Document specialist

Applicants must have a minimum of five years of document control experience in a regulated pharmaceutical / biotechnology environment. An understanding of cGMPs documentation control is essential. This position requires excellent organizational and people interaction skills. The appropriate candidates should be self-starters with good verbal and written communication skills, attention to details, strong computer skills and documentation skills. The successful candidate will have the ability to work on several projects concurrently, and maintain strong interpersonal and project management skills.Computer literate: MS Office including Word, Excel, PowerPoint and Access is required.Past experience in life sciences is required.Working knowledge of cGMP documentation system is required. Working knowledge with GCP and GLP practices is desirable.Email your resumePlease click here,or copy and paste the following link into your email browser, to email your resume. SunnyvaleCABioSource.95210.479@manpowerna.aplitrak.com At Manpower, our mission is to serve as trusted advisors in the changing world of work. Work with us and make a change for the better. us.manpower.com manpowerprofessional.com