Description
This Quality Assurance and Compliance role requires the majority of the allowing abilities:-Excellent working knowledge and understanding of GMP related requirements, proficiency of regulatory and ICH guidelines. Broad experience in the pharmaceutical industry with a strong analytical and/or manufacturing background, some R&D is a plus
-Background in batch record review
-Detail-oriented with excellent review skills of production records for lot disposition
-Experience in clinical API is highly desired
-Excellent working knowledge of Quality Systems and cGMP standards
-Small molecule experience is a plus!
3+ years of pharmaceutical experience in a GMP quality (QA/QC) environment
This highly desirable position within the pharmaceutical industry is a 6 month contract but can transform into a permanent role. The company is offering a very competitive compensation.
This urgent and coveted position will fill quickly so please be in contact as soon as possible.
Only California applicants please
To find out more about Real Staffing please visit www.realstaffing.com