Senior Validation Engineer
Job
United Consulting Hub
Taunton, MA (In Person)
Full-Time
Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
70
out of 100
Average of individual scores
Skill Insights
Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
Job Description
Senior Validation Engineer at United Consulting Hub Senior Validation Engineer at United Consulting Hub in Taunton, Massachusetts Posted in 1 day ago.
Type:
full-timeJob Description:
Overview We are seeking a Senior CQV Specialist to lead commissioning, qualification, and validation (CQV) activities for GMP facilities, equipment, and computerized systems supporting cell therapy manufacturing. This role will own qualification strategy and execution, ensuring compliant, risk?based validation aligned withUSP , GAMP
5, and industry best practices. The ideal candidate can step into multiple projects quickly and operate with minimal oversight in a fast?paced GMP environment. Key Responsibilities Lead and execute CQV activities across facilities, process equipment, QC equipment, and computerized systems. Perform cleanroom qualifications including smoke studies and environmental assessments. Develop and execute risk?based qualification strategies in alignment withUSP , GAMP
5, and system impact assessments. Author and execute validation plans, protocols (IQ/OQ/PQ), reports, risk assessments, and GxP documentation. Drive execution activities and proactively resolve issues, deviations, and remediation actions during qualification. Lead deviation investigations, impact assessments, and corrective/preventive actions. Support qualification of cell therapy-specific and QC systems (e.g., qPCR, BacT, Faxitron, microplate readers). Independently manage validation activities from planning through final approval. Support internal and regulatory inspections related to CQV activities. Requirements 8+ years of CQV/validation experience in GMP pharmaceutical, biotech, or cell therapy manufacturing (cell therapy experience strongly preferred). Hands?on experience qualifying facilities, utilities, process equipment, QC equipment, and computerized systems. Strong working knowledge ofUSP , GAMP
5, and risk?based validation methodologies. Proven experience owning validation programs, writing protocols, executing testing, and managing deviations. Ability to assess complex systems, define qualification impact, and implement compliant execution strategies. Strong communication skills with the ability to work independently and manage multiple deliverables simultaneously.Similar remote jobs
Fujifilm
Pierre, SD
Posted2 days ago
Updated12 hours ago
Anywhere Real Estate
San Antonio, TX
Posted2 days ago
Updated12 hours ago
Farmers Insurance Careers
Posted2 days ago
Updated12 hours ago
Similar jobs in Taunton, MA
Taco Bell
Taunton, MA
Posted3 days ago
Updated1 day ago
Similar jobs in Massachusetts
Massasoit Community College
Canton, MA
Posted2 days ago
Updated12 hours ago