Senior Manager, Regulatory Affairs - PMA Products - San Diego

San Diego  ‐ Onsite
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Description

Job Responsibilities:

You will manage several direct reports and work both on new product development as well as sustaining and making changes to the existing product line. You will work closely with other departments and act as a primary liaison for important matters. You will communicate extensively with the FDA and you will also work with other countries' regulatory agencies. Your responsibilities will extend to playing a major role in planning what is to come for the company as it expands its large pipeline of innovative and life-saving technology. Your job will often consist of managing several projects at once.

Qualifications:

Minimum five years of regulatory affairs experience. PMA submissions experience is essential as well as experience working back and forth with the FDA. Experience supervising and managing others is preferred, as is international submissions experience. Bachelor's degree in science or engineering is preferred.

Looking for a person who is supportive, positive, and creative. If this sounds like a good fit for you, we look forward to hearing from you.

To find out more about Real please visit www.realstaffing.com
Start date
12/2013
From
Real Staffing
Published at
08.11.2013
Project ID:
623969
Contract type
Permanent
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