Join a growing QA Validation group at a leading biotechnology company in Boston, Massachusetts. You will provide QA oversight of commissioning, qualification and validation for a cGMP cell and gene therapy manufacturing facility and its QC laboratories.

What you'll do

• Provide QA oversight of CQV, periodic review and requalification.
• Review and approve validation protocols and reports (IQ, OQ, PQ, CSV, process and cleaning validation).
• Review CMMS records for asset release, database requests and work orders.
• Author and review SOPs in Veeva.
• Support change controls, risk assessments, deviations, audits and inspections.

Requirements

• Bachelor's degree in a technical discipline + 5 years of validation and/or QA experience (or 7+ years equivalent).
• 21 CFR, ICH, EU regulations, GAMP 5 and risk-based validation.
• Kneat strongly preferred.
• Cell and gene therapy or contract manufacturing experience preferred.

Benefits

• Contract: 6-12 months, with possible extension
• Shift: Administrative, Monday-Friday
• Start: Immediate