BS/BA or equivalent in Chemistry, Biochemistry or Biological Sciences
and 0-3 years experience in Manufacturing in a cGMP environment of the biotech or pharmaceutical
industry or 5+ years relevant work experience in a cGMP environment of the biotech or pharmaceutical
industry.
Skills:
GMP trained.
Computer literate.
Good verbal and written communication skills.
Ability to work as part of a team as well as independently.
Ability to carry out detailed written and oral instructions in English.
Ability to speak effectively in English.
Essential Functions:
Perform functional testing of in process and final product.
Perform inspection of raw materials and in process material.
Perform daily calibrations and maintain logbooks.
Coordinate with Group Leader in determining work assignments to meet production
timelines.
Cross train in auditing/inspection.
Assist with customer complaint testing.
Perform environmental monitoring.
Additional Responsibilities
Participate on one TQM team.
Train new personnel in spool testing.
Regularly clean laboratory and work areas.
Perform additional duties as necessary.
Physical Demands
Position requires the ability to sit, stand, walk, talk and hear.
Specific vision abilities include close vision and the ability to adjust focus.
Work Environment
While performing the duties of this job, the employee will work with human
blood serum and chemicals.
Submit Resume or CV to:
Human Resources
Hitachi Chemical Diagnostics
630 Clyde Court
Mountain View, CA 94043
Fax: 650 969 2745
E-mail: webmaster@hcdiagnostics.com
Subject: QA Chemist I
hitachi.com 
Global Network
