Minimum requirements: Bachelor's degree in Engineering, Chemistry, Life Science or related subject with 7+ years of experience in either of the following industries biopharm, medical device and pharmaceutical.
A thorough understanding of the GMP regulatory environment, validation, and associated subjects.
An ability to work independently and follow instructions
Excellent verbal and written communication skills.
Proficiency in Windows and Microsoft Office applications.
A thorough understanding of the GMP regulatory environment and computer validation
Must understand U.S. and European Regulations.
Must have project management experience and be able to manage staff.
