VALIDATION SUPERVISOR, BIOPHARM
SUMMARY: We have been engaged to find a Validation Supervisor for one
of our client biopharmaceutical companies. This Supervisor will be
responsible for the validation programs for our client's facilities,
including their new manufacturing site, equipment, and utility
systems. He/She will interpret validation data and will author
reports reflecting the validations performed. Our client has
therapeutics and vaccines in the market and a strong pipeline of
products in various stages of development and clinical trials.
· BS/BA degree in science-related discipline, technical school or 5
years experience in related field of work.
· Familiarity with FDA regulations for biotechnology or drug
· 5+ years in validation
· Knowledge of FDA cGMP and related regulations and guidelines,
especially validation methodologies and principles.
If you have an interest in this or other opportunities, please send us
your resume/CV as an Attached File to an email or send by mail/FAX to
RS&A to the attention of Ann Rathbun, Managing Director. All
correspondence is held in strict confidence.
Rathbun, Sapir & Associates
P.O. Box 2337
Sedona, AZ 86339-2337 * USA
(520) 284-3360 Office (520) 284-3361 FAX
E-mail: rathbun at sedona.net