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Software Verification Engineer Jobs Near Me

Ascent Placement Partners

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Remote Software Engineer - Technical Advisor

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$150/hr

Remote Software Engineer - Technical Advisor $150.00 USD/hour | 100% Remote (USA Only) | Mostly ... Reviewing full coding-agent session logs to assess what a model investigated, verified, assumed, or ...

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Verista, Inc.

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Columbus, OH · On-site

... Engineer Responsibilities: * Authoring, editing, and executing technical commissioning ... Completing user interface testing, software verification, and complete alarm testing on automated ...

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Senior Embedded Software Engineer FULL-TIME/PART-TIME: Full Time LOCATION: Dublin, OH (Hybrid ... Write/review/execute Software Design Verification test protocols * Write/support development of ...

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How much do software verification engineer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for software verification engineer in the United States is $42.50, according to ZipRecruiter salary data. Most workers in this role earn between $34.62 and $46.88 per hour, depending on experience, location, and employer.

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Software Verification Engineer jobs near you
A map of the United States highlighting the number of Software Verification Engineer job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Software Verification Engineer job openings in each state, with California having the most at 2 and Hawaii the least at 0.

6461 - Senior CQV Engineer / Senior Validation Engineer

Columbus, OH

Verista, Inc.
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees
Learn more about Verista, Inc.external

$100K - $138K/yr

Full-time

Re-posted 20 days ago

Job description

Senior CQV Engineer Responsibilities:

  • Designing validation plans
  • Conducting and documenting impact and risk assessments with a full understanding of equipment/system/software operation and ability to assess direct, indirect, and no impact systems and functions within complex processes
  • Maintaining (and ensuring the team maintains) clear, detailed records of qualification and validation, and change control activities for future compliance audits
  • Designing and executing engineering studies for critical process parameter definition and verification prior to validation
  • Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader
  • Running test scripts and documenting results
  • Adherence with project schedule for all assigned activities
  • Maintaining clear, detailed records qualification and validation
  • Documenting impact and risk assessments as part of a team
  • Completing user interface testing, software verification, and complete alarm testing on automated systems
  • Developing, reviewing, and executing testing documentation
  • Making recommendations for design or process modification based on test results when executing test scripts
  • General understanding of capital equipment implementation and process knowledge
  • Understanding validation documents, URS, IQ, OQ, PQ

Requirements:

  • Must be able/willing to work onsite in the Indianapolis metropolitan area
  • Must be willing to meet potential future travel requirements (10-50%)
  • Bachelor's Degree or equivalent required
  • Ability to mentor and guide less experienced team members
  • Ability to communicate effectively with clients
  • Proven ability to identify areas of business expansion and report to management team for follow-up
  • Obvious business maturity and interpersonal skills to be able to effectively communicate and collaborate
  • Experience and capability of effectively communicating requirements (written and orally) with rationale to different levels of the client's organization
  • 4 - 6 years of demonstrated role relevant experience
  • Demonstrated experience in leading CQV activities specific to pharmaceutical manufacturing requirements
  • Proficiency using PC and Microsoft Office tools
  • Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms
  • Ability to work as part of a team
  • Strong problem-solving and critical thinking skills
  • Excellent organizational and time management skills
  • Strong attention to detail
  • GMP and Good Documentation Practice
  • Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes)
  • Basic skills with EXCEL and PowerPoint
  • Strong interpersonal skills and clear communication capabilities
  • Experience with and tolerance for high levels of challenge and change
  • Experience in GMP regulated environment
  • Proven attention to detail and organization in project work
  • Capable of working on assigned tasks without mentorship

Apply