Senior Manager, Quality Validation
CRISPR Therapeutics(2 months ago)
About this role
A Senior Manager, Quality Validation at CRISPR Therapeutics leads the Validation and Compliance Program for the company's GMP manufacturing site in Framingham, MA. The role sits within Site Quality Assurance and focuses on ensuring regulatory compliance and quality standards for facilities, utilities, and equipment.
Required Skills
- Validation
- Commissioning
- Documentation Review
- Compliance
- Gap Analysis
- CAPA
- Change Control
- Calibration
- Supplier Audits
- Regulatory Inspections
+4 more
Qualifications
- Bachelor of Science
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