considered, please use the 'Apply' button and attach your latest CV. Alternatively, talk to us in confidence about this opportunity and other suitable positions by contacting a member of the Medical Devices Division on 01423 813450.

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