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Senior Commissioning, Qualification & Validation (CQV) Engineer

Verista, Inc. · Indianapolis, IN · Life sciences client projects

Compensation

$70k – $110k /yr

Employment type

Full-time

Work setting

On-site

Location

Indianapolis, IN

Schedule

Day shift

Posted

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Job overview

The Senior Commissioning, Qualification & Validation (CQV) Engineer role is onsite in Indianapolis, IN. Compensation is $70,491–$109,900 per year. Verista supports life sciences clients working to address healthcare challenges. The role develops and executes validation and qualification work that helps clients implement and document compliant equipment, systems, software, and processes. It contributes through risk assessments, testing, detailed records, and recommendations based on test results.

What you'll do

  • Design validation plans
  • conduct and document impact and risk assessments
  • maintain qualification, validation, and change-control records
  • design and execute engineering studies
  • author, edit, and execute commissioning, qualification, and validation documentation
  • run test scripts and document results
  • perform user-interface, software-verification, and alarm testing
  • develop, review, and execute testing documentation
  • recommend design or process modifications based on test results
  • mentor less experienced team members.

What we're looking for

Skills & competencies
senior cqv engineer
commissioning
qualification
validation
pharmaceutical manufacturing
gmp
revit? no
indianapolis in
verista
full-time
onsite
$70,491–$109,900/year
bachelor's degree or equivalent
10–50% potential travel
Work arrangement
  • Weekend coverage required

Benefits & perks

  • Medical, dental, and vision insurance
  • company-paid life and disability insurance
  • FSA, dependent care, commuter benefits, HSA
  • supplemental insurance
  • 401(k) with employer match
  • paid time off and holidays
  • sick time
  • tuition reimbursement
  • paid parental leave and bereavement
  • performance-based incentives.

Why this role

Requires a bachelor's degree or equivalent, 4–6 years of relevant experience, and experience leading CQV activities for pharmaceutical manufacturing. Onsite in the Indianapolis metropolitan area; potential future travel of 10–50%.

About the employer

Verista, Inc. is hiring for this role. Industry: Engineering Services. Sector: 54.

Additional details

Industry sector
54
Industry
Engineering Services
Occupation code
17-2112.00
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