- Bedford, New Hampshire, United States
- Full-time · Senior
- 7–9 years
Lead analyst responsible for environmental monitoring and quality control in a cGMP pharmaceutical setting.
Responsibilities
- Perform routine environmental monitoring of classified clean rooms
- Conduct utility sampling and analysis of water and steam systems
- Monitor clean rooms during manufacturing operations
- Perform monitoring and analysis of clean compressed air system
- Write and execute protocols, experiments, and notebook studies
Requirements
- High school Diploma
- AS degree
- BS degree in Microbiology or related scientific field
- Nice to have: AS degree or BS degree in Microbiology