Description
Experience:
- 3-5 years professional experience.
Education:
- Bachelor's Degree or equivalent unless otherwise specified.
Description:
- Assist Quality and Regulatory along with other engineering and production personnel in the Investigation and Implementation of Corrective Action and Preventive Action (CAPA) activities. Additionally, write, execute and consult on Software and Process validations.
- Write, execute and consult on IQ/OQ and PQ activities. Assist with documentation of new and existing Engineering projects to assure compliance to FDA GMP.