CQV Engineer / Validation Engineer
Description For CQV Engineer / Validation Engineer
Verista is a leading life science industry solutions provider with a team of 600 experts working with the world's most recognizable brands. We focus on solving pressing healthcare challenges and empowering growth and innovation within the scientific community. The CQV Engineer role involves technical commissioning, qualification, and validation of equipment, systems, and software in a GMP-regulated environment.
The ideal candidate will be responsible for documentation, test execution, and quality assurance activities. You'll work in a collaborative environment where attention to detail and strong technical skills are essential. The role offers opportunities to impact healthcare solutions while working with cutting-edge technologies and processes.
Verista offers a people-focused culture with excellent growth potential and comprehensive benefits. The company values empowerment, client success, and continuous learning. Team members enjoy a supportive environment that encourages professional development and innovation.
The position is based in Columbus, OH, offering competitive compensation and extensive benefits including healthcare coverage, retirement plans, and work-life balance provisions. Join a dynamic team that's making a difference in the life sciences industry while building a rewarding career in validation engineering.
Responsibilities For CQV Engineer / 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
- Completing user interface testing, software verification, and alarm testing
- Developing, reviewing, and executing testing documentation
- Making recommendations for design or process modification based on test results
Requirements For CQV Engineer / Validation Engineer
- Bachelor's Degree or equivalent required
- Demonstrated experience in leading CQV activities specific to Process Equipment
- Proficiency using PC and Microsoft Office tools
- Strong problem-solving and critical thinking skills
- GMP and Good Documentation Practice
- Experience in GMP regulated environment
- Must be willing to work onsite in Columbus, OH
- Strong interpersonal skills and clear communication capabilities
Benefits For CQV Engineer / Validation Engineer
- 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 with Employer Matching
- Paid Time Off with Rollover Option and Holidays
- As Needed Sick Time
- Tuition Reimbursement
- Paid Parental Leave and Bereavement
