St. Louis, MO
Our client is a pharmaceutical company currently seeking an expert with GMP Pharmaceutical experience to write investigations and deviations.
Day to Day Responsibilities:
The consultant we are seeking will be responsible for writing and closing out all root cause investigations in accordance with FDA & GMP standards. They will also be writing CAPAs as well as closing them out throughout the term of the project. This person will also help review SOPs as well as perform root cause analysis.
- Pharmaceutical/Combo Product Experience 5+ years
- Write Investigations/Deviations/CAPA’ s
- Aseptic Processing
- Quality Assurance
Job Type: Contract