Company: Barrington James Europe
Closing Date: 29 Dec 16
Salary (£): Competitive
Regulatory Affairs Specialist **Medical Device – Exclusive**
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!!
Rowan House Smallfield Road Horley Surrey
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