Senior CQV Engineer - Lead Validation & CQV Delivery

Verista

Wichita (KS)

Hybrid

USD 79,000 - 123,000

Full time

13 days ago

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Benefits offered by this job

Competitive pay

Company-paid Life, Short‑Term, andLong

Disability Insurance

Health Savings Account

Paid Time Off and Holidays

Tuition Reimbursement

Parental Leave

Team Events

Job summary

Verista is seeking an experienced CQV Engineer in Wichita, KS to lead commissioning and qualification activities for GMP-regulated facilities, utilities, and equipment. You will author IQ/OQ/PQ protocols, coordinate field execution, and ensure regulatory compliance across QA, Engineering, and Operations teams.

Ideal candidates have 5+ years in CQV within life sciences, strong technical writing, and a track record of delivering validated systems on time and within budget. Relocation not specified.

Qualifications

Hands-on CQV experience in pharma/biotech or regulated life sciences.
Strong IQ/OQ/PQ protocol development and execution.
Experience with deviations, change control, and data integrity.

Responsibilities

Lead CQV activities for facilities, utilities, equipment, and systems.
Author and review qualification documentation per GDP and cGMP.
Coordinate with Engineering, Quality, Operations, and vendors.

Skills

CQV experience

IQ/OQ/PQ protocols

GxP regulatory compliance

Technical writing

Project leadership

Deviations management

Education

Bachelor’s degree in Engineering, Life Sciences, or related

Tools

GAMP 5

ASTM E2500

P&ID familiarity

Documentation control systems

Job description

Ideal candidates have 5+ years in CQV within life sciences, strong technical writing, and a track record of delivering validated systems on time and within budget. Relocation not specified.

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