Pharmaceutical Facilities Utilities Quality Compliance SME
St. Louis, MO
Pharmaceutical Facilities/Utilities Validation SME
Our client is a large pharmaceutical company who is converting their clinical site into a commercial manufacturing site for a solid oral dosage product.
Day to Day Responsibilities:
The client is looking for a quality compliance SME with experience converting clinical sites into manufacturing. The consultant will be looking at floor plans, equipment flow, and personnel to assess the SOPs and revise and edit as necessary. The consultant must have experience with facilities and utilities as well as doing gap assessments for facility conversions. The consultant must be a high energy person who will take the initiative and is comfortable doing the hands on technical writing as well. This will be the first steps in a large project initiative to convert this site. The consultant should have an understanding of qualification of solid dosage equipment as well as SOPs for facilities and utilities.
- Clinical-Commercial plant conversion
- Facilities Utilities
- Quality Compliance
- SOP Technical writing
- Gap Assessments
- Solid oral dose
Job Type: Contract