Senior Regulatory Affairs Manager job Santa Rosa California
Senior Regulatory Affairs Manager job Santa Rosa California
Home
Contacting Us
F. A. Q.
Links
Log In
Scam Awareness
 
 
Job Seekers
Browse Jobs
Search Jobs
Post a Resume
Modify Resume
Delete Resume
Job Alerts
 
Employers
Browse Resumes
Search Resumes
Post a Job
Modify Job Ad
Delete Job Ad
 
Resources
Employment Directory

Senior Regulatory Affairs Manager Job


Employer Name: BiotechCrossing SpiderID: 2339032
Location: Santa Rosa, California Date Posted: 7/4/2008
Wage: Category: Biotech
Job Code: 6022931

Job Description:
The specific emphasis of this position is to ensure that the appropriate clinical aspects of regulatory affairs are operating to support the world-class regulatory organization, and to continue to improve these systems over time as a vital interface with the Clinical Research Department. These systems address ongoing support of currently commercialized products, ongoing regulatory compliance, and support of new product development & commercialization worldwide. Position Responsibilities The Senior Manager, Regulatory Affairs will plan and implement policies, procedures, practices, and business process strategy for the Regulatory Affairs department of Medtronic Vascular. This includes managing comprehensive regulatory activities, developing regulatory strategy, and supervising the preparation of regulatory submissions necessary to introduce new products to market and thereafter maintain post-market compliance. The Senior Manager, Regulatory Affairs will provide senior level management expertise, direction, and leadership to the Regulatory Affairs Department and Medtronic Vascular. The specific emphasis of this position is to ensure that the appropriate clinical aspects of regulatory affairs are operating to support the world-class regulatory organization, and to continue to improve these systems over time as a vital interface with the Clinical Research Department. These systems address ongoing support of currently commercialized products, ongoing regulatory compliance, and support of new product development & commercialization worldwide. Primary Responsibilities * Contribute to the development and implementation of business unit strategic and operating plan. * Lead and manage activities that create and improve regulatory business systems, as appropriate, in order to facilitate accurate, timely, and sustainable regulatory compliance, submissions, and reporting activities.

For more information, please click here to visit us at BiotechCrossing

For further information, please visit us online at http://www.biotechcrossing.com

Sign Up Now


Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:


Contact Information:
Contact Name: - Company Type: Employer
Company: BiotechCrossing
City: Pasadena
State: California
Zip:
Web Site: http://www.biotechcrossing.com

Send ad to a friend
Report a Problem


    



© 2003 CC Marketing and Classified Systems
Privacy Policy | CC Marketing Sites | Site Map