Regulatory Affairs Program Director - Device

A leading multinational developer, manufactor and marketer of innovative, life-enhancing medical devices needs an experienced regulatory affairs program director.

Develop regulatory policies, goals, and executive reports. Determine effective regulatory procedures.

FDA submissions.

Manage the regulatory affairs department.

Must possess knowledge of physical science, manufacturing, biology, and regulatory affairs.

Experienced in managing in the regulatory affairs device.

4 year degree a must - Masters degree a plus.

Minimum of 10 years experience in regulatory affairs in medical devices.

Class II 510k and Class III ID/PMA submissions

120-150K Plus Bonus


Email updated resume to: Larry@cooperstaffing.com in Atlanta