Verista, Inc.

Verista, Inc.

6498 - Senior CQV Engineer / Senior Validation Engineer

Wichita, KS · Senior

Sponsorship not specified$79k-$123kDetected 37 days ago
Manual TestingGMPMedical DevicesProblem SolvingMentoringWritingGxP

Stay score

odds of building a lasting career here

47Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds (Level II)66
Fits your clock70

Sponsors, but it's cap-subject — you still face the weighted lottery (~30% per draw at Level II). Good if you win; have a cap-exempt backup on your list.

Lottery odds assume a STEM candidate.

Personalize to your clock →

H-1B wage level

the lottery is wage-weighted — each level is one more entry

Level I · 1×
Level I$74,3601 entry
Level II$88,5462 entries
Level III$102,7313 entries
Level IV$116,9174 entries

$9,621 more — $88,546 — moves this role to Level II and 2 lottery entries. That figure is inside the range the employer already advertised.

Based on the DOL prevailing wage for this occupation and worksite, a base salary of $88,546 would place this position at wage Level II. That figure is within the posted range, and I'd like to target it. This role classifies under "Industrial Engineers" for prevailing-wage purposes.

DOL prevailing wage, 2026-27 wage year · Industrial Engineers (17-2112) · Wichita, KS. Wage level is derived by USCIS from the offered wage, occupation and worksite; the occupation shown is inferred from the job title.

Community outcomes

No reports yet — be the first to help the next applicant.

About the role

  • Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
  • Our talented and dedicated professionals are committed to making an impact every day.
  • For US geography, the salary range for this position is shown below.

Responsibilities

  • Lead and/or support the execution of CQV activities for facilities, utilities, manufacturing equipment, laboratory systems, and computerized systems within GxP-regulated environments.
  • Author, review, and execute CQV documentation, including URS, risk assessments, qualification plans, protocols, test scripts, IQ/OQ/PQ documentation, commissioning documents, deviations, and validation/qualification summary reports.
  • Develop and execute qualification and testing activities, including IQ/OQ/PQ, functional testing, system walkdowns, field verification, punch-list management, and acceptance testing.
  • Coordinate and perform hands-on field execution, ensuring protocols are followed, test results are properly documented, and discrepancies are identified, investigated, and resolved.
  • Review engineering and vendor documentation, drawings, specifications, manuals, and test records to support CQV planning and execution.
  • Manage and support deviations, discrepancies, change controls, and corrective actions associated with commissioning and qualification activities.
  • Provide technical guidance and mentorship to junior CQV engineers and support the development of standardized CQV processes and templates.
  • Support multiple projects and priorities while maintaining quality, schedule, and execution commitments.
  • Maintain accurate documentation and ensure all executed records meet Good Documentation Practices (GDP) and client quality requirements.
  • We empower and support our colleagues

Requirements

  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline.
  • Demonstrated experience with both authoring and field execution of CQV/qualification documentation.
  • Experience with facilities, utilities, manufacturing equipment, laboratory systems, and/or computerized systems.
  • Strong understanding of cGMP requirements and the equipment/system qualification lifecycle.
  • Experience with deviation management, change control, punch-list management, and resolution of qualification issues.
  • Experience leading CQV activities or workstreams within large pharmaceutical or biotechnology capital projects.
  • Experience with GAMP 5, ASTM E2500, risk-based qualification approaches, and data integrity/ALCOA+ principles.
  • Experience working with engineering drawings, P&IDs, equipment specifications, and vendor documentation.

Nice to have

  • Competitive pay plus performance-based incentive programs

Compensation

  • For US geography, the salary range for this position is shown below.

Benefits

  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • Tuition Reimbursement
  • Paid Parental Leave and Bereavement

Company info

  • Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives.

This listing is sourced directly from Verista, Inc.'s careers page and normalized into a canonical job model.