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Posted by Jeiven Pharmaceutical Consulting Inc on October 14, 1996 at 10:22:23:
In Reply to: Help Wanted posted by Webmaster on September 14, 1996 at 00:30:00:
Challenging opportunity to join a small (bur growing) 7 year old pharmaceutical consulting firm. We are seeking individuals, full and part time, permanent employees and consultants, who will, coordinate clinical supplies operations, audit and monitor contractors for GMP compliance, write SOPs, design patient and site compliant labeling and packaging, and review manufacturing, packaging, and labeling documentaion. Individuals should have a degree in pharmacy or chemstry, excellent coordinationa and communication skills, a working knowledge of GMPs, and 3 to 5 years experience in one or more of the following areas: QA/QC, clinical manufacturing, clinical project coordination, and clinical packaging and labeling. Please e mail us or sen a resume to: Jeiven Pharmaceutical Consulting, Inc. PO Box 302, Garwood, NJ 07027