Description
We are currently looking for a Sr. Manager of Quality Systems/Document Control. Depending on the candidate this position could be made an Associate Director. This role also requires a lot of work with the GXP quality systems. In this hands-on position, you will report to the VP of Regulatory Affairs and manage and lead all aspects of Quality Assurance, including documentation systems, our GXP training program and product lot release from our Contract Manufacturing Organizations.Requirements:
- Position requires a PhD in a relevant scientific discipline (biology, biochemistry, chemistry)
- Candidates must be PC computer literate and have experience with statistical and database software.
- Excellent communication, writing, and organizational skills required.
- At least 7 years of Quality Assurance experience in the pharmaceutical or biotechnology (preferred) industry and a minimum of 2 years of managing a QA group.
To find out more about Real please visit www.realstaffing.com