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CQV Engineer - Senior Validation Engineer

Verista's 600 experts team up with the world's most recognizable brands in the life science industry to solve their business needs.
$70,491 - $118,941
Backend
Senior Software Engineer
In-Person
501 - 1,000 Employees
5+ years of experience
Healthcare · Biotech
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Description For CQV Engineer - Senior Validation Engineer

Verista is seeking a CQV Engineer - Senior Validation Engineer to join their team. This role involves authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/software, and processes. The ideal candidate will have a Bachelor's Degree or equivalent, demonstrated experience in leading CQV activities specific to Process Equipment, and proficiency in using PC and Microsoft Office tools.

Key responsibilities include:

  • Running test scripts and documenting results
  • Maintaining clear, detailed records of qualification and validation
  • Documenting impact and risk assessments as part of a team
  • Completing user interface testing, software verification, and alarm testing on automated systems
  • Developing, reviewing, and executing testing documentation
  • Making recommendations for design or process modification based on test results

The role requires strong problem-solving and critical thinking skills, excellent organizational and time management abilities, and a strong attention to detail. Experience in a GMP regulated environment and the ability to work as part of a team are essential.

Verista offers a competitive benefits package including medical, dental & vision insurance, 401(k) with employer matching, paid time off, and tuition reimbursement. The company culture emphasizes empowering and supporting colleagues, committing to client success, and encouraging an inclusive environment.

This is an on-site position located in Columbus, Ohio, with a salary range of $70,491-$118,941, depending on qualifications and experience. Join Verista to be part of a high-growth, fast-paced organization with a people-focused culture in the life sciences industry.

Last updated 9 months ago

Responsibilities For CQV Engineer - Senior Validation Engineer

  • Authoring, editing, and executing technical commissioning, qualification and validation documentation
  • Running test scripts and documenting results
  • Maintaining clear, detailed records qualification and validation
  • Documenting impact and risk assessments as part of a team
  • Completing user interface testing, software verification, and alarm testing on automated systems
  • Developing, reviewing, and executing testing documentation
  • Making recommendations for design or process modification based on test results

Requirements For CQV Engineer - Senior Validation Engineer

  • Bachelor's Degree or equivalent
  • Demonstrated experience in leading CQV activities specific to Process Equipment
  • Proficiency using PC and Microsoft Office tools
  • Strong problem-solving and critical thinking skills
  • Excellent organizational and time management skills
  • Strong attention to detail
  • Experience in GMP regulated environment
  • Intermediate skills with WORD
  • Basic skills with EXCEL and PowerPoint
  • Strong interpersonal skills and clear communication capabilities

Benefits For CQV Engineer - Senior Validation Engineer

401k
Commuter Benefits
Dental Insurance
Education Budget
Medical Insurance
Parental Leave
Vision Insurance
  • Competitive pay plus performance-based incentive programs
  • 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
  • As Needed Sick Time
  • Tuition Reimbursement
  • Paid Parental Leave and Bereavement

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