Join our team as a Document Coordinator. If you have a strong background in biotechnology, process validation, or quality assurance, we want to hear from you!
Key Responsibilities:
- Develop and implement procedures and best practices for Biologics Process Validation.
- Act as a Project Manager, tracking and monitoring Process Validation deliverables.
- Coordinate and manage Process Validation documentation, ensuring alignment across teams.
- Perform Data Verification on completed studies and reports.
What We're Looking For:
- Bachelor's degree in life sciences or a related field.
- Minimum of four years of experience in biotechnology, process validation, or a related area.
- Strong understanding of GMP principles and process validation in regulated environments.
