Description
I am currently in charge of finding the next Sr. Specialist of Batch record Review for a very exciting pharmaceutical oncology company in the Bay Area. They currently have over 20 on-going clinical trials, with several drugs in the pipeline. Their most succesful drug is currently fairing very well in Phase III clinical trials and is well on its way to going commercial by next year. This company has a very fast paced environment and expects anyone joining the team to hit the ground running. The best candidate should have the following attributes:- 3-5 years in a GMP Quality Enviroment
- Lots of experience and knowledhge of GMP requirements and a strong analytical background
- Working knowledge of quality systems and CAPA
- 3+ years hands-on batch record review/release experience
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