6078 - Senior CQV Engineer / Senior Validation Engineer
Verista, Inc.(20 days ago)
About this role
The Senior CQV Engineer at Verista leads and executes Commissioning, Qualification, and Validation activities with a focus on Clean-In-Place systems used in Drug Substance Manufacturing. This role serves as a technical subject matter expert in CIP system qualification and cleaning validation, ensuring compliance with GMP, regulatory, and internal quality standards.
Required Skills
- CQV
- Validation
- CIP Systems
- GMP Compliance
Qualifications
- Bachelor’s Degree in Engineering
- Chemistry
- Biology or related field
About Verista, Inc.
verista.comVerista is a life‑sciences consulting and engineering firm that supports pharmaceutical, biotech, medical device, and consumer‑health companies across the entire product lifecycle. They specialize in validation, quality and regulatory compliance, engineering and automation, commissioning/qualification, computer system validation, and digital transformation. Verista combines domain‑specific technical expertise and regulatory know‑how with hands‑on implementation to reduce risk, accelerate timelines, and ensure GxP compliance for complex manufacturing, clinical, and commercial operations.
Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Verista, Inc.
Vice President of Business Development
Verista, Inc.(1 day ago)
6153 - Lead CQV Engineer/ Lead Validation Engineer
Verista, Inc.(1 day ago)
6170 - Batch Disposition Associate / Quality Specialist
Verista, Inc.(7 days ago)
6176 - CIP Senior Process Engineer / Senior Process Engineer
Verista, Inc.(8 days ago)