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Verista
Cqv Engineer
Indianapolis, IN · On-site · Full time · Entry level
$69.3k–$103k / year
About the role
Support change control and deviation management activities in a regulated cGMP environment. Ensure manufacturing changes are assessed, documented, and executed properly.
What you’ll do
• Author and manage change controls for systems and processes. • Perform impact assessments on product quality and regulatory impact. • Collaborate with cross-functional teams for compliant change implementation. • Support execution and documentation of change control deliverables. • Participate in audits and provide SME support for change control.
What you’ll bring
• Bachelor’s degree in Chemistry, Engineering, or Life Sciences. • 1-3 years experience in CQV or Quality Engineering. • Experience with change control systems and cGMP/GDP environments. • Strong technical writing and documentation skills. • Excellent communication and collaboration abilities.
Life at Verista
Competitive pay with performance incentives, comprehensive insurance benefits, 401(k) with matching, paid time off, tuition reimbursement, and team social activities.
About Verista
Verista, Inc. provides innovative solutions and services to life science clients, empowering growth and innovation to solve healthcare challenges.