What are the responsibilities and job description for the Quality Documentation Optimization position at ProPharma?
Quality Documentation Optimization Resource
Responsibilities
- Observation aggregation
- Training/process insight, and stage-gate visibility
- Gather observations from Manufacturing and Quality review
- Convert themes into training/process recommendations
- Build cycle-time and stage-gate visibility
- Prepare sustainment tools for leadership governance.
Requirements
- 5-10 years of Quality Manufacturing experience within pharma industry
- 8 week contract opportunity; full-time weekly hours; onsite in Memphis, TN