Sunday 17 February 2019       info@tesladuo.com

Regulatory Affairs Specialist 1

Description:

Assess manufacturing process, design, and labeling changes for regulatory reporting impact. Write, edit and/publish various types of submission documents to FDA and EU regulatory bodies, including but not limited to INDs, BLAs, Annual Reports, CBE-30s, Technical Files, and Design Dossiers. Product design and manufacturing change assessments for regulatory reporting....
 
 

Details of the ad

Ref:
d6526354b3fea4b3

Date of publish:
14-Dec-2018 11:51

Company:
Grifols

Work location:
San Diego, CA 92101

Experience:
Not assigned

Etudes:
Not assigned


Back to Top