Be part of a transformative project by joining our client's expansion and play a key role in transitioning this site into a fully operational facility delivering life-saving products.
What You'll Do:
- Lead CQV activities for sterile vial and syringe operations.
- Drive cleaning validation, sterilization, and equipment qualification.
- Collaborate with cross-functional teams to meet regulatory and market standards.
- Ensure seamless facility introduction from Operational Qualification (OQ) to commercial readiness.
What We're Looking For:
- 6+ years of C&Q/QA/Validation experience in regulated industries.
- Expertise in sterile operations, single-use technologies, and cleaning/sterilization validation.
- Strong project leadership and regulatory compliance skills
Apply now for access to the full job description.
