Our company seeks an individual to conduct Quality Assurance audits/inspections of non-clinical labs and tissue manufacturing areas for compliance to GMP/GTP regs and ISO standards.  Additional quality compliance duties include conducting GLP final report reviews.   The ideal candidate would have BA/BS degree or equivalent experience with Toxicology Studies and final reports, biology or microbiology, 3-5 years auditing or lab experience and experience in a cGMP regulated and ISO environment.  Requires excellent organizational skills, be detail orientated, have good computer skills, especially with Microsoft office programs (word, excel & power point).  Please submit your resume and cover letter with salary requirements to the contact info above.