I3 INFOTEK
Location: all cities,NY, USA
Date: 2024-11-21T15:24:41Z
Job Description:
Responsibilities:
- Support and execute life cycle documents.
- Manage change controls and ensure compliance with Quality Assurance.
- Draft change control and validation documents for client review.
- Route documents for approval and request performance copies for protocols.
- Execute approved protocols.
Qualifications:
- Bachelor's or master's degree in a scientific or healthcare field.
- 5-10 years of experience as a Senior Validation Analyst or Lead in the pharmaceutical or life sciences industry.