Be part of a transformative project! Join the 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
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
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