Verista is seeking a detail-oriented Validation / CQV Engineer with strong experience in change management and documentation control within regulated pharmaceutical manufacturing environments
Job Summary
Verista is seeking a detail-oriented Validation / CQV Engineer with strong experience in change management and documentation control within regulated pharmaceutical manufacturing environments.
This role supports commissioning, qualification, validation, and lifecycle change activities to ensure systems, equipment, and processes meet GMP, regulatory, and client requirements.
The ideal candidate brings hands-on experience managing validation documentation, coordinating cross-functional stakeholders, and leading change control activities to support compliant and efficient project execution.
Matching Summary
Verista is seeking a detail-oriented Validation / CQV Engineer with strong experience in change management and documentation control within regulated pharmaceutical manufacturing environments.
Salary
$59,951—$102,623 USD
Skills & Requirements
Must-have
GMP, regulatory, and client requirements
change management and documentation control
validation documentation
electronic document management systems (EDMS)
Good Documentation Practices (GDP)
Nice-to-have
empower growth and innovation
team environment
inclusive environment
Key Requirements
2-4 years of experience
Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline
Demonstrated experience with change management
Proficiency with EDMS platforms and Microsoft SharePoint