Position Summary
Responsible for facilitating the validation lifecycle process for the Validation Department as a Level II resource to support cGMP manufacturing operations for biopharmaceutical products. This position will provide support for more than one area of subject matter expertise for validation disciplines which may include:
- Facilities qualification
- Utilities qualification
- Equipment qualification
- Manufacturing process control system qualification
- Cleaning validation
- Steaming Validation
- Air Visualization Studies
- Mixing Studies.
Staff will actively develop subject matter expertise in at least one discipline.
Position Responsibilities
