We are seeking quality assurance professionals with 2-7 years of demonstrated experience in Good Manufacturing Practice (cGMP) regulations, including procedure development and implementation, CAPA, investigations, deviations and risk assessment.
This position requires a scientific degree. The right candidate will be capable of working with our client's staff to achieve compliance with these regulations within their organization, and design a plan to implement appropriate procedures and systems to achieve that goal.
Experience in a pharmaceutical or biologics manufacturing environment is a must for this position.
No phone calls, please.