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Job Details

Regulatory Affairs Specialist **Medical Device – Exclusive** SWITZERLAND

Company: Barrington James Europe
Location:
Reference: 510kpmalh
Closing Date: 29 Dec 16
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

Regulatory Affairs Specialist **Medical Device – Exclusive**

Requirements:

Are you looking to work in a dynamic and innovative medical device company? Looking to work in a supportive, communicative environment? Ready to utilize your medical device experience in a family run company?

 

THEN I HAVE THE OPPORTUNITY FOR YOU!

 

After a recent, exclusive partnership with a family run company that specializes in the development, manufacturing and customization of precision medical devices, I am looking for experienced Regulatory Affairs professionals to join them in a specialist role!

 

The highly innovative, family run company specialize in the respiratory therapeutic area. With strong goals of being the number one in their area, due to how niche they are, they are looking to add to their growing Regulatory Affairs/R &D department.

As a Regulatory affairs specialist you will be responsible for developing, coordinating and preparing US medical device submissions such as 510K and PMA’s. As well as reporting into the Regulatory Affairs Director.

 

To qualify and apply for the role you need the following:

Minimum of a Bachelors’ degree
Minimum of 3 years Regulatory Affairs experience in Medical Device industry.
Experience with 510K submissions and/or PMAs

 

For more information on what this role can offer you, APPLY NOW!!

Apply for this job: Regulatory Affairs Specialist **Medical Device – Exclusive** SWITZERLAND

Contact Information:

Address:  Head Office
Rowan House Smallfield Road Horley Surrey
RH6 9AU
England
Tel:  01293 776644
Fax:  01293 822333

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