I've been telling ya, come work with me! Of course California sucks right now, 'cept for everything but pharma and biotech
LINK
We really need some QA personell
In case you were lazy:
Description
The incumbent will review all batch records in preparation for final batch release. They will obtain corrections to ensure compliance, as well as review deviation reports, non-conforming material reports, and component envelopes for adherence to SOPs.
The QA Associate will work with other departments to clarify and correct documentation to ensure compliance. The incumbent will also review controlled documents for adherence to SOPs, as well as suggest process improvements. This position will make strong contributions to cross-functional teams.
In addition to conducting batch record audits, the QA Associate will perform walk-through audits of the production areas to ensure compliance with cGMPs and internal procedures.
Qualifications
BS/BA or equivalent in a related science discipline required. One to five years? of related experience preferably in a Quality Assurance or Manufacturing role in a cGMP environment required. Experience in Parentaral manufacturing is preferable. The candidate must possess a strong knowledge of quality systems and cGMP regulations. Additionally, they should be comfortable with computer systems. Excellent writing, as well as exceptional attention to detail, is also a strong requirement. This position will interact with all levels of the organization and across departments.
So I will have to confirm when I can move and sort out somewhere to live, but with the pay I am getting I should be able to live pretty comfortably.
